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通过放射受体分析法评估大鼠不同给药途径后阿托品和异丙托溴铵的血浆动力学。

Plasma kinetics of atropine and ipratropium in rats after different routes of administration evaluated by a radioreceptor assay.

作者信息

Urso R, Segre G, Bianchi E, Bruni G, Dal Pra P, Fiaschi A I

机构信息

Instituro di Farmacologia, Universita di Siena, Italia.

出版信息

Eur J Drug Metab Pharmacokinet. 1991;Spec No 3:111-5.

PMID:1840322
Abstract

Plasma kinetics of atropine and ipratropium was assessed in rat after i.v. (10 mg/kg), oral and i.p. (50 mg/kg) administration by a radioreceptor assay (RRA). The volume of the central compartment and the clearance of both drugs were very similar (about 3 L/kg and 3.5 L/h/kg respectively) while the steady state volume of distribution and the terminal half-life of atropine were higher than those of ipratropium. After i.p. administration the kinetics of ipratropium was very different from what was expected after the i.v. experiment.

摘要

通过放射受体分析法(RRA)评估了大鼠静脉注射(10毫克/千克)、口服和腹腔注射(50毫克/千克)后阿托品和异丙托溴铵的血浆动力学。两种药物的中央室容积和清除率非常相似(分别约为3升/千克和3.5升/小时/千克),而阿托品的稳态分布容积和终末半衰期高于异丙托溴铵。腹腔注射后,异丙托溴铵的动力学与静脉注射实验后的预期情况非常不同。

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