Construction of an In Vitro Air-Liquid Interface Exposure System to Assess the Toxicological Impact of Gas and Particle Phase of Semi-Volatile Organic Compounds.

Anthropogenic activities and industrialization render continuous human exposure to semi-volatile organic compounds (SVOCs) inevitable. Occupational monitoring and safety implementations consider the inhalation exposure of SVOCs as critically relevant. Due to the inherent properties of SVOCs as gas/particle mixtures, risk assessment strategies should consider particle size-segregated SVOC association and the relevance of released gas phase fractions. We constructed an in vitro air-liquid interface (ALI) exposure system to study the distinct toxic effects of the gas and particle phases of the model SVOC dibutyl phthalate (DBP) in A549 human lung epithelial cells. Cytotoxicity was evaluated and genotoxic effects were measured by the alkaline and enzyme versions of the comet assay. Deposited doses were assessed by model calculations and chemical analysis using liquid chromatography tandem mass spectrometry. The novel ALI exposure system was successfully implemented and revealed the distinct genotoxic effects of the gas and particle phases of DBP. The empirical measurements of cellular deposition and the model calculations of the DBP particle phase were concordant.The model SVOC DBP showed that inferred oxidative DNA damage may be attributed to particle-related effects. While pure gas phase exposure may follow a distinct mechanism of genotoxicity, the contribution of the gas phase to total aerosol was comparably low.

Novel Graphene Wool Gas Adsorbent for Volatile and Semivolatile Organic Compounds.

Volatile and semivolatile organic compounds in ambient air and occupational settings are of great concern due to their associated adverse human health and environmental impacts. Novel graphene wool samplers have been developed and tested to overcome limitations of commercially available sorbents that can only be used once and typically require solvent extraction. Graphene wool (GW) was synthesized by non-catalytic chemical vapor deposition with optimized conditions, resulting in a novel fibrous graphene wool that is very easy to manage and less rigid than other forms of graphene, lending itself to a wide range of potential applications. Here, the air pollutant sampling capabilities of the GW were of interest. The optimal packing weight of GW inside a glass tube (length 178 mm, i.d. 4 mm, o.d. 6 mm) was investigated by the adsorption of vaporized alkane standards on the GW, using a condensation aerosol generator in a temperature-controlled chamber and subsequent detection using a flame ionization detector. The optimized GW packing density was found to be 0.19 mg mm-3 at a flow rate of 500 mL min-1, which provided a gas collection efficiency of >90% for octane, decane, and hexadecane. The humidity uptake of the sampler is less than 1% (m/m) for ambient humidities <70%. Breakthrough studies showed the favorable adsorption of polar molecules, which is attributed to the defective nature of the graphene and the inhomogeneous coating of the graphene layers on the quartz wool, suggesting that the polar versus non-polar uptake potential of the GW can be tuned by varying the graphene layering on the quartz wool substrate during synthesis. Oxidized domains at the irregular edges of the graphene layers, due to a broken, non-pristine sp2 carbon network, allow for adsorption of polar molecules. The GW was applied and used in a combustion sampling campaign where the samplers proved to be comparable to frequently used polydimethylsiloxane sorbents in terms of sampling and thermal desorption of non-polar semivolatile organic compounds. The total alkane concentrations detected after thermal desorption of GW and PDMS samplers were found to be 17.96 ± 13.27 and 18.30 ± 16.42 µg m-3, respectively; thus, the difference in the alkane sampling concentration between the two sorbent systems was negligible. GW provides a new, exciting possibility for the monitoring of organic air pollutants with numerous advantages, including high sampling efficiencies, simple and cost-effective synthesis of the thermally stable GW, solvent-free and environmentally friendly analysis, and, importantly, the reusability of samplers.

In vitro genotoxicity of dibutyl phthalate on A549 lung cells at air-liquid interface in exposure concentrations relevant at workplaces.

