Nebulizer-spray chamber apparatus and method for production of multi-component particle types and their use in affecting cellular responses

A particle generation apparatus and methodology is described for its application to prepare heterogeneous particles of defined chemical composition and their subsequent delivery to human lung cell cultures. A concentric type nebulizer was used together with a single pass spray chamber that was operated at two different temperature settings, either room temperature or to produce intact particles, at nonuniform temperature with the central axis measuring 54°C. Silica (SiO₂) particles in the micrometer size range were produced from the aggregation of nanoparticles. Tumor necrosis factor (TNF)-α, a well-characterized cytokine, was incorporated as a secondary soluble component within host silica particles for application as a proof-of-concept heterogeneous particle type. The overall particle deposition and wetting efficiency into media was 2.0 ± 0.4%, and the average size of particles that impacted and sank in the growth medium was 3.4 µm. The particle dose, reported as particle-to-cell ratio, spanned 0.1 to ～2.5. Co-cultures of A549 and differentiated human monocytic cells (THP-1*) exposed to silica particles caused IL-6 upregulation, but not IL-8. For the silica plus TNF-α particle type, ICAM-1 signal increased in A549 mono-cultures as the particle-to-cell ratio increased, yet an estimated 90% of the TNF-α was denatured or possibly bound to the silica particle host, and was therefore bio-unavailable. Method quantitation using particles having two different chemical compositions has been described, illustrating capability for subsequent systematic investigation of the role of particles having different chemical composition in the human health aspects of the particulate air pollution issue.

Copyright © 2016 American Association for Aerosol Research     

Design and validation of an air-liquid interface (ALI) exposure device based on thermophoresis

In vitro, direct aerosol nanoparticle exposure of cells cultured at the air-liquid interface (ALI) has shown great potential over the conventional submerged cell exposure methods due to exposure relevancy and more accurate dose determination. Here, we present a design of an ALI cell exposure device, the thermocollector, which applies thermophoresis to deposit aerosol particles onto the cells. Computational numerical simulations were used to estimate the deposition flux and how it depended on particle properties. The deposition flux was approximately 250 particles/m²s for particles smaller than 100?nm, corresponding to an aerosol concentration of 1 #/cm³. This was also confirmed with experimental studies. For larger particles, the deposition rate depended more on particle properties; however, for fractal combustion derived soot particles, the deposition rate is practically size independent at the size range studied here. Finally, epithelial cells were exposed with wood combustion aerosol, and the toxicologic responses were investigated. The cell viability decrease and DNA damage were detected after the exposure. These effects were not detected in cells after the exposure to clean air in this cell exposure system.

Copyright © 2019 American Association for Aerosol Research     

Dose estimation methodology for the UV inactivation of bioaerosols in a Continuous-Flow reactor

Indoor air microbial pollution may be responsible for various human allergies and diseases. To reduce exposure, airborne bacteria can be directly controlled through devices that employ ultraviolet-C (UV-C) radiation. In this study, a continuous annular photo-reactor was used to evaluate the inactivation dose for two species: Gram-negative Escherichia coli and Pseudomonas aeruginosa. In order to provide meaningful results, a comprehensive kinetic modeling was performed, which included the evaluation of optical properties of the microorganisms and the calculation of radiation field inside the reactor. In this way, intrinsic inactivation rates could be obtained. From the reactor modeling and the experimental data sets, the first order inactivation rate or UV susceptibility for E. coli was 0.1055?m² J^?1, while for P. aeruginosa the obtained value was 0.2579?m² J^?1. The approach used allows a straightforward scaling-up of the process for real applications and microorganism species involved.

