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Atmospheric particulate matter is a concern in most of the European towns because it has potential negative effects on human health (Davidson et al., 2005; Lelieveld et al., 2015). Although the toxic effects of PM have been correlated with some of its chemical and physical properties, the toxicity mechanisms are not yet fully known. Different in vitro toxicological tests are often necessary to characterise potential health effects and, often, it is found significant correlation only among a few of the possible tests. In addition, contrasting results could be obtained comparing in vitro tests with acellular assays like those used to determine oxidative potential (Steenhof et al., 2011; Van Den Heuvel et al., 2018). The aim of the work was to study the oxidative potential (OP) of PM10, determined with the acellular DTT assay, in relationship with its ecotoxicological and cytotoxicological potential. The study was carried out on aqueous extracts of 10 samples of airborne PM10 randomly selected among the samples collected between 16/09/2017 and 25/12/2017. Samples were collected using a low-volume (2.3 m3 /h) sampler (SWAM, Fai Instruments srl) on 47 mm quartz fibre filters (Whatman) pre-fired at 700 °C for 2 hours in order to reduce contamination. Samples were exposed for 24 hours (starting at midnight) at the Environmental-Climate Observatory of ISAC-CNR in Lecce (Southern Italy), regional station of the Global Atmosphere Watch (GAW) network, characterised as an urban background site (Cesari et al., 2018). The aqueous extraction was performed in an ultrasonic bath for 80 min using 10 ml Milli-Q water. The ecotoxicological potential of PM10 was assessed by the bioluminescence inhibition assay based on the Gram-negative non-pathogenic bacterium Vibrio fischeri (Microtox® test), which physiologically emits light as a results of its metabolic activity. The natural bioluminescence of V. fisheri is inhibited by the exposure to a number of chemical pollutants, including organic and inorganic compounds (Abbass et al., 2018). Different exposure times (5, 15, and 30 mins) were used and inhibition results, obtained with five repetitions, are reported as a net effect corrected using field blanks. The cytotoxicological potential of PM10 was assessed on the same extracts by the MTT assay on the cell line A549. The MTT assay is based on a colorimetric reaction dependent on mitochondrial respiration of the cells and indirectly allows assessing the cellular energy capacity of a cell (Stockert et al., 2012). The MTT assay was applied to the A549 cell line, representative of the alveolar type II pneumocytes of the human lung (Foster et al., 1998). Cell mortality after 24h exposition is evaluated, in relative terms, considering the net effect of PM10 using field blanks for correction. Six repetitions were done. The water-soluble fraction of PM10 was also used for the analysis of the OP, performed with the dithiothreitol assay (DTT), a surrogate for cellular antioxidants, which analyses the rate of DTT depletion catalysed by chemical species present in the PM (Chirizzi et al., 2017). An aliquot of the extracts was diluted with deionised water (1:4 factor). Diluted samples were incubated at 37 °C with DTT (0.1 mM) in 0.1 M potassium phosphate buffer at pH 7.4 for times varying from 5 to 90 min. At designated times (specifically at 5, 10, 15, 20, 30, 45, 60, and 90 min) an aliquot of incubation mixture was picked up and 10% trichloroacetic acid was added to stop the reaction. Then, this reaction mixture was mixed with a solution containing 10 mM DTNB. The concentration of the formed 5-mercapto-2-nitrobenzoic acid was measured by its optical density absorption at 412 nm using a Eon BioTek Microplate Spectrophotometer. The consumption of DTT over time was determined through the linear fitting of the absorbance with the time in which it was made the withdrawal. The DTT depletion rate was used to determine OP values as DTT-activity 21 normalized in terms of sampled air volume (OPV) or in terms of mass of collected aerosols (OPM). The OPV and OPM values were comparable with previous measurements in this area or in other Italian towns (Chirizzi et al., 2017). In all the 10 samples analysed a significant inhibition of the Vibrio fisheri bioluminescence was observed as a results of the exposure of bacteria to the undiluted extracts for 5, 15 and 30 min, suggesting the presence in the PM10 of components able to induce an ecotoxic effect. Four samples (samples n. 2,3,4, and 7) showed a % of inhibition ranging from 30% to 50%, ascribable to a slight toxic effect, while six samples (samples 1,5,6, 8,9, and 10) showed a % of inhibition above 50% after 30 min exposure, suggesting the presence of a toxic effect. The correlation analysis between the sampled mass and the Vibrio fisheri bioluminescence inhibition showed a significant positive correlation (p

Long and short-term exposure to atmospheric particulate matter (PM) has detrimental effects on human health. The effective mechanisms leading to PM toxicity are still not fully understood, even if it is known that physical-chemical properties, strongly influenced by sources and atmospheric processes, are known to play an important role. In this work, PM10 samples were collected, at an urban background site in southern Italy, to determine cytotoxicity (using MTT test on A549 cells), genotoxicity (using the comet assay), and intracellular oxidative stress on A549 cells exposed for 24 h to aqueous extracts of PM10 samples. Organic carbon (OC) and elemental carbon (EC) content of PM10 and acellular determination of oxidative potential with DTT assay were performed to compare results of acellular and cellular biological assays. Cellular (OSGCV and MTTV) and acellular (OPDTTV) outcomes, normalized in volume, are well correlated (statistically significant results) with carbon content suggesting that combustion sources play an important role in determining cellular oxidative stress and cytotoxicity of PM10. Even if the number of data is limited, genotoxicity results are well correlated (Pearson r &gt, 0.95) with OSGCV and MTTV, and a weaker, but statistically significant correlation was observed with OPDTTV. OSGCV is well correlated with the cell mortality observed with the MTTV test and a lower, but still statistically significant correlation is observed between MTTV and OPDDTV. A statistically significant correlation was found between OPDTTV and OSGCV results. When the outcomes of the cellular and acellular assay are compared normalized in mass (i.e., intrinsic values), the correlations become significantly weaker suggesting that the different sources acting on the site produces particulate matter with different toxicological potential influencing differently the biological tests studied.

Silica sheathed SnO 2 microcables were grown directly on a Si substrate via a simple one-step vapor phase method, with high yield and uniform distribution, using gold as a catalyst. The morphology, the microstructure and the chemical composition of the microcables were characterized by means of scanning electron microscopy coupled with an X-ray microanalysis equipment, transmission electron microscopy, selected area diffraction pattern, X-ray diffraction and UV–vis and Raman spectroscopies. A possible growth mechanism of the microcables was also proposed on the basis of study of the products obtained at different thermal treatment times in the furnace.