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Influence of non-degradable and degradable microplastics on the bioavailability of per- and polyfluoroalkyl substance in mice: Mechanism exploration

The Science of The Total Environment 2025 3 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 58 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Pengfei Zhou, Yi Kong, Dengke Zhang, Albert L. Juhasz, Qian Zhang, Qian Zhang, Xinyi Cui

Summary

Researchers studied how microplastics in food affect the body's absorption of per- and polyfluoroalkyl substances (PFAS), a class of persistent chemicals found in drinking water. They found that high doses of polystyrene microplastics significantly increased PFAS absorption in mice while reducing the amount excreted, essentially making these harmful chemicals more bioavailable. The study suggests that microplastics in the diet could amplify the health risks posed by co-occurring chemical contaminants.

Polymers
Models
Study Type In vivo

Per- and polyfluorinated alkyl substances (PFAS) contamination in drinking water and their associated health risks have received extensive global attention. Microplastics (MPs), which commonly coexist with PFAS in the daily diet, remain poorly understood in terms of their effects on PFAS bioavailability. Here, we investigated the effect of non-biodegradable (PS) and biodegradable (PBS) MPs on PFAS bioavailability using a mouse model, with PFAS level in drinking water being at 20 μg/L. High-dose dietary MPs (50 mg/g) significantly increased PFAS bioavailability, especially for PS co-exposure (29.2 ± 5.09 % vs 19.4 ± 3.66 % in control, p < 0.05), while reducing fecal excretion by 0.34 and 0.31-fold (p < 0.05). Mechanistic studies showed that high-dose PS significantly (p < 0.05) increased mouse serum albumin concentrations, which were closely related with the in vivo absorption of PFAS. Both PS and PBS downregulated the expression of efflux proteins (Mrp2 and Mrp4) by 0.10-0.22 fold, thereby increasing PFAS bioavailability. Molecular docking further showed that legacy PFASs (PFOA and PFOS) exhibited higher binding affinities to transport-related proteins than emerging alternatives (HFPO-TA and 6:2 FTSA), explaining their greater susceptibility to MPs co-exposure. These findings provide novel mechanistic insights into the modulation of PFAS bioavailability by co-exposure of MPs. While high MP doses were used to elucidate the mechanism, future studies using environmentally relevant exposure levels are necessary to assess the health risks of PFAS-MP co-exposure and support science-based risk management.

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