State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing, China.
E.I. du Pont de Nemours & Company, Inc., Newark, DE, USA.
Chemosphere. 2014 Oct;112:34-41. doi: 10.1016/j.chemosphere.2014.02.068. Epub 2014 Apr 21.
6:2 Fluorotelomer iodide [6:2 FTI, F(CF2)6CH2CH2I] is the industrial raw material used to manufacture 6:2 fluorotelomer alcohol [6:2 FTOH, F(CF2)6CH2CH2OH] and 6:2 FTOH-based products. During its manufacture and industrial use, workers may be exposed to via oral, dermal or inhalation of 6:2 FTI. Therefore it is useful to understand how 6:2 FTI may be metabolized and into what transformation products. 6:2 FTI in vitro rat liver microsomal metabolism was explored for the first time to compare its biotransformation potential with that of [1,2-(14)C] 6:2 FTOH [F(CF2)6(14)CH2(14)CH2OH]. 6:2 FTI and 6:2 FTOH metabolite yields were determined in closed-bottle systems using Sprague Dawley and Wistar Han rat microsomes after incubation at 37 °C for up to 6h with NADPH (reduced form of nicotinamide adenine dinucleotide phosphate)-addition and NADPH-regenerating systems, respectively. 5:3 acid [F(CF2)5CH2CH2COOH] was the most abundant metabolite for 6:2 FTI (3.3-6.3 mol%) and 6:2 FTOH (9-12 mol%). Perfluorobutanoic acid (PFBA), perfluoropentanoic acid (PFPeA), and perfluorohexanoic acid (PFHxA) in sum accounted for 1.3-2.2 mol% from 6:2 FTI and 2.7-4.4 mol% from 6:2 FTOH biotransformation. Perfluoroheptanoic acid (PFHpA) accounted for 0.14-0.36 mol% from 6:2 FTI but only 0.01-0.06 mol% from 6:2 FTOH biotransformation. These results suggest that mammalian systems exposed to 6:2 FTI or 6:2 FTOH would form 5:3 acid, PFBA, PFPeA, PFHxA as the primary stable metabolites, whereas more PFHpA would be expected from 6:2 FTI biotransformation.
6:2 氟调聚物碘化物[6:2 FTI,F(CF2)6CH2CH2I]是用于制造 6:2 氟调聚物醇[6:2 FTOH,F(CF2)6CH2CH2OH]和 6:2 FTOH 基产品的工业原料。在制造和工业使用过程中,工人可能通过口服、皮肤或吸入 6:2 FTI 而接触到 6:2 FTI。因此,了解 6:2 FTI 可能如何代谢并转化为哪些转化产物是有用的。首次探索了 6:2 FTI 在大鼠肝微粒体中的体外代谢,以比较其生物转化潜力与[1,2-(14)C] 6:2 FTOH[F(CF2)6(14)CH2(14)CH2OH]的生物转化潜力。在 37°C 下用 NADPH(烟酰胺腺嘌呤二核苷酸磷酸的还原形式)-添加和 NADPH 再生系统分别孵育 Sprague Dawley 和 Wistar Han 大鼠微粒体 6 小时后,在封闭瓶系统中确定了 6:2 FTI 和 6:2 FTOH 代谢产物的产率。5:3 酸[F(CF2)5CH2CH2COOH]是 6:2 FTI(3.3-6.3 mol%)和 6:2 FTOH(9-12 mol%)的最丰富代谢物。全氟丁酸(PFBA)、全氟戊酸(PFPeA)和全氟己酸(PFHxA)合计占 6:2 FTI 生物转化的 1.3-2.2 mol%,6:2 FTOH 生物转化的 2.7-4.4 mol%。全氟庚酸(PFHpA)占 6:2 FTI 生物转化的 0.14-0.36 mol%,但仅占 6:2 FTOH 生物转化的 0.01-0.06 mol%。这些结果表明,暴露于 6:2 FTI 或 6:2 FTOH 的哺乳动物系统会形成 5:3 酸、PFBA、PFPeA、PFHxA 作为主要稳定的代谢物,而 6:2 FTI 生物转化预计会产生更多的 PFHpA。