{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T00:28:27Z","timestamp":1791332907789,"version":"4.3.1"},"reference-count":30,"publisher":"Wiley","issue":"8","license":[{"start":{"date-parts":[[2004,9,13]],"date-time":"2004-09-13T00:00:00Z","timestamp":1095033600000},"content-version":"vor","delay-in-days":3696,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J. Biomed. Mater. Res."],"published-print":{"date-parts":[[1994,8]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Cartilage implants which could potentially be used to resurface damaged joints were created using rabbit articular chondrocytes and synthetic, biodegradable polymer scaffolds. Cells were serially passaged and then cultured <jats:italic>in vivo<\/jats:italic> on fibrous polyglycolic acid (PGA) scaffolds. Cell\u2010PGA constructs were implanted <jats:italic>in vivo<\/jats:italic> as allografts to repair 3\u2010mm diameter, full thickness defects in the knee joints of adult rabbits, and cartilage repair was assessed histologically over 6 months. <jats:italic>In vitro<\/jats:italic>, chondrocytes proliferated on PGA and regenerated cartilaginous matrix. Collagen and glycosaminoglycan (GAG) represented 20 to 8% of the implant dry weight (dw), respectively, at the time of <jats:italic>in vivo<\/jats:italic> implantation; the remainder was PGA and unspecified components. Implants based on passaged chondrocytes had 1.7\u2010times as much GAG and 2.6\u2010times as much collagen as those based on primary chondrocytes. <jats:italic>In vivo<\/jats:italic>, cartilaginous repair tissue was observed after implantation of PGA both with and without cultured chondrocytes. Six month repair was qualitatively better for cell\u2010PGA allografts than for PGA alone, with respect to: (1) surface smoothness, (2) columnar alignment of chondrocytes, (3) spatially uniform GAG distribution, (4) reconstitution of the subchondral plate, and (5) bonding of the repair tissue to the underlying bone. These pilot studies demonstrate that it is feasible to use cell\u2010polymer allografts for joint resurfacing <jats:italic>in vivo<\/jats:italic>. \u00a9 1994 John Wiley &amp; Sons, Inc.<\/jats:p>","DOI":"10.1002\/jbm.820280808","type":"journal-article","created":{"date-parts":[[2005,5,27]],"date-time":"2005-05-27T19:37:50Z","timestamp":1117222670000},"page":"891-899","source":"Crossref","is-referenced-by-count":334,"title":["Joint resurfacing using allograft chondrocytes and synthetic biodegradable polymer scaffolds"],"prefix":"10.1002","volume":"28","author":[{"given":"L. 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