Simultaneous quantification of 5-hydroxyindoleacetic acid and 5-hydroxytryptamine by capillary electrophoresis with quantum dot and horseradish peroxidase enhanced chemiluminescence detection

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Sep 15:967:190-4. doi: 10.1016/j.jchromb.2014.07.002. Epub 2014 Jul 26.

Abstract

A capillary electrophoresis (CE) with chemiluminescence (CL) detection method was developed for the simultaneous quantification of 5-hydroxyindoleacetic acid (5-HIAA) and 5-hydroxytryptamine (5-HT). In this method, CdTe quantum dot (QD) and horseradish peroxidase (HRP) were used as enhancing reagents to co-catalyze the post-column CL reaction between luminol and hydrogen peroxide, achieving highly efficient CL emission. 5-HIAA and 5-HT inhibit the CL emission resulting to the formation of negative peaks in electropherogram. The degree of CL suppression is proportional to the concentration of 5-HT and 5-HIAA. The linear ranges for the determination of 5-HIAA and 5-HT were 2.5×10(-8)-2.5×10(-6) M and 2.5×10(-8)-5.0×10(-6) M with detection limits (signal/noise=3) of 7.0×10(-9) M and 6.0×10(-9) M, respectively. Intraday precision do not exceed 5.0%. The accuracy was confirmed by the recoveries ranged from 98% to 104%. The present method was successfully applied for the quantification of 5-HIAA and 5-HT in human urine. The concentrations of 5-HT and 5-HIAA in human urine were found to be in the range of 0.78-1.2 μM and 3.2-5.1 μM, respectively.

Keywords: 5-Hydroxyindoleacetic acid; 5-Hydroxytryptamine; Capillary electrophoresis; Chemiluminescence; Human urine; Quantum dot.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Electrophoresis, Capillary / methods*
  • Horseradish Peroxidase / metabolism
  • Humans
  • Hydroxyindoleacetic Acid / urine*
  • Limit of Detection
  • Linear Models
  • Luminescent Measurements / methods*
  • Quantum Dots
  • Reproducibility of Results
  • Serotonin / urine*

Substances

  • Serotonin
  • Hydroxyindoleacetic Acid
  • Horseradish Peroxidase