An integrated assessment of ecological and human health risks of per- and polyfluoroalkyl substances through toxicity prediction approaches

生物累积 生物监测 大型水蚤 全氟辛酸 环境毒理学 环境化学 生物 水生毒理学 毒性 化学 有机化学
作者
Naima Hamid,Muhammad Junaid,Rakia Manzoor,Marriya Sultan,Meng Chuan Ong,Jun Wang
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:905: 167213-167213 被引量:24
标识
DOI:10.1016/j.scitotenv.2023.167213
摘要

Per- and polyfluoroalkyl substances (PFAS) are also known as “forever chemicals” due to their persistence and ubiquitous environmental distribution. This review aims to summarize the global PFAS distribution in surface water and identify its ecological and human risks through integrated assessment. Moreover, it provides a holistic insight into the studies highlighting the human biomonitoring and toxicological screening of PFAS in freshwater and marine species using quantitative structure-activity relationship (QSAR) based models. Literature showed that PFOA and PFOS were the most prevalent chemicals found in surface water. The highest PFAS levels were reported in the US, China, and Australia. The TEST model showed relatively low LC50 of PFDA and PFOS for Pimephales promelas (0.36 and 0.91 mg/L) and high bioaccumulation factors (518 and 921), revealing an elevated associated toxicity. The risk quotients (RQs) values for P. promelas and Daphnia magna were found to be 269 and 23.7 for PFOS. Studies confirmed that long-chain PFAS such as PFOS and PFOA undergo bioaccumulation in aquatic organisms and induce toxicological effects such as oxidative stress, transgenerational epigenetic effects, disturbed genetic and enzymatic responses, perturbed immune system, hepatotoxicity, neurobehavioral toxicity, altered genetic and enzymatic responses, and metabolism abnormalities. Human biomonitoring studies found the highest PFOS, PFOA, and PFHxS levels in urine, cerebrospinal fluid, and serum samples. Further, long-chain PFOA and PFOS exposure create severe health implications such as hyperuricemia, reduced birth weight, and immunotoxicity in humans. Molecular docking analysis revealed that short-chain PFBS (−11.84 Kcal/mol) and long-chain PFUnDA (−10.53 Kcal/mol) displayed the strongest binding interactions with human serum albumin protein. Lastly, research challenges and future perspectives for PFAS toxicological implications were also discussed, which helps to mitigate associated pollution and ecological risks.
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