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终末期肾病患者中劳卡尼的动力学及蛋白结合情况

Lorcainide kinetics and protein binding in patients with end-stage renal disease.

作者信息

Somani P, Simon V, Gupta R K, King P, Shapiro R S, Stockard H

出版信息

Int J Clin Pharmacol Ther Toxicol. 1984 Mar;22(3):121-5.

PMID:6715079
Abstract

Lorcainide is a new antiarrhythmic drug undergoing clinical investigation for management of patients with ventricular arrhythmias. In this study we investigated the kinetic profile of lorcainide in nine patients with end-stage renal disease. A single intravenous bolus of 100 mg of the drug was injected while the patients were undergoing hemodialysis or during the off-dialysis period. Renal disease did not alter the kinetic properties of lorcainide; the elimination t1/2 beta during hemodialysis was 8.61 +/- 6.35 h, not significantly different from 7.04 +/- 4.12 h off-dialysis. Serum protein binding of lorcainide was investigated in vitro, and the percent binding of lorcainide to serum proteins of normal volunteers and renal or cardiac patients was not significantly different. These data suggest that renal disease should not alter either the dose or the dosing interval of lorcainide.

摘要

劳卡尼是一种正在进行临床研究的新型抗心律失常药物,用于治疗室性心律失常患者。在本研究中,我们调查了9例终末期肾病患者体内劳卡尼的动力学情况。在患者进行血液透析期间或非透析期,静脉注射100mg该药物的单次推注剂量。肾病并未改变劳卡尼的动力学特性;血液透析期间的消除半衰期β为8.61±6.35小时,与非透析期的7.04±4.12小时无显著差异。我们在体外研究了劳卡尼与血清蛋白的结合情况,劳卡尼与正常志愿者、肾病患者或心脏病患者血清蛋白的结合百分比无显著差异。这些数据表明,肾病不应改变劳卡尼的剂量或给药间隔。

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