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A novel liposomal drug delivery system for PMMA bone cements

The population in developed countries is ageing and the number of people experiencing joint‐related conditions, such as osteoarthritis, is expected to increase. Joint replacements are currently the most effective treatment for severe joint conditions and although many of these procedures are success...

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Autores principales: Ayre, Wayne Nishio, Birchall, James C., Evans, Samuel L., Denyer, Stephen P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082562/
https://www.ncbi.nlm.nih.gov/pubmed/26256271
http://dx.doi.org/10.1002/jbm.b.33488
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author Ayre, Wayne Nishio
Birchall, James C.
Evans, Samuel L.
Denyer, Stephen P.
author_facet Ayre, Wayne Nishio
Birchall, James C.
Evans, Samuel L.
Denyer, Stephen P.
author_sort Ayre, Wayne Nishio
collection PubMed
description The population in developed countries is ageing and the number of people experiencing joint‐related conditions, such as osteoarthritis, is expected to increase. Joint replacements are currently the most effective treatment for severe joint conditions and although many of these procedures are successful, infection developing after the procedure is still an issue, requiring complex and expensive revisions. Whilst incorporating a powdered antibiotic within the bone cement can reduce infection rates, the powder frequently agglomerates, resulting in poor antibiotic release characteristics and compromised mechanical performance of the cement. To overcome these issues, a novel delivery system consisting of antibiotic‐loaded nano‐sized liposomes was developed for inclusion into polymethyl methacrylate (PMMA) bone cement. This system was tested in a commercial cement (Palacos R) and consistently delivered a higher percentage (22%) of the incorporated antibiotic when compared to the powdered antibiotic cement (9%), meaning less antibiotic needs to be incorporated than with conventional cement. The novel system resulted in a controlled and gradual release of antibiotic over a longer, 30‐day period and enhanced the toughness, bending strength and Vickers hardness of the cement, without altering its polymerization or molecular structure. This new material has the potential to significantly reduce infections in cemented joint replacements leading to enhanced patient quality of life and reduced healthcare costs. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 1510–1524, 2016.
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spelling pubmed-50825622016-11-09 A novel liposomal drug delivery system for PMMA bone cements Ayre, Wayne Nishio Birchall, James C. Evans, Samuel L. Denyer, Stephen P. J Biomed Mater Res B Appl Biomater Original Research Reports The population in developed countries is ageing and the number of people experiencing joint‐related conditions, such as osteoarthritis, is expected to increase. Joint replacements are currently the most effective treatment for severe joint conditions and although many of these procedures are successful, infection developing after the procedure is still an issue, requiring complex and expensive revisions. Whilst incorporating a powdered antibiotic within the bone cement can reduce infection rates, the powder frequently agglomerates, resulting in poor antibiotic release characteristics and compromised mechanical performance of the cement. To overcome these issues, a novel delivery system consisting of antibiotic‐loaded nano‐sized liposomes was developed for inclusion into polymethyl methacrylate (PMMA) bone cement. This system was tested in a commercial cement (Palacos R) and consistently delivered a higher percentage (22%) of the incorporated antibiotic when compared to the powdered antibiotic cement (9%), meaning less antibiotic needs to be incorporated than with conventional cement. The novel system resulted in a controlled and gradual release of antibiotic over a longer, 30‐day period and enhanced the toughness, bending strength and Vickers hardness of the cement, without altering its polymerization or molecular structure. This new material has the potential to significantly reduce infections in cemented joint replacements leading to enhanced patient quality of life and reduced healthcare costs. © 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 1510–1524, 2016. John Wiley and Sons Inc. 2015-08-10 2016-11 /pmc/articles/PMC5082562/ /pubmed/26256271 http://dx.doi.org/10.1002/jbm.b.33488 Text en © 2015 The Authors Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Reports
Ayre, Wayne Nishio
Birchall, James C.
Evans, Samuel L.
Denyer, Stephen P.
A novel liposomal drug delivery system for PMMA bone cements
title A novel liposomal drug delivery system for PMMA bone cements
title_full A novel liposomal drug delivery system for PMMA bone cements
title_fullStr A novel liposomal drug delivery system for PMMA bone cements
title_full_unstemmed A novel liposomal drug delivery system for PMMA bone cements
title_short A novel liposomal drug delivery system for PMMA bone cements
title_sort novel liposomal drug delivery system for pmma bone cements
topic Original Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082562/
https://www.ncbi.nlm.nih.gov/pubmed/26256271
http://dx.doi.org/10.1002/jbm.b.33488
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