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      Size-Dependent Bioactivity of Silver Nanoparticles: Antibacterial Properties, Influence on Copper Status in Mice, and Whole-Body Turnover

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          Abstract

          Purpose

          The ability of silver nanoparticles (AgNPs) of different sizes to influence copper metabolism in mice is assessed.

          Materials and Methods

          AgNPs with diameters of 10, 20, and 75 nm were fabricated through a chemical reduction of silver nitrate and characterized by UV/Vis spectrometry, transmission and scanning electronic microscopy, and laser diffractometry. To test their bioactivity, Escherichia coli cells, cultured A549 cells, and C57Bl/6 mice were used. The antibacterial activity of AgNPs was determined by inhibition of colony-forming ability, and cytotoxicity was tested using the MTT test (viability, %). Ceruloplasmin (Cp, the major mammalian extracellular copper-containing protein) concentration and enzymatic activity were measured using gel-assay analyses and WB, respectively. In vitro binding of AgNPs with serum proteins was monitored with UV/Vis spectroscopy. Metal concentrations were measured using atomic absorption spectrometry.

          Results

          The smallest AgNPs displayed the largest dose- and time-dependent antibacterial activity. All nanoparticles inhibited the metabolic activity of A549 cells in accordance with dose and time, but no correlation between cytotoxicity and nanoparticle size was found. Nanosilver was not uniformly distributed through the body of mice intraperitoneally treated with low AgNP concentrations. It was predominantly accumulated in liver. There, nanosilver was included in ceruloplasmin, and Ag-ceruloplasmin with low oxidase activity level was formed. Larger nanoparticles more effectively interfered with the copper metabolism of mice. Large AgNPs quickly induced a drop of blood serum oxidase activity to practically zero, but after cancellation of AgNP treatment, the activity was rapidly restored. A major fraction of the nanosilver was excreted in the bile with Cp. Nanosilver was bound by alpha-2-macroglobulin in vitro and in vivo, but silver did not substitute for the copper atoms of Cp in vitro.

          Conclusion

          The data showed that even at low concentrations, AgNPs influence murine copper metabolism in size-dependent manner. This property negatively correlated with the antibacterial activity of AgNPs.

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          Most cited references95

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          Silver Nanoparticles: Synthesis, Characterization, Properties, Applications, and Therapeutic Approaches

          Recent advances in nanoscience and nanotechnology radically changed the way we diagnose, treat, and prevent various diseases in all aspects of human life. Silver nanoparticles (AgNPs) are one of the most vital and fascinating nanomaterials among several metallic nanoparticles that are involved in biomedical applications. AgNPs play an important role in nanoscience and nanotechnology, particularly in nanomedicine. Although several noble metals have been used for various purposes, AgNPs have been focused on potential applications in cancer diagnosis and therapy. In this review, we discuss the synthesis of AgNPs using physical, chemical, and biological methods. We also discuss the properties of AgNPs and methods for their characterization. More importantly, we extensively discuss the multifunctional bio-applications of AgNPs; for example, as antibacterial, antifungal, antiviral, anti-inflammatory, anti-angiogenic, and anti-cancer agents, and the mechanism of the anti-cancer activity of AgNPs. In addition, we discuss therapeutic approaches and challenges for cancer therapy using AgNPs. Finally, we conclude by discussing the future perspective of AgNPs.
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            A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases.

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              Mechanistic Basis of Antimicrobial Actions of Silver Nanoparticles

              Multidrug resistance of the pathogenic microorganisms to the antimicrobial drugs has become a major impediment toward successful diagnosis and management of infectious diseases. Recent advancements in nanotechnology-based medicines have opened new horizons for combating multidrug resistance in microorganisms. In particular, the use of silver nanoparticles (AgNPs) as a potent antibacterial agent has received much attention. The most critical physico-chemical parameters that affect the antimicrobial potential of AgNPs include size, shape, surface charge, concentration and colloidal state. AgNPs exhibits their antimicrobial potential through multifaceted mechanisms. AgNPs adhesion to microbial cells, penetration inside the cells, ROS and free radical generation, and modulation of microbial signal transduction pathways have been recognized as the most prominent modes of antimicrobial action. On the other side, AgNPs exposure to human cells induces cytotoxicity, genotoxicity, and inflammatory response in human cells in a cell-type dependent manner. This has raised concerns regarding use of AgNPs in therapeutics and drug delivery. We have summarized the emerging endeavors that address current challenges in relation to safe use of AgNPs in therapeutics and drug delivery platforms. Based on research done so far, we believe that AgNPs can be engineered so as to increase their efficacy, stability, specificity, biosafety and biocompatibility. In this regard, three perspectives research directions have been suggested that include (1) synthesizing AgNPs with controlled physico-chemical properties, (2) examining microbial development of resistance toward AgNPs, and (3) ascertaining the susceptibility of cytoxicity, genotoxicity, and inflammatory response to human cells upon AgNPs exposure.
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                Author and article information

                Journal
                Nanotechnol Sci Appl
                Nanotechnol Sci Appl
                nsa
                nsa
                Nanotechnology, Science and Applications
                Dove
                1177-8903
                31 December 2020
                2020
                : 13
                : 137-157
                Affiliations
                [1 ]International Research Center of Functional Materials and Devices of Optoelectronics, ITMO University , St. Petersburg, Russia
                [2 ]Department of Molecular Genetics, Research Institute of Experimental Medicine , St. Petersburg, Russia
                [3 ]Higher Engineering Physics School of the Institute of Physics, Nanotechnology and Telecommunications, Peter the Great St. Petersburg Polytechnic University , St. Petersburg, Russia
                [4 ]Department of Experimental Physiology and Pharmacology, Almazov National Medical Research Centre , St. Petersburg, Russia
                [5 ]Laboratory of Blood Circulation Biophysics, Pavlov First Saint Petersburg State Medical University , St. Petersburg, Russia
                [6 ]Center of Nanoheterostructures Physics, Ioffe Institute, Russian Academy of Sciences , St. Petersburg, Russia
                [7 ]Laboratory of Cell Protection Mechanisms, Institute of Cytology, Russian Academy of Sciences , St. Petersburg, Russia
                [8 ]Telethon Institute of Genetics and Medicine , Pozzuoli, Naples, Italy
                Author notes
                Correspondence: Ekaterina Yu Ilyechova Department of Molecular Genetics, Research Institute of Experimental Medicine , Acad. Pavlov Street, 12, St. Petersburg197376, RussiaTel +79217605274Fax +78122322307 Email ilichevaey@itmo.ru
                Author information
                http://orcid.org/0000-0003-1959-7110
                http://orcid.org/0000-0002-5623-2156
                Article
                287658
                10.2147/NSA.S287658
                7781014
                33408467
                7fe19417-3dff-4154-be8f-fba63cd72f7a
                © 2020 Skomorokhova et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 21 October 2020
                : 04 December 2020
                Page count
                Figures: 10, References: 95, Pages: 21
                Funding
                Funded by: the Russian Science Foundation;
                Funded by: Russian Foundation for Basic Research, open-funder-registry 10.13039/501100002261;
                This work was supported by the Russian Science Foundation [grant number 20-74-10087] and Russian Foundation for Basic Research [grant numbers 18-515-7811, 18-015-00481, 19-315-90129].
                Categories
                Original Research

                silver nanoparticles,copper status,ceruloplasmin,alpha-2-macroglobulin,bile,urine

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