PVA-PAA hydrogels
The invention provides fabricated PVA-hydrogels, PVA-hydrogel-containing compositions, and methods of making the same. The invention also provides methods of implanting or administering the PVA-hydrogels, or the PVA-hydrogel-containing compositions to treat a subject in need. Methods of cross-linking pre-solidified or pre-gelled hydrogel particles and making cross-linked PVA-hydrogels, and cross-linked PVA-hydrogel-containing compositions also are disclosed herein.
1. A method of making a PVA-hydrogel comprising:
a) contacting an aqueous solution of poly(vinyl alcohol) (PVA) with an aqueous solution of poly(acrylic acid) (PAA) at a temperature above the room temperature, thereby forming a homogenous PVA-PAA solution wherein the PVA-PAA solution includes no polyethylene glycol (PEG);
b) pouring the PVA-PAA solution onto a mold followed by cooling down to room temperature, thereby allowing formation of the PVA-hydrogel;
c) cooling the PVA-hydrogel by freezing at a temperature below 0° C.;
d) thawing the PVA-hydrogel to a temperature above 0° C.; and
e) immersing PVA-hydrogel in a PEG solution, thereby allowing diffusion of the PEG into the PVA-hydrogel.
2. The method according to claim 1 , wherein the PVA:PAA ratio is about 99.9:0.1 to 5:5.
3. The method according to claim 1 , wherein the total polymer content in PVA-PAA solution is about 10% to about 50%.
4. The method according to claim 1 , wherein the PVA-PAA solution is poured into a pre-heated mold followed by cooling down to room temperature, thereby allowing formation of the PVA-hydrogel.
5. The method according to claim 1 , wherein the PVA-PAA solution is heated to a temperature above room temperature to about 90° C.
6. The method according to claim 1 , wherein the PVA-PAA solution is poured into a pre-heated mold followed by freezing below 0° C. and thawing to a temperature above 0° C., thereby allowing formation of the PVA-hydrogel.
7. The method according to claim 1 , wherein the PVA-PAA solution is poured into a pre-heated mold followed by freezing below 0° C. and thawing to a temperature above 0° C., thereby allowing formation of the PVA-hydrogel.
8. The method according to claim 1 , wherein the PVA-hydrogel is re-hydrated in water or saline.
9. The method according to claim 1 , wherein the freeze-thaw step is repeated for at least 2 to 100 cycles.
10. The method according to claim 1 , wherein the freeze-thaw step is repeated for at least 2, 3, 4, 5, 6, 7, 8, 9, 10, or more cycles.
11. The method according to claim 1 , wherein the PVA-hydrogel is dehydrated to remove part or all of the water content.
12. The method according to claim 1 , wherein the PVA-hydrogel is dehydrated by a method comprising the steps of:
a) contacting the PVA-hydrogel with an organic solvent, wherein the hydrogel comprises a polymer which is not soluble in the solvent, and wherein the solvent is at least partially miscible in water; and
b) air-drying the hydrogel at room temperature or heat drying the hydrogel.
13. The method according to claim 1 , wherein the PVA-hydrogel is dehydrated by a method comprising the steps of:
a) contacting the PVA-hydrogel with an organic solvent, wherein the hydrogel comprises a polymer which is not soluble in the solvent, and wherein the solvent is at least partially miscible in water; and
b) subjecting the hydrogel to at least one freeze-thaw cycle and allowing the hydrogel to warm-up room to temperature.
14. The method according to claim 11 , wherein the dehydration is carried out by placing the hydrogel in:
a) a non-solvent, wherein
i) the non-solvent is PEG, alcohols, acetones, saturated salinated water, vitamin, or carboxylic acid, aqueous solution of a salt of an alkali metal, and
ii) the non-solvent contains more than one ingredient including water, PEG, vitamin, polymer, ester, proteoglycan, and carboxylic acid, or
b) in a supercritical fluid.
15. The method according to claim 11 , wherein the dehydration is carried out at about 40° C. to above 200° C.
16. The method according to claim 11 , wherein the dehydration is carried out in an atmosphere containing 100% air, 100% inert gas, a mixture of one or more inert gases mixed with 0.1% to 99.9% air, or a mixture of one or more inert gases containing 0.1% to 99.9% oxygen.
17. The method according to claim 11 , wherein the dehydrated hydrogel is re-hydrated by placing the dehydrated hydrogel:
i) in water, saline solution, Ringer's solution, salinated water, buffer solution, and the like,
ii) in a humid chamber, and/or
iii) at room temperature or at an elevated temperature.
18. The method according to claim 1 , wherein the PVA-hydrogel is re-hydrated to reach an equilibrium.
19. The method according to claim 1 , wherein the pH mt of a PVA-PAA solution containing 1.654 w/w % aqueous PAA solution and 25% total polymer having a PVA:PAA ratio of 19:1 is between about 3.0 and about 5.5.
20. The method according to claim 1 , wherein the PVA-hydrogel comprises one or more hydrophilic polymers selected from the group consisting of: PVA-PAA copolymer, poly(ethylene oxide) (PEO)-PAA copolymer, Poly(methacrylic acid) (PMAA), polyvinylpyrrolidone (PVP), hyaluronic acid (HA), and poly(allylamine hydrochloride) (PAH).
21. The method according to claim 1 , wherein the hydrogel comprises water and/or one or more other ingredients, wherein the ingredient is PEG of different molecular weights or a blend of PEGs of different molecular weights.
22. The method of claim 1 further comprising dehydrating the hydrogel.
23. The method of claim 1 further comprising forming a medical implant from the PVA-hydrogel.