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Dosage method validation using UV for prednisone active ingredien | 10783
Drug Designing: Open Access

Drug Designing: Open Access
Open Access

ISSN: 2169-0138

+44 1223 790975

Dosage method validation using UV for prednisone active ingredient in 5 mg, PRECORTYL generic pill- Princeps dissolution kinetic study


JOINT EVENT ON 3rd International Conference and Expo on DRUG DISCOVERY & DESIGNING and 9th Annual PHARMACEUTICAL CHEMICAL ANALYSIS CONGRESS

October 02-03, 2017 | Vienna, Austria

R. Ketrane and N. Bouchara

Universit�?© de Bejaia, Algeria

Posters & Accepted Abstracts: Drug Des

Abstract :

PRECORTYL�?® 5 mg is a generic presented as pills where CORTANCYL is its princeps. It consists of an active ingredient, which is Prednisone, and five excipients. PRECORTYL�?® 5 mg is a glucocorticoid drug. It is used to treat a large spectrum of immunologic, allergic and inflammatory diseases, including asthma and arthritis this is what makes its financial interest. To optimize the production costs a new method that consists on UV spectrophotometry is validated to be used in routine tests. The aim of this study is to validate an assay method of the active ingredient using a UV spectrophotometry as well as doing a comparative dissolution kinetic study. The obtained results of both tests are compliant according European pharmacopeia standards.

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