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拉曼光谱和太赫兹光谱对吡拉西坦与3-羟基苯甲酸共晶形成过程的研究

Raman and terahertz spectroscopical investigation of cocrystal formation process of piracetam and 3-hydroxybenzoic acid.

作者信息

Du Yong, Zhang Huili, Xue Jiadan, Fang Hongxia, Zhang Qi, Xia Yi, Li Yafang, Hong Zhi

机构信息

Centre for THz Research, China Jiliang University, Hangzhou 310018, China.

Centre for THz Research, China Jiliang University, Hangzhou 310018, China.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2015 Mar 15;139:488-94. doi: 10.1016/j.saa.2014.11.109. Epub 2014 Dec 25.

Abstract

Cocrystallization can improve physical and chemical properties of active pharmaceutical ingredient, and this feature has great potential in pharmaceutical development. In this study, the cocrystal of piracetam and 3-hydroxybenzoic acid under grinding condition has been characterized by Raman and terahertz spectroscopical techniques. The major vibrational modes of individual starting components and cocrystal are obtained and assigned. Spectral results show that the vibrational modes of the cocrystal are different from those of the corresponding parent materials. The dynamic process of such pharmaceutical cocrystal formation has also been monitored directly with Raman and THz spectra. The formation rate is pretty fast in first several 20 min grinding time, and then it becomes slow. After ∼35 min, such process has been almost completed. These results offer us the unique means and benchmark for characterizing the cocrystal conformation from molecule-level and also provide us rich information about the reaction dynamic during cocrystal formation process in pharmaceutical fields.

摘要

共结晶可以改善活性药物成分的物理和化学性质,这一特性在药物开发中具有巨大潜力。在本研究中,采用拉曼光谱和太赫兹光谱技术对研磨条件下的吡拉西坦与3-羟基苯甲酸共晶体进行了表征。获得并归属了各个起始组分和共晶体的主要振动模式。光谱结果表明,共晶体的振动模式与相应母体材料的振动模式不同。还利用拉曼光谱和太赫兹光谱直接监测了这种药物共晶体形成的动态过程。在最初的20分钟研磨时间内,形成速率相当快,然后变慢。约35分钟后,该过程几乎完成。这些结果为我们从分子水平表征共晶体构象提供了独特的手段和基准,也为我们提供了关于药物领域共晶体形成过程中反应动力学的丰富信息。

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