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Preparation and evaluation of amorphous cefdinir solid dispersions

机译:非晶形头孢地尼固体分散体的制备与评价

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Amorphous solid dispersion of cefdinir was developedto improve its solubility and stability. Super-saturationscreening study of binary solid dispersions was performedto find proper additives of enhancing the solubility.Among the chosen additives, stability study wasperformed in solution and solid state, and the ratio of drugand additives were optimized by further study. Ternarysolid dispersions were prepared by mixing vitamin ETPGSand d-mannitol which had stabilizing effect ofamorphous form in binary solid dispersions. Ternary soliddispersion maintained its amorphous form for 75 days ofstability study at 40°C, 75% and its solubility wasimproved. Therefore, this solid dispersion formulationmight be the alternative promising candidate for cefdinir.
机译:开发了头孢地尼的非晶态固体分散体 以提高其溶解度和稳定性。超饱和 进行了二元固体分散体的筛选研究 寻找合适的添加剂以增加溶解度。 在所选的添加剂中,稳定性研究为 以溶液和固体状态进行,药物的比例 并通过进一步研究对添加剂进行了优化。三元 通过混合维生素ETPGS制备固体分散体 和d-甘露醇具有稳定作用 二元固体分散体的无定形形式。三元固体 分散液在75天内保持其无定形形式 在40°C,75%时的稳定性研究及其溶解度为 改善。因此,这种固体分散体配方 可能是头孢地尼的有前途的候选药物。

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