Sample stacking in CZE using dynamic thermal junctions I. Analytes with low dp K a / d T crossing a single thermally induced pH junction in a BGE with high dpH/d T

• Published in: Electrophoresis Vol. 30; no. 9; pp. 1501 - 1509
• Main Authors: Mandaji, Marcos, Rübensam, Gabriel, Hoff, Rodrigo Barcellos, Hillebrand, Sandro, Carrilho, Emanuel, Kist, Tarso Ledur
• Format: Journal Article
• Language: English
• Published: 01.05.2009
• ISSN: 0173-0835; 1522-2683
• DOI: 10.1002/elps.200800584

Abstract The possibility to compress analyte bands at the beginning of CE runs has many advantages. Analytes at low concentration can be analyzed with high signal‐to‐noise ratios by using the so‐called sample stacking methods. Moreover, sample injections with very narrow initial band widths (small initial standard deviations) are sometimes useful, especially if high resolutions among the bands are required in the shortest run time. In the present work, a method of sample stacking is proposed and demonstrated. It is based on BGEs with high thermal sensitive pHs (high dpH/d T ) and analytes with low dp K a / d T . High thermal sensitivity means that the working p K a of the BGE has a high dp K a / d T in modulus. For instance, Tris and Ethanolamine have dpH/d T =−0.028/°C and −0.029/°C, respectively, whereas carboxylic acids have low dp K a / d T values, i.e . in the −0.002/°C to+0.002/°C range. The action of cooling and heating sections along the capillary during the runs affects also the local viscosity, conductivity, and electric field strength. The effect of these variables on electrophoretic velocity and band compression is theoretically calculated using a simple model. Finally, this stacking method was demonstrated for amino acids derivatized with naphthalene‐2,3‐dicarboxaldehyde and fluorescamine using a temperature difference of 70°C between two neighbor sections and Tris as separation buffer. In this case, the BGE has a high pH thermal coefficient whereas the carboxylic groups of the analytes have low p K a thermal coefficients. The application of these dynamic thermal gradients increased peak height by a factor of two (and decreased the standard deviations of peaks by a factor of two) of aspartic acid and glutamic acid derivatized with naphthalene‐2,3‐dicarboxaldehyde and serine derivatized with fluorescamine. The effect of thermal compression of bands was not observed when runs were accomplished using phosphate buffer at pH 7 (negative control). Phosphate has a low dpH / d T in this pH range, similar to the d K a /d T of analytes. It is shown that ∣d K a /d T −dpH/d T ∣≫0 is one determinant factor to have significant stacking produced by dynamic thermal junctions.