Dispersive solid-phase extraction as a simplified clean-up technique for biological sample extracts. Determination of polybrominated diphenyl ethers by gas chromatography-tandem mass spectrometry

被引:83
作者
Fontana, Ariel R. [1 ]
Camargo, Alejandra [3 ,4 ,5 ]
Martinez, Luis D. [2 ]
Altamirano, Jorgelina C. [1 ,3 ]
机构
[1] CCT CONICET Mendoza, LISAMEN, Grp Invest & Desarrollo Quim Analit QUIANID, RA-5500 Mendoza, Argentina
[2] Univ Nacl San Luis, Fac Quim Bioquim & Farm, Dept Quim Analit, INQUISAL CONICET, San Luis, Argentina
[3] Univ Nacl Cuyo, Inst Ciencias Basicas, RA-5500 Mendoza, Argentina
[4] Univ Nacl Cuyo, Fac Ciencias Agr, IBAM CONICET, RA-5500 Mendoza, Argentina
[5] Univ Nacl Cuyo, Fac Ciencias Agr, Lab Anal Residuos Tox, RA-5500 Mendoza, Argentina
关键词
Polybrominated diphenyl ethers; QuEChERS; Dispersive solid-phase extraction; Biological samples; Fish; Gas chromatography-mass spectrometry; BROMINATED FLAME RETARDANTS; PESTICIDE-RESIDUE ANALYSIS; ELECTRON-CAPTURE DETECTION; POLYCHLORINATED-BIPHENYLS; BIOTA SAMPLES; BOVINE-MILK; MICROEXTRACTION; ENVIRONMENT; WINE; OIL;
D O I
10.1016/j.chroma.2011.02.058
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Dispersive solid-phase extraction (DSPE) is proposed for the first time as a simplified, fast and low cost clean-up technique of biological sample extracts for polybrominated diphenyl ethers (PBDEs) determination. The combination of a traditional extraction technique, such as ultrasound-assisted leaching (USAL) with DSPE was successfully applied for sample preparation prior to gas chromatography-tandem mass spectrometry (GC-MS/MS) analysis. The analytes were first extracted from 1 g homogenized sample in n-hexane:dichloromethane (8:2) by applying USAL technique and further cleaned-up using DSPE with 0.20 g C(18)-silica as sorbent material. Different solvent mixtures, sorbent type and amount, and lipid digestion procedures were evaluated in terms of clean-up and extraction efficiency. Under optimum conditions, the method detection limits (MDLs) for PBDEs, calculated as three times the signal-to-noise ratio (S/N) were within the range 9-44 pg g(-1) wet weight. The calibration graphs were linear within the concentration range of 53-500,000 pg g(-1), 66-500,000 pg g(-1), 89-500,000 pg g(-1) and 151-500,000 pg g(-1) for BDE-47, BDE-100, BDE-99 and BDE-153, respectively; and the coefficient of determination (r(2)) exceeded 0.9992 for all analytes. The proposed methodology was compared with a reference solid-phase extraction technique. The applicability of the methodology for the screening of PBDEs has been demonstrated by analyzing spiked and real samples of biological nature (fish, egg and chicken) with different lipid content as well as reference material (WELL-WMF-01). Recovery values ranged between 75% and 114% and the measured concentrations in certified material showed a reasonable agreement with the certified ones. BDE-47, BDE-100 and BDE-99 were quantified in three of the seven analyzed samples and the concentrations ranged between 91 and 140 pg g(-1). In addition, this work is the first description of PBDEs detected in fish of Argentinean environment. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2490 / 2496
页数:7
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