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米诺环素和万古霉素在兔体内的药代动力学

Pharmacokinetics of minocycline and vancomycin in rabbits.

作者信息

Nicolau D P, Freeman C D, Nightingale C H, Quintiliani R

机构信息

Department of Pharmacy, Hartford Hospital, CT 06115.

出版信息

Lab Anim Sci. 1993 Jun;43(3):222-5.

PMID:8355481
Abstract

The pharmacokinetic disposition of minocycline and vancomycin was studied in New Zealand White rabbits before initiating an experimental staphylococcal endocarditis protocol. Minocycline was administered in a multiple-dose regimen of 3 mg/kg i.v. every 12 h, 3 mg/kg i.v. every 8 h, and 6 mg/kg i.v. every 8 h. Vancomycin was given in a similar fashion using regimens of 75 mg/kg i.v. every 12 h and 50 mg/kg i.v. every 8 h. Multiple serum samples were obtained after the fifth dose and drug concentrations were analyzed by microbiologic assay. The pharmacokinetic parameters for each of the drug regimens were calculated using a two-compartment model by nonlinear least-squares regression. No statistically significant differences were noted in the volume of distribution or the half-life of the individual dosing regimens for either agent. As a result of this study, it appears that a minocycline regimen of 6 mg/kg i.v. every 8 h and a vancomycin regimen of 50 mg/kg i.v. every 8 h are appropriate dosing schemes for a comparative study of these agents in rabbits.

摘要

在启动实验性葡萄球菌性心内膜炎方案之前,对新西兰白兔进行了米诺环素和万古霉素的药代动力学研究。米诺环素采用多剂量方案给药,静脉注射剂量分别为每12小时3mg/kg、每8小时3mg/kg和每8小时6mg/kg。万古霉素采用类似方式给药,静脉注射方案分别为每12小时75mg/kg和每8小时50mg/kg。在第五剂给药后采集多个血清样本,并通过微生物测定法分析药物浓度。使用二室模型通过非线性最小二乘法回归计算每种药物方案的药代动力学参数。两种药物的各个给药方案在分布容积或半衰期方面均未观察到统计学上的显著差异。作为本研究的结果,每8小时静脉注射6mg/kg米诺环素方案和每8小时静脉注射50mg/kg万古霉素方案似乎是在兔中对这些药物进行比较研究的合适给药方案。

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