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茶叶中硫丹及硫丹硫酸酯的ELISA快速测定

  • 吕潇 ,
  • 任凤山 ,
  • 王文博 ,
  • 杜红霞 ,
  • 李慧冬 ,
  • 丁蕊艳 ,
  • 朱端卫 ,
  • LEENanjuA ,
  • SHEILDRoss ,
  • KENNEDYIvanR
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  • 1. 华中农业大学资源与环境学院,湖北 武汉 430070;
    2. 山东省农业科学院中心实验室,山东 济南 250100;
    3. Department of Food Science & Technology, University of NSW, Sydney, NSW, 2050, Australia;
    4. Agrisearch Analytical, Sydney NSW 2039, Australia;
    5. Faculty of Agriculture, Food and Natural Resources, University of Sydney, Sydney, NSW, 2006, Australia
吕潇(1957- ),女,研究员,在读博士生,主要从事农药残留分析与环境行为研究。

收稿日期: 2005-12-12

  修回日期: 2006-01-12

  网络出版日期: 2019-09-10

基金资助

国家留学基金2002

Determination of Endosulfan and Endosulfan Sulfate in Tea by ELISA

  • LU Xiao ,
  • REN Feng-shan ,
  • WANG Wen-bo ,
  • DU Hong-xia ,
  • LI Hui-dong ,
  • DING Rui-yan ,
  • ZHU Duan-wei ,
  • LEE Nanju A ,
  • SHEILD Ross ,
  • KENNEDY Ivan R
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  • 1. Faculty of Natural Resources & Environment, Huazhong Agricultural University, Wuhan 430070, China;
    2. Central Laboratory, Shandong Academy of Agricultural Sciences, Ji’nan 250100, China;
    3. Department of Food Science & Technology, University of NSW, Sydney, NSW, 2050, Australia;
    4. Agrisearch Analytical, Sydney, NSW, 2039, Australia;
    5. Faculty of Agriculture, Food and Natural Resources, University of Sydney, Sydney, NSW, 2006, Australia

Received date: 2005-12-12

  Revised date: 2006-01-12

  Online published: 2019-09-10

摘要

研究应用酶联免疫方法,快速检测茶叶中硫丹及硫丹硫酸酯。茶叶提取后,不净化,用PBS缓冲液稀释500倍后,进行酶联免疫方法测定,方法平均回收率为86.6%~91.1%;经SPE净化后,回收率68.7%~123%。标准曲线IC50为2βµg/L,线性范围1~10βµg/L。直接提取法最低检测限2βmg/kg,净化法为0.06βmg/kg。经气相色谱/质谱联用方法验证,灵敏度、精密度和准确度均符合快速检测要求。该法具有快速、简便、低耗、易操作等特点。

本文引用格式

吕潇 , 任凤山 , 王文博 , 杜红霞 , 李慧冬 , 丁蕊艳 , 朱端卫 , LEENanjuA , SHEILDRoss , KENNEDYIvanR . 茶叶中硫丹及硫丹硫酸酯的ELISA快速测定[J]. 茶叶科学, 2006 , 26(2) : 141 -146 . DOI: 10.13305/j.cnki.jts.2006.02.013

Abstract

A rapid method based on Enzyme-linked immunosorbent assay (ELISA) was developed for determination of endosulfan isomers and endosulfan sulfate in commercial black and green tea. The average recoveries obtained from crude extracts ranged from 86.6% to 91.1%, which from purified extracts ranged from 68.7% to 123%. The liner range of the standard curve was from 1βµg/L to 10βµg/L. The detection limit of crude extract was 2βmg/kg and the purified was 0.06βmg/kg. This study showed a validation of endosulfan analyzed in tea by ELISA and GC-MS at different levels and proved that ELISA is a quick, low cost and practical technique for monitoring pesticides in tea.

Key words: endosulfan; ELISA; tea; GC/MS

参考文献

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