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终末期肾衰竭患者硝苯地平的总稳态血浆水平、游离稳态血浆水平及药代动力学

Total and free steady-state plasma levels and pharmacokinetics of nifedipine in patients with terminal renal failure.

作者信息

van Bortel L, Böhm R, Mooij J, Schiffers P, Rahn K H

机构信息

Department of Pharmacology, University of Limburg, Maastricht, The Netherlands.

出版信息

Eur J Clin Pharmacol. 1989;37(2):185-9. doi: 10.1007/BF00558229.

Abstract

The total and free steady-state plasma levels of nifedipine in patients with renal failure have been compared with those in subjects with normal renal function. Studies were done after administration of nifedipine 10 mg t.d.s. p.o. for 5 days, after i.v. infusion of 4.4 mg, and after a single 10 mg oral dose. The systemic clearance of nifedipine after a single i.v.-dose was higher in subjects with renal insufficiency (854 ml/min) than in those with normal renal function (468 ml/min). After the single oral dose the AUC (6100 ng.min.ml-1) and maximum plasma concentration (75.0 ng.ml-1) were lower than in subjects with normal renal function (19300 ng.ml-1; 122 ng.ml-1). The plasma protein binding of nifedipine averaged 95.5% in normal subjects and 94.8% in patients with renal failure. Although free and total steady-state plasma levels of nifedipine tended to be somewhat lower than normal in renal failure, the changes in pharmacokinetics and decreased protein binding of nifedipine did not result in a significantly different steady-state plasma level of the drug. The blood pressure response to a given plasma nifedipine level appeared to be enhanced in renal failure.

摘要

已将肾衰竭患者硝苯地平的总稳态血浆水平和游离稳态血浆水平与肾功能正常的受试者进行了比较。研究在口服硝苯地平10毫克,每日三次,持续5天之后、静脉输注4.4毫克之后以及单次口服10毫克剂量之后进行。单次静脉给药后,肾功能不全受试者硝苯地平的全身清除率(854毫升/分钟)高于肾功能正常者(468毫升/分钟)。单次口服给药后,曲线下面积(6100纳克·分钟·毫升-1)和最大血浆浓度(75.0纳克·毫升-1)低于肾功能正常的受试者(19300纳克·毫升-1;122纳克·毫升-1)。硝苯地平在正常受试者中的血浆蛋白结合率平均为95.5%,在肾衰竭患者中为94.8%。尽管肾衰竭时硝苯地平的游离和总稳态血浆水平往往略低于正常水平,但硝苯地平的药代动力学变化和蛋白结合率降低并未导致该药物的稳态血浆水平有显著差异。肾衰竭患者对给定血浆硝苯地平水平的血压反应似乎增强。

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