Planche Christelle, Ratel Jérémy, Mercier Frédéric, Blinet Patrick, Debrauwer Laurent, Engel Erwan
INRA, UR370 QuaPA, MASS group, F-63122 Saint-Genès-Champanelle, France; INRA, UMR 1331 Toxalim, Research Centre in Food Toxicology, F-31027 Toulouse, France; Universitè de Toulouse, INPT, UPS, UMR 1331, F-31062 Toulouse, France.
INRA, UR370 QuaPA, MASS group, F-63122 Saint-Genès-Champanelle, France.
J Chromatogr A. 2015 May 1;1392:74-81. doi: 10.1016/j.chroma.2015.02.054. Epub 2015 Feb 24.
This paper evaluates different multiresidue methods based on comprehensive two-dimensional gas chromatography coupled to time-of-flight mass spectrometry (GC×GC-TOF/MS) to analyze dioxin-related micropollutants in complex food matrices. In a first step, the column sets Rtx-PCB/BPX-50 and Rtx-Dioxin2/BPX-50 were compared in terms of peak shape (width and symmetry) and resolution for the separation of polychlorinated biphenyls (PCBs) and polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs) in solvent. A satisfactory separation of 206 dioxin-related micropollutants including the 17 toxic PCDD/Fs was achieved in 75 min with the column set Rtx-Dioxin2/BPX-50. In a second time, the GC×GC-TOF/MS method was spread to the analysis of dioxin-related micropollutants in complex food matrices. An extraction procedure including accelerated solvent extraction (ASE), centrifugal evaporation and gel permeation chromatography (GPC) was optimized. Starting with meat as a model matrix, a micropollutant spiking method was then set up by comparing seven methods in terms of recoveries and reproducibility. The method combining immersion of the meat in a large volume of solvent containing micropollutants followed by homogenization by blender induced recoveries in the acceptable range of 70-130% and satisfactory standard deviations (≤10%) for most of the compounds studied. Limits of detection of the GC×GC-TOF/MS method ranged between 50 and 100 pg/g of spiked fresh meat for PCBs and between 65 and 227 pg/g for PCDD/Fs. Potential applications of this method are discussed.
本文评估了基于全二维气相色谱-飞行时间质谱联用仪(GC×GC-TOF/MS)的不同多残留方法,以分析复杂食品基质中的二噁英相关微污染物。第一步,比较了Rtx-PCB/BPX-50和Rtx-Dioxin2/BPX-50两种色谱柱组合在溶剂中分离多氯联苯(PCBs)和多氯二苯并对二噁英/二苯并呋喃(PCDD/Fs)时的峰形(宽度和对称性)及分离度。使用Rtx-Dioxin2/BPX-50色谱柱组合在75分钟内实现了包括17种有毒PCDD/Fs在内的206种二噁英相关微污染物的良好分离。第二步,将GC×GC-TOF/MS方法扩展至复杂食品基质中二噁英相关微污染物的分析。优化了包括加速溶剂萃取(ASE)、离心蒸发和凝胶渗透色谱(GPC)在内的萃取程序。以肉类为模型基质,通过比较七种方法的回收率和重现性,建立了一种微污染物加标方法。该方法是将肉类浸泡在含有微污染物的大量溶剂中,然后用搅拌器匀浆,对大多数研究的化合物而言,回收率在可接受的70 - 130%范围内,标准偏差令人满意(≤10%)。GC×GC-TOF/MS方法对PCBs的检测限在加标鲜肉中为50至100 pg/g,对PCDD/Fs为65至227 pg/g。讨论了该方法的潜在应用。