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人静脉注射利福平的药代动力学研究。

Pharmacokinetic study on intravenous rifampicin in man.

作者信息

Acocella G, Segre G, Conti R, Pagani V, Pallanza R, Perna G, Simone P

出版信息

Pharmacol Res Commun. 1984 Jul;16(7):723-36. doi: 10.1016/s0031-6989(84)80050-8.

Abstract

A pharmacokinetic study was carried out in 18 male patients in order to assess the blood concentrations of rifampicin after intravenous administration of 3 different doses (600, 900 and 1200 mg) over 3 different periods of infusion (1, 2 and 3 hours). The results show that, by increasing the dose and the rate of infusion higher and earlier peak concentrations are obtained. A kinetic analysis based on a one-compartment open model gives a good fitting of the data obtained experimentally. From these data one obtains for the volume of distribution a value of 48.1 +/- 17.2 liters and for the serum disappearance rate the value of 0.212 +/- 0.070 h-1 in adult subjects. It is possible to predict the time course of serum kinetics of the drug by using the equation (formula; see text).

摘要

对18名男性患者进行了一项药代动力学研究,以评估在3个不同输注时间段(1小时、2小时和3小时)静脉注射3种不同剂量(600毫克、900毫克和1200毫克)利福平后的血药浓度。结果表明,通过增加剂量和输注速率,可以更早、更高地获得峰值浓度。基于单室开放模型的动力学分析与实验获得的数据拟合良好。从这些数据中,成年受试者的分布容积值为48.1±17.2升,血清消除率值为0.212±0.070 h⁻¹。使用该方程(公式;见正文)可以预测药物血清动力学的时间进程。

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