Hygroscopicity, phase solubility and dissolution of various substituted sulfobutylether β-cyclodextrins (SBE) and danazol-SBE inclusion complexes

被引:38
作者
Jain, AC [1 ]
Adeyeye, MC [1 ]
机构
[1] Duquesne Univ, Grad Sch Pharmaceut Sci, Pittsburgh, PA 15282 USA
关键词
sulfobutylether beta-cyclodextrins (SBE); danazol; inclusion complexes; moisture sorption desorption isotherms; surface area analysis; porosity; X-ray diffraction; differential scanning calorimetry; phase solubility analysis; dissolution;
D O I
10.1016/S0378-5173(00)00607-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the present work was to characterize hygroscopicity, phase solubility and dissolution properties for various substituted sulfobutylether beta -cyclodextrins (SBEs) and danazol-SBE inclusion complexes. Moisture sorption was measured using a symmetric gravimetric analyzer. The complexes were characterized by powder X-ray diffraction (XRD) and differential scanning calorimetry (DSC). Moisture sorption isotherms for the SBEs and the complexes showed low moisture sorption at RH < 60%. The moisture absorption desorption isotherms for the various SBEs showed very little hysteresis, indicating almost complete desorption. Moisture adsorbed by the various SBE was in the order SEE 7 > SBE 4 > SBE 5 at 95% RH. Powder XRD data for complexes showed the disappearance of characteristic crystalline peaks for danazol or the formation of amorphous entities and DSC showed the disappearance of the peak of fusion of danazol indicating complex formation. Phase solubility of danazol with various substituted SBEs indicated 1:1 stoichiometry of complexes. The apparent stability constant, as determined by the method of Higuchi and Conners, increased as the degree of substitution of SBEs increased and decreased as the temperature increased. The dissolution of the complexes was significantly greater than that of the corresponding physical mixtures indicating that the formation of amorphous complex increased the solubility of poorly soluble danazol. More than 85% of danazol was released in < 10 min, compared to 15% danazol release from the physical mixtures. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:177 / 186
页数:10
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