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Inactivation characteristics of a 280 nm Deep-UV irradiation dose on aerosolized SARS-CoV-2

A non-filter virus inactivation unit was developed that can control the irradiation dose of aerosolized viruses by controlling the lighting pattern of a 280 nm deep-UV (DUV)-LED and the air flowrate. In this study, the inactivation properties of aerosolized SARS-CoV-2 were quantitatively evaluated b...

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Autores principales: Takamure, Kotaro, Iwatani, Yasumasa, Amano, Hiroshi, Yagi, Tetsuya, Uchiyama, Tomomi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Ltd. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241504/
https://www.ncbi.nlm.nih.gov/pubmed/37301046
http://dx.doi.org/10.1016/j.envint.2023.108022
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author Takamure, Kotaro
Iwatani, Yasumasa
Amano, Hiroshi
Yagi, Tetsuya
Uchiyama, Tomomi
author_facet Takamure, Kotaro
Iwatani, Yasumasa
Amano, Hiroshi
Yagi, Tetsuya
Uchiyama, Tomomi
author_sort Takamure, Kotaro
collection PubMed
description A non-filter virus inactivation unit was developed that can control the irradiation dose of aerosolized viruses by controlling the lighting pattern of a 280 nm deep-UV (DUV)-LED and the air flowrate. In this study, the inactivation properties of aerosolized SARS-CoV-2 were quantitatively evaluated by controlling the irradiation dose to the virus inside the inactivation unit. The RNA concentration of SARS-CoV-2 remained constant when the total irradiation dose of DUV irradiation to the virus exceeded 16.5 mJ/cm(2). This observation suggests that RNA damage may occur in regions below the detection threshold of RT-qPCR assay. However, when the total irradiation dose was less than 16.5 mJ/cm(2), the RNA concentration monotonically increased with a decreasing LED irradiation dose. However, the nucleocapsid protein concentration of SARS-CoV-2 was not predominantly dependent on the LED irradiation dose. The plaque assay showed that 99.16% of the virus was inactivated at 8.1 mJ/cm(2) of irradiation, and no virus was detected at 12.2 mJ/cm(2) of irradiation, resulting in a 99.89% virus inactivation rate. Thus, an irradiation dose of 23% of the maximal irradiation capacity of the virus inactivation unit can activate more than 99% of SARS-CoV-2. These findings are expected to enhance versatility in various applications. The downsizing achieved in our study renders the technology apt for installation in narrow spaces, while the enhanced flowrates establish its viability for implementation in larger facilities.
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spelling pubmed-102415042023-06-06 Inactivation characteristics of a 280 nm Deep-UV irradiation dose on aerosolized SARS-CoV-2 Takamure, Kotaro Iwatani, Yasumasa Amano, Hiroshi Yagi, Tetsuya Uchiyama, Tomomi Environ Int Full Length Article A non-filter virus inactivation unit was developed that can control the irradiation dose of aerosolized viruses by controlling the lighting pattern of a 280 nm deep-UV (DUV)-LED and the air flowrate. In this study, the inactivation properties of aerosolized SARS-CoV-2 were quantitatively evaluated by controlling the irradiation dose to the virus inside the inactivation unit. The RNA concentration of SARS-CoV-2 remained constant when the total irradiation dose of DUV irradiation to the virus exceeded 16.5 mJ/cm(2). This observation suggests that RNA damage may occur in regions below the detection threshold of RT-qPCR assay. However, when the total irradiation dose was less than 16.5 mJ/cm(2), the RNA concentration monotonically increased with a decreasing LED irradiation dose. However, the nucleocapsid protein concentration of SARS-CoV-2 was not predominantly dependent on the LED irradiation dose. The plaque assay showed that 99.16% of the virus was inactivated at 8.1 mJ/cm(2) of irradiation, and no virus was detected at 12.2 mJ/cm(2) of irradiation, resulting in a 99.89% virus inactivation rate. Thus, an irradiation dose of 23% of the maximal irradiation capacity of the virus inactivation unit can activate more than 99% of SARS-CoV-2. These findings are expected to enhance versatility in various applications. The downsizing achieved in our study renders the technology apt for installation in narrow spaces, while the enhanced flowrates establish its viability for implementation in larger facilities. The Authors. Published by Elsevier Ltd. 2023-07 2023-06-05 /pmc/articles/PMC10241504/ /pubmed/37301046 http://dx.doi.org/10.1016/j.envint.2023.108022 Text en © 2023 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Full Length Article
Takamure, Kotaro
Iwatani, Yasumasa
Amano, Hiroshi
Yagi, Tetsuya
Uchiyama, Tomomi
Inactivation characteristics of a 280 nm Deep-UV irradiation dose on aerosolized SARS-CoV-2
title Inactivation characteristics of a 280 nm Deep-UV irradiation dose on aerosolized SARS-CoV-2
title_full Inactivation characteristics of a 280 nm Deep-UV irradiation dose on aerosolized SARS-CoV-2
title_fullStr Inactivation characteristics of a 280 nm Deep-UV irradiation dose on aerosolized SARS-CoV-2
title_full_unstemmed Inactivation characteristics of a 280 nm Deep-UV irradiation dose on aerosolized SARS-CoV-2
title_short Inactivation characteristics of a 280 nm Deep-UV irradiation dose on aerosolized SARS-CoV-2
title_sort inactivation characteristics of a 280 nm deep-uv irradiation dose on aerosolized sars-cov-2
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10241504/
https://www.ncbi.nlm.nih.gov/pubmed/37301046
http://dx.doi.org/10.1016/j.envint.2023.108022
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