Delgado F A, Stout R L, Whelton A
J Antimicrob Chemother. 1983 May;11 Suppl B:79-88. doi: 10.1093/jac/11.suppl_b.79.
Systemic and urinary pharmacokinetic studies of the disposition of azlocillin were performed in seven male and six female healthy volunteers. Four separate studies identified the kinetics of the drug following a single 2, 3 or 4 g administration and during the repetitive administrations of 3 g of the drug over a five-day period. Peak plasma concentrations were 174 +/- 19 mg/l, 214 +/- 17 mg/l and 286 +/- 11 mg/l in the 2, 3 and 4 g single dose studies respectively. Trough values at 4 h post-dosing were 6 +/- 1 mg/l, 10 +/- 1 mg/l and 26 +/- 3 mg/l respectively. The plasma half-life of azlocillin was approximately 60 min. A dose-dependent phenomenon was observed. This was characterized by a slight but significant progressive increase in the plasma half-life of the drug as increasing amounts of drug were given and as the same amount was given repeatedly. No significant systemic accumulation of azlocillin was noted during the repetitive dosing study. The urinary excretion of the compound was prompt with most of the bioactive drug being eliminated in the first 4-6 h following dosing. The apparent volume of distribution of azlocillin was slightly greater than the extracellular fluid compartment. For the therapy of systemic infections in adults with normal renal function a 4 h or 6 h dosing cycle would be appropriate.
在7名男性和6名女性健康志愿者身上进行了阿洛西林处置的全身和尿液药代动力学研究。四项独立研究确定了单次给予2克、3克或4克药物后以及在5天内重复给予3克药物期间该药物的动力学。在2克、3克和4克单剂量研究中,血浆峰值浓度分别为174±19毫克/升、214±17毫克/升和286±11毫克/升。给药后4小时的谷值分别为6±1毫克/升、10±1毫克/升和26±3毫克/升。阿洛西林的血浆半衰期约为60分钟。观察到了剂量依赖性现象。其特征是随着给药量增加以及重复给予相同剂量,药物的血浆半衰期出现轻微但显著的逐渐增加。在重复给药研究中未观察到阿洛西林有明显的全身蓄积。该化合物的尿液排泄迅速,大部分生物活性药物在给药后的最初4至6小时内被清除。阿洛西林的表观分布容积略大于细胞外液腔室。对于肾功能正常的成人全身感染的治疗,4小时或6小时的给药周期是合适的。