Porous structures useful for growing living tissue, and methods of manufacture

• US 7,105,580 B2
• Filed: 12/05/2002
• Issued: 09/12/2006
• Est. Priority Date: 12/06/2001
• Status: Expired due to Fees

• Current Assignee: University of Washington, Georgia Tech Research Corporation (University System of Georgia)
• Original Assignee: University of Washington
• Inventors: Nair, Prabha D., Ratner, Buddy D., Vogel, Viola, Nerem, Robert M.
• Primary Examiner(s): Saucier, Sandra E.
• Assistant Examiner(s): BARNHART, LORA ELIZABETH
• Application Number:
  US10/314,453
• Publication Number:
  US 20030215946A1
• Time in Patent Office: 1,377 Days
• Field of Search: None
• US Class Current: 516/98
• 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: A61L 27/58 Materials at least partially resorbable by the body

Abstract

In one aspect the present invention provides biodegradable, porous structures that each include a structural framework, wherein the structural framework includes: (a) a solidified mixture of polymer molecules and amino acid molecules, wherein at least some of the amino acid molecules are linked to other amino acid molecules within the framework; and (b) a multiplicity of interconnected spaces defined by the structural framework. In some embodiments, the porous structures of the invention are adapted to physically support the growth of living cells in vitro or in vivo, and can be used to grow living tissue and/or living organs. The present invention also provide methods for making the biodegradable, porous structures of the invention.

Claims

1. A method of making a biodegradable porous structure comprising a multiplicity of interconnected spaces defined by a structural framework, said method comprising:

(a) stirring an aqueous solution in a colloidal aphron generator to form an aphron comprising a viscous foam, said aqueous solution selected from the group consisting of a solution of biodegradable polymer molecules and a solution of a mixture of amino acids and polymer molecules;

(b) placing said aphron into a mold;

(c) freezing the molded aphron to form a porous structure;

(d) lyophilizing the porous structure; and

(e) causing the porous structure to gel, yielding a lyophilized, biodegradable, porous structure comprising a multiplicity of interconnected spaces defined by a structural framework.

2. The method of claim 1 further comprising the step of covalently linking at least some of the amino acid molecules present in the lyophilized structure to other amino acid molecules present in the lyophilized structure.

3. The method of claim 1 wherein the biodegradable, porous structure is adapted to physically support the growth of living cells.

4. The method of claim 1 wherein the polymer molecules are selected from the group consisting of collagen, proteins, polysaccharide, fibrin, chitosan, poly(lactic acid), poly(glycolic acid), poly(lactic acid-glycolic acid copolymers), polyglycolides, aliphatic polyesters, poly(esteramides), polyamides, polyanhydrides, polyorthoesters, polyurethanes, and polyphosphazenes.

5. The method of claim 1 wherein the amino acid molecules are selected from the group consisting of aspartic acid, isoleucine, threonine, leucine, seine, tyrosine, glutamic acid, phenylalanine, proline, histidine, glycine, lysine, alanine, arginine, cysteine, tryptophan, valine, glutamine, methionine, and asparagine.

6. The method of claim 1 wherein the average diameter of the interconnected spaces is from 1 μ

m to 300 μ

m.

7. The method of claim 1 wherein the average diameter of the interconnected spaces is from 1 μ

m to 100 μ

m.

8. The method of claim 1 wherein the ratio of polymer molecules to amino acid molecules within the lyophilized, porous, structure is at least 25:

75.

9. The method of claim 1 wherein the ratio of polymer molecules to amino acid molecules within the lyophilized, porous, structure is from 25:

75 to 100;

1.

10. The method of claim 1 further comprising covalently or non-covalently attaching biologically active molecules to the biodegradable polymer molecules or to the amino acid molecules that comprise said aphron, wherein said biologically active molecules are selected from the group consisting of growth factors, fibronectin, laminin, vitronectin, integrins, nucleic acid molecules, lipids, sugars, antisense molecules, antiinflammatory agents, immunomodulatory agents, molecules that promote cell migration, molecules that promote cell division, molecules that promote cell proliferation and differentiation, molecules that stimulate phenotypic modification of cells, molecules that promote angiogenesis, molecules that promote vascularization and molecules that promote extracellular matrix disposition.

11. The method of claim 1 wherein the aphron is made from a population of molecules comprising a mixture of amino acid molecules and polymer molecules, frozen in a mold to yield a frozen, porous, structure and lyophilized, and further wherein at least some of the amino acid molecules are linked to other amino acid molecules.

12. The method of claim 1 wherein the average diameter of the interconnected spaces is from 10 μ

m to 50 μ

m.

22. The method of claim 11, further comprising lyophilizing the cross-linked porous structure containing the linked amino acids.

13. A method of making a biodegadable porous structure comprising a multiplicity of interconnected spaces defined by a structural framework, said method comprising:

(a) stiring an aqueous solution in a colloidal aphron generator to form an aphron comprising a viscous foam, said aqueous solution comprising alginate, glycine, lysine, isoluecine, and sodium docecyl sulfate;

(b) placing said aphron into a mold;

(c) freezing the molded aphron to form a porous structure;

(d) lyophilizing the porous structure; and

(e) causing the porous structure to gel.

14. The method of claim 13 further comprising drying the gelled porous structure.

15. The method of claim 14 further comprising crosslinking the amino acids in the porous structure.

16. The method of claim 15 further comprising lyophilizing the porous structure.

17. The method of claim 13, wherein the alginate in the aqueous solution is 2% alginic acid (w/v) or 5% alginic acid (w/v).

18. The method of claim 13, wherein the aqueous solution comprises 2% alginate (w/v) and alginate, glycine, lysine, and isoleucine are present in proportions of about 33.94:

59.39;

5.94;

0.73, respectively.

19. The method of claim 13, wherein the aqueous solution comprises 2% alginate (w/v) and alginate, glycine, lysine, and isoleucine are present in proportions of about 32.81:

56.24;

7.63;

3.32, respectively.

20. The method of claim 13 wherein the amount of sodium dodecyl sulfate is about 1.25% (weight/volume).

21. A method of making a porous structure comprising a multiplicity of interconnected spaces defined by a structural framework, said method comprising:

(a) stirring an aqueous solution in a colloidal aphron generator to form an aphron, said aqueous solution comprising polyvinyl alcohol, glycine, and lysine;

(b) placing said aphron in a mold;

(c) freezing the molded aphron to form a porous structure;

(d) lyophilizing the porous structure; and

(e) cross-linking the lyophilized porous structure using dicyclohexyl carbodiimide.