Gao S, Li P, Liu G L, Wang S X, Chui R L, Yang J P
Department of Clinical Pharmacology, Changhai Hospital, Shanghai, China.
Zhongguo Yao Li Xue Bao. 1992 Jul;13(4):377-80.
The pharmacokinetics of ceftizoxime (Cef) and its diffusivity across the peritoneal membrane were studied in 10 chronic kidney failure patients undergoing continuous ambulatory peritoneal dialysis. Cef was determined by HPLC. The results showed that the disposition of Cef could be described with a 2-compartment open model after 1 g intravenous infusion. VD = 20 +/- 5 L, AUC = 1237 +/- 327 micrograms.ml-1.h. T1/2 beta = 16.9 +/- 4.5 h, which was much longer than that of patients with normal renal function. Therefore, the regulation of dose regimen was necessary when treating patients with renal failure. Cef was partly eliminated by peritoneal dialysis with the ClD of 2.9 +/- 1.0 ml.min-1. The bidirectional exchange of Cef was seen between blood and dialysate. It is more suitable to describe the diffusive characteristics of Cef from dialysate (or blood) into blood (or dialysate) with a zero order constant rate model. The absorption percentage of Cef after 0.5 g instilled with peritoneal dialysate was 90.4 +/- 7.0%.
在10例接受持续性非卧床腹膜透析的慢性肾衰竭患者中研究了头孢唑肟(Cef)的药代动力学及其在腹膜的扩散性。采用高效液相色谱法测定头孢唑肟。结果显示,静脉输注1g后,头孢唑肟的处置可用二室开放模型描述。分布容积(VD)=20±5L,药时曲线下面积(AUC)=1237±327μg·ml⁻¹·h。消除半衰期(T1/2β)=16.9±4.5h,这比肾功能正常的患者长得多。因此,治疗肾衰竭患者时调整给药方案是必要的。头孢唑肟部分通过腹膜透析清除,清除率(ClD)为2.9±1.0ml·min⁻¹。在血液和透析液之间可见头孢唑肟的双向交换。用零级恒速模型描述头孢唑肟从透析液(或血液)进入血液(或透析液)的扩散特性更合适。腹膜透析液注入0.5g后头孢唑肟的吸收百分率为90.4±7.0%。