Gertz C, Böschemeyer L
Z Lebensm Unters Forsch. 1980;171(5):335-40. doi: 10.1007/BF01087127.
A simple analytical method for multiple mycotoxins was developed for detecting aflatoxin B1, B2, G1, G2, M1, and M2, sterigmatocystin, penicillin acid, ochratoxin A and patulin. These mycotoxins were extracted with ethyl acetate. The extract was cleaned up by chromatography on silica mini-column. Each fraction was separated by thin-layer chromatography. The final evaluation of the TLC-plates was carried out by fluorodensitometry. A considerable increase in fluorescence intensity was achieved by spraying the plates with paraffin after development. The detection limits of fluorescent mycotoxins and the fluorescent derivates of penicillic acid and sterigmatocystin were lowered to 1:10 up to 1:100. Spots of patulin were measured by fluorescence quenching.
开发了一种用于多种霉菌毒素的简单分析方法,用于检测黄曲霉毒素B1、B2、G1、G2、M1和M2、杂色曲霉素、青霉素酸、赭曲霉毒素A和展青霉素。这些霉菌毒素用乙酸乙酯提取。提取物通过硅胶微型柱色谱进行净化。每个馏分通过薄层色谱分离。通过荧光密度测定法对薄层板进行最终评估。展开后用石蜡喷雾板可使荧光强度显著增加。荧光霉菌毒素以及青霉素酸和杂色曲霉素的荧光衍生物的检测限降低到1:10至1:100。展青霉素的斑点通过荧光猝灭进行测量。