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罂粟碱的生物利用度可变。

Variable bioavailability of papaverine.

作者信息

Berg G, Jönsson K A, Hammar M, Norlander B

机构信息

Department of Obstetrics and Gynaecology, Linköping University, Sweden.

出版信息

Pharmacol Toxicol. 1988 May;62(5):308-10. doi: 10.1111/j.1600-0773.1988.tb01893.x.

Abstract

The plasma concentration curves of papaverine have been studied in nine healthy males and seven patients after administration of single intravenous (80 mg) and oral (80 mg) doses. The bioavailability of the drug was highly variable with a mean of 28% (range 5-99%) but reproducible within the same individual (4 of the volunteers) after a repeated (80 mg) oral dose. The calculated half-life after intravenous administration ranged between 1.2-6.6 hours (mean 3.0). The mean apparent volume of distribution was 3.1 l/kg and the mean total plasma clearance was 836 ml/min. It is concluded that papaverine shows an unacceptable inter-individual variation in the bioavailability after oral administration of 80 mg tablets.

摘要

在9名健康男性和7名患者单次静脉注射(80毫克)和口服(80毫克)剂量后,研究了罂粟碱的血浆浓度曲线。该药物的生物利用度高度可变,平均值为28%(范围为5%-99%),但在同一受试者(4名志愿者)重复口服(80毫克)剂量后具有可重复性。静脉给药后的计算半衰期在1.2至6.6小时之间(平均3.0小时)。平均表观分布容积为3.1升/千克,平均总血浆清除率为836毫升/分钟。得出的结论是,口服80毫克片剂后,罂粟碱的生物利用度存在个体间差异,这种差异是不可接受的。

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