Copyright © 2018 American Association for Aerosol Research     

Inter-comparison of low-cost sensors for measuring the mass concentration of occupational aerosols

Low-cost sensors are effective for measuring the mass concentration of ambient aerosols and second-hand smoke in homes, but their use at concentrations relevant to occupational settings has not been demonstrated. We measured the concentrations of four aerosols (salt, Arizona road dust, welding fume, and diesel exhaust) with three types of low-cost sensors (a DC1700 from Dylos and two commodity sensors from Sharp), an aerosol photometer, and reference instruments at concentrations up to 6500 µg/m³. Raw output was used to assess sensor precision and develop equations to compute mass concentrations. EPA and NIOSH protocols were used to assess the mass concentrations estimated with low-cost sensors compared to reference instruments. The detection efficiency of the DC1700 ranged from 0.04% at 0.1 µm to 108% at 5 µm, as expected, although misclassification of fine and coarse particles was observed. The raw output of the DC1700 had higher precision (lower coefficient of variation, CV = 7.4%) than that of the two sharp devices (CV = 25% and 17%), a finding attributed to differences in manufacturer calibration. Aerosol type strongly influenced sensor response, indicating the need for on-site calibration to convert sensor output to mass concentration. Once calibrated, however, the mass concentration estimated with low-cost sensors was highly correlated with that of reference instruments (R²= 0.99). These results suggest that the DC1700 and Sharp sensors are useful in estimating aerosol mass concentration for aerosols at concentrations relevant to the workplace.

© 2016 American Association for Aerosol Research     

Application of a quaternary ammonium agent on surgical face masks before use for pre-decontamination of nosocomial infection-related bioaerosols

Surgical face masks are commonly used by the general public in indoor environments. However, masks could be contaminated, resulting in secondary microbial infections when they act as touchable fomites. Therefore, we evaluated the ability and durability of a covalently bound antimicrobial surfactant coated onto mask surfaces before use to reduce the bacterial burden upon exposure to aerosols. With regard to bacteria that settled onto the mask surface, this antimicrobial product provided >99.3% efficiency for all three tested bacterial species. In addition, the antimicrobial ability of the coated mask maintained efficacy at least one week after coating. For bioaerosols that came into contact with the mask (10³ CFU/m³), the antimicrobial agent reduced the average colony rates by 91.8%, but the rates decreased with increased bioaerosol concentrations. Moreover, regardless of whether the coated mask was processed with the bioaerosol penetration test or the National Institute for Occupational Safety and Health-certified sodium chloride aerosol test, the filtration performance of the surgical mask was not significantly altered. These results demonstrate that this antimicrobial product has a durable inhibitory activity for the reduction of bacterial burdens on masks.

Copyright © 2016 American Association for Aerosol Research     

Toxicological characterization of particulate emissions from straw,Miscanthus, and poplar pellet combustion in residential boilers

Wood pellets have been used in domestic heating appliances for three decades. However, because the share of renewable energy for heating will likely rise over the next several years, alternative biomass fuels, such as short-rotation coppice or energy crops, will be utilized. We tested particulate emissions from the combustion of standard softwood pellets and three alternative pellets (poplar, Miscanthus sp., and wheat straw) for their ability to induce inflammatory, cytotoxic, and genotoxic responses in a mouse macrophage cell line. Our results showed clear differences in the chemical composition of the emissions, which was reflected in the toxicological effects. Standard softwood and straw pellet combustion resulted in the lowest PM₁ mass emissions. Miscanthus sp. and poplar combustion emissions were approximately three times higher. Emissions from the herbaceous biomass pellets contained higher amounts of chloride and organic carbon than the emissions from standard softwood pellet combustion. Additionally, the emissions of the poplar pellet combustion contained the highest concentration of metals. The emissions from the biomass alternatives caused significantly higher genotoxicity than the emissions from the standard softwood pellets. Moreover, straw pellet emissions caused higher inflammation than the other samples. Regarding cytotoxicity, the differences between the samples were smaller. Relative toxicity was generally highest for the poplar and Miscanthus sp. samples, as their emission factors were much higher. Thus, in addition to possible technical problems, alternative pellet materials may cause higher emissions and toxicity. The long-term use of alternative fuels in residential-scale appliances will require technological developments in both burners and filtration.

