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A surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption
A 100% water-soluble surfactant polymer dressing (SPD) that is bio-compatible and non-ionic has been reported to improve wound closure in preliminary clinical studies. The mechanism of action of SPD in wound healing remains unclear. Biofilm infection is a significant problem that hinders proper woun...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772662/ https://www.ncbi.nlm.nih.gov/pubmed/29343818 http://dx.doi.org/10.1038/s41598-018-19175-7 |
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author | Das Ghatak, Piya Mathew-Steiner, Shomita S. Pandey, Priyanka Roy, Sashwati Sen, Chandan K. |
author_facet | Das Ghatak, Piya Mathew-Steiner, Shomita S. Pandey, Priyanka Roy, Sashwati Sen, Chandan K. |
author_sort | Das Ghatak, Piya |
collection | PubMed |
description | A 100% water-soluble surfactant polymer dressing (SPD) that is bio-compatible and non-ionic has been reported to improve wound closure in preliminary clinical studies. The mechanism of action of SPD in wound healing remains unclear. Biofilm infection is a significant problem that hinders proper wound closure. The objective of this study was to characterize the mechanism of action of SPD inhibition of bacterial biofilm development. Static biofilms (48 h) of the primary wound pathogens Pseudomonas aeruginosa (PA01), Staphylococcus aureus (USA300) were grown on polycarbonate membranes and treated with SPD with and without antibiotics for an additional 24 h. The standard antibiotics – tobramycin (10 μg/ml) for PA01 and rifampicin (10 μg/ml) for USA300, were used in these studies. Following 24 h treatment with and without antibiotics, the biofilms were characterized using scanning electron microscopy (SEM) structural imaging, in vitro imaging system (IVIS) proliferation imaging, colony forming units (CFU), viability assay, quantitative PCR (qPCR) for virulence gene expression. Because SPD is a surfactant based dressing, it potentially has a direct effect on Gram negative bacteria such as Pseudomonas primarily due to the lipid-based outer membrane of the bacteria. SPD is a surfactant based dressing that has potent anti-biofilm properties directly or in synergy with antibiotics. |
format | Online Article Text |
id | pubmed-5772662 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57726622018-01-26 A surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption Das Ghatak, Piya Mathew-Steiner, Shomita S. Pandey, Priyanka Roy, Sashwati Sen, Chandan K. Sci Rep Article A 100% water-soluble surfactant polymer dressing (SPD) that is bio-compatible and non-ionic has been reported to improve wound closure in preliminary clinical studies. The mechanism of action of SPD in wound healing remains unclear. Biofilm infection is a significant problem that hinders proper wound closure. The objective of this study was to characterize the mechanism of action of SPD inhibition of bacterial biofilm development. Static biofilms (48 h) of the primary wound pathogens Pseudomonas aeruginosa (PA01), Staphylococcus aureus (USA300) were grown on polycarbonate membranes and treated with SPD with and without antibiotics for an additional 24 h. The standard antibiotics – tobramycin (10 μg/ml) for PA01 and rifampicin (10 μg/ml) for USA300, were used in these studies. Following 24 h treatment with and without antibiotics, the biofilms were characterized using scanning electron microscopy (SEM) structural imaging, in vitro imaging system (IVIS) proliferation imaging, colony forming units (CFU), viability assay, quantitative PCR (qPCR) for virulence gene expression. Because SPD is a surfactant based dressing, it potentially has a direct effect on Gram negative bacteria such as Pseudomonas primarily due to the lipid-based outer membrane of the bacteria. SPD is a surfactant based dressing that has potent anti-biofilm properties directly or in synergy with antibiotics. Nature Publishing Group UK 2018-01-17 /pmc/articles/PMC5772662/ /pubmed/29343818 http://dx.doi.org/10.1038/s41598-018-19175-7 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Das Ghatak, Piya Mathew-Steiner, Shomita S. Pandey, Priyanka Roy, Sashwati Sen, Chandan K. A surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption |
title | A surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption |
title_full | A surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption |
title_fullStr | A surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption |
title_full_unstemmed | A surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption |
title_short | A surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption |
title_sort | surfactant polymer dressing potentiates antimicrobial efficacy in biofilm disruption |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5772662/ https://www.ncbi.nlm.nih.gov/pubmed/29343818 http://dx.doi.org/10.1038/s41598-018-19175-7 |
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