Abstract
A mutual prodrug is the association in a unique molecule of two,
usually synergetic drugs attached to each other. Mutual prodrug of aspirin
with paracetamol as a model oral prodrug was prepared and identified
and many pharmaceutical steps were applied including: solubility studies,
hydrolysis of the prodrug in different pH from 1 to 9 to simulate the pH
of the GIT and hydrolysis of the prodrug by human plasma. The results
showed that the stability of the compound in the GIT should be more than
its transient time in the GIT in order to be absorbed before it is
hydrolyzed, and the compound should be hydrolyzed after it is absorbed
from the GIT with in suitable time in comparison to its elimination half
life. These studies can be considered as quick pharmaceutical studies for
preliminary evaluation of any suggested prodrug, if the compound passes
these steps successfully then further pharmaceutical studies is suggested
for the final recommendation.
usually synergetic drugs attached to each other. Mutual prodrug of aspirin
with paracetamol as a model oral prodrug was prepared and identified
and many pharmaceutical steps were applied including: solubility studies,
hydrolysis of the prodrug in different pH from 1 to 9 to simulate the pH
of the GIT and hydrolysis of the prodrug by human plasma. The results
showed that the stability of the compound in the GIT should be more than
its transient time in the GIT in order to be absorbed before it is
hydrolyzed, and the compound should be hydrolyzed after it is absorbed
from the GIT with in suitable time in comparison to its elimination half
life. These studies can be considered as quick pharmaceutical studies for
preliminary evaluation of any suggested prodrug, if the compound passes
these steps successfully then further pharmaceutical studies is suggested
for the final recommendation.