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PLA-HPG based coating enhanced anti-biofilm and wound healing of Shikonin in MRSA-infected burn wound
Burn wounds are susceptible to bacterial infections, including Methicillin-resistant Staphylococcus aureus (MRSA), which typically form biofilms and exhibit drug resistance. They also have specific feature of abundant exudate, necessitating frequent drug administration. Shikonin (SKN) has been repor...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448828/ https://www.ncbi.nlm.nih.gov/pubmed/37635995 http://dx.doi.org/10.3389/fbioe.2023.1243525 |
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author | Han, Huiyu Chen, Lianheng Liang, Shu Lü, Jiawei Wu, Yashi Wang, Xiongjun Xu, Fei Ge, Lanlan Xiao, Lingyun |
author_facet | Han, Huiyu Chen, Lianheng Liang, Shu Lü, Jiawei Wu, Yashi Wang, Xiongjun Xu, Fei Ge, Lanlan Xiao, Lingyun |
author_sort | Han, Huiyu |
collection | PubMed |
description | Burn wounds are susceptible to bacterial infections, including Methicillin-resistant Staphylococcus aureus (MRSA), which typically form biofilms and exhibit drug resistance. They also have specific feature of abundant exudate, necessitating frequent drug administration. Shikonin (SKN) has been reported to reverse MRSA drug resistance and possesses anti-biofilm and wound healing properties, however, it suffers from drawbacks of low solubility and instability. In this study, we developed PLA-HPG based bioadhesive nanoparticles SKN/BNP, which demonstrated a drug loading capacity of about 3.6%, and exhibited sustained-release behavior of SKN. The aldehyde groups present on the surface of BNP improved the local adhesion of SKN/BNP both in vitro and in vivo, thereby reducing the frequency of drug dosing in exudate-rich burn wounds. BNP alone enhanced proliferation and migration of the fibroblast, while SKN/BNP promoted fibroblast proliferation and migration as well as angiogenesis. Due to its bioadhesive property, BNP directly interacted with biofilm and enhanced the efficacy of SKN against MRSA biofilm in vitro. In a mouse model of MRSA-infected burn wounds, SKN/BNP demonstrated improved anti-biofilm and wound healing efficiency. Overall, our findings suggest that SKN/BNP holds great promise as a novel and effective treatment option for clinical applications in MRSA-infected burn wounds. |
format | Online Article Text |
id | pubmed-10448828 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104488282023-08-25 PLA-HPG based coating enhanced anti-biofilm and wound healing of Shikonin in MRSA-infected burn wound Han, Huiyu Chen, Lianheng Liang, Shu Lü, Jiawei Wu, Yashi Wang, Xiongjun Xu, Fei Ge, Lanlan Xiao, Lingyun Front Bioeng Biotechnol Bioengineering and Biotechnology Burn wounds are susceptible to bacterial infections, including Methicillin-resistant Staphylococcus aureus (MRSA), which typically form biofilms and exhibit drug resistance. They also have specific feature of abundant exudate, necessitating frequent drug administration. Shikonin (SKN) has been reported to reverse MRSA drug resistance and possesses anti-biofilm and wound healing properties, however, it suffers from drawbacks of low solubility and instability. In this study, we developed PLA-HPG based bioadhesive nanoparticles SKN/BNP, which demonstrated a drug loading capacity of about 3.6%, and exhibited sustained-release behavior of SKN. The aldehyde groups present on the surface of BNP improved the local adhesion of SKN/BNP both in vitro and in vivo, thereby reducing the frequency of drug dosing in exudate-rich burn wounds. BNP alone enhanced proliferation and migration of the fibroblast, while SKN/BNP promoted fibroblast proliferation and migration as well as angiogenesis. Due to its bioadhesive property, BNP directly interacted with biofilm and enhanced the efficacy of SKN against MRSA biofilm in vitro. In a mouse model of MRSA-infected burn wounds, SKN/BNP demonstrated improved anti-biofilm and wound healing efficiency. Overall, our findings suggest that SKN/BNP holds great promise as a novel and effective treatment option for clinical applications in MRSA-infected burn wounds. Frontiers Media S.A. 2023-08-10 /pmc/articles/PMC10448828/ /pubmed/37635995 http://dx.doi.org/10.3389/fbioe.2023.1243525 Text en Copyright © 2023 Han, Chen, Liang, Lü, Wu, Wang, Xu, Ge and Xiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Han, Huiyu Chen, Lianheng Liang, Shu Lü, Jiawei Wu, Yashi Wang, Xiongjun Xu, Fei Ge, Lanlan Xiao, Lingyun PLA-HPG based coating enhanced anti-biofilm and wound healing of Shikonin in MRSA-infected burn wound |
title | PLA-HPG based coating enhanced anti-biofilm and wound healing of Shikonin in MRSA-infected burn wound |
title_full | PLA-HPG based coating enhanced anti-biofilm and wound healing of Shikonin in MRSA-infected burn wound |
title_fullStr | PLA-HPG based coating enhanced anti-biofilm and wound healing of Shikonin in MRSA-infected burn wound |
title_full_unstemmed | PLA-HPG based coating enhanced anti-biofilm and wound healing of Shikonin in MRSA-infected burn wound |
title_short | PLA-HPG based coating enhanced anti-biofilm and wound healing of Shikonin in MRSA-infected burn wound |
title_sort | pla-hpg based coating enhanced anti-biofilm and wound healing of shikonin in mrsa-infected burn wound |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448828/ https://www.ncbi.nlm.nih.gov/pubmed/37635995 http://dx.doi.org/10.3389/fbioe.2023.1243525 |
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