Solute diffusion in hydrogels is important in many biotechnology field
s. Solute behavior in hydrogels has been explained in terms of reducti
on in hydrogel free volume, enhanced hydrodynamic drag on the solute,
increased path length due to obstruction, and a combination of hydrody
namic drag and obstruction effects. In this article the various mathem
atical models derived to explain and predict solute diffusion in hydro
gels are reviewed and tested against literature data. These models can
be divided into those applicable to hydrogels composed of flexible po
lymer chains (i.e., homogeneous hydrogels) and those composed of rigid
polymer chains (i.e., heterogeneous hydrogels). For homogeneous hydro
gels it was determined that a scaling hydrodynamic model provided the
best explanation for solute diffusion, while for heterogeneous hydroge
ls obstruction models were more consistent with the experimental data.
Both the scaling hydrodynamic model and the most appropriate obstruct
ion model contain undefined parameters which must be clarified in orde
r for these models to gain widespread acceptance.