BIFUNCTIONAL MODIFIED BIOPOLYMER BASED POLYMERS AND HYDROGELS OBTAINABLE FROM SUCH BIFUNCTIONAL MODIFIED BIOPOLYMER BASED POLYMERS

Abstract

The invention relates to a bifunctional modified biopolymer based polymer, comprising at least one polymer chain comprising n first functional groups and m second functional groups. The first functional groups comprise groups able of being radically cross-linked following a free radical chain- growth polymerisation. The second functional groups comprise groups able to thiol-ene crosslinking. Preferred bifunctional modified biopolymer based polymers comprise bifunctional modified gelatin and bifunctional modified collagen. The invention further relates to a method to prepare such a bifunctional modified biopolymer based polymer and to a method to prepare a hydrogel starting from such bifunctional modified biopolymer based polymer. Furthermore the invention relates to hydrogels obtainable starting from such bifunctional modified biopolymer based polymers and to the use of such hydrogels.

Claims

1-15. (canceled)

16. A bifunctional modified biopolymer based polymer comprising at least one polymer chain, wherein: the at least one polymer chain comprises n first functional groups and m second functional groups, with both n and m not being zero; the first functional groups comprise groups that are radically cross-linkable following a free radical chain-growth polymerization; and the second functional groups comprise thiol-ene cross-linkable groups that remain unreacted during free radical chain-growth polymerization of the first functional groups.

17. The bifunctional modified biopolymer based polymer of claim 16, wherein the biopolymer based polymer is selected from the group consisting of polypeptides, proteins, polysaccharides, nucleic acids, gelatins, collagens, alginates, dextrans, agarose, glycosaminoglycans, chitosans and carrageenans, derivates thereof, recombinant analogues thereof, and synthetic analogues thereof.

18. The bifunctional modified biopolymer based polymer of claim 16, wherein the first functional groups comprise methacrylamide functional groups, acrylamide functional groups, methacrylate functional groups, acrylate functional groups, or combinations thereof.

19. The bifunctional modified biopolymer based polymer of claim 16, wherein the second functional groups comprise norbornene functional groups, vinylether functional groups, vinyl ester functional groups, allyl ether functional groups, propenyl ether functional groups, alkene functional groups, N-vinylamide functional groups, or combinations thereof.

20. The bifunctional modified biopolymer based polymer of claim 16, wherein: the first functional groups comprise methacrylamide functional groups, acrylamide functional groups, methacrylate functional groups, acrylate functional groups, or combinations thereof; and the second functional groups comprise norbornene functional groups, vinylether functional groups, vinyl ester functional groups, allyl ether functional groups, propenyl ether functional groups, alkene functional groups, N-vinylamide functional groups, or combinations thereof.

21. The bifunctional modified biopolymer based polymer of claim 16, wherein the biopolymer based polymer comprises exactly one polymer chain.

22. A method to prepare a bifunctional modified biopolymer based polymer according to claim 16 from a biopolymer based polymer comprising at least one polymer chain comprising primary functional groups, the method comprising: functionalizing a first part of the primary functional groups to introduce n first functional groups, with n not being zero, the first functional groups being radically cross-linkable following a free radical chain-growth polymerization; and functionalizing a second part of the primary functional groups to introduce m second functional groups, with m not being zero, the second functional groups comprising thiol-ene cross-linkable groups that remain unreacted during free chain-growth polymerization of the primary functional groups, wherein the functionalizing the first part of the primary functional groups and the functionalizing the second part of the primary functional groups are performed simultaneously or sequentially in any order.

23. The method of claim 22, wherein: the primary functional groups comprise amine functional groups and/or carboxylic acid functional groups and/or hydroxyl functional groups; and functionalizing the first part of the primary functional groups comprises a reaction of the amine functional groups and/or a reaction of the carboxylic acid functional groups and/or a reaction of the hydroxyl functional groups.

24. The method of claim 22, wherein: the primary functional groups comprise amine functional groups and/or carboxylic acid functional groups and/or hydroxyl functional groups; and functionalizing the second part of the primary functional groups comprises a reaction of the amine functional groups and/or a reaction of the carboxylic acid functional groups and/or a reaction of the hydroxyl functional groups.

25. The method of claim 24, wherein the reaction of the amine functional groups and/or the reaction with the carboxylic acid functional groups and/or the reaction with the hydroxyl functional groups comprises a carbodiimide coupling reaction.

