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作 者:Pefia Maria Angeles Escalera Begofia Torrado Guillermo Natalini Paola
机构地区:[1]Department of Biomedical Science, Facultad de Farmacia, Universidad de Alcal~, Alcal6 de Henares, Madrid, Spain [2]Planta Piloto de Ingenieria Quimica (Plapiqui-Uns-Conicet), Bahia Blanca, Argentina
出 处:《Journal of Pharmacy and Pharmacology》2016年第7期351-358,共8页药剂与药理学(英文版)
摘 要:Abstract: The objective was to obtain solid dispersion to improve the dissolution rate, solubility and oral absorption of MB (mebendazole), poor water-soluble drugs. The new formulation was characterized by DSC (differential scanning calorimetry), PXRD (powder X-ray diffraction), FT-1R (fourier transform infrared spectroscopy) and STEM (scanning transmission electron microscopy) methods. Solid dispersions of MB with polyvinylpyrrolidone K-30 (PVP K30) were prepared by solvent evaporation method. The solubility of MB (original powder) and that of the solid dispersions was measured at 25℃ in ethanol-water. The aqueous solubility of MB was favoured by the presence of the polymer in solvent mixtures. Combination of solid dispersions with co-solvents increased the water solubility of MB in a larger extent that each method separately. Solubility parameter (o) was used to relate to solubility profiles. MB and the solid dispersions show a solubility curve with a single peak at 51 = 30.78 MPav2. Solid state characterizations indicated that the solid dispersion exist an amorphous material entrapped in polymer matrix getting highest improvement in wettability and solubility.
关 键 词:MEBENDAZOLE PVP K30 SOLUBILITY solid dispersion solubility parameter.
分 类 号:TQ460.6[化学工程—制药化工] TS236.9[轻工技术与工程—粮食、油脂及植物蛋白工程]
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