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A Cooperative Method for Detemination of Aflatoxin Bi in Tea by Immunoaffinity Column Purification and HPLC-FLD with Post-Column Photochemical Derivatization

机译:用免疫亲和力柱纯化和HPLC-FLD与柱后光化学衍生化测定黄曲霉毒素BI的合作方法

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A method for determination of aflatoxin B1 in tea by using HPLC-FLD with photochemical derivatization after immunoaffinity column purification was developed, and the determination conditions of sample were optimized in this paper. The sample was purified by immunoaffinity column using the mobile phase composed of methanol and water (60:40, v/v), then quantified with fluorescence detection after photochemical derivatization. The results showed that this method to determine aflatoxin Bi was finished within 12.5 min under the optimum conditions. The standard curve had a good linearity when the aflatoxin Bi was in the range of 0.2—20 pg/L. The correlation coefficient, the limits of detection and quantification, the recovery rate and the relative standard deviation of the method were 0.9999, 0.03 ng/g (S/N=3), 0.11ng/g (S/N=10), 80%—90% and 1.4%—2.4% (n=5), respectively. This is a very simple method and it has high sensitivity and good repeatability, which is applicable to determine the content of aflatoxin Bi in tea sample.
机译:开发了通过使用HPLC-FLD测定茶叶中黄曲霉毒素B1的方法,在显影衍生中进行了显影性衍生化,并在本文中优化了样品的测定条件。使用由甲醇和水组成的流动相(60:40,V / V)组成的流动相,通过免疫亲和力柱纯化样品,然后在光化学衍生化后用荧光检测量化。结果表明,在最佳条件下,该方法在12.5分钟内完成1mlAlatoxin Bi的方法。当黄曲霉毒素BI为0.2-20 pg / L时,标准曲线具有良好的线性。该方法的相关系数,检测率和定量的限制,方法的回收率和相对标准偏差为0.9999,0.03ng / g(s / n = 3),0.11ng / g(s / n = 10),80 %-90%和1.4%-2.4%(n = 5)。这是一种非常简单的方法,它具有高灵敏度和良好的重复性,这适用于确定茶样品中的黄曲霉毒素BI的含量。

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