Spray-dried voriconazole-cyclodextrin complexes: Solubility, dissolution rate and chemical stability

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• 作者：Tijana Miletic ; Kachrimanis Kyriakos ; Adrijana Graovac ; Svetlana Ibric
• 关键词：Voriconazole ; Cyclodextrins ; Solubility ; Dissolution ; Stability ; Molecular docking
• 刊名：Carbohydrate Polymers
• 出版年：2013
• 出版时间：15 October, 2013
• 年：2013
• 卷：98
• 期：1
• 页码：122-131
• 全文大小：2490 K

文摘

The present work investigates the effect of complexation with hydroxypropyl-beta-cyclodextrin (HPBCD) and 2-O-methyl-beta-cyclodextrin (2-O-MBCD), on voriconazole solubility, dissolution rate and chemical stability. Drug-cyclodextrin complexes were prepared as aqueous solutions, which were spray-dried, and their properties were compared to wet ground samples and physical mixtures. DSC analysis revealed absence of crystalline voriconazole from spray-dried complexes. FTIR spectroscopy indicated changes in the H-bonding network of the hydroxyl groups of cyclodextrin following drug inclusion. Dissolution rate of voriconazole was significantly higher from spray-dried complexes with either cyclodextrin in comparison with free drug, physical mixtures, or wet ground mixtures. However, two degradation impurities were found in aged samples, with slightly higher impurity level with HPBCD. Performed solubility studies suggested that 2-O-MBCD is more efficient solubilizer. Molecular docking simulations showed a difference in the 1:1 binding affinities and sites, with HPBCD surprisingly forming complexes of much lower energy, thus suggesting a multiple rather than a 1:1 complexation.