RT info:eu-repo/semantics/article T1 Glibornuride-ß-cyclodextrin inclusion complexes: Preparation, structural characterization and in vitro dissolution behaviour A1 Echezarreta López, María Magdalena A1 Torres-Labandeira, Juan J. A1 Santana-Penín, Lourdes A1 Vila-Jato, José L. A2 Ingeniería Química y Tecnología Farmacéutica AB Phase·solubility studies of the complexation of glibornuride (GB) with α-, β- and γ-cydodextrin (CyD) showed that the most stable complex is formed with β-CyD. The effects of β-CyD on chemical shift values in 1H-NMR spectra of GB in aqueous médium suggest that it ís the bornyl part of the drug which is bound inside the CyD cavity. Solid inclusion complexes were obtained by coprecipitation and freeze-drying methods, and characterized by X-ray diffractometry and differential scanning calorimetry. Druq solubility was improved by inclusion in solid complexes obtained by either method YR 1993 FD 1993 LK http://riull.ull.es/xmlui/handle/915/37326 UL http://riull.ull.es/xmlui/handle/915/37326 LA en DS Repositorio institucional de la Universidad de La Laguna RD 23-jun-2024