| Literature DB >> 26995353 |
Emily Caton1, Elizabeth Nenortas1, Rahul P Bakshi1, Theresa A Shapiro1.
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.Entities:
Keywords: Plasmodium falciparum; drug development; dynamic PK/PD; hollow-fiber cartridge system; malaria; pharmacodynamics; pharmacokinetics
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Year: 2016 PMID: 26995353 PMCID: PMC4811375 DOI: 10.1002/9780470559277.ch150194
Source DB: PubMed Journal: Curr Protoc Chem Biol ISSN: 2160-4762