This submission belongs to the session a. Advances in the solid state field of the event The 2nd Electronic Conference on Pharmaceutical Sciences
Published date
24 Apr, 2012
Citation
Kyriakos Kachrimanis, Zorica Djuric, Svetlana Ibric, Ioannis Nikolakakis, Jelena Djuris, Preparation and characterization of carbamazepine-polyethylene oxide hot-melt extruded solid dispersions, in Proceedings of The 2nd Electronic Conference on Pharmaceutical Sciences, 1 May–31 May 2012, MDPI: Basel, Switzerland, doi: 10.3390/ecps2012-00795
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Preparation and characterization of carbamazepine-polyethylene oxide hot-melt extruded solid dispersions
Jelena Djuris 1
Ioannis Nikolakakis 2
Svetlana Ibric 1
Zorica Djuric 1
Kyriakos Kachrimanis 2
1. Department of Pharmaceutical Technology and Cosmetology, Faculty of Pharmacy, University of Belgrade
2. Department of Pharmaceutical Technology, School of Pharmacy, Aristotle University of Thessaloniki
Abstract
The aim of the presented study was to investigate the possibility of usage of polyethylene oxide polymer (PEO, Polyox® WSR 301, DOW, USA) in the preparation of carbamazepine hot-melt extruded solid dispersions. Hot-melt extrusion (HME) is a simple, solvent free and continuous processing technique used to produce variety of dosage forms. Thermoplastic materials, such as PEO polymers, are required for the process feasibility. Poloxamer 407 (Lutrol® F127, BASF, Germany) was used as a plasticizer to facilitate the HME process, by reducing the processing temperature and lowering the monitored torque. Physico-chemical properties of carbamazepine and polymers, their physical mixtures and dispersions made by melt-mixing or HME were characterized in detail. A hot-melt extruder with one rotating screw was used for the preparation of solid dispersions by HME technique (RCP-0250 Microtruder, Randcastle extrusion systems, USA). Samples were analyzed by differential scanning calorimetry (DSC), thermo-gravimetric analysis (TGA), FT-IR spectroscopy and hot-stage microscopy (HSM) methods. Obtained results indicate that the addition of plasticizer enables preparation of carbamazepine-PEO hot-melt extrudates using a single-screw extruder configuration. It was demonstrated that there is no degradation of CBZ upon heating in the HME processing temperature range (90-110°C). Furthermore, the crystalline form of CBZ was not altered during the HME processing. The presence of CBZ form III crystals, homogeneously dispersed in the hot-melt extrudates, was confirmed. Dispersion of CBZ crystals in the polymers mixtures was visualized using the polarizing HSM technique. Presented study demonstrates the potential of PEO WSR 301 application in the preparation of carbamazepine hot-melt extruded solid dispersions.
Keywords
carbamazepine
hot-melt extrusion
polyethylene oxide
solid dispersions
Laminar Dispersive and Distributive Mixing with Dissolution and Applications to Hot-melt Extrusion
The Artificial Stomach and Duodenum (ASD): A physiologically relevant in vitro dissolution tool