Fanali S, Rudaz S, Veuthey J L, Desiderio C
Istituto di Cromatografia, Consiglio Nazionale delle Ricerche, Area della Ricerca di Roma, Rome, Italy.
J Chromatogr A. 2001 Jun 1;919(1):195-203. doi: 10.1016/s0021-9673(01)00781-6.
A capillary electrochromatography method, using vancomycin chiral stationary phase packed capillary, was optimized for the simultaneous chiral separation of the antidepressant drug venlafaxine and its main active metabolite O-desmethylvenlafaxine. Simultaneous baseline enantiomeric separation of the two compounds was obtained using a mobile phase composed of 100 mM ammonium acetate buffer pH 6/water/acetonitrile (5:5:90, v/v). The electrokinetic injection for sample introduction provided a limit of quantitation for both the compounds of 0.05 microg/ml racemate concentration suitable for the analysis of venlafaxine and metabolite in biological samples. The acetonitrile mobile phase concentration was found to modulate the analytes elution times, the enantiomeric resolution and the efficiency of the separation. The column was tested for repeatability and linearity showing RSD values (%) in the range of 0.13-0.24, 2.47-3.66 and 1.35-2.50 for migration time, sample/internal standard peak area ratio and enantiomeric resolution, respectively and correlation coefficients higher than 0.9990. The method was applied to the analysis of clinical samples of patients under depression therapy showing a stereoselective metabolism for venlafaxine.
采用万古霉素手性固定相填充毛细管的毛细管电色谱法,针对抗抑郁药物文拉法辛及其主要活性代谢物O-去甲基文拉法辛的同时手性分离进行了优化。使用由100 mM pH 6的醋酸铵缓冲液/水/乙腈(5:5:90,v/v)组成的流动相,实现了两种化合物的同时基线对映体分离。用于样品引入的电动进样为两种化合物提供了0.05 μg/ml外消旋体浓度的定量限,适用于生物样品中文拉法辛和代谢物的分析。发现乙腈流动相浓度可调节分析物的洗脱时间、对映体分辨率和分离效率。对该色谱柱进行了重复性和线性测试,迁移时间、样品/内标峰面积比和对映体分辨率的RSD值(%)分别在0.13 - 0.24、2.47 - 3.66和1.35 - 2.50范围内,相关系数高于0.9990。该方法应用于抑郁症治疗患者临床样品的分析,结果表明文拉法辛存在立体选择性代谢。