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Pharmacologic Modeling

  • Ronald GieschkeEmail author
  • Daniel Serafin
Chapter
  • 2.9k Downloads

Abstract

Pharmacologic modeling deals with pharmacokinetics (PK) and pharmacodynamics (PD). PK describes “what the body does to a drug,” i.e., how it is absorbed, distributed and eliminated, and PD “what a drug does to the body,” i.e., how it interacts with receptors and their signaling pathways up to the whole body level. The time course of drug concentrations and drug effects is modeling outcomes. PK uses compartmental models either in an empirical way to get a satisfactory fit to experimental data, or in a physiologic manner to create predictive models across species (physiologically-based PK, or PBPK). PD models turn drug concentrations at the pharmacologic site of action, or biophase, into biological effects using direct and/or indirect response mechanisms. Taken together, PK-PD models provide a powerful tool to link dosage regimens to clinical effects and vice versa.

Keywords

Drug Concentration PBPK Model Drug Amount Oseltamivir Carboxylate Mammillary Model 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 2014

Authors and Affiliations

  1. 1.Pharma Research and Early DevelopmentF. Hoffmann-La Roche LtdBaselSwitzerland
  2. 2.Pharma Research and Early DevelopmentF. Hoffmann-La Roche LtdBaselSwitzerland

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