Pharmacodynamics — Receptor Theory, Dose-Response & PK/PD Integration
Chemistry
PhD-level pharmacodynamics: receptor occupancy theory, Hill–Emax dose-response model and its derivation from the law of mass action, Schild analysis for competitive antagonists, time-delayed PK/PD models with effect-compartment linking, tolerance and sensitisation, and applications to therapeutic window design and clinical trial endpoint selection.
Learning Objectives
- Derive the Hill–Emax equation from the law of mass action and receptor occupancy theory
- Apply Schild regression to quantify competitive antagonism and compute the pA2 value
- Distinguish direct-effect PK/PD models from effect-compartment (biophase) models and indirect-response models
- Compute the effect-site equilibration half-life (t½keo) and predict the temporal dissociation between PK and PD
- Design a dosing regimen to maintain drug effect within the therapeutic window throughout the dosing interval
Lessons
Quick Practice
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