首页|期刊导航|贵州农业科学|基于QuEChERS-UPLC-MS/MS法的茶叶农药残留检测与分析研究

基于QuEChERS-UPLC-MS/MS法的茶叶农药残留检测与分析研究OA

Determination and Analysis of Pesticide Residues in Tea Based on QuEChERS-UPLC-MS/MS

中文摘要英文摘要

[目的]建立可同时检测茶叶中多种农药残留的 QuEChERS-UPLC-MS/MS方法,为茶叶中多类别农药残留的快速筛查提供技术支持.[方法]以绿茶为研究对象,通过优化液相色谱条件与质谱条件,并结合提取溶剂与净化剂的筛选试验,对样品前处理条件进行优化,建立可同时检测 65种农药残留的QuEChERS-UPLC-MS/MS方法,并采用该方法对 43批样品进行检测分析.[结果]65种农药在 0.001~1.000 mg/L体积浓度范围内,色谱峰面积与体积浓度间均呈良好线性关系,R2 均大于 0.990 0(除乙羧氟草醚),定量限均为 5 μg/kg.在 3个浓度(5 μg/kg、25 μg/kg、250 μg/kg)水平下,65种农药的回收率为71%~120%,相对标准偏差为 0.98%~19.63%,低于 NY/T 788-2018规定的 20%,符合要求.43批茶叶共检出10种农药,检出含量范围为 0.001~0.012 mg/kg.其中,啶虫脒检出率最高(14.0%),在 6批茶叶样品中被检出;噻嗪酮次之(9.3%),在 4批茶叶样品中被检出.所有检出样品中的农药残留量均低于茶叶中农药最大残留限量标准.[结论]基于 QuEChERS-UPLC-MS/MS的茶叶农药残留检测法精密度、准确度和灵敏度均满足农药残留检测分析要求,可简单快速地检测茶叶中多种农药残留.

[Objective]The QuEChERS-UPLC-MS/MS method for simultaneously detecting multiple pesticide residues in tea was established to provide technical support for rapid screening of multiple types of pesticide residues in tea.[Method]The pre-treatment conditions of green tea samples were optimized by optimizing the liquid chromatography conditions and mass spectrometry conditions,and combining with the screening experiments of extraction solvents and purification agents,and the established QuEChERS-UPLC-MS/MS method of simultaneously detecting 65 pesticide residues was used to analyze 43 batches of green tea samples.[Result]There was a good linear relationship between the chromatographic peak area and the volume concentration when the volume concentration of 65 pesticides was 0.001-1.000 mg/L.The R2 values all were greater than 0.990 0(except fluoroglycofen)and the quantitative limits were all 5 μg/kg.At three concentration levels of 5 μg/kg,25 μg/kg,and 250 μg/kg,the recovery rates of 65 pesticides ranged from 71%to 120%,and the relative standard deviations were 0.98%-19.63%,which were lower than the 20%specified in NY/T 788-2018 and met the requirements.A total of 10 pesticides were detected in 43 batches of tea samples,and the detected content ranged from 0.001 to 0.012 mg/kg.Among them,acetamiprid had the highest detection rate(14.0%),and was detected in 6 batches of tea samples.Buprofezin had the second highest detection rate(9.3%),and was detected in 4 batches of tea samples.The pesticide residues detected in tested tea samples all were below the maximum residue limit standard for pesticides in tea.[Conclusion]The precision,accuracy and sensitivity of the pesticide residue detection method based on QuEChERS-UPLC-MS/MS all meet the requirements for pesticide residue detection analysis,and it can simply and quickly detect various pesticide residues in tea.

张海艳;朱兴义;宋邦燕;龙育鋆;廖国会;陈明贵;陈湘燕;秦立新;朱峰

贵州省植物保护研究所,贵州 贵阳 550006||贵州省农药风险监测中心,贵州 贵阳 550006贵州大学,贵州 贵阳 550025贵州省植物保护研究所,贵州 贵阳 550006||贵州省农药风险监测中心,贵州 贵阳 550006贵州省植物保护研究所,贵州 贵阳 550006||贵州省农药风险监测中心,贵州 贵阳 550006贵州省植物保护研究所,贵州 贵阳 550006||贵州省农药风险监测中心,贵州 贵阳 550006贵州省植物保护研究所,贵州 贵阳 550006||贵州省农药风险监测中心,贵州 贵阳 550006贵州省植物保护研究所,贵州 贵阳 550006||贵州省农药风险监测中心,贵州 贵阳 550006贵州省植物保护研究所,贵州 贵阳 550006||贵州省农药风险监测中心,贵州 贵阳 550006贵州省植物保护研究所,贵州 贵阳 550006||贵州省农药风险监测中心,贵州 贵阳 550006

农业科技

茶叶农药残留QuEChERSUPLC-MS/MS基质效应检出率

teapesticide residueQuEChERSUPLC-MS/MSmatrix effectdetectable rate

《贵州农业科学》 2026 (9)

58-68,11

贵州省农业科学院青年基金项目(黔农科一般基金[2024]05)贵州省农业科学院"关键核心技术"项目(黔农科 GJHX[2025]05)贵州省优秀青年科技人才项目(黔科合平台人才-YQK[2023]026)2023年省辣椒专班科技支撑项目(品目九)

10.3969/j.issn.1001-3601.2026.09.007

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