环糊精
溶解度
化学
溶解
药品
共沉淀
劳拉西泮
包合物
增溶
生物利用度
苯二氮卓
色谱法
核化学
有机化学
药理学
医学
麻醉
生物化学
受体
作者
N. M. Sanghavi,K. B. Choudhari,Rajinder Singh Matharu,Latha Viswanathan
标识
DOI:10.3109/03639049309062976
摘要
AbstractThe preparation of an inclusion complex of Lorazepam, a benzodiazepine antianxiety agent with β -cyclodextrin is described. The inclusion compound was prepared by the homogeneous coprecipitation method in the molar ratio of 1:2 of the drug and β -cyclodextrin respectively. The formation of inclusion complex was evaluated by UV spectral studies, IR studies, X-ray diffractometry, and Differential Thermal Analysis. The solubility and in-vitro drug release studies indicated that the complex form of the drug significantly increase the solubility and the dissolution rate compared to the free form. Tablets prepared with Lorazepam- β -cyclodextrin complex also showed a significant increase in dissolution of the drug indicating that P-cyclodextrin plays an important role in the solubilization of the drug.
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