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Hemolytic Activity, Cytotoxicity, and Antimicrobial Effects of Human Albumin- and Polysorbate-80-Coated Silver Nanoparticles

In this study, we aimed to develop a technique for colloidal silver nanoparticle (AgNP) modification in order to increase their stability in aqueous suspensions. For this purpose, 40-nm spherical AgNPs were modified by the addition of either human albumin or Tween-80 (Polysorbate-80). After detailed...

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Autores principales: Korolev, Dmitry, Shumilo, Michael, Shulmeyster, Galina, Krutikov, Alexander, Golovkin, Alexey, Mishanin, Alexander, Gorshkov, Andrew, Spiridonova, Anna, Domorad, Anna, Krasichkov, Alexander, Galagudza, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227625/
https://www.ncbi.nlm.nih.gov/pubmed/34205084
http://dx.doi.org/10.3390/nano11061484
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author Korolev, Dmitry
Shumilo, Michael
Shulmeyster, Galina
Krutikov, Alexander
Golovkin, Alexey
Mishanin, Alexander
Gorshkov, Andrew
Spiridonova, Anna
Domorad, Anna
Krasichkov, Alexander
Galagudza, Michael
author_facet Korolev, Dmitry
Shumilo, Michael
Shulmeyster, Galina
Krutikov, Alexander
Golovkin, Alexey
Mishanin, Alexander
Gorshkov, Andrew
Spiridonova, Anna
Domorad, Anna
Krasichkov, Alexander
Galagudza, Michael
author_sort Korolev, Dmitry
collection PubMed
description In this study, we aimed to develop a technique for colloidal silver nanoparticle (AgNP) modification in order to increase their stability in aqueous suspensions. For this purpose, 40-nm spherical AgNPs were modified by the addition of either human albumin or Tween-80 (Polysorbate-80). After detailed characterization of their physicochemical properties, the hemolytic activity of the nonmodified and modified AgNPs was investigated, as well as their cytotoxicity and antimicrobial effects. Both albumin- and Tween-80-coated AgNPs demonstrated excellent stability in 0.9% sodium chloride solution (>12 months) compared to nonmodified AgNPs, characterized by their rapid precipitation. Hemolytic activity of nonmodified and albumin-coated AgNPs was found to be minimal, while Tween-80-modified AgNPs produced significant hemolysis after 1, 2, and 24 h of incubation. In addition, both native and Tween-80-covered AgNPs showed dose-dependent cytotoxic effects on human adipose-tissue-derived mesenchymal stem cells. The albumin-coated AgNPs showed minimal cytotoxicity. The antimicrobial effects of native and albumin-coated AgNPs against S. aureus, K. pneumonia, P. aeruginosa, Corynebacterium spp., and Acinetobacter spp. were statistically significant. We conclude that albumin coating of AgNPs significantly contributes to improve stability, reduce cytotoxicity, and confers potent antimicrobial action.
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spelling pubmed-82276252021-06-26 Hemolytic Activity, Cytotoxicity, and Antimicrobial Effects of Human Albumin- and Polysorbate-80-Coated Silver Nanoparticles Korolev, Dmitry Shumilo, Michael Shulmeyster, Galina Krutikov, Alexander Golovkin, Alexey Mishanin, Alexander Gorshkov, Andrew Spiridonova, Anna Domorad, Anna Krasichkov, Alexander Galagudza, Michael Nanomaterials (Basel) Article In this study, we aimed to develop a technique for colloidal silver nanoparticle (AgNP) modification in order to increase their stability in aqueous suspensions. For this purpose, 40-nm spherical AgNPs were modified by the addition of either human albumin or Tween-80 (Polysorbate-80). After detailed characterization of their physicochemical properties, the hemolytic activity of the nonmodified and modified AgNPs was investigated, as well as their cytotoxicity and antimicrobial effects. Both albumin- and Tween-80-coated AgNPs demonstrated excellent stability in 0.9% sodium chloride solution (>12 months) compared to nonmodified AgNPs, characterized by their rapid precipitation. Hemolytic activity of nonmodified and albumin-coated AgNPs was found to be minimal, while Tween-80-modified AgNPs produced significant hemolysis after 1, 2, and 24 h of incubation. In addition, both native and Tween-80-covered AgNPs showed dose-dependent cytotoxic effects on human adipose-tissue-derived mesenchymal stem cells. The albumin-coated AgNPs showed minimal cytotoxicity. The antimicrobial effects of native and albumin-coated AgNPs against S. aureus, K. pneumonia, P. aeruginosa, Corynebacterium spp., and Acinetobacter spp. were statistically significant. We conclude that albumin coating of AgNPs significantly contributes to improve stability, reduce cytotoxicity, and confers potent antimicrobial action. MDPI 2021-06-03 /pmc/articles/PMC8227625/ /pubmed/34205084 http://dx.doi.org/10.3390/nano11061484 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Korolev, Dmitry
Shumilo, Michael
Shulmeyster, Galina
Krutikov, Alexander
Golovkin, Alexey
Mishanin, Alexander
Gorshkov, Andrew
Spiridonova, Anna
Domorad, Anna
Krasichkov, Alexander
Galagudza, Michael
Hemolytic Activity, Cytotoxicity, and Antimicrobial Effects of Human Albumin- and Polysorbate-80-Coated Silver Nanoparticles
title Hemolytic Activity, Cytotoxicity, and Antimicrobial Effects of Human Albumin- and Polysorbate-80-Coated Silver Nanoparticles
title_full Hemolytic Activity, Cytotoxicity, and Antimicrobial Effects of Human Albumin- and Polysorbate-80-Coated Silver Nanoparticles
title_fullStr Hemolytic Activity, Cytotoxicity, and Antimicrobial Effects of Human Albumin- and Polysorbate-80-Coated Silver Nanoparticles
title_full_unstemmed Hemolytic Activity, Cytotoxicity, and Antimicrobial Effects of Human Albumin- and Polysorbate-80-Coated Silver Nanoparticles
title_short Hemolytic Activity, Cytotoxicity, and Antimicrobial Effects of Human Albumin- and Polysorbate-80-Coated Silver Nanoparticles
title_sort hemolytic activity, cytotoxicity, and antimicrobial effects of human albumin- and polysorbate-80-coated silver nanoparticles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227625/
https://www.ncbi.nlm.nih.gov/pubmed/34205084
http://dx.doi.org/10.3390/nano11061484
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