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磷霉素对人类志愿者静脉注射和口服后的动力学。

Fosfomycin kinetics after intravenous and oral administration to human volunteers.

作者信息

Goto M, Sugiyama M, Nakajima S, Yamashina H

出版信息

Antimicrob Agents Chemother. 1981 Sep;20(3):393-7. doi: 10.1128/AAC.20.3.393.

Abstract

The pharmacokinetics of fosfomycin, administered intravenously and orally at two different doses (20 and 40 mg/kg of body weight), was studied in seven volunteers. The elimination profile of this antibiotic, when administered intravenously, followed a two-compartment kinetic model, independent of dosage, giving an elimination half-life of 2.23 +/- 0.62 h and an average total volume of distribution at steady state of 0.34 liter/kg. Peak serum levels after rapid intravenous administration of 20 and 40 mg/kg were 132.1 +/- 31.8 and 259.3 +/- 32.5 micrograms/ml, respectively. Peak serum levels after oral administration were 7.1 +/- 1.6 and 9.4 +/- 3.6 micrograms/ml for the 20 and 40 mg/kg doses, respectively. During the first 24 h after administration, an average of 80% of the intravenous doses and less than 25% of the oral doses were recovered in the urine.

摘要

在7名志愿者中研究了以两种不同剂量(20和40mg/kg体重)静脉注射和口服磷霉素后的药代动力学。静脉给药时,这种抗生素的消除曲线符合二室动力学模型,与剂量无关,消除半衰期为2.23±0.62小时,稳态时平均总体分布容积为0.34升/千克。快速静脉注射20和40mg/kg后,血清峰值水平分别为132.1±31.8和259.3±32.5μg/ml。口服给药后,20和40mg/kg剂量的血清峰值水平分别为7.1±1.6和9.4±3.6μg/ml。给药后的头24小时内,静脉注射剂量平均80%经尿液回收,口服剂量回收不到25%。

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