4.4 Article

Capillary Electrophoresis Coupling with Electrochemiluminescence for Bisoprolol, Emolol, Propranolol Enantioseparation and Detection

Journal

Publisher

ESG
DOI: 10.20964/2021.10.09

Keywords

Enantioseparation; I3-blocker drugs; capillary electrophoresis; electrochemiluminescence

Funding

  1. Doctoral Research Initiation Fund of Hezhou University [HZUBS202105]
  2. Natural Science Foundations of Hainan Province [219QN290]
  3. Guangxi Province College Students Innovation and Entrepreneurship Training Plan Project [202111838032]

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A simple and flexible capillary electrophoresis with electrochemiluminescence (CE-ECL) detection method was developed for simultaneous enantioseparation of three β-blocker drugs. By optimizing buffer conditions, the separation efficiency and detection sensitivity were improved, achieving successful analysis of enantiomers in urine samples with high recoveries and stability.
A simple, convenient and flexibility capillary electrophoresis coupling with electrochemiluminescence (CE-ECL) detection method was carried out for simultaneous enantioseparation of three I3-blocker drugs (bisoprolol, esmolol, propranolol). In CE-ECL system, the buffers of the capillary outside and inside was not the same including the buffer composition, pH value, and concentrations. In order to simultaneously improve the detection sensitivity and enantiomer separation, the conditions of capillary inlet and outlet buffer were optimized in detail. Under the optimized conditions, the separation efficiency for enantiomers of three I3-blocker drugs were improved and baseline resolution was achieved. The limit of detection (LOD) were in the range of 0.01-0.08 ng/mL for bisoprolol, esmolol, propranolol enanotiomers. The RSDs of peak areas peak, heights, and migration time were in the range of 2.1-2.5 %, 2.0-2.3 %, and 1.9-2.2 % for enanotiomers, respectively. The separation-detection techniques was applied to analysis enantiomers of bisoprolol, esmolol, propranolol in urine sample successfully, the recoveries of the six enantiomers were in the range of 94.0 %-100.7 % with RSDs less than 3.1 %.

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