Scaffold for tissue engineering, artificial blood vessel, cuff, and biological implant covering member

• US 20050107868A1
• Filed: 09/28/2004
• Published: 05/19/2005
• Est. Priority Date: 03/28/2002
• Status: Abandoned Application

• Current Assignee: Bridgestone Corporation, National Cardiovascular Center Japan, National Cerebral And Cardiovascular Center
• Original Assignee: Bridgestone Corporation, National Cerebral And Cardiovascular Center
• Inventors: Nemoto, Yasushi, Tatsumi, Eisuke, Nakayama, Yasuhide
• Application Number:
  US10/950,620
• Publication Number:
  US 20050107868A1
• Time in Patent Office: Days
• US Class Current: 623/1.390
• CPC Class Codes: A61L 27/38 containing added animal cells organs or tissue containing native cells A61L27/36
• CPC Class Codes: A61L 27/507 for artificial blood vessels apparatus for applying cells on a blood vessel prosthesis A61F2/062
• CPC Class Codes: A61L 27/56 Porous materials, e.g. foams or sponges

Abstract

The invention provides a porous scaffold for tissue engineering which allows easy cell engraftment and cell culture and thus enables stable organization and an artificial blood vessel which exhibits high patency rate even if the inner diameter is small. The scaffold for tissue engineering is made of thermoplastic resin which forms a porous three-dimensional network structure having communication property, wherein the porous three-dimensional network structure has an average pore diameter of from 100 to 650 μm and an apparent density of from 0.01 to 0.5 g/cm³. The artificial blood vessel is composed of this scaffold.

The invention provides a cuff which allows easy infiltration of cells from living subcutaneous tissues, easy engraftment of cells, and neovascularization of capillary vessels so as to obtain robust bonding with subcutaneous tissues and, as a result, ensures separation of a wounded portion from the outside, thereby blocking exacerbation factors such as bacterial infection on healing and inhibiting progression of downgrowth. That is, the invention provides a cuff with none or little infection trouble such as tunnel infection. The cuff comprises a porous three-dimensional network structure which is made of thermoplastic resin or thermosetting resin and has communication property, wherein the porous three-dimensional network structure has an average pore diameter of from 100 to 1000 μm and apparent density of from 0.01 to 0.5 g/cm³.

The invention provides a biological implant covering member which allows easy infiltration of cells from living subcutaneous tissues, easy engraftment of cells, and organization, thereby obtaining robust bonding with native tissues and therefore protecting a living body from adverse effect which may occur due to the insertion of a biological implantation member into the living body. The biological implant covering member comprises a porous three-dimensional network structure which is made of thermoplastic resin or thermosetting resin and has communication property, wherein the porous three-dimensional network structure has an average pore diameter of from 100 to 1000 μm and apparent density of from 0.01 to 0.5 g/cm³.

Claims

1. A scaffold material for tissue engineering made of thermoplastic resin which forms a porous three-dimensional network structure having communication property, wherein the porous three-dimensional network structure has an average pore diameter of from 100 to 650 μ

m and an apparent density of from 0.01 to 0.5 g/cm³.

2. A scaffold material for tissue engineering as claimed in claim 1, wherein the average pore diameter of said porous three-dimensional network structure is from 100 to 400 μ

m and the apparent density thereof is from 0.01 to 0.5 g/cm³.

3. A scaffold material for tissue engineering as claimed in claim 2, wherein the average pore diameter of said porous three-dimensional network structure is from 100 to 300 μ

m.

4. A scaffold material for tissue engineering as claimed in any one of claim 1 through 3, wherein the apparent density of said porous three-dimensional network structure is from 0.01 to 0.2 g/cm³.

5. A scaffold material for tissue engineering as claimed in claim 4, wherein the apparent density of said porous three-dimensional network structure is from 0.01 to 0.1 g/cm³.

6. A scaffold material for tissue engineering as claimed claim 1, wherein the contribution ratio of pores of 150-300 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 10% or more.

7. A scaffold material for tissue engineering as claimed in claim 6, wherein the contribution ratio of pores of 150-300 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 20% or more.

8. A scaffold material for tissue engineering as claimed in claim 7, wherein the contribution ratio of pores of 150-300 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 30% or more.

