Van Egmond H P, Paulsch W E, Schuller P L
J Assoc Off Anal Chem. 1978 Jul;61(4):809-12.
The identity of aflatoxin M1 can easily be confirmed directly on a thin layer plate by reacting aflatoxin M1 with trifluoroacetic acid (TFA). This confirmation reaction is carried out on the thin layer plate which has been developed in 2 dimensions and used for the quantitation of aflatoxin M1 in the sample. TFA is superimposed on the separated M1 spot. The plate is kept in the dark 3 min, heated to 75 degrees C for 5 min, and developed with chloroform-methanol-acetic acid-water (92 + 8 + 2 + 0.8). The Rf value of the blue-fluorescent derivative is compared with that for the M1 standard. The method was used successfully on extracts of milk, cheese, and liver. M1 quantities on the plate as low as 0.5 ng can be confirmed by this method. The method is also suitable for simultaneous confirmation of aflatoxin B1.
通过使黄曲霉毒素M1与三氟乙酸(TFA)反应,可在薄层板上直接轻松确认黄曲霉毒素M1的身份。此确认反应在已进行二维展开并用于定量样品中黄曲霉毒素M1的薄层板上进行。将TFA叠加在分离出的M1斑点上。将板子置于暗处3分钟,加热至75摄氏度5分钟,然后用氯仿 - 甲醇 - 乙酸 - 水(92 + 8 + 2 + 0.8)展开。将蓝色荧光衍生物的比移值与M1标准品的比移值进行比较。该方法已成功应用于牛奶、奶酪和肝脏的提取物。通过该方法可确认板上低至0.5纳克的M1含量。该方法也适用于同时确认黄曲霉毒素B1。