Engineered scaffolds for promoting growth of cells

• US 20040126405A1
• Filed: 12/30/2002
• Published: 07/01/2004
• Est. Priority Date: 12/30/2002
• Status: Abandoned Application

• Current Assignee: Boston Scientific Scimed (Boston Scientific Corporation)
• Original Assignee: Scimed Life Systems Incorporated (Boston Scientific Corporation)
• Inventors: Dao, Kinh-Luan D., Chin, Yem, Sahatjian, Ronald A., Freyman, Toby, Zhong, Sheng-Ping, Banik, Michael S., Vu, Liem
• Application Number:
  US10/334,096
• Publication Number:
  US 20040126405A1
• Time in Patent Office: Days
• US Class Current: 424/423
• CPC Class Codes: A61L 27/3839 characterised by the site of application in the body materials for artificial blood vessels A61L27/507; materials for use in artificial skin A61L27/60
• CPC Class Codes: A61P 1/04 for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: C12M 25/14 Scaffolds; Matrices in general C12N5/0068

Abstract

A three dimensional cell scaffold is provided including a biocompatible polymer formed from a plurality of fibers configured so as to form a non-woven three dimensional open celled matrix having a predetermined shape, a predetermined pore volume fraction, a predetermined pore shape, and a predetermined pore size, with the matrix having a plurality of connections between the fibers.

Claims

1. A three dimensional cell scaffold, comprising:

a biocompatible polymer formed from a plurality of fibers configured so as to form a non-woven three dimensional open celled matrix having a predetermined shape, a predetermined pore volume fraction, a predetermined pore size, and a predetermined pore shape, wherein said matrix includes a plurality of connections between said plurality of fibers.

2. The cell scaffold according to claim 1, wherein said biocompatible polymer is a synthetic polymer, a natural polymer, or a combination thereof.

3. The cell scaffold according to claim 2, wherein said biocompatible polymer is biodegradable, or a combination of biodegradable and biostable.

4. The cell scaffold according to claim 3, wherein said biodegradable polymer is at least one of the group consisting of poly L-lactic acid (PLA), polyglycolic acid (PGA), alginate, hyaluronic acid, and copolymers and blends thereof.

5. The cell scaffold according to claim 4, wherein said biodegradable polymer comprises alginate or collagen.

6. The cell scaffold according to claim 1, wherein said predetermined pore shape is uniform throughout said matrix.

7. The cell scaffold according to claim 6, wherein said uniform shape is substantially circular, oval or rectilinear.

8. The cell scaffold according to claim 1, wherein said predetermined pore size is in the range of from about 0.5 micron to about 100 microns.

9. The cell scaffold according to claim 8, wherein said predetermined pore size is in the range of from about 1 micron to about 50 microns.

10. The cell scaffold according to claim 1, wherein said pore volume fraction is from about 60% to about 98%

11. The cell scaffold according to claim 10, wherein said pore volume fraction is from about 80% to about 98%.

12. The cell scaffold according to claim 1, wherein said predetermined shape is selected from the group consisting of a sheet, a tube, a cylinder, a sphere, a semi-circle, a cube, a rectangle, a wedge, and an irregular shape.

13. The cell scaffold according to claim 12, wherein said predetermined shape is a tube having an interior wall, an exterior wall, and a wall thickness, said wall thickness being from about 1 micron to about 50 microns, wherein said predetermined pore size is a gradient from a first pore size to a second pore size.

14. The cell scaffold according to claim 13, wherein said first pore size is about 2 μ

m to about 5 μ

m and said second pore size is from about 30 μ

m to about 60 μ

m.

15. The cell scaffold according to claim 14, wherein said predetermined pore size comprises one of said interior wall and said exterior wall having said first pore size and the other of said interior wall and said exterior wall having said second pore size.

16. The cell scaffold according to claim 15, wherein said gradient comprises one of a substantially gradual transition from said first pore size to said second pore size across said wall thickness and a substantially abrupt transition from said first pore size to said second pore size across said wall thickness.

17. The cell scaffold according to claim 1, wherein said biocompatible polymer comprises a plurality of polymers added sequentially to form said scaffold.

18. The cell scaffold according to claim 17, wherein said plurality of polymers includes at least one biodegradable polymer A and at least one biostable polymer B.

19. The cell scaffold according to claim 18, wherein said biodegradable polymer A is selected from the group consisting of a poly L-lactic acid (PLA), a polyglycolic acid (PGA), a collagen, a zein, a casein, a gelatin, a gluten, a serum albumen, an alginate, a hyaluronic acid, and blends and copolymers thereof.

20. The cell scaffold according to claim 18, wherein said biostable polymer B is selected from the group consisting of a poly(3-hydroxyalkanoate), a poly(3-hydroxyoctanoate), a poly(3-hydroxyfatty acid), a polyphosphazene, a poly(vinyl alcohol), a polyamide, a polyester amide, a polyamino acid, a polyanhydride, a polycarbonate, a polyacrylate, a polyalkylene, a polyalkylene glycol, a polyalkylene oxide, a polyalkylene terephthalates, a polyortho ester, a polyvinyl ether, a polyvinyl ester, a polyvinyl halide, a polyester, a polylactide, a polyglyxolide, a polysiloxane, a polyurethane, a SIBS block polymers, and blends and copolymers thereof.