9. A scaffold material for tissue engineering as claimed in claim 8, wherein the contribution ratio of pores of 150-300 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 40% or more.

10. A scaffold material for tissue engineering as claimed in claim 9, wherein the contribution ratio of pores of 150-300 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 50% or more.

11. A scaffold material for tissue engineering as claimed in claim 1, wherein said thermoplastic resin is one or more selected from a group composing of polyurethane resin, polyamide resin, polylactide resin, polyolefin resin, polyester resin, fluorocarbon resin, acrylic resin, methacrylic resin, and derivatives thereof.

12. A scaffold material for tissue engineering as claimed in claim 11, wherein the thermoplastic resin is polyurethane resin.

13. A scaffold material for tissue engineering as claimed in claim 12, wherein the polyurethane resin is segmented polyurethane resin.

14. A scaffold material for tissue engineering as claimed in claim 1, wherein one or more selected from a group composing of collagen Type I, collagen Type II, collagen Type III, collagen Type IV, atelocollagen, fibronectin, gelatin, hyaluronic acid, heparin, keratin acid, chondroitin, chondroitin sulfate, condroitin sulfate B, copolymer of hydroxyethyl methacrylate and dimethylaminoethyl methacrylate, copolymer of hydroxyethyl methacrylate and methacrylic acid, alginic acid, polyacrylamide, polydimethylacrylamide, and polyvinyl pyrrolidone is held in the porous three-dimensional network structure.

15. A scaffold material for tissue engineering as claimed in claim 14, wherein one or more selected from a group composing of fibrocyte growth factor, interleukin-1, tumor growth factor-β

, epidermal growth factor, and diploidic fibrocyte growth factor is further held in the porous three-dimensional network structure.

16. A scaffold material for tissue engineering as claimed in claim 15, wherein cells are adhered on the porous three-dimensional network structure.

17. A scaffold material for tissue engineering as claimed in claim 16, wherein said cells are cells of one or more kinds selected from a group composing of embryo-Nakayama stem cell, vascular endothelial cell, mesodermal cell, smooth muscle cell, peripheral vessel cell, and mesothelial cell.

18. A scaffold material for tissue engineering as claimed in claim 17, wherein said embryo-stem cell is dividing cell.

19. A scaffold material for tissue engineering as claimed in claim 1, wherein the scaffold takes the form of a tubular body.

20. A scaffold material for tissue engineering as claimed in claim 19, wherein the tubular body is from 0.3 to 15 mm in inner diameter and from 0.4 to 20 mm in outer diameter.

21. A scaffold material for tissue engineering as claimed in claim 20, wherein the tubular body is from 0.3 to 10 mm in inner diameter and from 0.4 to 15 mm in outer diameter.

22. A scaffold material for tissue engineering as claimed in claim 21, wherein the tubular body is from 0.3 to 6 mm in inner diameter and from 0.4 to 10 mm in outer diameter.

23. A scaffold material for tissue engineering as claimed in claim 22, wherein the tubular body is from 0.3 to 2.5 mm in inner diameter and from 0.4 to 10 mm in outer diameter.

24. A scaffold material for tissue engineering as claimed in claim 23, wherein the tubular body is from 0.3 to 1.5 mm in inner diameter and from 0.4 to 10 mm in outer diameter.

25. An artificial blood vessel being composed of A scaffold material as claimed in claim 1.

26. An artificial blood vessel as claimed in claim 25, wherein the outside of the scaffold is covered by another tubular body.

27. An artificial blood vessel as claimed in claim 26, wherein the tubular body covering the outside of the scaffold is a tube made of one or more selected from a group composing of chitosan, polylactide resin, polyester resin, polyamide resin, polyurethane resin, fibronectin, gelatin, hyaluronic acid, keratin acid, chondroitin, chondroitin sulfate, condroitin sulfate B, copolymer of hydroxyethyl methacrylate and dimethylaminoethyl methacrylate, copolymer of hydroxyethyl methacrylate and methacrylic acid, alginic acid, polyacrylamide, polydimethylacrylamide, and polyvinyl pyrrolidone, cross-linked collagen, and fibroin.

