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Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties
INTRODUCTION: Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most predominant and fatal pathogens at wound infection sites. MRSA is difficult to treat because of its antibiotic resistance and ability to form biofilms at the wound site. METHODS: In this study, a novel nanoscale liqu...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128272/ https://www.ncbi.nlm.nih.gov/pubmed/30214202 http://dx.doi.org/10.2147/IJN.S161680 |
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author | Yang, Sha Yang, Yun Cui, Sixin Feng, Ziqi Du, Yuzhi Song, Zhen Tong, Yanan Yang, Liuyang Wang, Zelin Zeng, Hao Zou, Quanming Sun, Hongwu |
author_facet | Yang, Sha Yang, Yun Cui, Sixin Feng, Ziqi Du, Yuzhi Song, Zhen Tong, Yanan Yang, Liuyang Wang, Zelin Zeng, Hao Zou, Quanming Sun, Hongwu |
author_sort | Yang, Sha |
collection | PubMed |
description | INTRODUCTION: Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most predominant and fatal pathogens at wound infection sites. MRSA is difficult to treat because of its antibiotic resistance and ability to form biofilms at the wound site. METHODS: In this study, a novel nanoscale liquid film-forming system (LFFS) loaded with benzalkonium bromide was produced based on polyvinyl alcohol and chitosan. RESULTS: This LFFS showed a faster and more potent effect against MRSA252 than benzalkonium bromide aqueous solution both in vitro and in vivo. Additionally, the LFFS had a stronger ability to destroy biofilms (5 mg/mL) and inhibit their formation (1.33 μg/mL). The LFFS inflicted obvious damage to the structure and integrity of MRSA cell membranes and caused increases in the release of alkaline phosphate and lactate dehydrogenase in the relative electrical conductivity and in K(+) and Mg(2+) concentrations due to changes in the MRSA cell membrane permeability. CONCLUSION: The novel LFFS is promising as an effective system for disinfectant delivery and for application in the treatment of MRSA wound infections. |
format | Online Article Text |
id | pubmed-6128272 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61282722018-09-13 Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties Yang, Sha Yang, Yun Cui, Sixin Feng, Ziqi Du, Yuzhi Song, Zhen Tong, Yanan Yang, Liuyang Wang, Zelin Zeng, Hao Zou, Quanming Sun, Hongwu Int J Nanomedicine Original Research INTRODUCTION: Methicillin-resistant Staphylococcus aureus (MRSA) is one of the most predominant and fatal pathogens at wound infection sites. MRSA is difficult to treat because of its antibiotic resistance and ability to form biofilms at the wound site. METHODS: In this study, a novel nanoscale liquid film-forming system (LFFS) loaded with benzalkonium bromide was produced based on polyvinyl alcohol and chitosan. RESULTS: This LFFS showed a faster and more potent effect against MRSA252 than benzalkonium bromide aqueous solution both in vitro and in vivo. Additionally, the LFFS had a stronger ability to destroy biofilms (5 mg/mL) and inhibit their formation (1.33 μg/mL). The LFFS inflicted obvious damage to the structure and integrity of MRSA cell membranes and caused increases in the release of alkaline phosphate and lactate dehydrogenase in the relative electrical conductivity and in K(+) and Mg(2+) concentrations due to changes in the MRSA cell membrane permeability. CONCLUSION: The novel LFFS is promising as an effective system for disinfectant delivery and for application in the treatment of MRSA wound infections. Dove Medical Press 2018-09-03 /pmc/articles/PMC6128272/ /pubmed/30214202 http://dx.doi.org/10.2147/IJN.S161680 Text en © 2018 Yang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Yang, Sha Yang, Yun Cui, Sixin Feng, Ziqi Du, Yuzhi Song, Zhen Tong, Yanan Yang, Liuyang Wang, Zelin Zeng, Hao Zou, Quanming Sun, Hongwu Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties |
title | Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties |
title_full | Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties |
title_fullStr | Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties |
title_full_unstemmed | Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties |
title_short | Chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates MRSA-infected wound healing by enhancing antibacterial and antibiofilm properties |
title_sort | chitosan-polyvinyl alcohol nanoscale liquid film-forming system facilitates mrsa-infected wound healing by enhancing antibacterial and antibiofilm properties |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6128272/ https://www.ncbi.nlm.nih.gov/pubmed/30214202 http://dx.doi.org/10.2147/IJN.S161680 |
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