Tablets of different hardnesses and compositions were prepared with an
original theophylline granulate previously coated with Eudragit RS 30
D. Dissolution studies of each tablet formulation were performed to ve
rity any kinetic variation from the dissolution profile. This was obta
ined by filling with the same coated granules in a hard gelatine capsu
le. While the dissolution profile of the capsules possesses very good
linearity, the tablet kinetics gradually deviate from this linearity w
ith an increase in the percentage of the coated granules in the formul
ation. Tablet hardness had only a marginal influence on this kinetic d
eviation.