28. A cuff comprising a porous three-dimensional network structure which is made of a substrate resin composed of thermoplastic resin or thermosetting resin and has communication property, wherein the porous three-dimensional network structure has an average pore diameter of from 100 to 1000 μ

m and apparent density of from 0.01 to 0.5 g/cm³.

29. A cuff as claimed in claim 28, wherein the average pore diameter of said porous three-dimensional network structure is from 200 to 600 μ

m and the apparent density is from 0.01 to 0.5 g/cm³.

30. A cuff as claimed in claim 29, wherein the average pore diameter of said porous three-dimensional network structure is from 200 to 500 μ

m and the apparent density is from 0.01 to 0.5 g/cm³.

31. A cuff as claimed in any one of claims 28 through 30, wherein the apparent density of said porous three-dimensional network structure is from 0.05 to 0.3 g/cm³.

32. A cuff as claimed in claim 31, wherein the apparent density of said porous three-dimensional network structure is from 0.05 to 0.2 g/cm³.

33. A cuff as claimed in claim 28, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 10% or more.

34. A cuff as claimed in claim 33, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 20% or more.

35. A cuff as claimed in claim 34, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 30% or more.

36. A cuff as claimed in claim 35, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 40% or more.

37. A cuff as claimed in claim 36, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 50% or more.

38. A cuff as claimed in any one of claims 28 through 37, wherein the thickness of the porous three-dimensional network structure is from 0.2 to 500 mm.

39. A cuff as claimed in claim 38, wherein the thickness of the porous three-dimensional network structure is from 0.2 to 100 mm.

40. A cuff as claimed in claim 39, wherein the thickness of the porous three-dimensional network structure is from 0.2 to 50 mm.

41. A cuff as claimed in claim 40, wherein the thickness of the porous three-dimensional network structure is from 0.2 to 10 mm.

42. A cuff as claimed in claim 41, wherein the thickness of the porous three-dimensional network structure is from 0.2 to 5 mm.

43. A cuff as claimed in claim 28, wherein said substrate resin is one or more selected from a group composing of polyurethane resin, polyamide resin, polylactide resin, polyolefin resin, polyester resin, fluorocarbon resin, urea resin, phenol resin, epoxy resin, polyamide resin, acrylic resin, methacrylic resin, and derivatives thereof.

44. A cuff as claimed in claim 43, wherein the substrate resin is polyurethane resin.

45. A cuff as claimed in claim 44, wherein the polyurethane resin is segmented polyurethane resin.

46. A cuff as claimed in claim 28, wherein the cuff is a lamination of a first layer composed of the porous three-dimensional network structure and a second layer different from the first layer.

47. A cuff as claimed in claim 46, wherein the second layer is one or more selected from a group composing of a fiber aggregation, a flexible film, and a porous three-dimensional network structure of which the average pore diameter and the apparent density are different from those of the porous three-dimensional network structure of the first layer.

48. A cuff as claimed in claim 47, wherein the fiber aggregation is unwoven fabric or woven fabric.

49. A cuff as claimed in claim 48, wherein the thickness of the unwoven fabric or woven fabric is 0.1-100 mm.

50. A cuff as claimed in claim 49, wherein the thickness of the unwoven fabric or woven fabric is 0.1-50 mm.

51. A cuff as claimed in claim 50, wherein the thickness of the unwoven fabric or woven fabric is 0.1-10.0 mm.

52. A cuff as claimed in claim 51, wherein the thickness of the unwoven fabric or woven fabric is 0.1-5.0 mm.

53. A cuff as claimed in any one of claims 48 through 52, wherein the porosity of the unwoven fabric or woven fabric is from 100 to 5000 cc/cm²/min.

54. A cuff as claimed in claim 46, wherein the fiber aggregation is made of one or more selected from a group composing of polyurethane resin, polyamide resin, polylactide resin, polyolefin resin, polyester resin, fluorocarbon resin, acrylic resin, methacrylic resin, and derivatives thereof.

55. A cuff as claimed in claim 46, wherein the fiber aggregation is made of one or more selected from a group composing of fibroin, chitin, chitosan, and cellulose, and derivatives thereof.

