tetano
Editor, Senior Moderator
Environ Sci Pollut Res Int. 2018 Jul 16. doi: 10.1007/s11356-018-2620-z. [Epub ahead of print]
[h=1]Inactivation of influenza A virus via exposure to silver nanoparticle-decorated silica hybrid composites.[/h] Park S[SUP]1,[/SUP][SUP]2[/SUP], Ko YS[SUP]3[/SUP], Lee SJ[SUP]1[/SUP], Lee C[SUP]1,[/SUP][SUP]4[/SUP], Woo K[SUP]3[/SUP], Ko G[SUP]5,[/SUP][SUP]6,[/SUP][SUP]7[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza A virus (IFV-A) is one of the main cause of seasonal flu and can infect various of host species via the reassortment of segmented RNA genomes. Silver nanoparticles (AgNPs) have been known as excellent antiviral agent against IFV. However, the use of free AgNPs has several major drawbacks, including the inherent aggregation among AgNPs and unwanted cytotoxic or genotoxic damages for human body via inhalation or ingestion. In this study, we assessed the efficacy of our novel ~ 30-nm-diameter AgNP-decorated silica hybrid composite (Ag30-SiO[SUB]2[/SUB]; ~ 400 nm in diameter) for IFV-A inactivation. Ag30-SiO[SUB]2[/SUB] particles can inhibit IFV-A effectively in a clear dose-dependent manner. However, when real-time RT-PCR assay was used, merely 0.5-log[SUB]10[/SUB] reduction of IFV-A was observed at both 5 and 20 ?C. Moreover, even after 1 h of exposure to Ag30-SiO[SUB]2[/SUB] particles, more than 80% of hemagglutinin (HA) damage and 20% of neuraminidase (NA) activities had occurred, and the infection of Madin-Darby Canine Kidney (MDCK) cells by IFV-A was reduced. The results suggested that the major antiviral mechanism of Ag30-SiO[SUB]2[/SUB] particles is the interaction with viral components located at the membrane. Therefore, Ag30-SiO[SUB]2[/SUB] particles can cause nonspecific damage to various IFV-A components and be used as an effective method for inactivating IFV-A.
[h=4]KEYWORDS:[/h] Antiviral agent; Disinfection; Influenza A virus; Silica hybrid composite; Silver nanoparticle; Virus inactivation
PMID: 30014367 DOI: 10.1007/s11356-018-2620-z
[h=1]Inactivation of influenza A virus via exposure to silver nanoparticle-decorated silica hybrid composites.[/h] Park S[SUP]1,[/SUP][SUP]2[/SUP], Ko YS[SUP]3[/SUP], Lee SJ[SUP]1[/SUP], Lee C[SUP]1,[/SUP][SUP]4[/SUP], Woo K[SUP]3[/SUP], Ko G[SUP]5,[/SUP][SUP]6,[/SUP][SUP]7[/SUP].
[h=3]Author information[/h]
[h=3]Abstract[/h] Influenza A virus (IFV-A) is one of the main cause of seasonal flu and can infect various of host species via the reassortment of segmented RNA genomes. Silver nanoparticles (AgNPs) have been known as excellent antiviral agent against IFV. However, the use of free AgNPs has several major drawbacks, including the inherent aggregation among AgNPs and unwanted cytotoxic or genotoxic damages for human body via inhalation or ingestion. In this study, we assessed the efficacy of our novel ~ 30-nm-diameter AgNP-decorated silica hybrid composite (Ag30-SiO[SUB]2[/SUB]; ~ 400 nm in diameter) for IFV-A inactivation. Ag30-SiO[SUB]2[/SUB] particles can inhibit IFV-A effectively in a clear dose-dependent manner. However, when real-time RT-PCR assay was used, merely 0.5-log[SUB]10[/SUB] reduction of IFV-A was observed at both 5 and 20 ?C. Moreover, even after 1 h of exposure to Ag30-SiO[SUB]2[/SUB] particles, more than 80% of hemagglutinin (HA) damage and 20% of neuraminidase (NA) activities had occurred, and the infection of Madin-Darby Canine Kidney (MDCK) cells by IFV-A was reduced. The results suggested that the major antiviral mechanism of Ag30-SiO[SUB]2[/SUB] particles is the interaction with viral components located at the membrane. Therefore, Ag30-SiO[SUB]2[/SUB] particles can cause nonspecific damage to various IFV-A components and be used as an effective method for inactivating IFV-A.
[h=4]KEYWORDS:[/h] Antiviral agent; Disinfection; Influenza A virus; Silica hybrid composite; Silver nanoparticle; Virus inactivation
PMID: 30014367 DOI: 10.1007/s11356-018-2620-z