A fast method for analysing six perfluoroalkyl substances in human serum by solid-phase extraction on-line coupled to liquid chromatography tandem mass spectrometry
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  • 作者:Mónica Bartolomé ; Alejandrina Gallego-Picó…
  • 关键词:Perfluoroalkyl substances ; On ; line solid ; phase extraction ; Turbo flow extraction ; Human serum ; Liquid chromatography with tandem spectrometry ; Human biomonitoring
  • 刊名:Analytical and Bioanalytical Chemistry
  • 出版年:2016
  • 出版时间:March 2016
  • 年:2016
  • 卷:408
  • 期:8
  • 页码:2159-2170
  • 全文大小:672 KB
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  • 作者单位:Mónica Bartolomé (1)
    Alejandrina Gallego-Picó (2)
    Olga Huetos (1)
    Miguel Ángel Lucena (1)
    Argelia Castaño (1)

    1. Environmental Toxicology, National Centre for Environmental Health, Instituto de Salud Carlos III, Carretera Majadahonda-Pozuelo km 2, 28220, Majadahonda, Spain
    2. Department of Analytical Sciences, Faculty of Sciences, National University of Distance Education (UNED), 28040, Madrid, Spain
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Analytical Chemistry
    Food Science
    Inorganic Chemistry
    Physical Chemistry
    Monitoring, Environmental Analysis and Environmental Ecotoxicology
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1618-2650
文摘
We have developed and validated an on-line TurboFlow solid-phase extraction procedure coupled to high-performance liquid chromatography with tandem mass spectrometry for the analysis of six perfluoroalkyl substances (PFAS), two sulfonates (perfluorooctane sulfonate and perfluorohexane sulfonate), three carboxylates (perfluorooctanoic acid, perfluorononanoic acid and perfluorodecanoic acid), and one sulfonamide (N-methylperfluorooctane sulfonamide), in human serum samples. This method requires only 100 μL of sample and involves a short pre-treatment with acetonitrile followed by addition of a labelled internal standard for quantification and ultracentrifugation. All PFAS were detected with a run time of 8.5 min. Linearity ranges stay between 0.1 and 20 μg L−1 (R 2 > 0.9960). Recoveries were determined by spiking blank serum samples with a mixture of six PFAS and found to be in the range 96–110 % for all compounds. Isotopic dilution was used to quantify the selected analytes. The low limits of quantification obtained, between 0.16 and 0.34 μg L−1, small volume of sample required and short run time used (from two to three times shorter than any other described method), make this validated method highly recommended for human biomonitoring studies.

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