Timonen J T, Pohjala E, Nikander H, Pakkanen T T
Department of Chemistry, University of Joensuu, Finland.
Pharm Res. 1998 Jan;15(1):110-5. doi: 10.1023/a:1011965107205.
31P CP/MAS NMR is used to characterize stability and changes in solid state properties of disodium clodronate tetrahydrate upon variable temperature and slow dehydration.
Variable temperature 31P CP/MAS NMR spectroscopy.
A fast rise in temperature leads to loss of lattice waters and produces an averaged structure characterized by a single 31P NMR resonance at 398 K. Slow room temperature dehydration converts the crystalline form to an anhydrous structure with two non-equivalent phosphorus atoms. The molecular skeleton of clodronate is stable within the temperature range 296 K-398 K of experiments. Rehydration of the anhydrous samples at room temperature restores the crystalline tetrahydrate form verified by a 31P CP/MAS NMR spectrum similar to that of a virginal sample.
Solid state NMR is a method which can offer both molecular and crystal scale information, when either bulk or dosage forms of a drug can be altered by temperature or by loss of lattice waters or solvents. The experiments are easy to perform, though time consuming, especially when low abundant nuclei are examined.
采用31P交叉极化/魔角旋转核磁共振(31P CP/MAS NMR)技术来表征氯膦酸二钠四水合物在变温和缓慢脱水过程中的稳定性及固态性质的变化。
变温31P CP/MAS NMR光谱法。
快速升温会导致晶格水的流失,并产生一种平均结构,其特征是在398 K时出现单一的31P NMR共振峰。室温下缓慢脱水会使晶体形式转变为具有两个不等价磷原子的无水结构。在296 K至398 K的实验温度范围内,氯膦酸的分子骨架是稳定的。室温下对无水样品进行再水化可恢复结晶四水合物形式,通过31P CP/MAS NMR光谱验证,该光谱与原始样品的光谱相似。
当药物的原料药或剂型可因温度、晶格水或溶剂的流失而改变时,固态核磁共振是一种能够提供分子和晶体尺度信息的方法。这些实验易于进行,尽管耗时,特别是在检测低丰度核时。