56. A cuff as claimed in claim 46, wherein the flexible film is a thermoplastic resin film.

57. A cuff as claimed in claim 56, wherein the thermoplastic resin is one or more selected from a group composing of polyurethane resin, polyamide resin, polylactide resin, polyolefin resin, polyester resin, fluorocarbon resin, urea resin, phenol resin, epoxy resin, polyimide resin, silicone resin, acrylic resin, methacrylic resin, and derivatives thereof.

58. A cuff as claimed in claim 57, wherein the thermoplastic resin is one or more selected from a group composing of polyvinyl chloride, polyurethane resin, fluorocarbon resin, and silicone resin.

59. A cuff as claimed in claim 46, wherein the thickness of the flexible film is 0.1-500 mm.

60. A cuff as claimed in claim 59, wherein the thickness of the flexible film is 0.1-100 mm.

61. A cuff as claimed in claim 60, wherein the thickness of the flexible film is 0.1-50 mm.

62. A cuff as claimed in claim 61, wherein the thickness of the flexible film is 0.1-10 mm.

63. A cuff as claimed in claim 46, wherein the porous three-dimensional network structure of the second layer has an average pore diameter of 0.1-200 μ

m and an apparent density of from 0.01 to 1.0 g/cm³.

64. A cuff as claimed in claim 46, wherein the thickness of the porous three-dimensional network structure of the second layer is from 0.2 to 20 mm.

65. A cuff as claimed in claim 28, wherein one or more selected from a group composing of collagen Type I, collagen Type II, collagen Type III, collagen Type IV, atelocollagen, fibronectin, gelatin, hyaluronic acid, heparin, keratin acid, chondroitin, chondroitin sulfate, condroitin sulfate B, elastin, heparan sulfate, laminin, thrombospondin, hydronectin, osteonectin, entactin, copolymer of hydroxyethyl methacrylate and dimethylaminoethyl methacrylate, copolymer of hydroxyethyl methacrylate and methacrylic acid, alginic acid, polyacrylamide, polydimethylacrylamide, and polyvinyl pyrrolidone is held in the porous three-dimensional network structure.

66. A cuff as claimed in claim 65, wherein one or more selected from a group composing of platelet-derived growth factor, epidermal growth factor, transforming growth factor-α

, insulin-like growth factor, insulin-like growth factor binding proteins, hepatocyte growth factor, vascular endothelial proliferation growth factor, angiopoietin, nerve growth factor, brain-derived neurotrophic factor, ciliary neurotrophic factor, transforming growth factor-β

, latent form transforming growth factor-β

, activin, bone plasma proteins, fibrocyte growth factor, tumor growth factor-β

, diploid fibrocyte growth factor, heparin-binding epidermal growth factor-like growth factor, schwannoma-derived growth factor, anfillegrin, betacellulin, epillegrin, lymphotoxin, erythropoietin, tumor necrosis factor-α

, interleukin-1β

, interleukin-6, interleukin-8, interleukin-17, interferon, antivirotic, antimicrobial agent, and antibacterial agent is further held in the porous three-dimensional network structure.

67. A cuff as claimed in claim 66, wherein cells are adhered on the porous three-dimensional network structure.

68. A cuff as claimed in claim 67, wherein said cells are cells of one or more kinds selected from a group composing of embryo-stem cell, vascular endothelial cell, mesodermal cell, smooth muscle cell, peripheral vessel cell, and mesothelial cell.

69. A cuff as claimed in claim 68, wherein the embryo-stem cell is dividing cell.

70. A biological implant covering member comprising a porous three-dimensional network structure which is made of a substrate resin composed of thermoplastic resin or thermosetting resin and has communication property, wherein the porous three-dimensional network structure has an average pore diameter of from 100 to 1000 μ

m and apparent density of from 0.01 to 0.5 g/cm³.

71. A biological implant covering member as claimed in claim 70, wherein the average pore diameter of said porous three-dimensional network structure is from 200 to 600 μ

m and the apparent density is from 0.01 to 0.5 g/cm³.

72. A biological implant covering member as claimed in claim 71, wherein the average pore diameter of said porous three-dimensional network structure is from 200 to 500 μ

m and the apparent density is from 0.01 to 0.5 g/cm³.

73. A biological implant covering member as claimed in any one of claims 70 through 72, wherein the apparent density of said porous three-dimensional network structure is from 0.05 to 0.3 g/cm³.

