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Pharmacokinetics of terbutaline after subcutaneous administration.

作者信息

Leferink J G, Lamont H, Wagemaker-Engels I, Maes R A, Pouwels R, van der Straeten M

出版信息

Int J Clin Pharmacol Biopharm. 1979 Apr;17(4):181-5.

PMID:447439
Abstract

The pharmacokinetics of terbutaline has been studied after subcutaneous adminsitration of a therapeutic dose of 250 microgram in 14 patients. Short absorption half-lives of about 7 min resulted in a fast uptake of the drug. Serum concentrations of terbutaline were measured up to 10 hr after administration, depending on the individual. An open one-compartment model appeared adequate for the mathematical description of the kinetics in most patients. Elimination constants of 0.27 +/- 0.07 hr-1 were observed. The elimination process was biphasic in 5 patients with a mean elimination constant of the second phase of 0.10 +/- 0.04 hr-1. This resulted in a comparatively high concentration of 0.7 ng/ml 10 hr after administration. Regular use of terbutaline did not influence the pharmacokinetic data in a significant way.

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