Emily Caton, Elizabeth Nenortas, Rahul P. Bakshi, Theresa A. Shapiro
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引用次数: 5
Abstract
Knowledge of pharmacokinetic/pharmacodynamic (PK/PD) relationships can enhance the speed and economy of drug development by enabling informed and rational decisions at every step, from lead selection to clinical dosing. For anti-infective agents in particular, dynamic in vitro hollow-fiber cartridge experiments permit exquisite control of kinetic parameters and the study of their consequent impact on pharmacodynamic efficacy. Such information is of great interest for the cost-restricted but much-needed development of new antimalarial drugs, especially since the major human pathogen Plasmodium falciparum can be cultivated in vitro but is not readily available in animal models. This protocol describes the materials and procedures for determining the PK/PD relationships of antimalarial compounds. © 2016 by John Wiley & Sons, Inc.
抗疟化合物药动学/药效学研究的中空纤维方法学
了解药代动力学/药效学(PK/PD)关系可以提高药物开发的速度和经济性,从先导物选择到临床给药的每一步都能做出明智和理性的决定。特别是对于抗感染药物,动态体外中空纤维药筒实验允许对动力学参数进行精确控制,并研究其对药效学效果的影响。这些信息对于成本有限但急需的新型抗疟药物的开发具有极大的兴趣,特别是因为主要的人类病原体恶性疟原虫可以在体外培养,但不易在动物模型中获得。本方案描述了测定抗疟疾化合物的PK/PD关系的材料和程序。©2016 by John Wiley &儿子,Inc。
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