Lin Ching-Erh, Fang I-Ju, Deng Yan-, Liao Wei-Ssu, Cheng Hsu-Tun, Huang Wen-Ping
Department of Chemistry, National Taiwan University, Taipei 10674, Taiwan.
J Chromatogr A. 2004 Oct 8;1051(1-2):85-94.
The migration behavior of cationic solutes and influences of the interactions of cationic solutes with sodium dodecyl sulfate (SDS) on the formation of micelles and its critical micelle concentration (CMC) were investigated by capillary electrophoresis at neutral pH. Catecholamines and structurally related compounds, including epinephrine, norepinephrine, dopamine, norephedrine, and tyramine, which involve different extents of hydrophobic, ionic and hydrogen-bonding interactions with SDS surfactant, are selected as cationic solutes. The dependence of the effective electrophoretic mobility of cationic solutes on the concentration of surfactant monomers in the premicellar region provides direct evidence of the formation of ion-pairs between cationic solutes and anionic dodecyl sulfate monomers. Three different approaches, based on the variations of either the effective electrophoretic mobility or the retention factor as a function of surfactant concentration in the premicellar and micellar regions, and the linear relationship between the retention factor and the product of a distribution coefficient and the phase ratio, were considered to determine the CMC value of SDS micelles. The suitability of the methods used for the determination of the CMC of SDS with these cationic solutes was discussed. Depending on the structures of cationic solutes and electrophoretic conditions, the CMC value of SDS determined varies in a wide concentration range. The results indicate that, in addition to hydrophobic interaction, both ionic and hydrogen-bonding interactions have pronounced effects on the formation of SDS micelles. Ionic interaction between cationic solutes and SDS surfactant stabilizes the SDS micelles, whereas hydrogen-bonding interactions weakens the solubilization of the attractive ionic interaction. The elevation of the CMC of SDS depends heavily on hydrogen-bonding interactions between cationic solutes and SDS surfactant. Thus, the CMC value of SDS is remarkably elevated with catecholamines, such as epinephrine and norepinephrine, as compared with norephedrine. In addition, the effect of methanol content in the sample solution of these cationic solutes on the CMC of SDS was also examined.
在中性pH条件下,采用毛细管电泳法研究了阳离子溶质的迁移行为以及阳离子溶质与十二烷基硫酸钠(SDS)的相互作用对胶束形成及其临界胶束浓度(CMC)的影响。选择儿茶酚胺及其结构相关化合物,包括肾上腺素、去甲肾上腺素、多巴胺、去氧麻黄碱和酪胺,作为阳离子溶质,它们与SDS表面活性剂存在不同程度的疏水、离子和氢键相互作用。阳离子溶质在胶束前区域的有效电泳迁移率对表面活性剂单体浓度的依赖性,为阳离子溶质与阴离子十二烷基硫酸酯单体之间形成离子对提供了直接证据。基于有效电泳迁移率或保留因子随胶束前和胶束区域表面活性剂浓度的变化,以及保留因子与分配系数和相比乘积之间的线性关系,考虑了三种不同的方法来测定SDS胶束的CMC值。讨论了用于测定SDS与这些阳离子溶质的CMC的方法的适用性。根据阳离子溶质的结构和电泳条件,所测定的SDS的CMC值在很宽的浓度范围内变化。结果表明,除疏水相互作用外,离子和氢键相互作用对SDS胶束的形成也有显著影响。阳离子溶质与SDS表面活性剂之间的离子相互作用使SDS胶束稳定,而氢键相互作用则削弱了有吸引力的离子相互作用的增溶作用。SDS的CMC升高在很大程度上取决于阳离子溶质与SDS表面活性剂之间的氢键相互作用。因此,与去氧麻黄碱相比,肾上腺素和去甲肾上腺素等儿茶酚胺可使SDS的CMC值显著升高。此外,还研究了这些阳离子溶质样品溶液中甲醇含量对SDS的CMC的影响。