Department of Physical Chemistry, Chair of Chemistry, Faculty of Pharmacy with Medical Analytics Division, Medical University of Lublin, 4a Chodźki St., 20-093 Lublin, Poland.
Department of Physical Chemistry, Chair of Chemistry, Faculty of Pharmacy with Medical Analytics Division, Medical University of Lublin, 4a Chodźki St., 20-093 Lublin, Poland.
J Chromatogr A. 2018 Jul 13;1558:77-84. doi: 10.1016/j.chroma.2018.05.023. Epub 2018 May 16.
In our previous papers we have investigated the influence of the mobile phase composition on mechanism of retention, selectivity and efficiency of peptide separation in various high-performance thin-layer chromatography (HPTLC) systems with commercially available silica-based adsorbents. We have also investigated the influence of pH of the mobile phase buffer on migration and separation of peptides in pressurized planar electrochromatography (PPEC). Here we investigate the influence of concentration of ion-pairing additive, and concentration and type of organic modifier of the mobile phase on migration of peptides in PPEC system with octadecyl silica-based adsorbent, and with the same set of the solutes as before. We compare our current results with the results obtained before for similar HPTLC and PPEC systems, and discuss the influence of particular variables on retention, electrophoretic mobility of solutes and electroosmotic flow of the mobile phase. We show, that the final selectivity of peptide separation results from co-influence of all the three factors mentioned. Concentration of organic modifier of the mobile phase, as well as concentration of ion-pairing additive, affect the retention, the electrophoretic mobility, and the electroosmotic flow simultaneously. This makes independent optimization of these factors rather difficult. Anyway PPEC offers much faster separation of peptides with quite different selectivity, in comparison to HPTLC, with similar adsorbents and similar mobile phase composition. However, we also present and discuss the issue of extensive tailing of peptide zones in the PPEC in comparison to similar HPTLC systems.
在之前的论文中,我们研究了流动相组成对各种市售硅胶基吸附剂高效薄层色谱(HPTLC)系统中保留机制、选择性和效率的影响。我们还研究了流动相缓冲液 pH 值对加压平面电色谱(PPEC)中肽迁移和分离的影响。在这里,我们研究了离子对添加剂浓度、流动相有机改性剂浓度和类型对十八烷基硅胶基吸附剂 PPEC 系统中肽迁移的影响,并使用与之前相同的溶质集。我们将当前的结果与之前类似的 HPTLC 和 PPEC 系统的结果进行比较,并讨论了特定变量对保留、溶质电泳迁移率和流动相电渗流的影响。我们表明,肽分离的最终选择性来自于上述三个因素的共同影响。流动相的有机改性剂浓度以及离子对添加剂的浓度同时影响保留、电泳迁移率和电渗流。这使得这些因素的独立优化变得相当困难。无论如何,与具有相似吸附剂和相似流动相组成的 HPTLC 相比,PPEC 提供了更快的肽分离,具有相当不同的选择性。然而,我们还提出并讨论了与类似 HPTLC 系统相比,PPEC 中肽区广泛拖尾的问题。