Collection efficiencies of an electrostatic sampler with superhydrophobic surface for fungal bioaerosols

We recently developed an electrostatic precipitator with superhydrophobic surface (EPSS), which collects particles into a 10‐ to 40‐μl water droplet allowing achievement of very high concentration rates (defined as the ratio of particle concentration in the collection liquid vs. the airborne particl...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Indoor air 2011-04, Vol.21 (2), p.110-120
Hauptverfasser: Han, T., Nazarenko, Y., Lioy, P. J., Mainelis, G.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 120
container_issue 2
container_start_page 110
container_title Indoor air
container_volume 21
creator Han, T.
Nazarenko, Y.
Lioy, P. J.
Mainelis, G.
description We recently developed an electrostatic precipitator with superhydrophobic surface (EPSS), which collects particles into a 10‐ to 40‐μl water droplet allowing achievement of very high concentration rates (defined as the ratio of particle concentration in the collection liquid vs. the airborne particle concentration per time unit) when sampling airborne bacteria. Here, we analyzed the performance of this sampler when collecting three commonly found fungal spores –Cladosporium cladosporioides, Penicillium melinii, and Aspergillus versicolor– under different operating conditions. We also adapted adenosine triphosphate (ATP)‐based bioluminescence for the analysis of collection efficiency and the concentration rates. The collection efficiency ranged from 10 to 36% at a sampling flow rate of 10 l/min when the airborne fungal spore concentration was approximately 105–106 spores/m3 resulting in concentration rates in the range of 1 × 105–3 × 105/min for a 10‐μl droplet. The collection efficiency was inversely proportional to the airborne spore concentration and it increased to above 60% for common ambient spore concentrations, e.g., 104–105 spores/m3. The spore concentrations determined by the ATP‐based method were not statistically different from those determined by microscopy and allowed us to analyze spore concentrations that were too low to be reliably detected by microscopy. Practical Implications The new electrostatic precipitator with superhydrophobic surface (EPSS) collects airborne fungal spores into small water droplets (10 and 40 μl) allowing achievement of concentration rates that are higher than those of most currently available bioaerosol samplers. Biosamplers with high concentration rates enable detection of low ambient aerial bioaerosol concentrations in various environments, including indoors air, and would be useful for improved exposure assessment. A successful adaptation of the adenosine triphosphate (ATP)‐based bioluminescence assay for the quantification of fungal spores from a specific species enables fast sample analysis in laboratory investigations. This rapid assay could be especially useful when investigating the performance of biological samplers as a function of multiple operational parameters.
doi_str_mv 10.1111/j.1600-0668.2010.00685.x
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4027968</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>869799113</sourcerecordid><originalsourceid>FETCH-LOGICAL-c5215-c70bf44d213ae75e90d73cf9a0ef79182726261222ed952700f0f1c420849e473</originalsourceid><addsrcrecordid>eNpdkVGL1DAUhYMo7uzqX5CADz51vEnTpgERlkF3F8r4ouxjyKTJNmOmGZPWnfn3ps46qIGQyz3fudxwEMIEliSf99slqQEKqOtmSSF3AeqmWh6eocVZeI4WIKAqasH4BbpMaQtAeCnKl-iCEgpMNHSB-lXw3ujRhQEba512Zsg34WCxyq1ZiyGNanQaJ7XbexPxoxt7nKa9if2xi2Hfh82sTtEqbbANEdtpeFAeb1xQJtuDT6_QC6t8Mq-f3iv07fOnr6vbov1yc7e6bgtdUVIVmsPGMtZRUirDKyOg46W2QoGxXJCGclrTmlBKTScqygEsWKIZhYYJw3h5hT6e5u6nzc502gxjVF7uo9upeJRBOfmvMrhePoSfkgHlom7ygHdPA2L4MZk0yp1L2nivBhOmJJtacCEIKTP59j9yG6Y45N9JUjGWGSpm6s3fC503-ZNBBj6cgEfnzfGsE5Bz1nIr50jlHKmcs5a_s5YHebe-zkW2Fye7S6M5nO0qfpc1L3kl79c38l6066pthWzLX2_lrWs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1544911293</pqid></control><display><type>article</type><title>Collection efficiencies of an electrostatic sampler with superhydrophobic surface for fungal bioaerosols</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Han, T. ; Nazarenko, Y. ; Lioy, P. J. ; Mainelis, G.</creator><creatorcontrib>Han, T. ; Nazarenko, Y. ; Lioy, P. J. ; Mainelis, G.