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Antiviral efficacy of cerium oxide nanoparticles
Nanomaterials are prospective candidates for the elimination of viruses due to their multimodal mechanisms of action. Here, we tested the antiviral potential of a largely unexplored nanoparticle of cerium dioxide (CeO(2)). Two nano-CeO(2) with opposing surface charge, (+) and (−), were assessed for...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637224/ https://www.ncbi.nlm.nih.gov/pubmed/36335167 http://dx.doi.org/10.1038/s41598-022-23465-6 |
Sumario: | Nanomaterials are prospective candidates for the elimination of viruses due to their multimodal mechanisms of action. Here, we tested the antiviral potential of a largely unexplored nanoparticle of cerium dioxide (CeO(2)). Two nano-CeO(2) with opposing surface charge, (+) and (−), were assessed for their capability to decrease the plaque forming units (PFU) of four enveloped and two non-enveloped viruses during 1-h exposure. Statistically significant antiviral activity towards enveloped coronavirus SARS-CoV-2 and influenza virus was registered already at 20 mg Ce/l. For other two enveloped viruses, transmissible gastroenteritis virus and bacteriophage φ6, antiviral activity was evidenced at 200 mg Ce/l. As expected, the sensitivity of non-enveloped viruses towards nano-CeO(2) was significantly lower. EMCV picornavirus showed no decrease in PFU until the highest tested concentration, 2000 mg Ce/l and MS2 bacteriophage showed slight non-monotonic response to high concentrations of nano-CeO(2)(−). Parallel testing of antiviral activity of Ce(3+) ions and SiO(2) nanoparticles allows to conclude that nano-CeO(2) activity was neither due to released Ce-ions nor nonspecific effects of nanoparticulates. Moreover, we evidenced higher antiviral efficacy of nano-CeO(2) compared with Ag nanoparticles. This result along with low antibacterial activity and non-existent cytotoxicity of nano-CeO(2) allow us to propose CeO(2) nanoparticles for specific antiviral applications. |
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