角色扮演
药代动力学
生物利用度
尿
药理学
化学
抗抑郁药
放射免疫分析
药品
医学
内分泌学
磷酸二酯酶
酶
生物化学
海马体
作者
W. Kŕause,G. Kühne,H. Matthes
出处
期刊:Xenobiotica
[Taylor & Francis]
日期:1989-01-01
卷期号:19 (6): 683-692
被引量:21
标识
DOI:10.3109/00498258909042306
摘要
1. The pharmacokinetics of rolipram were studied in healthy male volunteers using 3H-rolipram and a radioimmunoassay for measurement of unchanged drug. 2. Rolipram was rapidly and completely absorbed after an oral dose of 1 mg. Bioavailability was 73%. 3. Plasma levels of the unchanged drug declined with a terminal half-life of 2 h. The total clearance of rolipram was 2 ml/min per kg. 4. Labelled rolipram was excreted rapidly and completely. The main route of elimination was via the urine.
科研通智能强力驱动
Strongly Powered by AbleSci AI