Abstract
The objective of this study was to obtain Controlled-release dosage forms of dipyridamole chosen as a model drug practically insoluble above pH 5. The coevaporates were prepared by the solvent method using enteric and insoluble acrylic polymers as well as their mixtures in different proportions. The in vitro dissolution test results were determined by the USP XXII paddle method at different pH values during a period of 8 h. These results showed that the progressive pH-dependent release of dipyridamole could only be achieved by blending enteric and insoluble polymers. To overcome the difficulty in maintaining sink conditions with the paddle method, the dissolution profiles of some of the formulations were investigated using the open flow-through cell method.
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