Research Institute for Pesticides and Water, University Jaume I, Avda. Sos Baynat, 12071 Castellón de la Plana, Castellón, Spain.
Anal Bioanal Chem. 2010 Aug;397(7):2873-91. doi: 10.1007/s00216-010-3597-8. Epub 2010 Mar 17.
A multi-residue method has been developed and validated for the simultaneous quantification and confirmation of around 130 multiclass pesticides in orange, nectarine and spinach samples by GC-MS/MS with a triple quadrupole analyzer. Compounds have been selected from different chemical families including insecticides, herbicides, fungicides and acaricides. Three isotopically labeled standards have been used as surrogates in order to improve accurate quantitation. Samples were extracted by using accelerated solvent extraction (ASE) with ethyl acetate. In the case of spinach, an additional clean-up step by gel permeation chromatography was applied. Determination was performed by GC-MS/MS in electron ionization mode acquiring two MS/MS transitions for each analyte. The intensity ratio between quantitation transition (Q) and identification transition (q) was used as confirmatory parameter (Q/q ratio). Accuracy and precision were evaluated by means of recovery experiments in orange, nectarine, and spinach samples spiked at two concentration levels (0.01 and 0.05 mg/kg). Recoveries were, in most cases, between 70% and 120% and RSD were below 20%. The limits of quantification objective for which the method was satisfactorily validated in the three samples matrices were for most pesticides 0.01 mg/kg. Matrix effects over the GC-MS/MS determination were tested by comparison of reference standards in pure solvent with matrix-matched standards of each matrix. Data obtained showed enhancement of signal for the majority of analytes in the three matrices investigated. Consequently, in order to reduce the systematic error due to this effect, quantification was performed using matrix-matched standard calibration curves. The matrix effect study was extended to other food matrices such as raisin, paprika, cabbage, pear, rice, legume, and gherkin, showing in all cases a similar signal enhancement effect.
建立并验证了一种多残留方法,可通过三重四极杆分析器的 GC-MS/MS 同时定量和确证橙汁、油桃和菠菜样品中的约 130 种多类农药。化合物选自不同的化学家族,包括杀虫剂、除草剂、杀菌剂和杀螨剂。为了提高准确定量,使用了三种同位素标记标准品作为替代物。样品通过乙酸乙酯加速溶剂萃取(ASE)进行提取。对于菠菜,还应用了凝胶渗透色谱(GPC)的额外净化步骤。通过电子电离模式的 GC-MS/MS 进行测定,每个分析物获取两个 MS/MS 跃迁。定量跃迁(Q)和鉴定跃迁(q)之间的强度比用作确认参数(Q/q 比)。通过在橙汁、油桃和菠菜样品中以两个浓度水平(0.01 和 0.05mg/kg)进行加标回收实验来评估准确性和精密度。回收率在大多数情况下在 70%至 120%之间,RSD 低于 20%。该方法在三种样品基质中均得到满意验证的定量限目标为大多数农药 0.01mg/kg。通过比较纯溶剂中的参考标准品与各基质的基质匹配标准品,测试了 GC-MS/MS 测定中的基质效应。获得的数据表明,在所研究的三种基质中,大多数分析物的信号增强。因此,为了减少由于这种效应引起的系统误差,使用基质匹配标准品校准曲线进行定量。还将基质效应研究扩展到其他食品基质,如葡萄干、辣椒粉、白菜、梨、大米、豆类和小黄瓜,在所有情况下均显示出类似的信号增强效应。