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dc.contributor.authorNefedova, Aleksandra
dc.contributor.authorRausalu, Kai
dc.contributor.authorZusinaite, Eva
dc.contributor.authorVanetsev, Alexander
dc.contributor.authorRosenberg, Merilin
dc.contributor.authorKoppel, Kairi
dc.contributor.authorLilla, Stevin
dc.contributor.authorVisnapuu, Meeri
dc.contributor.authorSmits, Krisjanis
dc.contributor.authorKisand, Vambola
dc.contributor.authorTätte, Tanel
dc.contributor.authorIvask, Angela
dc.date.accessioned2023-01-12T18:15:19Z
dc.date.available2023-01-12T18:15:19Z
dc.date.issued2022
dc.identifier.issn2045-2322
dc.identifier.urihttps://www.nature.com/articles/s41598-022-23465-6
dc.identifier.urihttps://dspace.lu.lv/dspace/handle/7/61729
dc.descriptionThe authors gratefully acknowledge the financial support by the Estonian Research Council Grants (COVSG2, PRG629, PRG1496), Estonian Centre of Excellence in Research project “Advanced materials and high-technology devices for sustainable energetics, sensorics and nanoelectronics” TK141 (2014-2020.4.01.15-0011) and University of Tartu Development Fund (PLTFYARENG53). The research was partly conducted using the NAMUR+ core facility funded by projects “Center of nanomaterials technologies and research” (2014-2020.4.01.16-0123) and TT13.en_US
dc.description.abstractNanomaterials 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 (CeO2). Two nano-CeO2 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-CeO2 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-CeO2(−). Parallel testing of antiviral activity of Ce3+ ions and SiO2 nanoparticles allows to conclude that nano-CeO2 activity was neither due to released Ce-ions nor nonspecific effects of nanoparticulates. Moreover, we evidenced higher antiviral efficacy of nano-CeO2 compared with Ag nanoparticles. This result along with low antibacterial activity and non-existent cytotoxicity of nano-CeO2 allow us to propose CeO2 nanoparticles for specific antiviral applications. © 2022, The Author(s). --//-- This is an open access article Nefedova A, Rausalu K, Zusinaite E, Vanetsev A, Rosenberg M, Koppel K, Lilla S, Visnapuu M, Smits K, Kisand V, Tätte T, Ivask A., "Antiviral efficacy of cerium oxide nanoparticles", Scientific Reports (2022); 12(1):18746, doi: 10.1038/s41598-022-23465-6 published under the CC BY 4.0 licence.en_US
dc.description.sponsorshipEstonian Research Council Grants (COVSG2, PRG629, PRG1496); Estonian Centre of Excellence in Research TK141 (2014-2020.4.01.15-0011); University of Tartu Development Fund (PLTFYARENG53); Institute of Solid-State Physics, University of Latvia has received funding from the European Union's Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-Teaming Phase 2 under grant agreement No. 739508, project CAMART2.en_US
dc.language.isoengen_US
dc.publisherNature Researchen_US
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/739508/EU/Centre of Advanced Material Research and Technology Transfer/CAMART²en_US
dc.relation.ispartofseriesScientific Reports;12 (1) 18746
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Physicsen_US
dc.titleAntiviral efficacy of cerium oxide nanoparticlesen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.identifier.doi10.1038/s41598-022-23465-6


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