期刊
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
卷 54, 期 2, 页码 931-933出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.01145-09
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After intravenous or oral administration of 10 mg/kg itraconazole to rats with streptozotocin-induced diabetes mellitus and to control rats, the total area under the plasma concentration-time curve from time 0 to 24 h (AUC(0-24)) for itraconazole and that for its metabolite, 7-hydroxyitraconazole, were similar between the two groups of rats. This may be explained by the comparable hepatic and intestinal intrinsic clearance rates for the disappearance of itraconazole and the formation of 7-hydroxyitraconazole in both groups of rats.
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