Absolute bioavailability
Absolute Bioavailability is a concept in pharmacokinetics that refers to the amount of a drug that reaches the systemic circulation after administration, compared to the amount that would reach the circulation if the drug were given intravenously. It is a measure of the efficiency of drug absorption and first-pass metabolism.
Definition[edit | edit source]
The absolute bioavailability of a drug is defined as the fraction of an administered dose of unchanged drug that reaches the systemic circulation. It is typically expressed as a percentage. The absolute bioavailability is calculated by comparing the area under the plasma concentration-time curve (AUC) after non-intravenous administration, to the AUC after intravenous administration.
Factors Influencing Absolute Bioavailability[edit | edit source]
Several factors can influence the absolute bioavailability of a drug. These include the drug formulation, the route of administration, the rate and extent of drug absorption, and the extent of first-pass metabolism in the liver and gut wall.
Importance in Drug Development[edit | edit source]
Understanding the absolute bioavailability of a drug is crucial in drug development. It helps in determining the correct dosage and route of administration for a new drug. It also aids in predicting the drug's pharmacodynamics and pharmacokinetics.
See Also[edit | edit source]
References[edit | edit source]
Navigation: Wellness - Encyclopedia - Health topics - Disease Index - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD is not a substitute for professional medical advice. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.Contributors: Prab R. Tumpati, MD