The quantitative study of the time course of a drug or hormone within the body, encompassing the four fundamental processes of Absorption, Distribution, Metabolism, and Excretion, used to determine the optimal dosing regimen and route of administration for an individual patient. This clinical assessment provides critical data on systemic exposure and half-life, ensuring therapeutic efficacy while minimizing the potential for adverse effects. It is an essential component of precision medicine, particularly in hormone replacement therapy.
Origin
The term is derived from the Greek words pharmakon (drug or poison) and kinetikos (putting in motion), establishing it as the study of drug movement. This field is a core discipline in pharmacology, and its application to endocrinology allows for the scientific individualization of hormonal treatments. The need for precise, personalized dosing in hormone therapy is the driving factor for its clinical use.
Mechanism
The assessment involves measuring the concentration of the administered compound and its active metabolites in the plasma or saliva over specific time intervals following administration. These data are used to calculate key parameters such as the area under the curve and clearance rate, which define the individual’s unique handling of the substance. This mechanism allows clinicians to tailor the dose and frequency to achieve and maintain the desired therapeutic concentration window, optimizing the biological response.
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