Novak Predrag, Tepes Predrag, Fistrić Ines, Bratos Igor, Gabelica Vesna
Department of Analytical Chemistry, Faculty of Natural Sciences, University of Zagreb, Horvatovac 102a, HR-10000 Zagreb, Croatia.
J Pharm Biomed Anal. 2006 Mar 18;40(5):1268-72. doi: 10.1016/j.jpba.2005.09.002. Epub 2005 Oct 25.
This work has demonstrated the usefulness of combining liquid chromatography-nuclear magnetic resonance spectroscopy (LC-NMR) and liquid chromatography-mass spectrometry (LC-MS) methodologies for a rapid identification of an unknown impurity (N1) in the drug 5-aminosalycilic acid. Complementary information obtained from the two methods has revealed plenty of structural information and led to the fast on-line structure determination of N1 prior to its isolation and purification. The analysis of LC-NMR and LC-MS spectra revealed that N1 and 5-aminosalycilic acid are structurally closely related compounds. The structure of N1 was later confirmed by high-resolution NMR spectroscopy of the isolated compound and the atom assignment was made. The approach described here has potential for 5-aminosalycilic acid impurity profiling and monitoring the production process.
这项工作证明了将液相色谱 - 核磁共振光谱法(LC - NMR)和液相色谱 - 质谱法(LC - MS)相结合用于快速鉴定药物5 - 氨基水杨酸中未知杂质(N1)的有效性。从这两种方法获得的互补信息揭示了大量结构信息,并在N1分离纯化之前实现了其快速在线结构测定。LC - NMR和LC - MS光谱分析表明,N1与5 - 氨基水杨酸是结构密切相关的化合物。N1的结构后来通过分离化合物的高分辨率核磁共振光谱得到证实,并完成了原子归属。本文所述方法在5 - 氨基水杨酸杂质分析和生产过程监测方面具有潜力。