초록

This invention relates to an implant for a musculoskeletal defect having a bioactive agent having a concentration gradient.

대표청구항 ▼

We claim: 1. An implant for repair of a musculoskeletal defect comprising: a) a foam matrix having a central region, an upper region, a lower region and a peripheral region, and b) a first bioactive agent present within a first of the regions of the foam matrix, c) a second bioactive agent present

We claim: 1. An implant for repair of a musculoskeletal defect comprising: a) a foam matrix having a central region, an upper region, a lower region and a peripheral region, and b) a first bioactive agent present within a first of the regions of the foam matrix, c) a second bioactive agent present within a second of the regions of the foam matrix, wherein the presence of the bioactive agents in different regions of the foam matrix is characterized by different controlled, gradual spatial concentration gradients. 2. The implant of claim 1 wherein at least one of the first and second bioactive agents is a chemotactic bioactive agent. 3. The implant of claim 2 wherein at least one of the spatial concentration gradients promotes cellular migration from native tissue adjacent the defect. 4. The implant of claim 2 wherein at least one of the spatial concentration gradients provides a highest bioactive agent concentration in the central region of the matrix. 5. The implant of claim 2 wherein at least one of the bioactive spatial concentration gradients provides a highest bioactive agent concentration in the peripheral region of the implant. 6. The implant of claim 2 wherein at least one of the bioactive spatial concentration gradients provides a high bioactive agent concentration in the central, upper and lower regions of the matrix and a low bioactive agent concentration in the peripheral region of the implant. 7. The implant of claim 2 wherein at least one of the bioactive spatial concentration gradients provides a highest bioactive agent concentration in the upper region of the matrix. 8. The implant of claim 2 wherein at least one of the bioactive spatial concentration gradients provides a bioactive agent concentration in the central region that is at least 10 times a concentration in the peripheral region. 9. The implant of claim 2 wherein at least one of the spatial concentration gradients provides a high first bioactive agent concentration in the central and peripheral regions of the matrix and a low first bioactive agent concentration in the upper and lower regions of the implant. 10. The implant of claim 2 wherein the second bioactive agent is a differentiation factor. 11. The implant of claim 2 wherein the first and second bioactive agents are different bioactive agents. 12. The implant of claim 10 wherein the first bioactive agent is the same bioactive agent as the second bioactive agent and has a first concentration in the first region, and has a second concentration in the second region. 13. The implant of claim 12 wherein the first bioactive agent is present in the first region in a concentration that avoids differentiation and has a concentration gradient in the second region that promotes cellular migration from native cartilage tissue adjacent the defect. 14. The implant of claim 13 wherein the first bioactive agent is the same bioactive agent as the second bioactive agent and further wherein the first bioactive agent is sequestered for delayed release. 15. The implant of claim 13 wherein the first bioactive agent is a different bioactive agent than the second bioactive agent and is sequestered for delayed release. 16. The implant of claim 10 wherein at least one of the first and second bioactive agents is a differentiation factor that is present in a concentration that stimulates production of extracellular matrix. 17. The implant of claim 10 wherein the differentiation factor is sequestered for delayed release. 18. The implant of claim 10 wherein the chemotactic bioactive agent is adapted for quick release. 19. The implant of claim 2 wherein the controlled, gradual spatial concentration gradients provide chemotaxis and differentiation to the same cell. 20. The implant of claim 2 wherein the bioactive agents are housed in quick and delayed release vehicles. 21. The implant of claim 1 wherein the first bioactive agent promotes bone formation. 22. The implant of claim 21 wherein the second bioactive agent is a chemotactic agent. 23. The implant of claim 22 wherein the first bioactive agent that promotes bone formation is rhGDF-5. 24. The implant of claim 23 wherein the chemotactic agent is TGF-β.