Lanao J M, Dominguez-Gil A, Tabernero J M, Corbacho L
Eur J Clin Pharmacol. 1981;19(5):367-70. doi: 10.1007/BF00544588.
The pharmacokinetics of amikacin was studied in 17 hospitalized patients with normal renal function (creatinine clearance greater than 90 ml/min), after the administration of a single dose of 7.5 mg/kg body weight. In 10 patients the antibiotic was administered intravenously and in the other 7 it was injected intramuscularly. After i.v. administration, the antibiotic followed an open two-compartment kinetic model, and after i.m. administration it followed a single compartment kinetic model. The route of administration did not significantly modify the pharmacokinetic parameters of amikacin. On the basis of the pharmacokinetic parameters thus established, an intravenous infusion for therapeutic use should have an administration rate of 2.5 [mg/kg/h] and a duration of 6 h.
对17名肾功能正常(肌酐清除率大于90 ml/分钟)的住院患者,在给予单剂量7.5 mg/千克体重的丁胺卡那霉素后,研究了其药代动力学。10名患者静脉注射该抗生素,另外7名患者肌肉注射。静脉注射后,抗生素遵循开放二室动力学模型,肌肉注射后遵循单室动力学模型。给药途径并未显著改变丁胺卡那霉素的药代动力学参数。基于如此确定的药代动力学参数,治疗用静脉输注的给药速率应为2.5 [mg/(kg·小时)],持续时间为6小时。