[quechers -在线凝胶渗透色谱-气相色谱-串联质谱法高通量筛选动物性食品中多种农药残留]。

IF 1.2 4区 化学 Q4 CHEMISTRY, ANALYTICAL 色谱 Pub Date : 2023-07-01 DOI:10.3724/SP.J.1123.2022.10010
Jie Li, Xiang Ju, Yan-Li Wang, Qi-Yan Tian, Xiu-Qing Liang, Hai-Xia Li, Yan-Ming Liu
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引用次数: 0

摘要

生活水平的提高导致了动物性食品消费的增加。在动物饲养和肉类生产加工过程中,为防治和保存有害生物,可能非法使用农药。施用于作物的农药也可能通过食物链在动物组织中富集,从而增加农药残留在肌肉和内脏组织中积累的风险,危害人体健康。中国规定了畜禽肉及其内脏中农药残留的最高限量。许多其他主要发达国家和组织,包括欧盟、食品法典委员会和日本,也制定了这些残留物的最大残留限量(分别为0.005-10、0.004-10和0.001-10 mg/kg)。植物源性食品中农药残留检测的预处理技术研究较为广泛,但对动物源性食品的农药残留检测重视不够。因此,动物源性食品中农药残留的高通量检测技术是有限的。干扰植物性食品检测过程的杂质主要有有机酸、极性色素等小分子化合物;相比之下,动物源性食品的基质要复杂得多。大分子蛋白质、脂肪、小分子氨基酸、有机酸和磷脂会干扰动物源性食品中农药残留的检测。因此,选择合适的预处理和净化技术是非常重要的。本研究将QuEChERS技术与在线凝胶渗透色谱-气相色谱-串联质谱(GPC-GC-MS/MS)相结合,对196种动物源性食品中的农药残留进行了检测。样品乙腈提取,QuEChERS技术联用在线GPC纯化,GC-MS/MS检测,多反应监测模式(MRM)测定,外标法定量。考察了萃取溶剂和纯化剂类型对萃取效率和基质去除率的影响。考察了在线GPC对样品溶液的净化效果。通过研究不同馏分接收周期内目标物质的回收率和基质效应,得到最佳馏分接收时间,实现目标物质的有效引入和基质的高效去除。进一步评价了QuEChERS技术与在线GPC技术相结合的优点。评价了196种农药的基质效应;10种农药残留表现为中等基质效应,4种农药残留表现为强基质效应。采用矩阵匹配标准溶液定量。196种农药在0.005 ~ 0.2 mg/L范围内呈良好的线性关系,相关系数大于0.996。检测限为0.002 mg/kg,定量限为0.005 mg/kg。196种农药在0.01、0.05和0.20 mg/kg加标水平下的加标回收率为65.3% ~ 126.2%,相对标准偏差(rsd)为0.7% ~ 5.7%。该方法快速、准确、灵敏;因此,适用于动物性食品中多种农药残留的高通量筛选和检测。
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[High-throughput screening of multi-pesticide residues in animal-derived foods by QuEChERS-online gel permeation chromatography-gas chromatography-tandem mass spectrometry].

Improvements in living standards have led to an increase in the consumption of animal-derived foods. Pesticides may be used illegally during animal breeding as well as meat production and processing for pest control and preservation. Pesticides applied to crops may also be enriched in animal tissues through the food chain, thereby increasing the risk of pesticide residue accumulation in muscles and visceral tissues and endangering human health. China has stipulated maximum residue limits for pesticide residues in livestock and poultry meat and their viscera. Many other major developed countries and organizations, including the European Union, Codex Alimentarius Commission, and Japan, have also set maximum residue limits for these residues (0.005-10, 0.004-10, and 0.001-10 mg/kg, respectively). Research on pretreatment technologies for pesticide residue detection in plant-derived foods is widely available, but insufficient attention has been paid to animal-derived foods. Thus, high-throughput detection technologies for pesticide residues in animal-derived foods are limited. The impurities that can interfere with the detection process for plant-derived foods mainly include organic acids, polar pigments, and other small molecular compounds; by contrast, the matrix of animal-derived foods is much more complex. Macromolecular proteins, fats, small molecular amino acids, organic acids, and phospholipids can interfere with the detection of pesticide residues in animal-derived foods. Thus, selecting the appropriate pretreatment and purification technology is of great importance. In this study, the QuEChERS technique was combined with online gel permeation chromatography-gas chromatography-tandem mass spectrometry (GPC-GC-MS/MS) to determine 196 pesticide residues in animal-derived foods. The samples were extracted with acetonitrile, purified using the QuEChERS technique coupled with online GPC, detected by GC-MS/MS, determined in multiple reaction monitoring mode (MRM), and quantified using the external standard method. The effects of the extraction solvent and purification agent type on the extraction efficiency and matrix removal of the method were optimized. The purification effect of online GPC on the sample solution was investigated. The optimal distillate receiving time was obtained by studying the recoveries of the target substances and matrix effects over different distillate receiving periods to achieve the effective introduction of target substances and efficient matrix removal. Further, the advantages of the QuEChERS technique combined with online GPC were evaluated. The matrix effects of 196 pesticides were assessed; ten pesticide residues showed moderate matrix effects, while four pesticide residues showed strong matrix effects. A matrix-matched standard solution was used for quantification. The 196 pesticides showed good linearity in the range of 0.005-0.2 mg/L, with correlation coefficients greater than 0.996. The limits of detection and quantification were 0.002 and 0.005 mg/kg, respectively. The recoveries of 196 pesticides at spiked levels of 0.01, 0.05, and 0.20 mg/kg were 65.3%-126.2%, with relative standard deviations (RSDs) of 0.7%-5.7%. The proposed method is rapid, accurate, and sensitive; thus, it is suitable for the high-throughput screening and detection of multiple pesticide residues in animal-derived foods.

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来源期刊
色谱
色谱 CHEMISTRY, ANALYTICAL-
CiteScore
1.30
自引率
42.90%
发文量
7198
期刊介绍: "Chinese Journal of Chromatography" mainly reports the basic research results of chromatography, important application results of chromatography and its interdisciplinary subjects and their progress, including the application of new methods, new technologies, and new instruments in various fields, the research and development of chromatography instruments and components, instrument analysis teaching research, etc. It is suitable for researchers engaged in chromatography basic and application technology research in scientific research institutes, master and doctoral students in chromatography and related disciplines, grassroots researchers in the field of analysis and testing, and relevant personnel in chromatography instrument development and operation units. The journal has columns such as special planning, focus, perspective, research express, research paper, monograph and review, micro review, technology and application, and teaching research.
期刊最新文献
[Off-line comprehensive two-dimensional countercurrent chromatography-liquid chromatography separation of Curcuma volatile oil]. [Advances in synthesis methods and applications of microporous organic networks for sample preparation]. [Application progress of on-line sample preparation techniques coupled with liquid chromatography-mass spectrometry system in the detection of food hazards]. [Chiral capillary gas chromatography for the separation of the enantiomers of 4-chloromethyl-2,2-dimethyl-1,3-dioxolane]. [Determination of 14 β-agonists in animal meat by ultra high performance liquid chromatography-tandem mass spectrometry].
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