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Long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep

BACKGROUND: Articular cartilage has limited capacity to repair. Defects greater than 3 mm heal with formation of inferior fibrous cartilage. Therefore, many attempts have been made to find the ideal graft for larger cartilage lesions. Different grafts, such as untreated or cryopreserved osteochondra...

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Autores principales: Akens, Margarete K, von Rechenberg, Brigitte, Bittmann, Pedro, Nadler, Daniel, Zlinszky, Kati, Auer, Jörg A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC61033/
https://www.ncbi.nlm.nih.gov/pubmed/11747477
http://dx.doi.org/10.1186/1471-2474-2-9
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author Akens, Margarete K
von Rechenberg, Brigitte
Bittmann, Pedro
Nadler, Daniel
Zlinszky, Kati
Auer, Jörg A
author_facet Akens, Margarete K
von Rechenberg, Brigitte
Bittmann, Pedro
Nadler, Daniel
Zlinszky, Kati
Auer, Jörg A
author_sort Akens, Margarete K
collection PubMed
description BACKGROUND: Articular cartilage has limited capacity to repair. Defects greater than 3 mm heal with formation of inferior fibrous cartilage. Therefore, many attempts have been made to find the ideal graft for larger cartilage lesions. Different grafts, such as untreated or cryopreserved osteochondral transplants, have been used with variable success. METHODS: Photo-oxidized osteochondral grafts were implanted in both femoral condyles of one ovine knee. Untreated xenogeneic and autogeneic grafts served as controls. Three groups of 8 sheep each were formed and they were sacrificed 6, 12 or 18 months after surgery. RESULTS: The macroscopic evaluation of the condyle and graft showed a well-maintained cartilage surface in most grafts at all time points. However, the host cartilage matrix deteriorated considerably in all xenogeneic, most autogeneic and fewer of the photo-oxidized grafts at 12 and 18 months, respectively. The blue colour of the photo-oxidized grafts resulting from the process of photo-oxidation was visible in all grafts at 6 months, had diminished at 12 months and had completely disappeared at 18 months after surgery. Histologically a loss of matrix staining was almost never noticed in untreated xenografts, transiently at 6 months in photo-oxidized grafts and increased at 12 and 18 months. Fusion between graft and host cartilage could be seen in photo-oxidized grafts at 12 and 18 months, but was never seen in autografts and xenografts. CONCLUSIONS: The photo-oxidation of osteochondral grafts and its use as transplant appears to have a beneficial effect on cartilage and bone remodelling. Osteochondral grafts pre-treated with photo-oxidation may be considered for articular cartilage replacement and therefore may delay artificial joint replacements in human patients.
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spelling pubmed-610332001-12-20 Long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep Akens, Margarete K von Rechenberg, Brigitte Bittmann, Pedro Nadler, Daniel Zlinszky, Kati Auer, Jörg A BMC Musculoskelet Disord Research Article BACKGROUND: Articular cartilage has limited capacity to repair. Defects greater than 3 mm heal with formation of inferior fibrous cartilage. Therefore, many attempts have been made to find the ideal graft for larger cartilage lesions. Different grafts, such as untreated or cryopreserved osteochondral transplants, have been used with variable success. METHODS: Photo-oxidized osteochondral grafts were implanted in both femoral condyles of one ovine knee. Untreated xenogeneic and autogeneic grafts served as controls. Three groups of 8 sheep each were formed and they were sacrificed 6, 12 or 18 months after surgery. RESULTS: The macroscopic evaluation of the condyle and graft showed a well-maintained cartilage surface in most grafts at all time points. However, the host cartilage matrix deteriorated considerably in all xenogeneic, most autogeneic and fewer of the photo-oxidized grafts at 12 and 18 months, respectively. The blue colour of the photo-oxidized grafts resulting from the process of photo-oxidation was visible in all grafts at 6 months, had diminished at 12 months and had completely disappeared at 18 months after surgery. Histologically a loss of matrix staining was almost never noticed in untreated xenografts, transiently at 6 months in photo-oxidized grafts and increased at 12 and 18 months. Fusion between graft and host cartilage could be seen in photo-oxidized grafts at 12 and 18 months, but was never seen in autografts and xenografts. CONCLUSIONS: The photo-oxidation of osteochondral grafts and its use as transplant appears to have a beneficial effect on cartilage and bone remodelling. Osteochondral grafts pre-treated with photo-oxidation may be considered for articular cartilage replacement and therefore may delay artificial joint replacements in human patients. BioMed Central 2001-11-30 /pmc/articles/PMC61033/ /pubmed/11747477 http://dx.doi.org/10.1186/1471-2474-2-9 Text en Copyright © 2001 Akens et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Akens, Margarete K
von Rechenberg, Brigitte
Bittmann, Pedro
Nadler, Daniel
Zlinszky, Kati
Auer, Jörg A
Long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep
title Long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep
title_full Long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep
title_fullStr Long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep
title_full_unstemmed Long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep
title_short Long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep
title_sort long term in-vivo studies of a photo-oxidized bovine osteochondral transplant in sheep
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC61033/
https://www.ncbi.nlm.nih.gov/pubmed/11747477
http://dx.doi.org/10.1186/1471-2474-2-9
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