Formulation and Evaluation of Etoricoxib Oro Dispersable Tablets by Direct Compression Method
Journal Title: IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) - Year 2016, Vol 11, Issue 2
Abstract
Oral disintegrating tablet (ODT) is defined as “A solid dosage form containing medical substances or active ingredient which disintegrates rapidly usually within a matter of seconds when placed upon the tongue”. The main aim of the present study is to formulate Etoricoxib oral disintegrating tablets. Etoricoxib is a selective COX-II inhibitor which acts by inhibiting the COX–2 enzyme and decreases the incidences of side effects associated with these agents. Conventional tablets of Etoricoxib are not capable of rapid action, which is required for faster drug effect onset and immediate relief from pain. Etoricoxib ODT’s are prepared by direct compression method using Cross povidone, Cross carmellose sodium, Sodium starch glycolate and Calcium silicate as the super disintegrants. The prepared tablets were characterized for their hardness, weight variation, disintegration time, wetting time, tablet thickness, friability, and in vitro dissolution studies.DSC Studies were also performed. The ability of the tablet to release the drug faster depends on the concentration and type of super disintegrant. In this study the oral disintegrating tablets containing Cross carmellose sodium as the super disintegrant in the concentration of 10% shows better release of drug. About 98.6% of the drug was released in 10 mins from the tablets. Therefore, based on the physico chemical properties, in vitro drug release profile and mouth feel formulation F 10 containing 10% of Cross carmellose sodium is optimised as the best formulation. DSC study shows no drug excipient interaction.
Authors and Affiliations
Lakshmi Usha Ayalasomayajula, Radha Rani Earle, Prasanthi T,, V. Harika,, N. RamyaSree
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