RADIOISOTOPES
Online ISSN : 1884-4111
Print ISSN : 0033-8303
ISSN-L : 0033-8303
Carcinogenic Azo Dyes—Detection of New Metabolites of 3'-Methyl-4- (methylamino) azobenzene in Rat Bile—
Yukio MORIMasanobu HORIEKazumi TOYOSHI
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1979 Volume 28 Issue 2 Pages 72-77

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Abstract

Metabolism of 3'-methyl-4- (methylamino) azobenzene (3'-Me-MAB) in the rat has been investigated by an ion cluster technique. A mixture of non-labeled and deuterium labeled 3'-Me-MAB in cottonseed oil was administered orally with a stomach tube. After administration, the rat bile was collected for 24 hr and enzymically hydrolyzed. This sample was applied to an Amberlite XAD-2 column and the column was washed with water. The metabolites were eluted with methanol and were separated by thin-layer chromatography. The mass spectrum of each metabolite was measured. By means of this technique, the metabolites oxidized at the 3'-methyl group were newly detected in the bile in addition to the N-demethylated, aryl hy-droxylated, and their azo-reduced metabolites. The effect of the ring methyl group on the carcinogenic action of aminoazo dyes is also discussed.

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© Japan Radioisotope Association
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