Cited by 45Per- and polyfluoroalkyl substances researchEnvironmental Toxicology and EcotoxicologyToxic Organic Pollutants Impact

Tissue-specific uptake, depuration kinetics, and suspected metabolites of three emerging per- and polyfluoroalkyl substances (PFASs) in marine Medaka

Wang, Qi, Ruan, Yuefei, Jin, Linjie, Lin, Huiju, Yan, Meng, Gu, Jiarui, Yuen, Calista N. T., Leung, Kenneth M. Y. +1 more·2022·Environmental Science & Technology

Abstract

Restrictions on legacy per- and polyfluoroalkyl substances (PFASs) have led to the widespread use of emerging PFASs. However, their toxicokinetics have rarely been reported. Here, tissue-specific uptake and depuration kinetics of perfluoroethylcyclohexanesulfonate (PFECHS) and 6:2 and 8:2 chlorinated polyfluoroalkyl ether sulfonates (Cl-PFESAs) were studied in marine medaka ( Oryzias melastigma ). The fish were exposed to these substances for 28 days (0.2 μg/L), followed by a clearance period of 14 days. The depuration constant ( k d ) of PFECHS [0.103 ± 0.009 day -1 (mean ± standard deviation)] was reported for the first time. Among the six studied tissues, the highest concentrations of 6:2 Cl-PFESA, 8:2 Cl-PFESA, and PFECHS were found in the liver [1540, 1230, and 188 ng (g of wet weight) -1 , respectively] on day 28 while the longest residence times were found in the eyes ( t 1/2 values of 21.7 ± 4.3, 23.9 ± 1.5, and 17.3 ± 0.8 days, respectively). No significant positive correlation was found between the bioconcentration factors of the studied PFASs and the phospholipid or protein contents in different tissues of the studied fish. Potential metabolites of Cl-PFESAs, i.e., their hydrogen-substituted analogues (H-PFESAs), were identified by time-of-flight mass spectrometry. However, the biotransformation rates were low (<0.19%), indicating the poor capacity of marine medaka to metabolize Cl-PFESAs to H-PFESAs.

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Crossref · 10.1021/acs.est.1c07643

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  • Unlike other POPs, PFAS are found predominantly in protein-rich compartments (e.g., blood and liver) rather than in lipid-rich tissues in biota.

    “Unlike other POPs, PFAS are found predominantly in protein-rich compartments (e.g., blood and liver) rather than in lipid-rich tissues in biota”

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Authors
Wang, Q., Ruan, Y., Jin, L., Lin, H., Yan, M., Gu, J., Yuen, C. N. T., Leung, K. M. Y., & Lam, P. K. S.
Affiliations
  • City University of Hong Kong (HK)
  • State Key Laboratory of Marine Pollution (SKLMP) and Department of Chemistry, City University of Hong Kong, Hong Kong 999077, Hong Kong SAR, China
Corresponding author
  • Ruan, Yuefei
  • Lam, Paul K. S.
Venue
Environmental Science & Technology
Published
2022-04-19
Volume
56
Issue
10
Pages
6182-6191
ISSN
  • 0013-936X (ISSN-L)
  • 1520-5851
OpenAlex
W4224261055
Cited by
45
References
6
Citations by year
2026: 6 · 2025: 10 · 2024: 12 · 2023: 14 · 2022: 3
FWCI
3.46
Type
journal article
Language
en
Open access
closed
Locations
  • Environmental Science & Technology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Research Grants Council, University Grants Committee (T21-602/16-R)
  • Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (SMSEGL20SC02)
  • Science, Technology and Innovation Commission of Shenzhen Municipality (JCYJ20190812155805559)
  • National Natural Science Foundation of China (41806125)
  • Guangdong Basic and Applied Basic Research Foundation (2021A1515012048)
Topics
  • Physical Sciences › Environmental Science › Environmental Chemistry › Per- and polyfluoroalkyl substances research
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Environmental Toxicology and Ecotoxicology
  • Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Toxic Organic Pollutants Impact
Keywords
per- and polyfluoroalkyl substances, emerging PFASs, depuration kinetics, residence time, bioconcentration factor, tissue distribution, biotransformation, marine medaka, Oryzias melastigma
MeSH terms
Alkanesulfonates, Animals, China, Ether, Ethers, Fluorocarbons, Kinetics, Oryzias, Alkanesulfonic Acids

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