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Far-UVC light (222 nm) efficiently and safely inactivates airborne human coronaviruses
A direct approach to limit airborne viral transmissions is to inactivate them within a short time of their production. Germicidal ultraviolet light, typically at 254 nm, is effective in this context but, used directly, can be a health hazard to skin and eyes. By contrast, far-UVC light (207–222 nm)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314750/ https://www.ncbi.nlm.nih.gov/pubmed/32581288 http://dx.doi.org/10.1038/s41598-020-67211-2 |
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author | Buonanno, Manuela Welch, David Shuryak, Igor Brenner, David J. |
author_facet | Buonanno, Manuela Welch, David Shuryak, Igor Brenner, David J. |
author_sort | Buonanno, Manuela |
collection | PubMed |
description | A direct approach to limit airborne viral transmissions is to inactivate them within a short time of their production. Germicidal ultraviolet light, typically at 254 nm, is effective in this context but, used directly, can be a health hazard to skin and eyes. By contrast, far-UVC light (207–222 nm) efficiently kills pathogens potentially without harm to exposed human tissues. We previously demonstrated that 222-nm far-UVC light efficiently kills airborne influenza virus and we extend those studies to explore far-UVC efficacy against airborne human coronaviruses alpha HCoV-229E and beta HCoV-OC43. Low doses of 1.7 and 1.2 mJ/cm(2) inactivated 99.9% of aerosolized coronavirus 229E and OC43, respectively. As all human coronaviruses have similar genomic sizes, far-UVC light would be expected to show similar inactivation efficiency against other human coronaviruses including SARS-CoV-2. Based on the beta-HCoV-OC43 results, continuous far-UVC exposure in occupied public locations at the current regulatory exposure limit (~3 mJ/cm(2)/hour) would result in ~90% viral inactivation in ~8 minutes, 95% in ~11 minutes, 99% in ~16 minutes and 99.9% inactivation in ~25 minutes. Thus while staying within current regulatory dose limits, low-dose-rate far-UVC exposure can potentially safely provide a major reduction in the ambient level of airborne coronaviruses in occupied public locations. |
format | Online Article Text |
id | pubmed-7314750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73147502020-06-25 Far-UVC light (222 nm) efficiently and safely inactivates airborne human coronaviruses Buonanno, Manuela Welch, David Shuryak, Igor Brenner, David J. Sci Rep Article A direct approach to limit airborne viral transmissions is to inactivate them within a short time of their production. Germicidal ultraviolet light, typically at 254 nm, is effective in this context but, used directly, can be a health hazard to skin and eyes. By contrast, far-UVC light (207–222 nm) efficiently kills pathogens potentially without harm to exposed human tissues. We previously demonstrated that 222-nm far-UVC light efficiently kills airborne influenza virus and we extend those studies to explore far-UVC efficacy against airborne human coronaviruses alpha HCoV-229E and beta HCoV-OC43. Low doses of 1.7 and 1.2 mJ/cm(2) inactivated 99.9% of aerosolized coronavirus 229E and OC43, respectively. As all human coronaviruses have similar genomic sizes, far-UVC light would be expected to show similar inactivation efficiency against other human coronaviruses including SARS-CoV-2. Based on the beta-HCoV-OC43 results, continuous far-UVC exposure in occupied public locations at the current regulatory exposure limit (~3 mJ/cm(2)/hour) would result in ~90% viral inactivation in ~8 minutes, 95% in ~11 minutes, 99% in ~16 minutes and 99.9% inactivation in ~25 minutes. Thus while staying within current regulatory dose limits, low-dose-rate far-UVC exposure can potentially safely provide a major reduction in the ambient level of airborne coronaviruses in occupied public locations. Nature Publishing Group UK 2020-06-24 /pmc/articles/PMC7314750/ /pubmed/32581288 http://dx.doi.org/10.1038/s41598-020-67211-2 Text en © The Author(s) 2020, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Buonanno, Manuela Welch, David Shuryak, Igor Brenner, David J. Far-UVC light (222 nm) efficiently and safely inactivates airborne human coronaviruses |
title | Far-UVC light (222 nm) efficiently and safely inactivates airborne human coronaviruses |
title_full | Far-UVC light (222 nm) efficiently and safely inactivates airborne human coronaviruses |
title_fullStr | Far-UVC light (222 nm) efficiently and safely inactivates airborne human coronaviruses |
title_full_unstemmed | Far-UVC light (222 nm) efficiently and safely inactivates airborne human coronaviruses |
title_short | Far-UVC light (222 nm) efficiently and safely inactivates airborne human coronaviruses |
title_sort | far-uvc light (222 nm) efficiently and safely inactivates airborne human coronaviruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314750/ https://www.ncbi.nlm.nih.gov/pubmed/32581288 http://dx.doi.org/10.1038/s41598-020-67211-2 |
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