METHOD FOR PREPARING INORGANIC NANOPARTICLE-GELATIN CORE-SHELL COMPOSITE PARTICLES

Abstract

The present disclosure provides a method for preparing inorganic nanoparticle-gelatin core-shell composite nanoparticles, comprising: dissolving gelatin in a aqueous solution (in which inorganic nanoparticles are dispersed in) to obtain the gelatin-contained aqueous solution, dropwise adding a polar organic solvent to obtain a suspension of inorganic nanoparticle-gelatin core-shell composite particles of nanometer size or submicrometer size, then adding a cross-linking agent thereto to cross-link the gelatin components of the composite particles, followed by washing step to finally obtain inorganic nanoparticle-gelatin core-shell composite micro/nano-particles with inorganic nanoparticles as the core and gelatin as the shell. The present invention firstly provides a process for preparing the core-shell composite nano-scaled particles with inorganic nanoparticles as the core and gelatin as the shell by using a co-precipitation method which is simple and convenient, and beneficial for applying to industrial mass production.

Claims

1. Method for preparing inorganic nanoparticle-gelatin core-shell composite particles, comprising the following steps: (1) dispersing inorganic nanoparticles uniformly in deionized water, maintaining the temperature of the solution at 3060 C. for more than 30 min, then dissolving gelatin in the inorganic nanoparticle dispersion solution at 3060 C. for at least 30 min to get a homogeneous gelation solution with inorganic nanoparticles evenly dispersed inside, thereafter adjusting the pH of this solution to either acidic 1-5 or basic 9-14, to obtain a gelatin aqueous solution with dispersed inorganic nanoparticles; (2) dropwise adding polar organic solvent to the gelatin aqueous solution with dispersed inorganic nanoparticles obtained in step (1), maintaining stirring during adding the organic solvent, to obtain a suspension of inorganic nanoparticle-gelatin core-shell composite micro/nano-particles; (3) adding a cross-linking agent of gelatin polymer to the suspension containing the composite particles, maintaining stirring to allow the cross-linking reaction lasting for 112 hr.; repeating centrifugation or ultrafiltration, and re-suspending in deionized water, to obtain inorganic nanoparticle-gelatin core-shell composite micro/nano-particles with the inorganic nanoparticle as core and gelatin as shell; wherein, the composite particles have an average diameter of 20 nm to 2 m.

2. The method according to claim 1, wherein the gelatin concentration is 0.5 to 20 w/v % in the gelatin aqueous solution with dispersed inorganic nanoparticles in step (1).

3. The method according to claim 1, wherein the inorganic nanoparticle is at least one of silicon dioxide nanoparticle, mesoporous silicon dioxide nanoparticle, lithium magnesium silicate nanoparticle, hydroxyapatite nanoparticle, calcium phosphate nanoparticles, graphene nanoparticle, black phosphorus nanosheet, carbon nanotube, iron oxide nanoparticle and barium titanate nanoparticle.

4. The method according to claim 1, wherein the mass ratio of the inorganic nanoparticles to the gelatin is 0.01 to 1 in the gelatin aqueous solution with dispersed inorganic nanoparticles obtained in step (1).

5. The method according to claim 1, wherein the polar organic solvent in step (2) is at least one of methanol, ethanol, isopropanol, butanol, acetone, acetonitrile or tetrahydrofuran; the volume of the polar organic solvent added is more than one time the volume of the gelatin aqueous solution with dispersed inorganic nanoparticles.

6. The method according to claim 1, wherein the cross-linking agent of gelatin polymer in step (3) is at least one of glutaraldehyde, glyceraldehyde, formaldehyde, carbodiimide, dihaloalkane, isocyanate, diisocyanate, transglutaminase and genipin.

7. The method according to claim 1, wherein in step (3), the molar ratio of the added cross-linking agent to the amine group in gelatin macromolecules is 0.25 to 10.0.

8. A method for preparing inorganic nanoparticle-gelatin core-shell composite particles using a microfluidic chip device, comprising the following steps: (1) preparing gelatin aqueous solution with dispersed inorganic nanoparticles according to the method in claim 1; and using the gelatin aqueous solution with dispersed inorganic nanoparticles as the disperse phase, using the polar organic solvent as the continuous phase, and the cross-linking agent as a third phase; (2) injecting the disperse phase through the inlet of the disperse-phase fluid microchannel into the microfluidic chip at a first flow rate, and injecting the continuous phase through the inlet of the continuous-phase fluid microchannel into the microfluidic chip at a second flow rate, mixing the disperse phase and the continuous phase when they flows into a mixing channel, thereby obtaining inorganic nanoparticle-gelatin core-shell composite particles; (3) injecting the third phase at a third flow rate into a third-phase fluid microchannel at the downstream of the microfluidic chip device, the third phase flows into the mixing channel and mixes with the suspension of the inorganic nanoparticle-gelatin core-shell composite particles in the mixing channel, thereby cross-link the gelatin phase of the composite particles, then after being out of the chip through the output channel, the mixed solution is collected in a container; (4) repeating centrifugation or ultrafiltration and re-suspending the resultant composite particles collected in step (3), repeating this step with multiple times to obtain inorganic nanoparticle-gelatin core-shell composite particles composed of inorganic nanoparticle as the core and gelatin as the shell; wherein, the composite particles have an average diameter of 20 nm to 2 m.

9. The method according to claim 8, wherein the disperse-phase fluid microchannel, the continuous-phase fluid microchannel, the third-phase fluid microchannel or the mixing channel has a cross-sectional area of 310.sup.55 mm.sup.2.

10. The method according to claim 8, wherein the first flow rate, the second flow rate, and the third flow rate are 0.0520 mL hr.sup.1, 0.1100 mL hr.sup.1 and 0.052000 L, hr.sup.1, respectively.

11. The method according to claim 8, wherein the flow rate ratio of the second flow rate relative to the first flow rate is ranging from 1.0 to 10.0.

12. The method according to claim 8, wherein after the disperse-phase and the continuous-phase being injected into the microfluidic chip through the corresponding microchannels, the disperse phase liquid is rapidly mixed with the continuous-phase liquid by forming laminar co-flow mode or by forming flow-focusing mode depending on the geometry of the microfluidic channels.

