Thermogelling polymer blends for biomaterial applications
View Patent ↗Thermogelling polymers are described containing poly (n-isopropyl acrylamide). Solutions of this polymer, copolymers or mixtures of the polymer with a second polymer such as poly(ethylene glycol), poly (vinyl pyrrolidone) or poly(vinyl alcohol) are liquids at room temperature and solids at body temperature. Thus, also provided are methods of implanting a hydrogel into a mammal by injecting the solution as a liquid at a temperature below body temperature into a selected site in the mammal at a temperature below body temperature, which then undergoes thermal phase transition to form a solid hydrogel in situ in the body as the implant warms to body temperature. Methods for using these thermal gelling materials in various applications including nucleus pulposus replacement/augmentation, wound care, disk replacement, cartilage replacement, joint replacement, surgical barriers, gastrointestinal devices, cosmetic and reconstructive surgery, and breast enlargement are also provided.
1. A spinal disc augmentation implant for insertion into an intervertebral disc of a mammal comprising an injectable polymer solution comprising a poly(N-isopropyl acrylamide) chemically cross linked by a polyethylene glycol-based polymeric crosslinking agent so that the polymer solution solidifies from a liquid at room temperature to a solid or semi-solid hydrogel at physiological body temperature; wherein the ratio of poly(N-isopropyl acrylamide) to the polymeric crosslinking agent is from about 20 to 1 to about 500 to 1 and the implant has a modulus of elasticity between about 50 KPa and about 1,500 KPa.
2. The spinal disc augmentation implant according to claim 1 , wherein the polymeric crosslinking agent is hydrophilic.
3. The spinal disc augmentation implant according to claim 1 , wherein the polymer solution further comprises from about 25% to about 50% weight by volume of water.
4. The spinal disc augmentation implant according to claim 1 further comprising an imaging agent.
5. The spinal disc augmentation implant according to claim 4 , wherein said imaging agent is selected from the group consisting of barium sulfate, iodine, and a heavy metal power.
6. A method of implanting a thermogelling hydrogel into an interior cavity of an intervertebral disc of a spinal column of a mammal, the method comprising injecting a hydrogel solution comprising poly(N-isopropyl acrylamide) chemically cross linked by a polyethylene glycol-based polymeric crosslinking agent into the interior cavity of the intervertebral disc of the spinal column; wherein the hydrogel solution is injected as a liquid at room temperature and solidifies to form a solid implant as the hydrogel solution warms to physiological body temperature; wherein the ratio of poly(N-isopropyl acrylamide) to the polymeric crosslinking agent is from about 20 to 1 to about 500 to 1 and the implant has a modulus of elasticity between about 50 KPa and about 1,500 KPa.
7. The method according to claim 6 , wherein the polymeric crosslinking agent is hydrophilic.
8. The method according to claim 6 , wherein the hydrogel solution further comprises from about 25% to about 50% weight by volume of water.
9. The method according to claim 6 , wherein said hydrogel solution further comprises an imaging agent.
10. The method according to claim 6 , wherein the thermogelling hydrogel is implanted for nucleus pulposus replacement.
11. The method according to claim 6 , wherein the thermogelling hydrogel is implanted for nucleus pulposus augmentation.
12. A spinal disc augmentation implant for insertion into an intervertebral disc of a mammal comprising an injectable polymer solution comprising a poly(N-isopropyl acrylamide) chemically cross linked by a polyethylene glycol-based polymeric crosslinking agent so that the polymer solution solidifies from a liquid at room temperature to a solid or semi-solid hydrogel at physiological body temperature; wherein the ratio of poly(N-isopropyl acrylamide) to the polymeric crosslinking agent is from about 20 to 1 to about 500 to 1 and the implant has a modulus of elasticity between about 50 KPa and about 1,500 KPa; wherein the polymeric crosslinking agent comprises polyethylene glycol dimethylacrylate.
13. The method according to claim 6 , wherein the polymeric crosslinking agent comprises polyethylene glycol dimethylacrylate.
14. A method of implanting a thermogelling hydrogel into an intervertebral disc space between adjacent vertebral bodies using a hydrogel solution comprising poly(N-isopropyl acrylamide) chemically cross linked by a polyethylene glycol-based polymeric crosslinking agent, wherein the ratio of poly(N-isopropyl acrylamide) to the polymeric crosslinking agent is from about 20 to 1 to about 500 to 1, the method comprising the steps of:
a) forming an incision;
b) inserting a cannula into communication with the intervertebral disc space to create a passageway to the disc space;
c) inserting a needle into the intervertebral disc space via the cannula;
d) injecting the hydrogel solution as a liquid at room temperature into the intervertebral disc space;
e) permitting the hydrogel solution to solidify to form a solid implant as the hydrogel solution warms to physiological body temperature such that the solid implant has a modulus of elasticity between about 50 KPa and about 1,500 KPa;
f) removing the needle and cannula; and
g) closing the incision.
15. The spinal disc augmentation implant according to claim 1 , wherein room temperature is between 22° C. and 27° C. and body temperature is between 29° C. and 37° C.
16. The method of claim 6 , wherein room temperature is between 22° C. and 27° C. and body temperature is between 29° C. and 37° C.
17. The method of claim 14 , wherein room temperature is between 22° C. and 27° C. and body temperature is between 29° C. and 37° C.