26. A method to prepare a hydrogel, the method comprising: crosslinking a bifunctional modified biopolymer based polymer according to claim 16 by free radical chain-growth polymerization of at least a part of the n first functional groups; and crosslinking and/or functionalizing at least a part of the m second functional groups.

27. The method of claim 26, wherein crosslinking and/or functionalizing at least a part of the m second functional groups comprises crosslinking of at least a part of the m second functional groups.

28. The method of claim 26, wherein crosslinking and/or functionalizing at least a part of the m second functional groups comprises functionalizing at least part of the m functional groups.

29. The method of claim 26, wherein crosslinking and/or functionalizing at least a part of the m second functional groups comprises crosslinking a first part of the m functional groups and functionalizing a second part of the m functional groups.

30. A hydrogel obtained by the method according to claim 26.

31. The hydrogel of claim 30, adapted as a wound dressing.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0094] The present invention will be discussed in more detail below, with reference to the attached drawings, in which:

[0095] FIG. 1 shows the storage modulus G′ (top) and the mass swelling ratio of different gelatin derivates (bottom) in equilibrium swollen state (all hydrogels were crosslinked at a 10 w/v % concentration in the presence of 2 mol % (relative to the amount of photocrosslinkable groups) Li-TPO-L photoinitiator;

[0096] FIG. 2 shows fluorescent microscopy images (left) and normal optical microscopy images (right) of the multiphoton assisted grafting of a fluorescent 7-methyl-4-mercaptocoumarin inside a crosslinked gel-MOD-NB pellet at different spatiotemporal energies;

[0097] FIG. 3 shows the cell viability using different gelatin concentrations for different gelatin derivates.

DESCRIPTION OF EMBODIMENTS

[0098] The present invention will be described with respect to particular embodiments and with reference to certain drawings but the invention is not limited thereto but only by the claims.

EXAMPLE 1

Method to Prepare and Bifunctional Gelatin (gel-MOD-NB)

Materials

[0099] The following chemicals were used: [0100] Gelatin type B, isolated from bovine hides by an alkaline treatment, provided by Rousselot (Ghent, Belgium). [0101] Methacrylic anhydride, 5-norbornene-2-carboxylic acid, 1-ethyl-3-(3-dimethylamino)propyl)-carbodiimide hydrochloride (EDC), D,L-dithiotreitol (DTT) from Sigma-Aldrich (Diegem, Belgium). [0102] Dimethyl sulfoxide (DMSO) (99.85%) and N-hydroxysuccinimide (98%) (NHS) purchased from Acros (Geel, Belgium). [0103] Irgacure 2959 (1-[4-(2-hydroxyethoxy)-phenyl]-2-hydroxy-2-methyl-1-propane-1-one) from BASF. [0104] Dialysis membranes Spectra/por (MWCO 12-14 kDa) were received from polylab (Antwerp, Belgium).

Preparation of Gel-MOD

[0105] Gel-MOD with a DS (degree of substitution) of 72% was synthesized following a protocol described in A. I. Van Den Bulcke, B. Bogdanov, N. De Rooze, E. H. Schacht, M. Cornelissen, and H. Berghmans, “Structural and Rheological Properties of Methacrylamide Modified Gelatin Hydrogels,” Biomacromolecules, vol. 1, no. 1, pp. 31-38, Mar. 2000 and according to the following reaction:

##STR00001##

[0106] Briefly, 100 g of gelatin type B was dissolved in 1 L phosphate buffer (pH 7.8) at 40° C. After complete dissolution, 1 equivalent of methacrylic anhydride, relative to the primary amines present in the (hydroxy-)lysine and ornithine side chains, was added and the mixture was stirred vigorously. After 1 h, the mixture was diluted using 1 L of double distilled water (DDW) and introduced in dialysis membranes (Spectra/por MWCO 12-14 kDa) during 24 h against DDW. After dialysis, the pH of the mixture was adjusted to 7.4 to mimic natural ECM more closely using NaOH and gel-MOD was isolated using lyophilization (Christ freeze-dryer Alpha 2-4 LSC).

Preparation of Gel-MOD-NB

[0107] For the preparation of 10 g gel-MOD-NB, first 5-norbornene-2-carboxylic acid was activated to its succinimidylester. To this end, first a 1.6 times excess of 5-norbornene-2-carboxylic acid (638 mg, 4.62 mmol), with respect to the EDC to be added was dissolved in 50 ml of dry DMSO (obtained via vacuum distillation using CaH.sub.2 as drying agent). After complete dissolution, 0.75 equivalents of EDC (555 mg, 2.9 mmol) (relative to the original primary amines present in 10 g gelatin, i.e. 0.38 mmol/g gelatin) and 1.5 equivalents of NHS (relative to EDC) were added followed by 3 times degassing. The reaction was performed for at least 25 hours to eliminate any unreacted EDC functionalities which can result in gelatin crosslinking during the next reaction step.

