The comprehensive clinical and scientific knowledge of how the human body processes a substance, encompassing the four primary stages of Absorption, Distribution, Metabolism, and Excretion (ADME). This understanding is crucial for determining the correct dosage, frequency, and route of administration for any therapeutic agent to ensure efficacy and minimize adverse effects. It is the quantitative foundation of rational drug and supplement use.
Origin
The term is derived from the Greek pharmakon (drug) and kinetikos (motion), literally meaning the movement of drugs. It is a core discipline in pharmacology and toxicology. ‘Understanding’ emphasizes the necessary clinical interpretation of the quantitative data to optimize patient outcomes.
Mechanism
Pharmacokinetics is governed by a complex interplay of physiological factors, including gastrointestinal pH, plasma protein binding capacity, liver enzyme activity (e.g., Cytochrome P450 systems), and renal clearance rates. These processes dictate the time-concentration curve of the substance in the systemic circulation. A thorough understanding allows clinicians to predict a compound’s half-life and its steady-state concentration, ensuring therapeutic levels are maintained.
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