A MEMS-enabled portable gas chromatography injection system for trace analysis.

Growing concerns about environmental conditions, public health, and disease diagnostics have led to the rapid development of portable sampling techniques to characterize trace-level volatile organic compounds (VOCs) from various sources. A MEMS-based micropreconcentrator (µPC) is one such approach that drastically reduces the size, weight, and power constraints offering greater sampling flexibility in many applications. However, the adoption of µPCs on a commercial scale is hindered by a lack of thermal desorption units (TDUs) that easily integrate µPCs with gas chromatography (GC) systems equipped with a flame ionization detector (FID) or a mass spectrometer (MS). Here, we report a highly versatile µPC-based, single-stage autosampler-injection unit for traditional, portable, and micro-GCs. The system uses µPCs packaged in 3D-printed swappable cartridges and is based on a highly modular interfacing architecture that allows easy-to-remove, gas-tight fluidic, and detachable electrical connections (FEMI). This study describes the FEMI architecture and demonstrates the FEMI-Autosampler (FEMI-AS) prototype (9.5 cm × 10 cm x 20 cm, ≈500 gms). The system was integrated with GC-FID, and the performance was investigated using synthetic gas samples and ambient air. The results were contrasted with the sorbent tube sampling technique using TD-GC-MS. FEMI-AS could generate sharp injection plugs (≈240 ms) and detect analytes with concentrations <15 ppb within 20 s and <100 ppt within 20 min of sampling time. With more than 30 detected trace-level compounds from ambient air, the demonstrated FEMI-AS, and the FEMI architecture significantly accelerate the adoption of µPCs on a broader scale.

Shower water contributes viable nontuberculous mycobacteria to indoor air.

Nontuberculous mycobacteria (NTM) are frequently present in municipal drinking water and building plumbing, and some are believed to cause respiratory tract infections through inhalation of NTM-containing aerosols generated during showering. However, the present understanding of NTM transfer from water to air is insufficient to develop NTM risk mitigation strategies. This study aimed to characterize the contribution of shower water to the abundance of viable NTM in indoor air. Shower water and indoor air samples were collected, and 16S rRNA and rpoB genes were sequenced. The sequencing results showed that running the shower impacted the bacterial community structure and NTM species composition in indoor air by transferring certain bacteria from water to air. A mass balance model combined with NTM quantification results revealed that on average 1/132 and 1/254 of NTM cells in water were transferred to air during 1 hour of showering using a rain and massage showerhead, respectively. A large fraction of the bacteria transferred from water to air were membrane-damaged, i.e. they had compromised membranes based on analysis by live/dead staining and flow cytometry. However, the damaged NTM in air were recoverable as shown by growth in a culture medium mimicking the respiratory secretions of people with cystic fibrosis, implying a potential infection risk by NTM introduced to indoor air during shower running. Among the recovered NTM, Mycobacterium mucogenicum was the dominant species as determined by rpoB gene sequencing. Overall, this study lays the groundwork for future pathogen risk management and public health protection in the built environment.

Survival of MS2 and Φ6 viruses in droplets as a function of relative humidity, pH, and salt, protein, and surfactant concentrations.

The survival of viruses in droplets is known to depend on droplets' chemical composition, which may vary in respiratory fluid between individuals and over the course of disease. This relationship is also important for understanding the persistence of viruses in droplets generated from wastewater, freshwater, and seawater. We investigated the effects of salt (0, 1, and 35 g/L), protein (0, 100, and 1000 µg/mL), surfactant (0, 1, and 10 µg/mL), and droplet pH (4.0, 7.0, and 10.0) on the viability of viruses in 1-µL droplets pipetted onto polystyrene surfaces and exposed to 20%, 50%, and 80% relative humidity (RH) using a culture-based approach. Results showed that viability of MS2, a non-enveloped virus, was generally higher than that of Φ6, an enveloped virus, in droplets after 1 hour. The chemical composition of droplets greatly influenced virus viability. Specifically, the survival of MS2 was similar in droplets at different pH values, but the viability of Φ6 was significantly reduced in acidic and basic droplets compared to neutral ones. The presence of bovine serum albumin protected both MS2 and Φ6 from inactivation in droplets. The effects of sodium chloride and the surfactant sodium dodecyl sulfate varied by virus type and RH. Meanwhile, RH affected the viability of viruses as shown previously: viability was lowest at intermediate to high RH. The results demonstrate that the viability of viruses is determined by the chemical composition of carrier droplets, especially pH and protein content, and environmental factors. These findings emphasize the importance of understanding the chemical composition of carrier droplets in order to predict the persistence of viruses contained in them.

