Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/117389
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dc.contributor.authorTorres Mata, Laura Beatrizen_US
dc.contributor.authorGarcía-Pérez, Omaren_US
dc.contributor.authorRodriguez-Esparragon, F.en_US
dc.contributor.authorBlanco, Ángelesen_US
dc.contributor.authorVillar, Jesúsen_US
dc.contributor.authorRuíz Apodaca, Fernandoen_US
dc.contributor.authorMartín Barrasa, José Luisen_US
dc.contributor.authorGonzález-Martín, Jesús M.en_US
dc.contributor.authorSerrano-Aguilar, Pedroen_US
dc.contributor.authorPiñero, Jose E.en_US
dc.contributor.authorCórdoba-Lanús, Elizabethen_US
dc.contributor.authorLorenzo-Morales, Jacoben_US
dc.contributor.authorClavo Varas, Bernardinoen_US
dc.date.accessioned2022-07-27T09:23:13Z-
dc.date.available2022-07-27T09:23:13Z-
dc.date.issued2022en_US
dc.identifier.issn1660-4601en_US
dc.identifier.urihttp://hdl.handle.net/10553/117389-
dc.description.abstractBackground: Severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) continues to cause profound health, economic, and social problems worldwide. The management and disinfection of materials used daily in health centers and common working environments have prompted concerns about the control of coronavirus disease 2019 (COVID-19) infection risk. Ozone is a powerful oxidizing agent that has been widely used in disinfection processes for decades. The aim of this study was to assess the optimal conditions of ozone treatment for the elimination of heat-inactivated SARS-CoV-2 from office supplies (personal computer monitors, keyboards, and computer mice) and clinical equipment (continuous positive airway pressure tubes and personal protective equipment) that are difficult to clean. (2) Methods: The office supplies and clinical equipment were contaminated in an area of 1 cm2 with 1 × 104 viral units of a heat-inactivated SARS-CoV-2 strain, then treated with ozone using two different ozone devices: a specifically designed ozonation chamber (for low–medium ozone concentrations over large volumes) and a clinical ozone generator (for high ozone concentrations over small volumes). SARS-CoV-2 gene detection was carried out using quantitative real-time polymerase chain reaction (RT-qPCR). (3) Results: At high ozone concentrations over small surfaces, the ozone eliminated SARS-CoV-2 RNA in short time periods—i.e., 10 min (at 4000 ppm) or less. The optimum ozone concentration over large volumes was 90 ppm for 120 min in ambient conditions (24 °C and 60–75% relative humidity). (4) Conclusions: This study showed that the appropriate ozone concentration and exposure time eliminated heat-inactivated SARS-CoV-2 RNA from the surfaces of different widely used clinical and office supplies, decreasing their risk of transmission, and improving their reutilization. Ozone may provide an additional tool to control the spread of the COVID-19 pandemicen_US
dc.languageengen_US
dc.relation.ispartofInternational Journal of Environmental Research and Public Healthen_US
dc.sourceInternational Journal of Environmental Research and Public Health [EISSN 1660-4601], v. 19 (14)en_US
dc.subject320505 Enfermedades infecciosasen_US
dc.subject331110 Instrumentos médicosen_US
dc.subject.otherCOVID-19en_US
dc.subject.otherSARS-CoV-2en_US
dc.subject.otherSurface disinfectionen_US
dc.subject.otherClinical equipmenten_US
dc.subject.otherOffice suppliesen_US
dc.subject.otherOzoneen_US
dc.titleOzone Eliminates SARS-CoV-2 from Difficult-to-Clean Office Supplies and Clinical Equipmenten_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.identifier.doi10.3390/ijerph19148672en_US
dc.contributor.orcid0000-0003-3304-4176-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid0000-0003-1663-3673-
dc.contributor.orcid0000-0001-6820-7698-
dc.contributor.orcid0000-0001-5687-3562-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid0000-0002-3280-9838-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid0000-0001-6233-8224-
dc.contributor.orcid0000-0001-5534-8280-
dc.contributor.orcid#NODATA#-
dc.contributor.orcid0000-0003-2522-1064-
dc.identifier.issue14-
dc.relation.volume19en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.identifier.external116137515-
dc.utils.revisionen_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-VETen_US
dc.description.sjr0,828
dc.description.jcr4,614
dc.description.sjrqQ2
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.ssciSSCI
dc.description.miaricds10,7
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptGIR IUSA-ONE HEALTH 2 - Sanidad Animal de la Acuicultura y Especies Silvestres, Enfermedades Infecciosas y Seguridad Alimentaria-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptDepartamento de Patología Animal, Producción Animal, Bromatología y Tecnología de Los Alimentos-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.orcid0000-0002-3280-9838-
crisitem.author.orcid0000-0003-2522-1064-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameTorres Mata, Laura Beatriz-
crisitem.author.fullNameMartín Barrasa, José Luis-
crisitem.author.fullNameClavo Varas,Bernardino-
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