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Highly Efficient Antimicrobial Activity of Cu(x)Fe(y)O(z) Nanoparticles against Important Human Pathogens

The development of innovative antimicrobial materials is crucial in thwarting infectious diseases caused by microbes, as drug-resistant pathogens are increasing in both number and capacity to detoxify the antimicrobial drugs used today. An ideal antimicrobial material should inhibit a wide variety o...

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Autores principales: Zhu, Lu, Pearson, David W., Benoit, Stéphane L., Xie, Jing, Pant, Jitendra, Yang, Yanjun, Mondal, Arnab, Handa, Hitesh, Howe, Jane Y., Hung, Yen-Con, Vidal, Jorge E., Maier, Robert J., Zhao, Yiping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699552/
https://www.ncbi.nlm.nih.gov/pubmed/33233512
http://dx.doi.org/10.3390/nano10112294
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author Zhu, Lu
Pearson, David W.
Benoit, Stéphane L.
Xie, Jing
Pant, Jitendra
Yang, Yanjun
Mondal, Arnab
Handa, Hitesh
Howe, Jane Y.
Hung, Yen-Con
Vidal, Jorge E.
Maier, Robert J.
Zhao, Yiping
author_facet Zhu, Lu
Pearson, David W.
Benoit, Stéphane L.
Xie, Jing
Pant, Jitendra
Yang, Yanjun
Mondal, Arnab
Handa, Hitesh
Howe, Jane Y.
Hung, Yen-Con
Vidal, Jorge E.
Maier, Robert J.
Zhao, Yiping
author_sort Zhu, Lu
collection PubMed
description The development of innovative antimicrobial materials is crucial in thwarting infectious diseases caused by microbes, as drug-resistant pathogens are increasing in both number and capacity to detoxify the antimicrobial drugs used today. An ideal antimicrobial material should inhibit a wide variety of bacteria in a short period of time, be less or not toxic to normal cells, and the fabrication or synthesis process should be cheap and easy. We report a one-step microwave-assisted hydrothermal synthesis of mixed composite Cu(x)Fe(y)O(z) (Fe(2)O(3)/Cu(2)O/CuO/CuFe(2)O) nanoparticles (NPs) as an excellent antimicrobial material. The 1 mg/mL Cu(x)Fe(y)O(z) NPs with the composition 36% CuFeO(2), 28% Cu(2)O and 36% Fe(2)O(3) have a general antimicrobial activity greater than 5 log reduction within 4 h against nine important human pathogenic bacteria (including drug-resistant bacteria as well as Gram-positive and Gram-negative strains). For example, they induced a >9 log reduction in Escherichia coli B viability after 15 min of incubation, and an ~8 log reduction in multidrug-resistant Klebsiella pneumoniae after 4 h incubation. Cytotoxicity tests against mouse fibroblast cells showed about 74% viability when exposed to 1 mg/mL Cu(x)Fe(y)O(z) NPs for 24 h, compared to the 20% viability for 1 mg/mL pure Cu(2)O NPs synthesized by the same method. These results show that the Cu(x)Fe(y)O(z) composite NPs are a highly efficient, low-toxicity and cheap antimicrobial material that has promising potential for applications in medical and food safety.
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spelling pubmed-76995522020-11-29 Highly Efficient Antimicrobial Activity of Cu(x)Fe(y)O(z) Nanoparticles against Important Human Pathogens Zhu, Lu Pearson, David W. Benoit, Stéphane L. Xie, Jing Pant, Jitendra Yang, Yanjun Mondal, Arnab Handa, Hitesh Howe, Jane Y. Hung, Yen-Con Vidal, Jorge E. Maier, Robert J. Zhao, Yiping Nanomaterials (Basel) Article The development of innovative antimicrobial materials is crucial in thwarting infectious diseases caused by microbes, as drug-resistant pathogens are increasing in both number and capacity to detoxify the antimicrobial drugs used today. An ideal antimicrobial material should inhibit a wide variety of bacteria in a short period of time, be less or not toxic to normal cells, and the fabrication or synthesis process should be cheap and easy. We report a one-step microwave-assisted hydrothermal synthesis of mixed composite Cu(x)Fe(y)O(z) (Fe(2)O(3)/Cu(2)O/CuO/CuFe(2)O) nanoparticles (NPs) as an excellent antimicrobial material. The 1 mg/mL Cu(x)Fe(y)O(z) NPs with the composition 36% CuFeO(2), 28% Cu(2)O and 36% Fe(2)O(3) have a general antimicrobial activity greater than 5 log reduction within 4 h against nine important human pathogenic bacteria (including drug-resistant bacteria as well as Gram-positive and Gram-negative strains). For example, they induced a >9 log reduction in Escherichia coli B viability after 15 min of incubation, and an ~8 log reduction in multidrug-resistant Klebsiella pneumoniae after 4 h incubation. Cytotoxicity tests against mouse fibroblast cells showed about 74% viability when exposed to 1 mg/mL Cu(x)Fe(y)O(z) NPs for 24 h, compared to the 20% viability for 1 mg/mL pure Cu(2)O NPs synthesized by the same method. These results show that the Cu(x)Fe(y)O(z) composite NPs are a highly efficient, low-toxicity and cheap antimicrobial material that has promising potential for applications in medical and food safety. MDPI 2020-11-20 /pmc/articles/PMC7699552/ /pubmed/33233512 http://dx.doi.org/10.3390/nano10112294 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhu, Lu
Pearson, David W.
Benoit, Stéphane L.
Xie, Jing
Pant, Jitendra
Yang, Yanjun
Mondal, Arnab
Handa, Hitesh
Howe, Jane Y.
Hung, Yen-Con
Vidal, Jorge E.
Maier, Robert J.
Zhao, Yiping
Highly Efficient Antimicrobial Activity of Cu(x)Fe(y)O(z) Nanoparticles against Important Human Pathogens
title Highly Efficient Antimicrobial Activity of Cu(x)Fe(y)O(z) Nanoparticles against Important Human Pathogens
title_full Highly Efficient Antimicrobial Activity of Cu(x)Fe(y)O(z) Nanoparticles against Important Human Pathogens
title_fullStr Highly Efficient Antimicrobial Activity of Cu(x)Fe(y)O(z) Nanoparticles against Important Human Pathogens
title_full_unstemmed Highly Efficient Antimicrobial Activity of Cu(x)Fe(y)O(z) Nanoparticles against Important Human Pathogens
title_short Highly Efficient Antimicrobial Activity of Cu(x)Fe(y)O(z) Nanoparticles against Important Human Pathogens
title_sort highly efficient antimicrobial activity of cu(x)fe(y)o(z) nanoparticles against important human pathogens
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699552/
https://www.ncbi.nlm.nih.gov/pubmed/33233512
http://dx.doi.org/10.3390/nano10112294
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