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用于测定乳制品中皮克级黄曲霉毒素M1的直接酶联免疫吸附测定法。

Direct enzyme-linked immunosorbent assay for determining aflatoxin M1 at picogram levels in dairy products.

作者信息

Fremy J M, Chu F S

出版信息

J Assoc Off Anal Chem. 1984 Nov-Dec;67(6):1098-101.

PMID:6440890
Abstract

Protocols for detecting picogram quantities of aflatoxin M1 in dairy products were established. Milk samples were subjected to a reverse phase Sep-Pak C18 cartridge treatment before analysis by an enzyme-linked immunosorbent assay (ELISA) according to previously published procedures. M1 in yogurt, brick cheddar, and ripened Brie cheese was extracted by a modified Pons method, subjected to a normal phase silica cartridge treatment, and analyzed by ELISA. The detection limits for M1 in milk, yogurt, cheddar, and Brie were 10, 10, 50, and 25 ppt (ng/kg), respectively. Recovery for M1 added to these products was in the range 70-110%. Good agreement was found for M1 levels in several naturally contaminated milk samples analyzed by both ELISA and liquid chromatography.

摘要

建立了检测乳制品中皮克级黄曲霉毒素M1的方法。牛奶样品在按照先前发表的程序通过酶联免疫吸附测定(ELISA)分析之前,先经过反相Sep-Pak C18柱处理。酸奶、块状切达干酪和成熟布里干酪中的M1通过改良的庞斯方法提取,经过正相硅胶柱处理,然后用ELISA分析。牛奶、酸奶、切达干酪和布里干酪中M1的检测限分别为10、10、50和25 ppt(纳克/千克)。添加到这些产品中的M1回收率在70%-110%之间。通过ELISA和液相色谱分析的几个天然污染牛奶样品中的M1水平结果吻合良好。

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