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US5842477A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for repairing cartilage

Assignee: Smith and Nephew Inc
•
Filing: 1996-02-21
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Granted: 1998-12-01
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Expires: 2016-02-21
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Abstract

Abstract The present invention relates to methods of making and/or repairing cartilage in vivo comprising implanting into a patient, at a site of cartilage damage or loss, a biocompatible, non-living three-dimensional scaffold or framework structure in combination with periosteal/perichondrial tissue that can be used to hold the scaffold in place and provides a source of chondrocyte progenitor cells, chondrocytes and other stromal cells for attachment to the scaffold in vivo. In addition, a preparation of cells that can include chondrocytes, chondrocyte progenitor cells or other stromal cells is administered, either before, during or after implantation of the scaffold and/or the periosteal perichondrial tissue; the cells are administered directly into the site of the implant in vivo and promote the induction of factors that enhance chondrogenesis and the migration of chondrocytes, progenitor cells and other stromal cells from the adjacent in vivo environment into the scaffold for the production of new cartilage at the site of implantation.

Inventors

  • 👤 Gail K. Naughton
  • 👤 Jane Willoughby

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 11:50
CPC Classifications
A; A61; A61L; A61L27/00; A61L27/36; A61L27/38; A61L27/3804; A61L27/3834; A61F; A61F2/00; A61F2/02; A61F2/30; A61F2/30756; A61L27/3604; A61L27/3641; A61L27/3645; A61L27/3654; A61L27/3683; A61L27/3687; A61L27/3839; A61L27/3843; A61L27/3852; A61F2002/30001; A61F2002/30003; A61F2002/3006; A61F2002/30062; A61F2002/30108; A61F2002/30199; A61F2002/30766; A61F2210/00; A61F2210/0004; A61F2230/00; A61F2230/0063; A61L2430/00; A61L2430/06; Y; Y10; Y10S; Y10S623/00; Y10S623/902

