Department of Applied Environmental Science (ITM), Stockholm University, SE-106 91 Stockholm, Sweden.
Department of Environmental Chemistry, NILU-Norwegian Institute for Air Research, FRAM-Centre, NO-9007 Tromsø, Norway; Department of Laboratory Medicine, University Hospital of North Norway, NO-9038 Tromsø, Norway.
Environ Int. 2014 Apr;65:63-72. doi: 10.1016/j.envint.2014.01.005. Epub 2014 Jan 25.
A method was developed for simultaneous analysis of perfluoroalkane sulfonic acids (PFSAs) and their sulfonamide-based precursors (perfluoroalkane sulfonamidoacetic acids (FASAAs), sulfonamides (FASAs), and sulfonamidoethanols (FASEs)) in fish muscle. Extraction was performed with acetonitrile followed by a clean-up and fractionation step and instrumental analysis by UPLC/MS/MS and GC/MS. Time trends of PFSAs and their precursors in herring muscle samples originating from the Kattegat at the west coast of Sweden were investigated covering the years 1991-2011. The following analytes were detected, all with decreasing or unchanged trends between 1991 and 2011: Perfluorobutane sulfonic acid (PFBS, below the method detection limit (<MDL)-10pg/g), perfluorohexane sulfonic acid (PFHxS, 9-38pg/g), perfluorooctane sulfonic acid (PFOS, 240-930pg/g), perfluorodecane sulfonic acid (PFDS, <MDL-4pg/g), N-methyl and N-ethyl perfluorooctane sulfonamidoacetic acid (MeFOSAA and EtFOSAA, 2-39 and 2-31pg/g, respectively) and perfluorooctane sulfonamide (FOSA, 78-920pg/g). The highest concentrations were found for PFOS and FOSA around the turn of the century. Shorter disappearance half-lives were observed for precursors compared to PFSAs. Assuming that these trend differences are representative for fish consumed by the general Swedish population, this observation suggests that the relative contribution of precursors to total human exposure to PFOS via fish intake has decreased in Sweden over the study period. PFOS precursors in fish may have constituted a significant indirect exposure pathway for PFOS in the 1990s. Isomer-specific analysis of PFOS and FOSA revealed <10% relative contributions of branched isomers to total PFOS and total FOSA. Furthermore, the percentage branched isomers decreased over time for both compounds. These findings are contrary to patterns and temporal trends of PFOS isomers commonly found in human serum. In combination with literature data on isomer patterns in other edible fish species and on isomer-specific human toxicokinetics, our results suggest that fish consumption alone cannot account for the PFOS isomer patterns and trends observed in humans.
建立了一种同时分析鱼肌肉中全氟烷磺酸(PFSAs)及其磺酰胺类前体(全氟烷磺酰胺基乙酸(FASAAs)、磺酰胺(FASAs)和磺酰胺基乙醇(FASEs))的方法。采用乙腈提取,经净化和分级后,采用 UPLC/MS/MS 和 GC/MS 进行仪器分析。研究了 1991 年至 2011 年间来自瑞典西海岸卡特加特的鲱鱼肌肉样本中 PFSAs 及其前体的时间趋势。检测到以下分析物,1991 年至 2011 年间均呈下降或不变趋势:全氟丁烷磺酸(PFBS,低于方法检测限(<MDL)-10pg/g)、全氟己烷磺酸(PFHxS,9-38pg/g)、全氟辛烷磺酸(PFOS,240-930pg/g)、全氟癸烷磺酸(PFDS,<MDL-4pg/g)、N-甲基和 N-乙基全氟辛烷磺酰胺基乙酸(MeFOSAA 和 EtFOSAA,分别为 2-39 和 2-31pg/g)和全氟辛烷磺酰胺(FOSA,78-920pg/g)。在世纪之交,PFOS 和 FOSA 的浓度最高。与 PFSAs 相比,前体的消失半衰期更短。如果这些趋势差异代表了瑞典一般人群食用的鱼类,那么这一观察结果表明,在研究期间,瑞典通过鱼类摄入导致人体对 PFOS 的总暴露中,前体的相对贡献已经减少。鱼类中的 PFOS 前体在 20 世纪 90 年代可能构成了 PFOS 间接暴露的一个重要途径。对 PFOS 和 FOSA 的同系物分析显示,总 PFOS 和总 FOSA 中支链异构体的相对贡献<10%。此外,两种化合物的支链异构体比例随时间下降。这些发现与在人类血清中常见的 PFOS 同系物模式和时间趋势相反。结合其他可食用鱼类物种的同系物模式和同系物特异性人体毒代动力学的文献数据,我们的结果表明,仅通过鱼类消费无法解释在人体中观察到的 PFOS 同系物模式和趋势。