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Pharmacokinetic characterization of amantadine in human brain tissue.

机译:金刚烷胺在人脑组织中的药代动力学表征。

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摘要

Amantadine concentrations in human brain tissue were assessed in order to estimate population pharmacokinetic parameters using the computer program NONMEM. The elimination constant in brain tissue was determined to be 0.00447 [1/h], resulting in a t1/2 of 6.5 days for the mean patient in the population investigated (n = 19). An estimate of 65.5 L was obtained for the apparent volume of distribution. The elimination half-life of amantadine from brain tissue is much longer than from blood and is comparable to the previously investigated neuroleptic drugs haloperidol and levomepromazine.
机译:使用计算机程序NONMEM评估人脑组织中金刚烷胺的浓度,以估计群体药代动力学参数。确定脑组织中的消除常数为0.00447 [1 / h],导致所调查人群中的平均患者的t1 / 2为6.5天(n = 19)。表观分布体积估计为65.5L。金刚烷胺从脑组织中消除的半衰期比从血液中消除的半衰期长得多,并且与先前研究的抗精神病药氟哌啶醇和左旋丙嗪相当。

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