Bromide ion-functionalized nanoprobes for sensitive and reliable pH measurement by surface-enhanced Raman spectroscopy.

4-Mercaptopyridine (4-Mpy) is a pH reporter molecule commonly used to functionalize nanoprobes for surface-enhanced Raman spectroscopy (SERS) based pH measurements. However, nanoprobes functionalized by 4-Mpy alone have low pH sensitivity and are subject to interference by halide ions in sample media. To improve nanoprobe pH sensitivity and reliability, we functionalized gold nanoparticles (AuNPs) with both 4-Mpy and bromide ion (Br-). Br- electrostatically stabilizes protonated 4-Mpy, thus enabling sensitive SERS detection of the protonation state of 4-Mpy as a function of pH while also reducing variability caused by external halide ions. Through optimization of the functionalization parameters, including suspension pH, [4-Mpy], and [Br-], the developed nanoprobes enable monitoring of pH from 2.1 to 10 with high SERS activity and minimal interference from halide ions within the sample matrix. As a proof of concept, we were able to track nanoprobe location and image the pH distribution inside individual cancer cells. This study provides a novel way to engineer reliable 4-Mpy-functionalized SERS nanoprobes for the sensitive analysis of spatially localized pH features in halide ion-containing microenvironments.

Emission of iron and aluminum oxide particles from ultrasonic humidifiers and potential for inhalation.

Ultrasonic humidifier use is a potential source of human exposure to inhalable particulates. This research evaluated the behavior of insoluble iron oxide and aluminum oxide particles in water used to fill room-sized ultrasonic humidifiers. Solutions of 10 mg/L Fe, as iron oxide particles, or 5 mg/L Al, as aluminum oxide suspension, were added into tap water used to fill ultrasonic humidifiers. The humidifiers were operated for 14 h; samples were obtained over time and monitored for soluble and particulate Fe and Al, as well as particle sizes in the humidifier reservoir and emitted in aerosols. Denser, settleable particles of approximately 1.5 µm diameter of iron or aluminum oxides accumulated at the bottom of the humidifier reservoir. Smaller, suspended metal oxide particles of 0.22-0.57 µm diameter were emitted as aerosols from the humidifier. Soluble anions and cations in tap water were also present in the aerosols emitted from humidifiers. The results indicate that a typical 1.6 MHz ultrasonic humidifier can emit 0.22-0.57 µm particles and dissolved minerals from fill water into breathable air.

Single-Cell Analysis Reveals that Chronic Silver Nanoparticle Exposure Induces Cell Division Defects in Human Epithelial Cells.

Multiple organizations have urged a paradigm shift from traditional, whole animal, chemical safety testing to alternative methods. Although these forward-looking methods exist for risk assessment and predication, animal testing is still the preferred method and will remain so until more robust cellular and computational methods are established. To meet this need, we aimed to develop a new, cell division-focused approach based on the idea that defective cell division may be a better predictor of risk than traditional measurements. To develop such an approach, we investigated the toxicity of silver nanoparticles (AgNPs) on human epithelial cells. AgNPs are the type of nanoparticle most widely employed in consumer and medical products, yet toxicity reports are still confounding. Cells were exposed to a range of AgNP doses for both short- and-long term exposure times. The analysis of treated cell populations identified an effect on cell division and the emergence of abnormal nuclear morphologies, including micronuclei and binucleated cells. Overall, our results indicate that AgNPs impair cell division, not only further confirming toxicity to human cells, but also highlighting the propagation of adverse phenotypes within the cell population. Furthermore, this work illustrates that cell division-based analysis will be an important addition to future toxicology studies.

Influenza Virus Infectivity Is Retained in Aerosols and Droplets Independent of Relative Humidity.

Pandemic and seasonal influenza viruses can be transmitted through aerosols and droplets, in which viruses must remain stable and infectious across a wide range of environmental conditions. Using humidity-controlled chambers, we studied the impact of relative humidity on the stability of 2009 pandemic influenza A(H1N1) virus in suspended aerosols and stationary droplets. Contrary to the prevailing paradigm that humidity modulates the stability of respiratory viruses in aerosols, we found that viruses supplemented with material from the apical surface of differentiated primary human airway epithelial cells remained equally infectious for 1 hour at all relative humidities tested. This sustained infectivity was observed in both fine aerosols and stationary droplets. Our data suggest, for the first time, that influenza viruses remain highly stable and infectious in aerosols across a wide range of relative humidities. These results have significant implications for understanding the mechanisms of transmission of influenza and its seasonality.

Particle/Gas Partitioning of Phthalates to Organic and Inorganic Airborne Particles in the Indoor Environment.

