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Bio-Dis and the Paddle Dissolution Apparatuses Applied to the Release Characterization of Ketoprofen from Hypromellose Matrices

机译:Bio-Dis和桨式溶出装置应用于羟丙甲纤维素基质中酮洛芬的释放特性

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摘要

The purposes of this work were: (1) to comparatively evaluate the effects of hypromellose viscosity grade and content on ketoprofen release from matrix tablets, using Bio-Dis and the paddle apparatuses, (2) to investigate the influence of the pH of the dissolution medium on drug release. Furthermore, since direct compression had not shown to be appropriate to obtain the matrices under study, it was also an objective (3) to evaluate the impact of granulation on drug release process. Six formulations of ketoprofen matrix tablets were obtained by compression, with or without previous granulation, varying the content and viscosity grade of hypromellose. Dissolution tests were carried out at a fixed pH, in each experiment, with the paddle method (pH 4.5, 6.0, 6.8, or 7.2), while a pH gradient was used in Bio-Dis (pH 1.2 to 7.2). The higher the hypromellose viscosity grade and content were, the lower the amount of ketoprofen released was in both apparatuses, the content effect being more expressive. Drug dissolution enhanced with the increase of the pH of the medium due to its pH-dependent solubility. Granulation caused an increase in drug dissolution and modified the mechanism of the release process.
机译:这项工作的目的是:(1)使用Bio-Dis和桨式装置比较评估羟丙甲纤维素粘度等级和含量对酮洛芬从基质片剂释放的影响,(2)研究溶出pH的影响介质释放药物。此外,由于未显示直接压缩适合获得所研究的基质,因此评估制粒对药物释放过程的影响也是目标(3)。通过压制获得六种酮洛芬基质片剂,无论是否进行制粒,均需改变羟丙甲纤维素的含量和粘度等级。在每个实验中,均采用桨法(pH 4.5、6.0、6.8或7.2)在固定的pH值下进行溶出度测试,而Bio-Dis使用pH梯度(pH 1.2至7.2)。羟丙甲纤维素粘度等级和含量越高,在两种设备中酮洛芬的释放量越低,含量效应更具表现力。由于其pH依赖性溶解度,药物的溶解度随介质pH值的增加而增强。制粒导致药物溶解增加,并改变了释放过程的机制。

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