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作 者:陈卉[1] 陈燕忠[1] 谢清春[1] 班俊峰[1]
机构地区:[1]广东药学院药物研究所/广东省药物新剂型重点实验室,广州510006
出 处:《中国药师》2012年第9期1281-1283,共3页China Pharmacist
摘 要:目的:研究两种不同类型环糊精羟丙基-β-环糊精(HP-β-CD)、γ-环糊精(γ-CD)对吲达帕胺的包合增溶作用,并进行包合物的鉴定。方法:运用相溶解度法考察不同类型环糊精对药物的增溶作用,并用差示扫描量热(DSC)法和红外光谱(IR)法对包合物进行鉴定。结果:确定了吲达帕胺与HP-β-CD和γ-CD包合物的相溶解度图,并计算了表观稳定常数,用DSC法和IR法确证2种不同类型环糊精的包合物均已形成。结论:2种不同类型环糊精对吲达帕胺都有显著的增溶作用,且都能形成包结比为1:1的包合物,γ-CD的增溶作用更强,形成的包合物更稳定。Objective: To investigate the solubilization effect of hydroxypropyl-β-cyclodextrin(HP-β-CD) and γ-cyclodextrin(γ-CD) on indapamide and identify the inclusion compounds.Method: The solubility of inclusion compounds were evaluated by phase solubility method.The inclusion compounds were identified by differential scanning calorimetry(DSC) and infrared spectroscopy(IR).Result: The phase-solubility diagrams of indapamide/HP-β-CD and indapamide/γ-CD inclusion compounds were drawn and the stability constants were calculated.The results of DSC and IR showed the inclusion compounds were prepared successfully.Conclusion: Both the cyclodextrins have significant solubilization effect on indapamide and can form inclusion compounds at the formation ratio of 1∶ 1.The solubilization effect of γ-CD is better and the inclusion compounds are more stable.
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