2000
DOI: 10.1080/027868200303722
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Survival of Airborne Microorganisms During Swirling Aerosol Collection

Abstract: ABSTRACT. An earlier study evaluated the physical performance of the Swirling Aerosol Collector, also known as the``BioSampler,'' and found it to have several advantages over the widely used AGI-30 impinger when tested with inert test particles. Th e present study was focused on the ph ysical and biological performan ce with laboratory-aerosolized microorganisms. The results showed th at the BioSampler has better physical collection ef® ciency for B. subtilis an d P.¯uo-rescens than the AGI-30 wh en water was … Show more

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Cited by 145 publications
(160 citation statements)
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“…The physical penetration correction factor (CF P ) was applied to compensate for unequal sampling train particle loss bias as described in detail in Lore et al (19) Viable Penetration All glass impingers (AGI-30; ACE Glass Inc., Vineland, N.J.) were chosen to sample the viable bioaerosols as they are a good compromise between collection efficiency, collection stress on microorganism viability, and volumetric sampling rate. (13,(20)(21)(22) The PEN V of each bioaerosol was measured by sampling its viable concentration upstream and downstream of each test FFR into an AGI-30 connected to the appropriate sampling port. Each AGI-30 was filled with 20 mL of either 1 × PBS for MS2 and B. atrophaeus bacteria or deionized water for B. atrophaeus spores.…”
Section: Aerosol Sampling Physical Penetrationmentioning
confidence: 99%
“…The physical penetration correction factor (CF P ) was applied to compensate for unequal sampling train particle loss bias as described in detail in Lore et al (19) Viable Penetration All glass impingers (AGI-30; ACE Glass Inc., Vineland, N.J.) were chosen to sample the viable bioaerosols as they are a good compromise between collection efficiency, collection stress on microorganism viability, and volumetric sampling rate. (13,(20)(21)(22) The PEN V of each bioaerosol was measured by sampling its viable concentration upstream and downstream of each test FFR into an AGI-30 connected to the appropriate sampling port. Each AGI-30 was filled with 20 mL of either 1 × PBS for MS2 and B. atrophaeus bacteria or deionized water for B. atrophaeus spores.…”
Section: Aerosol Sampling Physical Penetrationmentioning
confidence: 99%
“…The widely used culture-based analysis method which reports the results as Colony Forming Units (CFUs) is potentially very sensitive (one organism), but time consuming, and organisms may become damaged and non-culturable during sample collection (Buttner et al 1991;Martinez et al 1988;Lin et al 2000). Moreover, the majority of naturally occurring microorganisms cannot be cultivated using standard culture methods (≥90-99%) or readily identified in culture (Amann et al 1995;DeLong and Pace 2001).…”
Section: Introductionmentioning
confidence: 99%
“…Exposure to bacteria and fungi is usually assessed by monitoring the concentration of viable biological aerosols. Commonly used inertial sampling techniques, such as impaction and impingement, have been shown to adversely affect the viability of the microorganisms being sampled (Stewart et al 1995;Lin et al 2000). In inertial samplers, the particle velocity toward the collection medium is usually tens or hundreds of meters per second.…”
Section: Introductionmentioning
confidence: 99%