Copyright © 2016 American Association for Aerosol Research     

Determination of the distribution of infectious viruses in aerosol particles using water-based condensational growth technology and a bacteriophage MS2 model

Inhalation of aerosols containing pathogenic viruses can result in morbidity, in some cases leading to mortality. The objective of this study was to develop a model for assessing how infectious viruses might distribute in airborne particles using bacteriophage MS2 as a surrogate for human viruses. Particle deposition in the respiratory system is size-dependent, and small virus-containing particles can be inhaled deeply into the lower lungs, potentially leading to more severe respiratory disease manifestations. Laboratory-generated virus-containing particles were size-selected by a differential mobility analyzer and then collected by the newly introduced Super-Efficient Sampler for Influenza Virus. The number of infectious and total viruses per particle as a function of particle size varied with the spraying medium: it approximated a cubic exponential value scaling for deionized (DI) water, a quartic exponential value for artificial saliva (AS), and between quadratic and cubic exponential value for beef extract solution (BES). The survivability of MS2 did not change significantly with particle size for DI water and BES, while that for AS was maximum at 120?nm. Viruses could be homogeneously distributed or aggregated inside or on the surface of the particles, depending on the composition of the spraying medium.

Copyright © 2019 American Association for Aerosol Research     

Experimental and numerical study of the performance of upper-room ultraviolet germicidal irradiation with the effective Z-value of airborne bacteria

Upper-room ultraviolet germicidal irradiation (UR-UVGI) is recommended for the defense against airborne pathogens in poorly ventilated rooms in public buildings or high risk environments, such as hospitals. Currently, there are few studies on the performance of UR-UVGI with the effective bacteria susceptibility constant (eZ-value) obtained from UR-UVGI experiment. In this study, the Eulerian model for the inactivation of UVGI was improved to consider the difference between exposure time and computational time, and was validated by our previous experiments. The method was applied to study numerically the performance of the UR-UVGI for 3, 6, and 10 air changes per hour (ACH) with the application of the eZ-value of airborne bacteria. Moreover, the eZ-values of commonly found bacteria, including Serratia marcescens, Staphylococcus epidermidis, Pseudomonas alcaligenes, and Micrococcus luteus, were obtained from a series of experiments in a full-scale environmental chamber equipped with a UR-UVGI fixture. The eZ-values were 0.0983, 0.0586, 0.0476, and 0.0115 m²/J, respectively. Compared with the data in the literature, these eZ-values of the tested bacteria are different from the Z-values obtained from single-pass UVGI. The simulation results show that UR-UVGI exhibited the highest inactivation efficiency on S. marcescens among the tested bacteria in this study. The percentage of bacteria inactivated by UR-UVGI decreased as the ventilation rate increased. The bacteria concentration in the breathing zone under low ventilation rate could be decreased using UR-UVGI. The findings demonstrate that high indoor air quality can be achieved with the application of UR-UVGI without the need to maintain high ventilation rate.

Copyright © 2017 American Association for Aerosol Research     

An integrative model for the filtration efficiencies in realistic tests with consideration of the filtration velocity profile and challenging particle size distribution

Many well-established models can be applied to calculate the filtration efficiencies. In these models the filtration velocity and challenging particle size are assumed to be known accurately. However, in realistic filtration tests, the filtration velocity has profiles dependent on the filter holder geometry and experimental conditions; the challenging particles have size distributions dependent on the instruments and operation conditions. These factors can potentially affect the measured filtration efficiency and lead to discrepancies with the models.

