Kang Xu-Sheng, Hou Di-Bo, Zhang Guang-Xin, Chen Xi-Ai, Yue Fei-Heng, Huang Ping-Jie, Zhou Ze-Kui
Department of Control Science and Engineering, Zhejiang University, Hangzhou 310027, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2012 Jul;32(7):1744-7.
The present article measured the absorption coefficient spectra and refractive index spectra of nitrofurantoin original drug, which is one kind of nitrofuran drugs, in the terahertz frequency range from 0.2 to 1.8 THz using terahertz time-domain spectroscopy. The results showed that there exist a number of characteristic absorption peaks of nitrofurantoin with different intensity in the range and the absorption coefficient spectra can be used to identify nitrofurantoin. The article also simulated absorption coefficient spectra of nitrofurantoin molecule within 0.2 - 1.8 THz using density functional theory by Gaussian software, and vibrational modes of some peaks in the experimental absorption coefficient spectra were analyzed and identified. The results show that the experimental absorption peaks at 1.25 and 1.60 THz correspond with the theoretical peaks at 1.30 and 1.67 THz, and these experimental peaks were caused by intramolecular vibrational modes of nitrofurantoin.
本文利用太赫兹时域光谱技术,在0.2至1.8太赫兹的太赫兹频率范围内测量了硝基呋喃妥因原药(一种硝基呋喃类药物)的吸收系数光谱和折射率光谱。结果表明,在此范围内存在多个不同强度的硝基呋喃妥因特征吸收峰,且吸收系数光谱可用于鉴别硝基呋喃妥因。本文还使用高斯软件通过密度泛函理论模拟了0.2 - 1.8太赫兹范围内硝基呋喃妥因分子的吸收系数光谱,并对实验吸收系数光谱中部分峰的振动模式进行了分析和识别。结果表明,1.25和1.60太赫兹处的实验吸收峰与1.30和1.67太赫兹处的理论峰相对应,这些实验峰是由硝基呋喃妥因的分子内振动模式引起的。