Chung M, Costello R, Symchowicz S
Antimicrob Agents Chemother. 1980 Feb;17(2):184-7. doi: 10.1128/AAC.17.2.184.
In a crossover study, single doses of netilmicin and gentamicin were administered intramuscularly, each at 1.0 and 2.5 mg/kg. The serum concentrations, analyzed by a two-compartment open model with a first-order absorption, indicated that the pharmacokinetics of the drugs are essentially the same. Both drugs were rapidly absorbed and distributed after administration. No significant differences were observed between the two drugs in disposition half-life, rate of distribution and elimination, area under the serum concentration-time curve, urinary excretion, total body clearance, and renal clearance. After 1.0 mg/kg, the maximum serum concentration of netilmicin (5.18 microgram/ml) was only slightly lower than that for gentamicin (5.76 microgram/ml), but no difference was found after the 2.5-mg/kg dose.
在一项交叉研究中,分别以1.0毫克/千克和2.5毫克/千克的剂量肌肉注射奈替米星和庆大霉素单剂量。通过具有一级吸收的二室开放模型分析血清浓度,结果表明这两种药物的药代动力学基本相同。给药后,两种药物均迅速吸收并分布。在处置半衰期、分布和消除速率、血清浓度-时间曲线下面积、尿排泄、总体清除率和肾清除率方面,两种药物之间未观察到显著差异。1.0毫克/千克剂量后,奈替米星的最大血清浓度(5.18微克/毫升)仅略低于庆大霉素(5.76微克/毫升),但2.5毫克/千克剂量后未发现差异。