The drug liberation of dissolved and suspended pharmacons was studied
from hydrogels, which contained gel-forming polymers. The process of l
iberation was studied on a flow-through membrane diffusion model. The
quantities of the liberated drugs were measured as a function of the f
low-through time and the cumulative curves were drawn. It was found th
at the relation between the quantity of the liberated pharmacon and th
e diffusion time could be described with a power function the exponent
of which was 0.5. The validity of the relation did not depend on the
type of the polymer, on the gel-forming concentration or on the type o
f pharmacon dispersion.