</creatorcontrib><description>We recently developed an electrostatic precipitator with superhydrophobic surface (EPSS), which collects particles into a 10‐ to 40‐μl water droplet allowing achievement of very high concentration rates (defined as the ratio of particle concentration in the collection liquid vs. the airborne particle concentration per time unit) when sampling airborne bacteria. Here, we analyzed the performance of this sampler when collecting three commonly found fungal spores –Cladosporium cladosporioides, Penicillium melinii, and Aspergillus versicolor– under different operating conditions. We also adapted adenosine triphosphate (ATP)‐based bioluminescence for the analysis of collection efficiency and the concentration rates. The collection efficiency ranged from 10 to 36% at a sampling flow rate of 10 l/min when the airborne fungal spore concentration was approximately 105–106 spores/m3 resulting in concentration rates in the range of 1 × 105–3 × 105/min for a 10‐μl droplet. The collection efficiency was inversely proportional to the airborne spore concentration and it increased to above 60% for common ambient spore concentrations, e.g., 104–105 spores/m3. The spore concentrations determined by the ATP‐based method were not statistically different from those determined by microscopy and allowed us to analyze spore concentrations that were too low to be reliably detected by microscopy. Practical Implications The new electrostatic precipitator with superhydrophobic surface (EPSS) collects airborne fungal spores into small water droplets (10 and 40 μl) allowing achievement of concentration rates that are higher than those of most currently available bioaerosol samplers. Biosamplers with high concentration rates enable detection of low ambient aerial bioaerosol concentrations in various environments, including indoors air, and would be useful for improved exposure assessment. A successful adaptation of the adenosine triphosphate (ATP)‐based bioluminescence assay for the quantification of fungal spores from a specific species enables fast sample analysis in laboratory investigations. This rapid assay could be especially useful when investigating the performance of biological samplers as a function of multiple operational parameters.</description><identifier>ISSN: 0905-6947</identifier><identifier>EISSN: 1600-0668</identifier><identifier>DOI: 10.1111/j.1600-0668.2010.00685.x</identifier><identifier>PMID: 21204982</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenosine Triphosphate - analysis ; Aerosols - analysis ; Air Microbiology ; Air Pollution, Indoor - analysis ; Aspergillus ; Aspergillus - isolation &amp; purification ; ATP bioluminescence ; Bioaerosols ; Cladosporium - isolation &amp; purification ; Collection efficiency ; Concentration rate ; Electrostatic precipitation ; Environmental Restoration and Remediation - instrumentation ; Environmental Restoration and Remediation - methods ; Fungi ; Hydrophobic and Hydrophilic Interactions ; Luminescent Measurements - methods ; Microscopy - methods ; Penicillium ; Penicillium - isolation &amp; purification ; Spores, Fungal - isolation &amp; purification ; Static Electricity ; Surface Properties</subject><ispartof>Indoor air, 2011-04, Vol.21 (2), p.110-120</ispartof><rights>2011 John Wiley &amp; Sons A/S</rights><rights>2011 John Wiley &amp; Sons A/S.</rights><rights>2011 John Wiley &amp; Sons A/S 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5215-c70bf44d213ae75e90d73cf9a0ef79182726261222ed952700f0f1c420849e473</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1600-0668.2010.00685.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-0668.2010.00685.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21204982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Han, T.</creatorcontrib><creatorcontrib>Nazarenko, Y.</creatorcontrib><creatorcontrib>Lioy, P. J.</creatorcontrib><creatorcontrib>Mainelis, G.</creatorcontrib><title>Collection efficiencies of an electrostatic sampler with superhydrophobic surface for fungal bioaerosols</title><title>Indoor air</title><addtitle>Indoor Air</addtitle><description>We recently developed an electrostatic precipitator with superhydrophobic surface (EPSS), which collects particles into a 10‐ to 40‐μl water droplet allowing achievement of very high concentration rates (defined as the ratio of particle concentration in the collection liquid vs. the airborne particle concentration per time unit) when sampling airborne bacteria. Here, we analyzed the performance of this sampler when collecting three commonly found fungal spores –Cladosporium cladosporioides, Penicillium melinii, and Aspergillus versicolor– under different operating conditions. We also adapted adenosine triphosphate (ATP)‐based bioluminescence for the analysis of collection efficiency and the concentration rates. The collection efficiency ranged from 10 to 36% at a sampling flow rate of 10 l/min when the airborne fungal spore concentration was approximately 105–106 spores/m3 resulting in concentration rates in the range of 1 × 105–3 × 105/min for a 10‐μl droplet. The collection efficiency was inversely proportional to the airborne spore concentration and it