Pharmacokinetic/Pharmacodynamic (PK/PD) Model
PK/PD models describe the relation between drug dosing, concentration, and efficacy.
Pharmacokinetic/pharmacodynamics (PK/PD) modeling, an integral component of the drug development process, is a mathematical technique for predicting the effect and efficacy of drug dosing over time. Broadly speaking, pharmacokinetic models describe how the body reacts to a drug in terms of absorption, distribution, metabolism, and excretion. Pharmacodynamic models describe how a drug affects the body by linking the drug concentration to an efficacy (or safety) metric. A well-characterized PK/PD model is an important tool in guiding the design of future experiments and trials.
You can represent PK/PD models with MATLAB and SimBiology, which provide an environment that streamlines and automates the modeling process. You can:
- Import, process, and visualize time-course data
- Select a PK model from a library, or create mechanism-based PK/PD models using the interactive block-diagram editor
- Estimate model parameters using nonlinear regression or NLME methods
- Explore system dynamics, using parameter sweeps and sensitivity analysis
- Simulate dosing strategies and what-if scenarios
Examples and How To
- PK/PD Model for Bacterial Growth Kinetics Under Therapy (Example)
- Model for Target–Mediated Drug Disposition (TMDD) (Example)
- PK/PD Model of Tumor Growth Kinetics Under Therapy (Example)
- Using SimBiology for Mechanism-Based PK/PD Modeling (Webinar)
- Using SimBiology for Pharmacokinetic and Mechanistic Modeling (Tutorial)
Software Reference
- Pharmacokinetic and Pharmacodynamic Modeling (Documentation)
- Pharmacokinetic Modeling (Functions)
See also: computational biology, biotech and pharmaceutical, Curve Fitting Toolbox, Statistics Toolbox