This study aims to develop an integrative model to predict the filtration efficiencies in realistic tests by incorporating the effects of the filtration velocity profile and challenging particle size distribution classified by a differential mobility analyzer (DMA) into the existing filtration models. Face velocity profile is modeled with fluid mechanics simulations; the initial generated particle size distribution, the particle charging status and the DMA transfer function are modeled to obtain the challenging particle size distribution. These results are then fed into the filtration models. Simulated results are compared with experimental ones to verify the model accuracy. This model can be used to reduce filtration test artifacts and to improve the experimental procedure.

The results reveal that the face velocity upstream the filter exhibits high degree of homogeneity not affecting the filtration efficiency if the filter pressure drop is not very low. The generated particle size distribution and the DMA selection size window could influence the challenging particle size distribution and therefore the measured filtration efficiency.

Copyright © 2017 American Association for Aerosol Research     

Influence of volatilization from mainstream tobacco smoke particles on the gas-particle distribution in annular denuders

The influence of volatilization from mainstream tobacco smoke particles in annular denuders on the gas-particle distribution was investigated by using multiple annular denuders coupled with a filter pack method (multiple-AD-FP method) under low flow volume conditions (1.05 and 1.65 L/min). Smoking experiments and model experiments using poly styrene latex (PSL) particles and generated gases were conducted to measure the particle loss ratio and gas collection efficiency in the denuders. In this research, we focused on the influence of XAD-4 slurry concentrations and particle volatility including tobacco smoke from a cigarette and vapor products on the volatilization from particles in the denuders, and have proposed a measurement method for considering volatilization. Our experimental results showed that volatilization depends on the particle volatility, targeted components, denuder length, particle concentration, and adsorbent amount, thereby suggesting the importance of selecting the proper measurement conditions and taking volatilization into account, so as to evaluate the appropriate gas-particle distribution. The gas-phase nicotine ratio obtained from calculating the volatilization rate in the multiple-AD-FP method agreed with previous research. This means that the calculation method was appropriate for the evaluation of gas-particle distribution. Furthermore, the gas-particle ratio determined through the multiple-AD-FP method was compared to that determined through a filter-impinger method that uses a glass fiber filter. The results revealed that most of the gases in the filter-impinger method were not collected in the impinger due to the condensation of gases on the surface of the filter fibers and collected particles.

© 2017 American Association for Aerosol Research     

Comparison of two size-differentiating air samplers for detecting airborne swine viruses under experimental conditions

Detection and quantification of dilute viral aerosols, as encountered outside animal housing facilities, requires methods that are able to detect small numbers of viruses in large volumes of air. This study compared the performance of two size-differentiating cascade impactors; an Andersen 8-stage (ACI; 28.3 L/min) and a high volume Tisch (TCI; 1,133 L/min) to assess sampling efficiency for detecting porcine reproductive and respiratory syndrome virus (PRRSV) and influenza A virus (IAV). Samples of particles sorted by aerodynamic diameter were analyzed by quantitative polymerase chain reaction (qPCR) and collection efficiency was assessed by particle size. Collection media (minimum essential medium [MEM] and beef extract [BE]), elution technique (active versus passive), and sampling times (10, 20, and 30 min) were variables assessed for the TCI sampler. Extraction efficiency was 35% higher with BE as compared to that of MEM (p = 0.0007); active extraction technique was 19% more efficient than the passive technique (p = 0.03); time of sampling did not significantly affect the amount of virus recovered. The ACI sampler was more efficient in detecting both viruses from small and medium sized airborne particles (≤3 μm) as compared to the TCI sampler (p < 0.001). The latter sampler, however, was more efficient at IAV detection from large airborne particles (>3 μm) (p = 0.0025) indicating the potential of this sampler in detecting the presence of small amounts of viruses in aerosols under field conditions.