[0108] After 25 h of reaction 10 g of gel-MOD with a known DS was dissolved in 150 ml dry DMSO (obtained via vacuum distillation using CaH.sub.2 as drying agent) at 50° C. under inert atmosphere (Ar) and reflux conditions. After addition, the set-up was degassed 3 times and brought under Argon atmosphere. Following complete dissolution, the prepared 5-norbornene-2-succimidylester mixture was added to the gelatin solution followed by 3 times degassing. The mixture was allowed to react at 50° C. under inert atmosphere and reflux conditions for 5-20 h.

[0109] After the reaction, the mixture was precipitated in a tenfold excess of acetone, filtered on filter paper (VWR, pore size: 12-15 μm) using a Büchner filter, dissolved in DDW and dialysed (Spectra/por 4: MWCO 12-14 kDa) during 24 h at 40° C. against DDW. After dialysis, the pH was adjusted to 7.4 using NaOH followed by freezing and lyophilization (Christ freeze-dryer Alpha2-4 LSC). The preparation of gel-MOD-NB is illustrated by reaction [2]:

##STR00002##

Properties of Gel-MOD-NB

[0110] FIG. 1 shows the storage modulus G′ (top) and the mass swelling ratio of different gelatin derivates (bottom). The storage modulus G′ corresponds with the storage modulus of 10 w/v % crosslinked gelatin in equilibrium swollen state after 30 minutes of crosslinking (using 2 mol % (relative to the amount of crosslinkable functionalities) of Li-TPO-L as photoinitiator and 24 hours of incubation in milliQ for respectively gel-MOD DS 72, gel-NB DS 90+DTT (thiol/ene: 1), gel-MOD-NB DS 72 before and after an additional 30 minutes crosslinking in the presence of 5 mM DTT followed by equilibrium swelling and gel-MOD DS 95.

[0111] The mass swelling ratio of gel-MOD DS 72, gel-MOD DS 95 and gel-MOD-NB DS 72 is shown in the bottom panel of FIG. 1.

[0112] After crosslinking the first methacrymide functionalities and equilibrium swelling, the gel-MOD-NB derivative exhibits slightly higher stiffness in comparison to gel-MOD with a similar DS, although only the methacrylamides were polymerised. Although the inventors do not want to be bound by any theory, it is anticipated that this increase in mechanical properties is a consequence of the presence of hydrophobic norbornene functionalities which result in a lower water uptake capacity of the gel in comparison to the normal gel-MOD as can be derived from FIG. 1.

[0113] Furthermore, it should be noted that the gel-MOD-NB exhibits a higher stiffness in comparison to fully crosslinked gel-NB with a higher degree of substitution (e.g. 90%). Additionally, the mechanical properties of gel-MOD-NB are in between these of gel-MOD with a similar DS, but below the stiffness of gel-MOD which is fully functionalized (see FIG. 1). Furthermore, as proof of concept of the bifunctional nature, additional stiffness could be introduced after UV-irradiation in the presence of DTT after equilibrium swelling thereby benefitting from the thiol-ene photografting (see FIG. 1). However, still lower mechanical properties are obtained due to the nature of the formed additional crosslinks, since thiol-ene crosslinking results in a more homogeneous network, characterised by a lower crosslink density in comparison conventional chain-growth hydrogels.

[0114] FIG. 2 shows the results of two-photon polymerization assisted photografting of a fluorescent 7-methyl-4-mercaptocoumarin inside a crosslinked bifunctional modified gelatin (gel-MOD-NB) pellet according to the present invention at different spatiotemporal energies, taking advantage of the norbornene functionalities.

[0115] The left picture of FIG. 2 shows fluorescent microscopy images. This images indicate the presence of coumarin with a high degree of spatiotemporal control.

[0116] The right picture of FIG. 2 shows normal microscopy images whereby the grafting of the coumarin leads to local shrinkage resulting in an observable difference in refractive index. It should be noted that besides no difference in refractive index is observed for all writing speeds at low laser power (e.g. 25 mW), the fluorescence microscopy clearly indicates successful grafting of the compound. From FIG. 2 (left and right picture) can be derived that the bifunctional modified gelatin (gel-MOD-NB) allows post-production grafting with a high degree of spatiotemporal control thereby proving that the norbornene functionalities are not affected by the initial crosslinking step.