The ubiquitous use of phthalates in various materials and the knowledge about their potential adverse effects is of great concern for human health. Several studies have uncovered their role in carcinogenic events and suggest various phthalate-associated adverse health effects that include pulmonary diseases. However, only limited information on pulmonary toxicity is available considering inhalation of phthalates as the route of exposure. While in vitro studies are often based on submerged exposures, this study aimed to expose A549 alveolar epithelial cells at the air-liquid interface (ALI) to unravel the genotoxic and oxidative stress-inducing potential of dibutyl phthalate (DBP) with concentrations relevant at occupational settings. Within this scope, a computer modeling approach calculating alveolar deposition of DBP particles in the human lung was used to define in vitro ALI exposure conditions comparable to potential occupational DBP exposures. The deposited mass of DBP ranged from 0.03 to 20 ng/cm2 , which was comparable to results of a human lung particle deposition model using an 8 h workplace threshold limit value of 580 µg/m3 proposed by the Scientific Committee on Occupational Exposure Limits for the European Union. Comet and Micronucleus assay revealed that DBP induced genotoxicity at DNA and chromosome level in sub-cytotoxic conditions. Since genomic instability was accompanied by increased generation of the lipid peroxidation marker malondialdehyde, oxidative stress might play an important role in phthalate-induced genotoxicity. The results highlight the importance of adapting in vitro studies to exposure scenarios relevant at occupational settings and reconsidering occupational exposure limits for DBP.

Development of a Personal Aerosol Sampler for Monitoring the Particle-Vapour Fractionation of SVOCs in Workplaces.

Semi-volatile organic compounds (SVOCs), partitioned between particulates and vapours of an aerosol, require special attention. The toxicological effects caused by the inhalation of such aerosols may depend on the concentration and in which phase the organic compounds are found. A personal denuder-gas-particle separation aerosol sampler was developed to provide information about the partitioning of aerosols from organic compounds. The sampler was tested in a series of controlled laboratory experiments, which confirmed the capability and accuracy of the sampler to measure gas-particle mixtures. An average difference of 14.8 ± 4.8% was found between sampler and reference laboratory instruments. The obtained results showed that our sampler enables a more accurate measurement of the SVOC aerosols' gas-particle fractionation, compared with that of conventional samplers.

Carbonaceous Monolithic Multi-Channel Denuders as Vapour-Particle Partitioning Tools for the Occupational Sampling of Semi-Volatile Organic Compounds.

Denuders are gas-particle partitioning tools and can be used in combination with filters and adsorbers for phase-separated collection of hazardous semi-volatile organic compound (SVOC) aerosols. Here, we investigated the suitability of carbonaceous monolithic multi-channel denuders for this approach. Particle transmission efficiency through the denuders was investigated using particles of polystyrene latex (PSL) and droplets of n-hexadecane and diethylene glycol. The time-dependent vapour collection efficiency was analysed for n-hexadecane and diethylene glycol vapours and also compared to calculated predictions. Our measurements showed an averaged transmission efficiency of 97 ± 4.4% for PSL particles with diameters of 0.51, 0.99, 1.93, and 3.00 µm. Measurements with one denuder and 1.08, 1.98, and 2.97 µm particles consisting of n-hexadecane or diethylene glycol resulted in an averaged transmission efficiency of 99 ± 6.5%. Regarding the vapour collection efficiency at a flow rate of 5 l min-1, n-hexadecane vapour could be adsorbed to a similar extent (91 ± 1.4% for one denuder, 98 ± 0.3% for two denuders) as diethylene glycol vapour (93 ± 1.8% for one denuder, 97 ± 0.9% for two denuders). The comparison between experimental and theoretical vapour collection efficiencies revealed differences around 2.8% for n-hexadecane and around 12.3% for diethylene glycol. The results show that the tested denuders can be used as vapour collection tools for SVOCs, and can be integrated in currently used personal air samplers for separated vapour and particle collection.

Multi-channel silicone rubber traps as denuders for gas-particle partitioning of aerosols from semi-volatile organic compounds.

During many measurements it is important to account for possible changes in the gas-particle distribution of aerosols containing semi-volatile organic compounds (SVOCs). If denuders are combined with currently used personal air samplers, a simultaneous differential sampling of the gas and particle phase is possible. Here we analysed the transmission efficiency of denuders based on multi-channel silicone rubber traps (setup: 9 cm long glass liner (ID 4 mm), containing 22 parallel silicone rubber tubes (55 mm long, ID 0.3 mm, OD 0.5 mm)) with polystyrene latex (PSL) particles for different scenarios. n-Hexadecane, dimethyl phthalate and diethylene glycol gases were used to measure the time-dependent gas phase collection efficiency of a denuder. Additionally, the evaporation of n-hexadecane aerosol particles passing through the denuders was investigated. Our results showed high transmission efficiencies from 91 to 100% (variation coefficients 3.69-9.65%) for the denuders operated vertically at a flow rate of 0.5 l min-1. With regard to the gas phase collection efficiency, nonpolar n-hexadecane gas was trapped with higher efficiency (87% after 22 h) than dimethyl phthalate gas (27% after 22 h), while for highly polar diethylene glycol the gas phase collection efficiency was 50% after 2 h. Regarding the evaporation of aerosol particles, smaller particles and lower flow rates led to higher particle volume reduction inside the denuders. In conclusion, the tested denuders are suitable for determining the gas-particle partitioning of SVOC aerosols of nonpolar substances and show above 90% transmission for all tested particle sizes.

