Hetmanski M T, Scudamore K A
ADAS Slough Laboratory, Berks, U.K.
Food Addit Contam. 1989 Jan-Mar;6(1):35-48. doi: 10.1080/02652038909373737.
A simple and sensitive procedure is described for the analysis of aflatoxins B1, B2, G1 and G2 in cereal and animal feedstuff samples. Aflatoxins are extracted with dichloromethane:water (10:1). Gel permeation chromatography (GPC) using a column packed with Bio-beads S-X3 and dichloromethane:hexane (3:1) as the eluent is used for clean-up of extracts prior to separation and quantification of aflatoxins by HPLC. The eluent fraction containing the aflatoxins is concentrated by evaporation under reduced pressure and the aflatoxins separated by reverse phase HPLC on an ODS column. Quantitative results have been obtained at levels down to 1 microgram/kg, and average recoveries from samples of wheat, maize and compound feed spiked at levels of 10 and 40 micrograms/kg were greater than 80%, 70% and 65% respectively.
本文描述了一种简单且灵敏的方法,用于分析谷物和动物饲料样品中的黄曲霉毒素B1、B2、G1和G2。黄曲霉毒素用二氯甲烷:水(10:1)萃取。在通过高效液相色谱法分离和定量黄曲霉毒素之前,使用装有Bio-beads S-X3的柱子和二氯甲烷:己烷(3:1)作为洗脱剂的凝胶渗透色谱法(GPC)对提取物进行净化。含有黄曲霉毒素的洗脱液部分通过减压蒸发浓缩,黄曲霉毒素在ODS柱上通过反相高效液相色谱法分离。已获得低至1微克/千克水平的定量结果,小麦、玉米和复合饲料样品在10和40微克/千克水平加标后的平均回收率分别大于80%、70%和65%。