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Janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms

Safe and efficient antibacterial materials are urgently needed to combat drug-resistant bacteria and biofilm-associated infections. The rational design of nanoparticles for flexible elimination of biofilms remains challenging. Herein, we propose the fabrication of Janus-structured nanoparticles targ...

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Autores principales: Liu, Zhiwen, Guo, Kangli, Yan, Liemei, Zhang, Kai, Wang, Ying, Ding, Xiaokang, Zhao, Nana, Xu, Fu-Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447547/
https://www.ncbi.nlm.nih.gov/pubmed/37612285
http://dx.doi.org/10.1038/s41467-023-40830-9
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author Liu, Zhiwen
Guo, Kangli
Yan, Liemei
Zhang, Kai
Wang, Ying
Ding, Xiaokang
Zhao, Nana
Xu, Fu-Jian
author_facet Liu, Zhiwen
Guo, Kangli
Yan, Liemei
Zhang, Kai
Wang, Ying
Ding, Xiaokang
Zhao, Nana
Xu, Fu-Jian
author_sort Liu, Zhiwen
collection PubMed
description Safe and efficient antibacterial materials are urgently needed to combat drug-resistant bacteria and biofilm-associated infections. The rational design of nanoparticles for flexible elimination of biofilms remains challenging. Herein, we propose the fabrication of Janus-structured nanoparticles targeting extracellular polymeric substance to achieve dispersion or near-infrared (NIR) light-activated photothermal elimination of drug-resistant biofilms, respectively. Asymmetrical Janus-structured dextran-bismuth selenide (Dex-BSe) nanoparticles are fabricated to exploit synergistic effects of both components. Interestingly, Janus Dex-BSe nanoparticles realize enhanced dispersal of biofilms over time. Alternatively, taking advantage of the preferential accumulation of nanoparticles at infection sites, the self-propelled active motion induced by the unique Janus structure enhances photothermal killing effect. The flexible application of Janus Dex-BSe nanoparticles for biofilm removal or NIR-triggered eradication in vivo is demonstrated by Staphylococcus aureus-infected mouse excisional wound model and abscess model, respectively. The developed Janus nanoplatform holds great promise for the efficient elimination of drug-resistant biofilms in diverse antibacterial scenarios.
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spelling pubmed-104475472023-08-25 Janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms Liu, Zhiwen Guo, Kangli Yan, Liemei Zhang, Kai Wang, Ying Ding, Xiaokang Zhao, Nana Xu, Fu-Jian Nat Commun Article Safe and efficient antibacterial materials are urgently needed to combat drug-resistant bacteria and biofilm-associated infections. The rational design of nanoparticles for flexible elimination of biofilms remains challenging. Herein, we propose the fabrication of Janus-structured nanoparticles targeting extracellular polymeric substance to achieve dispersion or near-infrared (NIR) light-activated photothermal elimination of drug-resistant biofilms, respectively. Asymmetrical Janus-structured dextran-bismuth selenide (Dex-BSe) nanoparticles are fabricated to exploit synergistic effects of both components. Interestingly, Janus Dex-BSe nanoparticles realize enhanced dispersal of biofilms over time. Alternatively, taking advantage of the preferential accumulation of nanoparticles at infection sites, the self-propelled active motion induced by the unique Janus structure enhances photothermal killing effect. The flexible application of Janus Dex-BSe nanoparticles for biofilm removal or NIR-triggered eradication in vivo is demonstrated by Staphylococcus aureus-infected mouse excisional wound model and abscess model, respectively. The developed Janus nanoplatform holds great promise for the efficient elimination of drug-resistant biofilms in diverse antibacterial scenarios. Nature Publishing Group UK 2023-08-23 /pmc/articles/PMC10447547/ /pubmed/37612285 http://dx.doi.org/10.1038/s41467-023-40830-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liu, Zhiwen
Guo, Kangli
Yan, Liemei
Zhang, Kai
Wang, Ying
Ding, Xiaokang
Zhao, Nana
Xu, Fu-Jian
Janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms
title Janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms
title_full Janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms
title_fullStr Janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms
title_full_unstemmed Janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms
title_short Janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms
title_sort janus nanoparticles targeting extracellular polymeric substance achieve flexible elimination of drug-resistant biofilms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10447547/
https://www.ncbi.nlm.nih.gov/pubmed/37612285
http://dx.doi.org/10.1038/s41467-023-40830-9
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