초록 ▼

Methods and apparatuses are provided for musculoskeletal tissue engineering. For example, a scaffold apparatus is provided which comprises microspheres of selected sizes and/or composition. The microspheres are layered to have a gradient of microsphere sizes and/or compositions. The scaffold provide

Methods and apparatuses are provided for musculoskeletal tissue engineering. For example, a scaffold apparatus is provided which comprises microspheres of selected sizes and/or composition. The microspheres are layered to have a gradient of microsphere sizes and/or compositions. The scaffold provides a functional interface between multiple tissue types.

대표청구항 ▼

What is claimed is: 1. A scaffold apparatus for musculoskeletal tissue engineering, said apparatus comprising microspheres of selected sizes and/or concentrations, wherein the microspheres are layered to have a gradient of microsphere sizes and/or concentrations, and wherein the scaffold promotes g

What is claimed is: 1. A scaffold apparatus for musculoskeletal tissue engineering, said apparatus comprising microspheres of selected sizes and/or concentrations, wherein the microspheres are layered to have a gradient of microsphere sizes and/or concentrations, and wherein the scaffold promotes growth and maintenance of a soft tissue and bone. 2. The scaffold apparatus of claim 1, wherein the scaffold supports growth, maintenance and differentiation of a soft tissue and bone. 3. The scaffold apparatus of claim 1, further comprising: a first region comprising composite microspheres of a first size and composition optimized to promote growth, proliferation, and differentiation of a first cell type for integration and growth of a first soft tissue and/or bone type; a second region joined to the first region, said second region comprising at least one of microspheres and a fibrous mesh, said one of microspheres and a fibrous mesh having a second size and a second composition; a third region joined to the second region, said third region comprising microspheres and/or a fibrous mesh, said microspheres and/or fibrous mesh having a third size and a third composition, and said second and third regions being optimized to promote growth, proliferation and differentiation of a second cell type for integration and formation of a second soft tissue and/or bone type; and a fourth region joined to the third region, said fourth region comprising at least one of microspheres and/or a fibrous mesh, said microspheres and/or fibrous mesh having a composition adapted to promote growth, proliferation, and differentiation of a third cell type for integration and growth of a third soft tissue and/or bone type, wherein said first, second, third and fourth regions are joined together through one of a solid state sintering process and a solvent aggregation process, in which selected growth factors or bioactive agents are incorporated into each region to promote formation, growth and integration of said first, second and third types of tissues. 4. The scaffold apparatus of claim 1, wherein the scaffold provides a functional interface between soft tissue and bone. 5. The scaffold apparatus of claim 4, wherein the scaffold has multiple phases including a first phase for supporting growth and maintenance of the soft tissue, a second phase for supporting growth and maintenance of the bone, and a third phase as an interfacial zone supporting growth of fibrocartilage between said first and second phases. 6. The scaffold apparatus of claim 1, wherein the first phase for supporting growth and maintenance of the soft tissue is seeded with at least one of fibroblasts, chondrocytes and stem cells. 7. The scaffold apparatus of claim 1, wherein the first phase of the scaffold includes a fiber mesh. 8. The scaffold apparatus of claim 7, wherein said fiber mesh is electrospun. 9. The scaffold apparatus of claim 1, wherein the second phase for supporting growth and maintenance of the bone is seeded with at least one of osteoblasts, osteoblast-like cells and stem cells. 10. The scaffold apparatus of claim 9, wherein said second phase contains at least one of osteogenic agents, osteogenic materials, osteoinductive agents, osteoinductive materials, osteoconductive agents, osteoconductive materials, growth factors and chemical factors. 11. The scaffold apparatus of claim 1, wherein the third phase includes at least some of said microspheres. 12. The scaffold apparatus of claim 11, wherein the third phase includes a gradient of microsphere sizes. 13. The scaffold apparatus of claim 11, wherein the third phase includes a gradient of microsphere compositions. 14. The scaffold apparatus of claim 11, wherein the microspheres in the third phase are joined by sintering in at least one stage. 15. The scaffold apparatus of claim 11, wherein the second phase of the scaffold further includes additional microspheres. 16. The scaffold apparatus of claim 15, wherein the at least some of said microspheres of the third phase are in a first range of diameters, and the additional microspheres of the second phase are in a second range of diameters, the second range being nonoverlapping with the first range. 17. The scaffold apparatus of claim 1, wherein said scaffold apparatus is integrated in a graft collar. 18. The scaffold apparatus of claim 17, wherein said graft collar is adapted for hamstring tendon-to-bone healing. 19. The scaffold apparatus of claim 17, wherein said graft collar is adapted for peridontal ligament repair. 20. The scaffold apparatus of claim 17, wherein said graft collar is adapted for spinal repair. 21. The scaffold apparatus of claim 1, wherein said first phase is seeded with human hamstring tendon fibroblasts. 22. The scaffold apparatus of claim 1, wherein at least one of said first phase and said second phase is seeded with one or more agents by using a microfluidic system. 23. The scaffold apparatus of claim 1, wherein the scaffold has multiple phases joined by a gradient of properties. 