A preliminary assessment of silver nanoparticle inhibition of monkeypox virus plaque formation

被引:321
作者
Rogers, James V. [1 ]
Parkinson, Christopher V. [1 ]
Choi, Young W. [1 ]
Speshock, Janice L. [2 ]
Hussain, Saber M. [2 ]
机构
[1] Battelle Mem Inst, Columbus, OH 43201 USA
[2] Human Effectiveness Directorate, Appl Biotechnol Branch, Wright Patterson AFB, OH 45433 USA
来源
NANOSCALE RESEARCH LETTERS | 2008年 / 3卷 / 04期
关键词
nanoparticle; monkeypox virus; silver; anti-viral therapeutic; plaque reduction assay;
D O I
10.1007/s11671-008-9128-2
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
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 (AgNO3) at concentrations of 100, 50, 25, and 12.5 mu g/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 mu g/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 mu g/mL AgNO3. 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.
引用
收藏
页码:129 / 133
页数:5
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