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机构地区:[1]武汉大学分析测试科学系
出 处:《色谱》1998年第5期424-426,共3页Chinese Journal of Chromatography
摘 要:将β-环糊精、2,6-二甲基-β-环糊精、2,3,6-三甲基-β-环糊精分别作为手性流动相添加剂,较系统地研究了D,L-肾上腺素、D,L-异丙肾上腺素、D,L-麻黄碱在反相HPLC系统中的拆分,建立了甲基化β-环糊精动态手性固定相法分离肾上腺素类药物对映体的方法。The enantiomeric resolution of epinephrine, isoproterenol, ephedrine was studied by reversed phase HPLC. β CD, DM β CD,TM β CD were used as chiral mobile phase additives. The effects of the concentration of DM β CD and the concentration of methanol on resolution of D,L epinephrine were investigated. The results showed: D,L epinephrine and D,L isoproterenol can be separated by β CD, DM β CD, TM β CD, but D,L ephedrine cant. Hydrogen bonding plays an important role in the chiral recognition mechanism. In the separation of isoproterenol, the enantioselectivity of TM β CD was better than those of β CD and DM β CD. As the concentration of DM β CD changed from 0 04mmol/L to 1 00mmol/L, the resolution varied slightly. The experiment of the effect of methanol concentration on R s showed: when the ratio of methanol/water was 40/60, the R s reached the maximum. The coefficients of variation of retention time of D epinephrine and L epinephrine were 1 3% and 1 4% respectively. It is demonstrated that the chromatographic systems with a dynamically generated stationary phase with methylated β cyclodextrin are versatile tools for enantiomer separation. This technique leads to column with excellent time stability and good reproducibility of the enantio selectivity.
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