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Preparation, characterization and evaluation in vitro of naringenin/ PVP k-30 solid dispersions

机译:柚皮素/ PVP K-30固体分散体体外的制备,表征和评价

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Solid dispersions (SD) were prepared with naringenin and polyvinyl pyrrolidone k-30 (PVP k-30) by the solvent evaporation method with three drying methods (microwave-vacuum drying, MVD;;and spray drying, SPD;;vacuum drying, VD). The physical state was characterized by DSC, PXRD, SEM, and FT-IR. The results showed that the vitro dissolution rate and extent of naringenin was improved significantly by SD as compared with the pure drug and physical mixtures (PM). The results of FT-IR showed that naringenin is possibly interacted with PVP k-30 via intermolecular hydrogen bond, the results of DSC and PXRD showed that all of the SD prepared with three drying methods was completely amorphous. Compared with other drying methods, the MVD method can save time and energy.
机译:通过具有三种干燥方法的溶剂蒸发法制备疣素和聚乙烯吡咯烷酮K-30(PVP K-30)制备固体分散体(SD)(微波真空干燥,MVD;;喷雾干燥,SPD ;;真空干燥,VD )。物理状态的特点是DSC,PXRD,SEM和FT-IR。结果表明,与纯药物和物理混合物(PM)相比,SD的体外溶解速率和鼻腔的程度明显改善。 FT-IR的结果表明,Naringenin可能通过分子间氢键与PVP K-30相互作用,DSC和PXRD的结果表明,用三种干燥方法制备的所有SD是完全无定形的。与其他干燥方法相比,MVD方法可以节省时间和能量。

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