Formulation development and evaluation of orodispersible tablet of Azelnidipine by factorial design and its comparison with the marketed formulation

The aim of the present investigation was to prepare an orodispersible tablet of Azelnidipine using superdisintegrant agents like croscarmellose sodium by direct compression method. These formulated tablets were evaluated for drug content, weight variation, friability, hardness, solubility study also...

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Bibliographic Details
Published in:Particulate science and technology Vol. 41; no. 7; pp. 1053 - 1061
Main Authors: Dolas, Ramdas T., Ware, Pooja D.
Format: Journal Article
Language:English
Published: Philadelphia Taylor & Francis 03-10-2023
Taylor & Francis Ltd
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Summary:The aim of the present investigation was to prepare an orodispersible tablet of Azelnidipine using superdisintegrant agents like croscarmellose sodium by direct compression method. These formulated tablets were evaluated for drug content, weight variation, friability, hardness, solubility study also, and drug excipient compatibility study. Based on data obtained from pre-compression and post-compression evaluation of batches as well as the factorial design model study f7 batch was selected as the optimized batch. Based on the result obtained from the dissolution profile study it was concluded that the formula responsible for Azelnidipine tablets gives the fastest disintegration as well as absorption of the drug as compared to the conventional marketed tablet dosage form.
ISSN:0272-6351
1548-0046
DOI:10.1080/02726351.2023.2173109