74. A biological implant covering member as claimed in claim 73, wherein the apparent density of said porous three-dimensional network structure is from 0.05 to 0.2 g/cm³.

75. A biological implant covering member as claimed in claim 70, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 10% or more.

76. A biological implant covering member as claimed in claim 75, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 20% or more.

77. A biological implant covering member as claimed in claim 76, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 30% or more.

78. A biological implant covering member as claimed in claim 77, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 40% or more.

79. A biological implant covering member as claimed in claim 78, wherein the contribution ratio of pores of 150-400 μ

m diameter in the average pore diameter of the porous three-dimensional network structure is 50% or more.

80. A biological implant covering member as claimed in claim 70, wherein the thickness of the porous three-dimensional network structure is from 0.5 to 500 mm.

81. A biological implant covering member as claimed in claim 80, wherein the thickness of the porous three-dimensional network structure is from 0.5 to 100 mm.

82. A biological implant covering member as claimed in claim 81, wherein the thickness of the porous three-dimensional network structure is from 0.5 to 50 mm.

83. A biological implant covering member as claimed in claim 82, wherein the thickness of the porous three-dimensional network structure is from 0.5 to 10 mm.

84. A biological implant covering member as claimed in claim 83, wherein the thickness of the porous three-dimensional network structure is from 0.5 to 5 mm.

85. A biological implant covering member as claimed in claim 70, wherein said substrate resin is one or more selected from a group composing of polyurethane resin, polyamide resin, polylactide resin, polymalate resin, polyglycolate resin, polyolefin resin, polyester resin, fluorocarbon resin, urea resin, phenol resin, epoxy resin, polyimide resin, acrylic resin, methacrylic resin, and derivatives thereof.

86. A biological implant covering member as claimed in claim 85, wherein the substrate resin is polyurethane resin.

87. A biological implant covering member as claimed in claim 86, wherein the polyurethane resin is segmented polyurethane resin.

88. A biological implant covering member as claimed in claim 70, wherein the biological implant covering member is a lamination of a first layer composed of the porous three-dimensional network structure and a second layer different from the first layer.

89. A biological implant covering member as claimed in claim 70, wherein one or more selected from a group composing of collagen Type I, collagen Type II, collagen Type III, collagen Type IV, atelocollagen, fibronectin, gelatin, hyaluronic acid, heparin, keratin acid, chondroitin, chondroitin sulfate, condroitin sulfate B, elastin, heparan sulfate, laminin, thrombospondin, hydronectin, osteonectin, entactin, copolymer of hydroxyethyl methacrylate and dimethylaminoethyl methacrylate, copolymer of hydroxyethyl methacrylate and methacrylic acid, alginic acid, polyacrylamide, polydimethylacrylamide, and polyvinyl pyrrolidone is held in the porous three-dimensional network structure.

90. A biological implant covering member as claimed in claim 89, wherein one or more selected from a group composing of platelet-derived growth factor, epidermal growth factor, transforming growth factor-α

, insulin-like growth factor, insulin-like growth factor binding proteins, hepatocyte growth factor, vascular endothelial proliferation growth factor, angiopoietin, nerve growth factor, brain-derived neurotrophic factor, ciliary neurotrophic factor, transforming growth factor-β

, latent form transforming growth factor-β

, activin, bone plasma proteins, fibrocyte growth factor, tumor growth factor-β

, diploid fibrocyte growth factor, heparin-binding epidermal growth factor-like growth factor, schwannoma-derived growth factor, anfillegrin, betacellulin, epighrelin, lymphotoxin, erythropoietin, tumor necrosis factor-α

, interleukin-1β

, interleukin-6, interleukin-8, interleukin-17, interferon, antivirotic, antimicrobial agent, and antibacterial agent is further held in the porous three-dimensional network structure.

91. A biological implant covering member as claimed in claim 90, wherein cells are adhered on the porous three-dimensional network structure.

92. A biological implant covering member as claimed in claim 91, wherein said cells are cells of one or more kinds selected from a group composing of embryo-stem cell, vascular endothelial cell, mesodermal cell, smooth muscle cell, peripheral vessel cell, and mesothelial cell.

93. A biological implant covering member as claimed in claim 92, wherein the embryo-stem cell is dividing cell.