Bioavailability
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Revision as of 01:19, 5 July 2014 by Panayiotis Stavrou (talk | contribs) (m)

Definition

Bioavailability (F) is a pharmacokinetic parameter representing the fraction of a drug dose that reaches the systemic circulation unaltered.

Characteristics

  • The greater the F, the greater the amount of drug that reaches the systemic circulation, and thus the greater the drug concentration in plasma and vice versa
  • The route with the highest F (F=1) is via intravenous (I.V.) administration.
  • The second highest F is achieved through inhalation.
  • The parenteral routes of drug administration have low F because all the drug absorbed by the GIT, passes through the hepatic circulation undergoing *first pass metabolism, prior entering to the systemic circulation.


Types

Absolute bioavailability

AUC IVPO.svg

It is the comparison of the per os bioavailability to the intavenous bioavailability