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Polymorphic properties of micronized carbamazepine produced by RESS.
Gosselin, P M; Thibert, R; Preda, M; McMullen, J N.
Afiliação
  • Gosselin PM; Faculté de Pharmacie, Université de Montréal, C.P. 6128, Succursale Centre-Ville, Que., Montreal, Canada. patrick.gosselin@umontreal.ca
Int J Pharm ; 252(1-2): 225-33, 2003 Feb 18.
Article em En | MEDLINE | ID: mdl-12550798
ABSTRACT
Carbamazepine microparticles were produced by the rapid expansion of supercritical carbon dioxide solutions (RESS) method. The characteristics of the resulting particles were studied by X-ray powder diffraction (XRPD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and image analysis. X-ray diffractograms and SEM photomicrographs revealed that the crystalline nature of the produced carbamazepine microparticles depended on operating pressure and temperature conditions. Different polymorphs were obtained under various operating conditions. Under certain temperature (below 40 degrees C) and pressure (below 240 bar) conditions, it was possible to form primarily the carbamazepine polymorph stipulated by US Pharmacopeia. A significant reduction was observed in the particle size and size distribution range of carbamazepine produced by RESS. The processed particles had a mean diameter smaller than 3 microm and a size distribution range between 0.5 and 2.5 microm compared to unprocessed starting material with a mean diameter of approximately 85 microm and a size distribution range between 15 and 336 microm. Thus, this study demonstrates that the polymorphic characteristics of carbamazepine microparticles produced by the RESS method can be controlled by varying operating pressure and temperature parameters.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carbamazepina / Tecnologia Farmacêutica Idioma: En Revista: Int J Pharm Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Canadá
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carbamazepina / Tecnologia Farmacêutica Idioma: En Revista: Int J Pharm Ano de publicação: 2003 Tipo de documento: Article País de afiliação: Canadá