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Health impacts of PM
Residential wood combustion (RWC) is one of the largest sources of fine particles (PM2.5) in the Nordic cities. The current study aims to calculate the related health effects in four studied city areas in Sweden, Finland, Norway, and Denmark.
BioMed Central (BMC)
2022
Health impacts and air pollution - An exploration of factors influencing estimates of air pollution impact upon the health of European citizens. ETC/ACC Technical Paper, 2008/13
2008
2015
2009
Health and Exposure to VOCs From Pinewood in Indoor Environments
Frontiers Media S.A.
2019
The contaminant situation in the Norwegian-Russian border has caused concern for several decades and considerable amount of data has been gathered during the Pasvik programme (Stebel et al., 2007; Pasvik programme, 2008) for the environmental pollution, but not in this extent for food safety and potential human health risks in this region. Through the compiling of the available literature the authors of this report have identified a number of issues that need further attention.
2013
2021
2022
Hazard identification and safety assessment of the huge variety of nanomaterials (NMs), calls for robust and validated toxicity screening tests in combination with cheminformatics approaches to identify factors that can drive toxicity. Cytotoxicity and genotoxicity of seventeen JRC repository NMs, derived from titanium dioxide, zinc oxide, silver and silica, were tested in vitro using human lung alveolar epithelial cells A549. Cytotoxicity was assessed with the AlamarBlue (AB) and colony forming efficiency (CFE) assays, and genotoxicity by the enzyme-linked version of the comet assay. Nanoparticle tracking analysis (NTA) was used to measure size of the NMs in stock and in cell culture medium at different time points. Categorization and ranking of cytotoxic and genotoxic potential were performed (EU-NanoREG2 project approach). Descriptors for prediction of NMs toxicity were identified by quantitative structure-activity relationship (QSAR) analysis. Our results showed that ZnO NMs (NM-110 and NM-111), and Ag NMs (NM-300K and NM-302) were cytotoxic, while the TiO2 and SiO2 NMs were non-cytotoxic. Regarding genotoxicity, TiO2 NM-100, ZnO NM-110, SiO2 NM-203 and Ag NM-300K were categorized as positive. Cheminformatics modeling identified electron properties and overall chemical reactivity as important descriptors for cytotoxic potential, HOMO-LUMO energy parameter, ionization potential, pristine size for the NMs´ genotoxic potential, and presence of surface coating as descriptor for induction of DNA oxidized base lesions.
Elsevier
2022
Background
Hazard and risk assessment of nanomaterials (NMs) face challenges due to, among others, the numerous existing nanoforms, discordant data and conflicting results found in the literature, and specific challenges in the application of strategies such as grouping and read-across, emphasizing the need for New Approach Methodologies (NAMs) to support Next Generation Risk Assessment (NGRA). Here these challenges are addressed in a study that couples physico-chemical characterization with in vitro investigations and in silico similarity analyses for nine nanoforms, having different chemical composition, sizes, aggregation states and shapes. For cytotoxicity assessment, three methods (Alamar Blue, Colony Forming Efficiency, and Electric Cell-Substrate Impedance Sensing) are applied in a cross-validation approach to support NAMs implementation into NGRA.
Results
The results highlight the role of physico-chemical properties in eliciting biological responses. Uptake studies reveal distinct cellular morphological changes. The cytotoxicity assessment shows varying responses among NMs, consistent among the three methods used, while only one nanoform gave a positive response in the genotoxicity assessment performed by comet assay.
Conclusions
The study highlights the potential of in silico models to effectively identify biologically active nanoforms based on their physico-chemical properties, reinforcing previous knowledge on the relevance of certain properties, such as aspect ratio. The potential of implementing in vitro methods into NGRA is underlined, cross-validating three cytotoxicity assessment methods, and showcasing their strength in terms of sensitivity and suitability for the testing of NMs.
BioMed Central (BMC)
2024
2022
The movement towards an animal-free testing approach for risk assessment represents a key paradigm shift in toxicology. Risk assessment of engineered and anthropogenic nanoscale materials (NM) is dependent on reliable hazard characterization, which requires validated test methods and models, and increasingly on mechanistic insights into the mode of action. The properties that make NMs so advantageous for a wide range of commercial and industrial applications also pose a challenge when it comes to safety testing under in vitro and in chemico experimental settings. Their large reactive surface area makes NMs prone to interactions with assay reagents, readout signals, or intermediate steps of many test assays, leading to the potential for biased results and data inconsistencies, collectively referred to as interferences. Therefore, methods and protocols developed and validated for conventional chemicals often require adaptation and checking for reliability in NMs' toxicity assessment. This review presents the collected scientific knowledge on NMs-induced interferences for the most common in vitro toxicity assays and methods related to cytotoxicity, oxidative stress and inflammatory response evaluation. Our analysis of existing scientific literature showed that the challenge of NMs-induced interference was not explicitly addressed in more than 90% of the papers published up to 2014 reporting the safety and toxicity of NMs. In later years, increasing number of studies tackled the interference challenge in toxicity testing of NMs, which initiated exhaustive work on standardization and validation of existing regulatory-relevant in vitro test protocols and guidelines. Due to the specificity of the different NMs and the range of ways they can potentially interfere with in vitro assays, interference and fit-for purpose controls should be included for each NM type and method applied, unless label-free assays are selected. Here, we provide a decision tree to guide researchers on how to design experiments to avoid interferences during in vitro testing by taking appropriate mitigation actions and how to include proper interference controls in their experimental design where complete avoidance is not possible. The application of this decision tree will improve the reliability, comparability and reusability of in vitro toxicity data on engineered NMs or ENMs, increasing the relevance of in silico hazard data for use in risk assessment and in science-based risk governance of NMs. The approach is applicable more broadly also, to advanced materials and to hazard assessment of anthropogenic nanoscale materials such as microplastic and tyre-wear particles.
Elsevier
2024
2025
2025
2022
Hazard and exposure assessment of do-it-yourself products forimpregnation
A large number of do-it-yourself impregnation products are marketed to Danish consumers. The products are typically used for re-impregnation of consumer products (e.g. footware and outdoor clothing) immediately after the products have been purchased or when the water and/or dirt-repellent effect begins to diminish.
The Danish Environmental Protection Agency has chosen to make a survey of the market, where 110 do-it-yourself impregnation products were identified within ten different application categories. Out of these products, 14 were included in initial chemical content analyzes, as well as hazard and exposure analyzes. The main components in the majority of the products were saturated hydrocarbons, but some of the products also contained oxygen-containing solvents (e.g. alcohols, ethers, esters or ketones). The potential hazard of 12 of the 14 selected impregnation spray products was performed by measuring acute respiratory toxicity. Of the 12 products tested, 10 inhibited the function of the lung surfactant and may therefore potentially be harmful by inhalation.
On the basis of this study, it could not be demonstrated that the products with PFAS resulted in an inhibition of the lung surfactant at lower doses as compared to products without PFAS; in fact, the lowest inhibitory doses were seen for impregnating agents based on siloxanes/silicones. The results show that the hazardous properties of an impregnation product cannot be determined solely on the basis of the ingredients, and it is therefore necessary to examine the ability of the individual products to inhibit the lung surfactant in connection with a hazard assessment.
Danish Environmental Protection Agency
2023
2011