Sri K Vijaya, Kondaiah A, Ratna J Vijaya, Annapurna A
College of Pharmaceutical Sciences, Andhra University, Visakhapatnam, India.
Drug Dev Ind Pharm. 2007 Mar;33(3):245-53. doi: 10.1080/03639040601150195.
The objective of the present study is to prepare and characterize cyclodextrin inclusion complexes of quercetin and rutin to improve their aqueous solubility and dissolution properties. Inclusion complexes of quercetin and rutin with beta-cyclodextrin (beta-CD) and hydroxyl propyl-beta-cyclodextrin (HP-beta-CD) were prepared by kneading and coevaporation methods. Characterization of inclusion complexes was done by phase solubility analysis and was supported by X-ray powder diffractometry (XRD), differential scanning calorimetry (DSC), and Fourier-transform infra red spectroscopy (FT-IR) analysis. Inclusion complexes exhibited higher rates of dissolution than the corresponding physical mixtures and pure drug. Higher dissolution rates were observed with HP-beta-CD kneaded complexes in comparison to the products with beta-CD.
本研究的目的是制备槲皮素和芦丁的环糊精包合物并对其进行表征,以改善它们的水溶性和溶解性能。采用捏合法和共蒸发法制备了槲皮素和芦丁与β-环糊精(β-CD)和羟丙基-β-环糊精(HP-β-CD)的包合物。通过相溶解度分析对包合物进行表征,并辅以X射线粉末衍射(XRD)、差示扫描量热法(DSC)和傅里叶变换红外光谱(FT-IR)分析。包合物的溶出速率高于相应的物理混合物和纯药物。与β-CD产品相比,HP-β-CD捏合复合物的溶出速率更高。