[Determination of 79 pesticide residues in fruits and vegetables by QuEChERS-ultra performance liquid chromatography-tandem mass spectrometry].

Le Zhao, Xian-Jun Liu, Hao Zhang, Jian Li, Liang Cai, Xiang Fan, Tan-Yao Li, Dong-Yang Chen
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Abstract

Pesticide residues in fruits and vegetables are becoming a serious issue. These residues can affect the quality of agricultural products and people's health. Therefore, it has become crucial to effectively monitor and control pesticide residues in the food safety field. In this study, a rapid and effective QuEChERS-ultra performance liquid chromatography-tandem mass spectrometry (QuEChERS-UPLC-MS/MS) method was established for the simultaneous determination of 79 typical pesticides in vegetables and fruits, including organophosphates, carbamates, and pyrethroids. The pretreatment, UPLC, and MS/MS conditions were optimized. The fruit and vegetable samples were extracted with frozen acetonitrile after pulverization and homogenization, cleaned up by the QuEChERS method, filtered through a centrifugal membrane, and analyzed by UPLC-MS/MS. The separation was carried out on an ACQUITY UPLC HSS T3 column (100 mm×2.1 mm, 1.8 μm) with gradient elution. The aqueous and organic phases were water-methanol (98∶2, v/v) and methanol-water (98∶2, v/v) respectively, both with 5 mmol/L ammonium acetate and 0.1% formic acid. A triple quadrupole mass spectrometer was used in positive-ion electrospray ionization (ESI+) scanning mode, with target pesticide residues quantified using the matrix-matched standard-curve method. The results showed that under the optimized conditions, the 79 target compounds were determined with good linearities in the range of 0.1-200 μg/L, and the correlation coefficients (r) were all greater than 0.990. The limits of detection (LODs) and limits of quantification (LOQs) of the 79 compounds were in the range of 0.01-4.0 μg/kg and 0.03-13.0 μg/kg. The recoveries at three spiked levels ranged from 78.2% to 119.8%, with relative standard deviations (RSDs) all less than 15.8%. The established method was successfully applied to 80 samples of fruits and vegetables from Hunan province. As a result, 19 pesticides were detected in 31 samples, and thiamethoxam, acetamiprid and clothianidin being the most highly detected with a content range of 0.012-2.62 mg/kg; According to the data of the Hunan province survey yearbook, the percentages of acceptable daily intake (%ADI) for chronic dietary exposure of the detected neonicotinoid insecticides (thiamethoxam and clothianidin) have been calculated. The results indicate that the %ADI of clothianidin in fruits and vegetables ranged from 5.74% to 0.36%, respectively, and the %ADI of thiamethoxam in fruits and vegetables ranged from 0.40% to 19.50%. The %ADI of both pesticides were found to be less than 100%, indicating they are within acceptable limits. The method is simple, sensitive, accurate, and suitable for the simultaneous determination of multiple pesticide residues in fruits and vegetables.

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[quechers -超高效液相色谱-串联质谱法测定果蔬中79种农药残留]。
水果和蔬菜中的农药残留正在成为一个严重的问题。这些残留物会影响农产品的质量和人们的健康。因此,有效监测和控制农药残留已成为食品安全领域的关键。本研究建立了一种快速有效的quechers -超高效液相色谱-串联质谱(QuEChERS-UPLC-MS/MS)同时测定蔬菜和水果中有机磷、氨基甲酸酯、拟除虫菊酯等79种典型农药的方法。对预处理条件、UPLC条件和MS/MS条件进行了优化。果蔬样品粉碎均质后用冷冻乙腈提取,QuEChERS法清洗,离心膜过滤,UPLC-MS/MS分析。采用ACQUITY UPLC HSS T3色谱柱(100 mm×2.1 mm, 1.8 μm)梯度洗脱。水相为水-甲醇(98∶2,v/v),有机相为甲醇-水(98∶2,v/v),乙酸铵为5 mmol/L,甲酸为0.1%。采用三联四极杆质谱仪,采用正离子电喷雾电离(ESI+)扫描模式,采用矩阵匹配标准曲线法定量目标农药残留。结果表明,在优化条件下,79个目标化合物在0.1 ~ 200 μg/L范围内具有良好的线性关系,相关系数(r)均大于0.990。79种化合物的检出限和定量限分别为0.01 ~ 4.0 μg/kg和0.03 ~ 13.0 μg/kg。加样回收率在78.2% ~ 119.8%之间,相对标准偏差(rsd)均小于15.8%。建立的方法成功地应用于湖南省80份水果和蔬菜样品。结果,在31份样品中检出19种农药,其中以噻虫脒、啶虫脒和噻虫脒检出率最高,含量范围为0.012 ~ 2.62 mg/kg;根据湖南省调查年鉴数据,计算出检测到的新烟碱类杀虫剂(噻虫脒和噻虫脒)慢性膳食暴露的可接受日摄入量百分比(%ADI)。结果表明,水果和蔬菜中噻虫胺的%ADI分别为5.74% ~ 0.36%,水果和蔬菜中噻虫嗪的%ADI为0.40% ~ 19.50%。两种农药的每日推荐摄入量均低于100%,均在可接受范围内。该方法简便、灵敏、准确,适用于果蔬中多种农药残留的同时测定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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