Photo-crosslinked hydrogel material and preparation, composition, and application thereof photo-crosslinked hydrogel

Abstract

This invention provides preparations, compositions, products, and applications of photo-crosslinked hydrogels. Component A—a photosensitive polymer derivative, component B—the photoinitiator, and auxiliary component C—other biocompatible polymer derivative each are respectively dissolved in a biocompatible medium to obtain solution A, solution B, and solution C. The solution A, the solution B, and the optional solution C are mixed homogenously to obtain a hydrogel precursor solution. The hydrogel precursor solution is subject to irradiation of the UV light for photocoupled crosslinking to form a photo-crosslinked hydrogel. The photo-crosslinked hydrogel exhibit rapid speed of photo-curing, strong tissue adhesion, excellent mechanical properties, good biocompatibility, and excellent clinical operability. In addition, this invention also provides a kit for making the photo-crosslinked hydrogel, and applications thereof in tissue engineering, regenerative medicine, 3D printing, and as a carrier of cell, protein, or drug.

Claims

1. A method of making a photo-crosslinked hydrogel material comprising: dissolving a component A including a photosensitive polymer derivative in a biocompatible medium to obtain a photosensitive polymer solution A; dissolving a component B including a photoinitiator in a biocompatible medium to obtain a photoinitiator solution B; obtaining a hydrogel precursor solution by homogeneously mixing solutions including the photosensitive polymer solution A and the photoinitiator solution B; and under an irradiation of light, performing free radical cross-linking reaction to form a hydrogel, wherein the photosensitive polymer derivative is selected from one or more of the following: (a) a photosensitive polymer derivative containing an o-nitrobenzyl phototrigger as shown in Formula A-I; and (b) a photosensitive polymer derivative containing both an o-nitrobenzyl phototrigger and double bond functional group as shown in Formula A-III, ##STR00194## wherein the Formula A-1 contains an o-nitrobenzyl phototrigger represented by Formula I selected from the group consisting of Formula I-1 and Formula I-2, the Formula I-2 represents a cyclic o-nitrobenzyl phototrigger, ##STR00195## where, in the Formula I-1 and the Formula I-2, when X═0, the o-nitrobenzyl phototrigger is an o-nitrobenzyl alcohol phototrigger; when X═S, the o-nitrobenzyl phototrigger is an o-nitrobenzyl sulphydryl phototrigger; and when X═N, the o-nitrobenzyl phototrigger is an o-nitrobenzyl amine phototrigger; in the Formula A-I, Formula A-III, Formula I, Formula I-1, and Formula I-2, R′ is selected from the group consisting of hydrogen atom, halogen atom, hydroxyl group, mercapto group, amine group, nitro group, cyano group, aldehyde group, ketone group, ester group, amide, phosphonic acid group, phosphonate ester group, sulfoacid group, sulfonate group, sulfone group, sulfoxide group, aryl group, heteroaryl group, alkyl group, alkylene group, modified alkyl group, and modified alkylene group; in the Formula I-1 and Formula I-2, R.sub.1 is selected from the group consisting of a hydrogen atom, an ether group, an ester group, a carbonate ester group, an amino formate ester group, a mercapto formate ester group, and a phosphonate ester group; in the Formula I-1 and Formula I-2, R.sub.2, R.sub.3, R.sub.4, R.sub.5 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, a hydroxyl group, a mercapto group, an amine group, a nitro group, a cyano group, an aldehyde group, a ketone group, a carboxyl group, an ester group, amide, a phosphonic acid group, phosphonate ester group, sulfoacid group, sulfonate group, sulfone group, sulfoxide group, aryl group, heteroaryl group, alkyl group, alkylene group, modified alkyl group, and modified alkylene group; in the Formula I-2, X is O, S or NH, R.sub.1 is connected to X and one of R.sub.2, R.sub.3, R.sub.4 and R.sub.5 to form a cyclic structure; in the Formula A-III, R.sub.1′, R.sub.2′, R.sub.3′ are selected from the group consisting of a hydrogen atom, an alkyl group, a modified alkyl or aryl group; R.sub.4′ is selected from the group consisting of an alkyl group, an ether group, an ester group, and an amide group; optionally, in Formula A-III, R.sub.1′, R.sub.2′, R.sub.3′ are connected with a carbon atom to form a saturated or unsaturated alicyclic ring or alicyclic heterocyclic ring; in the Formula A-I and the Formula A-III, n≥2, P.sub.1 is independently a hydrophilic or water-soluble natural polymer or synthetic polymer; the photoinitiator is a substance capable of generating free radicals under irradiation by light.

2. The method of claim 1, wherein the component A further comprises a polymer derivative containing double bond functional group as shown in Formula A-II: ##STR00196## where, in the Formula A-II, R′.sub.1, R′.sub.2, R′.sub.3 and are selected from hydrogen, alkyl, modified alkyl or aryl; R′.sub.4 is selected from alkyl, an ether group, an ester group, an amide group; optionally, in the Formula A-II, R′.sub.1, R′.sub.2, R′.sub.3 are connected together with a carbon atom to form a saturated or unsaturated alicyclic ring or alicyclic heterocycle; and in Formula A-II, n≥2, P.sub.1 is a hydrophilic or water-soluble natural polymer, or a hydrophilic or water-soluble synthetic polymer.

3. The method of claim 1, further comprising dissolving an auxiliary component C including another biocompatible polymer derivative in a biocompatible medium to obtain a polymer solution C, wherein the another biocompatible polymer derivative is a polymer derivative containing an amine, hydrazine, hydrazide, or hydroxylamine functional group, the solutions further include the solution C, aldehyde or ketone group produced by irradiation of the o-nitrobenzyl phototrigger in component A is capable of reacting with the amine, hydrazine, hydrazide, or hydroxylamine functional group in component C through photocoupling crosslinking, nitroso group produced by irradiation of the o-nitrobenzyl phototrigger in component A is capable of reacting with the sulphydryl group in component C through photoinduced S-nitrosylation crosslinking.

4. The method of claim 1, Wherein the alkyl group of R′, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.1′, R.sub.2′, and R.sub.3′ is a saturated or unsaturated aliphatic linear or branched alkyl group having 1 to 30 carbon atoms, the alkylene group of R′, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.1′, R.sub.2′, and R.sub.3′ is a saturated or unsaturated aliphatic linear chain or branched alkylene group with 1-30 carbon atoms, the modified alkyl group of R′, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.1′, R.sub.2′, and R.sub.3′ has a carbon atom at least substituted by a halogen atom, —OH, —SH, —NO.sub.2, —CN, —CHO, —COOH, ester, amide, aromatic, arylidene —CO—, —O—, —S—, —SO—, —SO.sub.2—, amino, secondary amine, tertiary amine, quaternary ammonium salt, saturated or unsaturated single or double cyclic alkylene, or bridged aliphatic heterocyclic, the modified alkyl group of R′, R.sub.2, R.sub.3, R.sub.4, R.sub.4, R.sub.1′, R.sub.2′, and R.sub.3′ has 1˜30 carbon atoms whose carbon-carbon single bond is optionally and independently replaced by a carbon-carbon double bond or a carbon-carbon triple bond, the modified alkylene group of R′, R.sub.2, R.sub.3, R.sub.4, and R.sub.5 has a carbon atom least substituted by a halogen atom, —OH, —SH, —NO.sub.2—CN, —CHO, —COOH, ester, amide, aromatic, arylidene, —CO—, —O—, —S—, —SO—, —SO.sub.2—, amino, secondary amine, tertiary amine, quaternary ammonium salt, saturated or unsaturated single or double cyclic alkylene, or bridged aliphatic heterocyclic, and the modified alkyl group has 1˜30 carbon atoms whose carbon-carbon single bond is optionally and independently replaced by a carbon-carbon double bond or a carbon-carbon triple bond, the ether group of R.sub.1 and R.sub.4′ is selected from the following structures: —(CH.sub.2).sub.xCH.sub.3, —(CH.sub.2CH.sub.2O).sub.xCH.sub.3,—(CH.sub.2).sub.x(CH.sub.2CH.sub.2O).sub.yCH.sub.3 and ##STR00197## wherein x and y≥0 and are integers, the ester group R′, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.1′, R.sub.2′, and R.sub.3′ is selected from the following structures: —CO(CH.sub.2).sub.xCH.sub.3, —CO(CH.sub.2CH.sub.2O).sub.xCH.sub.3, —CO(CH.sub.2).sub.x(CH.sub.2CH.sub.2O).sub.yCH.sub.3, wherein x and y≥0 and are integers, the carbonate group of R.sub.1 is selected from the following structures: —COO(CH.sub.2).sub.xCH.sub.3, —COO(CH.sub.2CH.sub.2O).sub.xCH.sub.3, —COO(CH.sub.2).sub.x(CH.sub.2CH.sub.2O).sub.yCH.sub.3, wherein x and y≥0 and are integers, the amino formate ester group of R.sub.1 is selected from the following structures: —CONH(CH.sub.2).sub.xCH.sub.3, —CONH(CH.sub.2CH.sub.2O).sub.xCH.sub.3, —CONH(CH.sub.2).sub.x(CH.sub.2CH.sub.2O).sub.yCH.sub.3, wherein x and y≥0 and are integers, the mercapto formate ester group is selected from the following structures: —COS(CH.sub.2).sub.xCH.sub.3, —COS(CH.sub.2CH.sub.2O).sub.xCH.sub.3, —COS(CH.sub.2).sub.x(CH.sub.2CH.sub.2O).sub.yCH.sub.3, wherein x and y≥0 and are integers, the phosphonate ester group is selected from the following structures: —POOO(CH.sub.2).sub.xCH.sub.3, —POOO(CH.sub.2CH.sub.2O).sub.xCH.sub.3, —POOO(CH.sub.2).sub.x(CH.sub.2CH.sub.2O).sub.yCH.sub.3, wherein x and y≥0 and are integers. the aryl group of R′, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.1′, R.sub.2′, and R.sub.3′ is a monocyclic or fused bicyclic ring of 5-10 atoms, the heteroaryl group of R′, R.sub.2, R.sub.3, R.sub.4, R.sub.5is a monocyclic or fused bicyclic ring containing 5 to 10 atoms, the ring contains at least one hetero atom selected from N, O, S or Si, the halogen atom is selected from F, Cl, Br or I, the alicyclic ring is a saturated or unsaturated monocyclic or polycyclic alicyclic ring of 3 to 10 atoms, and the heteroalicyclic ring is a saturated or unsaturated monocyclic or polycyclic alicyclic ring of 3 to 10 atoms, and the ring contains at least one hetero atom selected from N, O, S or Si, when the heteroalicyclic ring contains an S atom, the S atom takes the form of —S—, —SO— or —SO.sub.2—; H on the alicyclic or alicyclic ring is optionally substituted by a halogen atom, a nitro group, an aryl group, an alkyl group, or a modified alkyl group.

5. The method of claim 1, wherein P.sub.1 forms a linkage bond, when the photosensitive polymer derivative has the structure of the Formula A-I, P.sub.1 is connected to one or more of R.sub.2, R.sub.3, R.sub.4 and R.sub.5, or connected to a saturated or unsaturated alicyclic or heteroalicyclic ring formed by R.sub.2, R.sub.3, R.sub.4 and/or R.sub.5, or connected to an aromatic ring or aromatic heterocyclic ring formed by R.sub.2, R.sub.3, R.sub.4 and/or R.sub.5 or connected to a cyclic chain formed by connecting R.sub.1 with one of R.sub.2, R.sub.3, R.sub.4 and/or R.sub.5 via a linkage bond, wherein the linkage bond is represented by —O—, —S—, —NH—, -alkyl group-, —COO—, or —CONH—; when the photosensitive polymer derivative has the structure of the Formula A-III, the linkage bond is represented by formula: A-P.sub.1-B, the linkage bond has a first end and a second end, the first end is connected to one or more of R.sub.2, R.sub.3, R.sub.4, and R.sub.5, or connected to a saturated or unsaturated alicyclic or heteroalicyclic ring formed by R.sub.2, R.sub.3, R.sub.4, and/or R.sub.5, or connected to an aromatic ring or aromatic heterocyclic ring formed by R.sub.2, R.sub.3, R.sub.4, and/or R.sub.5, or connected to a cyclic chain formed by connecting R.sub.1 with one of R.sub.2, R.sub.3, R.sub.4, and R.sub.5, and the second end is connected to R.sub.4′; wherein A and B are each independently selected from the group consisting of O, S, NH, alkyl group, COO, and CONH.

6. The method of claim 1, wherein the natural hydrophilic or water-soluble polymer comprises a natural polysaccharide, a protein, or a modification or degradation thereof, wherein the natural polysaccharide includes at least one selected from the group consisting of hyaluronic acid, carboxymethyl cellulose, methyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, alginate, dextran, agarose, heparin, chondroitin sulfate, glycol chitosan, propylene glycol chitosan, chitosan lactate, carboxymethyl chitosan, and quaternary ammonium salt of chitosan, and the protein includes at least one selected from the group consisting of a hydrophilic or water-soluble animal or plant protein, collagen, serum protein, silk fibroin protein or elastin, and a protein degradate including gelatin or polypeptide, and the hydrophilic or water-soluble synthetic polymer includes at least one selected from the group consisting of two-arm or multi-arm poly (ethylene glycol), poly (ethylene imine), dendrites, synthetic peptides, polylysine, poly (glutamic acid), poly (acrylic acid), poly (methacrylic acid), polyacrylate, poly (methacrylate), poly (acrylamide), poly (methacrylamide poly (vinyl alcohol), and poly (vinyl pyrrolidone).

7. The method of claim 1, wherein the polymer derivative is selected from the following structures: ##STR00198## ##STR00199## ##STR00200## ##STR00201## ##STR00202## ##STR00203## ##STR00204## ##STR00205## ##STR00206## ##STR00207## ##STR00208## ##STR00209## ##STR00210## ##STR00211## ##STR00212## ##STR00213## ##STR00214## ##STR00215## ##STR00216## ##STR00217## where, in Component A-1 to Component A-106 and Component A-116 to Component A-154; n≥2, HA represents hyaluronic acid; CMC represents carboxymethyl cellulose, Alg represents alginic acid, CS represents chondroitin sulfate, PGA represents polyglutamic acid, PEG represents poly ethylene-glycol, PLL represents polylysine, and Dex represents dextran; Hep represents heparin.

8. The method of claim 3, wherein the polymer derivative containing amino, diammonium, hydrazide, and hydroxyamine group respectively have the structure of Formula C-I, Formula C-II, Formula C-III, and Formula C-IV: ##STR00218## the polymer derivatives containing sulphydryl group have the structure of Formula C-V: ##STR00219## where, in Formula C-I, C-II, C-V, n≥2; P.sub.2, P.sub.3, P.sub.4, P.sub.5 and P.sub.6 each independently are a hydrophilic or water-soluble natural polymer, or a hydrophilic or water-soluble synthetic polymer, the hydrophilic or water-soluble natural polymer includes natural polysaccharide, decoration or degradation of the natural polysaccharide, protein, or decoration, modifier or degradation of the protein, the natural polysaccharide includes hyaluronic acid, carboxymethyl cellulose, methyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, alginate, dextran, agarose, heparin, chondroitin sulfate, glycol chitosan, propylene glycol chitosan, chitosan lactate, carboxymethyl chitosan, or quaternary ammonium salt of chitosan, the protein includes a hydrophilic or water-soluble animal or plant protein, a collagen, a serum protein, or a silk fibroin protein and elastin, and the protein degradation include a gelatin or a polypeptide, the hydrophilic or water-soluble synthetic polymers include two-arm of multi-arm poly (ethylene glycol), poly (ethylene imine), dendrites, synthetic peptides, polylysine, poly (glutamic acid), poly (acrylic acid), poly (methacrylic acid), polyacrylate, poly (methacrylate), poly (acrylamide), poly (methacrylamide), poly (vinyl alcohol), or poly (vinyl pyrrolidone), the Formula C-I is selected from the following structure of Component C-1 to Component C-9, the Formula C-II is selected from the following structure of Component C-10, the Formula C-III is selected from the following structure of Component C-11 to Component C-13, the Formula C-IV is selected from the following structure of Component C-14 to C-15, the Formula C-V is selected from the following structure of Component C-16 to Component C-21, ##STR00220## ##STR00221## ##STR00222## where, in Component C-1 to Component C-21, n≥2.

9. The method of claim 1, wherein, for Formula I-1 and Formula I-2, R.sub.2, R.sub.3, R.sub.4, and R.sub.5 are connected with a carbon atom to form a saturated or unsaturated alicyclic ring or alicyclic heterocycle, or form an aromatic ring or an aromatic heterocyclic ring.

10. The method of claim 1, wherein the photoinitiator is selected from Component B-1, Component B-2, Component B-3, and a derivative thereof; ##STR00223##

11. The method of claim 2, further comprising dissolving an auxiliary component C including another biocompatible polymer derivative in a biocompatible medium to obtain a polymer solution C, wherein the another biocompatible polymer derivative is a polymer derivative containing an amine, hydrazine, hydrazide, or hydroxylamine functional group, the solutions further include the solution C, aldehyde or ketone group produced by irradiation of the o-nitrobenzyl phototrigger in component A is capable of reacting with the amine, hydrazine, hydrazide, or hydroxylamine functional group in component C through photocoupling crosslinking, nitroso group produced by irradiation of the o-nitrobenzyl phototrigger in component A is capable of reacting with the sulphydryl group in component C through photoinduced S-nitrosylation crosslinking.

12. The method of claim 2, wherein the polymer derivative is selected from the group consisting of Component A-107 to Component A-115; ##STR00224## ##STR00225##

13. The method of claim 1, wherein the photosensitive polymer derivative is the photosensitive polymer derivative containing both an o-nitrobenzyl phototrigger and double bond functional group as shown in Formula A-III.

14. The method of claim 9, wherein the aromatic ring is a monocyclic or fused bicyclic ring of 5-10 atoms, the aromatic heterocyclic ring is a monocyclic or fused bicyclic ring containing 5 to 10 atoms, the aromatic heterocyclic ring contains at least one hetero atom selected from the group consisting of N, O, S, and Si, and the aromatic ring or the aromatic heterocyclic ring is optionally substituted by a halogen atom, a nitro group, an aryl group, an alkyl group, or a modified alkyl group.

Description

DESCRIPTION OF DRAWINGS

(1) Note: NB is o-nitrobenzyl phototriggers in Component A-1 of the invention; cNB is cyclic o-nitrobenzyl phototriggers in Component A-88 of the invention; cNB-MA is cyclic o-nitrobenzyl phototriggers and double bond functional group in Component A-144 of invention. Among them, HA-NB is Component A-1; HA-cNB is Component A-88; HA-cNB-MA is Component A-144.

(2) FIG. 1 is a dynamic time sweep rheological diagram of a hydrogel precursor solution (2% HA-NB/6% Gelatin/1% HAMA/0.2% LAP 2% HA-cNB/1% HA-cNB-MA/0.2% LAP) which is illuminated to form a gel.

(3) FIG. 2 is a adhesion test graph of the hydrogel (2% HA-NB/6% Gelatin/1% HAMA/0.2% LAP 2% HA-cNB/1% HA-cNB-MA/0.2% LAP).

(4) FIG. 3 is a compression test diagram of the hydrogel (2% HA-NB/6% Gelatin/1% HAMA/0.2% LAP 2% HA-cNB/1% HA-cNB-MA/0.2% LAP).

(5) FIG. 4 is a graph of biocompatibility testing of the hydrogel (HA-NB/Gelatin/HAMA/LAP HA-cNB/HA-cNB-MA/LAP).

(6) FIG. 5 is a visual representation of the effect of wound closure of the hydrogel (Component A-1/Component A-107/Component C-4/Component B-2).

(7) FIG. 6 is an effect view of the hydrogel as postoperative anti-adhesion (Component A-1/Component A-107/Component C-4/Component B-2).

(8) FIG. 7 is an effect view of the hydrogel as hemostasis in the liver (Component A-1/Component A-107/Component C-4/Component B-2).

(9) FIG. 8 is an effect view of the hydrogel as bone/cartilage tissue engineering scaffold material (Component A-1/Component A-107/Component C-4/Component B-2).

(10) FIG. 9 is an effect view of the hydrogel as bio-ink (Component A-1/Component A-107/Component C-4/Component B-2).

EXAMPLES

(11) The following use example s to describe the present invention in more detail. The invention will be further described in conjunction with the accompanying drawings and example s as following. However, the examples are merely illustrative of the preferred example s of the invention, but not intended to limit the scope of the invention. Any other changes and modifications made by technical personnel in the field without deviation of the spirit and scope in the invention are still included in the scope of the invention.

Example 1: Synthesis of Component A-1

(12) ##STR00042##

(13) (1) Synthesis of Compound 1. The synthesis was carried out according to the method disclosed in the reference (Yunlong Yang; Jieyuan Zhang; Zhenzhen Liu; Qiuning Lin; Xiaolin Liu; Chunyan Bao; Yang Wang; Linyong Zhu. Adv. Mater. 2016, 28, 2724). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 328.1507.

(14) (2) Synthesis of Component A-1. To a solution of hyaluronic acid (2 g, 340 kDa) in 100 mL 0.01 mol/L 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 1 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). 4-(4, 6-Dimethoxytriazin-2-yl)-4-methylmorpholine hydrochloride (DMTMM, 0.4 g, 1.5 mmol) dissolved in 3 mL MES buffer was added to the above reaction solution by three times (every 1 h), and the mixture was reacted at 35° C. for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain the photosensitive hyaluronic acid derivative Compound A-1 (1.85 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 1 could be calculated to be about 3.42%.

Example 2: Synthesis of Component A-2

(15) ##STR00043##

(16) (1) Synthesis of Compound 2. The synthesis was carried out according to the method disclosed in the reference (James F. Cameron; Jean M. J. Frechet. J. Am. Chem. Soc. 1991, 113, 4303).

(17) (2) Synthesis of Compound 3. The solution of Compound 2 (1 g, 3.2 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were reluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in ethyl acetate and washed with a saturated solution of NaCl. After removing the solvent by rotary evaporation under reduced pressure, the crude product was dissolved in methanol and re-precipitated from ethyl acetate. Compound 3 (0.89 g, 82%) was obtained by filtration and vacuum drying after repeated dissolution and heavy precipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.33 (d, J=6.9 Hz, 3H). MS (ESI): [M+H] 342.1624.

(18) (3) Synthesis of Component A-2. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.3) was added Compound 1 (68 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.6 g, 2 mmol) dissolved in 9 mL water was added into the above solution three times with an interval of 30 min, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-1 (1.92 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 1 could be calculated to be about 3.29%.

Example 3: Synthesis of Component A-3

(19) ##STR00044##

(20) (1) Synthesis of Compound 4. The synthesis was carried out according to the method disclosed in the reference (Michael C. Pirrung; Yong Rok Lee; Kaapjoo; James B. Springer. J. Org. Chem. 1999, 64, 5042).

(21) (2) Synthesis of Compound 5. The solution of Compound 4 (1 g, 2.7 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 5 (0.80 g, 74%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 6.35 (dd, J=10.0, 15.0 Hz, 1H), 6.04 (m, 1H), 5.8 (m, 1H), 5.4 (m, 1H), 4.96 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.75 (d, J=6.5 Hz, 3H). MS (ESI): [M+H] 394.1908.

(22) (3) Synthesis of Component A-3. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 5 (79 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-3 (1.73 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 5 can be calculated to be about 2.97%.

