Lou G, Montgomery P R, Sitar D S
Department of Pharmacology and Therapeutics, University of Manitoba, Winnipeg, Canada.
J Psychiatry Neurosci. 1996 Nov;21(5):334-9.
The pharmacokinetic disposition of intravenous and oral doses of tacrine was determined in 5 elderly patients (aged 64 to 96 y) with the clinical diagnosis of Alzheimer's disease. The bioavailability of the oral formulation was low (9.9% to 36.4%), and the plasma half-life was not altered by route of drug delivery. These data indicate that tacrine elimination occurs by a 1st-order process. Plasma clearance of tacrine varied more than its half-life, which is consistent with a modulating effect of apparent volume of distribution (Vd). Our findings, together with other limited published studies, suggest that use of tacrine for the treatment of Alzheimer's disease (AD) will be confounded by the high interindividual variability in its kinetic disposition.
在5名临床诊断为阿尔茨海默病的老年患者(年龄64至96岁)中测定了静脉注射和口服他克林剂量后的药代动力学情况。口服制剂的生物利用度较低(9.9%至36.4%),且药物给药途径未改变血浆半衰期。这些数据表明他克林的消除是通过一级过程进行的。他克林的血浆清除率变化大于其半衰期,这与表观分布容积(Vd)的调节作用一致。我们的研究结果与其他有限的已发表研究共同表明,他克林用于治疗阿尔茨海默病(AD)时,其动力学情况存在高度个体间变异性,这将使治疗受到干扰。