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Characterization of α-Glucosidase Inhibitor/Cyclodextrin Complex Prepared by Freeze-Drying

机译:冷冻干燥制备的α-葡萄糖苷酶抑制剂/环糊精复合物的表征

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Miglitol (MT) is an α-glucosidase inhibitor with a postmeal blood glucose level lowering effect that is used to treat type 2 diabetes. In addition, α-cyclodextrin (αCD) has been reported to inhibit increases in postmeal blood glucose. The aim of this study was to prepare a freeze-dried product (FD) composed of MT and αCD or γCD (molar ratio of MT/αCD = 1/1, MT/γCD = 1/1) and to evaluate the physicochemical properties and biological activity of the FD. The PXRD profile of FD exhibited a halo pattern, and characteristic peaks derived from MT, αCD, and γCD were not observed. The TG-DTA results for FD indicated an increased weight loss temperature and the absence of an endothermic peak for MT. The NIR absorption spectrum measurement suggested an intermolecular interaction between MT and αCD or γCD in the FD. 1H-1H NOESY NMR spectroscopy (D2O) revealed an intermolecular interaction in the FD. The results of the α-glucosidase activity inhibition test and the α-amylase activity inhibition test indicated that the FD exhibited the same inhibition rate as MT alone and the effects of MT were not altered by the freeze-drying method.
机译:米格列醇(MT)是一种具有餐后血糖降低作用的α-葡萄糖苷酶抑制剂,用于治疗2型糖尿病。另外,据报道α-环糊精(αCD)抑制餐后血糖的升高。这项研究的目的是制备由MT和αCD或γCD(MT /αCD的摩尔比= 1/1,MT /γCD= 1/1)组成的冻干产品(FD)并评估其理化性质和FD的生物活性。 FD的PXRD轮廓显示出晕轮图案,未观察到源自MT,αCD和γCD的特征峰。 FD的TG-DTA结果表明减肥温度升高,MT没有吸热峰。 NIR吸收光谱测量表明FD中MT与αCD或γCD之间存在分子间相互作用。 1H-1H NOESY NMR光谱(D2O)显示了FD中的分子间相互作用。 α-葡糖苷酶活性抑制试验和α-淀粉酶活性抑制试验的结果表明,FD显示出与单独的MT相同的抑制率,并且冷冻干燥方法没有改变MT的作用。

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