The study of how an externally administered substance, such as a therapeutic peptide, hormone, or drug, is absorbed, distributed throughout the body, metabolized, and ultimately excreted over a period of time. This quantitative analysis is essential for determining the optimal route of administration, the correct dosage, and the appropriate frequency to achieve a stable and therapeutically effective concentration at the target receptor site. Understanding pharmacokinetics minimizes adverse effects and maximizes clinical efficacy.
Origin
The term is a compound of “exogenous agent,” meaning a substance originating outside the body, and “pharmacokinetics,” which itself derives from the Greek words pharmakon (drug/poison) and kinetikos (moving/putting in motion). This discipline has been fundamental to pharmacology since the mid-20th century, providing the mathematical basis for rational drug design and dosing schedules.
Mechanism
The pharmacokinetic mechanism follows the ADME paradigm: Absorption dictates the substance’s entry into systemic circulation; Distribution determines its movement into tissues and target organs; Metabolism involves enzymatic transformation, primarily in the liver, often rendering the agent inactive; and Excretion, typically renal or biliary, removes the agent and its metabolites from the body. These four processes collectively determine the concentration-time curve of the agent.
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