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基于动物数据预测碱性药物在人体中的分布容积。

Prediction of the volumes of distribution of basic drugs in humans based on data from animals.

作者信息

Sawada Y, Hanano M, Sugiyama Y, Harashima H, Iga T

出版信息

J Pharmacokinet Biopharm. 1984 Dec;12(6):587-96. doi: 10.1007/BF01059554.

Abstract

The apparent volume of distribution-after distribution equilibrium and the ratio of distributive tissue volume to the unbound fraction in the tissue (VT/fuT) of 10 weak basic drugs, i.e., chlorpromazine, imipramine, propranolol, disopyramide, lidocaine, quinidine, meperidine, pentazocine, chlorpheniramine, and methacyclin were compared in animal species and humans. In these two parameters, a statistically significant correlation between animals and humans was obtained, when the parameters were plotted on a log-log scale. The correlation coefficient between VT/fuT was significantly higher than that between the apparent volumes of distribution (p less than 0.05). In general, there was little difference between VT/fuT of various basic drugs in animals and that in humans. Prediction of the apparent volume of distribution in humans using animal data of VT/fuT, plasma unbound fraction, blood volume, and blood-to-plasma concentration ratio in humans was successful for most of drugs studied.

摘要

比较了10种弱碱性药物,即氯丙嗪、丙咪嗪、普萘洛尔、双异丙吡胺、利多卡因、奎尼丁、哌替啶、喷他佐辛、氯苯那敏和甲烯土霉素在动物和人体中的分布平衡后表观分布容积以及组织分布容积与组织中游离分数的比值(VT/fuT)。当以对数-对数尺度绘制这些参数时,在动物和人体之间获得了统计学上显著的相关性。VT/fuT之间的相关系数显著高于表观分布容积之间的相关系数(p小于0.05)。一般来说,各种碱性药物在动物和人体中的VT/fuT差异不大。利用人体的VT/fuT、血浆游离分数、血容量和血药浓度比的动物数据预测人体的表观分布容积,对大多数研究药物来说是成功的。

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