Surface directed cellular attachment

• US 8,002,830 B2
• Filed: 02/07/2005
• Issued: 08/23/2011
• Est. Priority Date: 02/06/2004
• Status: Active Grant

• Current Assignee: Georgia Tech Research Corporation (University System of Georgia)
• Original Assignee: Georgia Tech Research Corporation (University System of Georgia)
• Inventors: Schwartz, Zvi, Kennedy, Stephen J., Boyan, Barbara D.
• Primary Examiner(s): Anderson; James
• Assistant Examiner(s): Polansky; Gregg
• Application Number:
  US11/053,410
• Publication Number:
  US 20050196452A1
• Time in Patent Office: 2,388 Days
• Field of Search: 623/16.11, 623/23.5, 623/23.71, 623/23.72, 623/23.74, 623/23.76, 514/738, 424/422
• US Class Current: 623/16.11
• CPC Class Codes: A61L 27/16 obtained by reactions only involving carbon-to-carbon unsaturated bonds
• CPC Class Codes: A61L 27/52 Hydrogels or hydrocolloids
• CPC Class Codes: A61L 27/56 Porous materials, e.g. foams or sponges
• CPC Class Codes: A61P 19/00 Drugs for skeletal disorders
• CPC Class Codes: B33Y 80/00 Products made by additive manufacturing
• CPC Class Codes: C08L 29/04 Polyvinyl alcohol; Partially hydrolysed homopolymers or copolymers of esters of unsaturated alcohols with saturated carboxylic acids

Abstract

Implantable biomaterials, particularly hydrogel substrates with porous surfaces, and methods for enhancing the compatibility of biomaterials with living tissue, and for causing physical attachment between biomaterials and living tissues are provided. Also provided are implants suitable for load-bearing surfaces in hard tissue repair, replacement, or augmentation, and to methods of their use. One embodiment of the invention relates to an implantable spinal disc prosthesis.

Claims

1. A hydrogel having an outer surface and a depth, the hydrogel comprising:

a plurality of first substantially uniform cavities along the outer surface of the hydrogel, each of said first cavities extending to a bottom surface of said first cavity; and

a plurality of second substantially uniform cavities located below at least one of the first cavities, each of said second cavities extending from the bottom surface of the first cavity;

wherein said first cavities are only located on the outer surface of the hydrogel and do not extend throughout the depth of said hydrogel;

wherein said second cavities do not extend throughout the depth of said hydrogel; and

wherein the hydrogel comprises polyvinyl alcohol.

2. The hydrogel of claim 1, wherein the hydrogel is a load bearing device that is configured for implantation in a knee, shoulder or spine.

3. The hydrogel of claim 1,

wherein a cross section of each of the first cavities is larger than a cross section of each of the second cavities;

wherein the first cavities promote differentiation of a first cell type; and

wherein the second cavities promote differentiation of a second cell type.

4. The hydrogel of claim 1,

wherein the first cavities are larger than the second cavities;

wherein the first cavities promote attraction of bone cells; and

wherein the second cavities promote anchoring and growth of said bone cells.

5. The hydrogel of claim 1,

wherein the hydrogel comprises bone and cartilage forming cells or precursor cells to bone and cartilage forming cells.

6. The hydrogel of claim 1,

wherein the hydrogel comprises one or more of the following cells types:

osteoblasts, chondrocytes, mesenchymal stem cells and osteoprogenitor cells.

7. The hydrogel of claim 1,

wherein said hydrogel comprises bioactive factors to stimulate growth or differentiation of cells.

8. The hydrogel of claim 1, wherein both the first and the second cavities are arranged in a regular repeating fashion.

9. The hydrogel of claim 1, wherein the first cavities and the second cavities are within 1 millimeter of the outer surface of the hydrogel.

10. The hydrogel of claim 1, wherein the first cavities and the second cavities are within 200 micrometers of the surface of the hydrogel.

11. The hydrogel of claim 1, wherein said hydrogel has a moisture content of at least 5% w/w of the overall hydrogel.

12. The hydrogel of claim 1, wherein said hydrogel has a moisture content of at least 30% w/w of the overall hydrogel.

13. The hydrogel of claim 1, wherein the first cavities have an average cross-section of between 10 to 300 micrometers.

14. The hydrogel of claim 1, wherein the first cavities have an average cross-section of between 30 and 100 micrometers.

15. The hydrogel of claim 1, wherein the second cavities have an average cross-section of between 1 to 10 micrometers.

16. The hydrogel of claim 1, wherein the second cavities have an average cross-section of between 2 to 5 micrometers.

17. A hydrogel having an outer surface and a depth, the hydrogel comprising:

a plurality of first substantially uniform cavities along the outer surface of the hydrogel, each of said first cavities extending to a bottom surface of said first cavity; and

a plurality of second substantially uniform cavities located below at least one of the first cavities, each of said second cavities extending from the bottom surface of the first cavity;

wherein said first cavities are only located along the outer surface of the hydrogel and do not extend throughout the depth of said hydrogel;

wherein said second cavities do not extend throughout the depth of said hydrogel; and

wherein the hydrogel is a load bearing device that is configured for implantation in a joint.

18. The hydrogel of claim 17,

wherein the first cavities are larger than the second cavities;

wherein the first cavities promote attraction of bone cells; and

wherein the second cavities promote anchoring and growth of said bone cells.

19. The hydrogel of claim 17, wherein the first cavities and the second cavities are within 1 millimeter of the outer surface of the hydrogel.

20. The hydrogel of claim 17, wherein the first cavities and the second cavities are within 200 micrometers of the surface of the hydrogel.