Original Research Article | OPEN ACCESS

Super-disintegrant activity of acid-modified millet starch in diclofenac tablet formulations

Sylvester O Eraga , Vincent N Nwajuobi, Magnus A Iwuagwu

Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmacy, University of Benin, PMB 1154, Benin City, 300001, Nigeria;

For correspondence:-  Sylvester Eraga   Email:  eragaso@uniben.edu   Tel:  +2348030884928

Published: 31 December 2017

Citation: Eraga SO, Nwajuobi VN, Iwuagwu MA. Super-disintegrant activity of acid-modified millet starch in diclofenac tablet formulations. J Sci Pract Pharm 2017; 4(1):161-168 doi: 10.47227/jsppharm.v4i1.3

© 2017 The author(s).
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). This license requires that reusers give credit to the creator. It allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, for noncommercial purposes only. .

Abstract

Purpose: To determine the effect of acid modification on the disintegrant activity of native millet starch in diclofenac sodium tablet formulation in comparison with sodium starch glycolate.
Methods: Diclofenac sodium tablets were prepared by direct compression using sodium starch glycolate, native and acid-modified millet starches at concentrations of 2.5 and 5 %w/w. The granules were evaluated for their flow properties while the tablets were evaluated for tablet dimensions, uniformity of weight, crushing strength, friability, disintegration time, wetting time and dissolution studies. Drug-excipient interaction using DSC and FTIR was also investigated.
Results: All the granules were free flowing with angles of repose and Carr's indices of < 31° and < 21 % respectively. The tablet hardness was between 4.3 - 6.5 kp while the friability values were < 1.0 %. They all showed good wetting and disintegration time of < 3 min and 7.5 min respectively. Only batches of tablets formulated with 5 %w/w of sodium starch glycolate and acid-modified millet starch met official specification for fast disintegrating tablets. Dissolution studies showed that all batches achieved over 90 % drug release in 30 min except tablets prepared with 2.5 %w/w of the native millet starch. DSC and FTIR analyses revealed no drug interactions with excipients.
Conclusion: The acid-modified millet starch showed a shorter disintegration time and a better dissolution profile when compared with the native millet starch. Acid modification imparts better disintegration and dissolution properties to the starch. The acid-modified millet starch can also be used as a cheaper alternative to sodium starch glycolate because of the comparable disintegration times and dissolution profiles of diclofenac sodium tablets formulated with these disintegrants

Keywords: Acid modification, millet starch, disintegrant, diclofenac, tablets

Journal Metrics
Impact Factors
» Thompson Reuters (ISI): 0.000
» H-5 index: 7 (2024)
» SCImago Journal Rank (SJR): 0.000


Manuscripts
» Submission to first review: 07-14 days
» Submission to acceptance: 20-30 days
» Acceptance to publication: 20-30 days

Article Tools

Share this article with



Archives

2022; 9: 
1.
2021; 8: 
1.
2020; 7: 
1.
2019; 6: 
1.
2018; 5: 
1, 2.
2017; 4: 
1.
2016; 3: 
1.
2015; 2: 
1.
2023; 10: 
1.
2014; 1: 
1.