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环苯咯啶对人体口服给药后的血浆浓度及药代动力学

Plasma levels and pharmacokinetics of cyclofenil after oral administration to man.

作者信息

Borgström L

出版信息

Eur J Clin Pharmacol. 1981 Feb;19(3):213-6. doi: 10.1007/BF00561952.

Abstract

Cyclofenil was given as a single oral dose of 200 mg, and also as 200 mg/day for eight days, to seven healthy female volunteers. Plasma was analyzed for the active metabolite and pharmacokinetic modelling was performed. A biological half life of 29 h was bound after the single dose and 18 h after the eighth day of continuous treatment. No significant difference was found in any of the calculated parameters when comparing the values from Day 1 and Day 8. The theoretically constructed steady-state curve fitted the experimented values.

摘要

给7名健康女性志愿者单次口服200毫克克罗米酚,也按200毫克/天的剂量服用8天。分析血浆中的活性代谢物并进行药代动力学建模。单次给药后测得生物半衰期为29小时,连续治疗第8天后为18小时。比较第1天和第8天的值时,在任何计算参数中均未发现显著差异。理论构建的稳态曲线与实验值相符。

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