Multi-composite disc prosthesis
View Patent ↗A multi-composite disc prosthesis is adapted to be implanted within the annulus of an evacuated disc nucleus space in a human spine. The disc prosthesis has a generally solid unitary body with a size and a shape adapted to be positioned within the annulus of the evacuated disc nucleus space. The body has an outer portion comprised of a first biomaterial and an inner portion comprised of a second biomaterial. The second biomaterial has a compressive modulus that is harder than a compressive modulus of the first biomaterial and the first and second biomaterials are chemically or physically bonded to form a multi-composite material that forms the solid body.
1. A disc prosthesis that is adapted to be implanted within the annulus of an evacuated disc nucleus space in a human spine, the evacuated disc nucleus space being defined at least in part by tissue superior to the evacuated disc nucleus space and tissue inferior to the evacuated disc nucleus space, the disc prosthesis comprising, a generally solid unitary body having a size and a shape adapted to be positioned within the annulus of the evacuated disc nucleus space, wherein the solid unitary body is comprised of a plurality of interconnected segments that are positioned situ within the evacuated disc space to form the size and the shape of the solid unitary body, the body having: an outermost portion comprised of a first biomaterial and presenting a surface adapted to contact at least one of the tissue superior to the evacuated disc nucleus space and the tissue inferior to the evacuated disc nucleus space; and an innermost portion defining an inner core that provides support and stability for the solid body, the inner core comprised of a second biomaterial, wherein the outermost portion surrounds the innermost portion in an assembled configuration in situ, the inner core being of a compressive modulus that is harder than a compressive modulus of the outermost portion, first biomaterial and wherein the first and second biomaterials together form a multi-composite material comprising the solid body, and wherein the first biomaterial and the second biomaterial are bonded together at an interface such that the outermost portions and the innermost portion are held in a fixed spatial relationship with respect to each other at said interface.
2. The disc prosthesis of claim 1 wherein the first biomaterial and the second biomaterial are chemically bonded.
3. The disc prosthesis of claim 1 wherein the first biomaterial and the second biomaterial are physically bonded.
4. The disc prosthesis of claim 1 wherein the first biomaterial and the second biomaterial are each polymers.
5. The disc prosthesis of claim 4 wherein the first biomaterial and the second biomaterial are each a polyurethane.
6. The disc prosthesis of claim 5 wherein the polyurethane is comprised of a diisocyanate and a polyol.
7. The disc prosthesis of claim 5 wherein the components of the polyurethane are selected from the group consisting of: diisocyanates, polyols, catalysts, chain extenders and cross-linking agents.
8. The disc prosthesis of claim 5 , wherein the polyurethane of the first biomaterial has a hard segment content in the range of about 15 to 25 weight percent.
9. The disc prosthesis of claim 5 , wherein the polyurethane of the second biomaterial has a hard segment content in the range of about 50 to 70 weight percent.
10. The disc prosthesis of claim 4 wherein the second biomaterial is selected from the group consisting of: a thermoplastic polyether-urethane, polycarbonate-urethane and poly-ether-ether-ketone.
11. The disc prosthesis of claim 4 , wherein the first biomaterial is selected from the group consisting of: a thermoplastic polyether-urethane and polycarbonate-urethane.
12. The disc prosthesis of claim 1 , wherein the compressive modulus of the first biomaterial is in the range of about 10-20 MPa.
13. The disc prosthesis of claim 1 , wherein the second biomaterial has a Shore D hardness of at least 55.
14. The disc prosthesis of claim 1 , wherein at least an outermost layer of the outer portion further comprises at least one medicant operably carried by the first biomaterial to be eluted after the prosthesis is implanted.
15. The disc prosthesis of claim 1 , wherein the compressive modulus of the second biomaterial is at least 200 Mpa.
16. A disc prosthesis that is adapted to be implanted within the annulus of an evacuated disc nucleus space in a human spine, the evacuated disc nucleus space being defined at least in part by tissue superior to the evacuated disc nucleus space and tissue inferior to the evacuated disc nucleus space, the disc prosthesis comprising, a generally solid unitary body having a size and shape adapted to be positioned within the annulus of the evacuated disc nucleus space, wherein the solid unitary body is comprised of a plurality of interconnected segments that are positioned in situ within the evacuated disc space to form the size and the shape of the unitary body, the body having: an outermost portion comprised of a first biomaterial and presenting a surface adapted to contact at least one of the tissue superior to the evacuated disc nucleus space and the tissue inferior to the evacuated disc nucleus space; and an innermost portion defining an inner core comprised of a second biomaterial and arranged as a structure that provides support and stability for the solid body, wherein the outermost portion surrounds the innermost portion in an assembled configuration in situ, the second biomaterial has a compressive modulus greater than 200 Mpa that is harder than a compressive modulus of the first biomaterial by at least an order of magnitude and the first and second biomaterials together form a multi-composite material comprising the solid body, and wherein the first biomaterial and the second biomaterial are bonded together at an interface such that the outermost portion and the innermost portion are held in a fixed spatial relationship with respect to each other at said interface.
17. The disc prosthesis of claim 16 wherein the first biomaterial and the second biomaterial are chemically bonded.
18. The disc prosthesis of claim 16 wherein the first biomaterial and the second biomaterial are physically bonded.
19. The disc prosthesis of claim 16 wherein the first biomaterial and the second biomaterial are each polymers.
20. The disc prosthesis of claim 19 wherein the first biomaterial and the second biomaterial are each polyurethane.
21. The disc prosthesis of claim 20 wherein the polyurethane is comprised of a diisocyanate and a polyol.
22. The prosthesis of claim 20 wherein the components of the polyurethane are selected from the group consisting of: diisocyanates, polyols, catalysts, chain extenders and cross-linking agents.
23. The disc prosthesis of claim 20 wherein the polyurethane of the first biomaterial has a hard segment content in the range of about 15 to 25 weight percent.
24. The disc prosthesis of claim 20 wherein the polyurethane of the second biomaterial has a hard segment content in the range of about 50 to 70 weight percent.
25. The disc prosthesis of claim 19 wherein the second biomaterial is selected from the group consisting of: a thermoplastic polyether-urethane, polycarbonate-urethane and poly-ether-ether-keytone.
26. The disc prosthesis of claim 19 wherein the first biomaterial is selected from the group consisting of: a thermoplastic polyether-urethane and polycarbonate-urethane.
27. The disc prosthesis of claim 16 wherein the compressive modulus of the first biomaterial is in the range of about 10-20 Mpa.
28. The disc prosthesis of claim 16 wherein the second biomaterial has a Shore D hardness of at least 55.
29. The disc prosthesis of claim 16 wherein at least an outermost layer of the outer portion further comprises at least one medicant operably carried by first biomaterial to be eluted after the prosthesis is implanted.