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Pharmacokinetics of trospectomycin sulphate in healthy subjects after single intravenous and intramuscular doses.

机译:单次静脉内和肌肉内给药后硫酸托斯帕霉素的药代动力学在健康受试者中。

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摘要

The pharmacokinetics of trospectomycin (75-1000 mg free base equivalents) were studied in 128 healthy males (eight per dose group), after a 20 min intravenous (i.v.) infusion and intramuscular (i.m.) injection of trospectomycin sulphate. The concentrations of trospectomycin in serum were described by bi- or tri-exponential disposition functions indicating an initial half-life of 1.1-1.4 h for the i.v. dose and 1.6-2.1 h for the i.m. dose and terminal half-lives of over 15 h. Most of the drug was eliminated rapidly (mean residence time 5-12 h). The distribution volume was 59-112% of body weight and clearance was 112-152 ml min-1. The absorption into blood after i.m. dosing was rapid. The area under the concentration-time curve and maximum concentration values were linearly related to dose. Serum drug concentrations fell below the minimum inhibitory concentration values for a variety of organisms by 8-12 h, which indicates that two or three times daily dosing would be appropriate. However, the long terminal half-life suggests that significant accumulation is likely in some tissues with an 8 h dose interval and this may prolong the action of trospectomycin.
机译:在静脉内(i.v.)输注和肌内(i.m.)注射硫酸托斯帕霉素硫酸盐20分钟后,对128名健康男性(每剂量组8个)研究了托斯帕霉素(75-1000 mg游离碱当量)的药代动力学。血清中托曲霉素的浓度通过双指数或三指数处理功能描述,表明静脉注射的初始半衰期为1.1-1.4小时。剂量和1.6-2.1小时剂量和最终半衰期超过15小时。大部分药物被快速清除(平均停留时间5-12小时)。分布体积为体重的59-112%,清除率为112-152 ml min-1。下午后吸收到血液中给药迅速。浓度-时间曲线下的面积和最大浓度值与剂量线性相关。血清药物浓度在8-12小时内降至各种生物体的最低抑菌浓度值以下,这表明每天给药两次或三次是适当的。但是,较长的终末半衰期表明,在某些组织中,以8小时的剂量间隔可能会出现明显的蓄积,这可能会延长托曲霉素的作用。

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