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The European Food Safety Authority (EFSA) has a goal to efficiently conduct aggregate exposure assessments (AEAs) for chemicals using both exposure models and human biomonitoring (HBM) data by 2030. To achieve EFSA's vision, a roadmap for action for advancing aggregate exposure (AE) in the EU was developed. This roadmap was created by performing a series of engagement and data collection activities to map the currently available methods, data, and tools for assessing AE of chemicals, against the needs and priorities of EFSA. This allowed for the creation of a AEA framework, identification of data and knowledge gaps in our current capabilities, and identification of the challenges and blockers that would hinder efforts to fill the gaps. The roadmap identifies interdependent working areas (WAs) where additional research and development are required to achieve EFSA's goal. It also proposes future collaboration opportunities and recommends several project proposals to meet EFSA's goals. Eight proposal projects supported by SWOT analysis are presented for EFSA's consideration. The project proposals inform high‐level recommendations for multi‐annual and multi‐partner projects. Recommendations to improve stakeholder engagement and communication of EFSA's work on AEA were gathered by surveying stakeholders on specific actions to improve EFSA's communication on AE, including webinars, virtual training, social media channels, and newsletters. [ABSTRACT FROM AUTHOR]

Characterization of toxicogenomic signatures of carcinogen exposure holds significant promise for mechanistic and predictive toxicology. In vitro transcriptomic studies allow the comparison of the response to chemicals with diverse mode of actions under controlled experimental conditions. We conducted an in vitro study in TK6 cells to characterize gene expression signatures of exposure to 15 genotoxic carcinogens frequently used in European industries. We also examined the dose-responsive changes in gene expression, and perturbation of biochemical pathways in response to these carcinogens. TK6 cells were exposed at 3 dose levels for 24 h with and without S9 human metabolic mix. Since S9 had an impact on gene expression (885 genes), we analyzed the gene expression data from cells cultures incubated with S9 and without S9 independently. The ribosome pathway was affected by all chemical-dose combinations. However in general, no similar gene expression was observed among carcinogens. Further, pathways, i.e. cell cycle, DNA repair mechanisms, RNA degradation, that were common within sets of chemical-dose combination were suggested by clustergram. Linear trends in dose-response of gene expression were observed for Trichloroethylene, Benz[a]anthracene, Epichlorohydrin, Benzene, and Hydroquinone. The significantly altered genes were involved in the regulation of (anti-) apoptosis, maintenance of cell survival, tumor necrosis factor-related pathways and immune response, in agreement with several other studies. Similarly in S9+ cultures, Benz[a]pyrene, Styrene and Trichloroethylene each modified over 1000 genes at high concentrations. Our findings expand our understanding of the transcriptomic response to genotoxic carcinogens, revealing the alteration of diverse sets of genes and pathways involved in cellular homeostasis and cell cycle control.

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Rising plastic consumption leads to widespread microplastic (MP) contamination. Raman spectroscopy is widely used for MP identification due to its ability to analyse particles as small as 1 μm. However, it faces challenges such as interference from pigments and additives. In this study, we aim to assess the accuracy of Raman micro-spectroscopy in identifying coloured plastic samples by applying various oxidative treatments to eliminate the possible interference effect caused by colourants associated with the sample. Standard and coloured microplastics were analysed using a Raman imaging microscope. Coloured plastics were treated with H 2 O 2 30%, Sodium hypochlorite 5%, and Fenton reagent (H2O2 30% and Ferrous sulphate 0.2 M) for 24, 48, and 72 h. The Raman spectra were acquired after treatment to assess the impact of the treatment procedure on the polymer identification. Our results revealed that colourants significantly impact Raman spectra by peak broadening and/or fluorescence effects, which reduces identification accuracy and match scores Red pigments particularly obscure polymer identification. Treatments like oxidation and Fenton's reagent showed limited effectiveness. Additives in plastic samples can affect the accuracy of polymer identification by the Raman spectroscopy technique. Common treatment procedures do not improve the accuracy of identification. In order to improve the reliability of Raman analysis, essential factors such as utilizing multiple excitation lasers and appropriate CCD detectors, establishing a comprehensive reference library of colourants and additives, and employing advanced techniques like time-gated Raman spectroscopy or Surface-Enhanced Raman Spectroscopy (SERS) should be considered. [Display omitted] • Polymer identification accuracy by Raman is affected by colourants used in plastic. • Colourants used in plastics can mask the identifying peaks of polymer. • Colourants used in plastics may increase the fluorescence effect in Raman Spectrum. • Oxidative treatments do not improve the identification accuracy by Raman. [ABSTRACT FROM AUTHOR]