伊曲康唑的药代动力学、血液分配和组织分布。

Joo H Lee, Jee H Shin, Myung G Lee
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引用次数: 0

摘要

以10 mg/kg剂量伊曲康唑给药1 min后,测定其在雄性新西兰大白兔体内的药代动力学。伊曲康唑的终末半衰期为524 min,伊曲康唑在家兔体内清除缓慢,全身清除率为3.26 ml/min/kg。测定了伊曲康唑在家兔血浆和血细胞之间的血液分配。伊曲康唑在兔血浆和血细胞之间迅速达到平衡。平衡血浆/血细胞浓度比与伊曲康唑、1、5和10 μ g/ml兔血药浓度无关;平均值为3.25。以10 mg/kg剂量给药1 min后测定伊曲康唑在大鼠体内的组织分布。伊曲康唑在给药后1和24 h除脂肪和胃外,其余大鼠组织中T/P均大于1,说明所研究的大鼠组织对伊曲康唑具有较高的亲和力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacokinetics, blood partition, and tissue distribution of itraconazole.

Pharmacokinetics of itraconazole was measured after 1-min intravenous infusion at a dose of 10 mg/kg to male New Zealand white rabbits. The terminal half-life of itraconazole was 524 min. Itraconazole was eliminated slowly in rabbits with total body clearance of 3.26 ml/min/kg. Blood partition of itraconazole between plasma and blood cells of rabbit blood was measured. Itraconazole reached equilibrium rapidly between plasma and blood cells of rabbit blood. The equilibrium plasma/blood cells concentration ratios were independent of initial rabbit blood concentrations of itraconazole, 1, 5, and 10 microg/ml; the mean value was 3.25. Tissue distribution of itraconazole was also measured after 1-min intravenous administration at a dose of 10 mg/kg to rats. The tissue-to-plasma (T/P) ratios of itraconazole were greater-than-unity in all rat tissues studied at both 1 and 24 h except in fat and stomach at 1 h. This indicated that rat tissues studied had a high affinity to itraconazole.

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