Koup J R, Keller E, Neumann H, Stoeckel K
Eur J Clin Pharmacol. 1986;30(3):303-7. doi: 10.1007/BF00541533.
The purpose of this study was to investigate the pharmacokinetics of intraperitoneally (IP) administered ceftriaxone (CRO) in patients maintained on chronic peritoneal dialysis. A single 2 g dose of CRO was administered IP to six adult patients who did not have peritonitis at the time of study. After a 5 hour dwell, the peritoneal fluid was exchanged with CRO-free fluid. Exchanges were carried out every 4 to 8 h, over a 24- to 28-h period. The peak total plasma CRO concentration was 104 micrograms/ml. An average of 74.1% of the IP dose of CRO was absorbed. Plasma protein binding was nonlinear; mean free fraction ranged from 12.8 to 17.9% at low and high concentrations. Dialysate concentrations at the end of subsequent exchanges ranged from means of 19.9 to 2.9 micrograms/ml. Total CRO clearance from plasma was 10.1 ml X kg-1 X h-1 and the mean terminal t 1/2 was 12.7 h. Dialytic clearance averaged 0.69 ml X kg-1 X h-1, only 6.9% of total clearance. A model which incorporates known characteristics of CRO binding and distribution in anuric patients was used to simulate plasma and peritoneal concentrations of CRO during multiple dose IP drug administration.
本研究的目的是调查在接受慢性腹膜透析的患者中腹腔内(IP)给予头孢曲松(CRO)的药代动力学。向6名在研究时未患腹膜炎的成年患者腹腔内给予单次2 g剂量的CRO。在留置5小时后,将腹腔液换成不含CRO的液体。在24至28小时内,每4至8小时进行一次更换。血浆中CRO的总浓度峰值为104微克/毫升。腹腔内给予的CRO剂量平均有74.1%被吸收。血浆蛋白结合呈非线性;在低浓度和高浓度下,平均游离分数范围为12.8%至17.9%。后续更换结束时透析液浓度范围为均值19.9至2.9微克/毫升。血浆中CRO的总清除率为10.1毫升×千克⁻¹×小时⁻¹,平均终末t 1/2为12.7小时。透析清除率平均为0.69毫升×千克⁻¹×小时⁻¹,仅占总清除率的6.9%。一个纳入了已知无尿患者中CRO结合和分布特征的模型被用于模拟多次腹腔内给药期间CRO的血浆和腹腔浓度。