21. The cell scaffold according to claim 20, wherein and said biostable polymer B is a SIBS block polymer.

22. The cell scaffold according to claim 18, wherein said scaffold includes layers of polymer A (A) and polymer B (B) according to a pattern selected from the group consisting of:

A-B, A-B-A, and A-B-A-B-A.

23. The cell scaffold according to claim 18, wherein said first pore size is sufficient to accommodate a diameter of an epithelial cell and said second pore size is sufficient to accommodate a diameter of a fibroblast cell.

24. The cell scaffold according to claim 12, wherein said predetermined shape is a tube and said predetermined pore size is sufficient to accommodate a diameter of an esophageal epithelial cell.

25. The cell scaffold according to claim 1, further comprising at least one biologically active agent selected from the group consisting of a nutrient, an angiogenic factor, an immunomodulatory factor, a drug, a cytokine, an extracellular protein, a proteoglycan, a glycosaminoglycan, a polysaccharide, a growth factor, and a RGD peptide.

26. The cell scaffold according to claim 25, wherein said extracellular protein is selected from the group consisting of a fibronectin, a laminin, a vitronectin, a tenascin, an entactin, a thrombospondin, an elastin, a gelatin, a collagen, a fibrillin, a merosin, an anchorin, a chondronectin, a link protein, a bone sialoprotein, an osteocalcin, an osteopontin, an epinectin, a hyaluronectin, an undulin, an epiligrin, and a kalinin.

27. The cell scaffold according to claim 25, wherein said growth factor is selected from the group consisting of a platelet derived growth factor, an insulin-like growth factor, a fibroblast growth factor, a transforming growth factor, a bone morphogenic protein, a vascular endothelial growth factor, a placenta growth factor, an epidermal growth factor, an interleukin, a colony stimulating factor, a nerve growth factor, a stem cell factor, a hepatocyte growth factor, and a ciliary neurotrophic factor.

28. The cell scaffold according to claim 25, wherein said drug is at least one of the group consisting of an immunosuppressant, an anticoagulant, and an antibiotic.

29. The cell scaffold according to claim 1, further comprising a support member selected from the group consisting of a stent, a rod, a hook, a band, and a coil.

30. The cell scaffold according to claim 1, further comprising a coating.

31. The cell scaffold according to claim 30, wherein said coating comprises hyaluronic acid.

32. The cell scaffold according to claim 1, further comprising a culture material containing cells.

33. The cell scaffold according to claim 32, wherein said cells are selected from the group consisting of epithelial cells, keratinocytes, adipocytes, hepatocytes, neurons, glial cells, astrocytes, podocytes, mammary epithelial cells, islet cells, endothelial cells, mesenchymal cells, dermal fibroblasts, mesothelial cells, stem cells, osteoblasts, smooth muscle cells, striated muscle cells, ligament fibroblasts, tendon fibroblasts, and chondrocytes.

34. A method for regenerating tissue in a mammal, comprising implanting the cell scaffold of claim 1 into said mammal.

35. The method according to claim 34, wherein said biocompatible polymer is at least one of the group consisting of a poly L-lactic acid (PLA), a polyglycolic acid (PGA), an alginate, a hyaluronic acid, a cellulose, a dextran, a pullane, a chitin, a poly(3-hydroxyalkanoate), a poly(3-hydroxyoctanoate), a poly(3-hydroxyfatty acid), a collagen, a zein, a casein, a gelatin, a gluten, a serum albumen, a polyphosphazene, a polyvinyl alcohol, a polyamide, a polyester amide, a poly amino acid, a polyanhydride, a polycarbonate, a polyacrylate, a polyalkylene, a polyalkylene glycol, a polyalkylene oxide, a polyalkylene terephthalate, a polyortho ester, a polyvinyl ether, a polyvinyl ester, a polyvinyl halide, a polyester, a polylactide, a polyglyxolide, a polysiloxane, a styrene isobutyl styrene block polymer, a polyurethane, and copolymers and blends thereof.

36. The method according to claim 35, wherein said scaffold is formed from a combination of:

(a) a biodegradable polymer selected from the group consisting of a poly L-lactic acid (PLA), a polyglycolic acid (PGA), an alginate, a hyaluronic acid, and copolymers and blends thereof, and

(b) a biostable polymer selected from the group consisting of a styrene isobutyl styrene block polymer, a polyurethane, and copolymers and blends thereof.

37. The method according to claim 34, wherein said predetermined shape is selected from the group consisting of a sheet, a tube, a cylinder, a sphere, a semi-circle, a cube, a rectangle, a wedge, and an irregular shape.

38. The method according to claim 34, further comprising the step of seeding cells into said cell scaffold prior to said implanting step.

