A method for the screening and identification of drug metabolites directly in crude urine and tissue extracts is described. The method, an application of an MS/MS technique, CAD MIKE spectrometry (collisionally activated decompostion mass analyzed ion kinetic energy spectrometry), greatly reduces the time of analysis and the amount of biological sample required. The structure of the metabolites is elucidated by interpretation of the CAD MIKE spectra obtained by selection and collision-induced decomposition of targeted molecular ions. Application of this technique to the study of biotransformation in the rat of the anthelmintic drug Nitroxynil (3-iodo-4-hydroxy-5-nitrobenzamide) has provided unequivocal identification of its metabolutes in urine and liver tissue in less than 3 days.

CAD MIKE spectrometry: a novel approach to the study of drug metabolism / R. Maffei Facino, M. Carini, P. Traldi. - In: CHIMICA OGGI-CHEMISTRY TODAY. - ISSN 0392-839X. - 12:(1985 Dec), pp. 23-29.

CAD MIKE spectrometry: a novel approach to the study of drug metabolism

R. Maffei Facino
Primo
;
M. Carini
Secondo
;
1985

Abstract

A method for the screening and identification of drug metabolites directly in crude urine and tissue extracts is described. The method, an application of an MS/MS technique, CAD MIKE spectrometry (collisionally activated decompostion mass analyzed ion kinetic energy spectrometry), greatly reduces the time of analysis and the amount of biological sample required. The structure of the metabolites is elucidated by interpretation of the CAD MIKE spectra obtained by selection and collision-induced decomposition of targeted molecular ions. Application of this technique to the study of biotransformation in the rat of the anthelmintic drug Nitroxynil (3-iodo-4-hydroxy-5-nitrobenzamide) has provided unequivocal identification of its metabolutes in urine and liver tissue in less than 3 days.
Mass spectrometry; drug metabolism
Settore CHIM/08 - Chimica Farmaceutica
dic-1985
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/270542
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