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[吡拉西坦与3-羟基苯甲酸药物共晶形成的光谱分析]

[Spectral Analysis about the Pharmaceutical Cocrystal Formation of Piracetam and 3-Hydroxybenzoic Acid].

作者信息

Zhang Hui-li, Xia Yi, Hong Zhi, Du Yong

出版信息

Guang Pu Xue Yu Guang Pu Fen Xi. 2015 Jul;35(7):1854-9.

Abstract

Pharmaceutical cocrystal can improve physical and chemical properties of active pharmaceutical ingredient (API), meanwhile this feature has shown great potential in improving the pharmaceutical's properties and characteristics. In this study, cocrystal formation between piracetam and 3-hydroxybenzoic acid (3HBA) using grinding method has been characterized by Fourier transform infrared (FTIR), Raman and terahertz (THz) spectroscopical techniques. The vibrational modes of different motions are obtained by the assignment of the peaks in the spectra of the starting materials and the cocrystal components. FTIR, Raman and THz spectroscopical results show that the vibrational modes of the cocrystal are different from those of the starting materials. In addition, the dynamic process of the above cocrystal formation is investigated in-depth with Raman and THz spec- tra. Piracetam-3HBA cocrystal is formed pretty fast in first several minutes, and then the formation rate becomes slow. After 35 minutes, such formation process has been completed. The results offer the theoretical benchmark and unique means for real-time monitoring pharmaceutical cocrystal formation and also the corresponding quantitative analysis in the pharmaceutical field.

摘要

药物共晶体可以改善活性药物成分(API)的物理和化学性质,同时这一特性在改善药物的性能和特点方面已显示出巨大潜力。在本研究中,采用研磨法制备了吡拉西坦与3-羟基苯甲酸(3HBA)的共晶体,并通过傅里叶变换红外(FTIR)、拉曼和太赫兹(THz)光谱技术对其进行了表征。通过对起始原料和共晶体成分光谱中的峰进行归属,获得了不同运动的振动模式。FTIR、拉曼和THz光谱结果表明,共晶体的振动模式与起始原料不同。此外,利用拉曼和THz光谱对上述共晶体形成的动态过程进行了深入研究。吡拉西坦-3HBA共晶体在最初几分钟内形成得相当快,然后形成速率变慢。35分钟后,该形成过程完成。这些结果为药物共晶体形成的实时监测以及药物领域相应的定量分析提供了理论基准和独特手段。

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