Example 4: Synthesis of Component A-4

(23) ##STR00045##

(24) (1) Synthesis of Compound 6. The synthesis was carried out according to the method disclosed in the reference (Isabelle Aujard; Chouaha Benbrahim; Ludovic Jullien. Chem. Eur. J. 2006, 12, 6865).

(25) (2) Synthesis of Compound 7. The solution of Compound 6 (1 g, 3.1 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 7 (0.85 g, 78%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 353.1426.

(26) (3) Synthesis of Component A-4. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added compound 7 (70 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-3 (1.78 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 7 can be calculated to be about 2.49%.

Example 5: Synthesis of Component A-5

(27) ##STR00046##

(28) (1) Synthesis of Compound 8. The synthesis was carried out according to the method disclosed in the reference (Alexander G. Russell; Dario M. Bassani; John S. Snaith. J. Org. Chem. 2010, 75, 4648).

(29) (2) Synthesis of Compound 9. The solution of Compound 8 (1 g, 2.9 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was redissolved in methanol and reprecipitated in ethyl acetate. Compound 9 (0.78 g, 72%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 372.1424.

(30) (3) Synthesis of Component A-5. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added compound 9 (74 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-5 (1.76 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 9 can be calculated to be about 3.08%.

Example 6: Synthesis of Component A-6

(31) ##STR00047##

(32) (1) Synthesis of Compound 10. The synthesis was carried out according to the method disclosed in the reference (Alexandre Specht; Maurice Goeldner. Angew. Chem. Int. Ed. 2004, 43, 2008.).

(33) (2) Synthesis of Compound 11. The solution of Compound 10 (1 g, 2.7 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 11 (0.68 g, 63%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 396.1374.

(34) (3) Synthesis of Component A-6. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 11 (79 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-6 (1.79 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 11 can be calculated to be about 2.34%.

Example 7: Synthesis of Component A-7

(35) ##STR00048##

(36) (1) Synthesis of Compound 12. The synthesis was carried out according to the method disclosed in the reference (Jack F. Baldwin; Adrian W. McConnaughie; Sung Bo Shin. Tetrahedron. 1990, 46, 6879.).

(37) (2) Synthesis of Compound 13. The solution of Compound 12 (1 g, 2.4 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 13 (0.61 g, 57%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.75 (ddd, J=8.2, 1.4, 0.4 Hz, 1H), 7.22 (s, 1H), 7.57 (tdd, J=7.3, 1.4, 0.7 Hz, 1H), 7.49 (dd, J=7.9, 1.4 Hz, 1H), 7.36 (ddd, J=8.1, 7.3, 1.4 Hz, 1H), 4.96 (s, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 449.1618.

(38) (3) Synthesis of Component A-7. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 13 (90 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-7 (1.72 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 13 can be calculated to be about 2.38%.

Example 8: Synthesis of Component A-8

(39) ##STR00049##

(40) (1) Synthesis of Compound 14. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Bamer-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.).

(41) (2) Synthesis of Compound 15. The solution of Compound 14 (1 g, 2.6 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 15 (0.90 g, 83%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.63-3.52 (m, 1H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 2.00-1.34 (m, 6H). MS (ESI): [M+H] 412.2027.

(42) (3) Synthesis of Component A-8. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added compound 15 (82 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-8 (1.86 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 15 can be calculated to be about 3.43%.

Example 9: Synthesis of Component A-9

(43) ##STR00050##

(44) (1) Synthesis of Compound 16. The synthesis was carried out according to the method disclosed in the reference (Patchomik Abraham; Amit B.; Woodward R. B. J. Am. Chem. Soc. 1970, 92, 6333.).

(45) (2) Synthesis of Compound 17. The solution of Compound 16 (1 g, 2.5 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 17 (0.80 g, 75%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.63-3.52 (m, 1H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 2.00-1.34 (m, 6H). MS (ESI): [M+H] 412.2027.

(46) (3) Synthesis of Component A-9. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 17 (86 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid Compound derivative Compound A-9 (1.82 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 17 can be calculated to be about 3.24%.

Example 10: Synthesis of Component A-10

(47) ##STR00051##

(48) (1) Synthesis of Compound 18. The synthesis was carried out according to the method disclosed in the reference (Patchornik Abraham; Amit B.; Woodward R. B. J. Am. Chem. Soc. 1970, 92, 6333.).

(49) (2) Synthesis of Compound 19. The solution of Compound 18 (1 g, 2.7 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 19 (0.76 g, 71%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.25 (q, J=6.5 Hz, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.32 (t, J=6.5 Hz, 3H). MS (ESI): [M+H] 400.1742.

(50) (3) Synthesis of Component A-10. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 19 (80 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-10 (1.88 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 19 can be calculated to be about 3.01%.

Example 11: Synthesis of Component A-11

(51) ##STR00052##

(52) (1) Synthesis of Compound 20. The synthesis was carried out according to the method disclosed in the reference (Kalbag, S. M.; Roeske, R. W. J. Am. Chem. Soc. 1975, 97, 440.).

(53) (2) Synthesis of Compound 21. The solution of Compound 20 (1 g, 2.3 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 21 (0.84 g, 79%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.63 (q, J=6.9 Hz, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.67 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.48 (d, J=6.9 Hz, 3H). MS (ESI): [M+H] 457.1976.

(54) (3) Synthesis of Component A-11. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 21 (91 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-11 (1.76 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 21 can be calculated to be about 3.15%.

Example 12: Synthesis of Component A-12

(55) ##STR00053##

(56) (1) Synthesis of Compound 22. The synthesis was carried out according to the method disclosed in the reference (Patchomik Abraham; Amit B.; Woodward R. B. J. Am. Chem. Soc. 1970, 92, 6333.).

(57) (2) Synthesis of Compound 23. The solution of Compound 22 (1 g, 2.7 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 23 (0.76 g, 71%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.25 (q, J=6.5 Hz, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.32 (t, J=6.5 Hz, 3H). MS (ESI): [M+H] 416.1422.

(58) (3) Synthesis of Component A-12. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 23 (80 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-12 (1.88 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 23 can be calculated to be about 3.01%.

Example 13: Synthesis of Component A-13

(59) ##STR00054##

(60) (1) Synthesis of Compound 24. The synthesis was carried out according to the method disclosed in the reference (Engels, J.; Schlaeger, E. J. J. Med. Chem. 1977, 20, 907.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.25 (q, J=6.5 Hz, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.32 (t, J=6.5 Hz, 3H). MS (ESI): [M+H]435.1432.

(61) (2) Synthesis of Component A-13. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 24 (87 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-13 (1.73 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 24 can be calculated to be about 3.08%.

Example 21: Synthesis of Component A-21

(62) ##STR00055##

(63) (1) Synthesis of Compound 32. The synthesis was carried out according to the method disclosed in the reference (Emmanuel Riguet; Christian G. Bochet. Org. Lett. 2007, 26, 5453.).

(64) (2) Synthesis of Compound 33. The solution of Compound 32 (1 g, 3.4 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were reluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 33 (0.85 g, 78%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=8.05 (d, J=9.54 Hz, 1H), 7.24 (d, J=2.72 Hz, 1H), 6.92 (dd, J=9.54, 2.72 Hz, 1H), 4.85 (s, 2H), 3.56-3.68 (m, 4H), 3.49-3.56 (m, 2H), 3.42-3.49 (m, 2H), 3.32 (t, J=5.9 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H). MS (ESI): [M+H] 346.1454.

(65) (3) Synthesis of Component A-21. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 33 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-21 (1.76 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 33 can be calculated to be about 2.84%.

Example 22: Synthesis of Component A-22

(66) ##STR00056##

(67) (1) Synthesis of Compound 34. The synthesis was carried out according to the method disclosed in the reference (Isabelle Aujard; Chouaha Benbrahim; Ludovic Jullien. Chem. Eur. J. 2006, 12, 6865.).

(68) (2) Synthesis of Compound 35. The solution of Compound 34 (1 g, 3.2 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 35 (0.96 g, 88%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=8.05 (d, J=9.54 Hz, 1H), 7.28 (d, J=8.00 Hz, 2H), 7.24 (d, J=2.72 Hz, 1H), 6.92 (dd, J=9.54, 2.72 Hz, 1H), 6.78 (d, 8.00 Hz, 2H), 4.96 (s, 2H), 4.83 (s, 2H), 3.32 (t, J=5.9 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H). MS (ESI): [M+H]346.1454.

(69) (3) Synthesis of Component A-22. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 35 (69 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-22 (1.83 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 35 can be calculated to be about 3.12%.

Example 25: Synthesis of Component A-25

(70) ##STR00057##

(71) (1) Synthesis of Compound 40. The synthesis was carried out according to the method disclosed in the reference (Emmanuel Riguet; Christian G. Bochet. Org. Lett. 2007, 26, 5453.).

(72) (2) Synthesis of Compound 41. The solution of Compound 10 (1 g, 3.6 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were refluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, and then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 41 (0.93 g, 85%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.24 (s, 2H), 3.32 (t, J=5.9 Hz, 2H), 3.27-3.21 (m, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.75 (t, J=6.3 Hz, 2H), 2.00-1.91 (m, 2H). MS (ESI): [M+H] 309.1522.

(73) (3) Synthesis of Component A-25: To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 41 (62 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-25 (1.82 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 41 can be calculated to be about 3.12%.

Example 26: Synthesis of Component A-26

(74) ##STR00058##

(75) (1) Synthesis of Compound 42. The synthesis was carried out according to the method disclosed in the reference (Singh, A. K.; Khade, P. K. Tetrahedron. 2005, 61, 10007.).

(76) (2) Synthesis of Compound 43. The solution of Compound 42 (1 g, 3.4 mmol) and ethylenediamine (1.1 mL) dissolved in methanol (50 mL) were reluxed overnight. The solvents were removed by rotary evaporation under reduced pressure, then the residue was re-dissolved in methanol and re-precipitated in ethyl acetate. Compound 43 (0.90 g, 82%) was obtained by filtration and vacuum drying after several times of dissolution-reprecipitation. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=8.31-7.12 (m, 5H), 4.96 (s, 2H), 4.83 (s, 2H), 3.32 (t, J=5.9 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H). MS (ESI): [M+H] 320.1254.

(77) (3) Synthesis of Component A-26. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 43 (64 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-26 (1.87 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 43 can be calculated to be about 3.21%.

Example 28: Synthesis of Component A-28

(78) ##STR00059##

(79) (1) Synthesis of Compound 46. The synthesis was carried out according to the method disclosed in the reference (Grazyna Groszek; Agnieszka Nowak-Krol; Barbara Filipek. Eur. J. Med. Chem. 2009, 44, 5103.).

(80) (2) Synthesis of Compound 47. Compound 46 (1 g, 3.3 mmol) and ethylenediamine (1.1 mL) were dissolved in methanol (50 mL) and refluxed overnight. After steaming by rotary evaporation under reduced pressure, the crude product was dissolved in methanol and re-precipitated from ethyl acetate. After several times of dissolution-reprecipitation, filtration and vacuum drying gave Compound 47 (0.97 g, 89%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=8.04 (s, 1H), 7.42 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 328.1507.

(81) (3) Synthesis of Component A-28. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 47 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-28 (1.85 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 47 can be calculated to be about 3.43%.

Example 29: Synthesis of Component A-29

(82) ##STR00060##

(83) (1) Synthesis of Compound 48. The synthesis was carried out according to the method disclosed in the reference (Thomas F. Greene; Shu Wang; Mary J. Meegan. J. Med. Chem. 2016, 59, 90.).

(84) (2) Synthesis of Compound 49. Compound 48 (1 g, 3.3 mmol) and ethylenediamine (1.1 mL) were dissolved in methanol (50 mL) and refluxed overnight. The solvent was removed by rotary evaporation under reduced pressure, the obtained crude product was dissolved in methanol and re-precipitated from ethyl acetate for several times to obtain Compound 49 (0.95 g, 87%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.95 (s, 1H), 7.12 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 328.1507.

(85) (3) Synthesis of Component A-29. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 49 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-29 (1.86 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 49 can be calculated to be about 3.52%.

Example 30: Synthesis of Component A-30

(86) ##STR00061##

(87) (1) Synthesis of Compound 50. The synthesis was carried out according to the method disclosed in the reference (Yu-Shan; Mohane Selvaraj Coumar; Hsing-Pang Hsieh. J. Med. Chem. 2009, 52, 4941.).

(88) (2) Synthesis of Compound 51. Compound 50 (1 g, 3.3 mmol) and ethylenediamine (1.1 mL) were dissolved in methanol (50 mL) and refluxed overnight. The solvent was removed by rotary evaporation under reduced pressure, the obtained crude product was dissolved in methanol and re-precipitated from ethyl acetate for several times to obtain Compound 51 (0.89 g, 81%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.64 (s, 1H), 7.02 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 328.1507.

(89) (3) Synthesis of Component A-30. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 51 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-30 (1.85 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 51 can be calculated to be about 3.39%.

Example 31: Synthesis of Component A-31

(90) ##STR00062##

(91) (1) Synthesis of Compound 52. The synthesis was carried out according to the method disclosed in the reference (Sarit S. Agasti; Apiwat Chompoosor; Vincent M. Rotello. J. Am. Chem. Soc. 2009, 131, 5728.).

(92) (2) Synthesis of Compound 53. Compound 52 (1 g, 2.9 mmol) and ethylenediamine (1.1 mL) were dissolved in methanol (50 mL) and refluxed overnight. After steaming by rotary evaporation under reduced pressure, the crude product was dissolved in methanol and re-precipitated from ethyl acetate for several times to obtain Compound 53 (0.91 g, 84%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.91 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 373.1373.

(93) (3) Synthesis of Component A-31. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 53 (75 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-31 (1.87 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 53 can be calculated to be about 3.45%.

Example 33: Synthesis of Component A-33

(94) ##STR00063##

(95) Synthesis of Component A-33. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added the mixture of Compound 1 and Compound 55 (60 mg, weight ratio 1:1) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-33 (1.87 g). According to the nuclear magnetic resonance spectrum, the grafting degree of the NB mixture (Compound 1/Compound 55) can be calculated to be about 3.52%.

Example 34: Synthesis of Component A-34

(96) ##STR00064##

(97) (1) Synthesis of Compound 56. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Bamer-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.).

(98) (2) Synthesis of Compound 57. Compound 56 (1 g, 3.3 mmol) and ethylenediamine (1.1 mL) were dissolved in methanol (50 mL) and refluxed overnight. After steaming by rotary evaporation under reduced pressure, the crude product was dissolved in methanol and re-precipitated from ethyl acetate. After several times of dissolution-reprecipitation, filtration and vacuum drying gave Compound 57 (0.93 g, 85%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 3.99 (s, 3H), 3.32 (t, J=5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.55 (t, J=6.1 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H]326.1721.

(99) (3) Synthesis of Component A-34. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 57 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-34 (1.82 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 57 can be calculated to be about 3.21%.

Example 35: Synthesis of Component A-35

(100) ##STR00065##

(101) (1) Synthesis of Compound 58. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Bamer-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.).

(102) (2) Synthesis of Compound 59. Compound 58 (1 g, 3.3 mmol) and ethylenediamine (1.1 mL) were dissolved in methanol (50 mL) and refluxed overnight. After steaming by rotary evaporation under reduced pressure, the crude product was dissolved in methanol and re-precipitated from ethyl acetate. After several times of dissolution-reprecipitation, filtration and vacuum drying gave Compound 59 (0.82 g, 75%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.03 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 360.1213.

(103) (3) Synthesis of Component A-35. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 59 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-35 (1.87 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 59 can be calculated to be about 2.76%.

Example 36: Synthesis of Component A-36

(104) ##STR00066##

(105) (1) Synthesis of Compound 60. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Bamer-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.).

(106) (2) Synthesis of Compound 61. Compound 60 (1 g, 3.3 mmol) and ethylenediamine (1.1 mL) were dissolved in methanol (50 mL) and refluxed overnight. After steaming by rotary evaporation under reduced pressure, the crude product was dissolved in methanol and re-precipitated from ethyl acetate. After several times of dissolution-reprecipitation, filtration and vacuum drying gave Compound 61 (0.80 g, 73%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 3.99 (s, 3H), 3.45 (t, J=6.1 Hz, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 327.1625.

(107) (3) Synthesis of Component A-36. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 61 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-36 (1.76 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 61 can be calculated to be about 3.21%.

Example 37: Synthesis of Component A-37

(108) ##STR00067##

(109) Synthesis of Component A-37: To a solution of carboxymethyl cellulose (2 g, 90 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 1 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethylcellulose derivative Compound A-37 (1.89 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 1 can be calculated to be about 2.25%.

Example 38: Synthesis of Component A-38

(110) ##STR00068##

(111) Synthesis of Component A-38: To a solution of alginic acid (2 g) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 1 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive alginic acid derivative Compound A-38 (1.82 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 1 can be calculated to be about 3.17%.

Example 39: Synthesis of Component A-39

(112) ##STR00069##

(113) Synthesis of Component A-39. To a solution of chondroitin sulfate (2 g) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 1 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive chondroitin sulfate derivative Compound A-39 (1.73 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 1 can be calculated to be about 2.98%.

Example 40: Synthesis of Component A-40

(114) ##STR00070##

(115) Synthesis of Component A-40. To a solution of polyglutamic acid (PGA, 1 g) in 50 mL distilled water was added hydroxybenzotriazole (HOBt, 0.3 g, 2.3 mmol). Then Compound 1 (0.5 g, 1.6 mmol) and 1-ethyl-(3-dimethylaminopropyl) carbodiimine hydrochloride (EDC-HCl, 0.5 g, 2.6 mmol) dissolved in methanol were added to the above solution, and the mixture was stirred at room temperature for 48 h. The solution was firstly dialyzed with dilute hydrochloric acid solution containing sodium chloride (pH=3.5) for 1 d, and then dialyzed against pure water for 1 d, then freeze-dried to obtain photosensitive polyglutamic acid derivative Compound A-40 (0.92 g). According to its nuclear magnetic resonance spectrum, the grafting degree of Compound 1 can be calculated to be about 21.3%.

Example 41: Synthesis of Component A-41

(116) ##STR00071##

(117) Synthesis of Component A-41. To a solution of four-arm polyglycol carboxylic acid derivative 4-PEG-COOH (0.5 g, 10 kDa) dissolved in 20 mL dry dimethyl sulfoxide (DMSO) was added Compound 1 (130 mg, 0.4 mmol) dissolved in 5 mL dimethyl sulfoxide (DMSO). And then, 0.2 ml triethylamine TEA and benzotriazol-1-yl-oxytripyrrolidinylphosphonium (PyBop, 210 mg, 0.4 mmol) were added into the above solution. The mixture was reacted at room temperature for 24 h. Then, it was re-precipitated in diethyl ether, and the crude product was re-dissolved in water and poured into a dialysis bag (MWCO 3500) to dialyze against deionized water for 2-3 d. The photosensitive polyethylene glycol derivative Compound A-41 (0.45 g) was obtained by freeze-drying. According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 1 can be calculated to be about 98%.

Example 42: Synthesis of Component A-42

(118) ##STR00072##

(119) (1) Synthesis of Compound 62. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Barner-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.79 (t, J=6.1 Hz, 2H), 3.70 (t, J=7.2 Hz, 2H), 3.63-3.52 (m, 1H), 3.56 (t, J=7.2 Hz, 2H), 2.00-1.34 (m, 6H). MS (ESI): [M+H] 372.1627.

(120) (2) Synthesis of Component A-42. To a solution of hyaluronic acid (1 g, 340 kDa) dissolved in 50 mL of water was sequentially added Compound 62 (0.2 g, 0.48 mmol), EDC-HCl (0.76 g, 3.96 mmol) and DPTS (0.12 g, 0.48 mmol), and the reaction was stirred at room temperature for 48 h. The reaction solution was re-precipitated in cold ethanol, and the crude product was re-dissolved in water and re-precipitated several times. The collected precipitate was dried and dissolved in anhydrous DMSO, and the above solution was added p-toluenesulfonic acid to remove dihydropyran protecting group to obtain the photosensitive hyaluronic acid derivative Compound A-42 (0.86 g). According to its nuclear magnetic resonance spectrum, the grafting degree of Compound 62 can be calculated to be about 10%.

Example 43: Synthesis of Component A-43

(121) ##STR00073##

(122) (1) Synthesis of Compound 63. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Bamer-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.63-3.52 (m, 1H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 2.00-1.34 (m, 6H). MS (ESI): [M+H] 370.1512.

(123) (2) Synthesis of Component A-43. To a suspension liquid of chitosan (1 g) dissolved in 75 mL isopropanol was sequentially added Compound 63 (0.2 g, 0.54 mmol), EDC-HCl (0.76 g, 3.96 mmol) and NHS (0.46 g, 4.0 mmol), and the reaction was stirred at room temperature for 48 h. After completion of the reaction, the mixture solution was filtered, and the filtrate was dialyzed three times with a methanol/water mixed solvent and twice with methanol, and then freeze-dried to obtain chitosan modified by Compound 63 (0.9 g). The chitosan modified by Compound 63 was dissolved in anhydrous DMSO, and the solution was added p-toluenesulfonic acid to remove dihydropyran protecting group to obtain the photosensitive chitosan derivative Compound A-43. According to its nuclear magnetic resonance spectrum, the grafting degree of the Compound 63 can be calculated to be about 12.5%.

Example 44: Synthesis of Component A-44

(124) ##STR00074##

(125) Synthesis of Component A-44. To a solution of polylysine (PLL, 1 g) dissolved in 50 mL water was sequentially added Compound 63 (0.2 g, 0.54 mmol), EDC-HCl (0.76 g, 3.96 mmol) and NHS (0.46 g, 4.0 mmol), and the reaction was stirred at room temperature for 48 h. After completion of the reaction, the reaction solution was reprecipitated in cold ethanol, and the crude product was re-dissolved in water and reprecipitated several times. The collected precipitate was dried and dissolved in anhydrous DMSO, and the above solution was added p-toluenesulfonic acid to remove dihydropyran protecting group to obtain the photosensitive hyaluronic acid derivative Compound A-44 (0.84 g). According to its nuclear magnetic resonance spectrum, the grafting degree of Compound 63 can be calculated to be about 15.6%.

Example 45: Synthesis of Component A-45

(126) ##STR00075##

(127) Synthesis of Component A-45: To a solution of gelatin (1 g) dissolved in 50 mL water was sequentially added Compound 63 (0.2 g, 0.54 mmol), EDC-HCl (0.76 g, 3.96 mmol) and NHS (0.46 g, 4.0 mmol), and the reaction was stirred at room temperature for 48 h. After completion of the reaction, the reaction solution was reprecipitated in cold ethanol, and the crude product was re-dissolved in water and reprecipitated several times. The collected precipitate was dried and dissolved in anhydrous DMSO, and the above solution was added p-toluenesulfonic acid to remove dihydropyran protecting group to obtain the photosensitive gelatin derivative Compound A-45 (0.83 g). According to its nuclear magnetic resonance spectrum, the grafting degree of Compound 63 can be calculated to be about 11.2%

Example 46: Synthesis of Component A-46

(128) ##STR00076##

(129) Synthesis of Component A-46: To a solution of dextran (1 g) dissolved in 50 mL water was sequentially added Compound 63 (0.2 g, 0.54 mmol), EDC-HCl (0.76 g, 3.96 mmol) and NHS (0.46 g, 4.0 mmol), and the reaction was stirred at room temperature for 48 h. After completion of the reaction, the reaction solution was reprecipitated in cold ethanol, and the crude product was re-dissolved in water and reprecipitated several times. The collected precipitate was dried and dissolved in anhydrous DMSO, and the above solution was added p-toluenesulfonic acid to remove dihydropyran protecting group to obtain the photosensitive hyaluronic acid derivative Compound A-46 (0.92 g). According to its nuclear magnetic resonance spectrum, the grafting degree of Compound 63 can be calculated to be about 18.2%.

