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Comparative study for the dissolution of Isosorbide dinitrate tablets in commercial products
Author(s) -
Kahtan Jassim Hasson
Publication year - 2011
Publication title -
al mustansiriyah journal of pharmaceutical sciences
Language(s) - English
Resource type - Journals
eISSN - 2959-183X
pISSN - 1815-0993
DOI - 10.32947/ajps.v9i1.267
Subject(s) - isosorbide dinitrate , dissolution , isosorbide , dissolution testing , chromatography , chemistry , medicine , organic chemistry , anesthesia , biopharmaceutics classification system
Isosorbide dinitrate is prepared as a solid dosage forms, and found in the market as a sublingual tablet or conventional tablet of 10mg for oral administration which is subjected to the dissolution study.In this present work, different commercial products of Isosorbide dinitrate tablets were subjected to dissolution test according to USP method which includes an HPLC determination. The dissolution profiles of three commercial products of isosorbide dintrate tablets and preformulated product were evaluated by comparing with that of reference standard (European product. Actavis Co.) .Due to low bioequivalenceis of all the commercial products relative to the reference standard, attempts were made to improve the formula of the experimental batch of isosorbide dinitrate tablet by enhancing the dissolution rate and increase the stability of the active substances via the Using of a direct compression method in manufacturing of isosorbide dinitrate tablet which on testing showed a high dissolution rate with optimal physical properties of tables.  

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