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采用QuEChERS萃取和GC/MS法测定鸡胸肉中多类农药的方法验证与应用

Validation and application of a method for determination of multi-class pesticides in muscle chicken breast fillets using QuEChERS extraction and GC/MS.

作者信息

Tasic Aleksandra Mihail, Ninković Milan, Pavlović Ivan

机构信息

Department of Chemistry, Biochemistry and Drug Testing, Belgrade, Serbia.

Department of Immunology, Belgrade, Serbia.

出版信息

J Vet Res. 2024 Jun 22;68(2):223-232. doi: 10.2478/jvetres-2024-0036. eCollection 2024 Jun.

DOI:10.2478/jvetres-2024-0036
PMID:38947162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11210362/
Abstract

INTRODUCTION

The occurrence of pesticide residues in animal products deserves attention because of the contamination by environmental pollutants and pesticides that may be present in the food that animals are fed. The goal of this work was the validation of a method for detection of residues of multiple classes of pesticide and determination of their residues in chicken breast fillets.

MATERIAL AND METHODS

Gas chromatography with mass spectrometry was used for analysis. A modified quick, easy, cheap, effective, rugged and safe (QuEChERS) method was put into practice for its validation and applied to real samples. The study optimised mass detection and investigated the effect of a freezing step during the preparation of samples. Pesticides were determined in samples from conventional and organic production.

RESULTS

The impact of the matrix effect decreased, with the largest number of pesticides and satisfactory recovery determined by the application of mixed solvent acetonitrile and ethyl acetate for extraction. Detection of pesticide residues was achieved in a linear range between 5 and 50 µg/kg with satisfactory excellent correlation coefficients greater than 0.99. The recovery of all the pesticide residues ranged between 71.2 and 118.80%. The relative standard deviation was from 2.9% to 18.1% for all validated pesticide residues. The limits of quantification were in the range of 3.0-4.9 µg/kg. Out of 56 pesticide residues analysed in real samples, 5 were detected: α endosulfan, cypermethrin, endosulfan sulphate, permethrin and ,-dichlorodiphenyltrichloroethane (DDT) and their concentrations ranged from 4.9 to 15.2 µg/kg.

CONCLUSION

All tested samples were compliant with the evaluation criteria, and detected values of pesticide residues were lower than the maximum residual levels.

摘要

引言

由于动物所食用的食物中可能存在环境污染物和农药污染,动物产品中农药残留的出现值得关注。这项工作的目标是验证一种检测多种农药残留的方法,并测定鸡胸肉片中的农药残留量。

材料与方法

采用气相色谱 - 质谱联用进行分析。实践了一种改进的快速、简便、廉价、有效、耐用且安全(QuEChERS)方法用于验证,并应用于实际样品。该研究优化了质谱检测,并研究了样品制备过程中冷冻步骤的影响。测定了常规生产和有机生产样品中的农药。

结果

基质效应的影响降低,通过应用乙腈和乙酸乙酯混合溶剂进行萃取,测定的农药数量最多且回收率令人满意。农药残留的检测在5至50μg/kg的线性范围内实现,相关系数大于0.99,令人满意。所有农药残留的回收率在71.2%至118.80%之间。所有验证的农药残留的相对标准偏差为2.9%至18.1%。定量限在3.0 - 4.9μg/kg范围内。在实际样品分析的56种农药残留中,检测到5种:α - 硫丹、氯氰菊酯、硫丹硫酸酯、氯菊酯和滴滴涕(DDT),其浓度范围为4.9至15.2μg/kg。

结论

所有测试样品均符合评估标准,检测到的农药残留值低于最大残留限量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/321b/11210362/a31485391092/j_jvetres-2024-0036_fig_001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/321b/11210362/a31485391092/j_jvetres-2024-0036_fig_001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/321b/11210362/a31485391092/j_jvetres-2024-0036_fig_001.jpg

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