The mathematical simulation used to predict and describe the time course of drug or hormone concentration within the body’s various compartments based on individual physiological parameters. This modeling utilizes parameters such as volume of distribution, clearance rates, and bioavailability to forecast drug exposure profiles. It is an essential tool for establishing personalized dosing strategies.
Origin
This term originates from quantitative pharmacology, utilizing mathematical principles to describe biological processes. “Pharmacokinetic” pertains to ADME processes. “Modeling” signifies the creation of a predictive mathematical framework, often using compartmental or physiologically based models, to rationalize drug behavior in complex biological systems.
Mechanism
The model uses differential equations to represent the movement of the substance between compartments, such as plasma, adipose tissue, and target cells. By inputting patient-specific variables like renal function or body fat percentage, the model simulates the expected plasma concentration curve following a given dose. This simulation allows clinicians to adjust the proposed regimen before empirical testing, optimizing therapeutic exposure.
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