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LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity
INTRODUCTION: Antibiotic-loaded poly(methyl methacrylate) bone cements (ALBCs) are widely used in total joint replacement (TJR), for local delivery of antibiotics to provide prophylaxis against prosthetic joint infections (PJI). One of the shortcomings of the current generation of ALBCs is that the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292632/ https://www.ncbi.nlm.nih.gov/pubmed/30543660 http://dx.doi.org/10.1371/journal.pone.0207753 |
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author | Al Thaher, Yazan Yang, Lirong Jones, Steve A. Perni, Stefano Prokopovich, Polina |
author_facet | Al Thaher, Yazan Yang, Lirong Jones, Steve A. Perni, Stefano Prokopovich, Polina |
author_sort | Al Thaher, Yazan |
collection | PubMed |
description | INTRODUCTION: Antibiotic-loaded poly(methyl methacrylate) bone cements (ALBCs) are widely used in total joint replacement (TJR), for local delivery of antibiotics to provide prophylaxis against prosthetic joint infections (PJI). One of the shortcomings of the current generation of ALBCs is that the antibiotic release profile is characterized by a burst over the first few hours followed by a sharp decrease in rate for the following several days (often below minimum inhibitory concentration (MIC)), and, finally, exhaustion (after, typically, ~ 20 d). This profile means that the ALBCs provide only short-term antimicrobial action against bacterial strains involved PJI. RATIONALE: The purpose of the present study was to develop an improved antibiotic delivery system for an ALBC. This system involved using a layer-by-layer technique to load the antibiotic (gentamicin sulphate) (GEN) on silica nanoparticles, which are then blended with the powder of the cement. Then, the powder was mixed with the liquid of the cement (NP-GEN cement). For controls, two GEN-loaded brands were used (Cemex Genta and Palacos R+G). Gentamicin release and a host of other relevant properties were determined for all the cements studied. RESULTS: Compared to control cement specimens, improved GEN release, longer antimicrobial activity (against clinically-relevant bacterial strains), and comparable setting time, cytocompatibility, compressive strength (both prior to and after aging in PBS at 37 (o)C for 30 d), 4-point bend strength and modulus, fracture toughness, and PBS uptake. CONCLUSIONS: NP-GEN cement may have a role in preventing or treating PJI. |
format | Online Article Text |
id | pubmed-6292632 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-62926322018-12-28 LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity Al Thaher, Yazan Yang, Lirong Jones, Steve A. Perni, Stefano Prokopovich, Polina PLoS One Research Article INTRODUCTION: Antibiotic-loaded poly(methyl methacrylate) bone cements (ALBCs) are widely used in total joint replacement (TJR), for local delivery of antibiotics to provide prophylaxis against prosthetic joint infections (PJI). One of the shortcomings of the current generation of ALBCs is that the antibiotic release profile is characterized by a burst over the first few hours followed by a sharp decrease in rate for the following several days (often below minimum inhibitory concentration (MIC)), and, finally, exhaustion (after, typically, ~ 20 d). This profile means that the ALBCs provide only short-term antimicrobial action against bacterial strains involved PJI. RATIONALE: The purpose of the present study was to develop an improved antibiotic delivery system for an ALBC. This system involved using a layer-by-layer technique to load the antibiotic (gentamicin sulphate) (GEN) on silica nanoparticles, which are then blended with the powder of the cement. Then, the powder was mixed with the liquid of the cement (NP-GEN cement). For controls, two GEN-loaded brands were used (Cemex Genta and Palacos R+G). Gentamicin release and a host of other relevant properties were determined for all the cements studied. RESULTS: Compared to control cement specimens, improved GEN release, longer antimicrobial activity (against clinically-relevant bacterial strains), and comparable setting time, cytocompatibility, compressive strength (both prior to and after aging in PBS at 37 (o)C for 30 d), 4-point bend strength and modulus, fracture toughness, and PBS uptake. CONCLUSIONS: NP-GEN cement may have a role in preventing or treating PJI. Public Library of Science 2018-12-13 /pmc/articles/PMC6292632/ /pubmed/30543660 http://dx.doi.org/10.1371/journal.pone.0207753 Text en © 2018 Al Thaher et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Al Thaher, Yazan Yang, Lirong Jones, Steve A. Perni, Stefano Prokopovich, Polina LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity |
title | LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity |
title_full | LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity |
title_fullStr | LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity |
title_full_unstemmed | LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity |
title_short | LbL-assembled gentamicin delivery system for PMMA bone cements to prolong antimicrobial activity |
title_sort | lbl-assembled gentamicin delivery system for pmma bone cements to prolong antimicrobial activity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6292632/ https://www.ncbi.nlm.nih.gov/pubmed/30543660 http://dx.doi.org/10.1371/journal.pone.0207753 |
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