The particle/gas partition coefficient Kp is an important parameter affecting the fate and transport of indoor semivolatile organic compounds (SVOCs) and resulting human exposure. Unfortunately, experimental measurements of Kp exist almost exclusively for atmospheric polycyclic aromatic hydrocarbons, with very few studies focusing on SVOCs that occur in indoor environments. A specially designed tube chamber operating in the laminar flow regime was developed to measure Kp of the plasticizer di-2-ethylhexyl phthalate (DEHP) for one inorganic (ammonium sulfate) and two organic (oleic acid and squalane) particles. The values of Kp for the organic particles (0.23 ± 0.13 m3/µg for oleic acid and 0.11 ± 0.10 m3/µg for squalane) are an order of magnitude higher than those for the inorganic particles (0.011 ± 0.004 m3/µg), suggesting that the process by which the particles accumulate SVOCs is different. A mechanistic model based on the experimental design reveals that the presence of the particles increases the gas-phase concentration gradient in the boundary layer, resulting in enhanced mass transfer from the emission source into the air. This novel approach provides new insight into experimental designs for rapid Kp measurement and a sound basis for investigating particle-mediated mass transfer of SVOCs.

Highly stable SERS pH nanoprobes produced by co-solvent controlled AuNP aggregation.

Production of gold nanoparticle (AuNP) surface-enhanced Raman spectroscopy (SERS) nanoprobes requires replicable aggregation to produce multimers with high signal intensity. Herein, we illustrate a novel, yet simple, approach to produce SERS nanoprobes through control of co-solvent composition. AuNP multimers were produced by mixing AuNP monomers in water : ethanol co-solvent for variable periods of time. By varying the water : ethanol ratio and the amount of 4-mercaptobenzoic acid (4-MBA) present, the aggregation rate can be systematically controlled. Thiolated poly(ethylene glycol) was then added to halt the aggregation process and provide steric stability. This approach was used to produce pH nanoprobes with excellent colloidal stability in high ionic strength environments and in complex samples. The pH probe exhibits broad pH sensitivity over the range 6-11 and we calculate that a single AuNP dimer in a 35 fL volume is sufficient to generate a detectable SERS signal. As a proof-of-concept, the probes were used to detect the intracellular pH of human prostate cancer cells (PC-3). The internalized probes exhibit a strong 4-MBA signal without any interfering bands from either the cells or the culture media and produce exceptionally detailed pH maps. pH maps obtained from 19 xy surface scans and 14 yz depth scans exhibit highly consistent intracellular pH in the range of 5 to 7, thus indicating the greater reliability and reproducibility of our pH probes compared with other probes previously reported in the literature. Our water : ethanol co-solvent production process is fast, simple, and efficient. Adjustment of solvent composition may become a powerful way to produce SERS tags or nanoprobes in the future.

Partitioning of Viruses in Wastewater Systems and Potential for Aerosolization.

To gain insight into the potential for aerosolization of viruses in wastewater systems, we investigated the partitioning of MS2 and Phi6 bacteriophages in synthetic sludge and anaerobically digested sludge from a wastewater treatment plant. We evaluated partitioning among the liquid, solids, and material surfaces of porcelain, concrete, polyvinyl chloride (PVC), and polypropylene. In all cases, at least 94% of the virions partitioned into the liquid fraction. In real sludge, no more than 0.8% of virions partitioned to the solids and no more than 6% to the material surface. Both MS2 and Phi6 partitioned more to the surface of concrete and polypropylene than to the surface of porcelain or PVC. Partitioning of viruses in wastewater among the liquid, biosolids, and material surface does not appear to mitigate the potential for aerosolization of virus, as most of the virus remains in the liquid phase.

Seasonal Dynamics of the Airborne Bacterial Community and Selected Viruses in a Children's Daycare Center.

Children's daycare centers appear to be hubs of respiratory infectious disease transmission, yet there is only limited information about the airborne microbial communities that are present in daycare centers. We have investigated the microbial community of the air in a daycare center, including seasonal dynamics in the bacterial community and the presence of specific viral pathogens. We collected filters from the heating, ventilation, and air conditioning (HVAC) system of a daycare center every two weeks over the course of a year. Amplifying and sequencing the 16S rRNA gene revealed that the air was dominated by Proteobacteria, Firmicutes, Actinobacteria, and Bacteroidetes that are commonly associated with the human skin flora. Clear seasonal differences in the microbial community were not evident; however, the community structure differed when the daycare center was closed and unoccupied for a 13-day period. These results suggest that human occupancy, rather than the environment, is the major driver in shaping the microbial community structure in the air of the daycare center. Using PCR for targeted viruses, we detected a seasonal pattern in the presence of respiratory syncytial virus that included the period of typical occurrence of the disease related to the virus; however, we did not detect the presence of adenovirus or rotavirus at any time.