13. An injectable, self-healing inorganic/organic composite colloidal gel, wherein the colloidal gel is obtained by directly blending lyophilized powders with aqueous solution or aqueous solution with suspended cells or aqueous solution with dissolved biologically active molecules, the lyophilized powders are powders of the inorganic nanoparticle-gelatin core-shell composite particles prepared according to the method of claim 1.

14. The colloidal gel according to claim 13, wherein the colloidal gel has an elastic modulus between 10 Pa to 200 kPa, and the self-healing efficiency of the composite colloidal gel is more than 50% within 30 minutes after being destroyed by shear forces.

15. Application of the colloidal gel according to claim 13 in the preparation of implantable filler materials for tissue repair and regeneration.

Description

DESCRIPTION OF DRAWINGS

[0046] FIG. 1 is a TEM photograph of the hydroxyapatite nanoparticles used in Embodiment 1.

[0047] FIG. 2 is a SEM photograph of the hydroxyapatite nanoparticles used in Embodiment 1.

[0048] FIG. 3 is a TEM photograph of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1.

[0049] FIG. 4 is a SEM photograph of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1.

[0050] FIG. 5 is an x-ray elemental analysis of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1.

[0051] FIG. 6 is an x-ray diffraction spectrum of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1.

[0052] FIG. 7 is an infrared spectrum analysis of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1.

[0053] FIG. 8 is a rheological characterization of the self-healing behavior of the hydroxyapatite-gelatin composite colloidal gel prepared in Embodiment 1.

[0054] FIG. 9 is an SEM photograph of gelatin nanoparticles prepared in Comparative Example 1.

[0055] FIG. 10 is a TEM photograph of gelatin nanoparticles prepared in Comparative Example 1.

[0056] FIG. 11 is a fluorescence micrograph of fluorescein-labeled silicon dioxide nanoparticles in Embodiment 2.

[0057] FIG. 12 is an SEM photograph of fluorescein-labeled silicon dioxide nanoparticles in Embodiment 2.

[0058] FIG. 13 is a fluorescence micrograph of core-shell composite nanoparticles with silica-core and gelatin-shell prepared in Embodiment 2. The scale in the figure is 5 m.

[0059] FIG. 14 is a SEM photograph of core-shell composite nanoparticles with silica-core and gelatin-shell prepared in Embodiment 2.

[0060] FIG. 15 is SEM photograph of different silicon dioxide nanoparticles in Embodiment 3.

[0061] FIG. 16 is a TEM photograph of three groups of silicon dioxide-gelatin composite colloidal particles with different silicon dioxide nanoparticles sizes prepared in Embodiment 3.

[0062] FIG. 17 is a TEM photograph of three groups of silicon dioxide-gelatin composite colloidal particles with different amounts of silicon dioxide nanoparticles prepared in Embodiment 4.

[0063] FIG. 18 is a TEM photograph of ferroferric oxide nanoparticles in Embodiment 5.

[0064] FIG. 19 is a TEM photograph of ferroferric oxide-gelatin core-shell composite nanoparticles prepared in Embodiment 5.

[0065] FIG. 20 is a TEM photograph of black phosphorus nanosheet-gelatin core-shell composite nanoparticles prepared in Embodiment 6.

[0066] FIG. 21 is SEM and EDS photograph of black phosphorus nanosheet-gelatin core-shell composite nanoparticles prepared in Embodiment 6.

[0067] FIG. 22 is an TEM photograph of polystyrene nanoparticles used in Embodiment 7.

[0068] FIG. 23 is a TEM photograph of polystyrene nanoparticles-gelatin composite colloidal particles prepared in Embodiment 7.

[0069] FIG. 24 is a fluid reaction chip device for preparing core-shell composite nanoparticles in Embodiment 8, wherein: 1the first microchannel, 2the second microchannel, 3the third microchannel, 4output channel, 5U-type mixing channel I, 6U-type mixing channel II, 11 inlet of the first microchannel, 21inlet of the second microchannel, 31inlet of the third microchannel, 41outlet of the output channel.

[0070] FIG. 25 is a schematic diagram of a capillary microfluidic chip device in Embodiment 9, wherein: 1disperse phase fluid microchannel, 2continuous phase fluid microchannel, 3cross-linking agent microchannel, 4output channel, 5exhaust port, 6base, 7sample inlet of disperse phase fluid, 8sample inlet of continuous phase fluid, 9outlet of the output channel.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0071] The following non-limiting embodiments are provided to enable a person of ordinary skill in the art to fully understand the disclosure, but not to limit the disclosure in any way. In the following embodiments, unless otherwise stated, the experimental methods used are all conventional methods, and all materials and reagents used can be purchased from a biological or chemical company.

Embodiment 1

[0072] The hydroxyapatite-gelatin core-shell composite nanoparticles are prepared according to the following steps:

[0073] (1) dispersing hydroxyapatite nanoparticles prepared by hydrothermal synthesis in 25 mL of deionized water to get a suspension with a concentration of hydroxyapatite at 0.005 g/mL, heating the nanoparticles suspension to 40 C. and dissolving 1.25 g of gelatin in it and maintaining at 40 C. continuously, adjusting the pH of the suspension to 10 to get gelatin aqueous solution with dispersed hydroxyapatite nanoparticles, of which, the mixing ratio of hydroxyapatite to gelatin is 0.1:1 (w/w);

[0074] (2) dropwise adding 75 mL of ethanol to the above gelatin aqueous solution with dispersed hydroxyapatite nanoparticles and stirring continuously (1000 rpm) to obtain a suspension of core-shell composite nanoparticles with hydroxyapatite nanoparticles as the core and gelatin as the shell;

[0075] (3) adding 74 L of 25% glutaraldehyde aqueous solution (cross-linking agent) to the suspension to crosslink the gelatin shell layer, keeping the cross-linking reaction for 12 hr. with continuous stirring at 1000 rpm at room temperature; then repeating centrifugation (or ultrafiltration) and re-suspending the resultant composite particles collected, and repeating this step with multiple times to obtain hydroxyapatite-gelatin core-shell composite particles, of which, the centrifugation conditions are 5000 rpm, room temperature, centrifugation for 30 minutes to separate the particles and the supernatant;

[0076] (4) obtaining lyophilized powder of hydroxyapatite-gelatin core-shell composite particles by freeze drying.

