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三种克林霉素磷酸酯给药方案的药代动力学比较。

Pharmacokinetic comparison of three clindamycin phosphate dosing schedules.

作者信息

Townsend R J, Baker R P

出版信息

Drug Intell Clin Pharm. 1987 Mar;21(3):279-81. doi: 10.1177/106002808702100310.

Abstract

In a randomized, three-way crossover study, six male volunteers received clindamycin phosphate 600 mg iv q6h (treatment A), 600 mg iv q8h (treatment B), or 900 mg iv q8h (treatment C). Plasma clindamycin concentrations were determined periodically for eight hours after achieving steady state. The results indicate that treatment C yielded significantly higher peak plasma clindamycin concentrations than treatments A or B. There were no significant differences in minimum plasma clindamycin concentrations (Cmin) or area under the plasma concentration versus time curve (AUC24) between treatments A and C. However, both treatments A and C yielded significantly greater Cmin and AUC24 values than treatment B. There were no significant differences among treatments for clindamycin clearance. It is concluded that clindamycin phosphate 900 mg q8h is a pharmacokinetically acceptable alternative to clindamycin phosphate 600 mg q6h.

摘要

在一项随机、三交叉研究中,六名男性志愿者接受了以下治疗:静脉注射磷酸克林霉素600毫克,每6小时一次(治疗A);静脉注射600毫克,每8小时一次(治疗B);或静脉注射900毫克,每8小时一次(治疗C)。在达到稳态后,每隔一段时间测定8小时的血浆克林霉素浓度。结果表明,治疗C产生的血浆克林霉素峰值浓度显著高于治疗A或治疗B。治疗A和治疗C之间的最低血浆克林霉素浓度(Cmin)或血浆浓度-时间曲线下面积(AUC24)没有显著差异。然而,治疗A和治疗C产生的Cmin和AUC24值均显著高于治疗B。各治疗组的克林霉素清除率没有显著差异。结论是,每8小时静脉注射900毫克磷酸克林霉素在药代动力学上是每6小时静脉注射600毫克磷酸克林霉素的可接受替代方案。

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