李 玮,贾彦博,林伟杰,王秀丽,金崇崇,马慧丽,洪春来.分散固相萃取净化-气相色谱-质谱联用法测定茶叶中7种杀螨杀虫类农药残留[J].食品安全质量检测学报,2017,8(9):3485-3490
分散固相萃取净化-气相色谱-质谱联用法测定茶叶中7种杀螨杀虫类农药残留
Determination of 7 pesticides residues in tea by gas chromatography-mass spectrometry combined with dispersive solid phase extraction
投稿时间:2017-07-25  修订日期:2017-09-12
DOI:
中文关键词:  分散固相萃取  气相色谱-质谱法  茶叶  噻螨酮  噻嗪酮  哒螨灵、喹瞒醚、苯醚甲环唑、联苯菊酯  氟氰戊菊酯
英文关键词:dispersive solid phase extraction  gas chromatography-mass spectrometry  tea  hexythiazox  buprofezin  pyridaben  fenazaquin  difenoconazole  bifenthrin  flucythrinate
基金项目:浙江省食药监管系统科技计划资助项目(SP201709)
作者单位
李 玮 杭州市食品药品检验研究院 
贾彦博 杭州市食品药品检验研究院 
林伟杰 杭州市食品药品检验研究院 
王秀丽 杭州市食品药品检验研究院 
金崇崇 杭州市食品药品检验研究院 
马慧丽 杭州市食品药品检验研究院 
洪春来 浙江省农业科学院 
AuthorInstitution
LI Wei Hangzhou Institute for Food and Drug Control 
JIA Yan-Bo Hangzhou Institute for Food and Drug Control 
LIN Wei-Jie Hangzhou Institute for Food and Drug Control 
WANG Xiu-Li Hangzhou Institute for Food and Drug Control 
JIN Chong-Chong Hangzhou Institute for Food and Drug Control 
MA Hui-Li Hangzhou Institute for Food and Drug Control 
HONG Chun-Lai Zhejiang Academy of Agricultural Sciences 
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中文摘要:
      目的 建立茶叶中7种农药残留的快速检测方法。方法 采用分散固相萃取净化, 气相色谱-质谱法(gas chromatography-mass spectrometry, GC-MS)测定茶叶中噻螨酮、噻嗪酮、哒螨灵、喹瞒醚、苯醚甲环唑、联苯菊酯和氟氰戊菊酯7种农药的残留。结果 7种农药在0.05~5.00 mg/kg范围有良好的线性关系, 相关系数均大于或等于0.9995。3个浓度的平均加标回收率为70%~115%, 相对标准偏差为5.0%~13.2%; 方法检出限(limit of detection, LOD)为0.005~0.05 mg/kg, 定量限(limit of quantitation, LOQ)为0.015~0.15 mg/kg。采用此方法抽检了我国不同地区市场上的110批次的茶叶样品, 其中有15批次样品检出联苯菊酯, 含量在24~1640 μg/kg之间; 有4批次样品中检出噻嗪酮, 含量在35~150 μg/kg之间; 3批次样品检出哒螨灵, 含量在70~200 μg/kg之间。结论 本方法符合农药残留分析标准的要求, 可用于茶叶中7种农药残留的快速检测和确证分析。
英文摘要:
      Objective To establish a rapid detection method for 7 pesticide residues in tea. Methods The residues of hexythiazox, buprofezin, pyridaben, fenazaquin, difenoconazole, bifenthrin and flucythrinate in tea were detected by dispersion solid phase extraction purification combined with gas chromatography-mass spectrometry (GC-MS). Results The 7 pesticides had good linear relationships in the range of 0.05~5.00 mg/kg, and the correlation coefficients were larger than or equal to 0.9995. The recoveries of 7 pesticides of 3 different spiked levels were 70%~115%, with the relative standard deviations of 5.0%~13.2%. The limits of detection for 7 pesticides were 0.005~0.05 mg/kg, and limits of quantitation, were 0.015~0.15 mg/kg. The results of application of the established method in the detection of 110 batches of tea samples in different regions of China showed that, flucythrinate was detected in 15 batches of samples, and the content was 24~1640 μg/kg, buprofezin was detected in 4 batches of samples, and the content was 35~150 μg/kg, and pyridaben was detected in 3 batches of samples, and the content was 70~200 μg/kg. Conclusion The established method meets the requirements of pesticide residue analysis standard, which is suitable for the rapid detection and corroboration analysis of 7 pesticide residues in tea.
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