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Research Article


 

Microencapsulation of Diclofenac Sodium by Non-solvent Addition Technique

 

G Murtaza1, M Ahmad1* and G Shahnaz2

 1Department of Pharmacy, Faculty of Pharmacy and Alternative Medicines, The Islamia University of Bahawalpur, Bahawalpur 63100, Pakistan, 2Department of Pharmaceutical Sciences, Faculty of Pharmacy,  University of Innsbruck, Austria.

 

*Corresponding author:  E-mail: gmdogar356@gmail.com  Tel: +92-300-9682258 (mobile), 62-9255243; Fax: +92-62-9255565

 

Received: 26 July 2009                                        Revised accepted: 21 January 2010

 

Tropical Journal of Pharmaceutical Research, April 2010; 9(2): 187-195

 

Abstract

 

Purpose: To prepare, using non-solvent addition technique, diclofenac sodium-ethylcellulose microparticles with modified drug release properties.

Methods: Microparticles were prepared by non-solvent addition phase separation method and characterized by micromeritics, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), x-ray diffraction (XRD), dissolution test and thermal analysis.

Results: The microparticles were whitish, irregular, aggregated, and in the size range of 390 - 442 µm size. Drug embedment efficiency was 89 - 91 %. Characterisation studies indicate that there was no strong chemical interaction between the drug and the polymer in the microparticles. Polymer concentration and sustained release behavior were directly proportional.

Conclusion: Non-solvent addition phase separation is a suitable method for preparing diclofenac sodium-ethylcellulose multi-unit controlled release drug delivery system.

 

Keywords: Phase separation, Diclofenac sodium, Ethylcellulose, Non-solvent addition, Characterisation.

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