| Literature DB >> 3244626 |
A Ryrfeldt1, E Nilsson, A Tunek, L A Svensson.
Abstract
The lung uptake and biotransformation of 3H-bambuterol, a prodrug to terbutaline, were studied using isolated perfused and ventilated guinea pig lungs. 14C-Sucrose was used as an extracellular marker. The lung uptake of bambuterol was significantly (0.05 greater than or equal to P greater than or equal to 0.001) higher than that found for sucrose in single-pass perfusion experiments. High-performance liquid chromatographic (HPLC) analysis showed that 95.6 +/- 3.6% of the effluent 3H radioactivity was attributable to bambuterol. In recirculating experiments (120 min) the lung biotransformation of 3H-bambuterol (8.5 pmol/ml) was studied. Both oxidative and hydrolytic metabolism took place. The dominating metabolites were hydroxylated bambuterol and the monocarbamate derivative which is a product of hydrolysis of bambuterol. Traces of terbutaline were also formed. The results show that bambuterol has a certain affinity to lung tissue and that the drug is, to some extent, biotransformed in the guinea pig lung.Entities:
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Year: 1988 PMID: 3244626 DOI: 10.1023/a:1015908822131
Source DB: PubMed Journal: Pharm Res ISSN: 0724-8741 Impact factor: 4.200