Floating Matrix Tablets of Domperidone Formulation and Optimization Using Simplex Lattice Design

AuthorShailesh Prajapatien
AuthorLaxmanbhai Patelen
AuthorChhaganbhai Patelen
Issued Date2011-07-31en
AbstractThe purpose of this research was to prepare a floating matrix tablet containing domperidone as a model drug. Polyethylene oxide (PEO) and hydroxypropyl methylcellulose (HPMC) were evaluated for matrix-forming properties. A simplex lattice design was applied to systemically optimize the drug release profile. The amounts of PEO WSR 303, HPMC K15M and sodium bicarbonate were selected as independent variables and floating lag time, time required to release 50% of drug (t50) and 80% of drug (t80), diffusion coefficient (n) and release rate (k) as dependent variables. The amount of PEO and HPMC both had significant influence on the dependent variables. It was found that the content of PEO had dominating role as drug release controlling factor, but using suitable concentration of sodium bicarbonate, one can tailor the desired drug release from hydrophilic matrixes. The linear regression analysis and model fitting showed that all these formulations followed Korsmeyer and Peppas model, which had a higher value of correlation coefficient (r). The tablets of promising formulation were found to be stable for 3 months under accelerated (40°C / 75% RH) stability testing.en
DOIhttps://doi.org/10.22037/ijpr.2010.892en
KeywordDomperidoneen
KeywordFloating matrix tabletsen
KeywordSimplex lattice designen
KeywordRelease kineticsen
KeywordPolyethylene oxideen
KeywordHydroxypropyl methylcelluloseen
KeywordFloating lag timeen
KeywordTotal floating time.en
PublisherBrieflandsen
TitleFloating Matrix Tablets of Domperidone Formulation and Optimization Using Simplex Lattice Designen
TypeOriginal Articleen

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