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基于气相色谱-高分辨率质谱联用技术的方法的开发与优化,用于灵敏测定动物源性食品中的十氯联苯及相关降冰片烯类阻燃剂。

Development and optimization of gas chromatography coupled to high resolution mass spectrometry based method for the sensitive determination of Dechlorane plus and related norbornene-based flame retardants in food of animal origin.

作者信息

Rjabova Jekaterina, Viksna Arturs, Zacs Dzintars

机构信息

Institute of Food Safety, Animal Health and Environment ''BIOR'', Lejupes Street 3, Riga, LV-1076, Latvia; University of Latvia, Jelgavas Street 1, Riga, LV-1004, Latvia.

University of Latvia, Jelgavas Street 1, Riga, LV-1004, Latvia.

出版信息

Chemosphere. 2018 Jan;191:597-606. doi: 10.1016/j.chemosphere.2017.10.095. Epub 2017 Oct 19.

DOI:10.1016/j.chemosphere.2017.10.095
PMID:29078185
Abstract

An analytical method has been developed for the trace determination of 10 dechlorane-related compounds (DRCs) in food products by gas chromatography - high resolution mass spectrometry (GC-HRMS). The highest sensitivity of this instrumental analysis method was achieved by selection of the GC column type, optimization of the heated zones within the instrument, and adjusting the electron impact energy. The efficiency of solid phase extraction as clean-up procedure was also optimized. Two different types of cartridges - neutral silica gel and Florisil, as well as seven organic solvents or their mixtures - n-hexane, cyclohexane, acetone, toluene, n-hexane/ethyl acetate, n-hexane/acetone, and n-hexane/dichloromethane - were evaluated. The analytical method was characterized as selective, precise, accurate, and linear over the concentration ranges from 1.00 to 100 pg μL for DRCs. Ultra-trace level sensitivity was achieved with the instrumental limits of quantification (i-LOQs) varying from ∼0.01 pg to ∼ 1 pg and method limits of quantification (m-LOQs) by the analysis of 10 g of sample varying from ∼0.04 to ∼ 5 pg g. The developed method was successfully applied for the analysis of food samples and the analyses revealed the presence of majority of selected DRCs, with the Dechlorane Plus (DP) isomers occurring to a greater extent, pointing to the highest levels in cod liver and other fish products.

摘要

已开发出一种分析方法,用于通过气相色谱-高分辨率质谱法(GC-HRMS)痕量测定食品中的10种脱氯烷相关化合物(DRCs)。通过选择气相色谱柱类型、优化仪器内的加热区以及调整电子轰击能量,实现了这种仪器分析方法的最高灵敏度。还对作为净化程序的固相萃取效率进行了优化。评估了两种不同类型的柱管——中性硅胶和弗罗里硅土,以及七种有机溶剂或其混合物——正己烷、环己烷、丙酮、甲苯、正己烷/乙酸乙酯、正己烷/丙酮和正己烷/二氯甲烷。该分析方法在DRCs浓度范围为1.00至100 pg μL时具有选择性、精密度、准确性和线性。通过分析10 g样品,仪器定量限(i-LOQs)在约0.01 pg至约1 pg之间,方法定量限(m-LOQs)在约0.04至约5 pg g之间,实现了超痕量水平的灵敏度。所开发的方法成功应用于食品样品分析,分析结果显示大多数选定的DRCs存在,其中十氯联苯(DP)异构体的含量更高,表明在鳕鱼肝和其他鱼类产品中的含量最高。

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