期刊
JOURNAL OF CHROMATOGRAPHY A
卷 1513, 期 -, 页码 107-117出版社
ELSEVIER
DOI: 10.1016/j.chroma.2017.07.024
关键词
Polyfluoroalkyl substances; Antarctica; Biomonitoring; Seabird; Plasma; On-line solid phase extraction; Method validation
资金
- French National Research Agency (PolarTOP project) [ANR-10-CESA-0016]
- Institut Polaire Francais [109]
- INSU-EC2CO Ecodyn program
- NTERREG ORQUE SUDOE project [SOE3/P2/F591]
- French National Research Agency (ANR) [ANR-10-LABX-45]
- IdEx Bordeaux [ANR-10-IDEX-03-02]
- Aquitaine Regional Council
- European Union (CPER A2E project)
- Agence Nationale de la Recherche (ANR) [ANR-10-CESA-0016] Funding Source: Agence Nationale de la Recherche (ANR)
We report on a fast, accurate and rugged analytical procedure to determine a wide span of perfluoroalkyl and polyfluoroalkyl substances (PFASs) in seabird plasma. The 26 investigated compounds included perfluoroalkyl carboxylates (C-5-C-14 PFCAs), perfluoroalkyl sulfonates (C-4, C-6, C-7, C-8, C-10 PFSAs), perfluorooctane sulfonamide (FOSA) and N-alkyl derivatives (MeFOSA, EtFOSA), N-alkyl perfluorooctane sulfonamido acetic acids (MeFOSAA, EtFOSAA), fluorotelomer sulfonates (4:2 FTSA, 6:2 FTSA, 8:2 FFSA), polyfluoroalkyl phosphate diesters (diPAPs) and perfluorooctane sulfonamide phosphate diester (diS-AmPAP). The method described herein requires a reduced sample amount (25 mu L) and involves rapid and simple sample preparation (protein precipitation with acetonitrile but without acidification) prior to analysis by on-line solid phase extraction (Oasis HLB sorbent) coupled to high performance liquid chromatography negative electrospray ionization tandem mass spectrometry. The optimization was conducted using experimental designs to account for potential interactions between variables. Out of the 26 target analytes, 23 compounds showed excellent accuracy (+/- 25% of the expected values). Intermediate precision and matrix effects remained acceptable for most analytes thanks to efficient internal standardization. A human serum standard reference material (NIST SRM 1957) was included in the validation scheme to evaluate method trueness, which proved satisfactory (vertical bar Z-scores vertical bar<2 for most compounds). Notwithstanding the small initial sample intake, limits of detection as low as 0.003-0.1 ngg(-1) plasma were obtained. This allowed the determination of 11 target PFASs in Antarctic seabird plasma samples. Sigma PFASs in Antarctic seabird plasma ranged from 0.37 to 19 ng g(-1), with a predominance of PFOS (>54% of Sigma PFASs on average). The reduced plasma amount required implies that the present method could also be applied to the analysis of PFASs in the plasma of smaller biological models. (C) 2017 Elsevier B.V. All rights reserved.
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