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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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