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双氯芬酸钠-β-环糊精包合物的研制
引用本文:谷福根,柳翠敬. 双氯芬酸钠-β-环糊精包合物的研制[J]. 中国药学杂志, 1998, 33(3): 153-155
作者姓名:谷福根  柳翠敬
作者单位:北京 100083 北京医科大学药剂教研室
摘    要: 目的:制备双氯芬酸钠-β-环糊精包合物考察其有关性质。方法:采用共沉淀法制备双氯芬酸钠-β-环糊精包合物。结果:经UV,IR,DSC及相溶解度图法鉴定,表明双氯芬酸钠与β-环糊精确已形成包合物,含量测定证明包合物主、客分子比为1:1。结论:双氯芬酸钠-β-环糊精包合物可明显提高双氯芬酸钠的溶解度、溶出速度,并减小其对胃粘膜的刺激性。

关 键 词:双氯芬酸钠  β-环糊精  包合物  胃刺激性
收稿时间:1997-02-12;

The preparation of inclusion compound of diclofenac sodium-β-cyclodextrin
Gu Fugen,Liu Cuijing. The preparation of inclusion compound of diclofenac sodium-β-cyclodextrin[J]. Chinese Pharmaceutical Journal, 1998, 33(3): 153-155
Authors:Gu Fugen  Liu Cuijing
Affiliation:(Gu FG),Liu Cuijing (Liu cJ
Abstract:OBJECTIVE: To prepare the inclusion compound of diclofenac sodium (DFS)-β-cyclodextrin (β-CD) and investigate its properties. METHOD: The inclusion compound of DFS-β-CD was prepared by the co-precipitation method. RESULTS: The inclusion compound of DFS-β-CD was confirmed by UV absorption spectrum, IR absorption spectroscopy, differential scanning calorimetry (DSC) and phase solubility diagram. Meanwhile, the content analysis of the inclusion compound showed that the molecular ratio of DFS to β-CD was 1∶1. CONCLUSION: The soluability and dissolution rate of DFS were increased and its irritation to stomach was reduced when the drug was included by β-CD.
Keywords:diclofenac sodium  β-cyclodextrin  inclusion compound  gastric irritation
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