Comparison of Different Superdisintegrants In Designing of Mouth Dissolving Tablets of Domperidone
Keywords:
Mouth dissolving tablets, Domperidone, SuperdisintegrantsAbstract
This research involves preparation of mouth dissolving tablets of of Domperidone by direct compression method using various concentrations of superdisintegrants sodium starch glycolate, croscarmellose and crospovidone (D1 – D9). The tablets were evaluated for parameters like thickness, hardness, friability, In vitro & In vivo disintegration time, wetting time, water absorption ratio, % drug content and In vitro drug release studies. Based on the results, formulation containing 6% superdisintegrants in combination (CCS, CP & SSG) (D-2) was identified as ideal and better formulation among all formulations developed for Domperidone Maleate tablets. In vitro release of optimized formulation of Domperidone Maleate Mouth dissolving tablets of D-2 was found to be 99.43% drug release within 10minutes and in-vitro disintegration time being ranges between 40 and 42sec. The final optimized formulation (D-2) was compared with marketed product of Domperidone Maleate tablets (DOMSTAL-MT) which shows 94.22% drug release in 10 minutes. It means the prepared formulation show quite satisfactory release with compared to Marketed Product.
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