Matrix solid-phase dispersion of polybrominated diphenyl ethers and their hydroxylated and methoxylated analogues in lettuce, carrot and soil

被引:17
|
作者
Iparraguirre, A. [1 ]
Rodil, R. [2 ]
Quintana, J. B. [2 ]
Bizkarguenaga, E. [1 ]
Prieto, A. [1 ]
Zuloaga, O. [1 ]
Cela, R. [2 ]
Fernandez, L. A. [1 ]
机构
[1] Univ Basque Country, Fac Sci & Technol, Dept Analyt Chem, UPV EHU, Bilbao 48080, Spain
[2] Univ Santiago de Compostela, Dept Analyt Chem Nutr & Food Sci, IIAA Inst Food Anal & Res, Santiago De Compostela 15782, Spain
关键词
Polybrominated diphenyl ethers; Matrix solid-phase extraction; Gas chromatography-negative chemical ionization-mass spectrometry; Soil; Lettuce; Carrot; HALOGENATED FLAME RETARDANTS; ASSISTED EXTRACTION; PBDE METABOLITES; BLUE MUSSELS; IDENTIFICATION; ENVIRONMENT; BDE-47; PLASMA; PLANT; WATER;
D O I
10.1016/j.chroma.2014.07.079
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the present work, a novel analytical method for the simultaneous determination of ten polybrominated diphenyl ethers (PBDEs), eight methoxylated PBDEs (MeO-PBDEs) and seven hydroxylated PBDEs (OH-PBDEs) in soil, lettuce and carrot samples was developed. The procedure was based on matrix solid-phase dispersion (MSPD) followed by gas chromatography coupled to negative chemical ionization-mass spectrometry (GC-NCI-MS). Under optimum conditions, 0.5 g of sample (freeze-dried in the case of lettuce and carrot samples) was dispersed with 0.5 g of octadecyl-functionalized silica (C-18) and 1.75 g of acidified silica (10% H2SO4, w/w) was used as clean-up sorbent. A two-step fractionated elution was carried out. First, PBDEs and MeO-PBDEs were eluted in 75:25% (v/v) n-hexane/dichloromethane mixture and, then, the retained OH-PBDEs were eluted in pure dichloromethane. Both extracts were analyzed by GC-NCI-MS separately, in the case of OH-PBDEs after derivatization with N-methyl-N-(trimethylsilyl) trifluoroacetamide. The developed method was validated in terms of accuracy for soil, lettuce and carrot matrices, spiked at two fortification levels (5 and 25 ng g(-1)). After correction with the corresponding surrogate, apparent recovery values (defined as the recovery obtained after correction with the corresponding surrogate) were in the 80-129% range. Precision (as relative standard deviation) in the 1-21% range and method detection limits (MDLs) in the 0.003 and 0.3 ng g(-1) range for soil and in the 0.003-0.4 ng g(-1) range (dry weight) for lettuce and carrot samples were obtained. For PBDEs the method was also validated with a standard reference material (SRM-2585) of house dust. Finally, the method was applied for the determination of target analytes in soil, lettuce and carrot. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:57 / 65
页数:9
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