[0077] FIG. 1 and FIG. 2 are TEM photograph and SEM photograph of raw material needle-like hydroxyapatite nanoparticles respectively.

[0078] FIG. 3 is a TEM photograph of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1. As shown in the figure, the dark needle-like crystals are hydroxyapatite nanoparticles, while the gelatin is high polymer composition and low contrast, it shows light gray, surrounds the surface of the dark needle-like crystals. It confirms that the core-shell composite nanoparticles with hydroxyapatite as the core and gelatin as the shell have been successfully prepared according to the method in Embodiment 1.

[0079] FIG. 4 is a SEM photograph of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1. It can be seen that the surface of the needle-like crystals is embedded by gelatin layer, confirming the composite nanoparticles having core-shell structure. FIG. 4 A to 4C show SEM photographs at magnifications of 500, 5000, and 30000 respectively.

[0080] FIG. 5 is an energy dispersive x-ray spectrometer analysis of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1. It can be seen that the main element compositions of the composite nanoparticles include C, N, O, Ca and P, wherein C, N and O are the main elements of gelatin, and Ca and P are the main elements of hydroxyapatite, confirming that the components in the composite material are gelatin and hydroxyapatite.

[0081] FIG. 6 is an x-ray diffraction spectrum of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1. Of which, the peaks at 2 of 25.9 and 31.8 are the characteristic peaks of 002 crystal face and 211 crystal face of hydroxyapatite crystal, respectively, and the peaks at 20 are the diffraction peaks of gelatin. Since gelatin is an amorphous polymer, its diffraction peaks present dispersive peaks with a broad distribution. In FIG. 6, the diffraction spectra of crosslinked and uncrosslinked hydroxyapatite/gelatin composite nanoparticles show diffraction peaks of hydroxyapatite at 2=25.9 and 2=31.8, and broad diffraction peaks of gelatin at 20=20, reconfirming that the composite nanoparticles contain the components of hydroxyapatite and gelatin.

[0082] FIG. 7 is an infrared spectrum analysis of the hydroxyapatite-gelatin core-shell composite nanoparticles prepared in Embodiment 1. In the figure, the peak at 3297 cm.sup.1 is the stretching vibration of the NH bond of the amide bond in gelatin, the peak at 1631 cm.sup.1 is the stretching vibration of CO in the amide bond, and the peak at 1527 cm.sup.1 is the bending vibration of NH in the amide bond. The peaks of PO.sub.4.sup.3- groups in pure hydroxyapatite nanoparticles at different positions are 3-1(1090 cm.sup.1) and 3-2(1040 cm.sup.1), respectively. These two characteristic peaks exist apparently in hydroxyapatite-gelatin composite nanoparticles, which reconfirming that composite particles contain the components of hydroxyapatite and gelatin.

[0083] The lyophilized powder of hydroxyapatite-gelatin composite colloidal particles prepared by the above method is blended respectively with different amounts of 10 mM NaCl aqueous solution and rapidly stirred to uniformly mix to obtain composite colloidal gel materials with different colloidal particle contents. The composite colloidal gel materials with different mass fractions can be obtained by changing the amount of the aqueous solution, and the viscoelastic properties of the obtained colloidal gel materials with different components are evaluated by rheometer. The results are shown in Table 1. As the mass fraction of composite colloids in the gel material increases, the storage (elastic) modulus of the gel material increases accordingly. When the mass fraction of colloidal particles is 25 wt. %, the hydroxyapatite-gelatin composite colloidal gel material has an elastic modulus of more than 120 kPa.

TABLE-US-00001 TABLE 1 Rheological storage (elastic) modulus G of hydroxyapatite-gelatin composite colloidal gel materials with different mass fractions Mass fraction of composite colloidal particles (wt. %) Storage (elastic) modulus G (Pa) 10 8329 561 20 79055 9803 25 121004 13293

[0084] The self-healing behavior of colloidal gel is characterized by rheometer. The test method is as follows. Continuous rheological testing of the colloidal gels: firstly, an oscillating time sweep is performed under an oscillatory shear force of 1 Hz and a strain of 0.5%, to test the storage modulus (or elastic modulus, G) and the loss modulus (or viscous modulus, G) of the sample. In this case, the gel exhibits a rigidity of the solid under low shear force, as evidenced by the higher storage modulus G value than the loss modulus G. The G value at this stage is the initial elastic modulus of the sample, then the applied strain is gradually increased from 0.1% to 1000%. During the process, the colloidal gel sample is destroyed by applying an continuously increased shear force, which resulted into the gradual decrease of elastic modulus G, and finally crossing over with G; this rheological response indicated that the colloidal gel changed from a rigid solid into a viscous flowable fluid-like material, as the colloidal network was destroyed. Then the shear force is removed immediately, and the recovery of elastic modulus was evaluated. After the shear force is released, the self-healing efficiency of gel is quantitatively assessed by the percentage of storage (elastic) modulus of sample recovery to its initial storage (elastic) modulus.

[0085] The self-healing efficiency of the hydroxyapatite-gelatin composite colloidal gel materials with different mass fractions of colloidal particles is shown in Table 2. Within 10 minutes after the composite colloidal gel materials are subjected to structural failure, the recovery ratio of the storage (elastic) modulus exceeds 60%. The self-healing process of the composite colloidal gel material is shown in FIG. 8. The elastic modulus of the gel material recovers instantaneously after shear failure, and the self-healing elastic modulus recovers more than 60% of the initial modulus within 10 minutes, and such self-healing behaviors can be repeated. Upon applying destructive shear forces for multiple cycles to the sample, followed by removal of the shear forces after the structural failure of the gels, a quick recovery of more than 60% of the initial elastic modulus of the gel is observed. These findings suggested the composite colloidal gels have remarkable self-healing capability.