39. The method according to claim 38, wherein said cells are selected from the group consisting of epithelial cells, keratinocytes, adipocytes, hepatocytes, neurons, glial cells, astrocytes, podocytes, mammary epithelial cells, islet cells, endothelial cells, mesenchymal cells, dermal fibroblasts, mesothelial cells, stem cells, osteoblasts, smooth muscle cells, striated muscle cells, ligament fibroblasts, tendon fibroblasts, chondrocytes, and fibroblasts.

40. The method according to claim 34, wherein said tissue is selected from the group consisting of nerve, skin, vascular, cardiac, pericardial, muscle, ocular, periodontal, bone, cartilage, tendon, ligament, breast, pancreatic, esophageal, stomach, kidney, hepatic, mammary, adrenal, urological, and intestinal.

41. The method according to claim 34, further comprising the step of treating said cell scaffold with at least one biologically active agent prior to said implanting step.

42. The method according to claim 41, wherein said biologically active agent is at least one of the group consisting of an extracellular protein, a growth factor, a nutrient, an angiogenic factor, an immunomodulatory factor, a drug, a cytokine, an extracellular protein, a proteoglycan, a glycosaminoglycan, and a polysaccharide.

53. A three dimensional cell scaffold according to claim 1, formed from the steps of:

admixing at least a biocomparible polymer with a compatible solvent to form a flowable polymer mixture;

applying at least one fiber formed from said polymer mixture to a table capable of motion in at least a first plane (x) and a second plane (y) perpendicular to said first plane; and

controlling movement of at least said table so as to form said matrix.

54. A tissue modeling kit, comprising:

a cell scaffold according to claim 1;

and

a plurality of viable cells from a tissue to be modeled, wherein said viable cells are cultured in said cell scaffold.

55. The tissue modeling kit according to claim 54, further comprising at least one biologically active agent selected from the group consisting of a nutrient, an angiogenic factor, an immunomodulatory factor, a drug, a cytokine, an extracellular protein, a proteoglycan, a glycosaminoglycan, a polysaccharide, a growth factor, and a RGD peptide.

56. A method of testing toxicity to a tissue, comprising:

forming a cell scaffold according to claim 1, wherein said shape resembles at least a portion of a tissue to be tested;

culturing cells derived from said tissue in said cell scaffold;

administering a predetermined dosage of a test agent to said cell scaffold; and

measuring a cellular response to said dosage.

57. The method according to claim 56, further comprising the steps of:

culturing cells derived from said tissue in a control cell scaffold;

administering a dosage of a control agent to said control scaffold;

measuring a control response to said dosage; and

comparing said cellular response to said control response.

58. The method according to claim 56, wherein said dosage is a series of dilutions of said agent, and further comprising the step of generating a dose response curve from cellular response results obtained in said measuring steps.

59. The method according to claim 56, wherein said cellular response is cell death.

60. The method according to claim 56, wherein said dosage is of a carcinogen.

61. The method according to claim 56, wherein said cells are disease state cells and said test agent is a drug candidate.

62. The method according to claim 56, wherein said cells are cancer cells.

43. A method of treating Gastro Esophageal Reflux Disease (GERD), comprising the steps of:

forming a biocompatible polymeric matrix formed from a plurality of fibers configured so as to form a non-woven three dimensional open celled tubular matrix, said matrix having a predetermined pore volume fraction, a predetermined pore shape, and a predetermined pore size sufficient to accommodate a diameter of esophageal epithelial cells, wherein said matrix includes a plurality of connections between said plurality of fibers;

seeding said matrix with esophageal epithelial cells or stem cells; and

implanting said matrix into a mammalian esophageal space.

44. The method according to claim 43, wherein said predetermined pore size includes a gradient of pore sizes ranging from about 2 μ

m to about 5 μ

m toward an internal diameter of said tubular matrix to from about 30 μ

m to about 60 μ

m toward an external diameter of the tubular matrix.

45. The method according to claim 43, wherein said biocompatible tubular matrix is made from alginate.

46. The method according to claim 43, further comprising the step of combining a tubular stent with said biocompatible matrix prior to said implanting step.

47. The method according to claim 43, further comprising the step of coating said biocompatible matrix with hyaluronic acid prior to said implanting step.

48. The method according to claim 43, further comprising the step of administering a bioactive agent to said biocompatible matrix prior to said implanting step.

49. The method according to claim 43, wherein said cells are selected from the group consisting of autologous, xenogeneic, allogenic, and syngeneic.

50. The method according to claim 49, wherein said cells are autologous.

52. The method according to claim 50, wherein said cell destroying compound is selected from the group consisting of a lye and a peroxide.

51. A method of removing diseased esophageal tissue, comprising the steps of:

forming a biocompatible polymeric matrix formed from a plurality of fibers configured so as to form a non-woven three dimensional tubular matrix, said matrix having a predetermined pore volume fraction, a predetermined pore shape, a predetermined pore shape and a predetermined pore size, wherein said matrix includes a plurality of connections between said plurality of fibers;

treating said matrix with a predetermined concentration of a cell destroying compound; and

implanting said matrix into a mammalian esophageal space.