Example 47: Synthesis of Component A-47

(130) ##STR00077##

(131) (1) Synthesis of Compound 64. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Bamer-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 286.0943.

(132) (2) Synthesis of Component A-47. To a solution of sulphydryl-modified heparin Hep-SH (1 g) dissolved in 50 mL distilled water was added hydroxybenzotriazole (HOBt, 0.3 g, 2.3 mmol). Then Compound 64 (0.5 g, 1.6 mmol) and 1-ethyl-(3-dimethyl amino propyl) carbodiimine hydrochloride (EDC-HCl, 0.5 g, 2.6 mmol) dissolved in methanol were added to the above solution, and the mixture was stirred at room temperature for 48 h. The solution was firstly dialyzed with dilute hydrochloric acid solution containing sodium chloride (pH=3.5) for 1 d, and then dialyzed against pure water for 1 d, then freeze-dried to obtain photosensitive heparin derivative Compound A-47 (0.86 g). According to its nuclear magnetic resonance spectrum, the grafting degree of Compound 64 can be calculated to be about 10.2%.

Example 48: Synthesis of Component A-48

(133) ##STR00078##

(134) (1) Synthesis of Compound 65. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Bamer-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.63-3.52 (m, 1H), 3.04 (t, J=7.2 Hz, 2H), 2.00-1.34 (m, 6H). MS (ESI): [M+H] 391.0518.

(135) (2) Synthesis of Component A-48. To a suspension liquid of chitosan (1 g) in 75 mL isopropanol was slowly added 25 mL of NaOH solution (10 mol/L) for five times, and the solution was stirred for 0.5 h. Compound 65 (0.2 g) was then added to the above solution and reacted at 60° C. for 3 h. After completion of the reaction, the mixture solution was filtered, and the filtrate was dialyzed three times with a methanol/water mixed solvent and twice with methanol, and then freeze-dried to obtain chitosan modified by Compound 65 (0.92 g). The chitosan modified by Compound 65 was dissolved in DMSO, and the solution was added p-toluenesulfonic acid to remove dihydropyran protecting group to obtain the photosensitive chitosan derivative Compound A-48 (0.84 g). According to its nuclear magnetic resonance spectrum, the grafting degree of the Compound 65 can be calculated to be about 12.4%.

Example 49: Synthesis of Component A-49

(136) ##STR00079##

(137) Synthesis of Component A-49: To a solution of PEG-4OH (1 g, 0.05 mmol) dissolved in anhydrous acetonitrile was added K.sub.2CO.sub.3 (55.3 mg, 0.4 mmol) and stirred for 30 min. Then the solution was added Compound 65 (0.17 g, 0.4 mmol) and continued to react at room temperature for 24 h. After the reaction was completed, most of the solvent was removed, the residue was polyreprecipitated in diethyl ether, and washed several times. The PEG-4OH modified by Compound 65 was dissolved in DMSO, and the solution was added p-toluenesulfonic acid to remove dihydropyran protecting group to obtain the photosensitive polyethelene glycol derivative Compound A-49 (0.93 g). According to its nuclear magnetic resonance spectrum, the grafting degree of the Compound 65 can be calculated to be about 95%.

Example 50: Synthesis of Component A-50

(138) ##STR00080## ##STR00081##

(139) (1) Synthesis of Compound 66. To a solution of Compound 65 (0.5 g, 1.29 mmol) and ethylene glycol (0.24 g, 3.87 mmol) dissolved in anhydrous acetonitrile was added K.sub.2CO.sub.3 (0.5 g, 3.87 mmol) as a base and refluxed overnight. After completion of the reaction, the solvent was removed by rotary evaporation under reduced pressure and purified by column chromatography to afford Compound 66 (0.34 g, 72%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.79 (t, J=6.1 Hz, 2H), 3.70 (t, J=7.2 Hz, 2H), 3.63-3.52 (m, 1H), 3.56 (t, J=7.2 Hz, 2H), 2.00-1.34 (m, 6H). MS (ESI): [M+H] 372.1627.

(140) (2) Synthesis of Compound 67. To a solution of Compound 66 (0.64 g, 1.72 mmol) and triethylamine (0.34 g, 3.44 mmol) dissolved in dry dichloromethane was slowly dropwise added methacryloyl chloride (0.27 g, 2.58 mmol) under ice bath conditions, and the reaction was carried out overnight at room temperature after the dropwise addition. After completion of the reaction, the solvent was removed by rotary evaporation under reduced pressure and purified to afford Compound 67 (0.49 g, 65%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 6.25 (s, 1H), 5.68 (s, 1H), 4.96 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.79 (t, J=6.1 Hz, 2H), 3.70 (t, J=7.2 Hz, 2H), 3.63-3.52 (m, 1H), 3.56 (t, J=7.2 Hz, 2H), 2.00-1.34 (m, 6H), 1.87 (s, 3H). MS (ESI): [M+H] 440.1942.

(141) (3) Synthesis of Component A-50. Compound 67 (0.28 g, 0.63 mmol), comonomer PEG-MA (0.882 g, 2.52 mmol) and the initiator azobisisobutyronitrile (11 mg) were added into the Shrek tube and dissolved by anhydrous THF. After repeated freeze-vacuum cycle operation, the reaction system was reacted at 75° C. for 24 h. After the reaction was completed, the reaction solution was poured into cold diethyl ether and reprecipitated several times. The collected precipitate was dried and dissolved in anhydrous DMSO, and the solution was added p-toluenesulfonic acid to remove dihydropyran protecting group to obtain the photosensitive polyethelene glycol derivative Compound A-50 (0.84 g). According to its nuclear magnetic resonance spectrum, it can be calculated that the content of the Compound 67 in the copolymer is about 15.5%. According to GPC, the molecular weight of the synthetic polymer is about 25 kDa. According to the feed ratio, n is 12, x is 10, and y is 40.

Example 51: Synthesis of Component A-51

(142) ##STR00082##

(143) (1) Synthesis of Compound 68. The synthesis was carried out according to the method disclosed in the reference (Kunihiko Morihiro; Tetsuya Kodama; Shohei Mori; Satoshi Obika. Org. Biomol. Chem. 2014, 12, 2468.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.03 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H]344.1207.

(144) (2) Synthesis of Component A-51. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 68 (69 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-51 (1.85 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 68 can be calculated to be about 3.34%.

Example 52: Synthesis of Component A-52

(145) ##STR00083##

(146) (1) Synthesis of Compound 69. The synthesis was carried out according to the method disclosed in the reference (Yunlong Yang; Jieyuan Zhang; Zhenzhen Liu; Qiuning Lin; Xiaolin Liu; Chunyan Bao; Yang Wang; Linyong Zhu. Adv. Mater. 2016, 28, 2724.)

(147) (2) Synthesis of Compound 70. To a solution of Compound 69 (1 g, 3.0 mmol) dissolved in 50 mL tetrahydrofuran was added carbon tetrabromide (CBr.sub.4, 2 g, 6.0 mmol) and triphenylphosphine (PPh.sub.3, 1.6 g, 6.0 mmol), and the reaction was stirred at room temperature for 2 h under the protection of argon. After completion of the reaction, 5 mL of water was added to quench the reaction. Then, the solvent was removed by rotary evaporation under reduced pressure, the crude was extracted with ethyl acetate and separated by column chromatography (PE:DCM=4:1) to obtain Compound 70 (1.0 g, yield 84%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.56 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 390.0623.

(148) (3) Synthesis of Compound 71. To a solution of Compound 70 (0.5 g, 1.3 mmol) dissolved in 50 mL acetone was added L-cysteine methyl ester hydrochloride (0.45 g, 2.6 mmol) and sodium hydroxide (0.2 g, 5.2 mmol), the reaction was stirred at room temperature for 2 h under the protection of argon. After completion of the reaction, the solution was added 4 M HCl to adjust the pH=7. The solvent was removed by ratary evaporation under reduced pressure, and the crude was extracted with ethyl acetate and purified by column chromatography (PE:DCM=4:1) to obtain Compound 71 (0.7 g, 88%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.43 (d, J=5.6, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.42 (s, 9H). MS (ESI): [M+H]545.2219.

(149) (4) Synthesis of Component A-52. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 71 (109 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-52 (1.92 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 71 can be calculated to be about 3.32%.

Example 53: Synthesis of Component A-53

(150) ##STR00084##

(151) (1) Synthesis of Compound 72. The synthesis was carried out according to the method disclosed in the reference (James F. Cameron; Jean M. J. Frechet. J. Am. Chem. Soc. 1991, 113, 4303.)

(152) (2) Synthesis of Compound 73. According to the method in Example 52, Compound 73 was obtained from Compound 72 (yield: 73%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.66 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.33 (d, J=6.9 Hz, 3H). MS (ESI): [M+H] 404.0863.

(153) (3) Synthesis of Compound 74. According to the method in Example 52, Compound 74 was obtained from Compound 73 (yield: 70%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.86 (m, 1H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.43 (d, J=5.6, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.42 (s, 9H), 1.33 (d, J=6.9 Hz, 3H). MS (ESI): [M+H]559.2402.

(154) (4) Synthesis of Component A-53. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 74 (112 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-53 (1.75 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 74 can be calculated to be about 2.34%.

Example 54: Synthesis of Component A-54

(155) ##STR00085##

(156) (1) Synthesis of Compound 75. The synthesis was carried out according to the method disclosed in the reference (Jack E. Baldwin; Adrian W. McConnaughie; Sung Bo Shin Tetrahedron. 1990, 46, 6879.)

(157) (2) Synthesis of Compound 76. According to the method in Example 52, Compound 76 was obtained from Compound 75 (yield: 64%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.75 (ddd, J=8.2, 1.4, 0.4 Hz, 1H), 7.22 (s, 1H), 7.57 (tdd, J=7.3, 1.4, 0.7 Hz, 1H), 7.49 (dd, J=7.9, 1.4 Hz, 1H), 7.36 (ddd, J=8.1, 7.3, 1.4 Hz, 1H), 4.66 (s, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 511.0881.

(158) (3) Synthesis of Compound 77. According to the method in Example 52, Compound 77 was obtained from Compound 76 (yield: 58%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.75 (ddd, J=8.2, 1.4, 0.4 Hz, 1H), 7.22 (s, 1H), 7.57 (tdd, J=7.3, 1.4, 0.7 Hz, 1H), 7.49 (dd, J=7.9, 1.4 Hz, 1H), 7.36 (ddd, J=8.1, 7.3, 1.4 Hz, 1H), 4.86 (s, 1H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.43 (d, J=5.6, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.42 (s, 9H). MS (ESI): [M+H] 666.2423.

(159) (4) Synthesis of Component A-54. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 77 (133 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-54 (1.8 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 77 can be calculated to be about 3.35%.

Example 55: Synthesis of Component A-55

(160) ##STR00086##

(161) (1) Synthesis of Compound 78. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Bamer-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.).sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.63-3.52 (m, 1H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 2.00-1.34 (m, 6H). MS (ESI): [M+H]428.1831.

(162) (2) Synthesis of Component A-55. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 78 (85 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-55 (1.85 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 78 can be calculated to be about 3.42%.

Example 56: Synthesis of Component A-56

(163) ##STR00087##

(164) (1) Synthesis of Compound 79. The synthesis was carried out according to the method disclosed in the reference (Patchomik Abraham; Amit B.; Woodward R. B. J. Am. Chem. Soc. 1970, 92, 6333.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=8.02-7.23 (m, 5H), 7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H]448.1561.

(165) (2) Synthesis of Component A-56. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 79 (89 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-56 (1.87 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 79 can be calculated to be about 3.21%.

Example 57: Synthesis of Component A-57

(166) ##STR00088##

(167) (1) Synthesis of Compound 80. The synthesis was carried out according to the method disclosed in the reference (Patchomrnik Abraham; Amit B.; Woodward R. B. J. Am. Chem. Soc. 1970, 92, 6333.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.25 (q, J=6.5 Hz, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.32 (t, J=6.5 Hz, 3H). MS (ESI): [M+H] 416.1432.

(168) (2) Synthesis of Component A-57. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 80 (83 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-57 (1.74 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 80 can be calculated to be about 2.34%.

Example 58: Synthesis of Component A-58

(169) ##STR00089##

(170) (1) Synthesis of Compound 81. The synthesis was carried out according to the method disclosed in the reference (Kalbag, S. M.; Roeske, R. W. J. Am. Chem. Soc. 1975, 97, 440.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.63 (q, J=6.9 Hz, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.67 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.48 (d, J=6.9 Hz, 3H). MS (ESI): [M+H] 473.1734.

(171) (2) Synthesis of Component A-58. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 81 (94 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-58 (1.72 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 81 can be calculated to be about 2.56%.

Example 59: Synthesis of Component A-59

(172) ##STR00090##

(173) (1) Synthesis of Compound 82. The synthesis was carried out according to the method disclosed in the reference (Patchomik Abraham; Amit B.; Woodward R. B. J. Am. Chem. Soc. 1970, 92, 6333.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.25 (q, J=6.5 Hz, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.32 (t, J=6.5 Hz, 3H). MS (ESI): [M+H] 432.1224.

(174) (2) Synthesis of Component A-59. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 82 (83 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-59 (1.74 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 82 can be calculated to be about 2.34%.

Example 60: Synthesis of Component A-60

(175) ##STR00091##

(176) (1) Synthesis of Compound 83. The synthesis was carried out according to the method disclosed in the reference (Engels, J.; Schlaeger, E. J. J. Med. Chem. 1977, 20, 907.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.25 (q, J=6.5 Hz, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.32 (t, J=6.5 Hz, 3H). MS (ESI): [M+H]451.1126.

(177) (2) Synthesis of Component A-60. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 83 (90 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-60 (1.72 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 83 can be calculated to be about 2.36%.

Example 62: Synthesis of Component A-62

(178) ##STR00092##

(179) (1) Synthesis of Compound 85. The synthesis was carried out according to the method disclosed in the reference (Grazyna Groszek; Agnieszka Nowak-Krol; Barbara Filipek. Eur. J. Med. Chem. 2009, 44, 5103.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=8.04 (s, 1H), 7.42 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.43 (d, J=5.6, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.42 (s, 9H). MS (ESI): [M+H] 545.2234.

(180) (2) Synthesis of Component A-62. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 85 (109 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-62 (1.92 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 85 can be calculated to be about 3.14%.

Example 63: Synthesis of Component A-63

(181) ##STR00093##

(182) (1) Synthesis of Compound 86. The synthesis was carried out according to the method disclosed in the reference (Thomas F. Greene; Shu Wang; Mary J. Meegan. J. Med. Chem. 2016, 59, 90.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.95 (s, 1H), 7.12 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.43 (d, J=5.6, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.42 (s, 9H). MS (ESI): [M+H] 545.2262.

(183) (2) Synthesis of Component A-63. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 86 (109 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-63 (1.88 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 68 can be calculated to be about 3.45%.

Example 64: Synthesis of Component A-64

(184) ##STR00094##

(185) (1) Synthesis of Compound 87. The synthesis was carried out according to the method disclosed in the reference (Yu-Shan; Mohane Selvaraj Coumar; Hsing-Pang Hsieh. J. Med. Chem. 2009, 52, 4941.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.64 (s, 1H), 7.02 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.43 (d, J=5.6, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.42 (s, 9H). MS (ESI): [M+H] 545.2231.

(186) (2) Synthesis of Component A-64. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 87 (109 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-64 (1.85 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 87 can be calculated to be about 3.32%.

Example 65: Synthesis of Component A-65

(187) ##STR00095##

(188) Synthesis of Component A-65: To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added NB mixture (Compound 68/Compound 71, 60 mg, weight ratio is 1:1) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-65 (1.89 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound NB mixture is calculated to be about 3.41%.

Example 66: Synthesis of Component A-66

(189) ##STR00096##

(190) Synthesis of Component A-66. To a solution of carboxymethylcellulose (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 71 (109 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethylcellulose derivative Compound A-66 (1.74 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 71 can be calculated to be about 2.34%.

Example 67: Synthesis of Component A-67

(191) ##STR00097##

(192) (1) Synthesis of Compound 88. According to the method in Example 52, Compound 88 was prepared by conventional chemical methods. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.43 (d, J=5.6, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.42 (s, 9H). MS (ESI): [M+H] 503.1732.

(193) (2) Synthesis of Component A-67. To a suspension liquid of chitosan (1 g) dissolved in 75 mL isopropanol was sequentially added Compound 88 (0.2 g, 0.54 mmol), EDC-HCl (0.76 g, 3.96 mmol) and NHS (0.46 g, 4.0 mmol), and the reaction was stirred at room temperature for 48 h. After completion of the reaction, the mixture solution was dialyzed with diluted hydrochloric acid solution for 1 d, dialyzed with distilled water for 1 d, and then freeze-dried to obtain photosensitive chitosan derivatives Compound A-67 (0.89 g). According to its nuclear PEG-4OHmagnetic resonance spectrum, the grafting degree of the Compound 88 can be calculated to be about 12.5%.

Example 68: Synthesis of Component A-68

(194) ##STR00098##

(195) (1) Synthesis of Compound 89. According to the method in Example 52, Compound 89 was prepared by conventional chemical methods. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.43 (d, J=5.6, 2H), 3.04 (t, J=7.2 Hz, 2H), 1.42 (s, 9H). MS (ESI): [M+H] 523.0731.

(196) (2) Synthesis of Component A-68. To a solution of PEG-4OH (1 g, 0.05 mmol) in anhydrous acetonitrile was added K.sub.2CO.sub.3 (55.3 mg, 0.4 mmol) and stirred for 30 min. Then the solution was added Compound 89 (0.20 g, 0.4 mmol) and continued to react at room temperature for 24 h. After completion of the reaction, most of the solvent was removed, reprecipitated in diethyl ether, and washed several times to obtain the photosensitive polyethelene glycol derivative Compound A-68 (0.85 g). According to its nuclear magnetic resonance spectrum, the grafting degree of the Compound 89 can be calculated to be about 95%.

Example 69: Synthesis of Component A-69

(197) ##STR00099## ##STR00100##

(198) (1) Synthesis of Compound 90. To a solution of Compound 89 (0.5 g, 1.29 mmol) and ethylene glycol (0.24 g, 3.87 mmol) dissolved in anhydrous acetonitrile was added K.sub.2CO.sub.3 (0.5 g, 3.87 mmol) as a base and refluxed overnight. After completion of the reaction, the solvent was removed by rotary evaporation under reduced pressure and purified by column chromatography to obtain Compound 90 (0.34 g, 72%).

(199) (2) Synthesis of Compound 91. To a solution of Compound 90 (0.64 g, 1.72 mmol) and triethylamine (0.34 g, 3.44 mmol) dissolved in anhydrous dichloromethane was slowly dropwise added methacryloyl chloride (0.27 g, 2.58 mmol) under ice bath conditions, and the reaction was carried out overnight at room temperature after the dropwise addition. After completion of the reaction, the solvent was removed by rotary evaporation under reduced pressure and purified by column chromatography to afford Compound 91 (0.49 g, 65%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 6.25 (s, 1H), 5.68 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.79 (t, J=6.1 Hz, 2H), 3.70 (t, J=7.2 Hz, 2H), 3.56 (t, J=7.2 Hz, 2H), 3.43 (d, J=5.6, 2H), 1.87 (s, 3H), 1.42 (s, 9H). MS (ESI): [M+H] 573.2125.

(200) (3) Synthesis of Component A-69. Compound 91 (0.28 g, 0.63 mmol), comonomer PEG-MA (0.882 g, 2.52 mmol) and the initiator azobisisobutyronitrile (11 mg) were added into the Shrek tube and dissolved by anhydrous THF. After repeated freeze-vacuum cycle operation, the reaction system was reacted at 75° C. for 24 h. After the reaction was completed, the reaction solution was poured into cold diethyl ether and reprecipitated several times to obtain the photosensitive copolymer derivative Compound A-69 (0.86 g). According to its nuclear magnetic resonance spectrum, it can be calculated that the content of the Compound 91 in the copolymer is about 15.3%. According to GPC, the molecular weight of the synthetic polymer is about 25 kDa. According to the feed ratio, n is 12, x is 10, and y is 40.

Example 70: Synthesis of Component A-70

(201) ##STR00101##

(202) (1) Synthesis of Compound 92. The synthesis was carried out according to the method disclosed in the reference (Takahiro Muraoka; Honggang Cui; Samuel I. Stupp. J. Am. Chem. Soc. 2008, 130, 2946.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.35 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 327.1617.

(203) (2) Synthesis of Component A-70. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 92 (65 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-70 (1.8 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 92 is calculated to be about 3.26%.

Example 71: Synthesis of Component A-71

(204) ##STR00102##

(205) (1) Synthesis of Compound 93. The synthesis was carried out according to the method disclosed in the reference (Takahiro Muraoka; Honggang Cui; Samuel I. Stupp. J. Am. Chem. Soc. 2008, 130, 2946.).

(206) (2) Synthesis of Compound 94. To a solution of Compound 93 (15.4 g, 36.24 mmol) dissolved in 100 mL methanol was dropwise added methyl amine acetate (7.0 g, 78.65 mmol) dissolved in 70 mL of methanol and NaOH (2 M, 50 mL), and the mixture was stirred at room temperature for 30 min. Then, NaBH.sub.4 (12 g, 317.2 mmol) was slowly added to the above solution at 0° C. and reacted for 2 h. The solvent was removed by rotary evaporation under reduced pressure and adjusted to pH 5 with 2 M HCl to precipitate white solid. The crude was washed by diethyl ether for several times and precipitated with diethyl ether to obtain Compound 94 (17.5 g, 97%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.74 (s, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.42 (s, 9H). MS (ESI): [M+H] 499.2442.

(207) (3) Synthesis of Compound 95. Compound 94 (15 g, 30 mmol) was dissolved in a mixed solution of dichloromethane/trifluoroacetic acid (3:1), and the reaction was stirred at room temperature for 30 min. Then the solvent was removed by reduced pressure, and the crude product was precipitated by ethyl ether to obtain Compound 95 (11.4 g, 95%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.74 (s, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 399.1823.

(208) (4) Synthesis of Component A-71. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 95 (80 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-71 (1.87 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 95 is calculated to be about 3.42%.

Example 72: Synthesis of Component A-72

(209) ##STR00103##

(210) (1) Synthesis of Compound 96. The synthesis was carried out according to the method disclosed in the reference (James F. Cameron; Jean M. J. Frechet. J. Am. Chem. Soc. 1991, 113, 4303.). H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.75 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.74 (s, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.33 (d, J=6.9 Hz, 3H). MS (ESI): [M+H] 413.2041.

(211) (2) Synthesis of Component A-72. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 96 (82 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-72 (1.84 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 96 is calculated to be about 3.21%.

