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Engineering surgical stitches to prevent bacterial infection
Surgical site infections (SSIs) account for a massive economic, physiological, and psychological burden on patients and health care providers. Sutures provide a surface to which bacteria can adhere, proliferate, and promote SSIs. Current methods for fighting SSIs involve the use of sutures coated wi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764053/ https://www.ncbi.nlm.nih.gov/pubmed/35039588 http://dx.doi.org/10.1038/s41598-022-04925-5 |
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author | Vieira, Daniela Angel, Samuel N. Honjol, Yazan Masse, Maude Gruenheid, Samantha Harvey, Edward J. Merle, Geraldine |
author_facet | Vieira, Daniela Angel, Samuel N. Honjol, Yazan Masse, Maude Gruenheid, Samantha Harvey, Edward J. Merle, Geraldine |
author_sort | Vieira, Daniela |
collection | PubMed |
description | Surgical site infections (SSIs) account for a massive economic, physiological, and psychological burden on patients and health care providers. Sutures provide a surface to which bacteria can adhere, proliferate, and promote SSIs. Current methods for fighting SSIs involve the use of sutures coated with common antibiotics (triclosan). Unfortunately, these antibiotics have been rendered ineffective due to the increasing rate of antibiotic resistance. A promising new avenue involves the use of metallic nanoparticles (MNPs). MNPs exhibit low cytotoxicity and a strong propensity for killing bacteria while evading the typical antibiotic resistance mechanisms. In this work, we developed a novel MNPs dip-coating method for PDS-II sutures and explored the capabilities of a variety of MNPs in killing bacteria while retaining the cytocompatibility. Our findings indicated that our technique provided a homogeneous coating for PDS-II sutures, maintaining the strength, structural integrity, and degradability. The MNP coatings possess strong in vitro antibacterial properties against P aeruginosa and S. aureus—varying the %of dead bacteria from ~ 40% (for MgO NPs) to ~ 90% (for Fe(2)O(3)) compared to ~ 15% for uncoated PDS-II suture, after 7 days. All sutures demonstrated minimal cytotoxicity (cell viability > 70%) reinforcing the movement towards the use MNPs as a viable antibacterial technology. |
format | Online Article Text |
id | pubmed-8764053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-87640532022-01-18 Engineering surgical stitches to prevent bacterial infection Vieira, Daniela Angel, Samuel N. Honjol, Yazan Masse, Maude Gruenheid, Samantha Harvey, Edward J. Merle, Geraldine Sci Rep Article Surgical site infections (SSIs) account for a massive economic, physiological, and psychological burden on patients and health care providers. Sutures provide a surface to which bacteria can adhere, proliferate, and promote SSIs. Current methods for fighting SSIs involve the use of sutures coated with common antibiotics (triclosan). Unfortunately, these antibiotics have been rendered ineffective due to the increasing rate of antibiotic resistance. A promising new avenue involves the use of metallic nanoparticles (MNPs). MNPs exhibit low cytotoxicity and a strong propensity for killing bacteria while evading the typical antibiotic resistance mechanisms. In this work, we developed a novel MNPs dip-coating method for PDS-II sutures and explored the capabilities of a variety of MNPs in killing bacteria while retaining the cytocompatibility. Our findings indicated that our technique provided a homogeneous coating for PDS-II sutures, maintaining the strength, structural integrity, and degradability. The MNP coatings possess strong in vitro antibacterial properties against P aeruginosa and S. aureus—varying the %of dead bacteria from ~ 40% (for MgO NPs) to ~ 90% (for Fe(2)O(3)) compared to ~ 15% for uncoated PDS-II suture, after 7 days. All sutures demonstrated minimal cytotoxicity (cell viability > 70%) reinforcing the movement towards the use MNPs as a viable antibacterial technology. Nature Publishing Group UK 2022-01-17 /pmc/articles/PMC8764053/ /pubmed/35039588 http://dx.doi.org/10.1038/s41598-022-04925-5 Text en © Crown 2022 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Vieira, Daniela Angel, Samuel N. Honjol, Yazan Masse, Maude Gruenheid, Samantha Harvey, Edward J. Merle, Geraldine Engineering surgical stitches to prevent bacterial infection |
title | Engineering surgical stitches to prevent bacterial infection |
title_full | Engineering surgical stitches to prevent bacterial infection |
title_fullStr | Engineering surgical stitches to prevent bacterial infection |
title_full_unstemmed | Engineering surgical stitches to prevent bacterial infection |
title_short | Engineering surgical stitches to prevent bacterial infection |
title_sort | engineering surgical stitches to prevent bacterial infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8764053/ https://www.ncbi.nlm.nih.gov/pubmed/35039588 http://dx.doi.org/10.1038/s41598-022-04925-5 |
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