RESUMO
Secondary organic matter (SOM) formed from gaseous precursors constitutes a major mass fraction of fine particulate matter. However, there is only limited evidence on its toxicological impact. In this study, air-liquid interface cultures of human bronchial epithelia were exposed to different series of fresh and aged soot particles generated by a miniCAST burner combined with a micro smog chamber (MSC). Soot cores with geometric mean mobility diameters of 30 and 90 nm were coated with increasing amounts of SOM, generated from the photo-oxidation of mesitylene and ozonolysis of α-pinene. At 24 h after exposure, the release of lactate dehydrogenase (LDH), indicating cell membrane damage, was measured and proteome analysis, i.e. the release of 102 cytokines and chemokines to assess the inflammatory response, was performed. The data indicate that the presence of the SOM coating and its bioavailability play an important role in cytotoxicity. In particular, LDH release increased with increasing SOM mass/total particle mass ratio, but only when SOM had condensed on the outer surface of the soot cores. Proteome analysis provided further evidence for substantial interference of coated particles with essential properties of the respiratory epithelium as a barrier as well as affecting cell remodeling and inflammatory activity.
Assuntos
Poluentes Atmosféricos , Fuligem , Humanos , Idoso , Poluentes Atmosféricos/toxicidade , Proteoma , Material Particulado/toxicidade , Mucosa Respiratória , Tamanho da PartículaRESUMO
In this study, we present a custom-made facility developed for evaluating the measurement efficiency of optical particle counters and other common aerosol instrumentation. The facility consists of an aerosol generation setup, a turbulent flow tube for particle homogenization, isokinetic sampling ports, and a home-built particle counter that serves as a reference instrument. Stable and reproducible aerosols of polystyrene latex particles can be produced in the size range 100 nm-10 µm and at concentrations between 0.5 cm-3 and a few thousand submicron particles per cm3 or a few tens of 10 µm particles per cm3. The flow characteristics in the homogenizer were investigated with laser Doppler velocimetry measurements and computational fluid dynamics simulations indicating a plug (turbulent) flow at the aerosol sampling location. The particle mixing characteristics were determined experimentally at various heights of the flow tube by parallel measurements with two condensation particle counters. A spatial homogeneity within 1.1% was found across the sampling area. The measurement uncertainties in the determination of the particle number concentration have been evaluated in detail and amount typically to 5.4% at 1 cm-3 and 2.1% at 100 cm-3 (95% confidence level).
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The industrial exploitation of high value nanoparticles is in need of robust measurement methods to increase the control over product manufacturing and to implement quality assurance. InNanoPart, a European metrology project responded to these needs by developing methods for the measurement of particle size, concentration, agglomeration, surface chemistry and shell thickness. This paper illustrates the advancements this project produced for the traceable measurement of nanoparticle number concentration in liquids through small angle X-ray scattering (SAXS) and single particle inductively coupled plasma mass spectrometry (spICPMS). It also details the validation of a range of laboratory methods, including particle tracking analysis (PTA), dynamic light scattering (DLS), differential centrifugal sedimentation (DCS), ultraviolet visible spectroscopy (UV-vis) and electrospray-differential mobility analysis with a condensation particle counter (ES-DMA-CPC). We used a set of spherical gold nanoparticles with nominal diameters between 10 nm and 100 nm and discuss the results from the various techniques along with the associated uncertainty budgets.
RESUMO
The authors wish to make the following corrections to this paper [...].