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Multi-residue determination of 130 multiclass pesticides in fruits and vegetables by gas chromatography coupled to triple quadrupole tandem mass spectrometry

机译:气相色谱 - 三重四极杆串联质谱法测定水果和蔬菜中130种多类农药残留量

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摘要

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 triple quadrupole analyzer. Compounds have been selected from different chemical families including insecticides, herbicides, fungicides and acaricides. Three isotopically labelled 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 adquiring 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 70-120 % 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.
机译:已经开发了一种多残留方法,并通过使用三重四极杆分析仪的GC-MS / MS对橙,油桃和菠菜样品中的约130种多类农药进行同时定量和确证,这一方法已得到验证。化合物选自不同的化学家族,包括杀虫剂,除草剂,杀真菌剂和杀螨剂。三种同位素标记的标准品已被用作替代品,以提高准确定量的效果。样品通过使用乙酸乙酯的加速溶剂萃取(ASE)进行萃取。在菠菜的情况下,通过凝胶渗透色谱法进行额外的清洁步骤。通过GC-MS / MS在电子电离模式下进行测定,要求每种分析物有两个MS / MS跃迁。定量转换(Q)和鉴定转换(q)之间的强度比用作确认参数(Q / q比)。通过回收实验对橙,油桃和菠菜样品中两个浓度水平(0.01和0.05 mg / Kg)加标的准确性和精密度进行了评估。在大多数情况下,回收率在70-120%之间,RSD低于20%。对于大多数农药,在三种样品基质中均能令人满意地验证该方法的定量目标限为0.01 mg / Kg。通过在纯溶剂与基质匹配的标准溶液中比较参比标准品,测试了基质对GC-MS / MS测定的影响每个矩阵的标准。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,为了减少由于该效应引起的系统误差,使用与矩阵匹配的标准校准曲线进行了定量。基质效应研究扩展到了其他食品基质,如葡萄干,辣椒粉,卷心菜,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作用。

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