TABLE-US-00002 TABLE 2 The self-healing efficiency of hydroxyapatite-gelatin composite colloidal gel materials with different mass fractions after shear failure Mass fraction of composite colloidal particles (wt. %) Self-healing efficiency (%)* 10 65 9 20 71 14 25 73 11 *Note: Self-healing efficiency is the percentage (%) of elastic modulus recovery detected within 10 minutes after the gel material is shorn by 1000% strain continuously for 60 s and the stress is released.

Comparative Example 1

[0086] Preparing gelatin nanoparticles according to the following steps:

[0087] (1) Dissolving 1.25 g of gelatin in 25 mL of deionized water and maintaining the temperature at 40 C. Adjusting the pH of the aqueous solution to 10 by dropwise adding NaOH solution, to obtain an gelatin aqueous solution;

[0088] (2) dropwise adding 75 mL of anhydrous ethanol to the above gelatin aqueous solution, maintaining the temperature at 40 C. and stirring at 1000 rpm, with the process of dropwise adding, forming a suspension of gelatin nanoparticles; after the completion of addition, adding 74 L of cross-linking agent glutaraldehyde (25 wt. % aqueous solution) to the above nanoparticle suspension to act a crosslinking reaction for 12 hr. Then adding 100 mM glycine to the reaction product, to terminate the end groups of glutaraldehyde that are not reacted completely;

[0089] (3) repeating centrifugation (or ultrafiltration), and re-suspending the resultant gelatin particles collected, and repeating this step with multiple times repeating centrifugation and washing to obtain gelatin particles, of which, the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant;

[0090] (4) obtaining dry powder of gelatin nanoparticles by freeze drying the above gelatin nanoparticles suspension at 60 C.

[0091] FIG. 9 is an SEM photograph of gelatin nanoparticles prepared in Comparative Example 1. It can be seen that the gelatin nanoparticles are spherical, and their particle sizes are 200 to 300 nm, which is completely different from that of hydroxyapatite-gelatin composite nanoparticles.

[0092] FIG. 10 is a TEM photograph of gelatin nanoparticles prepared by the method described in Comparative Embodiment 1. As shown from the figure, the gelatin nanoparticles are spherical, and the particle size of microspheres is in the range of 200 to 300 nm. The morphology is completely different from that of hydroxyapatite-gelatin composite nanoparticles.

Embodiment 2

[0093] FIG. 11 is a TEM photograph of fluorescein-labeled silicon dioxide nanoparticles.

[0094] FIG. 12 is an SEM photograph of fluorescein-labeled silicon dioxide nanoparticles. It can be seen that the particle size of the silicon dioxide nanoparticles is 80 to 100 nm and particles are in spherical shape.

[0095] Silica-gelatin core-shell composite nanoparticles are prepared using the above fluorescein-labeled silicon dioxide nanoparticles according to the following steps:

[0096] (1) dispersing fluorescein-labeled silicon dioxide nanoparticles in 25 mL of deionized water to get a suspension with a concentration of silicon dioxide at 0.01 g/mL, heating the nanoparticles suspension to 40 C., dissolving 1.25 g of gelatin in the nanoparticles suspension and maintaing at 40 C., adjusting the pH of the solution to 3 to get gelatin aqueous solution with dispersed silicon dioxide nanoparticles, of which, the mixing ratio of silicon dioxide to gelatin is 0.2:1 (w/w);

[0097] (2) dropwise adding 75 mL of acetone to the above gelatin aqueous solution with dispersed silicon dioxide nanoparticles and stirring continuously (1000 rpm) to obtain a dispersion suspension of core-shell composite nanoparticles with silica nanoparticles as the core and gelatin as the shell;

[0098] (3) adding 74 L of 25% glutaraldehyde aqueous solution (cross-linking agent) to the suspension to crosslink the gelatin shell layer, keeping cross-linking reaction for 12 hrs with stirring at 1000 rpm at room temperature, then adding 100 ml of 100 mM aqueous solution of glycine to terminate the end groups of glutaraldehyde that are not reacted completely; then repeating centrifugation and washing to obtain silicon dioxide-gelatin core-shell composite nanoparticles, of which, the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant;

[0099] (4) obtaining lyophilized powders of silicon dioxide-gelatin core-shell composite particles by freeze drying.

[0100] FIG. 13 is a fluorescence micrograph of silicon dioxide-gelatin core-shell composite nanoparticles prepared in Embodiment 2. As shown in FIG. 13, the green fluorescent silicon dioxide particles agglomerate into spherical agglomerates with a particle size close to 1 m, which indicates that the silicon dioxide nanoparticles are successfully embedded by gelatin to form silicon dioxide-gelatin core-shell composite particles. The scale is 5 m in both FIG. 13A and FIG. 13B.

[0101] FIG. 14 is a SEM photograph of silicon dioxide-gelatin core-shell composite nanoparticles prepared in Embodiment 2. As shown in FIG. 14, silicon dioxide nanoparticles with a size of about 100 nm are embedded in gelatin microspheres.

[0102] The lyophilized powder of silicon dioxide-gelatin composite colloidal particles prepared by the above method is blended with deionized water and rapidly stirred to uniformly mix to obtain injectable composite colloidal gel material. The composite colloidal gel materials with different mass fractions can be obtained by changing the amount of the deionized water, and the viscoelastic properties of the obtained colloidal gel materials of different components are evaluated by rheometer. The results are shown in Table 3. As the mass fraction of composite colloid in the gel material increases, the storage (elastic) modulus of the gel material increases accordingly. When the mass fraction of colloidal particles is 25 vol %, the silicon dioxide-gelatin composite colloidal gel material has an elastic modulus of about 150 kPa.