© 2017 American Association for Aerosol Research     

Nanoscale aerovirology: An efficient yet simple method to analyze the viral distribution of single bioaerosols

The aerosolization mechanisms of viruses are poorly known, because of the challenges related to their sampling and observation. For example, single particle studies are needed to improve our understanding of bioaerosol enrichment processes. Such studies would help to develop models of airborne disease propagation. We propose a novel approach to study viral aerosols in single particles using a combination of fluorescence and transmission electron microscopy (TEM). This method allows for rapid analysis of labeled bacteriophages aerosolized and captured on a black membrane filter. It also requires performing image analyses on fluorescent spots. TEM is necessary to determine a single bacteriophage dimensions. Thus, the clustering of bacteriophage PP01 in a single aerosol particle was investigated and found to give a comparable number of virions to what was observed with TEM. The impact of the GFP (green fluorescent protein) in the head of PP01 virion compared to wild type (WT) PP01 was also tested by comparing the clustering of similar bioaerosol sizes generated by the aerosolization of PP01 WT, PP01-GFP, and PP01-GFP labeled with syto-red dye. Surprisingly, the PP01 WT bioaerosols were enriched compared to the PP01-GFP ones (64.9?±?17.5% more). PP01-GFPs were also found to be more numerous compared to those produced by PP01-GFP labeled with syto-red dye (28.9?±?16.9% more). The aerosolization process might be dependent on the electrochemical properties of the viruses and the environment. Changes of this nature could affect the mechanism of the aerosol formation in natural forming aerosols as demonstrated in this study for artificially generated aerosols.

© 2016 American Association for Aerosol Research     

Re-aerosolization in liquid-based air samplers induces bias in bacterial diversity

Bioaerosols collected in a liquid-based sampler can be re-aerosolized into the airflow during collection and lost or concentrated in the collection fluid and overestimated during the subsequent analyses. Very little information is available concerning the specific impact on bioaerosol quantification and diversity and wrong evaluation of pathogens or potentially harmful microorganisms concentration could lead to incorrect data interpretation and inaccurate exposure risk assessment. The aim of this two-part study was to better understand how evaporation impacts the results obtained from liquid-based samplers. Bacterial consortium was spiked in the collection vessels of the Coriolisµ^® and the BioSampler^® and the bacterial concentration was monitored after running the samplers in vitro. Relative ratios of the bacteria were analyzed using qPCR (before/after). A field study in which liquid-based air samplers in a natural environment were compared to filter-based samplers was performed. This allowed for the relative characterization of either concentration or the re-aerosolization between the two samplers using high throughput sequencing methods. Amongst the four strains of bacteria examined in vitro, results suggest differential behavior between concentration or re-aerosolization from the liquid. Re-aerosolization of bacteria is difficult to predict as the cell-surface hydrophobicity, the liquid-based air sampler and its flowrate can influence it. The sequencing results from field samples confirmed the loss of entire genera by re-aerosolization (Brevundimonas, Clostridium, Mycobacterium, and Smithella) out of the BioSampler^® while concentration of several other genera were reduced (Bradyrhizobium, Delftia, Propionibacterium, and Sphingomonas). These observations suggest that evaporation in liquid samplers might lead to over- or underestimation of the prevalence of some genera.

Copyright © 2019 American Association for Aerosol Research     

Changes of fluorescence spectra and viability from aging aerosolized E. coli cells under various laboratory-controlled conditions in an advanced rotating drum

An advanced rotating aerosol chamber was developed to study the changes of fluorescence spectral profile and intensity, the viability and the quantitative polymerase chain reaction (qPCR) signal of Escherichia coli aerosol particles as they are exposed to simulated atmospheric conditions over time. These conditions included relative humidity (RH) below 30% or ～75%, ozone ～100?ppb, volatile organic compounds (VOCs) α–pinene (～5?ppb) or toluene (～45?ppb), and simulated solar (SS) irradiation. Individual experiments examined the effects of these conditions applied individually and in combination. Experimental results demonstrate that the 263?nm laser excited UV fluorescence band (280–400?nm) showed the greatest rate of decrease, and the visible band (400–580?nm) generally had a smaller change rate which followed the change in the UV band. The 351?nm excited visible band (380–650?nm) had the smallest decay rates, and sometimes increased, when exposed to ozone, high RH, and VOCs. Generally, the viability, qPCR signal intensity, and the fluorescence intensity decayed faster when more variables were applied in combination. Simulated solar irradiation was the most dominant factor in the aging process, followed by the combination of high RH and ozone. Interestingly, the decay of fluorescence and qPCR signal do not appear to correlate directly with loss in viability. Therefore, additional studies are expected to further understand the mechanisms by which atmospheric chemical processes impact viability, qPCR signal intensity, and the fluorescence of biological aerosols.     

