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Br J Clin Pharmacol ; 51(2): 143-6, 2001 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-11259985

RESUMEN

AIMS: To describe the oral disposition of the dietary flavonoid chrysin in healthy volunteers. METHODS: Oral 400 mg doses of chrysin were administered to seven subjects. Chrysin and metabolites were assayed in plasma, urine and faeces by h.p.l.c. RESULTS: Peak plasma chrysin concentrations were only 3-16 ng ml(-1) with AUCs of 5-193 ng ml(-1) h. Plasma chrysin sulphate concentrations were 30-fold higher (AUC 450-4220 ng ml(-1) h). In urine, chrysin and chrysin glucuronide accounted for 0.2-3.1 mg and 2-26 mg, respectively. Most of the dose appeared in faeces as chrysin. Parallel experiments in rats showed high bile concentrations of chrysin conjugates. CONCLUSIONS: These findings, together with previous data using Caco-2 cells, suggest that chrysin has low oral bioavailability, mainly due to extensive metabolism and efflux of metabolites back into the intestine for hydrolysis and faecal elimination.


Asunto(s)
Fármacos Anti-VIH/farmacocinética , Flavonoides/farmacocinética , Administración Oral , Adulto , Animales , Fármacos Anti-VIH/metabolismo , Flavonoides/metabolismo , Humanos , Masculino , Modelos Animales , Ratas , Ratas Sprague-Dawley
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