Example 74: Synthesis of Component A-74

(212) ##STR00104##

(213) (1) Synthesis of Compound 98. The synthesis was carried out according to the method disclosed in the reference (Pauloehrl, T.; Delaittre, G.; Bruns, M.; Meißler, M.; Börner, H. G.; Bastmeyer, M.; Barner-Kowollik, C. Angew. Chem. Int. Ed. 2012, 51, 9181.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.90-3.80 (m, 1H), 3.63-3.52 (m, 1H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 2.00-1.34 (m, 6H). MS (ESI): [M+H]411.2231.

(214) (2) Synthesis of Component A-74. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 98 (82 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-74 (1.88 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 98 is calculated to be about 3.38%.

Example 75: Synthesis of Component A-75

(215) ##STR00105##

(216) (1) Synthesis of Compound 99. The synthesis was carried out according to the method disclosed in the reference (Patchomrnik Abraham; Amit B.; Woodward R. B. J. Am. Chem. Soc. 1970, 92, 6333.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=8.02-7.23 (m, 5H), 7.71 (s, 1H), 7.22 (s, 1H), 4.55 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H]431.1926.

(217) (2) Synthesis of Component A-75. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 99 (86 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-75 (1.85 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 99 is calculated to be about 3.21%.

Example 76: Synthesis of Component A-76

(218) ##STR00106##

(219) (1) Synthesis of Compound 100. The synthesis was carried out according to the method disclosed in the reference (Patchomik Abraham; Amit B.; Woodward R. B. J. Am. Chem. Soc. 1970, 92, 6333.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.55 (s, 2H), 4.25 (q, J=6.5 Hz, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.32 (t, J=6.5 Hz, 3H). MS (ESI): [M+H] 399.1818.

(220) (2) Synthesis of Component A-76. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 100 (80 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-76 (1.69 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 92 is calculated to be about 2.31%.

Example 77: Synthesis of Component A-77

(221) ##STR00107##

(222) (1) Synthesis of Compound 101. The synthesis was carried out according to the method disclosed in the reference (Kalbag, S. M.; Roeske, R. W. J. Am. Chem. Soc. 1975, 97, 440.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.55 (s, 2H), 4.63 (q, J=6.9 Hz, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.67 (s, 3H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H), 1.48 (d, J=6.9 Hz, 3H). MS (ESI): [M+H] 456.2036.

(223) (2) Synthesis of Component A-77. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 101 (91 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-77 (1.82 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 92 is calculated to be about 3.21%.

Example 80: Synthesis of Component A-80

(224) ##STR00108##

(225) (1) Synthesis of Compound 104. The synthesis was carried out according to the method disclosed in the reference (Grazyna Groszek; Agnieszka Nowak-Krol; Barbara Filipek. the J. Med. Chem. 2009, 44, 5103.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=8.04 (s, 1H), 7.42 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.74 (s, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (i, 2H). MS (ESI): [M+H] 399.1832.

(226) (2) Synthesis of Component A-80. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 104 (80 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-80 (1.8 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 104 is calculated to be about 3.32%.

Example 81: Synthesis of Component A-81

(227) ##STR00109##

(228) (1) Synthesis of Compound 105. The synthesis was carried out according to the method disclosed in the reference (Thomas F. Greene; Shu Wang; Mary J. Meegan. J. Med. Chem. 2016, 59, 90.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.95 (s, 1H), 7.12 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.74 (s, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H]399.1832.

(229) (2) Synthesis of Component A-81. To a solution of hyaluronic acid sodium (2 g, 340 kDa) in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 105 (80 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-81 (1.89 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 105 is calculated to be about 3.28%.

Example 82: Synthesis of Component A-82

(230) ##STR00110##

(231) (1) Synthesis of Compound 106. The synthesis was carried out according to the method disclosed in the reference (Yu-Shan; Mohane Selvaraj Coumar; Hsing-Pang Hsieh. J. Med. Chem. 2009, 52, 4941.). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.64 (s, 1H), 7.02 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.74 (s, 2H), 3.32 (dd, J=11.6, 5.7 Hz, 2H), 2.82 (t, J=5.9 Hz, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 399.1832.

(232) (2) Synthesis of Component A-82. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 106 (80 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-82 (1.91 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 106 is calculated to be about 3.26%.

Example 83: Synthesis of Component A-83

(233) ##STR00111##

(234) Synthesis of Component A-83. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added nNB mixture (Compound 92/Compound 95, 60 mg, weight ratio is 1:1) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-83 (1.89 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound NB mixture is calculated to be about 3.42%.

Example 84: Synthesis of Component A-84

(235) ##STR00112##

(236) Synthesis of Component A-84. To a solution of carboxymethyl cellulose (2 g, 90 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 95 (80 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-84 (1.72 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 95 is calculated to be about 2.21%.

Example 85: Synthesis of Component A-85

(237) ##STR00113##

(238) (1) Synthesis of Compound 107. According to the method in Example 71, Compound 107 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.74 (s, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+H] 357.1342.

(239) (2) Synthesis of Component A-85. To a suspension liquid of chitosan (1 g) dissolved in 75 mL isopropanol was sequentially added Compound 107 (0.2 g, 0.56 mmol), EDC-HCl (0.76 g, 3.96 mmol) and NHS (0.46 g, 4.0 mmol), and the reaction was stirred at room temperature for 48 h. After completion of the reaction, the mixture solution was dialyzed with diluted hydrochloric acid solution containing sodium chloride (pH=3.5) for 1 d, dialyzed with distilled water for 1 d, and then freeze-dried to obtain photosensitive chitosan derivatives Compound A-85 (0.82 g). According to its nuclear magnetic resonance spectrum, the grafting degree of the Compound 107 can be calculated to be about 11.3%.

Example 86: Synthesis of Component A-86

(240) ##STR00114##

(241) (1) Synthesis of Compound 108. According to the method in Example 71, Compound 108 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.74 (s, 2H), 3.04 (t, J=7.2 Hz, 2H). MS (ESI): [M+H] 377.0346.

(242) (2) Synthesis of Component A-86. To a solution of PEG-4OH (1 g, 0.05 mmol) dissolved in anhydrous acetonitrile was added K.sub.2CO.sub.3 (55.3 mg, 0.4 mmol) and stirred for 30 min. Then the solution was added Compound 108 (0.15 g, 0.4 mmol) and continued to react at room temperature for 24 h. After completion of the reaction, most of the solvent was removed, reprecipitated in diethyl ether, and washed several times to obtain the photosensitive polyethelene glycol derivative Compound A-86 (0.93 g). According to its nuclear magnetic resonance spectrum, the grafting degree of the Compound 89 can be calculated to be about 95%.

Example 87: Synthesis of Component A-87

(243) ##STR00115## ##STR00116##

(244) (1) Synthesis of Compound 109. To a solution of Compound 108 (0.5 g, 1.29 mmol) and ethylene glycol (0.24 g, 3.87 mmol) dissolved in anhydrous acetonitrile was added K.sub.2CO.sub.3 (0.5 g, 3.87 mmol) as a base and refluxed overnight. After completion of the reaction, the solvent was removed by rotary evaporation under reduced pressure and purified by column chromatography to afford Compound 109 (0.34 g, 72C %). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.79 (t, J=6.1 Hz, 2H), 3.74 (s, 2H), 3.70 (t, J=7.2 Hz, 2H), 3.56 (t, J=7.2 Hz, 2H). MS (ESI): [M+H] 359.1462.

(245) (2) Synthesis of Compound 110. To a solution of Compound 109 (0.64 g, 1.72 mmol) and triethylamine (0.34 g, 3.44 mmol) dissolved in anhydrous dichloromethane was slowly dropwise added methacryloyl chloride (0.27 g, 2.58 mmol) under ice bath conditions, and the reaction was carried out overnight at room temperature. After completion of the reaction, the solvent was removed by rotary evaporation under reduced pressure and purified by column chromatography to afford Compound 110 (0.49 g, 65C %). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.22 (s, 1H), 6.25 (s, 1H), 5.68 (s, 1H), 4.55 (s, 2H), 4.13 (t, J=6.1 Hz, 2H), 3.99 (s, 3H), 3.95 (s, 3H), 3.79 (t, J=6.1 Hz, 2H), 3.74 (s, 2H), 3.70 (t, J=7.2 Hz, 2H), 3.56 (t, J=7.2 Hz, 2H), 1.87 (s, 3H). MS (ESI): [M+H] 427.1725.

(246) (3) Synthesis of Component A-87. Compound 110 (0.28 g, 0.63 mmol), comonomer PEG-MA (0.882 g, 2.52 mmol) and the initiator azobisisobutyronitrile (11 mg) were added into the Shrek tube and dissolved by anhydrous THF. After repeated freeze-vacuum cycle operation, the reaction system was reacted at 75° C. for 24 h. After completion of the reaction, the solution was poured into cold diethyl ether and reprecipitated several times to obtain the photosensitive copolymer derivative Compound A-87 (0.85 g). According to its nuclear magnetic resonance spectrum, it can be calculated that the content of the Compound 110 in the copolymer is about 14.6%. According to GPC, the molecular weight of the synthetic polymer is about 25 kDa. According to the feed ratio, n is 12, x is 10, and y is 40

Example 88: Synthesis of Component A-88

(247) ##STR00117## ##STR00118##

(248) (1) Synthesis of Compound 111. To a solution of vanillin (25 g, 165 mmol) and potassium carbonate (11.4 g, 83 mmol) dissolved in 200 mL acetone was dropwise added benzyl bromide (21.2 g, 181 mmol), and the solution was refluxed at 90° C. for 8 h. Then the reaction was cooled to room temperature, the solvent was removed by rotary evaporation under reduced pressure. The crude was added 100 mL water and extracted three times with ethyl acetate. The combined organic layers were dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent under reduced pressure to give the colorless liquid. It was then recrystallized from 100 mL ethanol to give Compound 111 as white powder (36.2 g, 91%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=9.83 (s, 1H), 7.39 (ddd, J=24.2, 20.7, 7.4 Hz, 7H), 6.98 (d, J=8.2 Hz, 1H), 5.24 (s, 2H), 3.94 (d, J=0.9 Hz, 3H). MS (ESI): [M+Na] 265.0824.

(249) (2) Synthesis of Compound 112. To a solution of Compound 111 (10 g, 41.3 mmol) dissolved in 50 mL acetic anhydride was dropwise added 50 mL nitric acid (65%) under ice bath. The mixture was reacted at room temperature for 30 min. After completion of the reaction, the reaction system was slowly poured into 600 mL ice water to precipitate a yellow solid. The crude was crystallised from ethanol to obtain yellow needle-like product as Compound 112 (9.72 g, 82%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=10.42 (s, 1H), 7.67 (s, 1H), 7.43-7.39 (m, 3H), 7.37 (d, J=7.0 Hz, 1H), 5.26 (s, 2H), 4.01 (s, 3H). MS (ESI): [M+Na]310.0689.

(250) (3) Synthesis of Compound 113. To a solution of Compound 112 (9 g, 31.3 mmol) dissolved in 200 mL methanol was slowly added sodium borohydride (2.37 g, 62.6 mmol) under ice bath, and the mixture was carried out for 30 min at room temperature. After completion of the reaction, the system was acidified with 2 mol/L hydrochloric acid to pH 7.0, and methanol was removed by rotary evaporation under reduced pressure. The crude was added 100 mL water and extracted three times with ethyl acetate, and the combined organic phases was dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent by rotary evaporation under reduced pressure to give Compound 113 as yellow solid (9.06 g, 92%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.77 (s, 1H), 7.49-7.42 (m, 2H), 7.40 (dd, J=8.1, 6.4 Hz, 3H), 7.18 (s, 1H), 5.20 (s, 2H), 4.95 (s, 2H), 4.00 (s, 3H). MS (ESI): [M+Na] 312.0834.

(251) (4) Synthesis of Compound 114. To a solution of Compound 113 (3 g, 10.4 mmol) dissolved in 100 mL anhydrous tetrahydrofuran under protection of Ar.sub.2 was simultaneously added triphenylphosphine (4.08 g, 15.6 mmol) and carbon tetrabromide (5.16 g, 15.6 mmol) under ice bath, and the reaction was carried out for 2 h at room temperature. After completion of the reaction, 6 mL of water was added to quench the reaction system, and then the tetrahydrofuran was removed by rotary evaporation under reduced pressure. The crude was extracted twice with saturated brine and ethyl acetate, and then extracted three times with water and ethyl acetate. The combined organic phases was dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent by rotary evaporation under reduced pressure, then purified by column chromatography (PE:CH.sub.2Cl.sub.2=4:1) to obtain Compound 114 as yellow powder (3.09 g, 85%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.46-7.41 (m, 2H), 7.40-7.30 (m, 3H), 6.93 (s, 1H), 5.17-5.13 (m, 2H), 4.8-4.79 (m, 2H), 3.95 (s, 3H), 1.42 (s, 9H). MS (ESI): [M+Na] 374.0003.

(252) (5) Synthesis of Compound 115. To a solution of Compound 114 (3 g, 8.5 mmol) dissolved in 120 mL acetone under protection of Ar.sub.2 was added L-cysteine methyl ester hydrochloride (2.9 g, 17 mmol) and sodium hydroxide (0.85 g, 21.25 mmol), and the mixture was reacted at room temperature for 2 h. After completion of the reaction, the system was acidified with 4 mol/L hydrochloric acid to pH 7.0, and the acetone was removed by rotary evaporation under reduced pressure. The crude was extracted three times with saturated brine and ethyl acetate, and then extracted three times with water and ethyl acetate. The combined organic phases was dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent by rotary evaporation under reduced pressure, then purified by column chromatography (CH.sub.2Cl.sub.2:CH.sub.3OH=100:3) to obtain Compound 115 as a yellow solid (2.71 g, 78%). .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.45 (d, J=7.0 Hz, 2H), 7.39 (t, J=7.2 Hz, 3H), 6.95 (s, 1H), 5.18 (s, 2H), 4.13 (q, J=13.6 Hz, 2H), 3.98 (s, 3H), 3.73 (s, 3H), 3.65 (m, 1H), 2.91 (dd, J=13.7, 4.6 Hz, 1H), 2.75 (dd, J=13.6, 7.5 Hz, 1H). MS (ESI): [M+H] 407.1277.

(253) (6) Synthesis of Compound 116. To a solution of triethylene glycol (22 g, 113.2 mmol) dissolved in dry tetrahydrofuran was added sodium metal (40 mg, 1.74 mmol), the mixture was stirred until sodium was completely dissolved. The mixture was added tert-butyl acrylate (8 g, 62.4 mmol) and reacted at room temperature for 20 h. After completion of the reaction, the system was acidified with 1 mol/L hydrochloric acid to pH 7.0, and tetrahydrofuran was removed by rotary evaporation under reduced pressure. The crude was extracted three times with saturated brine and ethyl acetate, and then extracted three times with water and ethyl acetate. The combined organic phases was dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent by rotary evaporation under reduced pressure. Without further purification, Compound 116 (16.0 g, 80%) as a colorless oily liquid was obtained. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=3.78-3.69 (m, 4H), 3.69-3.54 (m, 14H), 2.52 (dd, J=4.3, 2.1 Hz, 2H), 1.45 (s, 9H). MS (ESI): [M+Na] 345.1872.

(254) (7) Synthesis of Compound 117. To a solution of Compound 116 (10 g, 31.2 mmol) dissolved in anhydrous dichloromethane was added anhydrous triethylamine (5.2 mm L, 37.4 mmol) and gradually dropwise added p-methylbenzenesulfonyl chloride (8.9 g, 46.8 mmol) in 40 mL dry dichloromethane under ice bath conditions, and the mixture was reacted at room temperature for 6 h. After completion of the reaction, the system was added 200 mL of water and extracted three times with dichloromethane. The combined organic phases were dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent by rotary evaporation under reduced pressure, then purified by column chromatography (CH.sub.2Cl.sub.2:CH.sub.3OH=50:1) to obtain Compound 117 (12.6 g, 85%) as a pale yellow oily liquid. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.79-7.74 (m, 2H), 7.32 (d, J=8.5 Hz, 2H), 4.21-3.90 (m, 2H), 3.66 (dd, J=5.7, 2.8 Hz, 4H), 3.62-3.35 (m, 12H), 2.47 (dd, J=8.3, 4.8 Hz, 2H), 2.42 (d, J=3.2 Hz, 3H), 1.42 (d, J=3.4 Hz, 9H). MS (ESI): [M+Na] 499.1964.

(255) (8) Synthesis of Compound 118. Compound 117 (10 g, 21.0 mmol) and lithium bromide (4.8 g, 31.5 mmol) were dissolved in 30 mL of N,N-dimethylformamide and heated to 80° C. to react for 1 h. After completion of the reaction, N,N-dimethylformamide was removed the solvent by rotary evaporation under reduced pressure. The crude was extracted three times with water and dichloromethane. The combined organic phases were dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent by rotary evaporation under reduced pressure, then purified by column chromatography to obtain Compound 118 (7.3 g, 90%) as a pale yellow oily liquid. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=3.72 (t, J=6.3 Hz, 2H), 3.62 (t, J=6.6 Hz, 2H), 3.58 (dd, J=2.6, 1.5 Hz, 8H), 3.54 (d, J=2.2 Hz, 4H), 3.39 (t, J=6.3 Hz, 2H), 2.42 (t, J=6.6 Hz, 2H), 1.36 (s, 9H). MS (ESI): [M+Na] 409.1005.

(256) (9) Synthesis of Compound 119. To a solution of Compound 118 (5 g, 13.0 mmol) dissolved in 30 mL anhydrous dichloromethane was added 10 mL trifluoroacetic acid, and the mixture was reacted at room temperature for 30 min. After completion of the reaction, the solvent was removed by rotary evaporation under reduced pressure. Then the crude was re-dissolved with dichloromethane and ethyl acetate and the solvent was removed by rotary evaporation under reduced pressure to absolutely remove trifluoroacetic acid. Without further purification, Compound 119 (3.9 g, 92%) as a yellow oily liquid was obtained. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=3.72 (t, J=6.3 Hz, 2H), 3.67 (t, J=6.3 Hz, 2H), 3.58 (dd, J=4.1, 1.7 Hz, 4H), 3.57 (s, 4H), 3.55 (s, 4H), 3.39 (t, J=6.3 Hz, 2H), 2.54 (t, J=6.3 Hz, 2H). MS (ESI): [M+Na] 353.0414.

(257) (10) Synthesis of Compound 120. To a solution of Compound 115 (2.0 g, 4.9 mmol) and Compound 119 (2.0 g, 5.9 mmol) dissolved in 40 mL anhydrous dichloromethane was added benzotriazol-1-yl-oxytripyrrolidinyl hexafluorophosphate (5.1 g, 9.8 mmol) and anhydrous triethylamine (1.4 mL, 9.8 mmol), and the mixture was reacted at room temperature for 1 h. After completion of the reaction, the system was extracted three times with dichloromethane and water. The combined organic phases were dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent by rotary evaporation under reduced pressure, then purified by column chromatography (CH.sub.2Cl.sub.2:CH.sub.3OH=100:3) to obtain Compound 120 (2.2 g, 62%) as a yellow solid. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.71 (s, 1H), 7.45 (d, J=7.0 Hz, 2H), 7.39 (t, J=7.2 Hz, 3H), 6.95 (s, 1H), 5.18 (s, 2H), 4.42 (m, 1H), 4.13 (q, J=13.6 Hz, 2H), 3.98 (s, 3H), 3.73 (s, 3H), 3.68-3.63 (m, 2H), 3.62-3.55 (m, 4H), 3.58-3.53 (m, 12H), 3.37 (t, J=6.3 Hz, 2H), 2.43 (t, J=5.8 Hz, 2H). MS (ESI): [M+Na] 741.1529.

(258) (11) Synthesis of Compound 121. Compound 120 (2 g, 2.8 mmol) was dissolved in 20 mL trifluoroacetic acid and reacted at 45° C. for 8 h. After completion of the reaction, trifluoroacetic acid was removed by rotary evaporation under reduced pressure and extracted three times with dichloromethane and water. The combined organic phases were dried over anhydrous Na.sub.2SO.sub.4, filtered and removed the solvent by rotary evaporation under reduced pressure, then purified by column chromatography (CH.sub.2Cl.sub.2:CH.sub.3OH=25:1) to obtain Compound 121 (1.4 g, 82%) as a yellow liquid. .sup.1H NMR (400 MHz, CDCl.sub.3): δ=7.60 (s, 1H), 6.79 (s, 1H), 4.73-4.66 (m, 1H), 3.99 (d, J=12.9 Hz, 2H), 3.97 (s, 3H), 3.73 (s, 3H), 3.70 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 4H), 3.58-3.53 (m, 12H), 3.37 (t, J=6.3 Hz, 2H), 2.43 (t, J=5.8 Hz, 2H). MS (ESI): [M+Na] 651.1026.

(259) (12) Synthesis of Compound 122. To a solution of Compound 121 (0.5 g, 0.8 mmol) in 400 mL acetone was added potassium carbonate (0.2 g, 1.6 mmol), and the mixture was refluxed at 75° C. for 4 h. After completion of the reaction, the system was filtrated to remove insoluble matter and removed solvent by rotary evaporation under reduced pressure. Then, the crude was purified by column chromatography (CH.sub.2Cl.sub.2:CH.sub.3OH=25:1) to obtain Compound 122 (0.27 g, 61%) as a yellow solid. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 3.97 (s, 3H), 3.73 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 4H), 3.52-3.39 (m, 14H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na]569.1782.

(260) (13) Synthesis of Compound 123. Compound 122 (0.2 g, 3.7 mmol) was dissolve in 20 mL anhydrous ethylenediamine and reacted at room temperature for 6 h. After completion of the reaction, the ethylenediamine was removed by rotary evaporation under reduced pressure. The crude was purified by column chromatography (CH.sub.2Cl.sub.2:CH.sub.3OH:triethylamine=100:8:0.5) to obtain Compound 123 (0.19 g, 89%) as a yellow powder. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 3.97 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 597.2211.

(261) ##STR00119##

(262) (14) Synthesis of Component A-88. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 123 (115 mg, 0.2 mmol) in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-88 (1.87 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 123 can be calculated to be about 3.49%.

Example 89: Synthesis of Component A-89

(263) ##STR00120##

(264) (1) Synthesis of Compound 124. According to the method in Example 88, Compound 124 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.96 (s, 2H), 4.42 (m, 1H), 3.97 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 559.2642.

(265) (2) Synthesis of Component A-89. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 124 (111 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-89 (1.82 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 124 can be calculated to be about 3.15%.

Example 90: Synthesis of Component A-90

(266) ##STR00121##

(267) (1) Synthesis of Compound 125. According to the method in Example 88, Compound 125 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.26 (s, 2H), 4.42 (m, 1H), 3.97 (s, 3H), 3.42 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 558.2725.

(268) (2) Synthesis of Component A-90. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 125 (111 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-90 (1.87 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 125 can be calculated to be about 3.27%.

Example 91: Synthesis of Component A-91

(269) ##STR00122##

(270) (1) Synthesis of Compound 126. According to the method in Example 88, Compound 126 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 5.16 (m, 1H), 4.42 (m, 1H), 3.97 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H), 1.33 (d, J=6.9 Hz, 3H). MS (ESI): [M+Na] 589.2517.

(271) (2) Synthesis of Component A-91. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 126 (118 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-91 (1.73 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 126 can be calculated to be about 3.14%.