Physical performances and kinetics of evaporation of the CIP 10-M personal sampler's rotating cup containing aqueous or viscous collection fluid

The CIP 10-M personal sampler measures worker exposure to airborne particles by collecting particles in a rotating metal cup containing a few milliliters of a collection fluid. This device is mainly used to sample microorganisms or microbial components to measure bioaerosol concentrations in various occupational environments. Aqueous liquids are generally used, but their rapid evaporation limits the duration of sampling; alternative collection fluids could alleviate this problem. Indeed, the particle-collection efficiency of the rotating cup has not been extensively studied, and the only data available relate to a discontinued model. This study aimed to measure the collection efficiency of the current rotating cup model containing an aqueous (water) or viscous (ViaTrap mineral oil) collection fluid. The kinetics of evaporation confirmed that ViaTrap does not evaporate, making 8-h sampling campaigns in constant volumes feasible. Particles with a wide range of aerodynamic diameters (between around 0.1 and 10 µm) were produced using various test rigs and mono- or polydisperse test aerosols. Both new and older cup models performed similarly, with a collection efficiency of >80% for larger particles (aerodynamic diameters >2.8 µm), progressively decreasing to around 50% for aerodynamic diameters of 2.1 µm; with aerodynamic diameters of <1 µm, the collection efficiency was generally <10%. In physical terms, collection efficiency was unaffected by the type (aqueous or viscous) or volume (between 0 and 3 mL) of collection fluid used. Bias maps indicated that the inhalable fraction may be underestimated in occupational settings, particularly with aerosols mainly composed of particles with aerodynamic diameters of less than around 3 µm.

Copyright © 2016 American Association for Aerosol Research     

Performance of wearable ionization air cleaners: Ozone emission and particle removal

Wearable ionization air cleaners are compact in size and marketed for personal respiratory protection by removing air pollutants from users' breathing zone. In this study, ozone emission and particle removal rates of four wearable ionization air cleaners (namely, AC1 through AC4) were evaluated inside a 0.46 m³ stainless steel chamber. Continuous measurements were conducted for ozone concentration, PM_2.5 concentration, and particle size distribution in the size range of 18.1–289 nm. Two of the four wearable air cleaners (i.e., AC1 and AC2) had detectable ozone emissions. The 10-h average ozone emission rates were quite different (i.e., 0.67 mg·h^?1 for AC1 and 3.40 × 10^?2 mg·h^?1 for AC2); however, the ozone emissions were negligible for AC3 and AC4. The number removal rates for particles within the measured size range were highly variable (i.e., 2.20 h^?1, 0.52 h^?1, 8.10 h^?1, and 27.9 h^?1 for AC1 through AC4, respectively). The corresponding mass removal rates of PM_2.5 were 1.85 h^?1, 0.48 h^?1_,1.52 h^?1, and 5.37 h^?1, respectively. Regulatory guidelines are needed to assure these devices can effectively remove particles without ozone emissions to protect public health.

