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Retention Mechanisms for Basic Drugs in the Submicellar and Micellar Reversed-Phase Liquid Chromatographic Modes

机译:亚胶束和胶束反相液相色谱模式下基本药物的保留机制

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摘要

The reversed-phase liquid chromatographic (RPLC) behavior (retention, elution strength, selectivity, efficiency, and peak asymmetry) for a group of basic drugs (beta-blockers), with mobile phases containing the anionic surfactant sodium dodecyl sulfate (SDS) and acetonitrile, revealed different separation environments, depending on the concentrations of both modifiers: hydro-organic, submicellar at low surfactant concentration and high concentration of organic solvent, micellar, and submicellar at high concentration of both surfactant and organic solvent. In the surfactant-mediated modes, the anionic surfactant layer adsorbed on the stationary phase interacts strongly with the positively charged basic drugs increasing the retention and masks the silanol groups that are the origin of the poor efficiencies and tailing peaks in hydro-organic RPLC with conventional columns. Also, the strong attraction between the cationic solutes and anionic SDS micelles or monomers in the mobile phase enhances the solubility and allows a direct transfer mechanism of the cationic solutes from micelles to the modified stationary phase, which has been extensively described for highly hydrophobic solutes.
机译:一组碱性药物(β受体阻滞剂)的反相液相色谱(RPLC)行为(保留,洗脱强度,选择性,效率和峰不对称性),流动相包含阴离子表面活性剂十二烷基硫酸钠(SDS)和乙腈显示出不同的分离环境,具体取决于两种改性剂的浓度:有机溶剂,低表面活性剂浓度和高浓度有机溶剂的胶束,胶束和高浓度表面活性剂和有机溶剂的胶束。在表面活性剂介导的模式下,吸附在固定相上的阴离子表面活性剂层与带正电荷的碱性药物发生强烈相互作用,从而增加了保留率并掩盖了硅烷醇基团,而后者是常规有机氢RPLC效率低下和拖尾峰的起因列。同样,在流动相中阳离子溶质和阴离子SDS胶束或单体之间的强吸引力增强了溶解性,并允许阳离子溶质从胶束直接转移到改性固定相,这已被广泛描述为高度疏水性溶质。

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