摘要
用分步法制备全苯异氰酸酯基-β-环糊精键合硅胶手性固定相.在高效液相色谱仪上,对氟西汀对映体进行拆分,并探讨流动相组成及配比、离子强度、pH值、流速和柱温等影响分离的因素.结果表明,在自制手性固定相上,外消旋氟西汀得以拆分;最优的流动相为甲醇-0.2%醋酸三乙胺缓冲液(体积比35∶65,pH 4.0),当流速为1.0 mL/min和柱温为35℃时可达到基线分离.
The perphenylcarbamoylated-β-cyclodextrin bonded silica gel chiral stationary phase (CSP) is prepared step by step. Then, fluoxetine enantiomers are separated by HPLC. The effects of mobile phase composition, ionic strength, pH, flow rate and column temperature on separation are studied systematically. By this CSP, fluoxetine enantiomers can be separated. The optimal mobile phase composition is methanol --0.2% TEAA (pH 4.0), and baseline resolution can be achieved under flow rate of 1.0 mL/min and at 35 ℃.
出处
《郑州大学学报(理学版)》
CAS
2008年第3期121-124,共4页
Journal of Zhengzhou University:Natural Science Edition
基金
教育部高等学校博士学科点专项科研基金资助项目
编号20040335045