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Biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study

This work establishes the in vivo performance of modified calcium phosphate bone cements for vertebroplasty of spinal fractures using a lapine model. A non-modified calcium phosphate bone cement and collagen-calcium phosphate bone cements composites with enhanced mechanical properties, utilising eit...

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Autores principales: Palmer, Iwan, Nelson, John, Schatton, Wolfgang, Dunne, Nicholas J., Buchanan, Fraser, Clarke, Susan A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108819/
https://www.ncbi.nlm.nih.gov/pubmed/27844306
http://dx.doi.org/10.1007/s10856-016-5806-2
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author Palmer, Iwan
Nelson, John
Schatton, Wolfgang
Dunne, Nicholas J.
Buchanan, Fraser
Clarke, Susan A.
author_facet Palmer, Iwan
Nelson, John
Schatton, Wolfgang
Dunne, Nicholas J.
Buchanan, Fraser
Clarke, Susan A.
author_sort Palmer, Iwan
collection PubMed
description This work establishes the in vivo performance of modified calcium phosphate bone cements for vertebroplasty of spinal fractures using a lapine model. A non-modified calcium phosphate bone cement and collagen-calcium phosphate bone cements composites with enhanced mechanical properties, utilising either bovine collagen or collagen from a marine sponge, were compared to a commercial poly(methyl methacrylate) cement. Conical cement samples (8 mm height × 4 mm base diameter) were press-fit into distal femoral condyle defects in New Zealand White rabbits and assessed after 5 and 10 weeks. Bone apposition and tartrate-resistant acid phosphatase activity around cements were assessed. All implants were well tolerated, but bone apposition was higher on calcium phosphate bone cements than on poly(methyl methacrylate) cement. Incorporation of collagen showed no evidence of inflammatory or immune reactions. Presence of positive tartrate-resistant acid phosphatase staining within cracks formed in calcium phosphate bone cements suggested active osteoclasts were present within the implants and were actively remodelling within the cements. Bone growth was also observed within these cracks. These findings confirm the biological advantages of calcium phosphate bone cements over poly(methyl methacrylate) and, coupled with previous work on enhancement of mechanical properties through collagen incorporation, suggest collagen-calcium phosphate bone cement composite may offer an alternative to calcium phosphate bone cements in applications where low setting times and higher mechanical stability are important.
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spelling pubmed-51088192016-12-09 Biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study Palmer, Iwan Nelson, John Schatton, Wolfgang Dunne, Nicholas J. Buchanan, Fraser Clarke, Susan A. J Mater Sci Mater Med Biocompatibility Studies This work establishes the in vivo performance of modified calcium phosphate bone cements for vertebroplasty of spinal fractures using a lapine model. A non-modified calcium phosphate bone cement and collagen-calcium phosphate bone cements composites with enhanced mechanical properties, utilising either bovine collagen or collagen from a marine sponge, were compared to a commercial poly(methyl methacrylate) cement. Conical cement samples (8 mm height × 4 mm base diameter) were press-fit into distal femoral condyle defects in New Zealand White rabbits and assessed after 5 and 10 weeks. Bone apposition and tartrate-resistant acid phosphatase activity around cements were assessed. All implants were well tolerated, but bone apposition was higher on calcium phosphate bone cements than on poly(methyl methacrylate) cement. Incorporation of collagen showed no evidence of inflammatory or immune reactions. Presence of positive tartrate-resistant acid phosphatase staining within cracks formed in calcium phosphate bone cements suggested active osteoclasts were present within the implants and were actively remodelling within the cements. Bone growth was also observed within these cracks. These findings confirm the biological advantages of calcium phosphate bone cements over poly(methyl methacrylate) and, coupled with previous work on enhancement of mechanical properties through collagen incorporation, suggest collagen-calcium phosphate bone cement composite may offer an alternative to calcium phosphate bone cements in applications where low setting times and higher mechanical stability are important. Springer US 2016-11-14 2016 /pmc/articles/PMC5108819/ /pubmed/27844306 http://dx.doi.org/10.1007/s10856-016-5806-2 Text en © The Author(s) 2016 This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Biocompatibility Studies
Palmer, Iwan
Nelson, John
Schatton, Wolfgang
Dunne, Nicholas J.
Buchanan, Fraser
Clarke, Susan A.
Biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study
title Biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study
title_full Biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study
title_fullStr Biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study
title_full_unstemmed Biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study
title_short Biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study
title_sort biocompatibility of calcium phosphate bone cement with optimised mechanical properties: an in vivo study
topic Biocompatibility Studies
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108819/
https://www.ncbi.nlm.nih.gov/pubmed/27844306
http://dx.doi.org/10.1007/s10856-016-5806-2
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