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Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant
Silver (Ag) is known to possess antimicrobial properties which is commonly attributed to soluble Ag ions. Here, we showed that Ag nanoparticles (NPs) potently inhibited SARS-CoV-2 infection using two different pseudovirus neutralization assays. We also evaluated a set of Ag nanoparticles of differen...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790969/ https://www.ncbi.nlm.nih.gov/pubmed/36578508 http://dx.doi.org/10.3389/fbioe.2022.1083232 |
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author | Gupta, Govind Hamawandi, Bejan Sheward, Daniel J. Murrell, Ben Hanke, Leo McInerney, Gerald Blosi, Magda Costa, Anna L. Toprak, Muhammet S. Fadeel, Bengt |
author_facet | Gupta, Govind Hamawandi, Bejan Sheward, Daniel J. Murrell, Ben Hanke, Leo McInerney, Gerald Blosi, Magda Costa, Anna L. Toprak, Muhammet S. Fadeel, Bengt |
author_sort | Gupta, Govind |
collection | PubMed |
description | Silver (Ag) is known to possess antimicrobial properties which is commonly attributed to soluble Ag ions. Here, we showed that Ag nanoparticles (NPs) potently inhibited SARS-CoV-2 infection using two different pseudovirus neutralization assays. We also evaluated a set of Ag nanoparticles of different sizes with varying surface properties, including polyvinylpyrrolidone (PVP)-coated and poly (ethylene glycol) (PEG)-modified Ag nanoparticles, and found that only the bare (unmodified) nanoparticles were able to prevent virus infection. For comparison, TiO(2) nanoparticles failed to intercept the virus. Proteins and lipids may adsorb to nanoparticles forming a so-called bio-corona; however, Ag nanoparticles pre-incubated with pulmonary surfactant retained their ability to block virus infection in the present model. Furthermore, the secondary structure of the spike protein of SARS-CoV-2 was perturbed by the Ag nanoparticles, but not by the ionic control (AgNO(3)) nor by the TiO(2) nanoparticles. Finally, Ag nanoparticles were shown to be non-cytotoxic towards the human lung epithelial cell line BEAS-2B and this was confirmed by using primary human nasal epithelial cells. These results further support that Ag nanoparticles may find use as anti-viral agents. |
format | Online Article Text |
id | pubmed-9790969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-97909692022-12-27 Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant Gupta, Govind Hamawandi, Bejan Sheward, Daniel J. Murrell, Ben Hanke, Leo McInerney, Gerald Blosi, Magda Costa, Anna L. Toprak, Muhammet S. Fadeel, Bengt Front Bioeng Biotechnol Bioengineering and Biotechnology Silver (Ag) is known to possess antimicrobial properties which is commonly attributed to soluble Ag ions. Here, we showed that Ag nanoparticles (NPs) potently inhibited SARS-CoV-2 infection using two different pseudovirus neutralization assays. We also evaluated a set of Ag nanoparticles of different sizes with varying surface properties, including polyvinylpyrrolidone (PVP)-coated and poly (ethylene glycol) (PEG)-modified Ag nanoparticles, and found that only the bare (unmodified) nanoparticles were able to prevent virus infection. For comparison, TiO(2) nanoparticles failed to intercept the virus. Proteins and lipids may adsorb to nanoparticles forming a so-called bio-corona; however, Ag nanoparticles pre-incubated with pulmonary surfactant retained their ability to block virus infection in the present model. Furthermore, the secondary structure of the spike protein of SARS-CoV-2 was perturbed by the Ag nanoparticles, but not by the ionic control (AgNO(3)) nor by the TiO(2) nanoparticles. Finally, Ag nanoparticles were shown to be non-cytotoxic towards the human lung epithelial cell line BEAS-2B and this was confirmed by using primary human nasal epithelial cells. These results further support that Ag nanoparticles may find use as anti-viral agents. Frontiers Media S.A. 2022-12-12 /pmc/articles/PMC9790969/ /pubmed/36578508 http://dx.doi.org/10.3389/fbioe.2022.1083232 Text en Copyright © 2022 Gupta, Hamawandi, Sheward, Murrell, Hanke, McInerney, Blosi, Costa, Toprak and Fadeel. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Gupta, Govind Hamawandi, Bejan Sheward, Daniel J. Murrell, Ben Hanke, Leo McInerney, Gerald Blosi, Magda Costa, Anna L. Toprak, Muhammet S. Fadeel, Bengt Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant |
title | Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant |
title_full | Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant |
title_fullStr | Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant |
title_full_unstemmed | Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant |
title_short | Silver nanoparticles with excellent biocompatibility block pseudotyped SARS-CoV-2 in the presence of lung surfactant |
title_sort | silver nanoparticles with excellent biocompatibility block pseudotyped sars-cov-2 in the presence of lung surfactant |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9790969/ https://www.ncbi.nlm.nih.gov/pubmed/36578508 http://dx.doi.org/10.3389/fbioe.2022.1083232 |
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