Physiological Modeling of Altered Pharmacokinetics of a Novel Anticancer Drug, UCN-01 (7-Hydroxystaurosporine), Caused by Slow Dissociation of UCN-01 from Human α1-Acid Glycoprotein

被引:0
|
作者
Eiichi Fuse
Akitoshi Hashimoto
Natsuko Sato
Hiromi Tanii
Takashi Kuwabara
Satoshi Kobayashi
Yuichi Sugiyama
机构
[1] Kyowa Hakko Kogyo Co.,Drug Development Research Laboratories, Pharmaceutical Research Institute
[2] Ltd.,Drug Development Research Laboratories, Pharmaceutical Research Institute
[3] Kyowa Hakko Kogyo Co.,Graduate School of Pharmaceutical Sciences
[4] Ltd.,undefined
[5] The University of Tokyo,undefined
来源
Pharmaceutical Research | 2000年 / 17卷
关键词
α1-acid glycoprotein; protein binding; dissociation rate; species difference; physiological model; pharmacokinetics;
D O I
暂无
中图分类号
学科分类号
摘要
Purpose. The extremely low clearance and small distribution volumeof UCN-01 in humans could be partly due to the high degree of bindingto hAGP (1,2). The quantitative effects of hAGP on the pharmacokineticsof UCN-01 at several levels of hAGP and UCN-01 were estimatedin rats given an infusion of hAGP to mimic the clinical situation anda physiological model for analysis was developed.
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页码:553 / 564
页数:11
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