Department of Instrumental Analysis and Environmental Chemistry, IQOG (CSIC), Juan de la Cierva 3, 28006 Madrid, Spain.
Laboratory of Dioxins, Environmental Chemistry Department, IDÆA (CSIC), Jordi Girona 18-26, 08034 Barcelona, Spain.
Anal Chim Acta. 2015 Aug 19;889:156-65. doi: 10.1016/j.aca.2015.07.039. Epub 2015 Aug 10.
This paper reports on the optimisation, characterisation, validation and applicability of gas chromatography coupled to triple quadrupole mass spectrometry in its tandem operation mode (GC-QqQ(MS/MS) for the quantification of polychlorinated dibenzo-p-dioxins and furans (PCDD/Fs, dioxins) and dioxin-like polychlorinated biphenyls (DL-PCBs) in environmental and food matrices. MS/MS parameters were selected to achieve the high sensitivity and selectivity required for the analysis of this type of compounds and samples. Good repeatability for areas (RSD = 1-10%, for PCDD/Fs and DL-PCBs) and for ion transition ratios (RSD = 0.3-10%, for PCDD/Fs, and 0.2-15%, for DL-PCBs) and low instrumental limits of detection, 0.07-0.75 pg μL(-1) (for dioxins) and 0.05-0.63 pg μL(-1) (for DL-PCBs), were obtained. A comparative study of the congener specific determination using both GC-QqQ(MS/MS) and gas chromatography-high resolution mass spectrometry (GC-HRMS) was also performed by analysing several fortified samples and certified reference materials (CRMs) with low (feed and foodstuffs), median (sewage sludge) and high (fly ash) toxic equivalency (TEQ) concentration levels, i.e. 0.60, 1.83, 72.9 and 3609 pg WHO-TEQ(PCDD/Fs) g(-1). The agreement between the results obtained for the total TEQs (dioxins) on GC-QqQ(MS/MS) and GC-HRMS in all the investigated samples were within the range of ±4%, and that of DL-PCBs at concentration levels of 0.84 pg WHO-TEQs (DL-PCBs) g(-1), in the case of feedstuffs, was 0.11%. Both instrumental methods have similar and comparable linearity, precision and accuracy. The GC-QqQ(MS/MS) sensitivity, lower than that of GC-HRMS, is good enough (iLODs in the down to low pg levels) to detect the normal concentrations of these compounds in food and environmental samples. These results make GC-QqQ(MS/MS) suitable for the quantitative analysis of dioxins and DL-PCBs and a real alternative tool to the reference sector HRMS instruments.
本文报告了气相色谱-串联三重四极杆质谱(GC-QqQ(MS/MS)在其串联操作模式下对环境和食品基质中多氯二苯并对二恶英和呋喃(PCDD/Fs,二恶英)和类似二恶英的多氯联苯(DL-PCBs)进行定量分析的优化、特征描述、验证和适用性。选择了 MS/MS 参数,以实现对这类化合物和样品进行分析所需的高灵敏度和选择性。对于面积(PCDD/Fs 和 DL-PCBs 的 RSD=1-10%)和离子跃迁比(PCDD/Fs 的 RSD=0.3-10%,DL-PCBs 的 RSD=0.2-15%)以及低仪器检测限(0.07-0.75pgμL(-1)(二恶英)和 0.05-0.63pgμL(-1)(DL-PCBs),都得到了很好的重复性。还通过对几种经过加标和用低(饲料和食品)、中(污水污泥)和高(飞灰)毒性等效浓度(TEQ)水平(即 0.60、1.83、72.9 和 3609pg WHO-TEQ(PCDD/Fs)g(-1)进行分析,对使用气相色谱-串联三重四极杆质谱(GC-QqQ(MS/MS)和气相色谱-高分辨率质谱(GC-HRMS)进行的同系物特异性测定进行了比较研究。在所有研究的样品中,GC-QqQ(MS/MS)和 GC-HRMS 获得的总 TEQs(二恶英)结果之间的一致性在±4%的范围内,而在饲料中,浓度水平为 0.84pg WHO-TEQs(DL-PCBs)的 DL-PCBs 的一致性为 0.11%。两种仪器方法都具有相似的线性度、精密度和准确度。GC-QqQ(MS/MS)的灵敏度低于 GC-HRMS,但足以检测食品和环境样品中这些化合物的正常浓度(低至 pg 级别的 iLODs)。这些结果表明 GC-QqQ(MS/MS)适用于二恶英和 DL-PCBs 的定量分析,是对参考部门 HRMS 仪器的真正替代工具。