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Characterization of the Antibacterial Activity of an SiO(2) Nanoparticular Coating to Prevent Bacterial Contamination in Blood Products
Technological innovations and quality control processes within blood supply organizations have significantly improved blood safety for both donors and recipients. Nevertheless, the risk of transfusion-transmitted infection remains non-negligible. Applying a nanoparticular, antibacterial coating at t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773057/ https://www.ncbi.nlm.nih.gov/pubmed/35052984 http://dx.doi.org/10.3390/antibiotics11010107 |
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author | Fonseca, Sahra Cayer, Marie-Pierre Ahmmed, K. M. Tanvir Khadem-Mohtaram, Nima Charette, Steve J. Brouard, Danny |
author_facet | Fonseca, Sahra Cayer, Marie-Pierre Ahmmed, K. M. Tanvir Khadem-Mohtaram, Nima Charette, Steve J. Brouard, Danny |
author_sort | Fonseca, Sahra |
collection | PubMed |
description | Technological innovations and quality control processes within blood supply organizations have significantly improved blood safety for both donors and recipients. Nevertheless, the risk of transfusion-transmitted infection remains non-negligible. Applying a nanoparticular, antibacterial coating at the surface of medical devices is a promising strategy to prevent the spread of infections. In this study, we characterized the antibacterial activity of an SiO(2) nanoparticular coating (i.e., the “Medical Antibacterial and Antiadhesive Coating” [MAAC]) applied on relevant polymeric materials (PM) used in the biomedical field. Electron microscopy revealed a smoother surface for the MAAC-treated PM compared to the reference, suggesting antiadhesive properties. The antibacterial activity was tested against selected Gram-positive and Gram-negative bacteria in accordance with ISO 22196. Bacterial growth was significantly reduced for the MAAC-treated PVC, plasticized PVC, polyurethane and silicone (90–99.999%) in which antibacterial activity of ≥1 log reduction was reached for all bacterial strains tested. Cytotoxicity was evaluated following ISO 10993-5 guidelines and L929 cell viability was calculated at ≥90% in the presence of MAAC. This study demonstrates that the MAAC could prevent bacterial contamination as demonstrated by the ISO 22196 tests, while further work needs to be done to improve the coating processability and effectiveness of more complex matrices. |
format | Online Article Text |
id | pubmed-8773057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87730572022-01-21 Characterization of the Antibacterial Activity of an SiO(2) Nanoparticular Coating to Prevent Bacterial Contamination in Blood Products Fonseca, Sahra Cayer, Marie-Pierre Ahmmed, K. M. Tanvir Khadem-Mohtaram, Nima Charette, Steve J. Brouard, Danny Antibiotics (Basel) Article Technological innovations and quality control processes within blood supply organizations have significantly improved blood safety for both donors and recipients. Nevertheless, the risk of transfusion-transmitted infection remains non-negligible. Applying a nanoparticular, antibacterial coating at the surface of medical devices is a promising strategy to prevent the spread of infections. In this study, we characterized the antibacterial activity of an SiO(2) nanoparticular coating (i.e., the “Medical Antibacterial and Antiadhesive Coating” [MAAC]) applied on relevant polymeric materials (PM) used in the biomedical field. Electron microscopy revealed a smoother surface for the MAAC-treated PM compared to the reference, suggesting antiadhesive properties. The antibacterial activity was tested against selected Gram-positive and Gram-negative bacteria in accordance with ISO 22196. Bacterial growth was significantly reduced for the MAAC-treated PVC, plasticized PVC, polyurethane and silicone (90–99.999%) in which antibacterial activity of ≥1 log reduction was reached for all bacterial strains tested. Cytotoxicity was evaluated following ISO 10993-5 guidelines and L929 cell viability was calculated at ≥90% in the presence of MAAC. This study demonstrates that the MAAC could prevent bacterial contamination as demonstrated by the ISO 22196 tests, while further work needs to be done to improve the coating processability and effectiveness of more complex matrices. MDPI 2022-01-14 /pmc/articles/PMC8773057/ /pubmed/35052984 http://dx.doi.org/10.3390/antibiotics11010107 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Fonseca, Sahra Cayer, Marie-Pierre Ahmmed, K. M. Tanvir Khadem-Mohtaram, Nima Charette, Steve J. Brouard, Danny Characterization of the Antibacterial Activity of an SiO(2) Nanoparticular Coating to Prevent Bacterial Contamination in Blood Products |
title | Characterization of the Antibacterial Activity of an SiO(2) Nanoparticular Coating to Prevent Bacterial Contamination in Blood Products |
title_full | Characterization of the Antibacterial Activity of an SiO(2) Nanoparticular Coating to Prevent Bacterial Contamination in Blood Products |
title_fullStr | Characterization of the Antibacterial Activity of an SiO(2) Nanoparticular Coating to Prevent Bacterial Contamination in Blood Products |
title_full_unstemmed | Characterization of the Antibacterial Activity of an SiO(2) Nanoparticular Coating to Prevent Bacterial Contamination in Blood Products |
title_short | Characterization of the Antibacterial Activity of an SiO(2) Nanoparticular Coating to Prevent Bacterial Contamination in Blood Products |
title_sort | characterization of the antibacterial activity of an sio(2) nanoparticular coating to prevent bacterial contamination in blood products |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773057/ https://www.ncbi.nlm.nih.gov/pubmed/35052984 http://dx.doi.org/10.3390/antibiotics11010107 |
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