Example 93: Synthesis of Component A-93

(272) ##STR00123##

(273) (1) Synthesis of Compound 128. According to the method in Example 88, Compound 128 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 5.82 (m, 1H), 4.76 (s, 2H), 3.97 (s, 3H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 589.2143.

(274) (2) Synthesis of Component A-93. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 128 (118 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-93 (1.73 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 128 can be calculated to be about 3.15%.

Example 94: Synthesis of Component A-94

(275) ##STR00124##

(276) (1) Synthesis of Compound 129. According to the method in Example 88, Compound 129 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.76 (s, 2H), 4.13 (t, J=7.2 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+Na] 575.2332.

(277) (2) Synthesis of Component A-94. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 129 (115 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-94 (1.84 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 129 can be calculated to be about 2.47%.

Example 95: Synthesis of Component A-95

(278) ##STR00125##

(279) (1) Synthesis of Compound 130. According to the method in Example 88, Compound 130 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.76 (s, 2H), 4.13 (t, J=7.2 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.69-2.55 (m, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+Na] 576.2242.

(280) (2) Synthesis of Component A-95. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 130 (115 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-95 (1.75 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 130 can be calculated to be about 3.07%.

Example 98: Synthesis of Component A-98

(281) ##STR00126##

(282) (1) Synthesis of Compound 133. According to the method in Example 88, Compound 133 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=8.11 (m, 1H), 7.27 (m, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 3.97 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 12H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 531.2143.

(283) (2) Synthesis of Component A-98. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 133 (106 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-98 (1.78 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 133 can be calculated to be about 3.31%.

Example 99: Synthesis of Component A-99

(284) ##STR00127##

(285) (1) Synthesis of Compound 134. According to the method in Example 88, Compound 134 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 3.97 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 575.2342.

(286) (2) Synthesis of Component A-99. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 134 (115 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-99 (1.84 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 134 can be calculated to be about 3.06%.

Example 100: Synthesis of Component A-100

(287) ##STR00128##

(288) (1) Synthesis of Compound 135. According to the method in Example 88, Compound 135 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.54 (m, 1H), 7.03 (m, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 3.97 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 20H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 619.2652.

(289) (2) Synthesis of Component A-100. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 135 (124 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-100 (1.84 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 135 can be calculated to be about 3.16%.

Example 101: Synthesis of Component A-101

(290) ##STR00129##

(291) (1) Synthesis of Compound 136. According to the method in Example 88, Compound 136 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=7.2 Hz, 2H), 3.73 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.86 (d, J=7.6 Hz, 2H), 2.76 (d, J=7.6 Hz, 2H), 2.49-2.35 (m, 2H), 2.44 (t, J=7.2 Hz, 2H), 2.26-2.17 (m, 2H). MS (ESI): [M+Na] 661.2745.

(292) (2) Synthesis of Component A-101. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 136 (132 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-101 (1.77 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 136 can be calculated to be about 3.21%.

Example 102: Synthesis of Component A-102

(293) ##STR00130##

(294) Synthesis of Component A-102. To a solution of hyaluronic acid sodium (2 g, 340 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added cNB mixture (Compound 123/Compound 136, 60 mg, mass ratio 1:1) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-102 (1.89 g). According to the nuclear magnetic resonance spectrum, the grafting degree of the cNB mixture (Compound 123/Compound 136) can be calculated to be about 3.52%.

Example 103: Synthesis of Component A-103

(295) ##STR00131##

(296) Synthesis of Component A-103. To a solution of carboxymethyl cellulose (2 g, 90 kDa) dissolved in 100 mL 0.01 M 2-(N-morpholine) mesylate (MES) buffer solution (pH=5.2) was added Compound 123 (115 mg, 0.2 mmol) dissolved in 10 mL dimethyl sulfoxide (DMSO). Then, DMTMM (0.4 g, 1.5 mmol) dissolved in 3 mL water was added into the above solution three times with an interval of 1 h, and the mixture was stirred for 24 hours in the dark 35° C. Then, the reaction solution was poured into a dialysis bag (MWCO 7000), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-103 (1.71 g). According to the nuclear magnetic resonance spectrum, the grafting degree of Compound 123 can be calculated to be about 2.41%.

Example 104: Synthesis of Component A-104

(297) ##STR00132##

(298) (1) Synthesis of Compound 137. According to the method in Example 88, Compound 137 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 3.97 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 533.1845.

(299) (2) Synthesis of Component A-104. To a suspension liquid of chitosan (1 g) dissolved in 75 mL isopropanol was sequentially added Compound 137 (0.2 g, 0.35 mmol), EDC-HCl (0.76 g, 3.96 mmol) and NHS (0.46 g, 4.0 mmol), and the reaction was stirred at room temperature for 48 h. After completion of the reaction, the mixture solution was dialyzed with diluted hydrochloric acid solution containing sodium chloride (pH=3.5) for 1 d, dialyzed with distilled water for 1 d, and then freeze-dried to obtain photosensitive chitosan derivatives Compound A-104 (0.82 g). According to its nuclear magnetic resonance spectrum, the grafting degree of the Compound 137 can be calculated to be about 12.5%.

Example 105: Synthesis of Component A-105

(300) ##STR00133##

(301) (1) Synthesis of Compound 138. According to the method in Example 88, Compound 138 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.93 (s, 3H), 3.72 (d, J=6.3 Hz, 2H), 3.62-3.55 (m, 2H), 3.52-3.39 (m, 16H), 3.04 (t, J=7.2 Hz, 2H), 2.49-2.35 (m, 2H). MS (ESI): [M+Na] 640.1134.

(302) (2) Synthesis of Component A-105. To a solution of PEG-4OH (1 g, 0.05 mmol) dissolved in anhydrous acetonitrile was added K.sub.2CO.sub.3 (55.3 mg, 0.4 mmol) and stirred for 30 min. Then the solution was added Compound 138 (0.23 g, 0.4 mmol) and continued to react at room temperature for 24 h. After the reaction was completed, most of the solvent was removed, reprecipitated in diethyl ether, and washed several times to obtain the photosensitive polyethelene glycol derivative Compound A-105 (0.85 g). According to its nuclear magnetic resonance spectrum, the grafting degree of the Compound 138 can be calculated to be about 95.3%.

Example 106: Synthesis of Component A-106

(303) ##STR00134##

(304) (1) Synthesis of Compound 139. According to the method in Example 88, Compound 139 was prepared by conventional chemical means. .sup.1H NMR (400 MHz, DMSO): δ=7.71 (s, 1H), 7.17 (s, 1H), 6.25 (s, 1H), 5.68 (s, 1H), 4.76 (s, 2H), 4.42 (m, 1H), 4.13 (t, J=6.1 Hz, 2H), 3.93 (s, 3H), 3.79 (t, J=6.1 Hz, 2H), 3.72 (d, J=6.3 Hz, 2H), 3.70 (t, J=7.2 Hz, 2H), 3.62-3.55 (m, 2H), 3.56 (t, J=7.2 Hz, 2H), 3.52-3.39 (m, 16H), 2.49-2.35 (m, 2H), 1.87 (s, 3H). MS (ESI): [M+Na] 689.2523.

(305) (2) Synthesis of Component A-106. Compound 139 (0.28 g, 0.63 mmol), comonomer PEG-MA (0.882 g, 2.52 mmol) and the initiator azobisisobutyronitrile (11 mg) were added into the Shrek tube and dissolved by anhydrous THF. After repeated freeze-vacuum cycle operation, the reaction system was reacted at 75° C. for 24 h. After completion of the reaction, the solution was poured into cold diethyl ether and reprecipitated several times to obtain the photosensitive copolymer derivative Compound A-106 (0.85 g). According to its nuclear magnetic resonance spectrum, it can be calculated that the content of the Compound 139 in the copolymer is about 15.4%. According to GPC, the molecular weight of the synthetic polymer is about 25 kDa. According to the feed ratio, n is 12, x is 10, and y is 40.

Example 107: Synthesis of Component A-107

(306) ##STR00135##

(307) Synthesis of Component A-107. To a solution of hyaluronic acid (1 g, 48 kDa) dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive hyaluronic acid derivative Compound A-107 (0.92 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 54%.

Example 108: Synthesis of Component A-108

(308) ##STR00136##

(309) Synthesis of Component A-108. To a solution of carboxymethyl cellulose (1 g, 90 kDa) dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-108 (0.89 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 43%.

Example 109: Synthesis of Component A-109

(310) ##STR00137##

(311) Synthesis of Component A-109. To a solution of alginate (1 g, 48 kDa) in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-109 (0.87 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 57%.

Example 110: Synthesis of Component A-110

(312) ##STR00138##

(313) Synthesis of Component A-110. To a solution of chondroitin sulfate (1 g) in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-110 (0.91 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 49%.

Example 111: Synthesis of Component A-111

(314) ##STR00139##

(315) Synthesis of Component A-111. To a solution of dextran (6 g, 70 kDa) dissolved in 60 mL anhydrous dimethyl sulfoxide (DMSO) was added 2 mL triethylamine (TEA) and 0.56 mL acryloyl chloride dissolved in 10 mL dichloromethane (DCM), the mixture was reacted for 10 h. After completion of the reaction, the reaction solution was poured into ethanol to reprecipitate. The crude product obtained by filtration was redissolved in deionized water and dialyzed for 2-3 d, and then lyophilized to obtain photosensitive dextran derivative Compound A-111 (5.8 g). According to the nuclear magnetic resonance spectrum, the content of the double bond can be calculated to be about 24%.

Example 112: Synthesis of Component A-112

(316) ##STR00140##

(317) Synthesis of Component A-112. To a solution of carboxymethylchitosan (1 g) dissolved in 100 mL deionized water was added 4 mL glycidyl methacrylate and 2 mL 5M NaOH at 40° C., the mixture was reacted for 2-3 h. The reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and freeze-dried to obtain a photosensitive carboxymethylchitosan derivative Compound A-112 (0.88 g). According to the nuclear magnetic resonance spectrum, the content of the double bond can be calculated to be about 32%.

Example 113: Synthesis of Component A-113

(318) ##STR00141##

(319) Synthesis of Component A-113. To a solution of gelatin (1 g) dissolved in 10 mL D-PBS was added 0.5 mL methacrylic anhydride, and the mixture was reacted for 2-3 h at 50° C. After completion of the reaction, the system was diluted with 40 mL D-PBS. Then, it was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive gelatin derivative Compound A-113 (0.93 g). According to the nuclear magnetic resonance spectrum, the content of the double bond can be calculated to be about 56%.

Example 114: Synthesis of Component A-114

(320) ##STR00142##

(321) Synthesis of Component A-114. To a solution of PEG-20H (10 kDa, 10 g) dissolved in anhydrous dichloromethane was added triethylamine (0.28 mL, 2 mmol) and then slowly dropwise added acryloyl chloride (0.18 g, 2 mmol) dissolved in dichloromethane, and the reaction was stirred for 12 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive polyethylene glycol derivative Compound A-114 (9.8 g). According to the nuclear magnetic resonance spectrum, the content of the double bond can be calculated to be about 98%.

Example 115: Synthesis of Component A-115

(322) ##STR00143##

(323) Synthesis of Component A-115. To a solution of PEG-4OH (10 kDa, 10 g) dissolved in anhydrous dichloromethane was added triethylamine (0.56 mL, 4 mmol) and slowly dropwise added acryloyl chloride (0.36 g, 4 mmol) dissolved in dichloromethane, and the reaction was stirred for 12 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive polyethylene glycol derivative Compound A-115 (9.3 g). According to the nuclear magnetic resonance spectrum, the content of the double bond can be calculated to be about 96%.

Example 116: Synthesis of Component A-116

(324) ##STR00144##

(325) Synthesis of Component A-116. To a solution of Component A-1 chondroitin sulfate (1 g) in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-116 (0.91 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 54%.

Example 117: Synthesis of Component A-117

(326) ##STR00145##

(327) Synthesis of Component A-117. To a solution of Component A-2 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-117 (0.87 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 51%.

Example 118: Synthesis of Component A-118

(328) ##STR00146##

(329) Synthesis of Component A-118. To a solution of Component A-8 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-118 (0.86 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 44%.

Example 119: Synthesis of Component A-119

(330) ##STR00147##

(331) Synthesis of Component A-119. To a solution of Component A-28 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-119 (0.85 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 43%.

Example 120: Synthesis of Component A-120

(332) ##STR00148##

(333) Synthesis of Component A-120. To a solution of Component A-29 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-120 (0.93 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 55%.

Example 121: Synthesis of Component A-121

(334) ##STR00149##

(335) Synthesis of Component A-121. To a solution of Component A-30 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-121 (0.85 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 49%.

Example 122: Synthesis of Component A-122

(336) ##STR00150##

(337) Synthesis of Component A-122. To a solution of Component A-37 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-122 (0.91 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 42%.

Example 123: Synthesis of Component A-123

(338) ##STR00151##

(339) Synthesis of Component A-123. To a solution of Component A-43 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-123 (0.84 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 56%.

Example 124: Synthesis of Component A-124

(340) ##STR00152##

(341) Synthesis of Component A-124. To a solution of Component A-45 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-124 (0.92 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 48%.

Example 125: Synthesis of Component A-125

(342) ##STR00153##

(343) Synthesis of Component A-125. To a solution of Component A-49 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-125 (0.94 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 24%.

Example 126: Synthesis of Component A-126

(344) ##STR00154##

(345) Synthesis of Component A-126. To a solution of Component A-51 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-126 (0.87 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 46%.

Example 127: Synthesis of Component A-127

(346) ##STR00155##

(347) Synthesis of Component A-127. To a solution of Component A-52 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-127 (0.85 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 57%.

Example 128: Synthesis of Component A-128

(348) ##STR00156##

(349) Synthesis of Component A-128. To a solution of Component A-53 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-128 (0.93 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 47%.

Example 129: Synthesis of Component A-129

(350) ##STR00157##

(351) Synthesis of Component A-129. To a solution of Component A-62 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-129 (0.90 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 58%.

Example 130: Synthesis of Component A-130

(352) ##STR00158##

(353) Synthesis of Component A-130. To a solution of Component A-63 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-130 (0.89 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 46%.

Example 131: Synthesis of Component A-131

(354) ##STR00159##

(355) Synthesis of Component A-131. To a solution of Component A-64 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-131 (0.87 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 58%.

Example 132: Synthesis of Component A-132

(356) ##STR00160##

(357) Synthesis of Component A-132. To a solution of Component A-66 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-132 (0.92 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 46%.

Example 133: Synthesis of Component A-133

(358) ##STR00161##

(359) Synthesis of Component A-133. To a solution of Component A-67 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-133 (0.91 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 47%.

Example 134: Synthesis of Component A-134

(360) ##STR00162##

(361) Synthesis of Component A-134. To a solution of Component A-68 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-134 (0.87 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 52%.

Example 135: Synthesis of Component A-135

(362) ##STR00163##

(363) Synthesis of Component A-135. To a solution of Component A-70 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-135 (0.92 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 47%.

Example 136: Synthesis of Component A-136

(364) ##STR00164##

(365) Synthesis of Component A-136. To a solution of Component A-71 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-136 (0.86 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 51%.

Example 137: Synthesis of Component A-137

(366) ##STR00165##

(367) Synthesis of Component A-137. To a solution of Component A-72 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-137 (0.93 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 45%.

Example 138: Synthesis of Component A-138

(368) ##STR00166##

(369) Synthesis of Component A-138. To a solution of Component A-80 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-138 (0.88 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 48%.

Example 139: Synthesis of Component A-139

(370) ##STR00167##

(371) Synthesis of Component A-139. To a solution of Component A-81 dissolved in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-139 (0.88 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 46%.

Example 140: Synthesis of Component A-140

(372) ##STR00168##

(373) Synthesis of Component A-140. To a solution of Component A-82 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-140 (0.91 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 57%.

Example 141: Synthesis of Component A-141

(374) ##STR00169##

(375) Synthesis of Component A-141. To a solution of Component A-84 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-141 (0.92 g). According to 5 the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 44%.

Example 142: Synthesis of Component A-142

(376) ##STR00170##

(377) Synthesis of Component A-142. To a solution of Component A-85 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-142 (0.87 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 56%.

Example 143: Synthesis of Component A-143

(378) ##STR00171##

(379) Synthesis of Component A-143. To a solution of Component A-86 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-143 (0.91 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 48%.

Example 144: Synthesis of Component A-144

(380) ##STR00172##

(381) Synthesis of Component A-144. To a solution of Component A-88 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-144 (0.89 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 52%.

Example 145: Synthesis of Component A-145

(382) ##STR00173##

(383) Synthesis of Component A-145. To a solution of Component A-89 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-145 (0.81 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 43%.

Example 146: Synthesis of Component A-146

(384) ##STR00174##

(385) Synthesis of Component A-146. To a solution of Component A-90 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-146 (0.84 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 49%.

Example 147: Synthesis of Component A-147

(386) ##STR00175##

(387) Synthesis of Component A-147. To a solution of Component A-91 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-147 (0.92 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 46%.

Example 148: Synthesis of Component A-148

(388) ##STR00176##

(389) Synthesis of Component A-148. To a solution of Component A-98 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5 M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-148 (0.94 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 56%.

Example 149: Synthesis of Component A-149

(390) ##STR00177##

(391) Synthesis of Component A-149. To a solution of Component A-99 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-149 (0.87 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 51%.

Example 150: Synthesis of Component A-150

(392) ##STR00178##

(393) Synthesis of Component A-150. To a solution of Component A-100 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-150 (0.88 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 47%.

Example 151: Synthesis of Component A-151

(394) ##STR00179##

(395) Synthesis of Component A-151. To a solution of Component A-101 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-151 (0.91 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 45%.

Example 152: Synthesis of Component A-152

(396) ##STR00180##

(397) Synthesis of Component A-152. To a solution of Component A-103 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-152 (0.84 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 43%.

Example 153: Synthesis of Component A-153

(398) ##STR00181##

(399) Synthesis of Component A-153. To a solution of Component A-104 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-153 (0.89 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 50%.

Example 154: Synthesis of Component A-154

(400) ##STR00182##

(401) Synthesis of Component A-154. To a solution of Component A-105 in 100 mL deionized water was added 4 mL methacrylic anhydride at 0-4° C. The solution was slowly added 2 mL 5M NaOH and reacted for 24 h. Then, the reaction solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain a photosensitive carboxymethyl cellulose derivative Compound A-154 (0.94 g). According to the nuclear magnetic resonance spectrum, the double bond content can be calculated to be about 43%.

Example 155: Synthesis of Photoinitiator-LAP

(402) ##STR00183##

(403) Synthesis of LAP. Dimethoxyphenylphosphine (3.0 g, 0.018 mol) placed in 250 mL three-necked flask under protection of argon was added 2, 4, 6-trimethylbenzoyl chloride (3.2 g, 0.018 mol), and the reaction was stirred at room temperature for 18 h. Then, lithium bromide (6.1 g, 0.072 mol) dissolved in 100 mL of 2-butanone was added to the above reaction solution and heated to 50° C. for 10 min, a precipitate formed. After cooling to room temperature for 4 h, it was filtered, and the obtained crude product was washed twice with 2-butanone, and dried to obtain LAP (6.0 g) as a white solid.

Example 156: Synthesis of Component C-10

(404) ##STR00184##

(405) Synthesis of Component C-10. To a solution of carboxymethylcellulose (CMC, 400 mg) in 50 mL distilled water was added hydroxybenzotriazole (HOBt, 153 mg), dihydrazine (90 mg) and 1-ethyl-(3-dimethyl amine propyl) carbodiimine hydrochloride (EDC-HCl, 90 mg), the mixture was stirred at room temperature for 48 h. After completion of the reaction, the reaction solution was added to a dialysis bag and dialyzed against dilute hydrochloric acid solution containing sodium chloride (pH=3.5) for 1 d, and dialyzed against distilled water for 1 d, then freeze-dried to obtain the carboxymethylcellulose photosensitive polymer derivative modified by hydrazine (410 mg). The grafting degree of hydrazine tested by TBNS method was about 10%.

Example 157: Synthesis of Component C-11

(406) ##STR00185##

(407) Synthesis of Component C-11. To a solution of hyaluronic acid (HA, 400 mg) in 50 mL distilled water was added hydroxybenzotriazole (HOBt, 153 mg), carbonyl hydrazide (CDH, 90 mg) and 1-ethyl-(3-dimethyl amine propyl) carbodiimine hydrochloride (EDC-HCl, 90 mg), the mixture was stirred at room temperature for 48 h. After completion of the reaction, the reaction solution was added to a dialysis bag and dialyzed against dilute hydrochloric acid solution containing sodium chloride (pH=3.5) for 1 d, and dialyzed against distilled water for 1 d, then freeze-dried to obtain the HA-CDH (410 mg). The grafting degree of hydrazine tested by TBNS method was about 10%.

Example 158: Synthesis of Component C-12

(408) ##STR00186##

(409) Synthesis of Component C-12. To a solution of hyaluronic acid (HA, 400 mg) in 50 mL distilled water was added hydroxybenzotriazole (HOBt, 153 mg), dihydrazide oxalate (ODH, 90 mg) and 1-ethyl-(3-dimethyl amine propyl) carbodiimine hydrochloride (EDC-HCl, 90 mg), the mixture was stirred at room temperature for 48 h. After completion of the reaction, the reaction solution was added to a dialysis bag and dialyzed against dilute hydrochloric acid solution containing sodium chloride (pH=3.5) for 1 d, and dialyzed against distilled water for 1 d, then freeze-dried to obtain HA-ODH (410 mg). The grafting degree of hydrazine tested by TBNS method was about 10%.

Example 159: Synthesis of Component C-13

(410) ##STR00187##

(411) Synthesis of Component C-13. To a solution of hyaluronic acid (HA, 400 mg) in 50 mL distilled water was added hydroxybenzotriazole (HOBt, 153 mg), dihydrazide adipate (ADH, 90 mg) and 1-ethyl-(3-dimethyl amine propyl) carbodiimine hydrochloride (EDC-HCl, 90 mg), the mixture was stirred at room temperature for 48 h. After completion of the reaction, the reaction solution was added to a dialysis bag and dialyzed against dilute hydrochloric acid solution containing sodium chloride (pH=3.5) for 1 d, and dialyzed against distilled water for 1 d, then freeze-dried to obtain HA-ADH (410 mg). The grafting degree of hydrazine tested by TBNS method was about 10%.

Example 160: Synthesis of Component C-14

(412) ##STR00188##

(413) Synthesis of Component C-14. To a solution of PEG-4OH (2 g, 97.3 μmol) and N-hydroxyphthalimide (634.6 mg, 3.89 mmol) in anhydrous dichloromethane was slowly added triphenylphosphine (1.02 g, 3.89 mmol) under ice bath, the mixture was reacted under ice bath for about 30 min. The above solution was slowly added diisopropyl azodicarboxylate (765.9 μL, 3.89 mmol) in dry dichloromethane and reacted at room temperature for 1 d. After completion of the reaction, the system was reprecipitated with diethyl ether. The above precipitate (0.25 g, 11.8 μmol) was re-dissolved in acetonitrile and added hydrazine monohydrate (22.9 μL, 473 μmol), the mixture was stirred for 2 h. The above mixture solution was added dichloromethane and filtered. The solvent was removed by rotary evaporation under reduced pressure to obtain four-arm polyethylene glycol modified by hydroxylamine (PEG-4ONH.sub.2).