increased to above 60% for common ambient spore concentrations, e.g., 104–105 spores/m3. The spore concentrations determined by the ATP‐based method were not statistically different from those determined by microscopy and allowed us to analyze spore concentrations that were too low to be reliably detected by microscopy. Practical Implications The new electrostatic precipitator with superhydrophobic surface (EPSS) collects airborne fungal spores into small water droplets (10 and 40 μl) allowing achievement of concentration rates that are higher than those of most currently available bioaerosol samplers. Biosamplers with high concentration rates enable detection of low ambient aerial bioaerosol concentrations in various environments, including indoors air, and would be useful for improved exposure assessment. A successful adaptation of the adenosine triphosphate (ATP)‐based bioluminescence assay for the quantification of fungal spores from a specific species enables fast sample analysis in laboratory investigations. This rapid assay could be especially useful when investigating the performance of biological samplers as a function of multiple operational parameters.</description><subject>Adenosine Triphosphate - analysis</subject><subject>Aerosols - analysis</subject><subject>Air Microbiology</subject><subject>Air Pollution, Indoor - analysis</subject><subject>Aspergillus</subject><subject>Aspergillus - isolation &amp; purification</subject><subject>ATP bioluminescence</subject><subject>Bioaerosols</subject><subject>Cladosporium - isolation &amp; purification</subject><subject>Collection efficiency</subject><subject>Concentration rate</subject><subject>Electrostatic precipitation</subject><subject>Environmental Restoration and Remediation - instrumentation</subject><subject>Environmental Restoration and Remediation - methods</subject><subject>Fungi</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Luminescent Measurements - methods</subject><subject>Microscopy - methods</subject><subject>Penicillium</subject><subject>Penicillium - isolation &amp; purification</subject><subject>Spores, Fungal - isolation &amp; purification</subject><subject>Static Electricity</subject><subject>Surface Properties</subject><issn>0905-6947</issn><issn>1600-0668</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkVGL1DAUhYMo7uzqX5CADz51vEnTpgERlkF3F8r4ouxjyKTJNmOmGZPWnfn3ps46qIGQyz3fudxwEMIEliSf99slqQEKqOtmSSF3AeqmWh6eocVZeI4WIKAqasH4BbpMaQtAeCnKl-iCEgpMNHSB-lXw3ujRhQEba512Zsg34WCxyq1ZiyGNanQaJ7XbexPxoxt7nKa9if2xi2Hfh82sTtEqbbANEdtpeFAeb1xQJtuDT6_QC6t8Mq-f3iv07fOnr6vbov1yc7e6bgtdUVIVmsPGMtZRUirDKyOg46W2QoGxXJCGclrTmlBKTScqygEsWKIZhYYJw3h5hT6e5u6nzc502gxjVF7uo9upeJRBOfmvMrhePoSfkgHlom7ygHdPA2L4MZk0yp1L2nivBhOmJJtacCEIKTP59j9yG6Y45N9JUjGWGSpm6s3fC503-ZNBBj6cgEfnzfGsE5Bz1nIr50jlHKmcs5a_s5YHebe-zkW2Fye7S6M5nO0qfpc1L3kl79c38l6066pthWzLX2_lrWs</recordid><startdate>201104</startdate><enddate>201104</enddate><creator>Han, T.</creator><creator>Nazarenko, Y.</creator><creator>Lioy, P. J.</creator><creator>Mainelis, G.</creator><general>Blackwell Publishing Ltd</general><general>Hindawi Limited</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7ST</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>KR7</scope><scope>SOI</scope><scope>M7N</scope><scope>5PM</scope></search><sort><creationdate>201104</creationdate><title>Collection efficiencies of an electrostatic sampler with superhydrophobic surface for fungal bioaerosols</title><author>Han, T. ; Nazarenko, Y. ; Lioy, P. J. ; Mainelis, G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5215-c70bf44d213ae75e90d73cf9a0ef79182726261222ed952700f0f1c420849e473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adenosine Triphosphate - analysis</topic><topic>Aerosols - analysis</topic><topic>Air Microbiology</topic><topic>Air Pollution, Indoor - analysis</topic><topic>Aspergillus</topic><topic>Aspergillus - isolation &amp; purification</topic><topic>ATP bioluminescence</topic><topic>Bioaerosols</topic><topic>Cladosporium - isolation &amp; purification</topic><topic>Collection efficiency</topic><topic>Concentration rate</topic><topic>Electrostatic precipitation</topic><topic>Environmental Restoration and Remediation - instrumentation</topic><topic>Environmental Restoration and Remediation - methods</topic><topic>Fungi</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Luminescent Measurements - methods</topic><topic>Microscopy - methods</topic><topic>Penicillium</topic><topic>Penicillium - isolation &amp; purification</topic><topic>Spores, Fungal - isolation &amp; purification</topic><topic>Static Electricity</topic><topic>Surface Properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, T.</creatorcontrib><creatorcontrib>Nazarenko, Y.