The specific method or route by which exogenous hormones are administered to a patient as part of a replacement or optimization therapy regimen. The chosen delivery method significantly influences the hormone’s pharmacokinetics, including its absorption rate, metabolic fate, and the resulting steady-state concentration in the bloodstream. Common delivery systems include transdermal patches, injectable solutions, oral capsules, and subcutaneous pellet implantation.
Origin
This term combines ‘hormonal replacement’—a clinical practice dating back to the early 20th century with the isolation of endocrine substances—with the pharmaceutical concept of ‘delivery.’ The evolution of delivery methods is driven by the clinical need to mimic the body’s natural, non-oral secretion patterns and to bypass hepatic first-pass metabolism. The choice of delivery system is a critical, personalized aspect of modern endocrinology.
Mechanism
Each delivery route utilizes different physiological barriers and transport mechanisms to introduce the hormone into the systemic circulation. Transdermal methods rely on passive diffusion through the skin to achieve stable, non-pulsatile levels, effectively avoiding the liver’s initial metabolic pass. Injectable methods provide a direct, high-concentration bolus or a slow-release depot effect depending on the ester. Oral delivery, while convenient, subjects the hormone to immediate hepatic metabolism, which can alter its biological activity and clearance profile.
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