Tripathy Vandana, Sharma Krishan Kumar, Yadav Rajbir, Devi Suneeta, Tayade Amol, Sharma Khushbu, Pandey Priya, Singh Gitansh, Patel Amar Nath, Gautam Rahul, Gupta Ruchi, Kalra Shobhita, Shukla Poonam, Walia Suresh, Shakil Najam Akhtar
a Project Coordinating Cell, Pesticide Residue Laboratory, All India Network Project on Pesticide Residues , ICAR (Indian Agricultural Research Institute) , New Delhi , India.
b Division of Agricultural Chemicals , ICAR (Indian Agricultural Research Institute) , New Delhi , India.
J Environ Sci Health B. 2019;54(5):394-406. doi: 10.1080/03601234.2019.1574169. Epub 2019 Feb 12.
Extraction and quantification of pesticide residue from the milk matrix at or below the established maximum residue limit (MRL) is a challenging task for both analytical chemists and the regulatory institutions to take corrective actions for the human health and safety. The main aim of the study is to develop a simple rapid and less expensive QuEChERS extraction and cleanup method for simultaneous analysis of 41 multiclass pesticide residue in milk by gas chromatography-electron capture detector (GC-ECD), followed by confirmation of the residues with gas chromatography-mass spectrometer (GC-MS). Effect of sorbent type, temperature, spiking concentration, matrix effect (ME), measurement uncertainty (MU), inter- and intra-assay repeatability, reproducibility of recovery, and trueness of the results were investigated to validate the effectiveness of the method. Limit of determination (LOD) and limit of quantitation (LOQ) for all the analytes ranged within 0.001-0.02 and 0.002-0.05 µg mL, respectively. The % recovery of all the pesticides ranged between 91.38 and 117.56% with relative standard deviation (RSD) below 2.79%. The MU for all the analytes was ≤29% of respective LOQs, and except for few pesticides, the ME was largely negative. The method fulfilled all the SANTE guidelines and thus can be extended for routine analysis of multiclass pesticide residue in milk.
从牛奶基质中提取和定量测定处于或低于既定最大残留限量(MRL)的农药残留,对于分析化学家和监管机构采取纠正措施以保障人类健康与安全而言,是一项具有挑战性的任务。本研究的主要目的是开发一种简单、快速且成本较低的QuEChERS提取和净化方法,用于通过气相色谱 - 电子捕获检测器(GC - ECD)同时分析牛奶中的41种多类农药残留,随后用气相色谱 - 质谱仪(GC - MS)对残留进行确证。研究了吸附剂类型、温度、加标浓度、基质效应(ME)、测量不确定度(MU)、批内和批间重复性、回收率的重现性以及结果的准确性,以验证该方法的有效性。所有分析物的测定限(LOD)和定量限(LOQ)分别在0.001 - 0.02和0.002 - 0.05 μg/mL范围内。所有农药的回收率在91.38%至117.56%之间,相对标准偏差(RSD)低于2.79%。所有分析物的MU≤各自LOQ的29%,除少数农药外,基质效应大多为负。该方法符合所有SANTE指南,因此可扩展用于牛奶中多类农药残留的常规分析。