Candioti Luciana Vera, Robles Juan C, Mantovani Víctor E, Goicoechea Héctor C
Laboratorio de Control de Calidad de Medicamentos, Cátedra de Química Analítica I, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, Ciudad Universitaria, Santa Fe, Argentina.
Talanta. 2006 Mar 15;69(1):140-7. doi: 10.1016/j.talanta.2005.09.021. Epub 2005 Oct 19.
Multiple response simultaneous optimization by using the desirability function was used for the development of a capillary electrophoresis method for the simultaneous determination of four active ingredients in pharmaceutical preparations: vitamins B(6) and B(12), dexamethasone and lidocaine hydrochloride. Five responses were simultaneously optimized: the three resolutions, the analysis time and the capillary current. This latter response was taken into account in order to improve the quality of the separations. The separation was carried out by using capillary zone electrophoresis (CZE) with a silica capillary and UV detection (240 nm). The optimum conditions were: 57.0 mmol l(-1) sodium phosphate buffer solution, pH 7.0 and voltage=17.2 kV. Good results concerning precision (CV lower than 2%), accuracy (recoveries ranged between 98.5 and 102.6%) and selectivity were obtained in the concentration range studied for the four compounds. These results are comparable to those provided by the reference high performance liquid chromatography (HPLC) technique.
采用期望函数法进行多响应同时优化,以开发一种毛细管电泳方法,用于同时测定药物制剂中的四种活性成分:维生素B6和B12、地塞米松和盐酸利多卡因。同时对五个响应进行了优化:三种分离度、分析时间和毛细管电流。考虑到后一个响应,以提高分离质量。采用硅胶毛细管和紫外检测(240nm)的毛细管区带电泳(CZE)进行分离。最佳条件为:57.0 mmol l(-1) 磷酸钠缓冲溶液,pH 7.0,电压 = 17.2 kV。在所研究的四种化合物浓度范围内,获得了关于精密度(变异系数低于2%)、准确度(回收率在98.5%至102.6%之间)和选择性的良好结果。这些结果与参考高效液相色谱(HPLC)技术提供的结果相当。