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US5624463A Expired / Lapsed US ⏱️ 0.0 years remaining

Prosthetic articular cartilage

Assignee: Regen Biologics Inc
•
Filing: 1994-04-25
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Granted: 1997-04-29
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Expires: 2014-04-25
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Abstract

Abstract A prosthetic, resorbable articular cartilage and methods of its fabrication and insertion are disclosed. The prosthetic articular cartilage, when implanted in a humanoid joint, acts as a resorbable scaffold for ingrowth of native articular chondrocytes and supports natural articulating joint forces. The prosthetic articular cartilage is a dry, porous, volume matrix of biocompatible and bioresorbable fibers. These fibers include a natural polymer or analogs thereof, at least a portion of which may be crosslinked. The matrix is adapted to have an in vivo outer surface contour substantially the same as that of natural articular cartilage in an articulating joint, and has a pore size in the approximate range of about 100 microns to about 400 microns.

Inventors

  • 👤 Kevin R. Stone
  • 👤 Shu-Tung Li

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-24 23:04
CPC Classifications
A; A61; A61L; A61L27/00; A61L27/50; A61L27/58; A61F; A61F2/00; A61F2/02; A61F2/28; A61F2/30; A61F2/30756; A61F2/38; A61F2/3872; A61F2/44; A61F2/442; A61L27/14; A61L27/20; A61L27/22; A61L27/227; A61L27/24; A61L27/26; A61L27/40; A61L27/44; A61L27/46; A61L27/48; A61L27/56; C; C08; C08L; C08L1/00; A61F2/30767; A61F2/30907; A61F2/3094; A61F2/30965; A61F2002/30001; A61F2002/30003; A61F2002/30004; A61F2002/30006; A61F2002/3006; A61F2002/30062; A61F2002/30108; A61F2002/3011; A61F2002/30112; A61F2002/30113; A61F2002/30131; A61F2002/30199; A61F2002/30205; A61F2002/30224; A61F2002/30225; A61F2002/3023; A61F2002/30667; A61F2002/30677; A61F2/30721; A61F2/30734; A61F2002/30736; A61F2002/30766; A61F2/30771; A61F2002/30795; A61F2002/30807; A61F2002/30808; A61F2002/3082; A61F2002/30822; A61F2002/30827; A61F2002/30878; A61F2002/30879; A61F2002/30881; A61F2002/30891; A61F2002/30904; A61F2/30942; A61F2002/30957; A61F2/42; A61F2/4261; A61F2002/4271; A61F2002/4274; A61F2002/4276; A61F2002/4279; A61F2002/4282; A61F2002/4284; A61F2002/4287; A61F2002/4289; A61F2002/4292; A61F2002/4294; A61F2002/4297; A61F2210/00; A61F2210/0004; A61F2230/00; A61F2230/0002; A61F2230/0004; A61F2230/0006; A61F2230/0013; A61F2230/0063; A61F2230/0067; A61F2230/0069; A61F2250/00; A61F2250/0014; A61F2250/0015; A61F2250/0057; A61F2310/00; A61F2310/00005; A61F2310/00365; A61L2430/00; A61L2430/06; A61L2430/38

