dc.creatorMartins, Rodrigo M.
dc.creatorSiqueira, Silvia
dc.creatorTacon, Luciana A.
dc.creatorFreitas, Luis A. P.
dc.date.accessioned2013-11-05T12:31:46Z
dc.date.accessioned2018-07-04T16:20:52Z
dc.date.available2013-11-05T12:31:46Z
dc.date.available2018-07-04T16:20:52Z
dc.date.created2013-11-05T12:31:46Z
dc.date.issued2012
dc.identifierPOWDER TECHNOLOGY, LAUSANNE, v. 215-16, n. 1, supl. 1, Part 6, pp. 156-165, JAN, 2012
dc.identifier0032-5910
dc.identifierhttp://www.producao.usp.br/handle/BDPI/41381
dc.identifier10.1016/j.powtec.2011.09.041
dc.identifierhttp://dx.doi.org/10.1016/j.powtec.2011.09.041
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1634674
dc.description.abstractThe aim of this study was to investigate the improvement of the aqueous solubility of carbamazepine by preparing microstructured ternary solid dispersions using polyoxylglycerides and colloidal silicon dioxide. Microstructured solid dispersions were obtained in a spray dryer. The influence of the spray drying conditions on the properties of the microparticles was investigated using a full 3(2) factorial design in which the factors studied were the silicon dioxide content and the air outlet temperature. The microparticles were thoroughly characterized in terms of yield, solubility, angle of repose, particle size, drug content, moisture content, sorption isotherms, morphology, thermal behavior, infrared spectroscopy and crystallinity. The dissolution rates of carbamazepine and of the microparticles in water were also determined. In general, the microstructured solid dispersions demonstrated good yield, adequate flow and moisture content (<3%), drug recovery (91.98 to 100.22%) and particle size (<142.90 mu m). Thermal and infrared analysis showed that there was no drug interaction during the process. On the other hand, the results of X-ray diffraction evidenced a partial polymorphic modification of carbamazepine. The solubility and dissolution rates of carbamazepine were remarkably improved. Therefore, the results confirm the high potential of the spray drying technique to obtain microstructured ternary solid dispersions. (C) 2011 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherELSEVIER SCIENCE SA
dc.publisherLAUSANNE
dc.relationPOWDER TECHNOLOGY
dc.rightsCopyright ELSEVIER SCIENCE SA
dc.rightsclosedAccess
dc.subjectFACTORIAL DESIGN
dc.subjectPOLYMORPHISM
dc.subjectSTEROYL MACROGOLGLYCERIDES
dc.subjectMICROSPHERES
dc.subjectDISSOLUTION TEST
dc.titleMicrostructured ternary solid dispersions to improve carbamazepine solubility
dc.typeArtículos de revistas


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