Tissue scaffolding comprising surface folds for tissue engineering

• US 20100303880A1
• Filed: 04/17/2006
• Published: 12/02/2010
• Est. Priority Date: 04/28/2005
• Status: Abandoned Application

• Current Assignee: Brendan Harley, Christopher J. Zagorski, Harry K. Reddy, Joannis V. Yannas
• Original Assignee: Brendan Harley, Christopher J. Zagorski, Harry K. Reddy, Joannis V. Yannas
• Inventors: Zagorski, Christopher J., Yannas, Joannis V., Reddy, Harry K., Harley, Brendan
• Application Number:
  US11/919,494
• Publication Number:
  US 20100303880A1
• Time in Patent Office: Days
• US Class Current: 424/423
• CPC Class Codes: A61L 27/38 containing added animal cells organs or tissue containing native cells A61L27/36
• CPC Class Codes: A61L 27/56 Porous materials, e.g. foams or sponges
• CPC Class Codes: A61P 17/00 Drugs for dermatological disorders
• CPC Class Codes: A61P 17/02 for treating wounds, ulcers, burns, scars, keloids, or the like

Abstract

The invention is directed to solid gradient scaffolds, methods of producing the same, and therapeutic applications arising from their utilization. Specifically, the gradient scaffolding includes, inter-alia, surface folds of various configuration for increasing surface area to volume of the scaffold.

Claims

1. A solid, biocompatible scaffold for implantation, comprising surface folds, wherein said surface folds increase said scaffold surface area to volume ratio (SA/V), by at least 20%.

2. The scaffold of claim 1, wherein said folds vary in terms of their depth, which may range from 1 mm-10 cm, their diameter, which may range from 1 mm-5 cm, or a combination thereof, within said scaffold.

3. The scaffold of claim 1, wherein said folds form a channel within said scaffold.

4. The scaffold of claim 3, wherein said channel may be oriented along an axis.

5. The scaffold of claim 3, wherein the diameter of said channel is greater at a point more proximal to the scaffold surface, than to its core.

6. The scaffold of claim 1, wherein said folds are randomly distributed throughout said scaffold.

7. The scaffold of claim 1, wherein said scaffold comprises at least one polymer.

8. The scaffold of claim 5, wherein said polymer comprises at least one synthetic or natural polymer, ceramic, metal, extracellular matrix protein or an analogue thereof.

9. The scaffold of claim 6, wherein said extracellular matrix proteins comprise a collagen, a glycosaminoglycan, or a combination thereof.

10. The scaffold of claim 1, wherein said scaffold is non-uniformly porous.

11. The scaffold of claim 10, wherein said scaffold varies in its pore diameter, from 0.75 to 3000 μ

m, its average pore size distribution, which may range from about 20 to 200 μ

m±

1 to about 50 μ

m, its cross-link density.

12. The scaffold of claim 1, wherein said scaffold further comprises cells, extracellular matrix components, growth factors, cytokines, hormones, inflammatory stimuli, angiogenic factors, or a combination thereof.

13. The scaffold of claim 1, wherein the size and shape of said scaffold is a function of the tissue into which the scaffold is to be implanted.

14. The scaffold of claim 1, wherein said scaffold, when implanted, promotes angiogenesis within, or proximal to the scaffold.

15. The scaffold of claim 1, wherein said scaffold is comprised of a material whose stiffness is sufficient to resist compressive forces of tissue proximal to a site of implantation.

23. A method of organ or tissue engineering in a subject, comprising the step of implanting a scaffold of any one of claim 1-15 or 22 in said subject.

24. The method of claim 23, further comprising the step of implanting cells in said subject.

25. The method of claim 24, wherein said cells are seeded on said scaffold.

26. The method of claim 25, wherein said cells are seeded at the periphery of said scaffold.

27. The method of claim 25, wherein said scaffold is cultured for a period of time prior to implantation in said subject.

28. The method of claim 25, wherein said cells are stem or progenitor cells.

29. The method of claim 25, wherein said engineering is of an organ or tissue comprised of heterogeneous cell types.

30. The method of claim 25, wherein said tissue is breast tissue or skin.

31. The method of claim 25, wherein said method is utilized in wound healing.

32. A method of organ or tissue repair or regeneration in a subject, comprising the step of implanting a scaffold of any of claim 1-15 or 22 in said subject.

33. The method of claim 32, further comprising the step of implanting cells in said subject.

34. The method of claim 32, wherein said cells are seeded on said scaffold.

35. The method of claim 34, wherein said scaffold is cultured for a period of time prior to implantation in said subject.

36. The method of claim 33, wherein said cells are seeded at the periphery of said scaffold.

37. The method of claim 33, wherein said cells are stem or progenitor cells.

38. The method of claim 33, further comprising the step of administering cytokines, growth factors, hormones or a combination thereof.

39. The method of claim 32, wherein said engineering is of an organ or tissue comprised of heterogeneous cell types.

40. The method of claim 32, wherein said tissue is skin or breast tissue.

41. The method of claim 32, wherein said method is used in wound healing

16. A process for preparing a solid scaffold comprising surface folds, the process comprising the steps of:

a. applying a polymeric suspension to a mold comprised of a conductive material, wherein a surface of said mold which is in contact with said suspension has numerous folds; and

b. subjecting the suspension-filled mold in (a) to conditions whereby said suspension is solidified.

17. The process of claim 16, wherein the mold is so constructed that the surface folds vary in depth, from 1 mm-10 cm, and diameter, which may range from 1 mm-5 cm, or a combination thereof, within said scaffold.

18. The process of claim 16, further comprising the step of super-cooling the suspension-filled mold in (a), at a constant temperature, for a period of time until said suspension is solidified, whereby ice crystals are formed in said solidified suspension, said crystals being oriented perpendicular to an edge of said scaffold

19. The process of claim 18, further comprising exposing the solidified suspension or a portion thereof, to conditions which enable sublimation in the exposed region, whereby pores are formed which are perpendicular to an edge of said scaffold.

20. The process of claim 18, wherein the pores form a channel.

21. The process of claim 18, wherein the pores are oriented along an axis.

22. A scaffold prepared according to the process of claim 16.