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线性和支化全氟辛烷磺酸 (PFOS) 异构体模式在几种北极熊组织和血液中存在差异。

Linear and branched perfluorooctane sulfonate (PFOS) isomer patterns differ among several tissues and blood of polar bears.

机构信息

Ecotoxicology and Wildlife Health Division, Wildlife and Landscape Science Directorate, Science and Technology Branch, National Wildlife Research Centre, Environment Canada, Carleton University, Ottawa, ON K1A 0H3, Canada.

出版信息

Chemosphere. 2013 Sep;93(3):574-80. doi: 10.1016/j.chemosphere.2013.07.013. Epub 2013 Aug 3.

DOI:10.1016/j.chemosphere.2013.07.013
PMID:23920361
Abstract

Perfluorooctane sulfonate (PFOS) is a globally distributed persistent organic pollutant that has been found to bioaccumulate and biomagnify in aquatic food webs. Although principally in its linear isomeric configuration, 21-35% of the PFOS manufactured via electrochemical fluorination is produced as a branched structural isomer. PFOS isomer patterns were investigated in multiple tissues of polar bears (Ursus maritimus) from East Greenland. The liver (n = 9), blood (n = 19), brain (n = 16), muscle (n = 5), and adipose (n = 5) were analyzed for linear PFOS (n-PFOS), as well as multiple mono- and di-trifluoromethyl-substituted branched isomers. n-PFOS accounted for 93.0 ± 0.5% of Σ-PFOS isomer concentrations in the liver, whereas the proportion was significantly lower (p<0.05) in the blood (85.4 ± 0.5%). Branched isomers were quantifiable in the liver and blood, but not in the brain, muscle, or adipose. In both the liver and blood, 6-perfluoromethylheptane sulfonate (P6MHpS) was the dominant branched isomer (2.61 ± 0.10%, and 3.26 ± 0.13% of Σ-PFOS concentrations, respectively). No di-trifluoromethyl-substituted isomers were detectable in any of the tissues analyzed. These tissue-specific isomer patterns suggest isomer-specific pharmacokinetics, perhaps due to differences in protein affinities, and thus differences in protein interactions, as well transport, absorption, and/or metabolism in the body.

摘要

全氟辛烷磺酸 (PFOS) 是一种在全球范围内分布的持久性有机污染物,已被发现在水生食物网中生物积累和生物放大。尽管主要以线性异构体构型存在,但通过电化学氟化制造的 PFOS 中有 21-35% 是以支化结构异构体的形式产生的。在东格陵兰的北极熊 (Ursus maritimus) 的多个组织中研究了 PFOS 异构体模式。对 9 只肝脏 (n = 9)、19 只血液 (n = 19)、16 只大脑 (n = 16)、5 只肌肉 (n = 5) 和 5 只脂肪 (n = 5) 中的线性 PFOS (n-PFOS) 以及多种单-和二-三氟甲基取代的支化异构体进行了分析。n-PFOS 占肝脏中 Σ-PFOS 异构体浓度的 93.0 ± 0.5%,而在血液中的比例明显较低 (p<0.05) (85.4 ± 0.5%)。支化异构体在肝脏和血液中是可量化的,但在大脑、肌肉或脂肪中则不可量化。在肝脏和血液中,6-全氟甲基庚烷磺酸 (P6MHpS) 是主要的支化异构体 (分别占 Σ-PFOS 浓度的 2.61 ± 0.10%和 3.26 ± 0.13%)。在所分析的组织中均未检测到二-三氟甲基取代的异构体。这些组织特异性的异构体模式表明存在异构体特异性的药代动力学,这可能是由于蛋白质亲和力的差异,从而导致蛋白质相互作用、以及体内的运输、吸收和/或代谢的差异所致。

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