Copyright © 2016 American Association for Aerosol Research     

Application of image analysis method to detection and counting of glass fibers from filter samples

Man-made vitreous fibers (MMVFs) are noncrystalline substances made of glass, rock or slag and are widely used as thermal or acoustic insulation materials. There is continued concern about their potential health impacts and thus, their dosimetry and behavior in the environment still require study using filters to collect fiber samples. After deposition or exposure measurements of MMVFs it is often necessary to analyze the filters with deposited fibers. This task is tedious, time-consuming, and requires skill. Therefore, many researchers have tried to simplify or automatize fiber detection and quantification. This article describes features of our in-house software, which automatically detects and counts fibers in images of filter samples. The image analysis is based on the use of a histogram equalization and an adaptive radial convolution filter that enhances fiber contrast and thus, improves the fiber identification. The accuracy of the software analysis was verified by comparison with manual counting using ordinary phase-contrast microscopy method. The correlation between the methods was very high (coefficient of determination was 0.977). However, there were some discrepancies caused by false identifications, which led to implementation of manual corrective functions.

Copyright © 2016 American Association for Aerosol Research     

Deposition method,relative humidity,and surface property effects of bacterial spore reaerosolization via pulsed air jet

Biological warfare incidents generate both immediate and delayed hazards, potentially resulting from reaerosolization of deposited hazardous particles from surfaces. Understanding the causes and effects of the initial deposition method and environmental conditions on reaerosolization is important in hazard prediction and selection of mitigation approaches. This study was conducted to determine the amount of reaerosolization of various bacterial spores and 1 µm polystyrene latex microspheres deposited wet or dry and incubated at 20 or 80% relative humidity (RH). The organisms used in this study were Bacillus atrophaeus var. globigii (Bg), B. thuringiensis (Bt), B. anthracis ΔSterne (Ba-ΔSterne), Ba-ΔSterne ΔbclA mutant (BclA), and Ba-ΔSterne ΔcotE mutant (CotE). These organisms represent a range of spore types with different outer surfaces: spores with exosporium hairs and a basal layer (Ba-ΔSterne and Bt), spores with a basal layer (BclA), and spores with a spore coat only (no exosporium, Bg and CotE). A pulsed air impinging jet was used to reaerosolize particles from gridded glass surfaces. The amount of reaerosolization was determined by counting the number of particles on the gridded surface before and after applying the air jet. Results indicate that, in general, higher reaerosolization was observed when particles were deposited dry and incubated at lower RH conditions. Our results indicate that Bt (has exosporium) was reaerosolized more readily than Bg (no exosporium) in all cases studied. This method can be used in laboratory studies to compare bacterial spore behavior and to study the relative effects of different spore outer layers and surface types on reaerosolization.

© 2017 Leidos, Inc.     

Recovery of culturable Escherichia coli O157:H7 during operation of a liquid-based bioaerosol sampler

Collection fluids used in liquid-based bioaerosol samplers can influence the viability of microorganisms. In this study we determined the recovery efficiency of vegetative E. coli O157:H7 cells that were spiked into low viscosity evaporating collection fluids during operation of a BioSampler® for up to 90 min at room temperature. The collection fluids tested were deionized (DI) water, DI water with 0.1% (w/w) antifoam B (AFB), phosphate-buffered saline (PBS), and osmoprotectants consisting of peptone (with and without AFB) or betaine at .1% (w/w) in DI water. Using DI water, there was a rapid decline in the recovery of culturable E. coli, with only 11, 3, and 0% being recovered after 30, 60, and 90 min, respectively. Recoveries were substantially greater with use of PBS (53, 25, and 16%, respectively) but not as high as with use of the osmoprotectants or AFB. Peptone and AFB alone or together allowed for the greatest recovery of E. coli, with average values ranging from 87 to 98% at 90 min. Betaine was also determined to be an effective osmoprotectant for runtimes of 30 and 60 min, with respective E. coli recoveries of 101 and 77% from the impingers. The results from this study support the incorporation of peptone, AFB, and betaine in collection fluids for BioSampler runtimes from 30 to 90 min. Runtimes longer than the recommend 30 min with low viscosity collection fluids are sometimes necessary when the airborne concentration of a target microorganism is low and one is trying to increase the probability of detection.