Example 161: Synthesis of Component C-15

(414) ##STR00189##

(415) Synthesis of Component C-15. To a solution of dextran (2 g, 97.3 μmol) and N-hydroxyphthalimide (634.6 mg, 3.89 mmol) in anhydrous dichloromethane was slowly added triphenylphosphine (1.02 g, 3.89 mmol) under ice bath, the mixture was reacted under ice bath for about 30 min. The above solution was slowly added diisopropyl azodicarboxylate (765.9 μL, 3.89 mmol) in dry dichloromethane and reacted at room temperature for 1 d. After completion of the reaction, the system was reprecipitated with diethyl ether. The above precipitate (0.25 g, 11.8 μmol) was re-dissolved in acetonitrile and added hydrazine monohydrate (22.9 μL, 473 μmol), the mixture was stirred for 2 h. The above mixture solution was added dichloromethane and filtered. The solvent was removed by rotary evaporation under reduced pressure to obtain dextran modified by hydroxylamine (Dex-ONH.sub.2).

Example 162: Synthesis of Component C-18

(416) ##STR00190##

(417) Synthesis of Component C-18. To a solution of hyaluronic acid (0.5 g, 48 kDa) in 50 mL distilled water was added hydroxybenzotriazole (HOBt, 0.2 g), 1-ethyl-(3-dimethylaminopropyl) carbodiimine hydrochloride (EDC-HCl, 0.1 g), 3, 3′-dithiobis (propionide) (DTP, 0.1 g). The mixture was adjusted to pH 4.75 with dilute hydrochloric acid solution and reacted for 24 h. Then, the solution was added DTT and continued to react for 5 h. After completion of the reaction, the solution was poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and freeze-dried to obtain HA-SH (0.45 g). According to the nuclear magnetic resonance spectrum, the grafting degree of sulfhydryl group can be calculated to be about 20%.

Example 163: Synthesis of Component C-19

(418) ##STR00191##

(419) Synthesis of Component C-19. To a solution of carboxymethyl chitosan (1 g) in 100 mL of deionized water was added N-acetylcysteine (1.77 g, 10 mmol) and 1-ethyl-(3-dimethylaminopropyl) carbodiimine hydrochloride (EDC-HCl, 1.91 g, 10 mmol). The mixture was adjusted to pH 5 with hydrochloric acid, and reacted at room temperature for 5 h. Then, the solution was poured into a dialysis bag (MWCO 3500), dialyzed against 5 mM HCl solution for 1 d, and dialyzed against 5 mM HCl/1% NaCl solution for 1 d, then dialyzed against 1 mM HCl solution for 1 d, lyophilized to obtain CMCh-SH (0.9 g). According to the nuclear magnetic resonance spectrum, the grafting degree of sulfhydryl group can be calculated to be about 10%.

Example 164: Synthesis of Component C-20

(420) ##STR00192##

(421) Synthesis of Component C-20. To a solution of dextran (40 kDa, 12 g, 0.3 mmol) in 50 mL DMSO was added 3-mercaptopropionic acid (636.8 mg, 6.0 mmol), 1, 3-dicyclohexyl carbodiimine (910.7 mg, 9.0 mmol) and 4-dimethylaminylpyridine (1099.5 mg, 9.0 mmol), and the solution was reacted at room temperature for 48 h. Then, it was reprecipitated in acetone. The crude product was dissolved in water, poured into a dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, and lyophilized to obtain Dex-SH (11.5 g). According to the nuclear magnetic resonance spectrum, the grafting degree of sulfhydryl group can be calculated to be about 20%.

Example 165: Synthesis of Component C-21

(422) ##STR00193##

(423) Synthesis of Component C-21. To a solution of heparin (0.5 g, 12 kDa) in 50 mL distilled water was added hydroxybenzotriazole (HOBt, 0.2 g), 1-ethyl-(3-dimethylamine-propyl) carbodiimine hydrochloride (EDC-HCl, 0.1 g) and mercaptoethylamine (0.1 g), the solution was adjusted to pH 5-6 with dilute hydrochloric acid solution and reacted for 24 h. The solution was poured into dialysis bag (MWCO 3500), dialyzed against deionized water for 2-3 d, freeze-dried to obtain Hep-SH (0.45 g). According to the nuclear magnetic resonance spectrum, the grafting degree of sulfhydryl group can be calculated to be about 20%.

Example 166: Photo-Crosslinking Method for Preparing Hydrogel

(424) Different hydrogel precursor solutions were prepared according to the process in the invention at 37° C. as shown in Table 1.

(425) TABLE-US-00001 TABLE 1 B Component Component Component Component B-1/ Component B-3/ Component B-3/ A B-1 B-2 B-3 Component C . . . Component C . . . Component C . . . concentration Component 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % A-1 Component 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % . . . Component 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % A-154 Component 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % A-1/ Component A-2 Component 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % A . . . . . . / Component A . . . . . . Component 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % 1-20 wt % A-153/ Component A-154

(426) The above different gel solutions are irradiated at 365 or 395 nm (20 mW/cm.sup.2) for a certain period of time to obtain hydrogels of different chemical compositions. Different gel materials have different biological effects, and the composition of the gel material can be selected in a targeted manner according to different applications.

(427) Note: Component A . . . is Component A-2˜A-153; Component A . . . is Component A-1˜A-154; Component C . . . is component C-1˜C-21.

(428) 1-20 wt % in Table 1 is a preferred range of mass concentration of the hydrogel precursor solution.

Example 167: Rheology Test of Photo-Crosslinked Hydrogel

(429) Rheology analysis was performed on a 37° C. test platform ((p=20 mm) using a HAAKE MARS rheometer. In this example, the effects of UV light time, light intensity and mass concentration of polymer derivatives on gelation time and storage modulus of hydrogels were investigated. FIG. 1 shows the gelation curve of the prepared hydrogel precursor solution under illumination of Component A-1 (i.e. HA-NB) prepared in Example 1, Component A-107 (i.e. HAMA) prepared in Example 107, Component C-4 (i.e. Gelatin) prepared in Example 107 and Component C-4 (i.e. Gelatin) and Component B-2 (i.e. LAP) prepared in Example 155, or Component A-88 prepared in Example 88 (i.e., HA-cNB), Component A-144 prepared in Example 144 (i.e., HA-cNB-MA) and Component B-2 (i.e., LAP) prepared in Example 155 (In the rheological test, G′ is the storage modulus, G″ is the loss modulus, and when G′ exceeds G″, it is the gel point.). Therefore, both the gelation rate and the gel strength are significantly better than those hydrogels prepared by free radical polymerization crosslinking and photocoupled crosslinking. As shown in FIG. 1, the solution starts to form gel at about 2 s, it is completely gelatinized in about 10 s, and the modulus at the time of complete gel formation can reach 3500-10000 Pa. Further, the strength of the gel is proportional to the mass concentration of the gel solution, and the greater the mass concentration of the gel is, the greater the strength of the gel is. The gel point and final modulus of hydrogel systems composed of other different materials are also different. The specific data are shown in Table 2.

(430) TABLE-US-00002 TABLE 2 Final Gel Modulus The composition of hydrogel material point (s) (Pa) HA-NB.sub.0/CMCh (2% wt:2% wt) 30 200 Component A-1/Component B-1 (2% wt:0.2% wt) <2 1100 Component A-1/Component B-3 (2% wt:0.2% wt) <2 900 Component A-1/Component B-2 (2% wt:0.2% wt) <2 1500 Component A-2/Component B-2 (2% wt:0.2% wt) <2 1400 Component A-8/Component B-2 (2% wt:0.2% wt) <2 1450 Component A-13/Component B-2 (2% wt:0.2% wt) <2 1640 Component A-28/Component B-2 (2% wt:0.2% wt) <2 1550 Component A-33/Component B-2 (2% wt:0.2% wt) <2 2100 Component A-37/Component B-2 (2% wt:0.2% wt) <2 1230 Component A-38/Component B-2 (2% wt:0.2% wt) <2 1050 Component A-39/Component B-2 (2% wt:0.2% wt) <2 990 Component A-40/Component B-2 (2% wt:0.2% wt) <2 860 Component A-41/Component B-2 (2% wt:0.2% wt) <2 880 Component A-43/Component B-2 (2% wt:0.2% wt) <2 1120 Component A-44/Component B-2 (2% wt:0.2% wt) <2 980 Component A-45/Component B-2 (2% wt:0.2% wt) <2 760 Component A-46/Component B-2 (2% wt:0.2% wt) <2 720 Component A-47/Component B-2 (2% wt:0.2% wt) <2 680 Component A-50/Component B-2 (2% wt:0.2% wt) <2 790 Component A-51/Component B-2 (2% wt:0.2% wt) <2 1700 Component A-52/Component B-2 (2% wt:0.2% wt) <2 1890 Component A-53/Component B-2 (2% wt:0.2% wt) <2 1760 Component A-55/Component B-2 (2% wt:0.2% wt) <2 1980 Component A-62/Component B-2 (2% wt:0.2% wt) <2 1680 Component A-65/Component B-2 (2% wt:0.2% wt) <2 2450 Component A-66/Component B-2 (2% wt:0.2% wt) <2 1540 Component A-67/Component B-2 (2% wt:0.2% wt) <2 1320 Component A-68/Component B-2 (2% wt:0.2% wt) <2 1100 Component A-69/Component B-2 (2% wt:0.2% wt) <2 1080 Component A-70/Component B-2 (2% wt:0.2% wt) <2 1670 Component A-71/Component B-2 (2% wt:0.2% wt) <2 1710 Component A-72/Component B-2 (2% wt:0.2% wt) <2 1730 Component A-74/Component B-2 (2% wt:0.2% wt) <2 1780 Component A-80/Component B-2 (2% wt:0.2% wt) <2 1670 Component A-83/Component B-2 (2% wt:0.2% wt) <2 2340 Component A-84/Component B-2 (2% wt:0.2% wt) <2 1310 Component A-85/Component B-2 (2% wt:0.2% wt) <2 1150 Component A-86/Component B-2 (2% wt:0.2% wt) <2 1020 Component A-87/Component B-2 (2% wt:0.2% wt) <2 890 Component A-88/Component B-2 (2% wt:0.2% wt) <2 2140 Component A-89/Component B-2 (2% wt:0.2% wt) <2 2010 Component A-90/Component B-2 (2% wt:0.2% wt) <2 1980 Component A-91/Component B-2 (2% wt:0.2% wt) <2 2040 Component A-93/Component B-2 (2% wt:0.2% wt) <2 1820 Component A-98/Component B-2 (2% wt:0.2% wt) <2 2140 Component A-102/Component B-2 (2% wt:0.2% wt) <2 2790 Component A-103/Component B-2 (2% wt:0.2% wt) <2 2110 Component A-104/Component B-2 (2% wt:0.2% wt) <2 2040 Component A-105/Component B-2 (2% wt:0.2% wt) <2 1890 Component A-106/Component B-2 (2% wt:0.2% wt) <2 1720 Component A-1/Component A-107/Component B-1 <2 2900 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/Component B-3 <2 2830 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/Component B-2 <2 3200 (2% wt:1% wt:0.2% wt) Component A-1/Component A-108/Component B-2 <2 2890 (2% wt:1% wt:0.2% wt) Component A-1/Component A-109/Component B-2 <2 2780 (2% wt:1% wt:0.2% wt) Component A-1/Component A-110/Component B-2 <2 2540 (2% wt:1% wt:0.2% wt) Component A-1/Component A-111/Component B-2 <2 2340 (2% wt:1% wt:0.2% wt) Component A-1/Component A-112/Component B-2 <2 2140 (2% wt:1% wt:0.2% wt) Component A-1/Component A-113/Component B-2 <2 1950 (2% wt:1% wt:0.2% wt) Component A-1/Component A-115/Component B-2 <2 1780 (2% wt:1% wt:0.2% wt) Component A-51/Component A-107/Component B-2 <2 3200 (2% wt:1% wt:0.2% wt) Component A-52/Component A-107/Component B-2 <2 3180 (2% wt:1% wt:0.2% wt) Component A-70/Component A-107/Component B-2 <2 3430 (2% wt:1% wt:0.2% wt) Component A-71/Component A-107/Component B-2 <2 3320 (2% wt:1% wt:0.2% wt) Component A-88/Component A-107/Component B-2 <2 8800 (2% wt:1% wt:0.2% wt) Component A-89/Component A-107/Component B-2 <2 7800 (2% wt:1% wt:0.2% wt) Component A-90/Component A-107/Component B-2 <2 6710 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/Component B-1 <2 4300 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/Component B-3 <2 4100 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/Component B-2 <2 4500 (2% wt:1% wt:0.2% wt) Component A-1/Component A-117/Component B-2 <2 4340 (2% wt:1% wt:0.2% wt) Component A-1/Component A-118/Component B-2 <2 4680 (2% wt:1% wt:0.2% wt) Component A-1/Component A-122/Component B-2 <2 4100 (2% wt:1% wt:0.2% wt) Component A-1/Component A-123/Component B-2 <2 4260 (2% wt:1% wt:0.2% wt) Component A-1/Component A-124 Component B-2 <2 3980 (2% wt:1% wt:0.2% wt) Component A-1/Component A-125/Component B-2 <2 3640 (2% wt:1% wt:0.2% wt) Component A-1/Component A-126/Component B-2 <2 5430 (2% wt:1% wt:0.2% wt) Component A-1/Component A-127/Component B-2 <2 5200 (2% wt:1% wt:0.2% wt) Component A-1/Component A-128/Component B-2 <2 4900 (2% wt:1% wt:0.2% wt) Component A-1/Component A-132/Component B-2 <2 4780 (2% wt:1% wt:0.2% wt) Component A-1/Component A-133/Component B-2 <2 4210 (2% wt:1% wt:0.2% wt) Component A-1/Component A-134/Component B-2 <2 4020 (2% wt:1% wt:0.2% wt) Component A-1/Component A-135/Component B-2 <2 5120 (2% wt:1% wt:0.2% wt) Component A-1/Component A-136/Component B-2 <2 4980 (2% wt:1% wt:0.2% wt) Component A-1/Component A-137/Component B-2 <2 4740 (2% wt:1% wt:0.2% wt) Component A-1/Component A-141/Component B-2 <2 3890 (2% wt:1% wt:0.2% wt) Component A-1/Component A-142/Component B-2 <2 3720 (2% wt:1% wt:0.2% wt) Component A-1/Component A-143/Component B-2 <2 3580 (2% wt:1% wt:0.2% wt) Component A-1/Component A-144/Component B-2 <2 8900 (2% wt:1% wt:0.2% wt) Component A-1/Component A-145/Component B-2 <2 8200 (2% wt:1% wt:0.2% wt) Component A-1/Component A-146/Component B-2 <2 7890 (2% wt:1% wt:0.2% wt) Component A-1/Component A-147/Component B-2 <2 8300 (2% wt:1% wt:0.2% wt) Component A-1/Component A-152/Component B-2 <2 7100 (2% wt:1% wt:0.2% wt) Component A-1/Component A-153/Component B-2 <2 6800 (2% wt:1% wt:0.2% wt) Component A-1/Component A-154/Component B-2 <2 6700 (2% wt:1% wt:0.2% wt) Component A-51/Component A-126/Component B-2 <2 5670 (2% wt:1% wt:0.2% wt) Component A-52/Component A-127/Component B-2 <2 5100 (2% wt:1% wt:0.2% wt) Component A-71/Component A-135/Component B-2 <2 4800 (2% wt:1% wt:0.2% wt) Component A-72/Component A-136/Component B-2 <2 4300 (2% wt:1% wt:0.2% wt) Component A-88/Component A-144/Component B-2 <2 10000 (2% wt:1% wt:0.2% wt) Component A-89/Component A-145/Component B-2 <2 9400 (2% wt:1% wt:0.2% wt) Component A-90/Component A-146/Component B-2 <2 8700 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/Component C-3/ <2 4600 Component B-1 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-3/ <2 3900 Component B-3 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-3/ <2 5100 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-4/ <2 3500 Component B-2 (2% wt:1% wt:6% wt:0.2 % wt) Component A-1/Component A-107/Component C-8/ <2 2300 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-10/ <2 1600 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-11/ <2 5400 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-14/ <2 2400 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-51/Component A-107/Component C-3/ <2 4500 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-52/Component A-107/Component C-3/ <2 4200 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-71/Component A-107/Component C-3/ <2 4100 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-72/Component A-107/Component C-3/ <2 3910 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-88/Component A-107/Component C-3/ <2 7600 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-89/Component A-107/Component C-3/ <2 7300 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-90/Component A-107/Component C-3/ <2 7100 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Note: NB.sub.0 is o-nitrobenzyl phototriggers used for constructing of hydrogels reported in the literature. (Yunlong Yang; Jieyuan Zhang; Zhenzhen Liu; Qiuning Lin; Xiaolin Liu; Chunyan Bao; Yang Wang; Linyong Zhu. Adv. Mater. 2016, 28, 2724.). HA-NB.sub.0 is hyaluronic acid polymer derivative modified by NB.sub.0. NB is o-nitrobenzyl phototriggers in Component A-1 of the invention; cNB is cyclic o-nitrobenzyl phototriggers in Component A-88 of the invention; cNB-MA is cyclic o-nitrobenzyl phototriggers and double bond functional group in Component A-144 of the invention. Among them, HA-NB is Component A-1; HA-cNB is Component A-88; HA-cNB-MA is Component A-144.

Example 168: Adhesion Test of Photo-Crosslinked Hydrogel

(431) Fresh pig casings were taken and cutted into 3.5 cm×2.5 cm casing pieces, and then fixed to 6.5 cm×2.5 cm tempered glass piece using 502 glue. The above tempered glass piece was taken, and 150 μL of a certain component of the hydrogel precursor solution was applied to one of the connected casing surfaces. Then, another piece of glass was placed over the above piece of glass to completely opposite, and the excess extruded hydrogel precursor solution was wiped off. The casing was irradiated for 5 min using a 395 nm UV LED source (20 mW/cm.sup.2) to allow the hydrogel precursor solution to gel in situ between the two casings. After the glue was completed, one end of the glass piece was vertically fixed, and the other end was connected to a container capable of holding water through a string. The metered water was then continuously added to the container until the two pieces of glass were broken. Thereafter, the mass of the water and the container at this time was recorded and converted into gravity, that was, the tensile force F when the glass piece was broken. The tissue adhesion of the hydrogel was calculated using the following formula:
Hydrogel tissue adhesion=F/A

(432) A is the adhesion area of the casing, and the test device is shown in FIG. 2. The tissue adhesion of hydrogel systems composed of other different materials is also different. The specific data is shown in Table 3.

(433) TABLE-US-00003 TABLE 3 Tissue adhesion Composition of hydrogel material (kPa) HA-NB.sub.0/CMCh (2% wt:2% wt) 24 Component A-1/Component B-1 (2% wt:0.2% wt) 80 Component A-1/Component B-3 (2% wt:0.2% wt) 81 Component A-1/Component B-2 (2% wt:0.2% wt) 84 Component A-2/Component B-2 (2% wt:0.2% wt) 78 Component A-8/Component B-2 (2% wt:0.2% wt) 79 Component A-13/Component B-2 (2% wt:0.2% wt) 74 Component A-28/Component B-2 (2% wt:0.2% wt) 72 Component A-33/Component B-2 (2% wt:0.2% wt) 88 Component A-37/Component B-2 (2% wt:0.2% wt) 82 Component A-38/Component B-2 (2% wt:0.2% wt) 77 Component A-39/Component B-2 (2% wt:0.2% wt) 73 Component A-40/Component B-2 (2% wt:0.2% wt) 68 Component A-41/Component B-2 (2% wt:0.2% wt) 66 Component A-43/Component B-2 (2% wt:0.2% wt) 74 Component A-44/Component B-2 (2% wt:0.2% wt) 63 Component A-45/Component B-2 (2% wt:0.2% wt) 67 Component A-46/Component B-2 (2% wt:0.2% wt) 63 Component A-47/Component B-2 (2% wt:0.2% wt) 65 Component A-50/Component B-2 (2% wt:0.2% wt) 61 Component A-51/Component B-2 (2% wt:0.2% wt) 67 Component A-52/Component B-2 (2% wt:0.2% wt) 63 Component A-53/Component B-2 (2% wt:0.2% wt) 62 Component A-55/Component B-2 (2% wt:0.2% wt) 61 Component A-62/Component B-2 (2% wt:0.2% wt) 65 Component A-65/Component B-2 (2% wt:0.2% wt) 69 Component A-66/Component B-2 (2% wt:0.2% wt) 67 Component A-67/Component B-2 (2% wt:0.2% wt) 66 Component A-68/Component B-2 (2% wt:0.2% wt) 62 Component A-69/Component B-2 (2% wt:0.2% wt) 60 Component A-70/Component B-2 (2% wt:0.2% wt) 68 Component A-71/Component B-2 (2% wt:0.2% wt) 66 Component A-72/Component B-2 (2% wt:0.2% wt) 64 Component A-74/Component B-2 (2% wt:0.2% wt) 62 Component A-80/Component B-2 (2% wt:0.2% wt) 67 Component A-83/Component B-2 (2% wt:0.2% wt) 69 Component A-84/Component B-2 (2% wt:0.2% wt) 66 Component A-85/Component B-2 (2% wt:0.2% wt) 64 Component A-86/Component B-2 (2% wt:0.2% wt) 61 Component A-87/Component B-2 (2% wt:0.2% wt) 60 Component A-88/Component B-2 (2% wt:0.2% wt) 78 Component A-89/Component B-2 (2% wt:0.2% wt) 76 Component A-90/Component B-2 (2% wt:0.2% wt) 74 Component A-91/Component B-2 (2% wt:0.2% wt) 75 Component A-93/Component B-2 (2% wt:0.2% wt) 73 Component A-98/Component B-2 (2% wt:0.2% wt) 75 Component A-102/Component B-2 (2% wt:0.2% wt) 77 Component A-103/Component B-2 (2% wt:0.2% wt) 72 Component A-104/Component B-2 (2% wt:0.2% wt) 71 Component A-105/Component B-2 (2% wt:0.2% wt) 68 Component A-106/Component B-2 (2% wt:0.2% wt) 62 Component A-1/Component A-107/Component B-1 85 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/Component B-3 81 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/Component B-3 84 (2% wt:1% wt:0.2% wt) Component A-1/Component A-108/Component B-2 82 (2% wt:1% wt:0.2% wt) Component A-1/Component A-109/Component B-2 80 (2% wt:1% wt:0.2% wt) Component A-1/Component A-110/Component B-2 79 (2% wt:1% wt:0.2% wt) Component A-1/Component A-111/Component B-2 81 (2% wt:1% wt:0.2% wt) Component A-1/Component A-112/Component B-2 82 (2% wt:1% wt:0.2% wt) Component A-1/Component A-113/Component B-2 81 (2% wt:1% wt:0.2% wt) Component A-1/Component A-115/Component B-2 80 (2% wt:1% wt:0.2% wt) Component A-51/Component A-107/Component B-2 76 (2% wt:1% wt:0.2% wt) Component A-52/Component A-107/Component B-2 74 (2% wt:1% wt:0.2% wt) Component A-70/Component A-107/Component B-2 73 (2% wt:1% wt:0.2% wt) Component A-71/Component A-107/Component B-2 71 (2% wt:1% wt:0.2% wt) Component A-88/Component A-107/Component B-2 99 (2% wt:1% wt:0.2% wt) Component A-89/Component A-107/Component B-2 92 (2% wt:1% wt:0.2% wt) Component A-90/Component A-107/Component B-2 91 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/Component B-1 88 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/Component B-3 86 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/Component B-2 84 (2% wt:1% wt:0.2% wt) Component A-1/Component A-117/Component B-2 82 (2% wt:1% wt:0.2% wt) Component A-1/Component A-118/Component B-2 81 (2% wt:1% wt:0.2% wt) Component A-1/Component A-122/Component B-2 78 (2% wt:1% wt:0.2% wt) Component A-1/Component A-123/Component B-2 74 (2% wt:1% wt:0.2% wt) Component A-1/Component A-124 Component B-2 71 (2% wt:1% wt:0.2% wt) Component A-1/Component A-125/Component B-2 69 (2% wt:1% wt:0.2% wt) Component A-1/Component A-126/Component B-2 84 (2% wt:1% wt:0.2% wt) Component A-1/Component A-127/Component B-2 82 (2% wt:1% wt:0.2% wt) Component A-1/Component A-128/Component B-2 79 (2% wt:1% wt:0.2% wt) Component A-1/Component A-132/Component B-2 80 (2% wt:1% wt:0.2% wt) Component A-1/Component A-133/Component B-2 76 (2% wt:1% wt:0.2% wt) Component A-1/Component A-134/Component B-2 74 (2% wt:1% wt:0.2% wt) Component A-1/Component A-135/Component B-2 82 (2% wt:1% wt:0.2% wt) Component A-1/Component A-136/Component B-2 80 (2% wt:1% wt:0.2% wt) Component A-1/Component A-137/Component B-2 79 (2% wt:1% wt:0.2% wt) Component A-1/Component A-141/Component B-2 76 (2% wt:1% wt:0.2% wt) Component A-1/Component A-142/Component B-2 74 (2% wt:1% wt:0.2% wt) Component A-1/Component A-143/Component B-2 71 (2% wt:1% wt:0.2% wt) Component A-1/Component A-144/Component B-2 86 (2% wt:1% wt:0.2% wt) Component A-1/Component A-145/Component B-2 82 (2% wt:1% wt:0.2% wt) Component A-1/Component A-146/Component B-2 88 (2% wt:1% wt:0.2% wt) Component A-1/Component A-147/Component B-2 83 (2% wt:1% wt:0.2% wt) Component A-1/Component A-152/Component B-2 82 (2% wt:1% wt:0.2% wt) Component A-1/Component A-153/Component B-2 76 (2% wt:1% wt:0.2% wt) Component A-1/Component A-154/Component B-2 72 (2% wt:1% wt:0.2% wt) Component A-51/Component A-126/Component B-2 81 (2% wt:1% wt:0.2% wt) Component A-52/Component A-127/Component B-2 78 (2% wt:1% wt:0.2% wt) Component A-71/Component A-135/Component B-2 76 (2% wt:1% wt:0.2% wt) Component A-72/Component A-136/Component B-2 79 (2% wt:1% wt:0.2% wt) Component A-88/Component A-144/Component B-2 85 (2% wt:1% wt:0.2% wt) Component A-89/Component A-145/Component B-2 82 (2% wt:1% wt:0.2% wt) Component A-90/Component A-146/Component B-2 81 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/Component C-3/ 85 Component B-1 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-3/ 83 Component B-3 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-3/ 84 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-4/ 81 Component B-2 (2% wt:1% wt:6% wt:0.2% wt) Component A-1/Component A-107/Component C-8/ 83 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-10/ 80 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-11/ 78 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/Component C-14/ 77 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-51/Component A-107/Component C-3/ 76 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-52/Component A-107/Component C-3/ 77 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-71/Component A-107/Component C-3/ 75 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-72/Component A-107/Component C-3/ 79 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-88/Component A-107/Component C-3/ 83 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-89/Component A-107/Component C-3/ 85 Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-90/Component A-107/Component C-3/ 87 Component B-2 (2% wt:1% wt:2% wt:0.2% wt)

