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Controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating Gram-positive drug-resistant bacteria and retaining biocompatibility
Infections caused by multidrug-resistant (MDR) bacteria are an increasing global healthcare concern. In this study, we developed a dual-ligand-functionalised Au(25)(SR(1))(x)(SR(2))(18−x)-type gold nanocluster and determined its antibacterial activity against MDR bacterial strains. The pyridinium li...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597861/ https://www.ncbi.nlm.nih.gov/pubmed/34820103 http://dx.doi.org/10.1039/d1sc03056f |
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author | Pang, Zeyang Li, Qizhen Jia, Yuexiao Yan, Weixiao Qi, Jie Guo, Yuan Hu, Fupin Zhou, Dejian Jiang, Xingyu |
author_facet | Pang, Zeyang Li, Qizhen Jia, Yuexiao Yan, Weixiao Qi, Jie Guo, Yuan Hu, Fupin Zhou, Dejian Jiang, Xingyu |
author_sort | Pang, Zeyang |
collection | PubMed |
description | Infections caused by multidrug-resistant (MDR) bacteria are an increasing global healthcare concern. In this study, we developed a dual-ligand-functionalised Au(25)(SR(1))(x)(SR(2))(18−x)-type gold nanocluster and determined its antibacterial activity against MDR bacterial strains. The pyridinium ligand (SR(1)) provided bactericidal potency and the zwitterionic ligand (SR(2)) enhanced the stability and biocompatibility. By optimising the ligand ratio, our gold nanocluster could effectively kill MDR Gram-positive bacteria via multiple antibacterial actions, including inducing bacterial aggregation, disrupting bacterial membrane integrity and potential, and generating reactive oxygen species. Moreover, combining the optimised gold nanocluster with common antibiotics could significantly enhance the antibacterial activity against MDR bacteria both in in vitro and animal models of skin infections. Furthermore, the fluorescence of the gold nanocluster at the second near-infrared (NIR-II) biological window allowed for the monitoring of its biodistribution and body clearance, which confirmed that the gold nanoclusters had good renal clearance and biocompatibility. This study provides a new strategy to combat the MDR challenge using multifunctional gold nanomaterials. |
format | Online Article Text |
id | pubmed-8597861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-85978612021-11-23 Controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating Gram-positive drug-resistant bacteria and retaining biocompatibility Pang, Zeyang Li, Qizhen Jia, Yuexiao Yan, Weixiao Qi, Jie Guo, Yuan Hu, Fupin Zhou, Dejian Jiang, Xingyu Chem Sci Chemistry Infections caused by multidrug-resistant (MDR) bacteria are an increasing global healthcare concern. In this study, we developed a dual-ligand-functionalised Au(25)(SR(1))(x)(SR(2))(18−x)-type gold nanocluster and determined its antibacterial activity against MDR bacterial strains. The pyridinium ligand (SR(1)) provided bactericidal potency and the zwitterionic ligand (SR(2)) enhanced the stability and biocompatibility. By optimising the ligand ratio, our gold nanocluster could effectively kill MDR Gram-positive bacteria via multiple antibacterial actions, including inducing bacterial aggregation, disrupting bacterial membrane integrity and potential, and generating reactive oxygen species. Moreover, combining the optimised gold nanocluster with common antibiotics could significantly enhance the antibacterial activity against MDR bacteria both in in vitro and animal models of skin infections. Furthermore, the fluorescence of the gold nanocluster at the second near-infrared (NIR-II) biological window allowed for the monitoring of its biodistribution and body clearance, which confirmed that the gold nanoclusters had good renal clearance and biocompatibility. This study provides a new strategy to combat the MDR challenge using multifunctional gold nanomaterials. The Royal Society of Chemistry 2021-10-25 /pmc/articles/PMC8597861/ /pubmed/34820103 http://dx.doi.org/10.1039/d1sc03056f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Pang, Zeyang Li, Qizhen Jia, Yuexiao Yan, Weixiao Qi, Jie Guo, Yuan Hu, Fupin Zhou, Dejian Jiang, Xingyu Controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating Gram-positive drug-resistant bacteria and retaining biocompatibility |
title | Controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating Gram-positive drug-resistant bacteria and retaining biocompatibility |
title_full | Controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating Gram-positive drug-resistant bacteria and retaining biocompatibility |
title_fullStr | Controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating Gram-positive drug-resistant bacteria and retaining biocompatibility |
title_full_unstemmed | Controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating Gram-positive drug-resistant bacteria and retaining biocompatibility |
title_short | Controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating Gram-positive drug-resistant bacteria and retaining biocompatibility |
title_sort | controlling the pyridinium–zwitterionic ligand ratio on atomically precise gold nanoclusters allowing for eradicating gram-positive drug-resistant bacteria and retaining biocompatibility |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8597861/ https://www.ncbi.nlm.nih.gov/pubmed/34820103 http://dx.doi.org/10.1039/d1sc03056f |
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