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Pharmacokinetic models use mathematical analysis to express a drug's time course in the body. These models can simulate rates of a drug's pharmacokinetic parameters and predict drug concentrations over time.
They help to optimize dosage regimens, correlate concentrations with pharmacologic activity, and estimate toxicity.
Different types of pharmacokinetic models include empirical, compartment, and physiological models.
Empirical models describe data with minimal assumptions, predicting pharmacokinetic parameters across species.
Compartment models represent the body as a series of compartments, having even drug distribution and reversible communication within compartments.
A central compartment represents plasma and highly perfused tissues, and a peripheral compartment depicts poorly perfused tissues.
Lastly, physiological models rely on anatomic and physiologic data to accurately represent drug disposition in various organs and tissues.
They utilize organ tissue size, blood flow, and drug tissue–blood ratios to predict drug concentrations in various tissues.
Pharmacokinetic models utilize mathematical analysis to achieve a detailed quantitative understanding of a drug's life cycle within the body. They are…
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