Isomer–Specific Distribution of Perfluoroalkyl Substances in Blood

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• 作者：Hangbiao Jin ; Yifeng Zhang ; Weiwei Jiang ; Lingyan Zhu ; Jonathan W. Martin
• 刊名：Environmental Science & Technology
• 出版年：2016
• 出版时间：July 19, 2016
• 年：2016
• 卷：50
• 期：14
• 页码：7808-7815
• 全文大小：375K
• 年卷期：0
• ISSN：1520-5851

文摘

Perfluoroalkyl substances (PFASs) such as perfluorohexanesulfonate (PFHxS), perfluorooctanoate (PFOA), perfluorooctanesulfonate (PFOS) and PFOS–precursors are routinely measured in human plasma and serum, but their relative abundance in the blood cell fraction has not been carefully examined, particularly at the isomer–specific level. Human plasma and whole blood were collected and partitioning behaviors of PFASs and their isomers between plasma and blood cells were investigated. In human samples, mass fraction in plasma (F_p) for PFASs increased among perfluoroalkyl carboxylates as the carbon chain length increased from C6 (mean 0.24) to C11 (0.87), indicating preference for the plasma fraction with increasing chain length. However, among perfluoroalkyl sulfonates, PFHxS (mean 0.87) had a slightly higher F_p than PFOS (0.85). In vitro assays with spiked Sprague–Dawley rat blood were also conducted, and the results showed that PFOS–precursors had lower F_p values than perfluoroalkyl acids, with perfluoroctanesulfonamide having the lowest F_p (mean 0.24). Consistently, linear isomers of PFOS and PFOS–precursors had lower mean F_p than their corresponding total branched isomers. Multiplying by a factor of 2 is not a reasonable method to convert from whole blood to plasma PFAS concentrations, and current ratios could be used as more accurate conversion factors.