Claims Analysis

Total Claims: 23
Claim 1
Independent Claim 164 words
A prosthetic articular cartilage device comprising a dry porous volume matrix of biocompatible and at least bioresorbable fibers and further comprising a base component, said fibers being natural polymers or analogs or mixtures thereof, said matrix being adapted to have an in vivo outer surface contour substantially the same as that of natural articular cartilage, and said matrix having a pore size in the approximate range of about 100 microns to about 400 microns, whereby said matrix establishes a bioresorbable scaffold adapted for the ingrowth of articular chondrocytes, and for supporting natural articulating joint forces, said base component configured to fit in a complementary aperture in cancellous bone thereby securing said articular cartilage device to said bone, said base component extending from portions of the outer surface of said matrix, said base component being a composite material comprising a dispersion of collagen and a composition which is selected from the group consisting of tricalcium phosphate, hydroxyapatite, and a combination of tricalcium phosphate and hydroxyapatite.
Claim 2
Dependent Claim 164 words
A prosthetic articular cartilage device comprising a dry porous volume matrix of biocompatible and at least bioresorbable fibers and further comprising a base component, said fibers being natural polymers or analogs or mixtures thereof, said matrix being adapted to have an in vivo outer surface contour substantially the same as that of natural articular cartilage, and said matrix having a pore size in the approximate range of about 100 microns to about 400 microns, whereby said matrix establishes a bioresorbable scaffold adapted for the ingrowth of articular chondrocytes, and for supporting natural articulating joint forces, said base component configured to fit in a complementary aperture in cancellous bone thereby securing said articular cartilage device to said bone, said base component extending from portions of the outer surface of said matrix, said base component being a composite material comprising a dispersion of collagen and a composition which is selected from the group consisting of tricalcium phosphate, hydroxyapatite, and a combination of tricalcium phosphate and hydroxyapatite.
Claim 3
Dependent Claim 16 words
The device of claim 1 further comprising crosslinks between at least a portion of said fibers.
Claim 4
Dependent Claim 16 words
The device of claim 1 further comprising a plurality of polysaccharide molecules interspersed with said fibers.
Claim 5
Dependent Claim 20 words
The device of claim 1 wherein at least a portion of said molecules provide crosslinks between ones of said fibers.
Claim 6
Dependent Claim 16 words
The device of claim 1 wherein said fibers are collagen, elastin, reticulin, cellulose, or mixtures thereof.
Claim 7
Dependent Claim 38 words
The device of claim 1 wherein said fibers are present at a concentration of about 75 to 100% by dry weight, and said polysaccharide molecules are present at a concentration of about 0 to 25% by dry weight.
Claim 8
Dependent Claim 29 words
The device of claim 1 wherein said polysaccharide molecules are chondroitin 4-sulfate, chondroitin 6-sulfate, keratan sulfate, dermatan sulfate, heparin sulfate, heparin, hyaluronic acid, alginic acid, chitosan, or mixtures thereof.
Claim 9
Dependent Claim 15 words
The device of claim 1 wherein said crosslinks are formed by a chemical crosslinking agent.
Claim 10
Dependent Claim 26 words
The device of claim 1 wherein said crosslinking agent is glutaraldehyde, formaldehyde, biocompatible bifunctional aldehydes, carbodiimides, hexamethylene diisocyanate, bisimidates, polyglycerol polyglycidyl ether, glyoxal, and mixtures thereof.
Claim 11
Dependent Claim 21 words
The device of claim 1 wherein said cartilage has a density of about 0.07 to 0.50 gram matrix per cubic centimeter.
Claim 12
Dependent Claim 24 words
The device of claim 1 wherein said cartilage has an intrafibrillary and interfibrillary space of about 2 to 14 cubic centimeters per gram matrix.
Claim 13
Dependent Claim 18 words
The device of claim 1 wherein said fibers are oriented in a substantially random fashion through said matrix.
Claim 14
Dependent Claim 18 words
The device of claim 1 wherein said fibers are oriented in a substantially ordered fashion through said matrix.
Claim 15
Dependent Claim 13 words
The device of claim 1 wherein said matrix comprises substantially circumferentially extending fibers.
Claim 16
Dependent Claim 13 words
The device of claim 1 wherein said matrix comprises substantially radially extending fibers.
Claim 17
Dependent Claim 17 words
The device of claim 1 wherein the density of said fibers is substantially uniform throughout said matrix.
Claim 18
Dependent Claim 16 words
The device of claim 1 wherein said polysaccharide molecules are dispersed substantially uniformly through said matrix.
Claim 19
Dependent Claim 15 words
The device of claim 1 wherein said polysaccharide molecules are dispersed nonuniformly through said matrix.
Claim 20
Dependent Claim 14 words
The device of claim 1 wherein the base component is at least partially resorbable.
Claim 21
Dependent Claim 16 words
The device of claim 1 wherein the base component includes a plurality of circumferentially extending ridges.
Claim 22
Dependent Claim 21 words
The device of claim 1 wherein the dispersion comprises about 90% by weight tricalcium phosphate and about 10% by weight collagen.
Claim 23
Dependent Claim 20 words
The device of claim 1 wherein the dispersion comprises about 90% by weight hydroxyapatite and about 10% by weight collagen.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 2000-04-28 2000-10-28 2001-04-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2004-04-28 2004-10-28 2005-04-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2008-04-28 2008-10-28 2009-04-29 $7700.00 Window Closed / Lapsed

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