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'''<big>Characteristics</big>'''
'''<big>Characteristics</big>'''
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 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.     
*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.     





Revision as of 01:19, 5 July 2014

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