Example 169: Mechanical Properties Test of Photo-Crosslinked Hydrogel

(434) The mechanical properties test was performed by GT-TCS-2000 tensile machine (including tensile test and compression test). The tensile test specimen is a dumbbell specimen with a length of 20 mm, a width of 3 mm and a thickness of 2 mm, and the test speed is 5 mm/min. The compression test sample is a cylindrical specimen with a diameter of 10 mm and a height of 3 mm, and the test speed is 1 mm/min. Take the hydrogel compared by Component A-1 (i.e., HA-NB) prepared in Example 1, Component A-107 (i.e., HAMA) prepared in Example 107, Component C-4 (i.e., gelatin) and Component B-2 (i.e., LAP) prepared in Example 155, or Component A-88 (i.e., HA-cNB) prepared in Example 88, Component A-144 (i.e., HA-cNB-MA) prepared in Example 144 and Component B-2 (i.e., LAP) prepared in Example 155 as an example to test the tensile and compressive properties of the hydrogel. As shown in FIG. 3, the hydrogel (HA-NB/HAMA/LAP) can be compressed to about 75% with the compression strength of about 2 MPa. Hydrogels (HA-cNB/HA-cNB-MA/LAP) can be compressed to about 88% with compression strength of about 1 MPa. The mechanical properties of hydrogel systems composed of other different materials are also different. The specific data are shown in Table 4.

(435) TABLE-US-00004 TABLE 4 Com- Com- pressive pression strength The composition of hydrogel material ratio (%) (kPa) HA-NB.sub.0/CMCh (2% wt:2% wt) 45 200 Component A-1/Component B-1 71 850 (2% wt:0.2% wt) Component A-1/Component B-3 68 780 (2% wt:0.2% wt) Component A-1/Component B-2 72 960 (2% wt:0.2% wt) Component A-2/Component B-2 70 880 (2% wt:0.2% wt) Component A-8/Component B-2 68 820 (2% wt:0.2% wt) Component A-13/Component B-2 67 800 (2% wt:0.2% wt) Component A-28/Component B-2 72 880 (2% wt:0.2% wt) Component A-33/Component B-2 75 990 (2% wt:0.2% wt) Component A-37/Component B-2 72 930 (2% wt:0.2% wt) Component A-38/Component B-2 67 850 (2% wt:0.2% wt) Component A-39/Component B-2 63 840 (2% wt:0.2% wt) Component A-40/Component B-2 61 760 (2% wt:0.2% wt) Component A-41/Component B-2 66 730 (2% wt:0.2% wt) Component A-43/Component B-2 71 760 (2% wt:0.2% wt) Component A-44/Component B-2 73 790 (2% wt:0.2% wt) Component A-45/Component B-2 68 820 (2% wt:0.2% wt) Component A-46/Component B-2 69 850 (2% wt:0.2% wt) Component A-47/Component B-2 65 760 (2% wt:0.2% wt) Component A-50/Component B-2 61 720 (2% wt:0.2% wt) Component A-51/Component B-2 72 880 (2% wt:0.2% wt) Component A-52/Component B-2 73 850 (2% wt:0.2% wt) Component A-53/Component B-2 68 810 (2% wt:0.2% wt) Component A-55/Component B-2 66 830 (2% wt:0.2% wt) Component A-62/Component B-2 65 800 (2% wt:0.2% wt) Component A-65/Component B-2 73 860 (2% wt:0.2% wt) Component A-66/Component B-2 67 870 (2% wt:0.2% wt) Component A-67/Component B-2 66 850 (2% wt:0.2% wt) Component A-68/Component B-2 62 750 (2% wt:0.2% wt) Component A-69/Component B-2 60 720 (2% wt:0.2% wt) Component A-70/Component B-2 68 820 (2% wt:0.2% wt) Component A-71/Component B-2 67 800 (2% wt:0.2% wt) Component A-72/Component B-2 64 790 (2% wt:0.2% wt) Component A-74/Component B-2 70 810 (2% wt:0.2% wt) Component A-80/Component B-2 72 830 (2% wt:0.2% wt) Component A-83/Component B-2 73 880 (2% wt:0.2% wt) Component A-84/Component B-2 66 850 (2% wt:0.2% wt) Component A-85/Component B-2 64 790 (2% wt:0.2% wt) Component A-86/Component B-2 61 770 (2% wt:0.2% wt) Component A-87/Component B-2 60 720 (2% wt:0.2% wt) Component A-88/Component B-2 78 980 (2% wt:0.2% wt) Component A-89/Component B-2 76 940 (2% wt:0.2% wt) Component A-90/Component B-2 74 920 (2% wt:0.2% wt) Component A-91/Component B-2 75 900 (2% wt:0.2% wt) Component A-93/Component B-2 73 910 (2% wt:0.2% wt) Component A-98/Component B-2 75 900 (2% wt:0.2% wt) Component A-102/Component B-2 77 970 (2% wt:0.2% wt) Component A-103/Component B-2 72 950 (2% wt:0.2% wt) Component A-104/Component B-2 71 850 (2% wt:0.2% wt) Component A-105/Component B-2 68 820 (2% wt:0.2% wt) Component A-106/Component B-2 62 800 (2% wt:0.2% wt) Component A-1/Component A-107/ 82 940 Component B-1 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/ 81 920 Component B-3 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/ 83 980 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-108/ 80 950 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-109/ 78 920 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-110/ 75 900 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-111/ 78 930 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-112/ 80 960 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-113/ 81 940 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-115/ 79 910 Component B-2 (2% wt:1% wt:0.2% wt) Component A-51/Component A-107/ 78 880 Component B-2 (2% wt:1% wt:0.2% wt) Component A-52/Component A-107/ 76 890 Component B-2 (2% wt:1% wt:0.2% wt) Component A-70/Component A-107/ 74 870 Component B-2 (2% wt:1% wt:0.2% wt) Component A-71/Component A-107/ 73 880 Component B-2 (2% wt:1% wt:0.2% wt) Component A-88/Component A-107/ 86 970 Component B-2 (2% wt:1% wt:0.2% wt) Component A-89/Component A-107/ 83 980 Component B-2 (2% wt:1% wt:0.2% wt) Component A-90/Component A-107/ 84 960 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/ 81 870 Component B-1 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/ 83 830 Component B-3 (2% wt:1% wt:0.2% wt) Component A-1/Component A-116/ 84 850 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-117/ 82 820 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-118/ 81 860 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-122/ 78 810 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-123/ 74 890 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-124 77 800 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-125/ 79 830 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-126/ 74 840 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-127/ 73 810 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-128/ 75 790 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-132/ 70 770 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-133/ 76 750 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-134/ 74 730 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-135/ 73 710 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-136/ 76 730 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-137/ 75 720 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-141/ 76 750 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-142/ 74 710 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-143/ 71 700 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-144/ 73 720 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-145/ 72 730 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-146/ 76 780 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-147/ 74 770 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-152/ 72 710 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-153/ 76 700 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-154/ 72 740 Component B-2 (2% wt:1% wt:0.2% wt) Component A-51/Component A-126/ 71 760 Component B-2 (2% wt:1% wt:0.2% wt) Component A-52/Component A-127/ 74 730 Component B-2 (2% wt:1% wt:0.2% wt) Component A-71/Component A-135/ 76 720 Component B-2 (2% wt:1% wt:0.2% wt) Component A-72/Component A-136/ 79 700 Component B-2 (2% wt:1% wt:0.2% wt) Component A-88/Component A-144/ 88 1000 Component B-2 (2% wt:1% wt:0.2% wt) Component A-89/Component A-145/ 87 980 Component B-2 (2% wt:1% wt:0.2% wt) Component A-90/Component A-146/ 83 970 Component B-2 (2% wt:1% wt:0.2% wt) Component A-1/Component A-107/ 74 1600 Component C-3/Component B-1 (2% wt:1% wt:2% wt:0.2% wt) Component A-1/Component A-107/ 71 1700 Component C-3/Component B-3 (2% wt:1% wt:2% wt: 0.2% wt) Component A-1/Component A-107/ 72 1500 Component C-3/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-1/Component A-107/ 75 2000 Component C-4/Component B-2 (2% wt:1% wt:6% wt: 0.2% wt) Component A-1/Component A-107/ 73 1800 Component C-8/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-1/Component A-107/ 70 1600 Component C-10/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-1/Component A-107/ 72 1300 Component C-11/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-1/Component A-107/ 71 1500 Component C-14/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-51/Component A-107/ 73 1400 Component C-3/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-52/Component A-107/ 71 1600 Component C-3/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-71/Component A-107/ 75 1200 Component C-3/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-72/Component A-107/ 73 1500 Component C-3/Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-88/Component A-107/ 73 1300 Component C-3/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt) Component A-89/Component A-107/ 75 1600 Component C-3/Component B-2 (2% wt:1% wt:2% wt:0.2% wt) Component A-90/Component A-107/ 77 1800 Component C-3/Component B-2 (2% wt:1% wt:2% wt: 0.2% wt)

Example 170: Biocompatibility Test of Photo-Crosslinked Hydrogel

(436) In this experiment, Component A-1 (i.e., HA-NB) prepared in Example 1, Component A-107 (i.e., HAMA) prepared in Example 107, Component C-4 (i.e., gelatin) and Component B-2 (i.e., LAP) prepared in Example 155, or Component A-88 prepared in Example 88 (i.e. HA-cNB), Component A-144 prepared in Example 144 (i.e. HA-cNB-MA) and Component B-2 prepared in Example 155 (i.e. LAP) were taken as example s to be evaluated by CCK-8 kit. First, fibroblast HDFs were seeded in a 96-well plate with a cell density of 5×10.sup.3 cells/well, then added the medium and cultured at 37° C./5% CO.sub.2 for 24 h. Each group of test samples diluted in a cell culture medium was added to well plate in which cells were cultured, and cultured for 24 h. Then, the cell fluid in the well was aspirated and added 100 μL of the medium and 10 μL of CCK-8 solution, and the cells were further incubated for 2 h. Finally, the absorbance at 450 nm in each well was measured using a microplate reader. Cell viability is calculated as follows:
Cell Viability (%)=(The average absorbance of the experimental group/the average absorbance of the control group)×100%

(437) As shown in FIG. 4, this Formula of photo-crosslinked hydrogel has good biocompatibility.

(438) In the in vivo immune inflammatory response test, Component A-1 (i.e., HA-NB) prepared in Example 1, Component A-107 (i.e., HAMA) prepared in Example 107, Component C-4 (i.e., gelatin) and Component B-2 (i.e., LAP) prepared in Example 155, or Component A-88 prepared in Example 88 (i.e. HA-cNB), Component A-144 prepared in Example 144 (i.e. HA-cNB-MA) and Component B-2 prepared in Example 155 (i.e. LAP) were taken as examples to be implanted under the skin of the rabbit, and the inflammatory reaction of the hydrogel on the body was analyzed by tissue section staining at different time points.

(439) The biocompatibility of other hydrogel systems compared by different materials is also different. The specific data is shown in Table 5.

(440) TABLE-US-00005 TABLE 5 Composition of Survival Composition of Survival hydrogel material rate (%) hydrogel material rate (%) Component A-1/ 98 Component A-1/ 96 Component B-1 Component A-107/ Component B-3 Component A-1/ 95 Component A-1/ 94 Component B-3 Component A-107/ Component B-2 Component A-1/ 94 Component A-1/ 98 Component B-2 Component A-108/ Component B-2 Component A-2/ 97 Component A-1/ 93 Component B-2 Component A-109/ Component B-2 Component A-8/ 93 Component A-1/ 97 Component B-2 Component A-110/ Component B-2 ComponentA-13/ 94 Component A-1/ 95 Component B-2 Component A-111/ Component B-2 Component A-28/ 97 Component A-1/ 96 Component B-2 Component A-112/ Component B-2 Component A-33/ 95 Component A-1/ 93 Component B-2 Component A-113/ Component B-2 Component A-37/ 92 Component A-1/ 93 Component B-2 Component A-115/ Component B-2 Component A-38/ 98 Component A-51/ 97 Component B-2 Component A-107/ Component B-2 Component A-39/ 92 Component A-52/ 98 Component B-2 Component A-107/ Component B-2 Component A-40/ 96 Component A-70/ 94 Component B-2 Component A-107/ Component B-2 Component A-41/ 92 Component A-71/ 93 Component B-2 Component A-107/ Component B-2 Component A-43/ 98 Component A-88/ 90 Component B-2 Component A-107/ Component B-2 Component A-44/ 92 Component A-89/ 91 Component B-2 Component A-107/ Component B-2 Component A-45/ 96 Component A-90/ 97 Component B-2 Component A-107/ Component B-2 Component A-46/ 98 Component A-1/ 95 Component B-2 Component A-116/ Component B-1 Component A-47/ 93 Component A-1/ 97 Component B-2 Component A-116/ Component B-3 Component A-50/ 90 Component A-1/ 93 Component B-2 Component A-116/ Component B-2 Component A-51/ 93 Component A-1/ 96 Component B-2 Component A-117/ Component B-2 Component A-52/ 91 Component A-1/ 98 Component B-2 Component A-118/ Component B-2 Component A-53/ 95 Component A-1/ 93 Component B-2 Component A-122/ Component B-2 Component A-55/ 94 Component A-1/ 96 Component B-2 Component A-123/ Component B-2 Component A-62/ 93 Component A-1/ 94 Component B-2 Component A-124 Component B-2 Component A-65/ 94 Component A-1/ 90 Component B-2 Component A-125/ Component B-2 Component A-66/ 93 Component A-1/ 95 Component B-2 Component A-126/ Component B-2 Component A-67/ 90 Component A-1/ 96 Component B-2 Component A-127/ Component B-2 Component A-68/ 94 Component A-1/ 93 Component B-2 Component A-128/ Component B-2 Component A-69/ 93 Component A-1/ 97 Component B-2 Component A-132/ Component B-2 Component A-69/ 99 Component A-1/ 95 Component B-2 Component A-133/ Component B-2 Component A-71/ 94 Component A-1/ 93 Component B-2 Component A-134/ Component B-2 Component A-72/ 96 Component A-1/ 96 Component B-2 Component A-135/ Component B-2 Component A-74/ 92 Component A-1/ 94 Component B-2 Component A-136/ Component B-2 Component A-80/ 98 Component A-1/ 90 Component B-2 Component A-137/ Component B-2 Component A-83/ 97 Component A-1/ 94 Component B-2 Component A-141/ Component B-2 Component A-84/ 94 Component A-1/ 95 Component B-2 Component A-142/ Component B-2 Component A-85/ 91 Component A-1/ 93 Component B-2 Component A-143/ Component B-2 Component A-86/ 94 Component A-1/ 91 Component B-2 Component A-144/ Component B-2 Component A-87/ 93 Component A-1/ 97 Component B-2 Component A-145/ Component B-2 Component A-88/ 98 Component A-1/ 98 Component B-2 Component A-146/ Component B-2 Component A-89/ 97 Component A-1/ 94 Component B-2 Component A-147/ Component B-2 Component A-90/ 91 Component A-1/ 97 Component B-2 Component A-152/ Component B-2 Component A-91/ 95 Component A-1/ 94 Component B-2 Component A-153/ Component B-2 Component A-93/ 95 Component A-1/ 93 Component B-2 Component A-154/ Component B-2 Component A-98/ 93 Component A-51/ 97 Component B-2 Component A-126/ Component B-2 Component A-102/ 95 Component A-52/ 94 Component B-2 Component A-127/ Component B-2 Component A-103/ 95 Component A-71/ 93 Component B-2 Component A-135/ Component B-2 Component A-104/ 92 Component A-72/ 96 Component B-2 Component A-136/ Component B-2 Component A-105/ 97 Component A-88/ 98 Component B-2 Component A-144/ Component B-2 Component A-106/ 95 Component A-89/ 94 Component B-2 Component A-145/ Component B-2 Component A-1/ 93 Component A-90/ 93 Component A-107/ Component A-146/ Component C-3/ Component B-2 Component B-1 Component A-1/ 95 Component A-51/ 97 Component A-107/ Component A-107/ Component C-3/ Component C-3/ Component B-3 Component B-2 Component A-1/ 97 Component A-52/ 94 Component A-107/ Component A-107/ Component C-3/ Component C-3/ Component B-2 Component B-2 Component A-1/ 95 Component A-71/ 92 Component A-107/ Component A-107/ Component C-4/ Component C-3/ Component B-2 Component B-2 Component A-1/ 97 Component A-72/ 90 Component A-107/ Component A-107/ Component C-8/ Component C-3/ Component B-2 Component B-2 Component A-1/ 98 Component A-88/ 91 Component A-107/ Component A-107/ Component C-10/ Component C-3/ Component B-2 Component B-2 Component A-1/ 95 Component A-89/ 96 Component A-107/ Component A-107/ Component C-11/ Component C-3/ Component B-2 Component B-2 Component A-1/ 97 Component A-90/ 92 Component A-107/ Component A-107/ Component C-14/ Component C-3/ Component B-2 Component B-2

(441) The relationship between component A and component B in the hydrogel materials of the above different components is 2% wt: 0.2% wt. The relationship between component A and component B and component C was 2% wt: 0.2% wt: 2% wt.

Example 171: Photo-Crosslinked Hydrogel for Wound Closure-Skin Repair

(442) In the experiment, a total skin defect wound with a diameter of 1.8 cm was constructed on the back of SD rats. Then 400 L hydrogel precursor solution (2% A-1/1% A-107/6% C-4/0.2% B-2) was filled into the wound site. Due to the good fluidity of the solution, the wound could be sufficiently filled and infiltrated by the hydrogel precursor solution. Then, under the illumination of 395 nm LED light source, the hydrogel was performed in situ in the skin defect, which closed the wound (as shown in FIG. 5). Then, the repair effects of in-situ hydrogels, preformed hydrogels and saline treatment on the back skin wounds of SD rats were compared within 7 days. The wound healing rate of in-situ hydrogels was significantly faster than the other two groups. The wound shrinkage area was the largest at 7 days, which played a good repairing effect. Preformed hydrogel materials was difficult to adequately fill the wound site. In addition, there is a lack of good organizational integration because of no seamless interface with covalent connections between organizations. And it is difficult for new cells and tissues to quickly enter the hydrogel material, so that the preformed hydrogel cannot fully play the role of the scaffold material. As a result, the repair rates and effects of pre-formed hydrogel were worse than in-situ hydrogels. The wound repair rate without hydrogel filling is the slowest, indicating that the photo-crosslinked hydrogel can promote wound repair as a cell scaffold material to.

(443) Hydrogel systems of different materials (Component A: Component A-1˜Component A-154; Component B: Component B-1˜Component B-3; Component C-1˜C-21) as photo-crosslinked hydrogel can also be used for wound closure and skin repair.

