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超高效液相色谱-串联质谱法测定茶叶中毒死蜱及其主要代谢物残留 被引量:8

Determination of Chlorpyrifos and Its Main Metabolite in Tea by Ultra-High Performance Liquid ChromatographyTandem Mass Spectrometry
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摘要 建立了超高效液相色谱-串联质谱(UPLC-MS/MS)法同时测定茶叶中毒死蜱(CPF)及其代谢产物3,5,6-三氯-2-羟基吡啶(TCP)残留量的分析检测方法。茶叶样品经4 mL水润湿后,用5%(V/V)乙酸酸化的乙腈提取,100 mg石墨化炭黑(GCB)和200 mg十八烷基硅烷(C_(18))净化,在仪器分析前用去离子水等体积稀释净化。CPF和TCP分别采用电喷雾正离子(ESI^+)和负离子(ESI^-)电离,可编程多反应监测(sM RM)模式监测,基质标准溶液内标法定量。结果表明,CPF和TCP分别在0.4~400.0μg/L和0.4~80.0μg/L浓度范围内线性关系良好(R^2> 0.99),方法的检出限(LOD,S/N=3)分别为0.06μg/kg和0.04~0.08μg/kg,定量限(LOQ,S/N=10)分别为0.20μg/kg和0.14~0.26μg/kg。在2.0、10.0和20.0μg/kg添加水平下,CPF和TCP的回收率分别为93.9%~111.4%和92.4%~118.4%,相对标准偏差(RSD,n=6)在3.2%~11.1%之间。本方法简便、快速、灵敏度高、重现性好,适用于茶叶中CPF和TCP的快速测定。 A sensitive method was developed for simultaneous determination of chlorpyrifos(CPF)and its main metabolite 3,5,6-trichloro-2-pyridinol(TCP)in tea samples by QuEChERS and ultra-high performance liquid chromatography coupled with tandem mass spectrometry.Tea samples were extracted with acidic acetonitrile(containing 5%acetic acid),and cleaned up by the mixture of adsorbents containing 100 mg of graphitized carbon black(GCB)and 200 mg of C18.The extracts were diluted with deionized water equally in volume prior to instrumental analysis.Scheduled multiple reaction monitoring in positive ion mode was applied to detection of chlorpyrifos and selected ion recording in negative mode was applied to detection of TCP.The matrix-matched internal standard method was used for quantification.The results showed that the method provided linear ranges from 0.4 to 400μg/kg and 0.4 to 80μg/kg for CPF and TCP respectively with the correlation coefficients of larger than 0.99.The limits of detection(S/N=3)were 0.06μg/kg for CPF and 0.04-0.08μg/kg for TCP,while the limits of quantification(S/N=10)were 0.20μg/kg for CPF and 0.14-0.26μg/kg for TCP.The recoveries were ranged from 93.9%to 111.4%for CPF and 92.4%to 118.4%for TCP respectively with the relative standard deviations(RSD,n=6)of 3.2%-11.1%.This method was sensitive,rapid,simple and had good reproducibility,indicating that it was suitable for simultaneous determination of CPF and TCP in tea samples.
作者 尹鹏 郭桂义 代金霞 诸力 高贯威 陈红平 刘新 YIN Peng;GUO Gui-Yi;DAI Jin-Xia;ZHU Li;GAO Guan-Wei;CHEN Hong-Ping;LIU Xin(Department of Tea Science,Xinyang Agriculture and Forestry University,Henan Key Laboratory of Tea Plant Comprehensive Utilization in South Henan,Xinyang 464000,China;Key Laboratory of Tea Quality and Safety Control,Ministry of Agriculture and Rural Affairs,Hangzhou 31008,China;Tea Research Institute,Chinese Academy of Agricultural Sciences,Hangzhou 31008,China;Tea Quality and Safety and Risk Assessment,Ministry of Agriculture and Rural Affairs,Hangzhou 31008,China)
出处 《分析化学》 SCIE EI CAS CSCD 北大核心 2019年第2期306-314,共9页 Chinese Journal of Analytical Chemistry
基金 农业农村部茶叶质量安全控制重点实验室开放课题(No.TRI20180101) 河南省科技攻关项目(No.182102110225) 茶叶产业技术体系(CARS-23) 茶叶质量与风险评估创新团队(No.CAAS-ASTIP-2014-TRICAAS)资助~~
关键词 茶叶 毒死蜱 3 5 6-三氯-2-羟基吡啶 超高效液相色谱-串联质谱 Tea Chlorpyrifos 3,5,6-Trichloro-2-pyridinol Ultra-high performance liquid chromatography coupled with tandem mass spectrometry
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