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Microplastics-sorbed phenanthrene and its derivatives are highly bioaccessible and may induce human cancer risks

Environment International 2022 75 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Xiaojie Hu, Qing Yu Jian Wang, Xiaojie Hu, Michael Gatheru Waigi, Michael Gatheru Waigi, Chao Qin, Jian Wang, Yanzheng Gao, Qing Yu Wanting Ling, Chao Qin, Jian Wang, Chao Qin, Xiaojie Hu, Jian Wang, Yanzheng Gao, Jian Wang, Wanting Ling, Qing Yu Yanzheng Gao, Qing Yu

Summary

Researchers studied how microplastics sorb phenanthrene and its derivatives, then measured the bioaccessibility and potential cancer risk of these contaminant-laden particles. The study found that microplastic-sorbed polycyclic aromatic hydrocarbons were highly bioaccessible during simulated digestion, suggesting they may pose meaningful human health risks when ingested.

Body Systems

Microplastics (MPs) are ubiquitous in environmental media and human diets and can enrich organic contaminants, including polycyclic aromatic hydrocarbons (PAHs) and their derivatives. The bioaccessibilities and triggering cancer risks of MP-sorbed PAHs and PAH derivatives are closely linked with human health, which, however, were rarely focused on. This study explored the sorption behaviors of phenanthrene (PHE) and PHE derivatives on polyethylene (PE), polypropylene (PP), and polystyrene (PS) MPs, and assessed their bioaccessibilities in gastrointestinal fluids as well as their inducing human cancer risks. PE MPs harbored the highest sorption capacity, secondly the PP MPs, then the PS ones. Sorption of PHE and PHE derivatives on MPs was positively correlated with their hydrophobicities. The bioaccessibilities of sorbed PHE and PHE derivatives could reach 53.59 %±0.46 %-90.28 %±0.92 % in gastrointestinal fluids and 81.34 %±0.77 %-98.72 %±1.44 % in gastrointestinal fluids with the addition of Tenax (more close to the bioavailability). The hydrophobicities also controlled the bioaccessibilities of PHE and PHE derivatives in gastric fluids, and those in intestinal fluids with Tenax for PS MPs. The incremental lifetime cancer risk (ILCR) values for PHE, PHE-Cl, and PHE-NO<sub>2</sub> on MPs at tested concentrations were all higher than the USEPA-suggested safety limit (10<sup>-6</sup>), and most of them were even higher than 10<sup>-4</sup>, which thus indicates serious cancer risks. This study promoted our understanding of the potential health threats posed by organic pollutant-bearing MPs in the environment.

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