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Original Research Article | OPEN ACCESS

Formulation and Optimization of Gastric Bioadhesive Tablets of Diltiazem Hydrochloride using Central Composite Design

Saurabh Sharma1 , Arun Nanda2, Lalit Singh3

1Department of Pharmacy, Vivek College of Technical Education, Bijnor; 2Department of Pharm Sci, M D University, Rohtak; 3SRMS CET, Bareilly, India.

For correspondence:-  Saurabh Sharma   Email: saurabhmpharm@rediffmail.com   Tel:+919927026893

Received: 5 September 2013        Accepted: 2 October 2013        Published: 24 December 2013

Citation: Sharma S, Nanda A, Singh L. Formulation and Optimization of Gastric Bioadhesive Tablets of Diltiazem Hydrochloride using Central Composite Design. Trop J Pharm Res 2013; 12(6):861-867 doi: 10.4314/tjpr.v12i6.1

© 2013 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 bioadhesive tablets of diltiazem hydrochloride with a unique combination of bioadhesion and drug release.
Method: Tablets were prepared by physical blending of diltiazem hydrochloride with two polymers, viz., carbopol and hydroxylpropyl methyl cellulose in different ratio along with other excipients. A 32 central composite design was employed to optimize the formulations on the basis of phycochemical properties, bioadhesive strength (measured as force of detachment from gastric mucosa) and in vitro drug release. HPMC K 4M and Carbopol 934P were taken as the independent variables. Contour plots were drawn and optimum formulations were selected by feasibility and grid searches.
Results: The tablets showed excellent bioadhesive strength which varied from 7.6 to 21 g. Both polymers had effect on the bioadhesive strength of the tablets and maximum bioadhesion was observed at the highest level of both the polymers. The drug release from the formulation varied from 79.74 to 94.54 % in 12 h. The diffusion exponent (n) of Korsmeyer-Peppas model ranged from 0.491 to 0.658 which indicates the mechanism of drug release was anomalous transport; the diffusion exponent (n) increased with increase in the amount of either polymer in the bioadhesive tablet.
Conclusion: Floating bioadhesive tablets of diltiazem hydrochloride with good bioadhesion and controlled release characteristics is feasible.

Keywords: Drug delivery, Gastroretentive, Bioadhesive, Diltiazem, Central composite design

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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