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      Smart antimicrobial efficacy employing pH-sensitive ZnO-doped diamond-like carbon coatings

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          Abstract

          One of the main challenges in endoprosthesis surgeries are implant-associated infections and aseptic-loosenings, caused by wear debris. To combat these problems, the requirements to surfaces of endoprostheses are wear-resistance, low cytotoxicity and antimicrobial efficacy. We here present antimicrobial coatings with a smart, adaptive release of metal ions in case of infection, based on ZnO-nanoparticles embedded in diamond-like carbon (DLC). The Zn 2+ ion release of these coatings in aqueous environments reacts and adapts smartly on inflammations accompanied by acidosis. Moreover, we show that this increased ion release comes along with an increased toxicity to fibroblastic cells (L929) and bacteria ( Staphylococcus aureus subsp. aureus, resistant to methicillin and oxacillin. (ATCC 43300, MRSA) and Staphylococcus epidermidis (ATCC 35984, S. epidermidis). Interestingly, the antimicrobial effect and the cytotoxicity of the coatings increase with a reduction of the pH value from 7.4 to 6.4, but not further to pH 5.4.

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          Most cited references31

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          Interpretation of Raman spectra of disordered and amorphous carbon

          Physical Review B, 61(20), 14095-14107
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            Environment-sensitive hydrogels for drug delivery

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              Antibacterial activity and mechanism of action of zinc oxide nanoparticles against Campylobacter jejuni.

              The antibacterial effect of zinc oxide (ZnO) nanoparticles on Campylobacter jejuni was investigated for inhibition and inactivation of cell growth. The results showed that C. jejuni was extremely sensitive to treatment with ZnO nanoparticles. The MIC of ZnO nanoparticles for C. jejuni was determined to be 0.05 to 0.025 mg/ml, which is 8- to 16-fold lower than that for Salmonella enterica serovar Enteritidis and Escherichia coli O157:H7 (0.4 mg/ml). The action of ZnO nanoparticles against C. jejuni was determined to be bactericidal, not bacteriostatic. Scanning electron microscopy examination revealed that the majority of the cells transformed from spiral shapes into coccoid forms after exposure to 0.5 mg/ml of ZnO nanoparticles for 16 h, which is consistent with the morphological changes of C. jejuni under other stress conditions. These coccoid cells were found by ethidium monoazide-quantitative PCR (EMA-qPCR) to have a certain level of membrane leakage. To address the molecular basis of ZnO nanoparticle action, a large set of genes involved in cell stress response, motility, pathogenesis, and toxin production were selected for a gene expression study. Reverse transcription-quantitative PCR (RT-qPCR) showed that in response to treatment with ZnO nanoparticles, the expression levels of two oxidative stress genes (katA and ahpC) and a general stress response gene (dnaK) were increased 52-, 7-, and 17-fold, respectively. These results suggest that the antibacterial mechanism of ZnO nanoparticles is most likely due to disruption of the cell membrane and oxidative stress in Campylobacter.
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                Author and article information

                Contributors
                christoph.westerhausen@gmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                21 November 2019
                21 November 2019
                2019
                : 9
                : 17246
                Affiliations
                [1 ]ISNI 0000 0001 2108 9006, GRID grid.7307.3, Chair for Experimental Physics 1, , University of Augsburg, ; Augsburg, 86159 Germany
                [2 ]ISNI 0000 0001 2180 3484, GRID grid.13648.38, Department of Dermatology and Venereology, , University Hospital Hamburg-Eppendorf, ; Hamburg, 20246 Germany
                [3 ]ISNI 0000000123222966, GRID grid.6936.a, Technical University of Munich, School of Medicine, Clinic of Orthopedics and Sportorthopedics, ; 81675 Munich, Germany
                [4 ]ISNI 0000 0004 1936 973X, GRID grid.5252.0, Center for NanoScience (CeNS), , Ludwig-Maximilians-Universität Munich, ; 80799 Munich, Germany
                [5 ]ISNI 0000 0001 2108 9006, GRID grid.7307.3, Chair for Physiology, University of Augsburg, ; Augsburg, 86159 Germany
                Author information
                http://orcid.org/0000-0002-1774-5194
                http://orcid.org/0000-0001-7103-7060
                Article
                53521
                10.1038/s41598-019-53521-7
                6872652
                31754198
                53b29943-0d0e-404a-b2f3-789d745c5f4e
                © 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/.

                History
                : 28 August 2019
                : 31 October 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft (German Research Foundation);
                Award ID: Projektnummer 263003590
                Award ID: Projektnummer 263003590
                Award ID: Projektnummer 263003590
                Award ID: Projektnummer 263003590
                Award ID: Projektnummer 263003590
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                antimicrobials,biomedical materials
                Uncategorized
                antimicrobials, biomedical materials

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