Dang Q X, Sun Z P, Ling D K
Shaanxi Institute for Drug Control, Xian, China.
J Chromatogr. 1992 Jun 19;603(1-2):259-66. doi: 10.1016/0021-9673(92)85369-5.
The separation and determination of seven sulphonamides and trimethoprim by micellar electrokinetic capillary chromatography were successfully achieved, employing sodium dodecyl sulphate (SDS) as a micellar phase and tetrabutylammonium bromide as additive. The effects of surfactant and modifier concentrations, pH and applied voltage on the retention behaviour of the solutes and the column efficiency were studied. The migration time of sulponamides increase with increasing SDS concentration and decreasing the applied voltage, but varies only slightly with pH. There is an optimum applied voltage at which a higher theoretical plate number is achieved, in contrast to the sulphonamides, the retention behaviour of trimethoprim gave a more obvious response to changes in the experimental conditions. The determination of three active ingredients in tablets was performed using sulphathiazole as an internal standard with good results. The theoretical plate number ranged between 2.0 x 10(5) and 2.8 x 10(5) with a 50-cm capillary.
以十二烷基硫酸钠(SDS)为胶束相,溴化四丁铵为添加剂,采用胶束电动毛细管色谱法成功实现了七种磺胺类药物和甲氧苄啶的分离与测定。研究了表面活性剂和改性剂浓度、pH值和施加电压对溶质保留行为和柱效的影响。磺胺类药物的迁移时间随SDS浓度的增加和施加电压的降低而增加,但随pH值变化较小。存在一个最佳施加电压,在此电压下可获得更高的理论塔板数。与磺胺类药物不同,甲氧苄啶的保留行为对实验条件的变化有更明显的响应。以磺胺噻唑为内标物对片剂中的三种活性成分进行了测定,结果良好。使用50 cm长的毛细管时,理论塔板数在2.0×10⁵至2.8×10⁵之间。