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Original Research Article | OPEN ACCESS

Formulation of Sustained-Release Diltiazem Matrix Tablets Using Hydrophilic Gum Blends

Afrasim Moin , H G Shivakumar

JSS College of Pharmacy, JSS University, Mysore, Karnataka-570015, India;

For correspondence:-  Afrasim Moin   Email: afrasimmoin@yahoo.co.in   Tel:+919886652844

Received: 27 August 2009        Accepted: 19 February 2010        Published: 24 June 2010

Citation: Moin A, Shivakumar HG. Formulation of Sustained-Release Diltiazem Matrix Tablets Using Hydrophilic Gum Blends. Trop J Pharm Res 2010; 9(3):283-291 doi: 10.4314/tjpr.v9i3.10

© 2010 The authors.
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 License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To develop sustained release matrix tablets of diltiazem hydrochloride (DTZ) using karaya gum (K) alone or in combination with locust bean gum (LB) and hydroxypropyl methylcellulose (H).
Methods: Matrix tablets of DTZ were prepared at different ratios of drug:gum (1:1, 1:2, and 1:4) and of the gum blends (K, K/LB, K/H and K/LB/H) by direct compression. The matrix tablets were evaluated for hardness, friability, in vitro release and drug content. The formulations were also characterised by scanning electron microscopy (SEM), Fourier transform infra-red spectroscopy (FTIR) and differential scanning calorimetry (DSC). A commercial diltiazem hydrochloride product Dilzem SR, was used as a reference for comparison.
Results: Tablets with only K or K/H had the highest mean dissolution time (MDT), the least dissolution efficiency (DE, 12 %), and released drug by swelling, diffusion and erosion mechanisms. Karaya gum or combinations with locust bean gum sufficiently controlled drug release, while combinations of KH and KLBH exhibited high and low drug release efficiency, respectively. SEM images of the tablets before and after dissolution showed morphological changes on the tablet surface while FTIR and DSC studies indicate that there was no chemical interaction between the drug and the polymers. Three of the formulations compared well with the reference (p < 0.05) in terms of release characteristics.
Conclusion: The results of the study demonstrate that karaya gum alone or in suitable combination with locust bean gum and hydroxypropyl methylcellulose is suitable for formulating sustained-release matrix tablets of diltiazem.

Keywords: Karaya gum, Locust bean gum, Diltiazem hydrochloride, Sustained release, Hydroxypropyl methylcellulose

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