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Multi-Stimulus Responsive Multilayer Coating for Treatment of Device-Associated Infections
Antibacterial coating with antibiotics is highly effective in avoiding device-associated infections (DAIs) which is an unsolved healthcare problem that causes significant morbidity and mortality rates. However, bacterial drug resistance caused by uncontrolled release of antibiotics seriously restric...
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/PMC8954600/ https://www.ncbi.nlm.nih.gov/pubmed/35323224 http://dx.doi.org/10.3390/jfb13010024 |
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author | Li, Wenlong Hua, Guanping Cai, Jingfeng Zhou, Yaming Zhou, Xi Wang, Miao Wang, Xiumin Fu, Baoqing Ren, Lei |
author_facet | Li, Wenlong Hua, Guanping Cai, Jingfeng Zhou, Yaming Zhou, Xi Wang, Miao Wang, Xiumin Fu, Baoqing Ren, Lei |
author_sort | Li, Wenlong |
collection | PubMed |
description | Antibacterial coating with antibiotics is highly effective in avoiding device-associated infections (DAIs) which is an unsolved healthcare problem that causes significant morbidity and mortality rates. However, bacterial drug resistance caused by uncontrolled release of antibiotics seriously restricts clinical efficacy of antibacterial coating. Hence, a local and controlled-release system which can release antibiotics in response to bacterial infected signals is necessary in antibacterial coating. Herein, a multi-stimulus responsive multilayer antibacterial coating was prepared through layer-by-layer (LbL) self-assembly of montmorillonite (MMT), chlorhexidine acetate (CHA) and Poly(protocatechuic acid-polyethylene glycol 1000-bis(phenylboronic acid carbamoyl) cystamine) (PPPB). The coating can be covered on various substrates such as cellulose acetate membrane, polyacrylonitrile membrane, polyvinyl chloride membrane, and polyurethane membrane, proving it is a versatile coating. Under the stimulation of acids, glucose or dithiothreitol, this coating was able to achieve controlled release of CHA and kill more than 99% of Staphylococcus aureus and Escherichia coli (4 × 10(8) CFU/mL) within 4 h. In the mouse infection model, CHA releasing of the coating was triggered by infected microenvironment to completely kill bacteria, achieving wounds healing within 14 days. |
format | Online Article Text |
id | pubmed-8954600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89546002022-03-26 Multi-Stimulus Responsive Multilayer Coating for Treatment of Device-Associated Infections Li, Wenlong Hua, Guanping Cai, Jingfeng Zhou, Yaming Zhou, Xi Wang, Miao Wang, Xiumin Fu, Baoqing Ren, Lei J Funct Biomater Article Antibacterial coating with antibiotics is highly effective in avoiding device-associated infections (DAIs) which is an unsolved healthcare problem that causes significant morbidity and mortality rates. However, bacterial drug resistance caused by uncontrolled release of antibiotics seriously restricts clinical efficacy of antibacterial coating. Hence, a local and controlled-release system which can release antibiotics in response to bacterial infected signals is necessary in antibacterial coating. Herein, a multi-stimulus responsive multilayer antibacterial coating was prepared through layer-by-layer (LbL) self-assembly of montmorillonite (MMT), chlorhexidine acetate (CHA) and Poly(protocatechuic acid-polyethylene glycol 1000-bis(phenylboronic acid carbamoyl) cystamine) (PPPB). The coating can be covered on various substrates such as cellulose acetate membrane, polyacrylonitrile membrane, polyvinyl chloride membrane, and polyurethane membrane, proving it is a versatile coating. Under the stimulation of acids, glucose or dithiothreitol, this coating was able to achieve controlled release of CHA and kill more than 99% of Staphylococcus aureus and Escherichia coli (4 × 10(8) CFU/mL) within 4 h. In the mouse infection model, CHA releasing of the coating was triggered by infected microenvironment to completely kill bacteria, achieving wounds healing within 14 days. MDPI 2022-02-28 /pmc/articles/PMC8954600/ /pubmed/35323224 http://dx.doi.org/10.3390/jfb13010024 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 Li, Wenlong Hua, Guanping Cai, Jingfeng Zhou, Yaming Zhou, Xi Wang, Miao Wang, Xiumin Fu, Baoqing Ren, Lei Multi-Stimulus Responsive Multilayer Coating for Treatment of Device-Associated Infections |
title | Multi-Stimulus Responsive Multilayer Coating for Treatment of Device-Associated Infections |
title_full | Multi-Stimulus Responsive Multilayer Coating for Treatment of Device-Associated Infections |
title_fullStr | Multi-Stimulus Responsive Multilayer Coating for Treatment of Device-Associated Infections |
title_full_unstemmed | Multi-Stimulus Responsive Multilayer Coating for Treatment of Device-Associated Infections |
title_short | Multi-Stimulus Responsive Multilayer Coating for Treatment of Device-Associated Infections |
title_sort | multi-stimulus responsive multilayer coating for treatment of device-associated infections |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954600/ https://www.ncbi.nlm.nih.gov/pubmed/35323224 http://dx.doi.org/10.3390/jfb13010024 |
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