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Nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents

Since its discovery nearly a century ago, antibiotics has been one of the most effective methods in treating infectious diseases and limiting pathogen spread. However, pathogens often build up antibiotic resistance over time, leading to serious failure of the treatment. Silver nanoparticle (AgNP) is...

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Autores principales: Chang, Be-Ming, Pan, Lei, Lin, Hsin-Hung, Chang, Huan-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739346/
https://www.ncbi.nlm.nih.gov/pubmed/31511584
http://dx.doi.org/10.1038/s41598-019-49675-z
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author Chang, Be-Ming
Pan, Lei
Lin, Hsin-Hung
Chang, Huan-Cheng
author_facet Chang, Be-Ming
Pan, Lei
Lin, Hsin-Hung
Chang, Huan-Cheng
author_sort Chang, Be-Ming
collection PubMed
description Since its discovery nearly a century ago, antibiotics has been one of the most effective methods in treating infectious diseases and limiting pathogen spread. However, pathogens often build up antibiotic resistance over time, leading to serious failure of the treatment. Silver nanoparticle (AgNP) is an appealing alternative, but successful treatment of the bacterial infection requires a plentiful supply of AgNP, which can negatively impact human health if people are excessively exposed to the particles. Here, we present a method to overcome this challenge by synthesizing nanodiamond-supported AgNP noncovalently conjugated with albumin molecules to achieve enhanced antibacterial activity and strengthened biocompatibility. Using Escherichia coli as a model bacterium, we found that the albumin-conjugated silver-diamond nanohybrids showed a long-term bactericidal effect after 36 days of the treatment at the AgNP concentration of 250 µg mL(−1). Moreover, the toxicity of the nanohybrids to human cells (including human fibroblasts, lung adenocarcinoma epithelial cells, and breast adenocarcinoma cells) is low even at the particle concentration of 500 µg mL(−1). The method provides a general and practical solution to the concerns of bacterial resistance against AgNP and issues associated with the size, shape, aggregation, and toxicity of AgNP are largely resolved. Finally, we demonstrate that the nanohybrids can be readily incorporated into natural polysaccharides (such as guar gum) to form three-in-one hydrogels, showing promising applications in nanomedicine.
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spelling pubmed-67393462019-09-22 Nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents Chang, Be-Ming Pan, Lei Lin, Hsin-Hung Chang, Huan-Cheng Sci Rep Article Since its discovery nearly a century ago, antibiotics has been one of the most effective methods in treating infectious diseases and limiting pathogen spread. However, pathogens often build up antibiotic resistance over time, leading to serious failure of the treatment. Silver nanoparticle (AgNP) is an appealing alternative, but successful treatment of the bacterial infection requires a plentiful supply of AgNP, which can negatively impact human health if people are excessively exposed to the particles. Here, we present a method to overcome this challenge by synthesizing nanodiamond-supported AgNP noncovalently conjugated with albumin molecules to achieve enhanced antibacterial activity and strengthened biocompatibility. Using Escherichia coli as a model bacterium, we found that the albumin-conjugated silver-diamond nanohybrids showed a long-term bactericidal effect after 36 days of the treatment at the AgNP concentration of 250 µg mL(−1). Moreover, the toxicity of the nanohybrids to human cells (including human fibroblasts, lung adenocarcinoma epithelial cells, and breast adenocarcinoma cells) is low even at the particle concentration of 500 µg mL(−1). The method provides a general and practical solution to the concerns of bacterial resistance against AgNP and issues associated with the size, shape, aggregation, and toxicity of AgNP are largely resolved. Finally, we demonstrate that the nanohybrids can be readily incorporated into natural polysaccharides (such as guar gum) to form three-in-one hydrogels, showing promising applications in nanomedicine. Nature Publishing Group UK 2019-09-11 /pmc/articles/PMC6739346/ /pubmed/31511584 http://dx.doi.org/10.1038/s41598-019-49675-z Text en © The Author(s) 2019 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/.
spellingShingle Article
Chang, Be-Ming
Pan, Lei
Lin, Hsin-Hung
Chang, Huan-Cheng
Nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents
title Nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents
title_full Nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents
title_fullStr Nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents
title_full_unstemmed Nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents
title_short Nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents
title_sort nanodiamond-supported silver nanoparticles as potent and safe antibacterial agents
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6739346/
https://www.ncbi.nlm.nih.gov/pubmed/31511584
http://dx.doi.org/10.1038/s41598-019-49675-z
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