[0117] It should be noted that at high energies, grafting is less successful as a consequence of local overexposure thereby removing part of the material.

[0118] FIG. 3 shows the metabolic activity measured on confluent adipose tissue derived stem cells using a presto blue assay after 2 hours in the presence of different precursors and after 24 hours recovery in the absence of the different precursors. To this end, first a confluent monolayer of GFP labelled adipose tissue derived stem cells (passage 17) was obtained by seeding 100 μL of a 2 million cells/mL of medium per 96 well. Next, the cells were allowed to reach confluency after 24 hours of incubation. Next, 100 μL of a solution containing a hydrogel precursor was placed on top followed by another 2 hours of incubation. After 24 hours of incubation, the metabolic activity was measured using a presto blue assay, after which the material was removed from the well plate. Following another 24 hours of incubation, the metabolic activity was measured using a presto blue assay, as an indication of induced cell damage during the first 2 hours of incubation in the presence of a hydrogel precursor.

[0119] FIG. 3 indicates that bifunctional modified gelatin according to the present invention (gel-MOD-NB) exhibits a comparable cytotoxicity as gel-MOD, which can be considered as one of the gold standards in the field of tissue engineering and regenerative medicine. Additionally, in general higher cell viability is obtained in comparison to gel-NB, which is conventionally considered cytocompatible in literature.

EXAMPLE 2

Method to Prepare and Bifunctional Collagen (Col-MOD-NB)

Preparation of Col-MOD

[0120] Col-MOD was synthesized by adapting a protocol described in A. I. Van Den Bulcke, B. Bogdanov, N. De Rooze, E. H. Schacht, M. Cornelissen, and H. Berghmans, “Structural and Rheological Properties of Methacrylamide Modified Gelatin Hydrogels,” Biomacromolecules, vol. 1, no. 1, pp. 31-38, Mar. 2000 and according to the following reaction:

##STR00003##

[0121] Briefly, 100 g of collagen was dissolved in 1 L phosphate buffer (pH 7.8) at 40° C. After complete dissolution, 1, 2 or 5 equivalent of methacrylic anhydride, relative to the primary amines present in the (hydroxy-)lysine side chains, was added and the mixture was stirred vigorously. After 1 h, the mixture was diluted using 1 L of double distilled water (DDW) and introduced in dialysis membranes (Spectra/por MWCO 12-14 kDa) during 24 h against DDW. After dialysis, the pH of the mixture was adjusted to 7.4 to mimic natural ECM more closely using NaOH and col-MOD was isolated using lyophilization (Christ freeze-dryer Alpha 2-4 LSC).

Preparation of Col-MOD-NB

[0122] For the preparation of 10 g col-MOD-NB, first 5-norbornene-2-carboxylic acid was activated to its succinimydilester. To this end, first a 1.6 times excess of 5-norbornene-2-carboxylic acid, with respect to the EDC to be added was dissolved in 50 ml of dry DMSO (obtained via vacuum distillation using CaH.sub.2 as drying agent). After complete dissolution, 0.75 equivalents of EDC (relative to the original primary amines present in 10 g collagen) and 1.5 equivalents of NHS (relative to EDC) were added followed by 3 times degassing. The reaction was performed for at least 25 hours to eliminate any unreacted EDC functionalities which can result in collagen crosslinking during the next reaction step.

[0123] After 25 h of reaction 10 g of col-MOD with a known DS was dissolved in 150 ml dry DMSO (obtained via vacuum distillation using CaH.sub.2 as drying agent) at 50° C. under inert atmosphere (Ar) and reflux conditions. After addition, the set-up was degassed 3 times and brought under Argon atmosphere. Following complete dissolution, the prepared 5-norbornene-2-succimidylester mixture was added to the collagen solution followed by 3 times degassing. The mixture was allowed to react at 50° C. under inert atmosphere and reflux conditions for 5-20 h.

[0124] After the reaction, the mixture was precipitated in a tenfold excess of acetone, filtered on filter paper (VWR, pore size: 12-15 μm)using a Büchner filter, dissolved in DDW and dialysed (Spectra/por 4: MWCO 12-14 kDa) during 24 h at 40° C. against DDW. After dialysis, the pH was adjusted to 7.4 using NaOH followed by freezing and lyophilization (Christ freeze-dryer Alpha2-4 LSC).The preparation of col-MOD-NB is illustrated by reaction [4]:

##STR00004##