Li Tong, Li Hui, Chen Jia, Yu Yongliang, Chen Shuai, Wang Jianhua, Qiu Hongdeng
CAS Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China; Department of Chemistry, Research Center for Analytical Sciences, College of Sciences, Northeastern University, Shenyang 110819, China.
CAS Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China.
J Chromatogr A. 2024 Jul 19;1727:465011. doi: 10.1016/j.chroma.2024.465011. Epub 2024 May 18.
Chiral enantiomers, especially the enantiomers of chiral drugs often exhibit different pharmacological activity, metabolism and toxicity, thus it is of great research significance to scientifically and reasonably develop single chiral drugs with low toxicity and high efficiency. Among them, high performance liquid chromatographic techniques based on chiral stationary phases (CSPs) has become one of the most attractive methods used to evaluate the enantiomeric purity of single-enantiomers compound of pharmacological relevance. In this work, pillar[5]arene functionalized with L- and D-histidine, respectively, were modified on the surface of mesoporous silica as novel chiral stationary phases called L/DHis-BP5-Sil. Notably, L/D-histidine had the characteristics of low steric hindrance and easy derivatization. Although the π-π interaction of imidazole group was weaker than that of benzene ring, the benzene ring bonding imidazole-conjugated ring in the structure produced better enantioseparation effect. The results showed that L/DHis-BP5-Sil can separate a variety of complex structural enantiomers with excellent reproducibility, thermal stability and separation performance. Hence, the unique advantage of the highly selective separation of L/DHis-BP5-Sil provides new insights into the enantioseparation field.
手性对映体,尤其是手性药物的对映体,往往表现出不同的药理活性、代谢特性和毒性,因此科学合理地开发低毒高效的单一手性药物具有重要的研究意义。其中,基于手性固定相(CSPs)的高效液相色谱技术已成为评估具有药理相关性的单一异构体化合物对映体纯度最具吸引力的方法之一。在这项工作中,分别用L-组氨酸和D-组氨酸功能化的柱[5]芳烃被修饰在介孔二氧化硅表面,作为新型手性固定相,称为L/DHis-BP5-Sil。值得注意的是,L/D-组氨酸具有空间位阻小、易于衍生化的特点。虽然咪唑基团的π-π相互作用比苯环弱,但结构中苯环连接咪唑共轭环产生了更好的对映体分离效果。结果表明,L/DHis-BP5-Sil能够分离多种结构复杂的对映体,具有出色的重现性、热稳定性和分离性能。因此,L/DHis-BP5-Sil高度选择性分离的独特优势为对映体分离领域提供了新的见解。