4.6 Article

Novel and sensitive reversed-phase high-pressure liquid chromatography method with electrochemical detection for the simultaneous and fast determination of eight biogenic amines and metabolites in human brain tissue

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1353, 期 -, 页码 28-39

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2014.05.004

关键词

Biogenic amines; Human brain tissue; HPLC-ECD; Method optimization; Method validation

资金

  1. Research Foundation-Flanders (FWO-Flanders)
  2. Interuniversity Poles of Attraction of the Belgian Federal Science Policy Office [P7/16]
  3. Methusalem excellence grant of the Flemish Government
  4. Medical Research Foundation Antwerp
  5. Neurosearch Antwerp
  6. Thomas Riellaerts Research Fund

向作者/读者索取更多资源

A fast and simple RP-HPLC method with electrochemical detection (ECD) and ion pair chromatography was developed, optimized and validated in order to simultaneously determine eight different biogenic amines and metabolites in post-mortem human brain tissue in a single-run analytical approach. The compounds of interest are the indolamine serotonin (5-hydroxytryptamine, 5-HT), the catecholamines dopamine (DA) and (nor)epinephrine ((N)E), as well as their respective metabolites, i.e. 3,4-dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA), 5-hydroxy-3-indoleacetic acid (5-HIAA) and 3-methoxy-4-hydroxyphenylglycol (MHPG). A two-level fractional factorial experimental design was applied to study the effect of five experimental factors (i.e. the ion-pair counter concentration, the level of organic modifier, the pH of the mobile phase, the temperature of the column, and the voltage setting of the detector) on the chromatographic behaviour. The cross effect between the five quantitative factors and the capacity and separation factors of the analytes were then analysed using a Standard Least Squares model. The optimized method was fully validated according to the requirements of SFSTP (Societe Francaise des Sciences et Techniques Pharmaceutiques). Our human brain tissue sample preparation procedure is straightforward and relatively short, which allows samples to be loaded onto the HPLC system within approximately 4 h. Additionally, a high sample throughput was achieved after optimization due to a total runtime of maximally 40 min per sample. The conditions and settings of the HPLC system were found to be accurate with high intra and inter-assay repeatability, recovery and accuracy rates. The robust analytical method results in very low detection limits and good separation for all of the eight biogenic amines and metabolites in this complex mixture of biological analytes. (C) 2014 Elsevier B.V. All rights reserved.

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