Claims Analysis

Total Claims: 49
Claim 1
Independent Claim 81 words
A method of producing cartilage at a cartilage defect site in vivo comprising: (a) implanting into the defect site a biocompatible, non- living three-dimensional scaffold structure in combination with periosteal tissue, perichondrial tissue or a combination of said tissues; and (b) separately administering into the defect site a preparation of stromal cells for attachment to the scaffold in vivo and for inducing chondrogenesis or migration of stromal cells from the in vivo environment adjacent to the defect site to the scaffold.
Claim 2
Independent Claim 81 words
A method of producing cartilage at a cartilage defect site in vivo comprising: (a) implanting into the defect site a biocompatible, non- living three-dimensional scaffold structure in combination with periosteal tissue, perichondrial tissue or a combination of said tissues; and (b) separately administering into the defect site a preparation of stromal cells for attachment to the scaffold in vivo and for inducing chondrogenesis or migration of stromal cells from the in vivo environment adjacent to the defect site to the scaffold.
Claim 3
Dependent Claim 30 words
The method of claim 1, wherein the scaffold is implanted into the defect site and the periosteal or perichondrial tissue is placed on top of and adjacent to the scaffold.
Claim 4
Dependent Claim 30 words
The method of claim 1, wherein the periosteal or perichondrial tissue is implanted into the defect site and the scaffold is placed on top of and adjacent to the tissue.
Claim 5
Dependent Claim 33 words
The method of claim 1, wherein the periosteal or perichondrial tissue is situated with respect to the scaffold such that stromal cells from the tissue can migrate from the tissue to the scaffold.
Claim 6
Dependent Claim 27 words
The method of claim 1, wherein the periosteal tissue is situated with respect to the scaffold such that the cambium layer of the tissue faces the scaffold.
Claim 7
Dependent Claim 30 words
The method of claim 1, wherein the perichondrial tissue is situated with respect to the scaffold such that the cambium or inner transition layers of the tissue face the scaffold.
Claim 8
Dependent Claim 23 words
The method of claim 1, wherein the preparation of stromal cells is administered prior to, during or after implantation of the scaffold structure.
Claim 9
Dependent Claim 25 words
The method of claim 1, wherein the preparation of stromal cells is administered prior to, during or after implantation of the periosteal or perichondrial tissue.
Claim 10
Dependent Claim 23 words
The method of claim 1, wherein the preparation of stromal cells is physically placed between the scaffold and the periosteal or perichondrial tissue.
Claim 11
Dependent Claim 15 words
The method of claim 1, wherein the scaffold structure is composed of a biodegradable material.
Claim 12
Dependent Claim 23 words
The method of claim 10, wherein the biodegradable material is polyglycolic acid, polylactic acid, cat gut sutures, cellulose, nitrocellulose, gelatin, collagen or polyhydroxyalkanoates.
Claim 13
Dependent Claim 15 words
The method of claim 1, wherein the scaffold structure is composed of a non-biodegradable material.
Claim 14
Dependent Claim 31 words
The method of claim 12, wherein the non-biodegradable material is a polyamide, a polyester, a polystyrene, a polypropylene, a polyacrylate, a polyvinyl, a polycarbonate, a polytetrafluorethylene, polyhydroxylakanoate, cotton or a cellulose.
Claim 15
Dependent Claim 11 words
The method of claim 1, wherein the scaffold is a felt.
Claim 16
Dependent Claim 11 words
The method of claim 1, wherein the scaffold is a mesh.
Claim 17
Dependent Claim 16 words
The method of claim 1, wherein the scaffold is treated with ethylene oxide prior to implantation.
Claim 18
Dependent Claim 17 words
The method of claim 1, wherein the scaffold is treated with an electron beam prior to implantation.
Claim 19
Dependent Claim 31 words
The method of claim 1, wherein the scaffold comprises or is modified to contain at least one substance capable of enhancing the attachment or growth of stromal cells on the scaffold.
Claim 20
Dependent Claim 40 words
The method of claim 18, wherein the substance is a bioactive agent selected from the group consisting of cellular growth factors, factors that stimulate migration of stromal cells, factors that stimulate chondrogenesis, factors that stimulate matrix deposition, anti-inflammatories, and immunosuppressants.
Claim 21
Dependent Claim 14 words
The method of claim 19, wherein the bioactive agent is a transforming growth factor-beta.
Claim 22
Dependent Claim 18 words
The method of claim 19, wherein the bioactive agent is a bone morphogenetic protein that stimulates cartilage formation.
Claim 23
Dependent Claim 15 words
The method of claim 19, wherein the bioactive agent further comprises a sustained release formulation.
Claim 24
Dependent Claim 18 words
The method of claim 22 further comprising a biocompatible polymer which forms a composite with the bioactive agent.
Claim 25
Dependent Claim 25 words
