Lee Joo H, Shin Jee H, Lee Myung G
College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, San 56-1, Shinlim-Dong, Kwanak-Gu, Seoul 151-742, South Korea.
Res Commun Mol Pathol Pharmacol. 2004;115-116:203-15.
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.
以10mg/kg的剂量对雄性新西兰白兔进行1分钟静脉输注后,测定了伊曲康唑的药代动力学。伊曲康唑的终末半衰期为524分钟。伊曲康唑在兔体内消除缓慢,全身清除率为3.26ml/(min·kg)。测定了伊曲康唑在兔血浆和血细胞之间的血液分配情况。伊曲康唑在兔血浆和血细胞之间迅速达到平衡。平衡时血浆/血细胞浓度比与伊曲康唑在兔血中的初始浓度1、5和10μg/ml无关;平均值为3.25。以10mg/kg的剂量对大鼠进行1分钟静脉给药后,也测定了伊曲康唑的组织分布。在1小时和24小时时,除脂肪和胃在1小时时外,在所研究的所有大鼠组织中,伊曲康唑的组织与血浆(T/P)比值均大于1。这表明所研究的大鼠组织对伊曲康唑具有高亲和力。