Publikation: Assessment of non-linear combination effect terms for drug-drug interactions
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Drugs interact with their targets in different ways. A diversity of modeling approaches exists to describe the combination effects of two drugs. We investigate several combination effect terms (CET) regarding their underlying mechanism based on drug-receptor binding kinetics, empirical and statistical summation principles and indirect response models. A list with properties is provided and the interrelationship of the CETs is analyzed. A method is presented to calculate the optimal drug concentration pair to produce the half-maximal combination effect. This work provides a comprehensive overview of typically applied CETs and should shed light into the question as to which CET is appropriate for application in pharmacokinetic/pharmacodynamic models to describe a specific drug-drug interaction mechanism.
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KOCH, Gilbert, Johannes SCHROPP, William J. JUSKO, 2016. Assessment of non-linear combination effect terms for drug-drug interactions. In: Journal of Pharmacokinetics and Pharmacodynamics. 2016, 43(5), pp. 461-479. ISSN 0090-466X. eISSN 1573-8744. Available under: doi: 10.1007/s10928-016-9490-0BibTex
@article{Koch2016-10Asses-36991,
year={2016},
doi={10.1007/s10928-016-9490-0},
title={Assessment of non-linear combination effect terms for drug-drug interactions},
number={5},
volume={43},
issn={0090-466X},
journal={Journal of Pharmacokinetics and Pharmacodynamics},
pages={461--479},
author={Koch, Gilbert and Schropp, Johannes and Jusko, William J.}
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<dcterms:abstract xml:lang="eng">Drugs interact with their targets in different ways. A diversity of modeling approaches exists to describe the combination effects of two drugs. We investigate several combination effect terms (CET) regarding their underlying mechanism based on drug-receptor binding kinetics, empirical and statistical summation principles and indirect response models. A list with properties is provided and the interrelationship of the CETs is analyzed. A method is presented to calculate the optimal drug concentration pair to produce the half-maximal combination effect. This work provides a comprehensive overview of typically applied CETs and should shed light into the question as to which CET is appropriate for application in pharmacokinetic/pharmacodynamic models to describe a specific drug-drug interaction mechanism.</dcterms:abstract>
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