Proline‐coated column for the capillary electrochromatographic separation of amino acids by in‐column derivatization

With 3‐trimethoxysilylpropyl chloride as the spacer, a proline‐coated capillary column was prepared for the capillary electrochromatographic (CEC) separation of amino acids by in‐column derivatization. Nine standard mixtures, including aspartic acid, glutamic acid, valine, phenylalanine, alanine, isoleucine, leucine, tyrosine, and tryptophan, were injected. o ‐Phthalaldehyde (OPA), OPA/2‐mercaptoethanol (2‐ME) and OPA/ N ‐acetylcysteine (NAC) in borate buffer were tested as the derivatizing agent. Among them, OPA (50 m M ) in borate buffer (pH 9.5, 50 m M ) gave the best performance. The formation of isoindole could be detected by UV detection. The sandwich‐type injection was carried out in hydrostatic mode (10 cm) with the program R(10 s)S(10 s) R(10 s)W(10 min) with R, S, and W being the reagent, sample, and waiting times. Mesityl oxide, benzyl alcohol, and acetone showed some interaction with the column. A current monitoring method was used instead of the determination of the electroosmotic flow (EOF). The direction of EOF was from anode to cathode even under acidic condition lower than the p I value (6.31) of the bonded group due to some unreacted silanol groups. Some parameters including pH, nature, and concentration of the mobile phase and the effect of organic modifier with regard to the CEC separation were investigated. With the proline‐coated column (75 (50) cm×75 μm ID) the best separation was performed in phosphate buffer (pH 4.00, 100 m M ) with an applied voltage of —15 kV. The established method was also compared with those precolumn derivatized prior to the separation with proline‐coated column as well as with in‐capillary derivatization and separation with a bare fused‐silica column.