24. The scaffold apparatus of claim 23, wherein the multiple phases of the scaffold are processed through one or more sintering stages. 25. The scaffold apparatus of claim 23, wherein the gradient of properties across the multiple phases of the scaffold includes mechanical properties. 26. The scaffold apparatus of claim 23, wherein the gradient of properties across the multiple phases of the scaffold includes chemical properties. 27. The scaffold apparatus of claim 23, wherein the gradient of properties across the multiple phases of the scaffold includes mineral content. 28. The scaffold apparatus of claim 23, wherein the gradient of properties across the multiple phases of the scaffold includes structural properties. 29. The scaffold apparatus of claim 23, wherein the gradient of properties across the multiple phases of the scaffold includes porosity. 30. The scaffold apparatus of claim 23, wherein the gradient of properties across the multiple phases of the scaffold includes geometry. 31. The scaffold apparatus of claim 1, wherein a first phase of the microspheres comprises polymer and a second phase of the microspheres comprises one of bioactive glass and calcium phosphate. 32. The scaffold apparatus of claim 31, wherein the calcium phosphate is selected from a group comprising tricalcium phosphate, hydroxyapatite, and a combination thereof. 33. The scaffold apparatus of claim 31, wherein the polymer is selected from a group comprising aliphatic polyesters, poly(amino acids), copoly(ether-esters), polyalkylenes oxalates, polyamides, poly(iminocarbonates), polyorthoesters, polyoxaesters, polyamidoesters, poly(ε-caprolactone)s, polyanhydrides, polyarylates, polyphosphazenes, polyhydroxyalkanoates, polysaccharides, and biopolymers, and a blend of two or more of the preceding polymers. 34. The scaffold apparatus of claim 33, wherein the polymer comprises at least one of poly(lactide-co-glycolide), poly(lactide) and poly(glycolide). 35. The scaffold apparatus of claim 1, wherein the first phase of the scaffold includes a fiber mesh, and the fiber mesh of the first phase and the microspheres of said third phase are sintered together. 36. The scaffold apparatus of claim 1, wherein the microspheres are processed through one or more sintering stages. 37. The scaffold apparatus of claim 1, wherein the scaffold includes a composite of said microspheres and a fiber mesh. 38. The scaffold apparatus of claim 37, wherein the fiber mesh is a degradable polymer. 39. The scaffold apparatus of claim 37, wherein said fiber mesh is electrospun. 40. The scaffold apparatus of claim 37, wherein at least one of bioactive agents and peptides coat the surface of the mesh. 41. The scaffold apparatus of claim 40, wherein the bioactive agents and peptides enhance differentiation, proliferation and attachment of cells and specific cell types. 42. The scaffold apparatus of claim 30, wherein at least one of bioactive agents and peptides are directly incorporated into the mesh. 43. The scaffold apparatus of claim 1, wherein the apparatus is biomimetic. 44. The scaffold apparatus of claim 1, wherein the apparatus is biodegradable. 45. The scaffold apparatus of claim 1, wherein the apparatus is osteointegrative. 46. The scaffold apparatus of claim 1, wherein the microspheres are degradable. 47. The scaffold apparatus of claim 1, wherein at least one of bioactive agents and peptides coat the surface of at least some of the microspheres. 48. The scaffold apparatus of claim 47, wherein the bioactive agents and peptides enhance at least one of differentiation, proliferation and attachment of cells and specific cell types. 49. The scaffold apparatus of claim 1, wherein at least one of bioactive agents and peptides are directly incorporated into at least some of the microspheres. 50. The scaffold apparatus of claim 1, wherein the microspheres additionally include one or more agents selected from a group comprising antiinfectives, hormones, analgesics, anti-inflammatory agents, growth factors, chemotherapeutic agents, anti-rejection agents and RGD peptides. 51. The scaffold apparatus of claim 1, wherein the second phase comprises one of polymeric and composite microspheres including a range of diameters or a gradient of diameter. 52. The scaffold apparatus of claim 1, wherein the second phase comprises polymeric hydrogels of one of polyethylene glycol and hydroxyethyl methacrylate. 53. The scaffold apparatus of claim 1, wherein the second phase comprises a hydrogel comprising one or more of poly(ethylene glycol), agarose, alginate, 2-hydroxyethyl methacrylate and polyacrylamide. 54. The scaffold apparatus of claim 1, wherein the second phase comprises collagen gels with varied mineral content. 55. The scaffold apparatus of claim 1, wherein varying concentrations of calcium phosphate are incorporated into the microspheres. 56. A multi-phased scaffold apparatus for providing a functional interface between bone and soft tissue, comprising: microspheres as one phase of the scaffold; and a mesh as another phase of the scaffold, wherein the microspheres and the mesh are sintered or solvent casted together and wherein the microspheres are layered to have a gradient of microsphere sizes and/or compositions. 57. The multi-phased scaffold apparatus of claim 56, wherein said mesh is electrospun. 58. The multi-phased scaffold apparatus of claim 56, wherein said multi-phased scaffold apparatus is integrated in a graft collar. 59. A scaffold apparatus for musculoskeletal tissue engineering, said apparatus comprising microspheres of selected sizes, wherein the microspheres are layered to have a gradient of microsphere sizes, and wherein the scaffold promotes growth and maintenance of a soft tissue, bone and fibrocartilage. 60. A scaffold apparatus for musculoskeletal tissue engineering, said apparatus comprising microspheres of selected concentrations, wherein the microspheres are layered to have a gradient of microsphere concentrations, and wherein the scaffold promotes growth and maintenance of a soft tissue, bone and fibrocartilage.