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作 者:王可[1] 魏永巨[2] 何燕[1] 曹丽玲[1] 左书梅[1]
机构地区:[1]石家庄市疾病预防控制中心理化检验所,河北050011 [2]河北师范大学化学与材料科学学院
出 处:《环境与健康杂志》2014年第8期718-720,共3页Journal of Environment and Health
基 金:石家庄市科学技术研究与发展计划(121461803)
摘 要:目的建立茶叶中黄曲霉毒素B1、B2、G1和G2的高效液相色谱串联质谱(HPLC-MS/MS)法。方法样品经70%甲醇超声提取15 min,免疫亲和柱净化后,用ZORBAX Eclipse Plus C18色谱柱(2.1 mm×100 mm,1.8μm)进行分离,流动相为甲醇-0.1%甲酸水(体积比为45∶55),采用多反应监测(MRM)正离子模式进行检测。结果在0.5~50.0 ng/ml的线性范围内,所得4种黄曲霉毒素的回归方程均具有良好的线性关系(r≥0.999 5)。该方法检出限为0.02~0.04μg/kg,定量下限为0.07~0.13μg/kg;平均回收率为75.6%~98.5%,RSD为3.9%~7.1%。结论该方法简单、准确、灵敏度高,适用于茶叶中黄曲霉毒素B1、B2、G1和G2的批量检测。Objective To establish a method for the determination of aflatoxins B1,B2,G1 and G2in tea by high performance liquid chromatography tandem mass spectrometry(HPLC-MS/MS). Methods The samples were extracted ultrasonically for 15 min by 70% methanol,then purified by immunoaffinity column. The analytes were seperated by ZORBAX Eclipse Plus C18column(2.1 mm×100 mm,1.8 μm),eluted with methanol-0.1% formic acid solution(45∶55,V/V),then determined by HPLCMS/MS with multiple reation monitoring(MRM) under positive ion mode of electrospray ionization. Results The good linearity of four aflatoxins were achieved in the range of 0.5-50 ng/ml(r≥0.999 5). The limits of detection were 0.02-0.04 μg/kg,and the limits of quantification were 0.07-0.13 μg/kg. The average recoveries of spiked samples were 75.6%-98.5% with the relative standard devitation of 3.9%-7.1%. Conclusion The method is simple,accurate, sensitive and applicable to the determination of aflatoxins B1,B2,G1 and G2in tea.
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