Development and Optimization of Sustained-Release Matrix Tablets of Diclofenac Sodium Using Carboxymethylated Chitosan Through Systematic Application of Design of Experiments

The study successfully developed a sustained-release matrix tablet of diclofenac sodium using CMCS as the primary matrix material. The optimized formulation demonstrated a dissolution profile comparable to the marketed product (>90% release in 8 hours), with f2 > 50 and f1 < 15, suggesting its potential as a generically equivalent alternative. Moreover, the findings indicate that CMCS is an effective carrier for sustainedrelease formulations and can potentially be applied to other drugs requiring controlled release.

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Publication Details

Journal
Drug Metabolism and Bioanalysis Letters
Published
2024-11-01
DOI
https://doi.org/10.2174/0118723128351869250213102431
Citations
2
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
0.42
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article

Development and Optimization of Sustained-Release Matrix Tablets of Diclofenac Sodium Using Carboxymethylated Chitosan Through Systematic Application of Design of Experiments

Debabrata Ghosh Dastidar, Amit Biswas, Arunima Das, Shovan Naskar et al.
2 citations
Drug Metabolism and Bioanalysis Letters
Drug Solubulity and Delivery Systems
0.42
article

Development and Optimization of Sustained-Release Matrix Tablets of Diclofenac Sodium Using Carboxymethylated Chitosan Through Systematic Application of Design of Experiments

Debabrata Ghosh Dastidar, Amit Biswas, Arunima Das, Shovan Naskar, Rupam Mahish
article en
2 citations

Abstract

The study successfully developed a sustained-release matrix tablet of diclofenac sodium using CMCS as the primary matrix material. The optimized formulation demonstrated a dissolution profile comparable to the marketed product (>90% release in 8 hours), with f2 > 50 and f1 < 15, suggesting its potential as a generically equivalent alternative. Moreover, the findings indicate that CMCS is an effective carrier for sustainedrelease formulations and can potentially be applied to other drugs requiring controlled release.

Drug Metabolism and Bioanalysis LettersVol. 17(3)
National Institute of Pharmaceutical Education and Research (IN)
Openalex Percentile: Top 40%
Drug Solubulity and Delivery Systems
0.42
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