Generation of living tissue in vivo using a mold

• US 20050123520A1
• Filed: 05/04/2004
• Published: 06/09/2005
• Est. Priority Date: 05/05/2003
• Status: Abandoned Application

• Current Assignee: Massachusetts Eye And Ear Infirmary (Foundation of The Massachusetts Eye and EAR Infirmary Incorporated), University Of Massachusetts
• Original Assignee: Massachusetts Eye And Ear Infirmary (Foundation of The Massachusetts Eye and EAR Infirmary Incorporated)
• Inventors: Aminuddin, Saim, Vacanti, Martin P., Vacanti, Charles A., Kamil, Syed H., Eavey, Roland D.
• Application Number:
  US10/838,758
• Publication Number:
  US 20050123520A1
• Time in Patent Office: Days
• US Class Current: 424/93.700
• CPC Class Codes: A61L 27/20 Polysaccharides
• CPC Class Codes: A61L 27/3804 characterised by specific cells or progenitors thereof, e.g. fibroblasts, connective tissue cells, kidney cells
• CPC Class Codes: A61L 27/52 Hydrogels or hydrocolloids
• CPC Class Codes: C08L 5/04 Alginic acid; Derivatives thereof
• CPC Class Codes: C12N 5/0697 Artificial constructs associating cells of different lineages, e.g. tissue equivalents blood vessels C12N5/0691

Abstract

The invention features methods of making living tissue constructs having a predetermined shape by obtaining a negative mold having a defined shape; suspending isolated tissue precursor cells in a hydrogel to form a liquid hydrogel-precursor cell composition; filling the liquid hydrogel-precursor cell composition into the mold; implanting the filled mold into a living host for incubation; removing the mold after a suitable incubation period; and removing the living tissue construct from the mold. The final living tissue construct can then be surgically implanted into a patient.

Claims

1. A method of making a living tissue construct having a predetermined shape, the method comprising

obtaining a negative mold having a defined shape;

suspending isolated tissue precursor cells in a hydrogel to form a liquid hydrogel-precursor cell composition;

filling the liquid hydrogel-precursor cell composition into the mold;

implanting the filled mold into a living host for a time sufficient to enable the tissue precursor cells to form tissue;

removing the mold from the living host; and

removing the living tissue construct from the mold.

2. The method of claim 1, wherein the tissue precursor cells are chondrocytes, osteocytes, osteoblasts, or adipocytes, or a combination thereof.

3. The method of claim 1, wherein the tissue precursor cells are chondrocytes.

4. The method of claim 1, wherein the hydrogel is selected from the group consisting of alginate, chitosan, pluronic, collagen, and agarose.

5. The method of claim 1, wherein the hydrogel is alginate.

6. The method of claim 5, wherein the alginate concentration is from 0.5% to 8%.

7. The method of claim 5, wherein the alginate concentration is from 1% to 4%.

8. The method of claim 5, wherein the alginate concentration is approximately 2%.

9. The method of claim 1, further comprising inducing gel formation of the liquid hydrogel-precursor cell composition either before or after filling the composition into the mold.

10. The method of claim 9, wherein inducing gel formation comprises contacting the liquid hydrogel with a suitable concentration of a divalent cation.

11. The method of claim 9, wherein the divalent cation is Ca⁺⁺.

12. The method of claim 1, wherein the filled mold is incubated in the host for a period of 8 to 20 weeks.

13. The method of claim 1, wherein the negative mold is prepared using CAD/CAM or rapid prototyping.

14. The method of claim 1, wherein the filled mold is incubated in the host for a time sufficient for at least 50 percent of the hydrogel to be degraded and removed from the tissue construct within the mold.

16. An injection-molded living tissue construct made by the process of claim 1.

17. A method of reconstructing an anatomical feature in a mammal, the method comprising

obtaining a living tissue construct having the shape of the anatomical feature;

and

implanting the tissue construct into the mammal, wherein the construct is prepared by the method of claim 1.

18. The method of claim 1, wherein the living tissue construct is shaped in the form of articular cartilage adjacent ajoint, a bone, a portion of a bone, or a bone defect.

19. The method of claim 1, wherein the hydrogel is selected from the group consisting of polysaccharides, proteins, polyphosphazenes, poly(oxyethylene)-poly(oxypropylene) block polymers, poly(oxyethylene)-poly(oxypropylene) block polymers of ethylene diamine, poly(acrylic acids), poly(methacrylic acids), copolymers of acrylic acid and methacrylic acid, poly(vinyl acetate), and sulfonated polymers.

20. The method of claim 1, wherein the tissue precursor cells are selected from the group consisting of epidermal cells, chondrocytes and other cells that form cartilage, macrophages, dermal cells, muscle cells, hair follicles, fibroblasts, organ cells, osteoblasts and other cells that form bone, endothelial cells, mucosal cells, pleural cells, ear canal cells, tympanic membrane cells, peritoneal cells, Schwann cells, corneal epithelial cells, gingiva cells, neural cells, neural stem cells, and tracheal epithelial cells.

21. The method of claim 1, wherein the tissue precursor cells are nervous system neural stem or progenitor cells.

15. A method of reconstructing an anatomical feature in a mammal, the method comprising

obtaining a suitable negative mold having a negative shape of the anatomical feature;

suspending isolated tissue precursor cells in a hydrogel to form a liquid hydrogel-precursor cell composition,

filling the liquid hydrogel-precursor cell composition into the mold;

inducing gel formation of the liquid hydrogel-precursor cell composition to form a living tissue construct;

implanting the filled mold into a living host for a time sufficient to enable the tissue precursor cells to form tissue;

removing the mold from the living host;

removing the tissue construct from the mold; and

implanting the tissue construct into the mammal.