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Bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses

The SARS-CoV-2 (COVID-19) pandemic has highlighted the urgent need for strategies that rapidly inactivate airborne respiratory viruses and break the transmission cycle of indoor spaces. Air ions can reduce viable bacteria, mold, and virus counts, however, most studies use small test enclosures with...

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Detalles Bibliográficos
Autores principales: Sobek, Edward, Elias, Dwayne A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664916/
https://www.ncbi.nlm.nih.gov/pubmed/37992037
http://dx.doi.org/10.1371/journal.pone.0293504
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author Sobek, Edward
Elias, Dwayne A.
author_facet Sobek, Edward
Elias, Dwayne A.
author_sort Sobek, Edward
collection PubMed
description The SARS-CoV-2 (COVID-19) pandemic has highlighted the urgent need for strategies that rapidly inactivate airborne respiratory viruses and break the transmission cycle of indoor spaces. Air ions can reduce viable bacteria, mold, and virus counts, however, most studies use small test enclosures with target microbes and ion sources in close vicinity. To evaluate ion performance in real-world spaces, experiments were conducted in a large, room-size BSL-3 Chamber. Negative and positive ions were delivered simultaneously using a commercially available bipolar air ion device. The device housed Needle Point Bipolar ionization (NPBI) technology. Large chamber studies often use unrealistically high virus concentrations to ensure measurable virus is present at the trial end. However, excessively high viral concentrations bias air cleaning devices towards underperformance. Hence, devices that provide a substantial impact for protecting occupants in real-world spaces with real-world virus concentrations are often dismissed as poor performers. Herein, both real-world and excessive virus concentrations were studied using Influenza A and B, Human Respiratory Syncytial Virus (RSV), and the SARS-CoV-2 Alpha and Delta strains. The average ion concentrations ranged from 4,100 to 24,000 per polarity over 60-minute and 30-minute time trials. The reduction rate was considerably greater for trials that used real-world virus concentrations, reducing infectivity for Influenza A and B, RSV, and SARS-CoV-2 Delta by 88.3–99.98% in 30 minutes, whereas trials using in-excess concentrations showed 49.5–61.2% in 30 minutes. These findings strongly support the addition of NPBI ion technology to building management strategies aimed to protect occupants from contracting and spreading infective respiratory viruses indoors.
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spelling pubmed-106649162023-11-22 Bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses Sobek, Edward Elias, Dwayne A. PLoS One Research Article The SARS-CoV-2 (COVID-19) pandemic has highlighted the urgent need for strategies that rapidly inactivate airborne respiratory viruses and break the transmission cycle of indoor spaces. Air ions can reduce viable bacteria, mold, and virus counts, however, most studies use small test enclosures with target microbes and ion sources in close vicinity. To evaluate ion performance in real-world spaces, experiments were conducted in a large, room-size BSL-3 Chamber. Negative and positive ions were delivered simultaneously using a commercially available bipolar air ion device. The device housed Needle Point Bipolar ionization (NPBI) technology. Large chamber studies often use unrealistically high virus concentrations to ensure measurable virus is present at the trial end. However, excessively high viral concentrations bias air cleaning devices towards underperformance. Hence, devices that provide a substantial impact for protecting occupants in real-world spaces with real-world virus concentrations are often dismissed as poor performers. Herein, both real-world and excessive virus concentrations were studied using Influenza A and B, Human Respiratory Syncytial Virus (RSV), and the SARS-CoV-2 Alpha and Delta strains. The average ion concentrations ranged from 4,100 to 24,000 per polarity over 60-minute and 30-minute time trials. The reduction rate was considerably greater for trials that used real-world virus concentrations, reducing infectivity for Influenza A and B, RSV, and SARS-CoV-2 Delta by 88.3–99.98% in 30 minutes, whereas trials using in-excess concentrations showed 49.5–61.2% in 30 minutes. These findings strongly support the addition of NPBI ion technology to building management strategies aimed to protect occupants from contracting and spreading infective respiratory viruses indoors. Public Library of Science 2023-11-22 /pmc/articles/PMC10664916/ /pubmed/37992037 http://dx.doi.org/10.1371/journal.pone.0293504 Text en © 2023 Sobek, Elias https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sobek, Edward
Elias, Dwayne A.
Bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses
title Bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses
title_full Bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses
title_fullStr Bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses
title_full_unstemmed Bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses
title_short Bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses
title_sort bipolar ionization rapidly inactivates real-world, airborne concentrations of infective respiratory viruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10664916/
https://www.ncbi.nlm.nih.gov/pubmed/37992037
http://dx.doi.org/10.1371/journal.pone.0293504
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