Gregory J F, Manley D
J Assoc Off Anal Chem. 1981 Jan;64(1):144-51.
A method was developed for the determination of aflatoxins, M1, B1, G1, B2, and G2 in animal tissues, meat, eggs, and dairy products by high performance liquid chromatography (HPLC). Previous extraction procedures were modified to optimize the precision and recovery of the method. HPLC is performed isocratically with a 5 micrometer microparticulate octadecylsilica column and fluorometric detection. The analysis is based on treatment of the purified sample extract or standard with trifluoroacetic acid (TFA) to catalyze the hydration of aflatoxins M1, B1, and G1 to the highly fluorescent M2a, B2a, and G2a derivatives. Analysis by HPLC with and without TFA treatment of the extract provides quantitative and qualitative data. The recovery of added aflatoxins and the precision of the recovery depend on the type of sample; mean coefficient of variation for all recovery values was 19.7 +/- 11.0% for the analysis of liver, ground beef, dairy products, and eggs. The method was sensitive, with a detection limit of 0.05 + 0.10 ng/g for each aflatoxin. This procedure provides an alternative to existing thin layer chromatographic methods for determining aflatoxins in animal tissues and products
开发了一种通过高效液相色谱法(HPLC)测定动物组织、肉类、蛋类和乳制品中黄曲霉毒素M1、B1、G1、B2和G2的方法。对先前的提取程序进行了改进,以优化该方法的精密度和回收率。使用5微米微粒十八烷基硅胶柱进行等度HPLC分离,并采用荧光检测。该分析基于用三氟乙酸(TFA)处理纯化的样品提取物或标准品,以催化黄曲霉毒素M1、B1和G1水合生成高荧光的M2a、B2a和G2a衍生物。对提取物进行TFA处理和未进行TFA处理的HPLC分析可提供定量和定性数据。添加黄曲霉毒素的回收率和回收精密度取决于样品类型;对肝脏、碎牛肉、乳制品和蛋类进行分析时,所有回收率值的平均变异系数为19.7±11.0%。该方法灵敏度高,每种黄曲霉毒素的检测限为0.05+0.10 ng/g。该程序为测定动物组织和产品中的黄曲霉毒素提供了一种替代现有薄层色谱法的方法。