Karenga Samuel, El Rassi Ziad
Department of Chemistry, Oklahoma State University, OK 74075, USA.
J Sep Sci. 2008 Aug;31(14):2677-85. doi: 10.1002/jssc.200800310.
A neutral octadecyl monolithic (ODM) column for RP capillary electrochromatography (RP-CEC) has been developed. The ODM column was prepared by the in situ polymerization of octadecyl acrylate (ODA) as the monomer and trimethylolpropanetrimethacrylate (TRIM) as the crosslinker, in a ternary porogenic solvent containing cyclohexanol, ethylene glycol, and water. The ODM column exhibited cathodal EOF over a wide range of pH and ACN concentration in the mobile phase despite the fact that it was devoid of any fixed charges. It is believed that the EOF is due to the adsorption of ions from the mobile phase onto the surface of the monolith thus imparting to the neutral ODM column the zeta potential necessary to support the EOF required for mass transport across the monolithic column. Furthermore, the adsorption of mobile phase ions to the neutral monolith modulated solute retention and affected the separation selectivity. The wide applications of the neutral ODM column were demonstrated by its ability to separate a wide range of small and large solutes, both neutral and charged. While the separation of the neutral solutes was based on RP retention mechanism, the charged solutes were separated on the basis of their electrophoretic mobility and hydrophobic interaction with the C18 ligands of the stationary phase. As a typical result, the neutral monolithic column was able to separate peptides quite rapidly with a separation efficiency of nearly 200,000 plates/m, and this efficiency was exploited in tryptic peptide mapping of standard proteins, e. g., lysozyme and cytochrome C, by isocratic elution.
已开发出一种用于反相毛细管电色谱(RP - CEC)的中性十八烷基整体柱(ODM柱)。该ODM柱是通过将丙烯酸十八酯(ODA)作为单体和三羟甲基丙烷三甲基丙烯酸酯(TRIM)作为交联剂,在含有环己醇、乙二醇和水的三元致孔溶剂中原位聚合制备而成。尽管该ODM柱没有任何固定电荷,但在流动相的广泛pH和乙腈浓度范围内均表现出阴极电渗流(EOF)。据信,EOF是由于流动相中的离子吸附到整体柱表面,从而赋予中性ODM柱支持整体柱内质量传输所需EOF的zeta电位。此外,流动相离子在中性整体柱上的吸附调节了溶质保留并影响了分离选择性。中性ODM柱能够分离各种大小的中性和带电溶质,这证明了其广泛的应用。中性溶质的分离基于反相保留机制,而带电溶质则根据其电泳迁移率以及与固定相C18配体的疏水相互作用进行分离。作为一个典型结果,中性整体柱能够以近200,000板/米的分离效率快速分离肽段,并且这种效率被用于标准蛋白质(如溶菌酶和细胞色素C)的胰蛋白酶肽图分析,采用等度洗脱。