</creatorcontrib><creatorcontrib>Lioy, P. J.</creatorcontrib><creatorcontrib>Mainelis, G.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Environment Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Environment Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Indoor air</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, T.</au><au>Nazarenko, Y.</au><au>Lioy, P. J.</au><au>Mainelis, G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Collection efficiencies of an electrostatic sampler with superhydrophobic surface for fungal bioaerosols</atitle><jtitle>Indoor air</jtitle><addtitle>Indoor Air</addtitle><date>2011-04</date><risdate>2011</risdate><volume>21</volume><issue>2</issue><spage>110</spage><epage>120</epage><pages>110-120</pages><issn>0905-6947</issn><eissn>1600-0668</eissn><abstract>We recently developed an electrostatic precipitator with superhydrophobic surface (EPSS), which collects particles into a 10‐ to 40‐μl water droplet allowing achievement of very high concentration rates (defined as the ratio of particle concentration in the collection liquid vs. the airborne particle concentration per time unit) when sampling airborne bacteria. Here, we analyzed the performance of this sampler when collecting three commonly found fungal spores –Cladosporium cladosporioides, Penicillium melinii, and Aspergillus versicolor– under different operating conditions. We also adapted adenosine triphosphate (ATP)‐based bioluminescence for the analysis of collection efficiency and the concentration rates. The collection efficiency ranged from 10 to 36% at a sampling flow rate of 10 l/min when the airborne fungal spore concentration was approximately 105–106 spores/m3 resulting in concentration rates in the range of 1 × 105–3 × 105/min for a 10‐μl droplet. The collection efficiency was inversely proportional to the airborne spore concentration and it increased to above 60% for common ambient spore concentrations, e.g., 104–105 spores/m3. The spore concentrations determined by the ATP‐based method were not statistically different from those determined by microscopy and allowed us to analyze spore concentrations that were too low to be reliably detected by microscopy. Practical Implications The new electrostatic precipitator with superhydrophobic surface (EPSS) collects airborne fungal spores into small water droplets (10 and 40 μl) allowing achievement of concentration rates that are higher than those of most currently available bioaerosol samplers. Biosamplers with high concentration rates enable detection of low ambient aerial bioaerosol concentrations in various environments, including indoors air, and would be useful for improved exposure assessment. A successful adaptation of the adenosine triphosphate (ATP)‐based bioluminescence assay for the quantification of fungal spores from a specific species enables fast sample analysis in laboratory investigations. This rapid assay could be especially useful when investigating the performance of biological samplers as a function of multiple operational parameters.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21204982</pmid><doi>10.1111/j.1600-0668.2010.00685.x</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0905-6947
ispartof Indoor air, 2011-04, Vol.21 (2), p.110-120
issn 0905-6947
1600-0668
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4027968
source MEDLINE; Access via Wiley Online Library
subjects Adenosine Triphosphate - analysis
Aerosols - analysis
Air Microbiology
Air Pollution, Indoor - analysis
Aspergillus
Aspergillus - isolation & purification
ATP bioluminescence
Bioaerosols
Cladosporium - isolation & purification
Collection efficiency
Concentration rate
Electrostatic precipitation
Environmental Restoration and Remediation - instrumentation
Environmental Restoration and Remediation - methods
Fungi
Hydrophobic and Hydrophilic Interactions
Luminescent Measurements - methods
Microscopy - methods
Penicillium
Penicillium - isolation & purification
Spores, Fungal - isolation & purification
Static Electricity
Surface Properties
title Collection efficiencies of an electrostatic sampler with superhydrophobic surface for fungal bioaerosols
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T14%3A17%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Collection%20efficiencies%20of%20an%20electrostatic%20sampler%20with%20superhydrophobic%20surface%20for%20fungal%20bioaerosols&rft.jtitle=Indoor%20air&rft.au=Han,%20T.&rft.date=2011-04&rft.volume=21&rft.issue=2&rft.spage=110&rft.epage=120&rft.pages=110-120&rft.issn=0905-6947&rft.eissn=1600-0668&rft_id=info:doi/10.1111/j.1600-0668.2010.00685.x&rft_dat=%3Cproquest_pubme%3E869799113%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1544911293&rft_id=info:pmid/21204982&rfr_iscdi=true