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Original scientific paper

DEVELOPMENT AND OPTIMIZATION OF CARVEDILOL FORMULATION USING EXPERIMENTAL DESIGN

By
Predrag Sibinovic ,
Predrag Sibinovic

Pharmaceutical and Chemical Industry Zdravlje-Actavis, Leskovac, Serbia

Valentina Marinkovic ,
Valentina Marinkovic

Pharmaceutical and Chemical Industry Zdravlje-Actavis, Leskovac, Serbia

Radoslav Palic ,
Radoslav Palic

Faculty of Science and Mathematics, University of Nis, Niš, Serbia

Ivan Savic ,
Ivan Savic

Faculty of Technology, University of Nis, Niš, Serbia

Ivana Savic -Gajic ,
Ivana Savic -Gajic
Contact Ivana Savic -Gajic

Faculty of Technology, University of Nis, Niš, Serbia

Dragan Milenovic ,
Dragan Milenovic

Pharmaceutical and Chemical Industry Zdravlje-Actavis, Leskovac, Serbia

Rada Jankovic
Rada Jankovic

Pharmaceutical and Chemical Industry Zdravlje-Actavis, Leskovac, Serbia

Abstract

The aim of this paper was to develop and optimize the carvedilol tablets formulation using the full factorial design. The content of binder (PVP K30), content of disintegrant (crospovidone) and main compression force were used as the independent variables. Tablets were prepared by wet granulation. The percentage of released carvedilol from prepared formulation after 10 minutes was defined as the response. It has been found that formulation with the low content of binding agents (4.8%), high content of disintegrant (4.5%) and compression force of 50 N has the best profile of drug. The optimal formulation was defined based on implementation of pharmaceuticaltechnological tests (testing strength, friability, disintegrating, contents of drug substance, drug release profiles). The stability of the optimal formulation with carvedilol was estimated using the aging tests.

Citation

Authors retain copyright. This work is made freely available online under an open-access model under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC-http://creativecommons.org/licenses/by-nc-nd/4.0/BY-NC-ND 4.0).

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