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采用离子色谱和串联质谱法分析动植物源性食品中的高极性阴离子农药,重点解决基质共提取物引起的不良反应。

Analysis of highly polar anionic pesticides in food of plant and animal origin by ion chromatography and tandem mass spectrometry with emphasis on addressing adverse effects caused by matrix co-extractives.

作者信息

Schäfer Ann-Kathrin, Vetter Walter, Anastassiades Michelangelo

机构信息

Section of Residues and Contaminants, Chemisches und Veterinäruntersuchungsamt Stuttgart, Fellbach, D-70736, Germany.

Institute of Food Chemistry (170b), University of Hohenheim, Stuttgart, D-70599, Germany.

出版信息

Anal Bioanal Chem. 2024 Aug;416(20):4503-4517. doi: 10.1007/s00216-024-05389-4. Epub 2024 Jun 19.

Abstract

Residues of various highly polar pesticides and their metabolites are commonly found in numerous food products. Some of these compounds, such as glyphosate, are not only used in large amounts in agriculture, but are also controversially discussed in public. Here, we present a method, employing ion chromatography (IC) coupled to tandem mass spectrometry (IC-MS/MS), for the analyses of glyphosate, aminomethyl phosphonic acid (AMPA), N-acetyl-glyphosate (NAGly), fosetyl, and 10 further highly polar pesticides and metabolites in various plant and animal matrices following a minimal sample preparation by means of the QuPPe method. Thorough investigations showed that an AS19 column enabled the analysis of all 14 compounds within 30 min. The best sensitivity could be obtained with the make-up solvent acetonitrile being admixed to the mobile phase at a 1:2 flow rate ratio. Matrix effects were thoroughly studied in terms of ion suppression and retention time shifts. Conductivity detection was used to monitor elution profiles of matrix co-extractives in comparison with matrix effect profiles obtained by continuous post-column infusion of a mix with 13 highly polar pesticides and metabolites. These tests indicated that a fivefold dilution of QuPPe extracts was suitable for the routine analysis of samples for MRL-conformity, as it considerably reduced matrix effects maintaining sufficient sensitivity and high recovery rates in eight different commodities. The suitability of the final method for its application in routine analysis was verified by the analysis of >130 samples containing incurred residues where the results were compared with two existing LC-MS/MS methods.

摘要

各种高极性农药及其代谢物的残留常见于众多食品中。其中一些化合物,如草甘膦,不仅在农业中大量使用,而且在公众中也存在争议性讨论。在此,我们介绍一种方法,该方法采用离子色谱(IC)与串联质谱(IC-MS/MS)联用,通过QuPPe方法进行最少的样品制备后,分析各种植物和动物基质中的草甘膦、氨甲基膦酸(AMPA)、N-乙酰草甘膦(NAGly)福赛得以及另外10种高极性农药和代谢物。深入研究表明,AS19柱能够在30分钟内分析所有14种化合物。以1:2的流速比将补充溶剂乙腈混入流动相时可获得最佳灵敏度。从离子抑制和保留时间偏移方面对基质效应进行了全面研究。与通过连续柱后注入含有13种高极性农药和代谢物的混合物获得的基质效应图谱相比,使用电导检测来监测基质共提取物的洗脱图谱。这些测试表明,将QuPPe提取物稀释五倍适用于符合最大残留限量的样品的常规分析,因为它在很大程度上降低了基质效应,同时在八种不同商品中保持了足够的灵敏度和高回收率。通过分析超过130个含有实际残留的样品,并将结果与两种现有的LC-MS/MS方法进行比较,验证了最终方法在常规分析中的适用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/578c/11294259/57f6ebd4f800/216_2024_5389_Fig1_HTML.jpg

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