Example 172: Photo-Crosslinked Hydrogel for Wound Closure-Postoperative Anti-Adhesion

(444) In the experiment, SD rats were used to construct an adhesion model of abdominal wall-cecum scraping. Because the cecum is the thickest, most accessible, and most abundant intestine in the abdominal cavity, the probability of abdominal adhesion is extremely high when the corresponding abdominal wall is simultaneously damaged and no measures are taken. The structural adhesion model is stable. During the surgery, the hydrogel precursor solution (2% Component A-1/1% Component A-107/6% Component C-4/0.2% component B-2) can adequately cover the cecal and abdominal wall wounds, and has sufficient residence time on the vertical tissue surface until it is lightly gelled. After giving 30 s of light, the obtained hydrogel was fixed at the wound site, and the hydrogel was not peeled off from the wound site with a certain force applied by a surgical blade. The above process from the administration of the hydrogel precursor solution to the complete gelation can be completed within 1 min (as shown in FIG. 6). After the surgery, the above SD rats were reared for 14 days in a sterile environment. After 14 days, the abdominal cavity of SD rats was opened again, and the abdominal adhesion was recorded. Among the 10 rats in the hydrogel-treated experimental group, 8 rats did not show any intestinal-abdominal wall and intestinal-intestinal adhesion after 14 days; One rat developed a moderate adhesion between the abdominal wall and the cecum; one rat developed a thin layer of adhesion between the intestine and the intestine. In addition, no residual hydrogel residue was observed in the above 9 SD rats without intestinal-abdominal adhesion, and the wound on the abdominal wall was completely healed. Severe abdominal and cecal adhesions occurred in 10 rats in the control group. Next, histological analysis of the tissue sections of the wound site in the experimental and control groups was performed by H&E staining. The injury of the cecum and abdominal wall was completely restored after 14 days in the SD rats in the experimental group, and the surface layer was re-epithelialized. In 14 days after SD rats in the control group, the smooth muscle of the cecum was completely fused with the muscle tissue of the abdominal wall, and fibroblasts and inflammatory cells were deposited at the adhesion site.

(445) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1 to C-21) belong to photo-crosslinked hydrogels, which can also be applied to wound closure-postoperative anti-adhesion.

Example 173: Photo-Crosslinked Hydrogel for Wound Closure-Oral Ulcer

(446) In the experiment, an oral ulcer defect wound with a diameter of 1.0 cm was constructed in the oral cavity of SD rats. Then fill the wound site with 200 μL of the hydrogel precursor solution ((2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2). Due to the good fluidity of the solution, the wound can be sufficiently filled and infiltrated by the hydrogel precursor solution. Then, under the illumination of a 395 nm LED light source, a hydrogel was prepared in situ at the oral cavity to achieve closure of the oral wound. Next, the repair effect of the in-situ hydrogel, the pre-formed hydrogel and the SD rat oral wound treated with physiological saline alone was compared in 7 days. The wound healing rate of in-situ hydrogels was significantly faster than the other two groups. The wound shrinkage area was the largest at 7 days, which played a good repairing effect. The pre-formed hydrogel material is difficult to fully fill the wound site; in addition, there is no seamless interface with covalent connections between the tissues, and lack of good tissue integration. It is difficult for new cells and tissues to quickly enter the hydrogel material, so that it can fully play the role of the scaffold material. As a result, pre-formed hydrogel repair rates and effects are worse than in-situ hydrogels. The wound repair rate without hydrogel filling is the slowest, indicating that the photo-crosslinked hydrogel acts as a cell scaffold material to promote oral ulcer repair.

(447) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels and can also be applied to wound closures-oral ulcers.

Example 174: Photo-Crosslinked Hydrogel Applied to Tissue Exudate Plugging-Intestinal Leakage Sealing

(448) New Zealand male white rabbits were used and divided into two groups for cecal leakage closure experiments: a: hydrogel treatment (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2) group; b: untreated control group. In the experiment, a model of leakage was made in the cecum of the rabbit, and then the hydrogel precursor solution was applied to the wound. After being fully infiltrated, the light was gelled in situ, and the hydrogel adhered firmly to the defect after gelation. No additional fixing is required. Four weeks after the operation, the rabbits in the experiment were sacrificed by intravenous injection of air, and the cecum was extracted to evaluate the effect of the experimental repair. The results showed that there was no leakage of the cecum blocked with hydrogel, and severe leakage occurred in the cecum without hydrogel treatment. After several weeks of repair, the original cecal defect has been repaired by hydrogel treatment. Therefore, the hydrogel can not only effectively block the leakage, but also facilitate the repair of damaged tissue after surgery.

(449) Hydrogel systems composed of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels, and can also be applied to tissue exudate plugging-intestinal leakage plugging.

Example 175: Photo-Crosslinked Hydrogel Applied to Tissue Exudate Plugging-Surgical Suture

(450) Male New Zealand white rabbits were used and divided into three groups for surgical suture experiments: a: hydrogel treatment (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2) group; b: surgical suture treatment group; c: no control group. In the experiment, a model of wound suture was made in the abdomen of the rabbit. In group a, the hydrogel precursor solution is applied to the wound, and after being fully infiltrated, the light is in situ gelled to achieve the sealing of the wound. Due to the excellent tissue adhesion of the hydrogel, the effect of tissue suturing can be achieved; group b was treated with conventional surgical sutures; group c was treated without treatment. Two weeks after the operation, the rabbits in the experiment were sacrificed by intravenous injection of air, and samples were taken to evaluate the effect of the experimental repair. The results showed that the wound treated with the hydrogel had a better suturing effect, which was almost the same as the surgical suture group, and the wounds that were not treated could not be effectively joined together. After 4 weeks of repair, the original wound defect site was hydrogel treated and the tissue was able to connect together and was significantly repaired. Therefore, the hydrogel can not only effectively suture the wound, but also facilitate the repair of the damaged tissue after surgery.

(451) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels, and can also be applied to tissue exudate plugging-surgical sutures.

Example 176: Photo-Crosslinked Hydrogel Applied to Hemostatic Material-Liver Hemostasis

(452) The SD rats were used to evaluate the hemostatic effect of the hydrogel, and the liver hemostasis experiments were divided into three groups: a: gelatin sponge group; b: hydrogel treatment (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2) group; c positive control group. The rats were anesthetized by intraperitoneal injection of chloral hydrate (4% aqueous solution). The injection was measured to be 0.9 ml/100 g. After deep anesthesia, the rat's anterior chest was shaved with a shaver and the iodine was disinfected. Then cut approximately 4 cm long incision along the midline of the chest, open the chest and expose the liver. Make an approximately 2 cm incision in the left lobe of the liver. Group a was treated with gelatin sponge to stop bleeding; group b was treated with hydrogel precursor solution at the incision to cover the section, and 395 nm LED light for 2 min to form a gel to stop bleeding; The c group did not do any treatment, so that the liver incision oozing naturally coagulated, and the oozing was sucked by gauze, and the amount of bleeding and the bleeding time were recorded by the weight loss method (as shown in FIG. 7). After the end of the experiment, group a adhered to the cut gelatin sponge and left in the rat for suturing. Group b hydrogels were cross-connected in situ in the incision and the wounds were isolated, the liver was placed back into the chest, and sutured. Group c was directly sutured without treatment. After 14 days, the liver recovery of SD rats was observed. The rats were sacrificed by intraperitoneal injection of excess anesthetic chloral hydrate (4% aqueous solution, 2.7 ml/100 g). The thoracic cavity was opened along the midline of the thoracic cavity, and the liver recovery of the three groups of rats was observed and photographed. At the same time, the liver injury site was sampled, and the specimen was fixed with 4% formalin solution for 2 days. After dehydration treatment, paraffin was embedded and sliced with a microtome. The thickness of the sample was 5 μm. Finally, the specimens were subjected to H&E staining, and photographs were taken with an optical microscope. The experimental results showed that the liver of group b recovered well, the hydrogel was completely degraded, no adhesion occurred, and the liver incision grew new liver tissue. The gelatin sponge in the rats in group a was still not degraded, and the adhesion between the organs and the omentum was severe. Hepatic and omental adhesions were common in group c. H&E staining showed that the liver surface of the experimental group was smooth and round, with abundant blood vessel distribution and clear liver interface. The liver of the adhesion was found by H&E staining, and the liver interface was uneven. The liver and the omentum were stuck together, and there were deposited inflammatory cells at the interface.

(453) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels, and can also be applied to hemostatic materials-liver hemostasis.

Example 177: Photo-Crosslinked Hydrogel Applied to Hemostatic Material-Bone Section Hemostasis

(454) Male New Zealand white rabbits were used and divided into three groups for bone section hemostasis experiments: a: hydrogel treatment (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2) group; b: bone wax treatment group; c: Control group not treated. In the experiment, a bone section bleeding model was made in the rabbit femur. In group a, the hydrogel precursor solution is applied to the wound, and after being fully infiltrated, the light is in situ gelatinized to achieve effective sealing of the bone section bleeding. Due to the excellent tissue adhesion and photocuring speed of the hydrogel, a timely and effective hemostatic effect can be achieved; Group b is the treatment of bleeding wounds with conventional bone wax; Group c is not treated for bleeding wounds. After 8 weeks of surgery, the rabbits in the experiment were sacrificed by intravenous injection of air, and samples were taken to evaluate the effect of the experimental repair. The results showed that the hydrogel-treated wounds had a better hemostatic effect, which was almost the same as the bone wax group, and the wounds that were not treated had sustained bleeding. After 2 weeks of repair, the original wound hemorrhage site was treated with hydrogel treatment, and the bone wax treated wound was not repaired, mainly because the bone wax did not degrade in the body. Therefore, the hydrogel can not only effectively achieve hemostasis of the bone section, but also facilitate the repair of damaged tissue after surgery.

(455) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels, and can also be applied to hemostasis materials-bone section hemostasis.

Example 178: Photo-Crosslinked Hydrogel Applied to Hemostatic Material-Arterial Hemostasis

(456) Male New Zealand white rabbits were used and divided into three groups for arterial hemostasis: a: hydrogel treatment (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2) group; b: hemostat treatment group; c: A control group that was not treated. In the experiment, a bleeding model was made in the rabbit femoral artery. In group a, the hydrogel precursor solution is applied to the wound, and after being fully infiltrated, the light is in situ gelatinized to achieve effective sealing of the femoral artery bleeding. Due to the excellent tissue adhesion and photocuring speed of the hydrogel, a timely and effective hemostatic effect can be achieved; group b was treated with conventional hemostatic forceps to treat bleeding wounds; group c was treated without bleeding wounds. Two weeks after the operation, the rabbits in the experiment were sacrificed by intravenous injection of air, and samples were taken to evaluate the effect of the experimental repair. The results show that the wound treated with hydrogel has a better hemostatic effect, which is almost the same as that of the hemostatic forceps, and the wound that is not treated will have a continuous bleeding condition. After 2 weeks of repair, the original wound hemorrhage site was treated with hydrogel and the tissue was repaired. Therefore, the hydrogel can not only effectively achieve femoral artery hemostasis, but also facilitate repair of damaged tissue after surgery.

(457) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels, and can also be applied to hemostatic materials-arterial hemostasis.

Example 179: Photo-Crosslinked Hydrogel Applied to Hemostatic Material-Cardiac Hemostasis

(458) New Zealand male white rabbits were used and divided into three groups for cardiac hemostasis experiments: a: hydrogel treatment (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2); b: gelatin sponge treatment group; c: control group not treated. In the experiment, a bleeding model was made in the rabbit heart. In group a, the hydrogel precursor solution is applied to the wound, and after being fully infiltrated, the light is in situ gelled to achieve effective sealing of the heart bleeding. Due to the excellent tissue adhesion and photocuring speed of the hydrogel, a timely and effective hemostatic effect can be achieved; Group b is to treat bleeding wounds with a conventional gelatin sponge; Group c is not treated for bleeding wounds. Two weeks after the operation, the rabbits in the experiment were sacrificed by intravenous injection of air, and samples were taken to evaluate the effect of the experimental repair. The results show that the wound treated with hydrogel has a better hemostatic effect, and the hemostatic effect of the gelatin sponge is better than that of the wound without treatment. After 2 weeks of repair, the original wound hemorrhage site was treated with hydrogel and the tissue was repaired significantly, and the repair effect was better than gelatin sponge. Therefore, the hydrogel can not only effectively achieve cardiac hemostasis, but also facilitate repair of damaged tissue after surgery.

(459) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels, and can also be applied to hemostatic materials-cardiac hemostasis.

Example 180: Photo-Crosslinked Hydrogel Applied to Tissue Engineering Scaffold Material-Cartilage Repair

(460) Male New Zealand white rabbits were used and divided into three groups for repair of articular cartilage: a: group of hydrogels (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2) wrapped with chondrocytes, that is, a group of Gel+ chondrocytes; b: pure hydrogel (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2) group, ie Gel group. c: The control group that is not processed, that is, the Control group. In the experiment, the hydrogel precursor solution can fully penetrate and fill the defect of the rabbit articular cartilage, and the glue adheres firmly to the defect after the glue is formed, and no additional fixation is needed. After 12 weeks of surgery, the rabbits in the experiment were sacrificed by intravenous injection of air, and the injured joints were extracted to evaluate the experimental repair effect. Gross photographs of rabbit articular cartilage lesions showed that after 12 weeks, the Gel+ chondrocyte group developed smooth neonatal cartilage tissue at the joint defect and was well integrated with the old cartilage tissue; The cartilage was also repaired in the Gel group, but the contour of the cartilage wound during surgery was also seen; In the Control group, the cartilage tissue was basically not repaired, and the lesion was still obvious. Next, we further evaluated the repair of cartilage in each of the above groups by H&E staining. H&E staining results showed that both the Gel+ chondrocyte group and the Gel group had new tissue formation and integrated well with the old cartilage tissue; however, the thickness of the new tissue of the Gel+ chondrocyte group was better than that of the Gel group, and the surface was flat; In the Control group, it is difficult to find obvious signs of new tissue. In addition, the components of neonatal cartilage were analyzed by Safranin-O and immunohistochemical staining. In the Gel+ chondrocyte group and the Gel group, the neonatal cartilage tissue showed a Safranin-O staining activity, and it was confirmed that the new cartilage tissue contained the glycoprotein component of normal cartilage. At the same time, the neonatal cartilage tissue of the Gel+ chondrocyte group and the Gel group showed staining activity of Formula II collagen, which proved that the cartilage tissue contained a large amount of Formula II collagen. The results of the above-mentioned Safranin-O and immunohistochemical staining demonstrated that the new cartilage tissue was hyaline cartilage when the new photo-crosslinked hydrogel material was used for cartilage repair.

(461) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels and can also be applied to tissue engineering scaffold materials-cartilage repair.

Example 181: Photo-Crosslinked Hydrogel Applied to Tissue Engineering Scaffold Material-Bone Repair

(462) SD rats were used for skull repair experiments, and the above SD rats were randomly divided into 3 groups: a: an experimental group of hydrogel (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2)+hydroxyapatite; b: hydrogel treatment (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2); c: Control group without material treatment. In the experiment, 4% chloral hydrate solution (0.9 mL per gram body weight) was used for abdominal anesthesia and iodine disinfection. The scalp at the skull of the rat is then opened using a surgical blade. A complete skull defect model with a diameter of 5 mm was made symmetrically around the skull of the mouse using a dental ring drill. In the experimental group, 200 μL of the hydrogel precursor solution was filled into the SD rat skull defect to fully penetrate into the wound edge; The 395 nm LED light source (20 mW/cm.sup.2) was used to illuminate it for 30 s to completely gel; the suture was used to suture the mouse's scalp. In the control group, after the SD rat skull defect model was made, the scalp was directly sutured without any other treatment. The above SD rats were kept in a sterile, 37° C. environment for 8 weeks. Then, the repair of the skull of SD rats in each group was evaluated by micro-CT scanning imaging.

(463) The results showed that in the control group without any treatment, the skull defect of the SD rat was not substantially repaired. There is new osteogenesis at the edge of the skull defect filled with hydrogel, but the amount of new bone tissue is small, and most of the defects are not well repaired. The skull defect filled with hydrogel+hydroxyapatite was basically repaired, and a large amount of new bone tissue was formed at the defect. The histological staining of the skull was then performed by Van Gieson staining. The results showed that both the hydrogel+hydroxyapatite-treated SD rats had intact new bone tissue in the skull defect, and only a small amount of new bone tissue was formed in the skull defect treated with hydrogel. Most of the defects were found. The bone tissue at the site is still defective. In the control group, almost no new bone tissue was formed. The tissue staining results further confirmed that the hydrogel coated with hydroxyapatite has a good repair effect on bone defects.

(464) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels and can also be applied to tissue engineering scaffold materials-bone repair.

Example 182: Photo-Crosslinked Hydrogel Applied to Tissue Engineering Scaffold Material-Bone/Cartilage Composite Defect Repair

(465) Pigs were used as animal models, cartilage phase materials were hydrogels+chondrocytes, bone phase materials were hydrogels+hydroxyapatite+BMSCs, and three groups were used to repair joint bone/cartilage complex defects: a: a hydrogel group (2% Component A-1/1% Component A-107/6% Component C-4/0.2% component B-2) in which chondrocytes and BMSCs are respectively wrapped, that is, a Gel+ cell group; b: a simple hydrogel (2% Component A-1/1% Component A-107/6% Component C-4/0.2% Component B-2) group, namely the Gel group. In the experiment, the bone phase material is first filled into the bone phase defect, and the gel precursor solution is fully infiltrated. After the light is gelatinized, the hydrogel adheres firmly to the bone defect, and then the cartilage phase material is filled into the cartilage phase defect. At the same time, the hydrogel adheres firmly to the cartilage defect after the light is glued (as shown in FIG. 8). Six months after the operation, the experimental pigs were sacrificed and the injured joints were extracted to evaluate the experimental repair effect. The Gel+ cell group developed smooth neonatal cartilage tissue and bone tissue at the joint defect, and was well integrated with the old cartilage/bone tissue. At the same time, the cartilage tissue and bone tissue were well integrated. In the Gel group, there was almost no repair of the bone/cartilage tissue, and the lesion was still a clear cavity. Next, the repair of the above-mentioned groups of cartilage was further evaluated by the method of H&E staining. H&E staining results showed that the Gel+ cell group had new tissue formation and was well integrated with the old cartilage tissue; however, it was difficult to find obvious signs of new tissue in the Gel group. In addition, the components of neonatal cartilage were analyzed by Safranin-O and immunohistochemical staining. In the Gel+ cell group, the neonatal cartilage tissue showed a Safranin-O staining activity, and it was confirmed that the new cartilage tissue contained the glycoprotein component of normal cartilage. At the same time, the neonatal cartilage tissue of the Gel+ cell group showed the staining activity of Formula II collagen, which proved that the cartilage tissue contained a large amount of Formula II collagen. The results of the above-mentioned Safranin-O and immunohistochemical staining demonstrated that the new cartilage tissue was hyaline cartilage when the new photo-crosslinked hydrogel material was used for cartilage repair. The histological staining of the bone tissue sections was then performed by Van Gieson staining. The results showed that the new bone tissue was formed in the bone defect treated by the Gel+ cell group, while only a small amount of new bone tissue was formed in the bone defect in the Gel group, and the bone tissue in most of the defect was still in a defect state. The tissue staining results further confirmed that the cell-added hydrogel has a good repair effect on bone defects.

(466) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels, and can also be applied to tissue engineering scaffold materials-bone/cartilage composite defect repair.

Example 183: Photo-Crosslinked Hydrogel for 3D Printing (FDM) Bio-Ink

(467) 3D printing technology is a three-dimensional molding technology that has been rapidly developed in recent years and has been widely used. Current 3D printing technologies include fused deposition (FDM), photocurable molding (SLA), laser sintering (SLS), continuous liquid level manufacturing (CLIP), and the like. But the way that is suitable for cell printing is currently mainly FDM. Materials with cell printing are primarily hydrogel materials, so developing bio-ink-printable hydrogel materials for 3D printing and increasing the resolution of hydrogel material printing are fundamental issues in this area of research. Component A-1 (i.e. HA-NB) prepared by Example 1, Component A-107 (i.e. HAMA) prepared by Example 107, component c-4 (i.e. Gelatin), and component b-2 (i.e. LAP) prepared by Example 155; Component A-88 from Example 88 (i.e. HA-cNB), Component A-144 from Example 144 (i.e. HA-cNB-MA), and component b-2 from Example 155 (i.e. LAP) are taken as example s. After uniformly mixing the hydrogel precursor solution of a certain mass concentration into the low temperature printing barrel, the printing temperature is controlled at about 25° C., and the viscosity of the bio ink is adjusted by the temperature to obtain the best printing state. Then determine the appropriate print pressure and print speed for bioprinting of different structures. After printing, the hydrogel was cross-connected by light (or by printing while printing) to obtain a cell-structured hydrogel with 3D cell culture (as shown in FIG. 9).

(468) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels and can also be applied to 3D printing (FDM) bio-inks.

Example 184: Photo-Crosslinked Hydrogel for 3D Printing (DLP) Bio-Ink

(469) DLP (Digital Light Processing) 3D printing technology is a new Formula of photo-curing printing method developed in recent years. Compared to SLA (stereo-curing) printers, DLP has the advantages of fast printing speed and high resolution, which is unmatched by most printing methods. Currently, it has certain application prospects in the fields of dental models and jewelry design. However, the printing inks currently used in the market are limited to photocurable resins, and hydrogels have not received much attention as an emerging bio-ink, mainly because there is no hydrogel material suitable for DLP printing. The composite photo-crosslinked hydrogel material proposed by the invention is very suitable for 3D printing with its fast photocuring speed and excellent mechanical properties, and has higher printing precision. Component A-1 (i.e. HA-NB) prepared by Example 1, Component A-107 (i.e. HAMA) prepared by Example 107, component c-4 (i.e. Gelatin), and component b-2 (i.e. LAP) prepared by Example 155; Component A-88 from Example 88 (i.e. HA-cNB), Component A-144 from Example 144 (i.e. HA-cNB-MA), and component b-2 from Example 155 (i.e. LAP) are taken as example s. After uniformly mixing the hydrogel precursor solution of a certain mass concentration into the liquid tank, By controlling the intensity of the light source, the exposure time and other parameters to adjust the printing of the bio-ink to obtain the best printing state, a hydrogel with both cells and structure can be obtained, and the 3D cell culture can be studied.

(470) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels and can also be applied to 3D printing (DLP) bio-inks.

Example 185: Photo-Crosslinked Hydrogel for Drug Wrapping and Release

(471) Hydrogel is a cross-linking polymer network that swells in water but does not dissolve. Since the hydrogel is mostly composed of water, it has very good biocompatibility and is Componenticularly suitable for carriers of drugs and biologically active macromolecules. The drug or biologically active macromolecule encapsulated in the hydrogel material achieves a sustained release of the drug by diffusion of the molecule and degradation of the material. Take the package and release of drugs as an example: Component A-1 (i.e., HA-NB) prepared in Example 1, Component A-107 (i.e., HAMA) prepared in Example 107, component c-4 (i.e., gelatin), and component b-2 (i.e., LAP) prepared in Example 155; Component A-88 from Example 88 (i.e. HA-cNB), Component A-144 from Example 144 (i.e. HA-cNB-MA), and component b-2 from Example 155 (i.e. LAP) are taken as example s. Dissolving it in physiological saline, Formulating a certain concentration of hydrogel precursor solution, adding a certain amount of drug molecules. 200 μL of the above solution was placed in a cyclic mold to light a hydrogel, and then placed in a 24-well cell culture plate, and a certain amount of physiological saline was added for drug release experiments. The release amount of the drug in the solution was analyzed by an ultraviolet test to evaluate the release effect of the material on the drug.

(472) Hydrogel systems of other different materials (Component A: Component A-1 to Component A-154; Component B: Component B-1 to Component B-3; Component C-1˜C-21) belong to photo-crosslinked hydrogels, which can also be applied to the wrapping and release of drugs.

(473) The above description of the example s is intended to facilitate the understanding and use of the invention by those skilled in the art. It will be apparent to those skilled in the art that various modifications can be readily made to these example s and the general principles described herein can be applied to other example s without the inventive work. Therefore, The invention is not limited to the example s described above, and those skilled in the art should be able to make modifications and changes within the scope of the invention without deComponenting from the scope of the invention.