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Solubilization and Solid-State Characterization of Modafinil Solid Dispersions using PVP K 30

机译:使用PVP K 30的莫达非尼固体分散体的增溶和固态表征

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The objective of the present study was to improve the dissolution rate of Modafinil by solid dispersion (SD) systems in PVP-K 30. Drug contents were determined by UV Spectrophotometry at λmax of 259.5 nm. The phase solubility behavior of Modafinil in presence of various concentrations of carriers in distilled water was obtained at 37±2°C. The dissolution of Modafinil increased with increasing amount of carriers. Gibbs free energy (G°tr) values were all negative, indicating the spontaneous nature of Modafinil solubilization. The SDs of Modafinil with the carrier was prepared at 1:1, 1:3 and 1:5 (Modafinil: carrier) ratio by lyophilization method. The FTIR spectroscopic studies and Differential Scanning Calorimetry (DSC) showed the stability of Modafinil and absence of well-defined drug polymer interaction. The dissolution rate increases with increasing the ratio of PVP-K 30.
机译:本研究的目的是通过在PVP-K 30中的固体分散(SD)系统提高莫达非尼的溶出度。通过紫外分光光度法在λmax为259.5 nm的条件下测定药物含量。在37±2°C下获得了莫达非尼在蒸馏水中各种浓度的载体存在下的相溶解行为。莫达非尼的溶出度随载体量的增加而增加。吉布斯自由能(G°tr)值均为负,表明莫达非尼的增溶是自发的。通过冻干法以1:1、1:3和1:5(莫达非尼:载体)的比例制备莫达非尼与载体的SD。 FTIR光谱研究和差示扫描量热法(DSC)显示莫达非尼的稳定性,并且没有明确定义的药物聚合物相互作用。溶出度随PVP-K 30比例的增加而增加。

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