首页> 外文期刊>Journal of Drug Delivery and Therapeutics >PREPARATION AND CHARACTERIZATION OF SOLID DISPERSION OF MODAFINIL USING PEG6000 AS HYDROPHILIC CARRIER FOR IMPROVEMENT OF DISSOLUTION PROFILE
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PREPARATION AND CHARACTERIZATION OF SOLID DISPERSION OF MODAFINIL USING PEG6000 AS HYDROPHILIC CARRIER FOR IMPROVEMENT OF DISSOLUTION PROFILE

机译:以聚乙二醇为亲水载体的PEG6000制备和表征莫达非尼的固体分散体,以改善溶出度

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Solid dispersions of modafinil were prepared using polyethyleneglycols, in various proportions by melting, solvent evaporation and kneading method. Based on the solubility, PEG6000 was selected and solid dispersion batch F6 containing drug:PEG6000 in 1:3 ration was formulated as tablet (batch TF6) and evaluated for in-vitro drug dissolution and six month stability; and the results were compared with that of tablet containing physical mixture of drug:PEG6000 in 1:3 ratio (batch TF24) and convention tablet (batch CT) containing pure drug. Tablet batch TF24 had shown significant improvement of dissolution profile of modafinil when compared with that of tablet batch TF6 and CT. Present study conclusively demonstrated that PEG6000 enhanced water solubility of modafinil by amorphisation, which was confirmed XRD and DSC; and also the melting method was found better than solvent evaporation.
机译:使用聚乙二醇通过熔融,溶剂蒸发和捏合方法以各种比例制备莫达非尼的固体分散体。根据溶解度,选择PEG6000,将含有药物:PEG6000的1:3比例的固体分散批次F6配制成片剂(批次TF6),并评估其在体外的药物溶出度和六个月的稳定性。并将结果与​​含有药物:PEG6000的物理混合物(比例为TF24)和常规片剂(成分为纯药物)的片剂(1:3)进行比较。与片剂批次TF6和CT相比,片剂批次TF24已显示莫达非尼的溶出度显着改善。本研究最终证明,PEG6000通过非晶化增强了莫达非尼的水溶性,这已通过XRD和DSC证实。并且发现熔融方法比溶剂蒸发更好。

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