Microbial community response of nitrifying sequencing batch reactors to silver, zero-valent iron, titanium dioxide and cerium dioxide nanomaterials.

As nanomaterials in consumer products increasingly enter wastewater treatment plants, there is concern that they may have adverse effects on biological wastewater treatment. Effects of silver (nanoAg), zero-valent iron (NZVI), titanium dioxide (nanoTiO2) and cerium dioxide (nanoCeO2) nanomaterials on nitrification and microbial community structure were examined in duplicate lab-scale nitrifying sequencing batch reactors (SBRs) relative to control SBRs that received no nanomaterials or ionic/bulk analogs. Nitrification function was not measurably inhibited in the SBRs by any of the materials as dosing was initiated at 0.1 mg/L and sequentially increased every 14 days to 1, 10, and 20 mg/L. However, SBRs rapidly lost nitrification function when the Ag⁺ experiment was repeated at a continuous high load of 20 mg/L. Shifts in microbial community structure and decreased microbial diversity were associated with both sequential and high loading of nanoAg and Ag⁺, with more pronounced effects for Ag⁺. Bacteroidetes became more dominant in SBRs dosed with Ag⁺, while Proteobacteria became more dominant in SBRs dosed with nanoAg. The two forms of silver also had distinct effects on specific bacterial genera. A decrease in nitrification gene markers (amoA) was observed in SBRs dosed with nanoAg and Ag⁺. In contrast, impacts of NZVI, nanoTiO2, nanoCeO2 and their analogs on microbial community structure and nitrification gene markers were limited. TEM-EDS analysis indicated that a large portion of nanoAg remained dispersed in the activated sludge and formed Ag­S complexes, while NZVI, nanoTiO2 and nanoCeO2 were mostly aggregated and chemically unmodified. Overall, this study suggests a high threshold of the four nanomaterials in terms of exerting adverse effects on nitrification function. However, distinct microbial community responses to nanoAg indicate potential long-term effects.

Oxidation of c60 aerosols by atmospherically relevant levels of o3.

Atmospheric processing of carbonaceous nanoparticles (CNPs) may play an important role in determining their fate and environmental impacts. This work investigates the reaction between aerosolized C60 and atmospherically relevant mixing ratios of O3 at differing levels of humidity. Results indicate that C60 is oxidized by O3 and forms a variety of oxygen-containing functional groups on the aerosol surface, including C60O, C60O2, and C60O3. The pseudo-first-order reaction rate between C60 and O3 ranges from 9 × 10(-6) to 2 × 10(-5) s(-1). The reaction is likely to be limited to the aerosol surface. Exposure to O3 increases the oxidative stress exerted by the C60 aerosols as measured by the dichlorofluorescein acellular assay but not by the uric acid, ascorbic acid, glutathione, or dithiothreitol assays. The initial prevalence of C60O and C60O2 as intermediate products is enhanced at higher humidity, as is the surface oxygen content of the aerosols. These results show that C60 can be oxidized when exposed to O3 under ambient conditions, such as those found in environmental, laboratory, and industrial settings.

Characterizing gas-particle interactions of phthalate plasticizer emitted from vinyl flooring.

Phthalates are widely used as plasticizers, and improved ability to predict emissions of phthalates is of interest because of concern about their health effects. An experimental chamber was used to measure emissions of di-2-ethylhexyl-phthalate (DEHP) from vinyl flooring, with ammonium sulfate particles introduced to examine their influence on the emission rate and to measure the partitioning of DEHP onto airborne particles. When particles were introduced to the chamber at concentrations of 100 to 245 µg/m(3), the total (gas + particle) DEHP concentrations increased by a factor of 3 to 8; under these conditions, emissions were significantly enhanced compared to the condition without particles. The measured DEHP partition coefficient to ammonium sulfate particles with a median diameter of 45 ± 5 nm was 0.032 ± 0.003 m(3)/µg (95% confidence interval). The DEHP-particle sorption equilibration time was demonstrated to be less than 1 min. Both the partition coefficient and equilibration time agree well with predictions from the literature. This study represents the first known measurements of the particle-gas partition coefficient for DEHP. Furthermore, the results demonstrate that the emission rate of DEHP is substantially enhanced in the presence of particles. The particles rapidly sorb DEHP from the gas phase, allowing more to be emitted from the source, and also appear to enhance the convective mass-transfer coefficient itself. Airborne particles can influence SVOC fate and transport in the indoor environment, and these mechanisms must be considered in evaluating exposure and human health.