Study of Drug Release of Diclofenac Sodium Matrix Tablets Using Synergistic Effect of HPMC and Xanthan Gum Polymer

Aims: To check the release efficacy of active pharmaceutical ingredients from tablet dosage form using synthetic and natural polymers. Introduction: Diclofenac sodium in sustained release manner tablets was created by Xanthan gum, HPMC, and mixed with both polymers to change the concentration ratio. The dosage form of the tablet was examined for the early stage formulation studies such as repose angle, apparent density, compressibility index, and some corporal properties like weight variant, friability, and content of the drug. For post-formulation studies, like in-vitro studies were implemented in a solution of phosphate buffer pH 7.4 for 8 hours. All the corporal properties of the diclofenac sodium tablets were within the limit of tolerance. Objective: The study checked the Diclofenac Sodium release kinetics from synthetic and natural polymer-modified tablets. Methods: Following the wet granulation method, we prepared a diclofenac sodium tablet using HPMC and Xanthan Gum Polymer. Results: The tablet that contained both HPMC and Xanthan gum (Batch C-I and C-II) shows the best drug content than other polymer-based batches like HPMC (Batch A-I, A-II) and Xanthan gum (Batch B-I, B-II). The great sustained drug release was shown in the HPMC and Xanthan gum mixed polymer-based matrix tablet (Batch C-I). The data showed that the mixing of polymers could lead to sustaining drug release from the formulation. Conclusion: From the research, we can conclude that the diclofenac release % was maximum when we used a combination of both polymers in the tablet dosage form.

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Publication Details

Journal
Current Applied Polymer Science
Published
2025-02-04
DOI
https://doi.org/10.2174/0124522716329448241226062454
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
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article

Study of Drug Release of Diclofenac Sodium Matrix Tablets Using Synergistic Effect of HPMC and Xanthan Gum Polymer

Mithun Bhowmick, Pratibha Bhowmick, Sumel Ashique, Shaik Abdul Rahaman et al.
Current Applied Polymer Science
Drug Solubulity and Delivery Systems
article

Study of Drug Release of Diclofenac Sodium Matrix Tablets Using Synergistic Effect of HPMC and Xanthan Gum Polymer

Mithun Bhowmick, Pratibha Bhowmick, Sumel Ashique, Shaik Abdul Rahaman, Mirazuddin Mollick
article en

Abstract

Aims: To check the release efficacy of active pharmaceutical ingredients from tablet dosage form using synthetic and natural polymers. Introduction: Diclofenac sodium in sustained release manner tablets was created by Xanthan gum, HPMC, and mixed with both polymers to change the concentration ratio. The dosage form of the tablet was examined for the early stage formulation studies such as repose angle, apparent density, compressibility index, and some corporal properties like weight variant, friability, and content of the drug. For post-formulation studies, like in-vitro studies were implemented in a solution of phosphate buffer pH 7.4 for 8 hours. All the corporal properties of the diclofenac sodium tablets were within the limit of tolerance. Objective: The study checked the Diclofenac Sodium release kinetics from synthetic and natural polymer-modified tablets. Methods: Following the wet granulation method, we prepared a diclofenac sodium tablet using HPMC and Xanthan Gum Polymer. Results: The tablet that contained both HPMC and Xanthan gum (Batch C-I and C-II) shows the best drug content than other polymer-based batches like HPMC (Batch A-I, A-II) and Xanthan gum (Batch B-I, B-II). The great sustained drug release was shown in the HPMC and Xanthan gum mixed polymer-based matrix tablet (Batch C-I). The data showed that the mixing of polymers could lead to sustaining drug release from the formulation. Conclusion: From the research, we can conclude that the diclofenac release % was maximum when we used a combination of both polymers in the tablet dosage form.

Current Applied Polymer ScienceVol. 08
Openalex Percentile: Top 98%
Drug Solubulity and Delivery Systems
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