Drugs of different solubilities were incorporated into porous cellulos
e matrices (PCMs) by solvent evaporation. The rate of release of the d
rugs from the PCMs was found to decrease with increasing drug concentr
ation and decreasing drug solubility. At low or moderate drug concentr
ations, the release rate remained moderately high except for drugs of
very low solubility. The mechanisms controlling release rate appeared
to include diffusion within the matrix but may be more complex.