Hydrogels, and particularly biopolymeric hydrogels, have recently rece
ived tremendous interest as controlled release systems for their pecul
iar features such as high biocompatibility, biodegradability, bioadhes
ivity, chemical and thermal resistance and good mechanical properties.
Among biopolymers, the exocellular microbial polysaccharide scleroglu
can appears to be particularly well suited for the formulation of mono
lithic hydrogel matrices for controlled drug release. In this work we
studied the macroscopic factors influencing the kinetics of a model dr
ug release (theophylline) from a scleroglucan hydrogel matrix (2%w/w)
and modeled the relevant experimental results. The evidences for the r
elease experiments indicate that the kinetics of the processes follow
an apparently non-Fickian behavior under different active drug concent
ration, temperature and stirring speed. However, by considering the pe
culiar nature of the hydrogel matrix and the geometrical features of t
he experimental setup in the formulation of the appropriate initial an
d boundary conditions, data can be satisfactorily modeled with the cla
ssical Fick's law.