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Detection of new urinary exemestane metabolites by gas chromatography coupled to mass spectrometry
Authors:Cavalcanti Gustavo de Albuquerque  Garrido Bruno Carius  Leal Felipe Dias  Padilha Monica Costa  de la Torre Xavier  de Aquino Neto Francisco Radler
Institution:1. Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan;2. Department of Material Science, Graduate School of Material Science, University of Hyogo, 3-2-1, Kouto, Kamigori, Ako 6781297, Japan;3. Department of Chemistry, Northeast Normal University, Changchun 130024, PR China;4. Center for Molecular Systems (CMS), Kyushu University, Fukuoka 819-0395, Japan;1. Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, Fukuoka 819-0395, Japan;2. Department of Material Science, Graduate School of Material Science, University of Hyogo, 3-2-1, Kouto, Kamigori, Ako 6781297, Japan;3. Department of Chemistry, Northeast Normal University, Changchun 130024, PR China;4. Center for Molecular Systems (CMS), Kyushu University, Fukuoka 819-0395, Japan
Abstract:Exemestane is an aromatase enzyme complex inhibitor. Its metabolism in humans is not fully described and there is only one known metabolite: 17β-hydroxyexemestane. In this work, excretion studies were performed with four volunteers aiming at the detection of new exemestane metabolites in human urine by gas chromatography coupled to mass spectrometry (GC-MS) after enzymatic hydrolysis and liquid-liquid extraction. Urine samples collected from four volunteers were analyzed separately. The targets of the study were mainly the 6-exomethylene oxidized metabolites. Two unreported metabolites were identified in both free and glucuconjugated urine fractions from all four volunteers, both of them were the result of the 6-exomethylene moiety oxidation: 6ξ-hydroxy-6ξ-hydroxymethylandrosta-1,4-diene-3,17-dione (metabolite 1) and 6ξ-hydroxyandrosta-1,4-diene-3,17-dione (metabolite 2). Furthermore, only in glucoconjugated fractions from all volunteers, one metabolite arising from the A-ring reduction was identified as well, 3ξ-hydroxy-5ξ-androst-1-ene-6-methylene-17-one (metabolite 3). The molecular formulae of all these metabolites were ascertained by the determination of exact masses using gas chromatography coupled to high resolution mass spectrometry (GC-HRMS). Moreover, all metabolites were confirmed using an alternative derivatization with methoxyamine and MSTFA/TMS-imidazole.
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