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固相萃取和液相色谱-质谱联用技术在水果和蔬菜中新烟碱类农药残留测定中的应用。

Application of solid-phase extraction and liquid chromatography-mass spectrometry to the determination of neonicotinoid pesticide residues in fruit and vegetables.

作者信息

Di Muccio Alfonso, Fidente Paola, Barbini Danilo Attard, Dommarco Roberto, Seccia Serenella, Morrica Patrizia

机构信息

ISS Istituto Superiore di Sanità (National Institute of Health), Viale Regina Elena 299, 00161 Rome, Italy.

出版信息

J Chromatogr A. 2006 Mar 3;1108(1):1-6. doi: 10.1016/j.chroma.2005.12.111. Epub 2006 Jan 31.

DOI:10.1016/j.chroma.2005.12.111
PMID:16448655
Abstract

A rapid and simple method for simultaneous analysis of four neonicotinoid insecticides including acetamiprid, imidacloprid, thiacloprid and thiamethoxam in fruit and vegetable matrices has been developed. For instance, ready-to-use cartridges filled with a macroporous diatomaceous material were used to extract in a single step insecticide residues with dichloromethane from aqueous-acetone extracts of fruits and vegetables. The eluate was evaporated, the residue redissolved with methanol and then analyzed by liquid chromatography-mass spectrometry in the electrospray ionization (ESI) positive mode. Average recoveries of the four pesticides were between 74.5 and 105% at both spiking levels 0.1 and 1.0 mg kg(-1) in peach, pear, courgette, celery and apricot. Relative standard deviations (RSDs) were less than 10% for all of the recovery tests. The calculated limits of quantitation (LOQs) (0.1-0.5 mg kg(-1)) were equal or lower then the maximum residue limits (MRLs) established by European legislation (0.1-0.5 mg kg(-1)). The proposed method is fast, easy to perform and could be utilized for monitoring of pesticides residues.

摘要

已开发出一种快速简便的方法,用于同时分析水果和蔬菜基质中的四种新烟碱类杀虫剂,包括啶虫脒、吡虫啉、噻虫啉和噻虫嗪。例如,使用填充有大孔硅藻土材料的即用型柱,从水果和蔬菜的水 - 丙酮提取物中用二氯甲烷一步提取杀虫剂残留。将洗脱液蒸发,残留物用甲醇重新溶解,然后通过液相色谱 - 质谱联用仪在电喷雾电离(ESI)正模式下进行分析。在桃子、梨、西葫芦、芹菜和杏子中,两种加标水平0.1和1.0 mg kg⁻¹下,四种农药的平均回收率在74.5%至105%之间。所有回收率测试的相对标准偏差(RSDs)均小于10%。计算出的定量限(LOQs)(0.1 - 0.5 mg kg⁻¹)等于或低于欧洲法规规定的最大残留限量(MRLs)(0.1 - 0.5 mg kg⁻¹)。所提出的方法快速、易于操作,可用于监测农药残留。

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