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Application of gas chromatography time-of-flight mass spectrometry for target and non-target analysis of pesticide residues in fruits and vegetables

机译:气相色谱飞行时间质谱技术在果蔬中农药残留目标和非目标分析中的应用

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摘要

In this work, the capability of gas chromatography coupled to time-of-flight mass spectrometry (GC–TOF MS) for quantitative analysis of pesticide residues has been evaluated. A multiclass method for rapid screening of pesticides (insecticides, acaricides, herbicides and fungicides) in fruit and vegetable matrices has been developed and validated, including detection, identification and quantification of the analytes. To this aim, several food matrices were selected: high water content (apples, tomatoes and carrots), high acid content (oranges) and high oil content (olives) samples. The well known QuEChERS procedure was applied for extraction of pesticides, and matrix-matched calibration using relative responses versus internal standard was used for quantification. The sample extracts were analyzed by GC–TOF MS. Up to five ions using narrow window (0.02 Da)-extracted ion chromatograms at the expected retention time were monitored using a target processing method. The most abundant ion was used for quantification while the remaining ones were used for confirmation of the analyte identity. Method validation was carried out for 55 analytes in the five sample matrices tested at three concentrations (0.01, 0.05 and 0.5 mg/kg). Most recoveries were between 70% and 120% with relative standard deviations (RSDs) lower than 20% at 0.05 and 0.5 mg/kg. At 0.01 mg/kg, roughly half of the pesticides could be satisfactorily validated due to sensitivity limitations of GC–TOF MS, which probably affected the ion ratios used for confirmation of identity. In the case of olive samples, results were not satisfactory due to the high complexity of the matrix. An advantage of TOF MS is the possibility to perform a non-target investigation in the samples by application of a deconvolution software, without any additional injection being required. Accurate-mass full-spectrum acquisition in TOF MS provides useful information for analytes identification, and has made feasible in this work the discovery of non-target imazalil, fluoranthene and pyrene in some of the samples analyzed.
机译:在这项工作中,已评估了气相色谱结合飞行时间质谱(GC-TOF MS)进行农药残留定量分析的能力。已经开发并验证了一种用于水果和蔬菜基质中农药(杀虫剂,杀螨剂,除草剂和杀真菌剂)快速筛选的多类方法,包括检测,鉴定和定量分析物。为此,选择了几种食品基质:高水分含量(苹果,西红柿和胡萝卜),高酸含量(橙色)和高油含量(橄榄)样品。将众所周知的QuEChERS程序用于农药的提取,并使用相对响应与内标的基质匹配校准进行定量。样品提取物通过GC-TOF MS分析。使用目标处理方法,在预期保留时间使用窄窗(0.02 Da)提取的离子色谱图最多可监测五个离子。最丰富的离子用于定量,而其余离子用于确认分析物身份。对三种浓度(0.01、0.05和0.5 mg / kg)的五个样品基质中的55种分析物进行了方法验证。在0.05和0.5 mg / kg时,大多数回收率在70%至120%之间,相对标准偏差(RSD)低于20%。在0.01 mg / kg下,由于GC–TOF MS的灵敏度限制,可以令人满意地验证大约一半的农药,这可能会影响用于确认身份的离子比率。对于橄榄样品,由于基质的高度复杂性,结果不令人满意。 TOF MS的一个优点是可以通过使用反卷积软件对样品执行非目标研究,而无需任何其他进样。在TOF MS中进行精确质量的全光谱采集可为分析物鉴定提供有用的信息,并且使这项工作在某些分析样品中发现非目标咪唑,荧蒽和pyr成为可能。

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