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健康年轻男性单次及重复口服格帕沙星后的药代动力学

Pharmacokinetics of grepafloxacin after oral administration of single and repeat doses in healthy young males.

作者信息

Efthymiopoulos C, Bramer S L, Maroli A

机构信息

Glaxo Wellcome R&D, Greenford, Middlesex, England.

出版信息

Clin Pharmacokinet. 1997;33 Suppl 1:1-8. doi: 10.2165/00003088-199700331-00003.

Abstract

The pharmacokinetics of grepafloxacin in healthy male subjects following single oral administration of doses ranging from 200 to 1200 mg, and following repeated oral administration of 400 and 800 mg doses are reported. Plasma levels of grepafloxacin reached a peak within 2 hours (on average) following drug administration and then declined bi-exponentially with concentrations being detectable (> 5 micrograms/L) in the plasma for at least up to 72 hours postdose. The high values for the apparent volume of distribution (5 to 8 L/kg) suggested extensive distribution of grepafloxacin in the tissues. Only a small percentage of the administered dose (ranging from 6% to 9.5%) was recovered in the urine as unchanged grepafloxacin, suggesting that metabolism, rather than urinary excretion, is the major elimination route. The half-life of grepafloxacin was about 12 hours after single doses and about 15 hours after repeat doses. The trough levels increased significantly over the first 3 days of repeat administration; thereafter, the changes were small, with steady-state being reached by the fifth day. The area under the concentration-time curve (AUC24 h) values observed on days 7 and 14 of repeat administration, at each dose level, were similar, suggesting that steady-state is maintained. The area values increased more than proportionally after administration of increasing single and repeat doses, suggesting nonlinear kinetics. The elimination half-life and renal clearance did not change with increasing doses. Saturation in the metabolism of grepafloxacin and possibly in the distribution into a peripheral compartment, as suggested by a decrease in the total plasma clearance and in the apparent volume of distribution, could be the origin of the nonlinear kinetics. However, this deviation from linearity is unlikely to be of clinical significance, since it was very small over the recommended range of therapeutic doses (400 to 600 mg once daily). Compared with other quinolones, grepafloxacin showed the longest half-life and the highest apparent volume of distribution. These features, together with the excellent bactericidal activity of grepafloxacin, support the recommended dosage regimen of grepafloxacin for the treatment of respiratory tract infections and sexually transmitted diseases.

摘要

报告了健康男性受试者单次口服200至1200毫克剂量以及多次口服400毫克和800毫克剂量后格帕沙星的药代动力学情况。给药后,格帕沙星血浆水平平均在2小时内达到峰值,然后呈双指数下降,给药后至少72小时血浆中浓度仍可检测到(>5微克/升)。表观分布容积的高值(5至8升/千克)表明格帕沙星在组织中广泛分布。给药剂量中只有一小部分(6%至9.5%)以未改变的格帕沙星形式在尿液中回收,这表明代谢而非尿排泄是主要的消除途径。单次给药后格帕沙星的半衰期约为12小时,多次给药后约为15小时。多次给药的前3天谷浓度显著升高;此后,变化较小,第5天达到稳态。在每个剂量水平,多次给药第7天和第14天观察到的浓度-时间曲线下面积(AUC24 h)值相似,表明维持了稳态。单次和多次增加剂量给药后,面积值增加超过比例,表明存在非线性动力学。消除半衰期和肾清除率不随剂量增加而改变。格帕沙星代谢的饱和以及可能在外周室分布的饱和,如总血浆清除率和表观分布容积的降低所示,可能是非线性动力学的起源。然而,这种与线性的偏差不太可能具有临床意义,因为在推荐的治疗剂量范围(每日一次400至600毫克)内偏差非常小。与其他喹诺酮类药物相比,格帕沙星显示出最长的半衰期和最高的表观分布容积。这些特征,连同格帕沙星出色的杀菌活性,支持了格帕沙星用于治疗呼吸道感染和性传播疾病的推荐给药方案。

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