TABLE-US-00003 TABLE 3 Rheological storage (elastic) modulus G of silicon dioxide- gelatin composite colloidal gel materials with different mass fractions Mass fraction of composite colloidal particles (wt. %) Storage (elastic) modulus G (Pa) 10 10772 6327 20 974036 12557 25 151865 9642

[0103] The self-healing behavior of colloidal gel is tested according to the method in Embodiment 1. The self-healing efficiency of the silicon dioxide-gelatin composite colloidal gel material is shown in Table 4. Within 10 minutes after the composite colloidal gel materials are subjected to structural failure be the applied destructive shearing force (increasing oscillatory shear strain from 0.1% to 1000%), the self-healing efficiency of the composite colloidal gels exceeds 50%. During the self-healing process of composite colloidal gel material, the elastic modulus of the gel recovers instantaneously after shear failure, and the self-healing storage (elastic) modulus recovers to around 50% of the initial modulus within 10 minutes, the self-healing efficiency is more than 50% in 30 minutes. Such self-healing behaviors can be repeated. Upon applying destructive shear forces for multiple cycles to the sample, followed by removal of the shear forces after the structural failure of the gels, a quick recovery of more than 50% of the initial elastic modulus of the composite gel is observed.

TABLE-US-00004 TABLE 4 The self-healing efficiency of silicon dioxide-gelatin composite colloidal gel materials with different mass fractions after shear failure Mass fraction of Self-healing efficiency Self-healing efficiency composite colloidal (%)within 10 min after (%)within 30 min after particles (wt. %) shear* shear* 10 43 16 52 7 20 51 9 58 12 25 49 13 56 14 *Note: The self-healing efficiency is the percentages (%) of elastic modulus recovery detected within 10 minutes and within 30 minutes respectively after the gel material is shorn by 1000% strain continuously for 60 s and the stress is released.

Embodiment 3

[0104] We prepared silicon dioxide nanoparticle with particle diameter of 20 nm, 50 nm, 150 nm by the classic Stober method, silicon dioxide-gelatin core-shell composite nanoparticles are prepared according to the following method:

[0105] (1) silicon dioxide nanoparticles of different sizes were dispersed in 25 mL of deionized water, and the sizes of silicon dioxide were 20 nm, 50 nm, and 150 nm, respectively, heating the nanoparticles suspensions to 40 C., and dissolving 1.25 g of gelatin in the nanoparticles suspensions and maintaining at 40 C. continuously, adjusting the pH of the suspensions to 3 to get gelatin aqueous solutions with different amounts of dispersed silicon dioxide nanoparticles, of which, the mixing ratio of silica to gelatin is 0.1:1 (w/w);

[0106] (2) dropwise adding 75 mL of acetone to the above three groups of gelatin aqueous solutions dispersed with silicon dioxide nanoparticles, and keeping stirring continuously (1000 rpm) to obtain a homogeneous suspensions of core-shell composite nanoparticles with silicon dioxide nanoparticles as the core and gelatin as the shell;

[0107] (3) adding 74 L of 25% glutaraldehyde aqueous solution (cross-linking agent) to the suspensions to crosslink the gelatin shell layer, keeping cross-linking reaction for 12 hr. with stirring at 1000 rpm at room temperature; then adding 100 ml of 100 mM aqueous solution of glycine to terminate the end groups of glutaraldehyde that is not reacted completely; and then repeating centrifugation (or ultrafiltration), and and re-suspending the resultant silica/gelatin particles collected, and repeating this step with multiple times repeating centrifugation and washing to obtain silica/gelatin composite particles, of which the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant;

[0108] (4) obtaining lyophilized powder of three groups of silicon dioxide-gelatin core-shell composite particles by freeze drying.

[0109] FIG. 15 is SEM photograph of different silicon dioxide nanoparticles, which is 20 nm, 50 nm, 150 nm from 15 A to 15C respectively. Each particle has uniform particle size and good dispersion.

[0110] FIG. 16 is a TEM photograph of three groups of silicon dioxide-gelatin composite colloidal particles with different silicon dioxide nanoparticles sizes prepared in Embodiment 3. The surface of the silicon dioxide is embedded by gelatin layer, confirming the composite nanoparticles having core-shell structure. We prepared single silicon dioxide-gelatin core-shell composite colloidal particles from 16C.

[0111] The lyophilized powders of three groups of silicon dioxide-gelatin composite colloidal particles with different silicon dioxide nanoparticles sizes are prepared by the above-mentioned method and blended respectively with deionized water or other aqueous solutions by rapidly stirring/mixing to obtain homogeneous injectable composite colloidal gel materials, of which the volume fraction of the composite colloidal particles in the colloidal gel is fixed at 20 v/v. % as an example. The viscoelastic properties of the obtained colloidal gel materials with different silicon dioxide nanoparticles sizes are evaluated by rheometer. The results are shown in Table 6. When the sizes of silicon dioxide in the composite colloidal particles increases from 20 nm to 150 nm, the storage (elastic) modulus G of the gel material increases accordingly. The self-healing efficiency of colloidal gel material also exhibits a different trend. When the size of silicon dioxide increases from 20 nm to 150 nm in the composite colloidal particles, the self-healing efficiency of gel material decreases from 1001% to 672% gradually within 30 minutes after shear failure.

TABLE-US-00005 TABLE 5 The rheological storage (elastic) modulus G of silicon dioxide-gelatin composite colloidal gel material over the change of silicon dioxide nanoparticles sizes Mass ratio of silicon dioxide to gelatin Storage (elastic) modulus G (Pa) 20 3779 1554 50 19415 1925 150 24443 2729

TABLE-US-00006 TABLE 6 The self-healing efficiency of silicon dioxide- gelatin composite colloidal gel material over the change of silicon dioxide nanoparticles sizes Mass ratio of silicon dioxide Self-healing efficiency (%) within 30 to gelatin minutes after shear failure* 20 100 1 50 69 6 150 67 2 *Note: The self-healing efficiency is the percentage (%) of elastic modulus recovery detected within 30 minutes after the gel material is shorn by 1000% strain continuously for 60 s and the stress is released.

