一步萃取法分析牛奶中手性和非手性农药的高通量多残留

IF 6.2
Massimo Giuseppe De Cesaris , Giulia Bertini , Chiara Dal Bosco , Nina Felli , Elena Lucci , Lorenzo Antonelli , Salvatore Fanali , Alessandra Gentili
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引用次数: 0

摘要

农药是牛奶的潜在污染物之一,但文献中缺乏针对手性农药的分析方法,即使其中许多农药被大量用作外消旋物。由于对映体的毒性和生物降解率不同,对牛奶等基本主食的分析是迫切需要的,特别是因为它是儿童大量消费的食物。下面的工作描述了一种同时分析11种农药的高通量方法,其中5种是光学异构体的外消旋混合物,1种是几何异构体的等摩尔混合物。尽管基质复杂,但由于提取过程的快速和简单,每小时可以处理18个牛奶样品。通常单独用于蛋白质沉淀的两种方法(用冷乙腈降低介质介电常数和用硫酸铵盐化作用)相结合,以最大限度地去除蛋白质。盐析现象也促进了水/乙腈的分离,有利于分析物转移到有机相。蒸发后,重组提取物通过对映选择高效液相色谱结合双极性串联质谱分析,在15分钟内完全分离了17个色谱峰。然后根据委员会决定2002/657/EC及其更新对该方法进行了验证。在三个强化水平下,绝对回收率在69.4%至88.5%之间。日内精度低于10.5%,日内精度低于17.5%。除决策限和检测能力外,还计算了检测限(0.011 ~ 1.622 μg/kg)和定量限(0.103 ~ 3.770 μg/kg)。在矩阵中建立了0.1 ~ 60 μg/kg的线性动态范围内的标定曲线,测定系数大于0.9924。最后用AgreePrep、BAGI、SPMS、complexMo-GAPI 4个指标对该方法进行评价,并与文献中其他方法进行比较,结果表明该方法具有较高的分析标准、通量和实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

One-step extraction for a high throughput multiresidue analysis of chiral and achiral pesticides in milk

One-step extraction for a high throughput multiresidue analysis of chiral and achiral pesticides in milk
Pesticides are among the potential contaminants of cow's milk, but the literature is lacking in methods aimed at the analysis of chiral pesticides even if many of them are massively used as racemates. Owing to the different toxicity and biodegradation rate of enantiomers, their analysis is a urgent need in a fundamental staple such as milk, especially because it is a food highly consumed by children. The following work describes a high throughput method for the simultaneous analysis of eleven pesticides, five out of which are racemic mixtures of optical isomers and one is an equimolar mixture of geometric isomers. The extraction procedure allows one to process 18 milk samples per hour thanks to its quickness and ease, albeit the matrix complexity. Two approaches, typically applied for protein precipitation separately (lowering of the medium dielectric constant with cold acetonitrile and salting out effect with ammonium sulphate), were combined to maximize protein removal. The salting out phenomenon also promoted the water/acetonitrile separation and favoured the analyte transfer into the organic phase. After evaporation, the reconstituted extracts were analysed by enantioselective high-performance liquid chromatography combined with dual-polarity tandem mass spectrometry, allowing the complete separation of seventeen chromatographic peaks in a 15-min run. The method was then validated following the Commission Decision 2002/657/EC and its updates. Absolute recoveries, evaluated at three fortification levels, spanned between 69.4 and 88.5 %. The intra-day and inter-day precision was lower than 10.5 % and 17.5 %, respectively. Besides decision limits and detection capabilities, limits of detection (0.011–1.622 μg/kg) and limits of quantitation (0.103–3.770 μg/kg) were also calculated. Calibration curves were built in matrix, in a linear dynamic range between 0.1–60 μg/kg, with determination coefficients higher than 0.9924. The method was finally evaluated with four metrics (AgreePrep, BAGI, SPMS, complexMo-GAPI) and compared with other methods from the literature, showing higher analytical standards, throughput and practicability.
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