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Development and evaluation of a novel bioaerosol amplification unit (BAU) for improved viral aerosol collection

A novel bioaerosol amplification unit (BAU) that increases the size of viral particles by condensational growth has been designed and evaluated for improved viral aerosol collection. In the BAU, water was used as the condensing vapor to preserve viability of virus, and supersaturation conditions for...

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Autores principales: Oh, Sewon, Anwar, Diandra, Theodore, Alexandros, Lee, Jin-Hwa, Wu, Chang-Yu, Wander, Joe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. Published by Elsevier Ltd. 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094383/
https://www.ncbi.nlm.nih.gov/pubmed/32226123
http://dx.doi.org/10.1016/j.jaerosci.2010.06.002
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author Oh, Sewon
Anwar, Diandra
Theodore, Alexandros
Lee, Jin-Hwa
Wu, Chang-Yu
Wander, Joe
author_facet Oh, Sewon
Anwar, Diandra
Theodore, Alexandros
Lee, Jin-Hwa
Wu, Chang-Yu
Wander, Joe
author_sort Oh, Sewon
collection PubMed
description A novel bioaerosol amplification unit (BAU) that increases the size of viral particles by condensational growth has been designed and evaluated for improved viral aerosol collection. In the BAU, water was used as the condensing vapor to preserve viability of virus, and supersaturation conditions for condensational growth of particles were achieved by either conductive cooling or mixing with hot, water-saturated air. MS2 bacteriophage (28 nm) was used as the test agent, and changes in collection efficiency of an SKC Biosampler with and without the BAU were determined by assaying plaque-forming units (PFUs) in the collection medium. Results showed that the mixing-type BAU (mBAU) was a promising device for improved viral aerosol sampling. The number of viruses (PFU) collected in the Biosampler increased 2–3 fold after passing through the mBAU. However, PFU increases in the cooling-type BAU (cBAU) were insignificant. APS results likewise showed that the mBAU was better in growing particles than the cBAU. After growth, number concentrations of particles larger than 327 nm in the cBAU and mBAU increased 1.3 and 15.0 fold, respectively. The relatively high molecular diffusivity of water vapor compared to the thermal diffusivity of air and the temperature gradient in the cBAU tube limited particle growth by causing condensation to occur predominantly at the colder wall.
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spelling pubmed-70943832020-03-25 Development and evaluation of a novel bioaerosol amplification unit (BAU) for improved viral aerosol collection Oh, Sewon Anwar, Diandra Theodore, Alexandros Lee, Jin-Hwa Wu, Chang-Yu Wander, Joe J Aerosol Sci Article A novel bioaerosol amplification unit (BAU) that increases the size of viral particles by condensational growth has been designed and evaluated for improved viral aerosol collection. In the BAU, water was used as the condensing vapor to preserve viability of virus, and supersaturation conditions for condensational growth of particles were achieved by either conductive cooling or mixing with hot, water-saturated air. MS2 bacteriophage (28 nm) was used as the test agent, and changes in collection efficiency of an SKC Biosampler with and without the BAU were determined by assaying plaque-forming units (PFUs) in the collection medium. Results showed that the mixing-type BAU (mBAU) was a promising device for improved viral aerosol sampling. The number of viruses (PFU) collected in the Biosampler increased 2–3 fold after passing through the mBAU. However, PFU increases in the cooling-type BAU (cBAU) were insignificant. APS results likewise showed that the mBAU was better in growing particles than the cBAU. After growth, number concentrations of particles larger than 327 nm in the cBAU and mBAU increased 1.3 and 15.0 fold, respectively. The relatively high molecular diffusivity of water vapor compared to the thermal diffusivity of air and the temperature gradient in the cBAU tube limited particle growth by causing condensation to occur predominantly at the colder wall. Elsevier Ltd. Published by Elsevier Ltd. 2010-09 2010-06-15 /pmc/articles/PMC7094383/ /pubmed/32226123 http://dx.doi.org/10.1016/j.jaerosci.2010.06.002 Text en Copyright © 2010 Elsevier Ltd. Published by Elsevier Ltd. All rights reserved. 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 Article
Oh, Sewon
Anwar, Diandra
Theodore, Alexandros
Lee, Jin-Hwa
Wu, Chang-Yu
Wander, Joe
Development and evaluation of a novel bioaerosol amplification unit (BAU) for improved viral aerosol collection
title Development and evaluation of a novel bioaerosol amplification unit (BAU) for improved viral aerosol collection
title_full Development and evaluation of a novel bioaerosol amplification unit (BAU) for improved viral aerosol collection
title_fullStr Development and evaluation of a novel bioaerosol amplification unit (BAU) for improved viral aerosol collection
title_full_unstemmed Development and evaluation of a novel bioaerosol amplification unit (BAU) for improved viral aerosol collection
title_short Development and evaluation of a novel bioaerosol amplification unit (BAU) for improved viral aerosol collection
title_sort development and evaluation of a novel bioaerosol amplification unit (bau) for improved viral aerosol collection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094383/
https://www.ncbi.nlm.nih.gov/pubmed/32226123
http://dx.doi.org/10.1016/j.jaerosci.2010.06.002
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