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首页> 外文期刊>Pharmaceutical development and technology >Solid-state compatibility screening of excipients suitable for development of indapamide sustained release solid-dosage formulation.
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Solid-state compatibility screening of excipients suitable for development of indapamide sustained release solid-dosage formulation.

机译:适合开发吲达帕胺缓释固体制剂的辅料的固态相容性筛选。

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摘要

Differential scanning calorimetry and Fourier transform infrared spectroscopy were applied as screening analytical methods to assess the solid-state compatibility of indapamide (4-chloro-N-(2-methyl-2,3-dihydroindol-1-yl)-3-sulfamoyl-benzamide) with several polymers aimed for development of 24?h sustained release solid-dosage formulation. After the initial research phase which was directed towards selection of suitable polymer matrices, based on their solid-state compatibility with the studied pharmaceutical active ingredient, the second phase of evaluation was intended for compatibility selection of other excipients required to complete a sustained release formulation. The preformulation studies have shown that polyvinylpyrrolydone/polyvinyl acetate might be considered incompatible with indapamide, and the implementation of this polymer career should be avoided in the case of the entitled development. The experimental data additionally have revealed that sorbitol is incompatible with indapamide. The obtained results afforded deeper insight in to the solid-state stability of the studied binary systems and pointed out directions for further development of indapamide sustained release solid-dosage formulation.
机译:差示扫描量热法和傅里叶变换红外光谱法用作筛选分析方法,以评估吲达帕胺(4-氯-N-(2-甲基-2,3-二氢吲哚-1-基)-3-氨磺酰基-苯甲酰胺)和几种旨在开发24小时持续释放固体制剂的聚合物。在最初的研究阶段旨在选择合适的聚合物基质之后,根据它们与所研究的药物活性成分的固态相容性,第二阶段的评估旨在选择完成持续释放制剂所需的其他赋形剂的相容性。配制前的研究表明,聚乙烯吡咯烷酮/聚乙酸乙烯酯可能被认为与吲达帕胺不相容,并且在有标题的开发情况下,应避免实施该聚合物事业。实验数据还表明山梨糖醇与吲达帕胺不相容。获得的结果为所研究的二元系统的固态稳定性提供了更深入的了解,并指出了吲达帕胺缓释固体制剂的进一步开发方向。

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