PT - JOURNAL ARTICLE AU - Kaori Hosoda AU - Takashi Furuta AU - Akitomo Yokokawa AU - Kenichiro Ogura AU - Akira Hiratsuka AU - Kazuo Ishii TI - Plasma Profiling of Intact Isoflavone Metabolites by High-Performance Liquid Chromatography and Mass Spectrometric Identification of Flavone Glycosides Daidzin and Genistin in Human Plasma after Administration of <em>Kinako</em> AID - 10.1124/dmd.108.021006 DP - 2008 Aug 01 TA - Drug Metabolism and Disposition PG - 1485--1495 VI - 36 IP - 8 4099 - http://dmd.aspetjournals.org/content/36/8/1485.short 4100 - http://dmd.aspetjournals.org/content/36/8/1485.full SO - Drug Metab Dispos2008 Aug 01; 36 AB - The roles of isoflavones in the prevention of several hormone-dependent cancers and osteoporosis are of great interest. Despite many pharmacokinetics studies of the isoflavones, the actual types of conjugates circulating in the body and the position(s) of conjugation sites on the flavone skeleton are still uncertain because, in general, conjugated compounds in biological fluids have been evaluated by measuring the free aglycones obtained after selective enzymatic hydrolysis. Using an high-performance (HPLC)-UV-diode-array detector (DAD) method combined with solid-phase extraction, we have obtained HPLC profiles of isoflavone glycosides [daidzin (Din) and genistin (Gin)] and of intact isoflavone metabolites in human plasma: daidzein, genistein, daizein-7-glucuronide, daidzein-4′-glucuronide, genistein-7-glucuronide, genistein-4′-glucuronide, daidzein-7-sulfate, daidzein-4′-sulfate, genistein-7-sulfate, and genistein-4′-sulfate. We investigated the plasma profile of intact isoflavone metabolites in plasma obtained 1 to-7 h after orally administration of 50 g of kinako (baked soybean powder) to two healthy volunteers. The results of DAD analysis indicated that the main isoflavone metabolite peaks were identified on the HPLC chromatogram. Furthermore, the intact glycosides Din and Gin were detected in 1-h plasma samples by their positive electrospray ionization mass spectra, demonstrating that the glycosides Din and Gin can be absorbed from the gut. The American Society for Pharmacology and Experimental Therapeutics