Oral Drug Administration

After oral administration, the amount of drug in the GIT at any time (Ai) is determined from the bioavailable dose (FD) which decreases at a rate dependent on the absorption rate constant.

Assuming first-order absorption:

Ai = FD e-kat

The amount of the drug in the body initially increases because the rate of absorption is larger than the rate of elimination and then decreases as the rate of elimination exceeds the rate of absorption.

The drug conc-time profile after single oral administration can be described by:

Cp =

F D ka

Vd (k a - k)
( e -kt - e -ka t)
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