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Preparation and Characterization of Solid Dispersions of Silymarin with Polyethylene Glycol 6000

机译:聚乙二醇6000水飞蓟素固体分散体的制备与表征

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Aim To prepare and characterize solid dispersions of silymarin with the intention of improving their dissolution properties. Methods The solid dispersions were prepared by the fusion method with polyethylene glycol 6000(PEG 6000) as the carrier. Evaluation of the properties of the dispersions was performed using dissolution studies, X-ray powder diffraction and Fourier-transform infrared (FT-IR) spectroscopy. Results The rate of dissolution of silymarin was considerably improved as compared with pure silymarin when formulated in solid dispersions with PEG 6000. The data of the X-ray diffraction showed some changes in the parameters of lattice spacing [d], peak position and relative intensities. FT-IR together with those from X-ray diffraction showed the absence of well-defined drug-polymer interactions. Conclusion The dissolution improvement of poorly soluble silymarin could be illuminated by the changes of the lattice parameters of PEG 6000 and the drug.
机译:目的制备和表征水飞蓟素的固体分散体,以改善其溶解性能。方法以聚乙二醇6000(PEG 6000)为载体,通过熔融法制备固体分散体。使用溶解度研究,X射线粉末衍射和傅立叶变换红外(FT-IR)光谱对分散体的性能进行评估。结果与纯水飞蓟素混合制成PEG 6000固体分散体后,水飞蓟素的溶解速率得到了显着提高。X射线衍射数据显示,晶格间距[d],峰位置和相对强度的参数有所变化。 。 FT-IR和X射线衍射结果表明,没有明确的药物-聚合物相互作用。结论改变PEG 6000和药物的晶格参数可以说明难溶性水飞蓟素的溶解性改善。

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