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A dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection
Increasing bacterial drug resistance to antibiotics has posed a major threat to contemporary public health, which resulted in a large number of people suffering from serious infections and ending up dying without any effective therapies every year. Here, a dynamic covalent polymeric antimicrobial, b...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191036/ https://www.ncbi.nlm.nih.gov/pubmed/37325499 http://dx.doi.org/10.1002/EXP.20210145 |
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author | Huang, Fan Cai, Xiaoyao Hou, Xiaoxue Zhang, Yumin Liu, Jinjian Yang, Lijun Liu, Yong Liu, Jianfeng |
author_facet | Huang, Fan Cai, Xiaoyao Hou, Xiaoxue Zhang, Yumin Liu, Jinjian Yang, Lijun Liu, Yong Liu, Jianfeng |
author_sort | Huang, Fan |
collection | PubMed |
description | Increasing bacterial drug resistance to antibiotics has posed a major threat to contemporary public health, which resulted in a large number of people suffering from serious infections and ending up dying without any effective therapies every year. Here, a dynamic covalent polymeric antimicrobial, based on phenylboronic acid (PBA)‐installed micellar nanocarriers incorporating clinical vancomycin and curcumin, is developed to overcome drug‐resistant bacterial infections. The formation of this antimicrobial is facilitated by reversible dynamic covalent interactions between PBA moieties in polymeric micelles and diols in vancomycin, which impart favorable stability in blood circulation and excellent acid‐responsiveness in the infection microenvironment. Moreover, the structurally similar aromatic vancomycin and curcumin molecules can afford π–π stacking interaction to realize simultaneous delivery and release of payloads. In comparison with monotherapy, this dynamic covalent polymeric antimicrobial demonstrated more significant eradication of drug‐resistant bacteria in vitro and in vivo due to the synergism of the two drugs. Furthermore, the achieved combination therapy shows satisfied biocompatibility without unwanted toxicity. Considering various antibiotics contain diol and aromatic structures, this simple and robust strategy can become a universal platform to combat the ever‐threatening drug‐resistant infectious diseases. |
format | Online Article Text |
id | pubmed-10191036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101910362023-06-14 A dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection Huang, Fan Cai, Xiaoyao Hou, Xiaoxue Zhang, Yumin Liu, Jinjian Yang, Lijun Liu, Yong Liu, Jianfeng Exploration (Beijing) Research Articles Increasing bacterial drug resistance to antibiotics has posed a major threat to contemporary public health, which resulted in a large number of people suffering from serious infections and ending up dying without any effective therapies every year. Here, a dynamic covalent polymeric antimicrobial, based on phenylboronic acid (PBA)‐installed micellar nanocarriers incorporating clinical vancomycin and curcumin, is developed to overcome drug‐resistant bacterial infections. The formation of this antimicrobial is facilitated by reversible dynamic covalent interactions between PBA moieties in polymeric micelles and diols in vancomycin, which impart favorable stability in blood circulation and excellent acid‐responsiveness in the infection microenvironment. Moreover, the structurally similar aromatic vancomycin and curcumin molecules can afford π–π stacking interaction to realize simultaneous delivery and release of payloads. In comparison with monotherapy, this dynamic covalent polymeric antimicrobial demonstrated more significant eradication of drug‐resistant bacteria in vitro and in vivo due to the synergism of the two drugs. Furthermore, the achieved combination therapy shows satisfied biocompatibility without unwanted toxicity. Considering various antibiotics contain diol and aromatic structures, this simple and robust strategy can become a universal platform to combat the ever‐threatening drug‐resistant infectious diseases. John Wiley and Sons Inc. 2022-05-23 /pmc/articles/PMC10191036/ /pubmed/37325499 http://dx.doi.org/10.1002/EXP.20210145 Text en © 2022 The Authors. Exploration published by Henan University and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Huang, Fan Cai, Xiaoyao Hou, Xiaoxue Zhang, Yumin Liu, Jinjian Yang, Lijun Liu, Yong Liu, Jianfeng A dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection |
title | A dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection |
title_full | A dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection |
title_fullStr | A dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection |
title_full_unstemmed | A dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection |
title_short | A dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection |
title_sort | dynamic covalent polymeric antimicrobial for conquering drug‐resistant bacterial infection |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191036/ https://www.ncbi.nlm.nih.gov/pubmed/37325499 http://dx.doi.org/10.1002/EXP.20210145 |
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