Höffken G, Tetzel H, Koeppe P, Lode H
J Antimicrob Chemother. 1985 Dec;16(6):763-71. doi: 10.1093/jac/16.6.763.
The pharmacokinetics of ticarcillin 5.0 g and clavulanic acid 0.2 g were examined both alone and combined (3.0 or 5.0 g ticarcillin + 0.2 g clavulanic acid as 3.2 or 5.2 g timentin) after a 15 min infusion in ten healthy volunteers. At the same time, the serum bactericidal activity of 5.0 g ticarcillin alone and 5.2 g Timentin was determined against two ticarcillin resistant strains each of Klebsiella oxytoca and Pseudomonas aeruginosa in the first and sixth hour after administration. The serum kinetics of both ticarcillin and clavulanic acid could best be described by an open 2-compartment model. Both substances showed similar kinetic behaviour in serum with a T 1/2 beta of 74.8 +/- 11.5 min for ticarcillin and 76.6 +/- 4.6 min for clavulanic acid. The total clearance of clavulanic acid was 158 +/- 23 ml/min and thus clearly exceeded that of ticarcillin (112 +/- 9 ml/min). The recovery rate in the 24 h urine was 41.3% for clavulanic acid as compared to 79.4% for ticarcillin. Concomitant administration of both substances led to a limited change in the kinetics of both ticarcillin and clavulanic acid. A significant enhancement of the serum bactericidal action of ticarcillin and clavulanic acid was only detected for both Klebsiella species and not for the Ps. aeruginosa species, and only in the first hour.
在10名健康志愿者中,静脉输注15分钟后,分别检测了替卡西林5.0 g和克拉维酸0.2 g单独使用及联合使用(3.0或5.0 g替卡西林 + 0.2 g克拉维酸,即3.2或5.2 g特美汀)时的药代动力学。同时,在给药后的第1小时和第6小时,分别测定了5.0 g替卡西林单独使用及5.2 g特美汀对产酸克雷伯菌和铜绿假单胞菌的两种耐替卡西林菌株的血清杀菌活性。替卡西林和克拉维酸的血清动力学均最适合用开放二室模型描述。两种物质在血清中的动力学行为相似,替卡西林的β半衰期为74.8±11.5分钟,克拉维酸为76.6±4.6分钟。克拉维酸的总清除率为158±23 ml/分钟,明显超过替卡西林(112±9 ml/分钟)。克拉维酸在24小时尿液中的回收率为41.3%,而替卡西林为79.4%。两种物质同时给药导致替卡西林和克拉维酸的动力学变化有限。仅在给药后的第1小时,检测到替卡西林和克拉维酸对两种克雷伯菌属的血清杀菌作用显著增强,而对铜绿假单胞菌则未增强。