4.8 Article

Significant Reductive Transformation of 6:2 Chlorinated Polyfluorooctane Ether Sulfonate to Form Hydrogen-Substituted Polyfluorooctane Ether Sulfonate and Their Toxicokinetics in Male Sprague-Dawley Rats

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 56, 期 10, 页码 6123-6132

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c00616

关键词

6; 2 Cl-PFESA; 6; 2 H-PFESA; biotransformation; reductive dechlorination; toxicokinetics; mammal

资金

  1. National Science Foundation of China (NSFC) [21737003, 41991313]
  2. Natural Science and Engineering Research Council of Canada (NSERC)

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The study found that 6:2 Cl-PFESA transformed into 6:2 H-PFESA as the sole metabolite in rat liver, with a reductive enzyme-dependent pathway. 6:2 H-PFESA was more prone to cumulative urinary excretion, suggesting a detoxification mechanism for organisms. The toxicokinetic properties of 6:2 Cl-PFESA and 6:2 H-PFESA were structure and dose dependent in blood and urine.
6:2 chlorinated polyfluorooctane ether sulfonate (6:2 Cl-PFESA) was previously shown to undergo limited dechlorination in rainbow trout to yield 6:2 hydrogen-substituted polyfluorooctane ether sulfonate (6:2 H-PFESA) as the sole metabolite. However, the biotransformation susceptibility of 6:2 Cl-PFESA has not been investigated in mammals and the biological behavior of 6:2 H-PFESA has not been defined in any species. We investigated the respective transformation products of 6:2 Cl-PFESA and 6:2 H-PFESA and their toxicokinetic properties in male Sprague-Dawley rats as a mammalian model. 6:2 H-PFESA was the sole detectable metabolite of 6:2 Cl-PFESA, with a transformation percentage of 13.6% in rat liver, but it resisted further degradation. 6:2 Cl-PFESA also transformed to 6:2 H-PFESA in reductive rat liver S9 incubations but remained stable under oxidative conditions, suggesting a reductive enzyme-dependent transformation pathway. 6:2 Cl-PFESA was more enriched in lipid-rich tissues, while 6:2 H-PFESA was more prone to cumulative urinary excretion. From this perspective, it may suggest a detoxification mechanism for organisms to form the less hydrophobic 6:2 H-PFESA to alleviate total burdens. To date, 6:2 Cl-PFESA was the second perfluoroalkyl acid reported to undergo biotransformation in mammals. The toxicokinetic properties determined for 6:2 Cl-PFESA and 6:2 H-PFESA in blood and urine were found to be structure and dose dependent.

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