The method of claim 23, wherein the biocompatible polymer is selected from the group consisting of polylactic acid, poly(lactic-co-glycolic acid), methylcellulose, hyaluronic acid, and collagen.
Claim 26
Dependent Claim 31 words
The method of claim 18, wherein the substance is selected from the group consisting of collagens, elastic fibers, reticular fibers, heparin sulfate, chondroitin-4-sulfate, chondroitin-6-sulfate, dermatan sulfate, keratin sulfate and hyaluronic acid.
Claim 27
Dependent Claim 32 words
The method of claim 1, further comprising the step of administering to the defect site at least one substance capable of enhancing the attachment or growth of stromal cells on the scaffold.
Claim 28
Dependent Claim 44 words
The method of claim 26, wherein the substance is a bioactive agent selected from the group consisting of cellular growth factors, factors that stimulate migration of stromal cells, factors that stimulate chondrogenesis, factors that stimulate chondrogenesis, factors that stimulate matrix deposition, anti-inflammatories, and immunosuppressants.
Claim 29
Dependent Claim 13 words
The method of claim 27, wherein the substance is a transforming growth factor-beta.
Claim 30
Dependent Claim 18 words
The method of claim 27, wherein the bioactive agent is a bone morphogenetic protein that stimulates cartilage formation.
Claim 31
Dependent Claim 17 words
The method of claim 1, wherein the periosteal or perichondrial tissue is autologous to the defect site.
Claim 32
Dependent Claim 13 words
The method of claim 1, wherein the preparation of stromal cells comprises chondrocytes.
Claim 33
Dependent Claim 15 words
The method of claim 1, wherein the preparation of stromal cells comprises chondrocyte progenitor cells.
Claim 34
Dependent Claim 16 words
The method of claim 1, wherein the preparation of stromal cells comprises fibroblasts or fibroblast-like cells.
Claim 35
Dependent Claim 51 words
The method of claim 1, wherein the preparation of stromal cells comprises a combination of cells selected from the group consisting of chondrocytes, chondrocyte progenitor cells, fibroblasts, fibroblast-like cells, endothelial cells, pericytes, macrophages, monocytes, leukocytes, plasma cells, mast cells, adipocytes, umbilical cord cells, and bone marrow cells from umbilical cord blood.
Claim 36
Dependent Claim 17 words
The method of claim 1, wherein the preparation of stromal cells comprises at least one bioactive agent.
Claim 37
Dependent Claim 38 words
The method of claim 35, wherein the bioactive agent is selected from the group consisting of cellular growth factors, factors that stimulate migration of stromal cells, factors that stimulate chondrogenesis, factors that stimulate matrix deposition, anti-inflammatories, and immunosuppressants.
Claim 38
Dependent Claim 14 words
The method of claim 36, wherein the bioactive agent is a transforming growth factor-beta.
Claim 39
Dependent Claim 18 words
The method of claim 36, wherein the bioactive agent is a bone morphogenetic protein that stimulates cartilage formation.
Claim 40
Dependent Claim 22 words
The method of claim 1, wherein the stromal cells of the preparation are genetically engineered to produce at least one bioactive agent.
Claim 41
Dependent Claim 38 words
The method of claim 39, wherein the bioactive agent is selected from the group consisting of cellular growth factors, factors that stimulate migration of stromal cells, factors that stimulate chondrogenesis, factors that stimulate matrix deposition, anti-inflammatories, and immunosuppressants.
Claim 42
Dependent Claim 25 words
The method of claim 1, wherein the stromal cells of the preparation are genetically engineered to express a gene that is deficiently expressed in vivo.
Claim 43
Dependent Claim 29 words
The method of claim 1, wherein the stromal cells of the preparation are genetically engineered to prevent or reduce the expression of a gene expressed by the stromal cells.
Claim 44
Dependent Claim 20 words
The method of claim 1, wherein the cartilage defect site is treated to degrade the existing cartilage at the site.
Claim 45
Dependent Claim 22 words
The method of claim 43, wherein the treatment is selected from the group consisting of enzyme treatment, abrasion, debridement, shaving, and microdrilling.
Claim 46
Dependent Claim 29 words
The method of claim 44, wherein the enzyme treatment utilizes at least one enzyme selected from the group consisting of trypsin, chymotrypsin, collagenase, elastase, hyaluronidase, DNAase, pronase and chondroitinase.
Claim 47
Dependent Claim 25 words
The method of claim 43, wherein the cartilage defect site is enzymatically treated prior to implantation of the scaffold or the periosteal or perichondrial tissue.
Claim 48
Dependent Claim 16 words
The method of claim 32 or 34 wherein the chondrocyte progenitor cells comprise mesenchymal stem cells.
Claim 49
Dependent Claim 13 words
The method of claim 19, 27 or 36 wherein the bioactive agent is

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3.5 Years (Year 4) 2001-11-30 2002-06-01 2002-12-01 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2005-11-30 2006-06-01 2006-12-01 $3760.00 Window Closed / Lapsed
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