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Prediction of drug-drug interaction from in vitro plasma protein binding and metabolism. A study of tolbutamide-sulfonamide interaction in rats.

作者信息

Sugita O, Sawada Y, Sugiyama Y, Iga T, Hanano M

出版信息

Biochem Pharmacol. 1981 Dec 15;30(24):3347-54. doi: 10.1016/0006-2952(81)90611-0.

DOI:10.1016/0006-2952(81)90611-0
PMID:7326045
Abstract
摘要

相似文献

1
Prediction of drug-drug interaction from in vitro plasma protein binding and metabolism. A study of tolbutamide-sulfonamide interaction in rats.基于体外血浆蛋白结合和代谢预测药物-药物相互作用。大鼠甲苯磺丁脲-磺胺类药物相互作用的研究。
Biochem Pharmacol. 1981 Dec 15;30(24):3347-54. doi: 10.1016/0006-2952(81)90611-0.
2
Kinetic analysis of tolbutamide-sulfonamide interaction in rabbits based on clearance concept. Prediction of species difference from in vitro plasma protein binding and metabolism.基于清除率概念对家兔中甲苯磺丁脲-磺胺相互作用的动力学分析。根据体外血浆蛋白结合和代谢预测种属差异。
Drug Metab Dispos. 1984 Jan-Feb;12(1):131-8.
3
Kinetics of drug-drug interactions in sheep: tolbutamide and sulfadimethoxine.绵羊体内药物相互作用的动力学：甲苯磺丁脲和磺胺二甲氧嘧啶。
J Pharm Sci. 1977 Aug;66(8):1063-70. doi: 10.1002/jps.2600660803.
4
Physiologically based pharmacokinetics of drug-drug interaction: a study of tolbutamide-sulfonamide interaction in rats.药物相互作用的基于生理学的药代动力学：大鼠中甲苯磺丁脲-磺胺类药物相互作用的研究
J Pharmacokinet Biopharm. 1982 Jun;10(3):297-316. doi: 10.1007/BF01059263.
5
The effect of sulfaphenazole and sulfadoxine on tolbutamide disposition in dwarf goats (Caprus hircus aegagrus).磺胺苯唑和周效磺胺对矮山羊（Caprus hircus aegagrus）中甲苯磺丁脲处置的影响。
Res Vet Sci. 1997 Nov-Dec;63(3):269-72. doi: 10.1016/s0034-5288(97)90032-1.
6
Mechanisms of inhibition of tolbutamide metabolism: phenylbutazone, oxyphenbutazone, sulfaphenazole.甲苯磺丁脲代谢抑制机制：保泰松、羟基保泰松、磺胺苯吡唑。
Clin Pharmacol Ther. 1977 Nov;22(5 Pt 1):573-9. doi: 10.1002/cpt1977225part1573.
7
[Binding of some sulfanilamides to blood proteins of man. 1. Determinations of low sulfanilamide concentrations in vitro at room temperature].[某些磺胺类药物与人血液蛋白的结合。1. 室温下体外低磺胺浓度的测定]
Arzneimittelforschung. 1966 Mar;16(3):346-54.
8
Prediction of in vivo drug-drug interactions between tolbutamide and various sulfonamides in humans based on in vitro experiments.基于体外实验预测甲苯磺丁脲与多种磺胺类药物在人体内的药物相互作用。
Drug Metab Dispos. 2000 Apr;28(4):475-81.
9
[Determination of t1/2 value for some sulfonamides in the mini-pig].[小型猪体内某些磺胺类药物t1/2值的测定]
Boll Soc Ital Biol Sper. 1978 Dec 30;54(24):2499-503.
10
[Blood levels of long-acting sufonamides in horses after oral or intravenous administration].[口服或静脉注射后马体内长效磺胺类药物的血药浓度]
Nihon Juigaku Zasshi. 1964 Dec;26(6):343-7. doi: 10.1292/jvms1939.26.343.

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An study to determine the impact of lipid emulsion on partitioning of a broad spectrum of drugs associated with overdose.一项旨在确定脂质乳剂对与过量用药相关的多种药物分配影响的研究。
BJA Open. 2024 Jun 12;10:100292. doi: 10.1016/j.bjao.2024.100292. eCollection 2024 Jun.
2
Quantitative prediction of in vivo drug-drug interactions from in vitro data based on physiological pharmacokinetics: use of maximum unbound concentration of inhibitor at the inlet to the liver.基于生理药代动力学，从体外数据对体内药物相互作用进行定量预测：利用肝脏入口处抑制剂的最大非结合浓度
Pharm Res. 2000 Mar;17(3):336-43. doi: 10.1023/a:1007509324428.
3
Physiologically based pharmacokinetics of drug-drug interaction: a study of tolbutamide-sulfonamide interaction in rats.
药物相互作用的基于生理学的药代动力学：大鼠中甲苯磺丁脲-磺胺类药物相互作用的研究
J Pharmacokinet Biopharm. 1982 Jun;10(3):297-316. doi: 10.1007/BF01059263.
4
Tolbutamide as a model drug for the study of enzyme induction and enzyme inhibition in the rat.甲苯磺丁脲作为大鼠体内酶诱导和酶抑制研究的模型药物。
Br J Pharmacol. 1984 Mar;81(3):557-62. doi: 10.1111/j.1476-5381.1984.tb10109.x.
5
Analysis of nonlinear tissue distribution of quinidine in rats by physiologically based pharmacokinetics.基于生理药代动力学对大鼠体内奎尼丁非线性组织分布的分析。
J Pharmacokinet Biopharm. 1985 Aug;13(4):425-40. doi: 10.1007/BF01061478.
6
Prediction of the disposition of nine weakly acidic and six weakly basic drugs in humans from pharmacokinetic parameters in rats.根据大鼠药代动力学参数预测九种弱酸性和六种弱碱性药物在人体内的处置情况。
J Pharmacokinet Biopharm. 1985 Oct;13(5):477-92. doi: 10.1007/BF01059331.