Navarro A S, Lanao J M, Dominguez-Gil A
J Antimicrob Chemother. 1987 Jun;19(6):799-806. doi: 10.1093/jac/19.6.799.
The pharmacokinetics of dibekacin were studied in the rabbit with a dosage regimen of 2 mg/kg at intervals of 12 h. The drug was administered by iv bolus injection, iv infusion and im injection. Twenty-four hours after the fifth dose, dibekacin concentrations in the renal cortex and medulla, liver, lung and heart were determined. The plasma concentrations showed significant differences between the first and fifth dose when the antibiotic was administered by iv bolus injection. The tissue concentrations also varied significantly according to the route of administration with higher tissue concentrations occurring after iv bolus injection. Tissue binding also varied according to the route of administration and was greatest for the renal cortex and medulla, followed by the lung, liver and heart.
以2mg/kg的剂量、12小时间隔的给药方案在兔体内研究了地贝卡星的药代动力学。药物通过静脉推注、静脉输注和肌肉注射给药。在第五次给药后24小时,测定肾皮质和髓质、肝脏、肺和心脏中的地贝卡星浓度。当通过静脉推注给药抗生素时,血浆浓度在第一次和第五次给药之间显示出显著差异。组织浓度也根据给药途径有显著变化,静脉推注后组织浓度更高。组织结合也根据给药途径而变化,在肾皮质和髓质中最大,其次是肺、肝脏和心脏。