| Literature DB >> 2669364 |
W Krause1, G Kühne, H Matthes.
Abstract
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.Entities:
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Year: 1989 PMID: 2669364 DOI: 10.3109/00498258909042306
Source DB: PubMed Journal: Xenobiotica ISSN: 0049-8254 Impact factor: 1.908