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在线萃取和 LC-MS/MS 同时分析极性和非极性农药的全球方法验证。

Validation of a global method for the simultaneous analysis of polar and non-polar pesticides by online extraction and LC-MS/MS.

机构信息

Department of Chemistry, Università di Roma La Sapienza, Piazzale Aldo Moro 5, 00185 Rome, Italy.

Department of Chemistry, Università di Roma La Sapienza, Piazzale Aldo Moro 5, 00185 Rome, Italy.

出版信息

Anal Chim Acta. 2024 Nov 15;1329:343231. doi: 10.1016/j.aca.2024.343231. Epub 2024 Sep 10.

Abstract

BACKGROUND

Multi-residue methods for pesticide analysis in food are available for many compounds, but polar pesticides are not generally included due to their specific properties, which include high polarity and low molecular weight. Single residue methods are therefore needed for sample preparation, while chromatographic separation often requires derivatization, ion paring, or dedicated methods suitable for polar compounds, mostly ion chromatography and hydrophilic interaction liquid chromatography (HILIC). These challenges affect the important pesticide glyphosate and the related compounds aminomethylphosphonic acid (AMPA) and glufosinate. There are only a few methods including these compounds in large-scale analysis, mostly complex methods based on multidimensional chromatography.

RESULTS

A new method, for the global online extraction and analysis of pesticides in beer was developed and validated. The method exploited an online trapping device, with reversed-phase (RP) and anion exchange properties, that can trap small molecules from liquid samples. The ion exchange mechanism was used to retain the very polar pesticides glyphosate, AMPA, and glufosinate. The hydrophobic properties of the trapping column were also exploited to trap pesticides suitable for multi-residue investigations. The chromatographic separation was optimized by comparison of HILIC and RP C30, which could separate pesticides, including the polar ones, with modulation by the trapping column after proper selection of the mobile phase composition and basic modifier. The validation for beer provided recoveries in the range 71-112 %, with <15 % RSD, and LOD and LOQ values of 0.02-1 and 0.3-3 μg L, respectively. The result was competitive with previous methods on polar pesticide analysis in beer.

SIGNIFICANCE

The method was validated for 15 pesticides, over the log K range from -4.4 to 4.5, using a methodology with single and fast chromatographic separation under conditions compatible with multi-residue analysis by RP-LC-MS/MS. In the case of beer, for which the method was validated, the sample preparation was also performed online, after simple degassing, and sample dilution.

摘要

背景

食品中农药多残留分析方法已经有很多,但由于极性农药具有高极性和低分子量等特殊性质,通常不包括这些农药。因此,需要进行单残留方法的样品前处理,而色谱分离通常需要衍生化、离子配对或专门针对极性化合物的方法,主要是离子色谱法和亲水相互作用液相色谱法(HILIC)。这些挑战影响了重要的农药草甘膦以及相关的氨基甲基膦酸(AMPA)和草铵膦。只有少数方法包括这些化合物的大规模分析,主要是基于多维色谱的复杂方法。

结果

开发并验证了一种新的用于啤酒中农药全球在线提取和分析的方法。该方法利用在线捕集装置,具有反相(RP)和阴离子交换特性,可从液体样品中捕集小分子。离子交换机制用于保留非常极性的农药草甘膦、AMPA 和草铵膦。还利用捕集柱的疏水性来捕集适合多残留研究的农药。通过比较亲水作用色谱法(HILIC)和 RP C30 对色谱分离进行了优化,通过适当选择流动相组成和碱性修饰剂,在捕集柱后进行调制,可以分离包括极性农药在内的农药。在啤酒中的验证结果表明,回收率在 71-112%之间,相对标准偏差(RSD)<15%,LOD 和 LOQ 值分别为 0.02-1 和 0.3-3 μg/L。与以前啤酒中极性农药分析的方法相比,该方法具有竞争力。

意义

该方法使用单步和快速色谱分离,在与 RP-LC-MS/MS 多残留分析兼容的条件下,验证了 15 种农药,其 log K 值范围为-4.4 至 4.5。在对啤酒进行验证的情况下,样品制备也可以在线进行,只需简单脱气和样品稀释。

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