Nanoparticulate mineral UV filters, such as titanium dioxide (TiO2) nanocomposites, are being increasingly used in sunscreens as an alternative to organic UV filters. However, there is still a lack of understanding regarding their fate and behavior in aquatic environments and potential environmental impacts after being released from a bather's skin during recreational activities. In this work, we assessed the release, fate, and transformation of two commercial nanocomposite TiO2 UV filters, one hydrophobic and one hydrophilic, in ultrapure water and simulated fresh- and seawater. The hydrophobic TiO2 nanocomposite, T-SA, was coated with a primary Al2O3 photopassivation layer and a secondary stearic acid layer, while the hydrophilic TiO2 nanocomposite, T-SiO2, was coated with a single SiO2 photopassivation layer. The influence of the sunscreen formulation was examined by dispersing the TiO2 nanocomposites in their typical continuous phase (i.e., oil for T-SA and water for T-SiO2) before introduction into the aqueous system. After 48 h of aqueous aging and 48 h of settling, 88-99% of the hydrophobic T-SA remained floating on top of the water column in all aqueous systems. On the other hand, 100% of the hydrophilic T-SiO2 settled out of the water column in the fresh- and seawaters. With respect to the photopassivation coatings, no loss of the T-SA Al2O3 layer was detected after aqueous aging, but 99-100% dissolution of the SiO2 layer on the T-SiO2 nanocomposite was observed after 48 h in the fresh- and seawaters. This dissolution left behind T-SiO2 by-products exhibiting a photocatalytic activity similar to that of bare rutile TiO2. Overall, the results demonstrated that the TiO2 surface coating and sunscreen formulation type drive environmental behavior and fate and that loss of the passivation layer can result in potentially harmful, photoactive by-products. These insights will help guide regulations and assist manufacturers in developing more environmentally safe sunscreens.

Sunscreens are emulsions of water and oil that contain filters capable of protecting against the detrimental effects of ultraviolet radiation (UV). The widespread use of cosmetic products based on nanoparticulate UV filters has increased concerns regarding their safety and compatibility with both the environment and human health. In the present work, we evaluated the effects of titanium dioxide nanoparticle (TiO₂ NP)-based UV filters with three different surface coatings on the development and immunity of the sea urchin, Paracentrotus lividus. A wide range of NP concentrations was analyzed, corresponding to different levels of dilution starting from the original cosmetic dispersion. Variations in surface coating, concentration, particle shape, and pre-dispersant medium (i.e., water or oil) influenced the embryonic development without producing a relevant developmental impairment. The most common embryonic abnormalities were related to the skeletal growth and the presence of a few cells, which were presumably involved in the particle uptake. Adult P. lividus immune cells exposed to silica-coated TiO₂ NP-based filters showed a broad metabolic plasticity based on the biosynthesis of metabolites that mediate inflammation, phagocytosis, and antioxidant response. The results presented here highlight the biosafety of the TiO₂ NP-based UV filters toward sea urchin, and the importance of developing safer-by-design sunscreens.

During the decommissioning and removal of radioactive material in nuclear facilities, fine, tritiated dusts of stainless steel, cement or tungsten are generated that could be accidently released to the environment. However, the potential radio- and ecotoxicological effects these tritiated particles may have are unknown. In this study, stainless steel particles (SSPs) representative of those likely to be tritiated are manufactured by hydrogenation and their tissue-specific bioaccumulation, release (depuration) and subsequent genotoxic response have been studied in the marine mussel, Mytilus galloprovincialis, as a baseline for future assessments of the potential effects of tritiated SSPs. Exposure to 1000 μg L^-1 of SSPs and adopting Cr as a proxy for stainless steel revealed relatively rapid accumulation (∼5 h) in the various mussel tissues but mostly in the digestive gland. Over longer periods up to 18 days, SSPs were readily rejected and egested as faecal material. DNA strand breaks, as a measure of genotoxicity, were determined at each time point in mussel haemocytes using single cell gel electrophoresis, or the comet assay. Lack of chemical genotoxicity was attributed to the rapid processing of SSP particles and limited dissolution of elemental components of steel. Further work employing tritiated SSPs will enable radio-toxicology to be studied without the confounding effects of chemical toxicity.

Assessing the environmental risks of emerging contaminants related to new technologies remains a major challenge due to the diversity of pollutants, their complex interactions, and the limitations of conventional testing frameworks. Among these contaminants, engineered nanomaterials (ENMs) stand out for their unique surface reactivities and transformation pathways, which can significantly alter their behavior and that of co-occurring pollutants. Although many studies have addressed the toxicity and fate of individual ENMs, real-world scenarios often involve complex mixtures, whose combined effects are less investigated. This study addresses this gap by investigating the fate, behavior, and ecological impacts of a mixture of two representative metal oxide ENMs i.e. an industrial TiO₂ and a combustion-derived CeO₂. This study shows that under environmentally relevant conditions using freshwater mesocosms, these two ENMs undergo primary hetero-aggregation. Co-exposure of the freshwater snail Planorbarius corneus revealed that ENM aggregates (homo- or primary hetero-aggregates) interact with egg layings, potentially affecting early developmental stages, while slight but measurable uptakes were also observed in co-exposed adult snails. Importantly, no quenching of reactive oxygen species generated by the photocatalytic TiO₂ was detected in the presence of CeO₂, suggesting that the combusted CeO₂ does not mitigate potentially TiO₂-induced phototoxicity. These findings underscore the importance of considering ENM mixtures in environmental risk assessments and the relevance of mesocosm experiments to capture realistic exposure scenarios. Future studies should prioritize investigating how unique surface reactivities and transformation mechanisms of ENM mixtures shape their ecological impacts throughout their life cycles.