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Adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection
The prodrug approach has emerged as a promising solution to combat bacterial resistance and enhance treatment efficacy against bacterial infections. Here, we report an adenosine triphosphate (ATP)-activated prodrug system for on-demand treatment of bacterial infection. The prodrug system benefits fr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372092/ https://www.ncbi.nlm.nih.gov/pubmed/35953495 http://dx.doi.org/10.1038/s41467-022-32453-3 |
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author | Weng, Yuhao Chen, Huihong Chen, Xiaoqian Yang, Huilin Chen, Chia-Hung Tan, Hongliang |
author_facet | Weng, Yuhao Chen, Huihong Chen, Xiaoqian Yang, Huilin Chen, Chia-Hung Tan, Hongliang |
author_sort | Weng, Yuhao |
collection | PubMed |
description | The prodrug approach has emerged as a promising solution to combat bacterial resistance and enhance treatment efficacy against bacterial infections. Here, we report an adenosine triphosphate (ATP)-activated prodrug system for on-demand treatment of bacterial infection. The prodrug system benefits from the synergistic action of zeolitic imidazolate framework-8 and polyacrylamide hydrogel microsphere, which simultaneously transports indole-3-acetic acid and horseradish peroxidase in a single carrier while preventing the premature activation of indole-3-acetic acid. The ATP-responsive characteristic of zeolitic imidazolate framework-8 allows the prodrug system to be activated by the ATP secreted by bacteria to generate reactive oxygen species (ROS), displaying exceptional broad-spectrum antimicrobial ability. Upon disruption of the bacterial membrane by ROS, the leaked intracellular ATP from dead bacteria can accelerate the activation of the prodrug system to further enhance antibacterial efficiency. In vivo experiments in a mouse model demonstrates the applicability of the prodrug system for wound disinfection with minimal side effects. |
format | Online Article Text |
id | pubmed-9372092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93720922022-08-13 Adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection Weng, Yuhao Chen, Huihong Chen, Xiaoqian Yang, Huilin Chen, Chia-Hung Tan, Hongliang Nat Commun Article The prodrug approach has emerged as a promising solution to combat bacterial resistance and enhance treatment efficacy against bacterial infections. Here, we report an adenosine triphosphate (ATP)-activated prodrug system for on-demand treatment of bacterial infection. The prodrug system benefits from the synergistic action of zeolitic imidazolate framework-8 and polyacrylamide hydrogel microsphere, which simultaneously transports indole-3-acetic acid and horseradish peroxidase in a single carrier while preventing the premature activation of indole-3-acetic acid. The ATP-responsive characteristic of zeolitic imidazolate framework-8 allows the prodrug system to be activated by the ATP secreted by bacteria to generate reactive oxygen species (ROS), displaying exceptional broad-spectrum antimicrobial ability. Upon disruption of the bacterial membrane by ROS, the leaked intracellular ATP from dead bacteria can accelerate the activation of the prodrug system to further enhance antibacterial efficiency. In vivo experiments in a mouse model demonstrates the applicability of the prodrug system for wound disinfection with minimal side effects. Nature Publishing Group UK 2022-08-11 /pmc/articles/PMC9372092/ /pubmed/35953495 http://dx.doi.org/10.1038/s41467-022-32453-3 Text en © The Author(s) 2022 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 Weng, Yuhao Chen, Huihong Chen, Xiaoqian Yang, Huilin Chen, Chia-Hung Tan, Hongliang Adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection |
title | Adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection |
title_full | Adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection |
title_fullStr | Adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection |
title_full_unstemmed | Adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection |
title_short | Adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection |
title_sort | adenosine triphosphate-activated prodrug system for on-demand bacterial inactivation and wound disinfection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372092/ https://www.ncbi.nlm.nih.gov/pubmed/35953495 http://dx.doi.org/10.1038/s41467-022-32453-3 |
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