Embodiment 4

[0112] By using silicon dioxide nanoparticles as described in Embodiment 2, silicon dioxide-gelatin core-shell composite nanoparticles are prepared according to the following method:

[0113] (1) dispersing different amounts of silicon dioxide nanoparticles in 25 mL of deionized water to get suspensions with the concentrations of silicon dioxide at 0.005 g/mL, 0.015 g/mL, and 0.025 g/mL, heating the nanoparticles suspensions to 40 C., respectively dissolving 1.25 g of gelatin in the nanoparticles suspensions and maintaining at 40 C. continuously, adjusting the pH of the suspensions to 3 to get gelatin aqueous solutions with different amounts of dispersed silicon dioxide nanoparticles, of which, the mixing ratios of silicon dioxide to gelatin are 0.1:1 (w/w), 0.3:1 (w/w), and 0.5:1 (w/w) respectively;

[0114] (2) dropwise adding 75 mL of acetone to the above three groups of gelatin aqueous solution with different amounts of dispersed silicon dioxide nanoparticles respectively, and stirring continuously (1000 rpm) to obtain dispersion suspensions of core-shell composite nanoparticles with silicon dioxide nanoparticles as the core and gelatin as the shell;

[0115] (3) respectively adding 74 L of 25% glutaraldehyde aqueous solution (cross-linking agent) to the suspensions to crosslink the gelatin shell layer, acting cross-linking reaction for 12 hr. with stirring at 1000 rpm at room temperature; then adding 100 ml of 100 mM aqueous solution of glycine to terminate the end groups of glutaraldehyde that are not reacted completely; and then repeating centrifugation (or ultrafiltration), and re-suspending the resultant silica/gelatin particles collected, and repeating this step with multiple times repeating centrifugation and washing to obtain silica/gelatin composite particles, of which the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant; obtaining lyophilized powder of three groups of silicon dioxide-gelatin core-shell composite particles by freeze drying.

[0116] FIG. 17 is a TEM photograph of three groups of silicon dioxide-gelatin composite colloidal particles with different amounts of silicon dioxide nanoparticles prepared in Embodiment 4. Compared with Three Groups of Silicon Dioxide-Gelatin Composite Colloidal Particles, the Inorganic Content of Core-Shell Particles was Significantly Different, which could Precisely Control the Composition of Core-Shell Particles.

[0117] The lyophilized powders of three groups of silicon dioxide-gelatin composite colloidal particles with different inorganic/organic contents prepared by the above method are blended respectively with deionized water and rapidly stirred to uniformly mix to obtain injectable composite colloidal gel materials, of which the volume fraction of the composite colloidal particles in the colloidal gel is fixed at 20 v/v. % as an example. The viscoelastic properties of the obtained colloidal gel materials with different components are evaluated by rheometer. The results are shown in Table 8. When the mass ratio of silicon dioxide to gelatin mixing in the composite colloidal particles increases from 0.1 to 0.3, the storage (elastic) modulus of the gel material increases accordingly. However, with the further increase of the mass ratio, the storage module of the colloidal gel material decreases, because the increased rigid inorganic component in the composite material reduces the elastic property of the gel material gradually The self-healing efficiency of colloidal gel material also exhibits a different trend. When the mass ratio of silicon dioxide to gelatin increases from 0.1 to 0.5 in the composite colloidal particles, the self-healing efficiency of gel material decreases from 728% to 6112% gradually within 30 minutes after shear failure.

TABLE-US-00007 TABLE 7 The rheological storage (elastic) modulus G of silicon dioxide-gelatin composite colloidal gel material over the change of mass ratio of silicon dioxide to gelatin Mass ratio of silicon dioxide to gelatin Storage (elastic) modulus G (Pa) 0.1 74338 9892 0.3 124036 35520 0.5 106380 23644

TABLE-US-00008 TABLE 8 The self-healing efficiency of silicon dioxide-gelatin composite colloidal gel material over the change of mass ratio of silicon dioxide to gelatin Mass ratio of silicon dioxide Self-healing efficiency (%) within 30 to gelatin minutes after shear failure* 0.1 72 8 0.3 67 11 0.5 61 12 *Note: The self-healing efficiency is the percentage (%) of elastic modulus recovery detected within 30 minutes after the gel material is shorn by 1000% strain continuously for 60 s and the stress is released.

Embodiment 5

[0118] FIG. 18 is a TEM photograph of ferroferric oxide nanoparticles. It can be seen that the particle size of the ferroferric oxide nanoparticles is 50 to 80 nm and particles are in spherical shape.

[0119] ferroferric oxide-gelatin core-shell composite nanoparticles are prepared using the above ferroferric oxide nanoparticles according to the following steps:

[0120] (1) dispersing ferroferric oxide nanoparticles in 25 mL of deionized water to get a suspension with a concentration of ferroferric oxide at 0.01 g/mL, heating the nanoparticles suspension to 40 C., dissolving 1.25 g of gelatin in the nanoparticles suspension and maintaing at 40 C., adjusting the pH of the solution to 10 to get gelatin aqueous solution with dispersed ferroferric oxide nanoparticles, of which, the mixing ratio of ferroferric oxide to gelatin is 0.2:1 (w/w);

[0121] (2) dropwise adding 75 mL of acetone to the above gelatin aqueous solution with dispersed ferroferric oxide nanoparticles and stirring continuously (1000 rpm) to obtain a dispersion suspension of core-shell composite nanoparticles with ferroferric oxide as the core and gelatin as the shell;

[0122] (3) adding 74 L of 25% glutaraldehyde aqueous solution (cross-linking agent) to the suspension to crosslink the gelatin shell layer, acting cross-linking reaction for 12 hrs with stirring at 1000 rpm at room temperature, then adding 100 ml of 100 mM aqueous solution of glycine to terminate the end groups of glutaraldehyde that are not reacted completely; and then repeating centrifugation (or ultrafiltration) and re-suspending the resultant ferroferric oxide/gelatin particles collected, and repeating this step with multiple times repeating centrifugation and washing to obtain ferroferric oxide/gelatin composite particles, of which, the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant;

[0123] (4) obtaining lyophilized powder of ferroferric oxide-gelatin core-shell composite particles by freeze drying.

[0124] FIG. 19 is a TEM photograph of ferroferric oxide-gelatin core-shell composite nanoparticles prepared in Embodiment 5. As shown in FIG. 18, ferroferric oxide nanoparticles with a size of about 50 nm are embedded in gelatin microspheres.