Development and field testing of a miniaturized sampling system for simultaneous sampling of vapours and droplets.

The sampling of semi volatiles (SV) in workplaces may lead to different results as measurements may be affected by sampling bias. The new European Standard EN 13936 defines "semi-volatiles" as substances with vapour pressures in the range between 0.001 and 100 Pa at room temperature. EN 13936 regulates the basic requirements for SV compounds that can occur as vapour and particle at the same time. Vapour and particles shall not be sampled separately and particles have to be sampled as inhalable fraction. Following EN 13936, the Institute for Occupational Safety and Health (Institut für Arbeitsschutz - IFA) has developed a miniaturized droplet-vapour sampler (GGP-Mini) which is designed to sample the inhalable aerosol fraction at low flow rates. The GGP-Mini uses 13 mm filters for particle sampling combined with adsorption tubes for vapour sampling. Laboratory tests were performed on 11 polar and non-polar compounds in a boiling point range from 188 °C to 318 °C. The substances were spiked directly on the filter followed by aspiration of 40 litres of air. Substances with boiling points below 230 °C were almost completely evaporated. Substances with boiling points above 230 °C up to 300 °C were found on both filter and charcoal tube. Lower-volatile compounds remained almost completely on the filter. For polar substances, the atmospheric humidity had a considerable influence upon the distribution of the liquid and vaporous components. A strong influence of the sampling temperature was found in the range from 0 °C to 50 °C. Droplet-vapour mixtures of n-hexadecane and diethylene glycol with droplet sizes between 1 µm and 4 µm were generated in a flow tube to verify the laboratory results. The aerosol concentrations were analysed on-line with a particle sizer and a flame ionisation detector, while parallel off-line samples were taken with the GGP-Mini. Evaporation losses from filters could be studied by comparing the on-line with off-line measurements. All sampling simulations, both spiking and tests on a droplet aerosol, have shown that the distribution between vapour and droplets is not constant and influenced e. g. by volatility, concentration, temperature and humidity. Only the sum of vapour and droplets constitutes a reproducible result.

An evaluation of the "GGP" personal samplers under semi-volatile aerosols: sampling losses and their implication on occupational risk assessment.

Semi-volatile (SV) aerosols still represent an important challenge to occupational hygienists due to toxicological and sampling issues. Particularly problematic is the sampling of hazardous SV that are present in both particulate and vapour phases at a workplace. In this study we investigate the potential evaporation losses of SV aerosols when using off-line filter-adsorber personal samplers. Furthermore, we provide experimental data showing the extent of the evaporation loss that can bias the workplace risk assessment. An experimental apparatus consisting of an aerosol generator, a flow tube and an aerosol monitoring and sampling system was set up inside a temperature controlled chamber. Aerosols from three n-alkanes were generated, diluted with nitrogen and sampled using on-line and off-line filter-adsorber methods. Parallel measurements using the on-line and off-line methods were conducted to quantify the bias induced by filter sampling. Additionally, two mineral oils of different volatility were spiked on filters and monitored for evaporation depending on the samplers flow rate. No significant differences between the on-line and off-line methods were detected for the sum of particles and vapour. The filter-adsorber method however tended to underestimate up to 100% of the particle mass, especially for the more volatile compounds and lower concentrations. The off-line sampling method systematically returned lower particle and higher vapour values, an indication for particle evaporation losses. We conclude that using only filter sampling for the assessment of semi-volatiles may considerably underestimate the presence of the particulate phase due to evaporation. Thus, this underestimation can have a negative impact on the occupational risk assessment if the evaporated particle mass is no longer quantified.