Pharmacokinetics of terbutaline after subcutaneous administration.

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

特布他林皮下给药后的药代动力学。
对14例患者皮下给予治疗剂量250微克特布他林后的药代动力学进行了研究。短的吸收半衰期约7分钟,导致药物的快速吸收。在给药后10小时测量特布他林的血清浓度,这取决于个体。一个开放的单室模型似乎足以对大多数患者的动力学进行数学描述。消除常数为0.27 +/- 0.07 hr-1。5例患者的消除过程为两期,第二期平均消除常数为0.10 +/- 0.04 hr-1。这导致给药10小时后相对较高的浓度为0.7 ng/ml。经常使用特布他林对药代动力学数据没有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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