Hazardous organic pollutants in indoor dust from elementary schools and kindergartens in Greece: Implications for children's health.

Children spend a significant portion of their day in school, where they may be exposed to hazardous organic compounds accumulated in indoor dust. The aim of this study was to evaluate the concentrations of major hazardous organic contaminants in dust collected from kindergartens and elementary schools in Northern Greece (n = 20). The sum concentrations of 20 targeted polybrominated diphenyl ether congeners (∑20PBDEs) in dust varied from 58 ng g-1 to 1480 ng g-1, while the sum of 4 novel brominated fire retardants (∑4NBFRs) ranged from 28 ng g-1 to 555 ng g-1. Correspondingly, the sum concentrations of phthalate esters (∑9PAEs) ranged between 265 µg g-1 and 2120 µg g-1, while the sum of organophosphate esters (∑11OPEs) was found between 2890 ng g-1 and 16,100 ng g-1. Finally, the sum concentrations of polycyclic aromatic hydrocarbons (∑16PAHs) were found within in the range 212 ng g-1 and 6960 ng g-1. Exposure to indoor dust contaminant via inhalation, ingestion and dermal absorption was investigated for children and adults (teachers). Carcinogenic and non-carcinogenic risks were also estimated. Children's estimated intakes of individual hazardous chemicals via the three exposure routes, were lower than the available health-based reference values.

Size-Resolved Redox Activity and Cytotoxicity of Water-Soluble Urban Atmospheric Particulate Matter: Assessing Contributions from Chemical Components.

Throughout the cold and the warm periods of 2020, chemical and toxicological characterization of the water-soluble fraction of size segregated particulate matter (PM) (<0.49, 0.49−0.95, 0.95−1.5, 1.5−3.0, 3.0−7.2 and >7.2 µm) was conducted in the urban agglomeration of Thessaloniki, northern Greece. Chemical analysis of the water-soluble PM fraction included water-soluble organic carbon (WSOC), humic-like substances (HULIS), and trace elements (V, Cr, Mn, Fe, Ni, Cu, Zn, As, Cd and Pb). The bulk (sum of all size fractions) concentrations of HULIS were 2.5 ± 0.5 and 1.2 ± 0.3 µg m−3, for the cold and warm sampling periods, respectively with highest values in the <0.49 µm particle size fraction. The total HULIS-C/WSOC ratio ranged from 17 to 26% for all sampling periods, confirming that HULIS are a significant part of WSOC. The most abundant water-soluble metals were Fe, Zn, Cu, and Mn. The oxidative PM activity was measured abiotically using the dithiothreitol (DTT) assay. In vitro cytotoxic responses were investigated using mitochondrial dehydrogenase (MTT). A significant positive correlation was found between OPmDTT, WSOC, HULIS and the MTT cytotoxicity of PM. Multiple Linear Regression (MLR) showed a good relationship between OPMDTT, HULIS and Cu.

Size-dependent in vitro inhalation bioaccessibility of PAHs and O/N PAHs - Implications to inhalation risk assessment.

Size segregated samples (<0.49, 0.49-0.95, 0.95-1.5, 1.5-3.0, 3.0-7.2 and > 7.2 µm) of atmospheric particulate matter (APM) were collected at a traffic site in the urban agglomeration of Thessaloniki, northern Greece, during the cold and the warm period of 2020. The solvent-extractable organic matter was analyzed for selected organic contaminants including polycyclic aromatic hydrocarbons (PAHs), and their nitro- and oxy-derivarives (NPAHs and OPAHs, respectively). Mean concentrations of ∑16PAHs, ∑6NPAHs and ∑10OPAHs associated to total suspended particles (TSP) were 18 ng m-3, 0.2 ng m-3 and 0.9 ng m-3, respectively, in the cold period exhibiting significant decrease (6.4, 0.2 and 0.09 ng m-3, respectively) in the warm period. The major amount of all compounds was found to be associated with the alveolar particle size fraction <0.49 µm. The inhalation bioaccessibility of PAHs and O/N PAHs was measured in vitro using two simulated lung fluids (SLFs), the Gamble's solution (GS) and the artificial lysosomal fluid (ALF). With both SLFs, the derived bioaccessible fractions (BAFs) followed the order PAHs > OPAHs > NPAHs. Although no clear dependence of bioaccessibility on particle size was obtained, increased bioaccessibility of PAHs and PAH derivatives in coarse particles (>7.2 µm) was evident. Bioaccessibility was found to be strongly related to the logKOW and the water solubility of individual compounds hindering limited mobilization of the most hydrophobic and less water-soluble compounds from APM to SLFs. The lifetime cancer risk due to inhalation exposure to bioaccessible PAHs, NPAHs and OPAHs was estimated and compared to those calculated from the particulate concentrations of organic contaminants.