Cargando…

A Preliminary Assessment of Silver Nanoparticle Inhibition of Monkeypox Virus Plaque Formation

The use of nanotechnology and nanomaterials in medical research is growing. Silver-containing nanoparticles have previously demonstrated antimicrobial efficacy against bacteria and viral particles. This preliminary study utilized an in vitro approach to evaluate the ability of silver-based nanoparti...

Descripción completa

Detalles Bibliográficos
Autores principales: Rogers, James V, Parkinson, Christopher V, Choi, Young W, Speshock, Janice L, Hussain, Saber M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244796/
http://dx.doi.org/10.1007/s11671-008-9128-2
_version_ 1782219759884959744
author Rogers, James V
Parkinson, Christopher V
Choi, Young W
Speshock, Janice L
Hussain, Saber M
author_facet Rogers, James V
Parkinson, Christopher V
Choi, Young W
Speshock, Janice L
Hussain, Saber M
author_sort Rogers, James V
collection PubMed
description The use of nanotechnology and nanomaterials in medical research is growing. Silver-containing nanoparticles have previously demonstrated antimicrobial efficacy against bacteria and viral particles. This preliminary study utilized an in vitro approach to evaluate the ability of silver-based nanoparticles to inhibit infectivity of the biological select agent, monkeypox virus (MPV). Nanoparticles (10–80 nm, with or without polysaccharide coating), or silver nitrate (AgNO(3)) at concentrations of 100, 50, 25, and 12.5 μg/mL were evaluated for efficacy using a plaque reduction assay. Both Ag-PS-25 (polysaccharide-coated, 25 nm) and Ag-NP-55 (non-coated, 55 nm) exhibited a significant (P ≤ 0.05) dose-dependent effect of test compound concentration on the mean number of plaque-forming units (PFU). All concentrations of silver nitrate (except 100 μg/mL) and Ag-PS-10 promoted significant (P ≤ 0.05) decreases in the number of observed PFU compared to untreated controls. Some nanoparticle treatments led to increased MPV PFU ranging from 1.04- to 1.8-fold above controls. No cytotoxicity (Vero cell monolayer sloughing) was caused by any test compound, except 100 μg/mL AgNO(3). These results demonstrate that silver-based nanoparticles of approximately 10 nm inhibit MPV infection in vitro, supporting their potential use as an anti-viral therapeutic.
format Online
Article
Text
id pubmed-3244796
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Springer
record_format MEDLINE/PubMed
spelling pubmed-32447962011-12-29 A Preliminary Assessment of Silver Nanoparticle Inhibition of Monkeypox Virus Plaque Formation Rogers, James V Parkinson, Christopher V Choi, Young W Speshock, Janice L Hussain, Saber M Nanoscale Res Lett Nano Perspectives The use of nanotechnology and nanomaterials in medical research is growing. Silver-containing nanoparticles have previously demonstrated antimicrobial efficacy against bacteria and viral particles. This preliminary study utilized an in vitro approach to evaluate the ability of silver-based nanoparticles to inhibit infectivity of the biological select agent, monkeypox virus (MPV). Nanoparticles (10–80 nm, with or without polysaccharide coating), or silver nitrate (AgNO(3)) at concentrations of 100, 50, 25, and 12.5 μg/mL were evaluated for efficacy using a plaque reduction assay. Both Ag-PS-25 (polysaccharide-coated, 25 nm) and Ag-NP-55 (non-coated, 55 nm) exhibited a significant (P ≤ 0.05) dose-dependent effect of test compound concentration on the mean number of plaque-forming units (PFU). All concentrations of silver nitrate (except 100 μg/mL) and Ag-PS-10 promoted significant (P ≤ 0.05) decreases in the number of observed PFU compared to untreated controls. Some nanoparticle treatments led to increased MPV PFU ranging from 1.04- to 1.8-fold above controls. No cytotoxicity (Vero cell monolayer sloughing) was caused by any test compound, except 100 μg/mL AgNO(3). These results demonstrate that silver-based nanoparticles of approximately 10 nm inhibit MPV infection in vitro, supporting their potential use as an anti-viral therapeutic. Springer 2008-04-09 /pmc/articles/PMC3244796/ http://dx.doi.org/10.1007/s11671-008-9128-2 Text en Copyright ©2008 to the authors
spellingShingle Nano Perspectives
Rogers, James V
Parkinson, Christopher V
Choi, Young W
Speshock, Janice L
Hussain, Saber M
A Preliminary Assessment of Silver Nanoparticle Inhibition of Monkeypox Virus Plaque Formation
title A Preliminary Assessment of Silver Nanoparticle Inhibition of Monkeypox Virus Plaque Formation
title_full A Preliminary Assessment of Silver Nanoparticle Inhibition of Monkeypox Virus Plaque Formation
title_fullStr A Preliminary Assessment of Silver Nanoparticle Inhibition of Monkeypox Virus Plaque Formation
title_full_unstemmed A Preliminary Assessment of Silver Nanoparticle Inhibition of Monkeypox Virus Plaque Formation
title_short A Preliminary Assessment of Silver Nanoparticle Inhibition of Monkeypox Virus Plaque Formation
title_sort preliminary assessment of silver nanoparticle inhibition of monkeypox virus plaque formation
topic Nano Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244796/
http://dx.doi.org/10.1007/s11671-008-9128-2
work_keys_str_mv AT rogersjamesv apreliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT parkinsonchristopherv apreliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT choiyoungw apreliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT speshockjanicel apreliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT hussainsaberm apreliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT rogersjamesv preliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT parkinsonchristopherv preliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT choiyoungw preliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT speshockjanicel preliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation
AT hussainsaberm preliminaryassessmentofsilvernanoparticleinhibitionofmonkeypoxvirusplaqueformation