Characterization of itraconazole/2-hydroxypropyl-β-cyclodextrin inclusion complex in aqueous propylene glycol solution

被引:68
作者
Miyake, K
Irie, T
Arima, H
Hirayama, F
Uekama, K
Hirano, M
Okamoto, Y
机构
[1] Kumamoto Univ, Fac Pharmaceut Sci, Kumamoto 8620973, Japan
[2] Janssen Kyowa Co Ltd, Nagaizumi, Shizuoka 4110932, Japan
关键词
itraconazole; 2-hydroxypropyl-beta-cyclodextrin; inclusion complexation; solubility; stability constants; stoichiometry;
D O I
10.1016/S0378-5173(98)00393-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The interaction of itraconazole, a triazole antifungal agent, with 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CyD) in water and 10% v/v propylene glycol/water solution at pH 2.0 was investigated by the solubility method and ultraviolet and H-1-nuclear magnetic resonance (NMR) spectroscopies. The solubility of itraconazole in water significantly increased as the concentrations of HP-beta-CyD were augmented, showing an A, type phase solubility diagram. The upward curvature closely corresponded to the simulation curve which was calculated on the basis of the 1:2 (guest:host) complexation model. The 1:2 complex was formed even in the presence of 10% v/v propylene glycol, although the co-solvent system made the interaction with HP-beta-CyD weaker due to the competitive inclusion. The ultraviolet spectroscopic studies also supported the 1:2 complex formation of itraconazole with HP-beta-CyD in 10% v/v propylene glycol/water solution at pH 2.0. The H-1-NMR spectroscopic studies suggested that the triazole and triazolone moieties of itraconazole are involved in the 1:2 inclusion complexation. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:237 / 245
页数:9
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