Embodiment 6

[0125] Black phosphorus-gelatin core-shell composite nanoparticles are prepared according to the following steps:

[0126] (1) dispersing black phosphorus nanosheet in 25 mL of deionized water to get a suspension with a concentration of black phosphorus nanosheet at 0.005 g/mL, heating the nanoparticles suspension to 40 C., dissolving 1.25 g of gelatin in the nanoparticles suspension and maintaing at 40 C., adjusting the pH of the solution to 3 to get gelatin aqueous solution with dispersed black phosphorus nanosheet, of which, the mixing ratio of black phosphorus nanosheet to gelatin is 0.1:1 (w/w);

[0127] (2) dropwise adding 75 mL of acetone to the above gelatin aqueous solution with dispersed black phosphorus nanosheet and stirring continuously (1000 rpm) to obtain a dispersion suspension of core-shell composite nanoparticles with black phosphorus nanosheet as the core and gelatin as the shell;

[0128] (3) adding 74 L of 25% glutaraldehyde aqueous solution (cross-linking agent) to the suspension to crosslink the gelatin shell layer, acting cross-linking reaction for 12 hrs with stirring at 1000 rpm at room temperature, then adding 100 ml of 100 mM aqueous solution of glycine to terminate the end groups of glutaraldehyde that are not reacted completely; and then repeating centrifugation (or ultrafiltration) and re-suspending the resultant black phosphorus/gelatin particles collected, and repeating this step with multiple times repeating centrifugation and washing to obtain black phosphorus/gelatin composite particles, of which, the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant;

[0129] (4) obtaining lyophilized powder of black phosphorus-gelatin core-shell composite particles by freeze drying.

[0130] FIG. 20 is a TEM photograph of black phosphorus nanosheet-gelatin core-shell composite nanoparticles prepared in Embodiment 6.

[0131] FIG. 21 is SEM and EDS photograph of black phosphorus nanosheet-gelatin core-shell composite nanoparticles prepared in Embodiment 6. It can be seen from the EDS figure that a large amount of phosphorus exists uniformly, confirming that the components in the composite material are gelatin and black phosphorus.

Embodiment 7

[0132] Polystyrene nanoparticles-gelatin core-shell composite nanoparticles are prepared according to the following steps:

[0133] (1) dispersing polystyrene nanoparticles in 25 mL of deionized water to get a suspension with a concentration of Polystyrene nanoparticles at 0.005 g/mL, heating the nanoparticles suspension to 40 C., dissolving 1.25 g of gelatin in the nanoparticles suspension and maintaing at 40 C., adjusting the pH of the solution to 10 to get gelatin aqueous solution with dispersed Polystyrene nanoparticles, of which, the mixing ratio of Polystyrene nanoparticles to gelatin is 0.1:1 (w/w);

[0134] (2) dropwise adding 75 mL of ethanol to the above gelatin aqueous solution with dispersed Polystyrene nanoparticles and stirring continuously (1000 rpm) to obtain a dispersion suspension of core-shell composite nanoparticles with Polystyrene nanoparticles as the core and gelatin as the shell;

[0135] (3) adding 74 L of 25% glutaraldehyde aqueous solution (cross-linking agent) to the suspension to crosslink the gelatin shell layer, acting cross-linking reaction for 12 hrs with stirring at 1000 rpm at room temperature, then adding 100 ml of 100 mM aqueous solution of glycine to terminate the end groups of glutaraldehyde that are not reacted completely; and then repeating centrifugation (or ultrafiltration) and re-suspending the resultant polystyrene/gelatin particles collected, and repeating this step with multiple times repeating centrifugation and washing to obtain polystyrene/gelatin composite particles, of which, the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant;

[0136] (4) obtaining lyophilized powder of polystyrene nanoparticles-gelatin core-shell composite particles by freeze drying.

[0137] FIG. 22 is an TEM photograph of polystyrene nanoparticles used in Embodiment 7. It can be seen that the polystyrene nanoparticles are finely dispersed, and their particle sizes are 90 to 120 nm.

[0138] FIG. 23 is a TEM photograph of polystyrene nanoparticles-gelatin composite colloidal particles prepared in Embodiment 7. As shown from the figure, The polystyrene nanoparticles are band together by the gelatin. The surface of the polystyrene nanoparticles is embedded by gelatin layer, confirming the composite nanoparticles having core-shell structure.

Embodiment 8

[0139] The microfluidic reaction chip can adopt a conventional microfluidic chip device (reactor) as shown in FIG. 24. The preparation method includes the following steps:

[0140] (1) preparing gelatin aqueous solution with dispersed hydroxyapatite nanoparticles, acetone solution and 25 wt. % aqueous solution of glutaraldehyde (cross-linking agent) according to the method described in Embodiment 1; using the gelatin aqueous solution with dispersed hydroxyapatite nanoparticles as disperse phase, acetone solution as continuous phase, and cross-linking agent as the third phase;

[0141] (2) injecting the disperse phase from the inlet of the first microchannel into the first microchannel in the chip reactor, injecting the continuous phase from the inlet of the second microchannel into the second microchannel, and the two solutions blending in the U-shaped mixing channel I in the reactor to form turbid nanoparticles suspension;

[0142] (3) injecting the third phase from the inlet of the third microchannel into the third microchannel, and blending with the above suspension in the U-shaped mixing channel II to obtain a suspension of crosslinked hydroxyapatite-gelatin core-shell nanoparticles;

[0143] (4) exporting the suspension out of the chip through the outlet of the output channel, collecting in the container with stirring, adding a 100 mM aqueous solution of glycine to the suspension to terminate the end groups of glutaraldehyde that are not reacted completely;

[0144] (5) repeating centrifugation (or ultrafiltration) the nanoparticles suspension obtained in step (4) and re-suspending in deionized water to finally obtain a suspension of hydroxyapatite-gelatin core-shell composite nanoparticles in deionized water, and repeating this washing/resuspending step for multiple times, of which the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant;

[0145] (6) obtaining lyophilized powder of hydroxyapatite-gelatin core-shell nanoparticles by freeze drying the above suspension.

[0146] Wherein, the microfluidic reaction chip, each channel is a circular pipe with uniform diameter, and the cross section thereof is 1 mm.sup.2. In step (2), the disperse phase injection speed is 1 mL/min, the continuous phase injection speed is 3 mL/min; and in step (3), the third phase injection speed is 0.013 mL/min.

