Wiedmer S K, Jumppanen J H, Haario H, Riekkola M L
Department of Chemistry, University of Helsinki, Finland.
Electrophoresis. 1996 Dec;17(12):1931-7. doi: 10.1002/elps.1150171221.
Selectivity and resolution were studied for the separation of seven corticosteroids by micellar electrokinetic capillary chromatography (MEKC) using a mixed micellar solution of sodium dodecyl sulfate (SDS) and sodium cholate (SC), buffered with 3-(N-morpholino)propanesulfonic acid (MOPS) or 3-[(1,1-dimethyl-2-hydroxyethyl)amino]-2-hydroxypropane sulfonic acid (AMPSO). The changes in selectivity were compared for the AMPSO-SDS-SC system by varying the pH and the concentrations of AMPSO, SDS and SC. The experimental design started with the central composite design and continued in a sequential manner. The optimum selectivity for the separation of the corticosteroids was calculated from the analyte migration times and the analyte velocities, by using empirical quadratic regression models. Satisfactory regression fits and coefficients of determination for prediction were obtained with cross-validated models. To optimize the resolution, the physical parameters of capillary length and analysis time were varied under the conditions optimal for the selectivity. In both the selectivity and the resolution, optimization the overall optimum was determined by using the desirability function technique. Analysis times were controlled by using 1,3-diaminopropane to influence the electroosmotic flow velocity (veo). The voltage was kept constant, which resulted in higher electric field strength in shorter capillaries. No changes in the selectivity were observed when 1,3-diaminopropane was used to control the electroosmotic flow velocity. Such an optimization technique, where the chemical and physical factors affecting the separation are treated independently, seemed to be effective for finding the best possible resolution for the corticosteroids.
采用十二烷基硫酸钠(SDS)和胆酸钠(SC)的混合胶束溶液,以3-(N-吗啉代)丙烷磺酸(MOPS)或3-[(1,1-二甲基-2-羟乙基)氨基]-2-羟丙烷磺酸(AMPSO)为缓冲剂,通过胶束电动毛细管色谱法(MEKC)研究了七种皮质类固醇的分离选择性和分离度。通过改变pH值以及AMPSO、SDS和SC的浓度,比较了AMPSO-SDS-SC体系中选择性的变化。实验设计从中心复合设计开始,并以连续的方式进行。通过使用经验二次回归模型,根据分析物迁移时间和分析物速度计算出皮质类固醇分离的最佳选择性。交叉验证模型获得了令人满意的回归拟合和预测决定系数。为了优化分离度,在选择性最佳的条件下改变毛细管长度和分析时间等物理参数。在选择性和分离度方面,通过使用合意函数技术确定总体最佳值。使用1,3-二氨基丙烷控制电渗流速度(veo)来控制分析时间。电压保持恒定,这导致较短毛细管中的电场强度更高。当使用1,3-二氨基丙烷控制电渗流速度时,未观察到选择性变化。这种将影响分离的化学和物理因素独立处理的优化技术,似乎对于找到皮质类固醇的最佳分离度是有效的。