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基于气相色谱/三重四极杆质谱法的食品中农药定量方法的验证

Validation of a gas chromatography/triple quadrupole mass spectrometry based method for the quantification of pesticides in food commodities.

作者信息

Martínez Vidal J L, Arrebola Liébanas F J, González Rodríguez M J, Garrido Frenich A, Fernández Moreno J L

机构信息

Department of Analytical Chemistry, University of Almería, 04071 Almería, Spain.

出版信息

Rapid Commun Mass Spectrom. 2006;20(3):365-75. doi: 10.1002/rcm.2315.

Abstract

A new multiresidue method has been validated in cucumber matrix for the routine analysis of 130 multiclass pesticide residues by gas chromatography/triple quadrupole mass spectrometry. The pesticides were extracted with ethyl acetate. A first identification of the pesticides was based on a tandem mass spectrometric (MS/MS) screening method, which monitors a single transition for each target compound, in less than 12 min. After that, potentially non-negative samples were analyzed again by the MS/MS confirmation/quantification method, which monitors two or three MS/MS transitions for each compound, also in less than 12 min. Performance characteristics, such as trueness, precision, linear range, detection limit (LOD) and quantification limit (LOQ), for each pesticide were calculated. The average recoveries obtained ranged between 70 and 120% at three different fortification levels (25, 200 and 500 microg/kg) with precision, expressed as relative standard deviation (RSD), values lower than 15%. The calculated LOD and LOQ were typically <3.2 and 9.6 microg/kg, respectively. Such limits were much lower than the maximum residue levels (MRLs) established by European legislation. The proposed methodology was applied to the determination of pesticides in real vegetable samples from Almería (Spain).

摘要

已在黄瓜基质中验证了一种新的多残留方法,用于通过气相色谱/三重四极杆质谱法对130种多类农药残留进行常规分析。用乙酸乙酯提取农药。首先基于串联质谱(MS/MS)筛选方法对农药进行鉴定,该方法在不到12分钟的时间内监测每种目标化合物的单个跃迁。之后,对潜在的非阴性样品再次采用MS/MS确证/定量方法进行分析,该方法同样在不到12分钟的时间内监测每种化合物的两个或三个MS/MS跃迁。计算了每种农药的性能特征,如准确性、精密度、线性范围、检测限(LOD)和定量限(LOQ)。在三个不同的加标水平(25、200和500微克/千克)下,获得的平均回收率在70%至120%之间,精密度以相对标准偏差(RSD)表示,其值低于15%。计算得出的LOD和LOQ通常分别<3.2和9.6微克/千克。这些限值远低于欧洲法规规定的最大残留限量(MRLs)。所提出的方法应用于测定来自西班牙阿尔梅里亚的实际蔬菜样品中的农药。

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