4.7 Article

Enhanced dissolution of Oxcarbazepine microcrystals using a static mixer process

Journal

COLLOIDS AND SURFACES B-BIOINTERFACES
Volume 59, Issue 2, Pages 208-214

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.colsurfb.2007.05.009

Keywords

static mixer; microcrystals; poorly soluble drugs; dissolution enhancement

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The purpose of this study was to form micronized powders of Oxcarbazepine (OXC), a poorly water-soluble drug, using a static mixer technique to enhance the dissolution rate. Controlled precipitation was achieved injecting the organic OXC solution rapidly into an aqueous methylcellulose (MC) protective solution by means of a static mixer thus providing turbulent and homogeneous mixing. Furthermore, a factorial design was implemented for data analysis. The physicochemical properties of the freeze-dried dispersions were evaluated by differential scanning calorimetry (DSC), infrared spectroscopy (FTIR) and X-ray diffraction (XRD). Drug microcrystals showed a narrow size distribution with approximately 2 mu m mean particle size and high drug loading. DSC and FTIR studies revealed that the drug remained in crystalline state and no drug-polymer interaction occurred. The dissolution studies showed enhanced dissolution of OXC microcrystals compared to the pure drug. The static mixer technique was proved capable for micro-sized polymeric particles. This is an inexpensive, less time consuming and fully scalable process for development of poorly soluble drugs. (C) 2007 Elsevier B.V. All rights reserved.

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