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    A capillary electrophoresis method for the determination of selected biogenic amines and amino acids in mammalian decomposition fluid

    137229_20293_A capillary electrophoresis method for the determination of selected.pdf (2.731Mb)
    Access Status
    Open access
    Authors
    Swann, Lisa
    Forbes, S.
    Lewis, Simon
    Date
    2010
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Swann, L.M. and Forbes, S.L. and Lewis, S.W. 2010. A capillary electrophoresis method for the determination of selected biogenic amines and amino acids in mammalian decomposition fluid. Talanta. 81 (4-5): pp. 1697-1702.
    Source Title
    Talanta
    DOI
    10.1016/j.talanta.2010.03.025
    ISSN
    00399140
    Faculty
    Department of Applied Chemistry
    School of Science and Computing
    Faculty of Science and Engineering
    Remarks

    The link to the journal’s home page is: http://www.elsevier.com/wps/find/journaldescription.cws_home/525438/description#description. Copyright © 2010 Elsevier B.V. All rights reserved

    URI
    http://hdl.handle.net/20.500.11937/34776
    Collection
    • Curtin Research Publications
    Abstract

    A simple capillary zone electrophoresis method for the determination of selected biogenic amines (tyramine and tryptamine) and amino acids (tryptophan, phenylalanine and tyrosine) in mammalian decomposition fluids is presented. Separations were carried out in a fused silica capillary (75μA i.d.,total length 65 cm, effective length 56 cm) with detection by ultraviolet absorbance spectrophotometry at 200 nm. In order to improve resolution and total analysis time, the method was subjected to optimisation utilising a chemometric approach. A screening design was carried out followed by a central composite design (CCD), using peak resolution and total analysis time as response factors. The influences of four experimental variables (pH, background electrolyte concentration, percentage of organic modifier(methanol) and applied voltage) were investigated. Optimum separation conditions were determined to be; a background electrolyte of boric acid (70mM) adjusted to pH 9.5 with 0.1 M sodium hydroxide with 32% methanol (v/v). Applied voltage was 30 kV, with the resulting current being less than 26μA. Under these conditions the analytes were separated within 12 min. Tryptamine, tyramine, tryptophan, tyrosine and phenylalanine were identified by migration time and spiking in porcine decomposition fluids.

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