Bioadhesive hydrogels
View Patent ↗A method of forming and the resulting bioadhesive hydrogel composition for repairing or supplementing a nucleus pulposus of an intervertebral disc comprises at least a first component, a second component and a third component, wherein the first component, the second component and the third component are crosslinked. The first component comprises an amine-containing polymer component at a concentration from about 0.1% weight by weight to about 13.65% weight by weight. The second component comprises a hydrophilic polymer or pre-polymer component at a concentration from about 3% weight by weight to about 35% weight by weight. The third component comprises an aldehyde component at a concentration from about 0.1% weight by weight to about 30% weight by weight. A method of repairing or supplementing a nucleus pulposus of an intervertebral disc comprises implanting the bioadhesive hydrogel composition in a patient.
1. A bioadhesive hydrogel composition for repairing or supplementing a nucleus pulposus of an intervertebral disc comprising at least a first component, a second component and a third component, the first component comprising an amine-containing polymer component at a concentration from about 0.1% weight by weight to about 13.65% weight by weight, the second component comprising a hydrophilic polymer or pre-polymer component comprising poly(vinyl alcohol) at a concentration from about 3% weight by weight to about 35% weight by weight, the third component comprising an aldehyde component at a concentration from about 0.1% weight by weight to about 30% weight by weight, wherein the first component, the second component and the third component are crosslinked.
2. The composition of claim 1 , wherein the amine-containing polymer component is selected from the group consisting of poly(ethylene imine), poly(diethyl aminoethyl methacrylate), poly(ethyl aminoethyl methacrylate), amine-grafted poly(vinyl alcohol) or amine-containing poly(ethylene glycol).
3. The composition of claim 1 , wherein the amine-containing polymer component is poly(ethylene imine).
4. The composition of claim 1 , wherein the hydrophilic polymer or pre-polymer component is selected from the group consisting of poly(vinyl alcohol) and poly(ethylene glycol).
5. The composition of claim 1 , wherein the hydrophilic polymer or pre-polymer component consists of poly(vinyl alcohol).
6. The composition of claim 1 , wherein the aldehyde component is selected from the group consisting of glutaraldehyde, poly(ethylene glycol)-dialdehyde, glyoxal, formaldehyde and malonaldehyde.
7. The composition of claim 1 , wherein the aldehyde component is glutaraldehyde.
8. The composition of claim 1 , wherein the first component and the second component are crosslinked by a method selected from the group consisting of cryogelation, dehydration processing, radiation and exposure to chemicals.
9. The composition of claim 1 , wherein the first, second and third components are injectable immediately after mixing but not after forty-eight hours.
10. The composition of claim 1 , wherein the amine-containing polymer component and the aldehyde component are combined in such a way as to achieve about a one to one molar ratio of reactive amine groups to aldehyde groups.
11. The composition of claim 1 , wherein the composition is pre-conditioned with an aqueous solution of poly(ethylene imine).
12. The composition of claim 1 , wherein the amine-containing polymer component is poly(ethylene imine) at a concentration from about 5% weight by weight to about 11% weight by weight, the hydrophilic polymer or pre-polymer component is poly(vinyl alcohol) at a concentration from about 4% weight by weight to about 15% weight by weight and the aldehyde component is at a concentration from about 2% weight by weight to about 7% weight by weight.
13. A bioadhesive hydrogel composition for repairing or supplementing a nucleus pulposus of an intervertebral disc comprising at least a first component, a second component and a third component, the first component comprising an amine-containing polymer component at a concentration from about 5% weight by weight to about 11% weight by weight, the second component comprising a hydrophilic polymer or pre-polymer component comprising poly(vinyl alcohol) at a concentration from about 4% weight by weight to about 15% weight by weight, the third component comprising an aldehyde component at a concentration from about 2% weight by weight to about 7% weight by weight, wherein the first component, the second component and the third component are crosslinked and the amine-containing polymer component and the aldehyde component are combined in such a way as to achieve about a one to one molar ratio of reactive amine groups to aldehyde groups.
14. A kit for forming a bioadhesive hydrogel composition comprising:
at least one first container containing an amine-containing polymer component at a sufficient concentration to be injectable at room temperature or under operating room conditions;
at least one second container containing a hydrophilic polymer or pre-polymer component comprising poly(vinyl alcohol) at a sufficient concentration to be injectable at room temperature or under operating room conditions; and
at least one third container containing an aldehyde component at a sufficient concentration to be injectable at room temperature or under operating room conditions,
wherein when the aldehyde component, the amine-containing polymer component and the hydrophilic polymer or pre-polymer component are mixed the composition is crosslinked and contains about 0.1% weight by weight to about 13.65% weight by weight of the amine-containing component, about 3% weight by weight to about 35% weight by weight of hydrophilic polymer or pre-polymer component and about 0.1% weight by weight to about 30% weight by weight of aldehyde component.
15. A kit for forming a bioadhesive hydrogel composition comprising:
at least one first container containing a precursor composition comprising an amine-containing polymer component crosslinked to a hydrophilic polymer or pre-polymer component comprising poly(vinyl alcohol); and
at least one second container loaded with an aldehyde component at a sufficient concentration to be injectable at room temperature or under operating room conditions,
wherein when the aldehyde component, the amine-containing polymer component and the hydrophilic polymer or pre-polymer component are mixed the composition is crosslinked and contains about 0.1% weight by weight to about 13.65% weight by weight of the amine-containing component, about 3% weight by weight to about 35% weight by weight of hydrophilic polymer or pre-polymer component and about 0.1% weight by weight to about 30% weight by weight of aldehyde component.
16. The kit of claim 15 , wherein the precursor composition is a hydrogel.
17. The kit of claim 15 , wherein the precursor composition is injectable at room temperature or under operating room conditions.
18. A method of repairing or supplementing a nucleus pulposus of an intervertebral disc comprising:
providing a bioadhesive hydrogel composition comprising at least a first component, a second component and a third component, the first component comprising an amine-containing polymer component at a concentration from about 0.1% weight by weight to about 13.65% weight by weight, the second component comprising a hydrophilic polymer or pre-polymer component comprising poly(vinyl alcohol) at a concentration from about 3% weight by weight to about 35% weight by weight, the third component comprising an aldehyde component at a concentration from about 0.1% weight by weight to about 30% weight by weight, wherein the first component, the second component and the third component are crosslinked; and
implanting the composition into a patient.
19. The method of claim 18 , wherein the bioadhesive hydrogel composition is implanted in the patient via injection.
20. The method of claim 18 , wherein the bioadhesive hydrogel composition solidifies in situ.
21. The method of claim 18 , wherein the bioadhesive hydrogel composition is implanted in the patient by inserting a solidified composition into the patient.
22. The method of claim 18 , wherein the composition is pre-conditioned with an aqueous solution of poly (ethylene imine) before implantation into the patient.
23. The method of claim 18 , wherein the amine-containing polymer component and the aldehyde component are combined in such a way as to achieve about a one to one molar ratio of reactive amine groups to aldehyde groups.