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免疫亲和柱净化/柱前衍生化-高效液相色谱荧光检测法测定粮谷中的T-2毒素
引用本文:李军,许烨,隋凯,卫锋,赵守成,王玉萍.免疫亲和柱净化/柱前衍生化-高效液相色谱荧光检测法测定粮谷中的T-2毒素[J].色谱,2006,24(3):256-259.
作者姓名:李军  许烨  隋凯  卫锋  赵守成  王玉萍
作者单位:1.Liaoning Entry & Exit Inspection and Quarantine Bureau, Dalian 116001, China; 2.Shenyang Agriculture University, Shenyang 110161, China
摘    要:建立了免疫亲和柱净化/柱前衍生化-高效液相色谱荧光检测器测定粮谷中T-2毒素含量的方法。样品经甲醇-水(体积比为80∶20)混合溶剂提取,通过免疫亲和柱(IAC)净化,以氰酸蒽(1-AN)为衍生化试剂、4-二甲基氨基吡啶(DMAP)为催化剂进行衍生,以ZORBAX Eclipse XDB-C18 柱为分离柱,乙腈-水(体积比为80∶20)为流动相进行高效液相色谱分离及荧光检测,荧光检测的激发波长为381 nm,发射波长为470 nm。T-2毒素的质量浓度为0.01~1.5 mg/L时与峰高呈良好的线性,相关系数为0.9985。在0.01~1.5 μg/g添加水平下,回收率为79.7%~94.5%,相对标准偏差小于7%;检出限(S/N=3)为0.01 μg/g。该方法净化效果好,灵敏度高,操作简便快速。

关 键 词:免疫亲和柱  柱前衍生化  高效液相色谱法  荧光检测  T-2毒素  粮谷
文章编号:1000-8713(2006)03-0256-04
收稿时间:2005-05-19
修稿时间:2005年5月19日

Determination of T-2 Toxin in Cereal Grains by High Performance Liquid Chromatography with Fluorescence Detection after Immunoaffinity Column Clean-Up and Precolumn Derivatization
LI Jun,XU Ye,SUI Kai,WEI Feng,ZHAO Shoucheng,WANG Yuping.Determination of T-2 Toxin in Cereal Grains by High Performance Liquid Chromatography with Fluorescence Detection after Immunoaffinity Column Clean-Up and Precolumn Derivatization[J].Chinese Journal of Chromatography,2006,24(3):256-259.
Authors:LI Jun  XU Ye  SUI Kai  WEI Feng  ZHAO Shoucheng  WANG Yuping
Institution:1.Liaoning Entry & Exit Inspection and Quarantine Bureau, Dalian 116001, China; 2.Shenyang Agriculture University, Shenyang 110161, China
Abstract:A method has been developed for the determination of T-2 toxin in cereal grains by high performance liquid chromatography with fluorescence detection after immunoaffinity column clean-up and precolumn derivatization. The derivatization reaction was used to develop a sensitive, reproducible and accurate method for the determination of T-2 toxin in wheat, corn, barley and rice. T-2 toxin was extracted with methanol-water (80: 20, v/v), purified by immunoaffinity columns containing antibodies specific for T-2 toxin, and quantified by reversed-phase high performance liquid chromatography with fluorescence detection (excitation wavelength, 381 nm; emission wavelength, 470 nm) after derivatization with 1-anthroylnitrile (1-AN) and 4-dimethylaminopyridine (DMAP). ZORBAX Eclipse XDB-C18 column and mobile phase of acetonitrile-water (80: 20, v/v) were used for the analysis. Recoveries from the different cereals spiked with T-2 toxin at levels ranging from 0.01 to 1.5 microg/g were from 79.7% to 94.5%, the relative standard deviations were lower than 7% and the limit of detection was 0.01 microg/g based on a signal-to-noise ratio of 3: 1.
Keywords:immunoaffinity column  precolumn derivatization  high performance liquid chromatography(HPLC)  fluorescence detection  T-2 toxin  cereal grains  
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