Optimized Dosing Kinetics describes the strategic administration schedule of exogenous compounds, such as hormones or supplements, designed to achieve plasma concentration profiles that closely mimic the desirable temporal pattern of endogenous production. This optimization aims to maximize therapeutic effect while minimizing exposure during periods where the compound might exert a detrimental or unnecessary signal. We seek to match the pharmacokinetic curve to the physiological need.
Origin
This term originates in pharmacology, specifically pharmacokinetics (PK), adapted for endocrine optimization where mimicking natural rhythmicity is the primary goal. It moves beyond simple half-life considerations to temporal patterning.
Mechanism
The mechanism involves calculating infusion or dosing rates that leverage the body’s absorption, distribution, metabolism, and excretion (ADME) properties to create desired peak-to-trough ratios. For example, frequent, small doses might be used to simulate the pulsatile release of a natural hormone. This fine-tuning ensures that receptor occupancy is achieved efficiently without inducing prolonged saturation or negative feedback.
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