Frydman A M, Le Roux Y, Lefebvre M A, Djebbar F, Fourtillan J B, Gaillot J
J Antimicrob Chemother. 1986 Apr;17 Suppl B:65-79. doi: 10.1093/jac/17.suppl_b.65.
Multiple-dose kinetics of pefloxacin was determined in 12 normal male subjects given 400 mg pefloxacin by iv 1 h-infusion every 12 h for 16 doses. Twelve other subjects (6 men and 6 women) were given 400 mg pefloxacin by mouth every 12 h for 18 doses. Plasma and urine concentrations of pefloxacin and its main metabolites (N-desmethyl pefloxacin or norfloxacin and pefloxacin N-oxide) were measured by high performance liquid chromatography. The bioavailability of pefloxacin was complete and plasma concentrations after iv or oral administration were similar. Pefloxacin was rapidly absorbed from the gastrointestinal tract and reached maximum plasma concentrations about 1 h after dosing. Pefloxacin elimination (T 1/2 beta) increased from 11.00 +/- 2.64 h after the first iv dose to 13.93 +/- 3.58 h after the last iv dose (P less than 0.01). Apparent total body clearance decreased from 148.5 +/- 47.6 to 106.9 +/- 39.2 ml/min (P less than 0.01) because of decreased non-renal clearance (apparent volume of distribution did not significantly change over the repeated pefloxacin administration). Similar results were obtained after repeated oral dosing. Renal clearance of pefloxacin was low (7.47 +/- 2.28 ml/min) indicating that non-renal clearance represents the major route of elimination of this quinolone. Urinary excretion of pefloxacin and N-desmethyl and N-oxide metabolites was approximately 31% of the pefloxacin dose and beta-elimination half-lives of these metabolites were very close to that of pefloxacin (13.34 +/- 2.72 h and 11.95 +/- 2.64 h respectively). Due to a possible saturable process in the metabolic pathway, some accumulation occurred during repeated iv or oral treatment (accumulation ratio = 1.37 +/- 0.20). These results show that concentrations of pefloxacin in excess of the minimum inhibitory concentrations for many important pathogens can be rapidly achieved in plasma and urine with the 400 mg bid regimen with both iv and oral routes.
对12名正常男性受试者进行了培氟沙星多剂量动力学研究,他们每12小时静脉滴注400毫克培氟沙星,持续1小时,共给药16次。另外12名受试者(6名男性和6名女性)每12小时口服400毫克培氟沙星,共给药18次。采用高效液相色谱法测定培氟沙星及其主要代谢产物(N-去甲基培氟沙星或诺氟沙星和培氟沙星N-氧化物)的血浆和尿液浓度。培氟沙星的生物利用度完全,静脉注射或口服后的血浆浓度相似。培氟沙星从胃肠道迅速吸收,给药后约1小时达到血浆最大浓度。培氟沙星的消除半衰期(T 1/2β)从首次静脉给药后的11.00±2.64小时增加到末次静脉给药后的13.93±3.58小时(P<0.01)。由于非肾清除率降低,表观全身清除率从148.5±47.6降至106.9±39.2毫升/分钟(P<0.01)(在重复给予培氟沙星的过程中,表观分布容积没有显著变化)。重复口服给药后也得到了类似的结果。培氟沙星的肾清除率较低(7.47±2.28毫升/分钟),这表明非肾清除是该喹诺酮类药物的主要消除途径。培氟沙星及其N-去甲基和N-氧化物代谢产物的尿排泄量约为培氟沙星剂量的31%,这些代谢产物的β消除半衰期与培氟沙星的非常接近(分别为13.34±2.72小时和11.95±2.64小时)。由于代谢途径中可能存在饱和过程,在重复静脉注射或口服治疗期间出现了一些蓄积(蓄积比=1.37±0.20)。这些结果表明,采用400毫克每日两次的静脉和口服给药方案,可使血浆和尿液中培氟沙星的浓度迅速超过许多重要病原体的最低抑菌浓度。