Tyczkowska K, Hutchins J E, Hagler W M
J Assoc Off Anal Chem. 1984 Jul-Aug;67(4):739-41.
The official AOAC method for aflatoxin M1 in milk was modified by replacing cellulose column chromatography with cartridge chromatographic cleanup and replacing thin layer chromatographic (TLC) determination with liquid chromatographic (LC) quantitation to yield a new method for bovine and porcine milk. An acetone extract of milk is treated with lead acetate and defatted with hexane, and M1 is partitioned into chloroform as in the AOAC method. Chloroform is removed by evaporation under a stream of nitrogen at 50 degrees C. The residue is dissolved in chloroform, the vessel is rinsed with hexane, and the 2 solutions are applied in sequence to a hexane-activated silica Sep-Pak cartridge. Less polar impurities are removed with hexane-ethyl ether, and M1 is eluted with chloroform-methanol, and determined by C18 reverse phase LC using fluorescence detection. Recoveries of M1 added to bovine milk at 0.25, 0.50, and 1.0 ng/mL were 90.8, 93.4, and 94.1%, respectively. The limit of detection was less than 0.1 ng M1/mL for both bovine and porcine milk.
美国官方分析化学师协会(AOAC)测定牛奶中黄曲霉毒素M1的方法经过了改进,用柱式色谱净化法替代了纤维素柱色谱法,并用液相色谱(LC)定量法替代了薄层色谱(TLC)测定法,从而产生了一种用于测定牛乳和猪乳的新方法。牛奶的丙酮提取物先用醋酸铅处理,再用己烷脱脂,然后按照AOAC方法将M1分配到氯仿中。在50℃下用氮气流蒸发除去氯仿。将残留物溶于氯仿中,用己烷冲洗容器,然后将这两种溶液依次加到经己烷活化的硅胶Sep-Pak柱上。用己烷 - 乙醚除去极性较小的杂质,用氯仿 - 甲醇洗脱M1,并用荧光检测的C18反相液相色谱法进行测定。向牛乳中添加浓度为0.25、0.50和1.0 ng/mL的M1时,回收率分别为90.8%、93.4%和94.1%。牛乳和猪乳中M1的检测限均小于0.1 ng/mL。