Direct tris(2,2'‐bipyridyl)ruthenium (II) electrochemiluminescence detection of polyamines separated by capillary electrophoresis

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Abstract
Capillary electrophoresis (CE) with tris(2,2`-bipyridyl) ruthenium (II) (Ru(bpy)32+) electrochemiluminescence (ECL) detection technique was developed for the analysis of four polyamines (putrescine (Put), cadaverine (Cad), spermidine (Spd), and spermine (Spm)) analysis. The four polyamines contain different amine groups, which have different ECL activity. There are several parameters which influence the resolution and ECL peak intensities, including the buffer pH and concentrations, separation voltage, sample injection, electrode materials, and Ru(bpy)32+ concentrations. Polyamines are separated by capillary zone electrophoresis in an uncoated fused-silica capillary (50 cm×25 μm (ID) filled with acidic phosphate buffer (200 mmol/L phosphate, pH 2.0) – 1mol/L phosphoric acid (9:1 v/v) and a separation voltage of 5 kV (25 μA), with end-column Ru(bpy)32+ ECL detection. A 5 mmol/L Ru(bpy)32+ solution plus 200 mmol/L phosphate buffer (pH 11.0) is added into the reagent reservoir. The calibration curve is linear over a concentration range of two or three orders of magnitude for the polyamines. The analysis time is less than 25 min. Detection limits for Put and Cad are 1.9×10−7 mol/L and 7.6×10−9 mol/L for Spd and Spm, respectively. Intraday and interday relative standard deviations of ECL peak intensities are less than 8%. The main advantages of this CE-ECL detection technique for polyamines analysis presented herein are the omission of chemical derivatization of the analytes and the high selectivity.

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