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首页> 外文期刊>Journal of Inclusion Phenomena and Macrocyclic Chemistry >Evaluation of host-guest complex formation between a benzimidazolic derivative and cyclodextrins by UV-VIS spectrophotometry and differential scanning calorimetry
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Evaluation of host-guest complex formation between a benzimidazolic derivative and cyclodextrins by UV-VIS spectrophotometry and differential scanning calorimetry

机译:通过紫外可见分光光度法和差示扫描量热法评估苯并咪唑衍生物和环糊精之间的客体复合物形成

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摘要

Interactions between a benzimidazolic derivative, omeprazole (OME), beta-cyclodextrin (βCD) and a chemically modified βCD, methyl-beta-cyclodextrin (MβCD) were investigated in aqueous solution by UV-VIS spectroscopy and in solid state by differential scanning calorimetry (DSC). Phase solubility studies were used to evaluate the complexation in aqueous solution. The two solubility diagrams obtained were AL type, indicating the formation of a drug-cyclodextrin complex with 1:1 stoichiometry. The complex of OME with MβCD showed a higher stability constant (K S) than those with βCD. Some evidences of inclusion complexation in solid state were obtained from DSC. Only in thermal curves of OME-βCD lyophilized product and in OME-MβCD spray-dried and lyophilized systems the melting point of the drug disappeared completely suggesting the possible formation of an inclusion complex.
机译:苯并咪唑衍生物,奥美拉唑(OME),β-环糊精(βCD)与化学修饰的βCD,甲基-β-环糊精(MβCD)在水溶液中的相互作用通过UV-VIS光谱法进行了研究,在固态下通过差示扫描量热法( DSC)。相溶解度研究用于评估水溶液中的络合度。所获得的两个溶解度图为AL 型,表明形成了化学计量比为1:1的药物-环糊精复合物。 OME与MβCD的复合物显示出比βCD更高的稳定性常数(K S )。从DSC获得了固态包裹体络合的一些证据。仅在OME-βCD冻干产品的热曲线以及在OME-MβCD喷雾干燥和冻干的系统中,药物的熔点完全消失,表明可能形成包合物。

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