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The commercial antibiotics with inherent AIE feature: In situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy

The research on pharmacology usually focuses on the structure-activity relationships of drugs, such as antibiotics, to enhance their activity, but often ignores their optical properties. However, investigating the photophysical properties of drugs is of great significance because they could be used...

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Detalles Bibliográficos
Autores principales: Wang, Bingnan, Wang, Lirong, Wu, Haozhong, Liu, Xiaolin, Zhu, Jiamiao, Hu, Rong, Ding, Dan, Qin, Anjun, Tang, Ben Zhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673049/
https://www.ncbi.nlm.nih.gov/pubmed/36439086
http://dx.doi.org/10.1016/j.bioactmat.2022.11.002
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author Wang, Bingnan
Wang, Lirong
Wu, Haozhong
Liu, Xiaolin
Zhu, Jiamiao
Hu, Rong
Ding, Dan
Qin, Anjun
Tang, Ben Zhong
author_facet Wang, Bingnan
Wang, Lirong
Wu, Haozhong
Liu, Xiaolin
Zhu, Jiamiao
Hu, Rong
Ding, Dan
Qin, Anjun
Tang, Ben Zhong
author_sort Wang, Bingnan
collection PubMed
description The research on pharmacology usually focuses on the structure-activity relationships of drugs, such as antibiotics, to enhance their activity, but often ignores their optical properties. However, investigating the photophysical properties of drugs is of great significance because they could be used to in situ visualize their positions and help us to understand their working metabolism. In this work, we identified a class of commercialized antibiotics, such as levofloxacin, norfloxacin, and moxifloxacin (MXF) hydrochloride, featuring the unique aggregation-induced emission (AIE) characteristics. By taking advantage of their AIE feature, antibiotic metabolism in cells could be in situ visualized, which clearly shows that the luminescent aggregates accumulate in the lysosomes. Moreover, after a structure-activity relationship study, we found an ideal site of MXF to be modified with a triphenylphosphonium and an antibiotic derivative MXF-P was prepared, which is able to specifically differentiate bacterial species after only 10 min of treatment. Moreover, MXF-P shows highly effective broad-spectrum antibacterial activity, excellent therapeutic effects and biosafety for S. aureus-infected wound recovery. Thus, this work not only discovers the multifunctionalities of the antibiotics but also provides a feasible strategy to make the commercialized drugs more powerful.
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spelling pubmed-96730492022-11-25 The commercial antibiotics with inherent AIE feature: In situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy Wang, Bingnan Wang, Lirong Wu, Haozhong Liu, Xiaolin Zhu, Jiamiao Hu, Rong Ding, Dan Qin, Anjun Tang, Ben Zhong Bioact Mater Article The research on pharmacology usually focuses on the structure-activity relationships of drugs, such as antibiotics, to enhance their activity, but often ignores their optical properties. However, investigating the photophysical properties of drugs is of great significance because they could be used to in situ visualize their positions and help us to understand their working metabolism. In this work, we identified a class of commercialized antibiotics, such as levofloxacin, norfloxacin, and moxifloxacin (MXF) hydrochloride, featuring the unique aggregation-induced emission (AIE) characteristics. By taking advantage of their AIE feature, antibiotic metabolism in cells could be in situ visualized, which clearly shows that the luminescent aggregates accumulate in the lysosomes. Moreover, after a structure-activity relationship study, we found an ideal site of MXF to be modified with a triphenylphosphonium and an antibiotic derivative MXF-P was prepared, which is able to specifically differentiate bacterial species after only 10 min of treatment. Moreover, MXF-P shows highly effective broad-spectrum antibacterial activity, excellent therapeutic effects and biosafety for S. aureus-infected wound recovery. Thus, this work not only discovers the multifunctionalities of the antibiotics but also provides a feasible strategy to make the commercialized drugs more powerful. KeAi Publishing 2022-11-16 /pmc/articles/PMC9673049/ /pubmed/36439086 http://dx.doi.org/10.1016/j.bioactmat.2022.11.002 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Wang, Bingnan
Wang, Lirong
Wu, Haozhong
Liu, Xiaolin
Zhu, Jiamiao
Hu, Rong
Ding, Dan
Qin, Anjun
Tang, Ben Zhong
The commercial antibiotics with inherent AIE feature: In situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy
title The commercial antibiotics with inherent AIE feature: In situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy
title_full The commercial antibiotics with inherent AIE feature: In situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy
title_fullStr The commercial antibiotics with inherent AIE feature: In situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy
title_full_unstemmed The commercial antibiotics with inherent AIE feature: In situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy
title_short The commercial antibiotics with inherent AIE feature: In situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy
title_sort commercial antibiotics with inherent aie feature: in situ visualization of antibiotic metabolism and specifically differentiation of bacterial species and broad-spectrum therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673049/
https://www.ncbi.nlm.nih.gov/pubmed/36439086
http://dx.doi.org/10.1016/j.bioactmat.2022.11.002
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