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Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms
We hypothesized that low concentrations of H(2)O(2) could be generated through the electrochemical conversion of oxygen by applying an electric potential to a conductive scaffold and produce a low, but constant, concentration of H(2)O(2) that would be sufficient to destroy biofilms. To test our hypo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604468/ https://www.ncbi.nlm.nih.gov/pubmed/26464174 http://dx.doi.org/10.1038/srep14908 |
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author | Sultana, Sujala T. Atci, Erhan Babauta, Jerome T. Mohamed Falghoush, Azeza Snekvik, Kevin R. Call, Douglas R. Beyenal, Haluk |
author_facet | Sultana, Sujala T. Atci, Erhan Babauta, Jerome T. Mohamed Falghoush, Azeza Snekvik, Kevin R. Call, Douglas R. Beyenal, Haluk |
author_sort | Sultana, Sujala T. |
collection | PubMed |
description | We hypothesized that low concentrations of H(2)O(2) could be generated through the electrochemical conversion of oxygen by applying an electric potential to a conductive scaffold and produce a low, but constant, concentration of H(2)O(2) that would be sufficient to destroy biofilms. To test our hypothesis we used a multidrug-resistant Acinetobacter baumannii strain, because this species is often implicated in difficult-to-treat biofilm infections. We used conductive carbon fabric as the scaffold material (“e-scaffold”). In vitro experiments demonstrated the production of a maximum constant concentration of ~25 μM H(2)O(2) near the e-scaffold surface. An e-scaffold was overlaid onto an existing A. baumannii biofilm, and within 24 h there was a ~4-log reduction in viable bacteria with an ~80% decrease in biofilm surface coverage. A similar procedure was used to overlay an e-scaffold onto an existing A. baumannii biofilm that was grown on a porcine explant. After 24 h, there was a ~3-log reduction in viable bacteria from the infected porcine explants with no observable damage to the underlying mammalian tissue based on a viability assay and histology. This research establishes a novel foundation for an alternative antibiotic-free wound dressing to eliminate biofilms. |
format | Online Article Text |
id | pubmed-4604468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46044682015-12-07 Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms Sultana, Sujala T. Atci, Erhan Babauta, Jerome T. Mohamed Falghoush, Azeza Snekvik, Kevin R. Call, Douglas R. Beyenal, Haluk Sci Rep Article We hypothesized that low concentrations of H(2)O(2) could be generated through the electrochemical conversion of oxygen by applying an electric potential to a conductive scaffold and produce a low, but constant, concentration of H(2)O(2) that would be sufficient to destroy biofilms. To test our hypothesis we used a multidrug-resistant Acinetobacter baumannii strain, because this species is often implicated in difficult-to-treat biofilm infections. We used conductive carbon fabric as the scaffold material (“e-scaffold”). In vitro experiments demonstrated the production of a maximum constant concentration of ~25 μM H(2)O(2) near the e-scaffold surface. An e-scaffold was overlaid onto an existing A. baumannii biofilm, and within 24 h there was a ~4-log reduction in viable bacteria with an ~80% decrease in biofilm surface coverage. A similar procedure was used to overlay an e-scaffold onto an existing A. baumannii biofilm that was grown on a porcine explant. After 24 h, there was a ~3-log reduction in viable bacteria from the infected porcine explants with no observable damage to the underlying mammalian tissue based on a viability assay and histology. This research establishes a novel foundation for an alternative antibiotic-free wound dressing to eliminate biofilms. Nature Publishing Group 2015-10-14 /pmc/articles/PMC4604468/ /pubmed/26464174 http://dx.doi.org/10.1038/srep14908 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Sultana, Sujala T. Atci, Erhan Babauta, Jerome T. Mohamed Falghoush, Azeza Snekvik, Kevin R. Call, Douglas R. Beyenal, Haluk Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms |
title | Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms |
title_full | Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms |
title_fullStr | Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms |
title_full_unstemmed | Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms |
title_short | Electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms |
title_sort | electrochemical scaffold generates localized, low concentration of hydrogen peroxide that inhibits bacterial pathogens and biofilms |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4604468/ https://www.ncbi.nlm.nih.gov/pubmed/26464174 http://dx.doi.org/10.1038/srep14908 |
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