[0147] In the above method, the channel of the microfluidic chip has a U-shaped mixng channel structure, and the fluids of disperse phase and continuous phase are blended in form of laminar flow. A turbulent flow is gradually formed by the irregular collection structure of the channel, to achieve physical blending of the two phase fluids.

Embodiment 9

[0148] The microfluidic reaction chip may adopt a capillary microfluidic chip device as shown in FIG. 16, which includes a disperse phase fluid microchannel, a continuous phase fluid microchannel, a cross-linking agent fluid microchannel, an output channel and a collection container. One end of the disperse phase fluid microchannel is unsealed inserted in one end of the continuous phase fluid microchannel, one end of the output channel is hermetically inserted in the other end of the continuous phase fluid microchannel, which is non end-to-end connected with the end of disperse phase fluid microchannel inserted into the continuous phase fluid microchannel. The cross-linking agent fluid microchannel is connected to the portion of output channel not inserted in the continuous phase fluid microchannel, and the other end (i.e. the outlet) of the output channel is connected to the collection container; the device can be fixed to a base for ease of use, and all channels are at the same horizontal level, the inner surface of each microchannel is subjected to a hydrophilic treatment.

[0149] The end of the disperse phase fluid microchannel inserted in the continuous phase fluid microchannel and the end of the output channel inserted in the continuous phase fluid microchannel are tapered; the disperse phase fluid microchannel, the continuous phase fluid microchannel and the cross-linking agent fluid microchannel are respectively connected to micro-peristaltic pump or micro-injector to achieve automatic sample injection; in the continuous phase fluid microchannel, the distance between the end of the disperse phase fluid microchannel to the end of the output channel is 200 m. A portion of the output channel that is not inserted in the continuous phase fluid microchannel is provided with an exhaust port for discharging the gas in the chip when the fluid is injected into the chip.

[0150] In the microfluidic chip device, the continuous phase fluid microchannel is a square glass capillary with a uniform inner diameter (inner diameter of 1.05 m). The disperse phase fluid microchannel is a cylindrical AIT glass capillary with a uniform inner diameter (inner diameter of 560 m), and the end inserted in the continuous phase fluid channel is a tapered end with an internal diameter of 30 m. The output channel is a cylindrical AIT glass capillary with a uniform inner diameter (inner diameter of 560 m), and the end inserted in the continuous phase fluid microchannel is a tapered end with an inner diameter of 60 m. FIG. 25B is a cross-sectional view on the a-a direction in FIG. 25A.

[0151] The preparation method includes the following steps:

[0152] (1) preparing gelatin aqueous solution with dispersed hydroxyapatite nanoparticles, acetone solution and 25 wt. % aqueous solution of glutaraldehyde (cross-linking agent) according to the method described in Embodiment 1;

[0153] (2) using the gelatin aqueous solution with dispersed hydroxyapatite nanoparticles as disperse phase, acetone solution as continuous phase, and cross-linking agent as the third phase;

[0154] (3) injecting the disperse phase to the disperse phase fluid microchannel from the sample inlet of disperse phase fluid and injecting the continuous phase to the continuous phase fluid microchannel from the sample inlet of continuous phase fluid respectively, the flow-focusing structure of the chip making the two phase solutions forming a concentric fluid in the chip, and blending by rapid material diffusion of the two-phase fluid in the microfluidic channel to form a turbid suspension of nanoparticles;

[0155] (4) injecting the third phase from the cross-linking agent microchannel disposed at the downstream of the output channel into the microfluidic chip device, and blending with the suspension formed in step (3) to obtain a suspension of crosslinked hydroxyapatite-gelatin core-shell nanoparticles.

[0156] (5) exporting the suspension from the chip through the outlet of output channel, and collecting in the container and continuous stirring;

[0157] (6) adding 100 mM glycine to the suspension to terminate the end groups of glutaraldehyde that are not reacted completely;

[0158] (7) repeating centrifugation (or ultrafiltration) the nanoparticles suspension obtained in step (4) and re-suspending in deionized water to finally obtain a suspension of hydroxyapatite-gelatin core-shell composite nanoparticles in deionized water, and repeating this washing/resuspending step for multiple times, of which, the centrifugation conditions are 5000 rpm, room temperature, and centrifugation for 30 minutes to separate the particles and the supernatant;

[0159] (8) obtaining a lyophilized powder of hydroxyapatite-gelatin core-shell composite nanoparticles by freeze drying the above suspension.

[0160] In step (2), the disperse phase injection speed is 500 L/hr., the continuous phase injection speed is 1.5 mL/hr.; and in step (3), the third phase injection speed is 6.5 L/hr.

[0161] In the above method, the microfluidic chip device has a flow-focusing microchannel structure capable of forming a concentric fluid, the disperse phase and continuous phase form a flow-focusing flow stype, of which the disperse phase (aqueous solution) is mixed with the continuous phase (organic solvent). Thereby, the two phases can be mixed by rapid material diffusion between the two phases, thereby promoting rapid nucleation of the gelatin molecules at the surfaces of the hydroxyapatite nanoparticles, and gradually growing to form a core-shell structure hydroxyapatite/gelatin composite nanoparticles.

[0162] Analyze the particle sizes of the hydroxyapatite-gelatin core-shell composite particles prepared by different methods in Embodiment 1, 3, and 4 by laser particle analyzer, as shown in Table 9.

TABLE-US-00009 TABLE 9 Analysis of particle size of hydroxyapatite-gelatin core-shell composite particles prepared by different methods in different embodiments Embodiment 1 Embodiment 3 Embodiment 4 (conventional (U-shaped hybrid (fluid focusing process) microfluidic chip) microfluidic chip) Particle size (nm) 234 47 211 18 228 23

[0163] The results in Table 9 show that the hydroxyapatite-gelatin core-shell nanoparticles prepared by conventional process in Embodiment 1 have a particle size of 23447 nm; and the hydroxyapatite-gelatin core-shell nanoparticles prepared by U-shaped mixed fluid reactor in Embodiment 4 have a similar particle size to those prepared by fluid focusing microfluidic chip in Embodiment 8, and have a narrow distribution of particle sizes.