Hydrogel scaffolds for tissue engineering
Disclosed herein are biodegradable hydrogel scaffolds for use in tissue engineering. The hydrogel scaffolds are composed of synthetic terpolymers complexed with polyvinyl alcohol (PVA), which facilitate cell-sheet and tissue growth. In the presence of a monosaccharide, the PVA-hydrogel is dissolved and cell-sheets are released for harvesting. Further disclosed herein are methods for producing PVA hydrogels which support tissue growth. Tissue engineering applications and methods are also disclosed.
1. A hydrogel scaffold composition comprising:
a hydrogel layer, the hydrogel layer comprising one or more polyvinyl alcohol polymers and one or more phenylboronate-containing copolymers, wherein the hydrogel layer is configured for cell growth into one or more of cell-sheets or tissues; and
a polyvinylidene fluoride membrane, wherein the polyvinylidene fluoride membrane overlays the hydrogel layer.
2. The composition of claim 1 , wherein the one more phenylboronate-containing copolymers includes one or more phenylboronate ligands, one or more acrylic monomers, and one or more alkaline tertiary amines.
3. The composition of claim 2 , wherein the one or more phenylboronate ligands are selected from the group consisting of 4-vinylphenylboronic acid, N-acryloyl-3-aminophenylboronic acid, 3-(2-carboxyvinyl)phenylboronic acid, 4-(1,6-dioxo-2,5-diaza-7-oxamyl)phenylboronic acid, and [2-(diethylamino)carbonyl-4-bromomethyl]phenylboronate, or any combination thereof.
4. The composition of claim 2 , wherein the one or more acrylic monomers are selected from the group consisting of acrylamide; N-isopropylacrylamide; N,N-dimethylacrylamide; 2-hydroxyethylmethacrylate; N-Hydroxyethyl acrylamide; methacrylamide; methacrylic acid; acrylic acid; N-vinyl-2-pyrrolidone; 4-pentenoic acid; N-isopropylmethacrylamide; N-methoxymethyl-N-isopropylacrylamide; and 2-(dimethylmaleimido)-N-ethylacrylamide, or any combination thereof.
5. The composition of claim 2 , wherein the one or more alkaline tertiary amines are selected from the group consisting of N,N-dimethylaminoethylmethacrylate; N,N-dimethylaminopropylacrylamide; N,N-diethylaminoethyl methacrylate; and 2-(N,N-Dimethylamino)ethyl methacrylate, or any combination thereof.
6. The composition of claim 1 , wherein the hydrogel scaffold is susceptible to degradation by saccharides.
7. The composition of claim 6 , wherein the saccharides are selected from the group consisting of fructose, glucose, mannitol, L-arabinose, D-xylose, D-galactose, D-mannose, L-fucose, N-acetyl-D-galactosamine, N-acetyl-D-glucosamine, and N-acetylneuraminic acid, or any combination thereof.
8. A method for producing the hydrogel scaffold of claim 1 comprising:
mixing one or more polyvinyl alcohol polymers with one or more phenylboronate-containing copolymers to form a mixture; and
allowing the mixture to congeal, wherein the scaffold is configured for cell growth into one or more of cell-sheets or tissues.
9. The method of claim 8 , wherein the one or more phenylboronate-containing copolymers includes one or more phenylboronate ligands, one or more acrylic monomers, and one or more alkaline tertiary amines.
10. The method of claim 8 , further comprising dissolving the one or more polyvinyl alcohol polymers prior to mixing the one or more polyvinyl alcohol polymers with the one or more phenylboronate-containing copolymers.
11. The method of claim 10 , wherein dissolving the one or more polyvinyl alcohol polymers prior to mixing the one or more polyvinyl alcohol polymers with the one or more phenylboronate-containing copolymers occurs at a temperature of at least 70° C.
12. The method of claim 11 , further comprising allowing the one or more polyvinyl alcohol polymers to cool to at least 40° C. after dissolving the one or more polyvinyl alcohol polymers and prior to mixing the one or more polyvinyl alcohol polymers with the one or more phenylboronate-containing copolymers.
13. The method of any of claim 8 , wherein mixing the one or more polyvinyl alcohol polymers with the one or more phenylboronate-containing copolymers to form the mixture occurs at a pH from 5 to 9.
14. A method for tissue engineering comprising:
culturing cells on the hydrogel scaffold of claim 1 to form one or more cell-layers, wherein the scaffold is configured for cell growth into one or more of cell-sheets or tissues;
dissolving the hydrogel scaffold with a saccharide solution; and
harvesting the one or more cell-layers.
15. The method of claim 14 , wherein the hydrogel scaffold includes one or more polyvinyl alcohol polymers.
16. The method of claim 14 , wherein the one or more phenylboronate-containing copolymers includes one or more phenylboronate ligands, one or more acrylic monomers, and one or more alkaline tertiary amines.
17. The method of claim 16 , wherein the one or more phenylboronate ligands are selected from the group consisting of 4-vinylphenylboronic acid, N-acryloyl-3-aminophenylboronic acid, 3-(2-carboxyvinyl)phenylboronic acid, 4-(1,6-dioxo-2,5-diaza-7-oxamyl)phenylboronic acid, and [2-(diethylamino)carbonyl-4-bromomethyl]phenylboronate, or any combination thereof.
18. The method of claim 16 , wherein the one or more acrylic monomers are selected from the group consisting of acrylamide; N-isopropylacrylamide; N,N-dimethylacrylamide; 2-hydroxyethylmethacrylate; N-Hydroxyethyl acrylamide; methacrylamide; methacrylic acid; acrylic acid; N-vinyl-2-pyrrolidone; 4-pentenoic acid; N-isopropylmethacrylamide; N-methoxymethyl-N-isopropylacrylamide; and 2-(dimethylmaleimido)-N-ethylacrylamide, or any combination thereof.
19. The method of claim 16 , wherein the one or more alkaline tertiary amines are selected from the group consisting of N,N-dimethylaminoethylmethacrylate; N,N-dimethylaminopropylacrylamide; N,N-diethylaminoethyl methacrylate; and 2-(N,N-Dimethylamino)ethyl methacrylate, or any combination thereof.
20. The method of claim 14 , wherein culturing the cells on the hydrogel scaffold occurs at a pH from 5 to 9.