This work examines the release of etodolac from various molecular weight fr
actions of polyethylene glycol (PEG) solid dispersions. Solid dispersions o
f etodolac were prepared in different molar ratios of drug/carrier by using
solvent and melting methods. The release rate of etodolac from the resulti
ng complexes was determined from dissolution studies by use of USP dissolut
ion apparatus 2 (paddle method). The physical state and drug:PEG interactio
n of solid dispersions and physical mixtures were characterized by X-ray di
ffraction (XRD), infrared spectroscopy (IR) and differential scanning calor
imetry (DSC). The dissolution rate of etodolac is increased in all of the s
olid dispersion systems compared to that of the pure drug and physical mixt
ures. The solid dispersion compound prepared in the molar ratio of 1:5 by t
he solvent method was found to have the fastest dissolution profile. The ph
ysical properties did not change after 9 months storage in normal condition
s. (C) 2000 Elsevier Science S.A. All rights reserved.