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Updated: Jun 1, 2026

On-chip Isotachophoresis for Separation of Ions and Purification of Nucleic Acids
Published on: March 2, 2012
Suppression of electroosmotic flow and prevention of wall adsorption in capillary zone electrophoresis using
1Department of Chemistry, The University of Calgary, 2500 University Drive NW, Calgary, Alberta, Canada T2N 1N4.
Abstract:
Addition of zwitterionic surfactants such as dodecyldimethyl(3-sulfopropyl)ammonium hydroxide, hexadecyldimethyl(3-sulfopropyl)ammonium hydroxide, and coco (amidopropyl)hydroxyldimethylsulfobetaine (Rewoteric AM CAS U) to an electrophoretic buffer suppress the electroosmotic flow by 50-90%. Onset of suppression occurs at approximately the critical micelle concentration of the surfactant. CAS U effectively suppresses the electroosmotic flow over the pH range 3-12. Addition of 2 mM CAS U to the electrophoretic buffer prevents adsorption of cationic proteins lysozyme, α-chymotrypsinogen A, cytochrome c, and ribonuclease A. Migration time reproducibility for these proteins is ∼1% RSD within 1 day and 2-5% from day to day. Efficiencies in excess of 750 000 plates/m and recoveries of >80% were observed for protein injections from distilled water. Alternatively if 2 mM CAS U is added to samples, recoveries were quantitative, although efficiencies decreased to 325 000-600 000 plates/m. The natural electroosmotic flow of the capillaries is regenerated simply by rinsing with sodium hydroxide.
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