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      Contact killing and antimicrobial properties of copper

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          Abstract

          With the emergence of antibiotic resistance, the interest for antimicrobial agents has recently increased again in public health. Copper was recognized in 2008 by the United States Environmental Protection Agency (EPA) as the first metallic antimicrobial agent. This led to many investigations of the various properties of copper as an antibacterial, antifungal and antiviral agent. This review summarizes the latest findings about 'contact killing', the mechanism of action of copper nanoparticles and the different ways micro-organisms develop resistance to copper.

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          Most cited references125

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          Copper: an essential metal in biology.

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            Size-dependent toxicity of metal oxide particles--a comparison between nano- and micrometer size.

            Toxicological studies have shown increased toxicity of nanoparticles (<100 nm) compared to micrometer particles of the same composition, which has raised concern about the impact on human health from nanoparticles. However, if this is true for a wide range of particles with different chemical composition is not clear. The aim of this study was to compare the toxicity of nano- and micrometer particles of some metal oxides (Fe(2)O(3), Fe(3)O(4), TiO(2) and CuO). The ability of the particles to cause cell death, mitochondrial damage, DNA damage and oxidative DNA lesions were evaluated after exposure of the human cell line A549. This study showed that nanoparticles of CuO were much more toxic compared to CuO micrometer particles. One key mechanism may be the ability of CuO to damage the mitochondria. In contrast, the micrometer particles of TiO(2) caused more DNA damage compared to the nanoparticles, which is likely explained by the crystal structures. The iron oxides showed low toxicity and no clear difference between the different particle sizes. In conclusion, nanoparticles are not always more toxic than micrometer particles, but the high toxicity of CuO nanoparticles shows that the nanolevel gives rise to specific concern.
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              Understanding the antibacterial mechanism of CuO nanoparticles: revealing the route of induced oxidative stress.

              To date, there is still a lack of definite knowledge regarding the interaction of CuO nanoparticles with bacteria and the possible permeation of the nanoparticles into bacterial cells. This study was aimed at shedding light on the size-dependent (from the microscale down to the small nanoscale) antibacterial activity of CuO. The potent antibacterial activity of CuO nanoparticles was found to be due to ROS-generation by the nanoparticles attached to the bacterial cells, which in turn provoked an enhancement of the intracellular oxidative stress. This paradigm was confirmed by several assays such as lipid peroxidation and reporter strains of oxidative stress. Furthermore, electron microscopy indicated that the small nanoparticles of CuO penetrated the cells. Collectively, the results reported herein may reconcile conflicting concepts in the literature concerning the antibacterial mechanism of CuO nanoparticles, as well as highlight the potential for developing sustainable CuO nanoparticles-based devices for inhibiting bacterial infections.
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                Author and article information

                Journal
                Journal of Applied Microbiology
                J Appl Microbiol
                Wiley
                13645072
                May 2018
                May 2018
                February 02 2018
                : 124
                : 5
                : 1032-1046
                Affiliations
                [1 ]CNRS, LEMTA, UMR 7563; Vandœuvre-lès-Nancy France
                [2 ]Université de Lorraine; LEMTA; UMR 7563; Vandœuvre-lès Nancy France
                [3 ]CNRS; UMR 7565; SRSMC; Vandœuvre-lès-Nancy France
                [4 ]Université de Lorraine; UMR 7565; SRSMC; Nancy France
                [5 ]ABC Platform; Nancy France
                [6 ]Faculté de Médecine; EA 7298; ERAMBO, DESP; Vandœuvre-lès-Nancy France
                Article
                10.1111/jam.13681
                29280540
                17debd3e-70ab-49fa-894e-5bd79ff56ac0
                © 2018

                http://doi.wiley.com/10.1002/tdm_license_1.1

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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