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Original Research Article | OPEN ACCESS

Dicyclomine-loaded Eudragit -based Microsponge with Potential for Colonic Delivery: Preparation and Characterization

Vikas Jain , Ranjit Singh

School of Pharmaceutical Sciences, Shobhit University, Meerut, Uttar Pradesh, 250110, India;

For correspondence:-  Vikas Jain   Email: vikasjain11118059@rediffmail.com   Tel:+911212575724

Received: 26 April 2009        Accepted: 21 December 2009        Published: 23 February 2010

Citation: Jain V, Singh R. Dicyclomine-loaded Eudragit -based Microsponge with Potential for Colonic Delivery: Preparation and Characterization. Trop J Pharm Res 2010; 9(1):67-72 doi: 10.4314/tjpr.v9i1.9

© 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: The purpose of this work was to develop a prolonged microsponge drug delivery system containing dicyclomine.
Methods: Dicyclomine-loaded, Eudragit-based microsponges were prepared using a quasi-emulsion solvent diffusion method. The compatibility of the drug with formulation components was established by differential scanning calorimetry (DSC) and Fourier transform infra-red (FTIR). Process parameters were modulated to optimise the formulation. Shape and surface morphology of the microsponges were examined using scanning electron microscopy.
Results: The results of compatibility tests showed that no chemical interaction or changes took place during preparation of the formulations; furthermore, the drug was stable in all the formulations. In increase in drug:polymer ratio resulted in a reduction in the release rate of the drug from the microsponges. Kinetic analysis showed that the main mechanism of drug release was by Higuchi matrix-controlled diffusion. Drug release was bi-phasic with an initial burst effect with 16 – 30 % of the drug was released in the first hour. Cumulative release for the microsponges over 8 hours ranged from 59 - 86 %. 
Conclusion: This study presents an approach for the modification of microsponges for prolonged drug release of dicyclomine. The unique compressibility of microsponges can be applied to achieve effective local action since microsponges may be taken up by macrophages present in colon.

Keywords: Microsponge; Dicyclomine; Quasi-emulsion solvent diffusion; Eudragit RS-100; Colonic drug release

Impact Factor
Thompson Reuters (ISI): 0.6 (2023)
H-5 index (Google Scholar): 49 (2023)

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