Quantitative determination of the neurotoxin β-N-methylamino-l-alanine (BMAA) by capillary electrophoresis–tandem mass spectrometry

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DOIResolve DOI: http://doi.org/10.1007/s00216-016-0091-y
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TypeArticle
Journal titleAnalytical and Bioanalytical Chemistry
ISSN1618-2642
1618-2650
Volume409
Issue6
Pages14811491
AbstractRecent reports of the widespread occurrence of the neurotoxin β-N-methylamino-l-alanine (BMAA) in cyanobacteria and particularly seafood have raised concerns for public health. LC–MS/MS is currently the analytical method of choice for BMAA determinations but incomplete separation of isomeric and isobaric compounds, matrix suppression and conjugated forms are plausible limitations. In this study, capillary electrophoresis (CE) coupled with MS/MS has been developed as an alternative method for the quantitative determination of free BMAA. Using a bare fused silica capillary, a phosphate buffer (250 mM, pH 3.0) and UV detection, it was possible to separate BMAA from four isomers, but the limit of detection (LOD) of 0.25 μg mL−1 proved insufficient for analysis of typical samples. Coupling the CE to a triple quadrupole MS was accomplished using a custom sheath-flow interface. The best separation was achieved with a 5 M formic acid in water/acetonitrile (9:1) background electrolyte. Strong acid hydrolysis of lyophilized samples was used to release BMAA from conjugated forms. Field-amplified stacking after injection was achieved by lowering sample ionic strength with a cation-exchange cleanup procedure. Quantitation was accomplished using isotope dilution with deuterium-labelled BMAA as internal standard. An LOD for BMAA in solution of 0.8 ng mL−1 was attained, which was equivalent to 16 ng g−1 dry mass in samples using the specified extraction procedure. This was comparable with LC–MS/MS methods. The method displayed excellent resolution of amino acid isomers and had no interference from matrix components. The presence of BMAA in cycad, mussel and lobster samples was confirmed by CE–MS/MS, but not in an in-house cyanobacterial reference material, with quantitative results agreeing with those from LC–MS/MS.
Publication date
PublisherSpringer
LanguageEnglish
AffiliationMeasurement Science and Standards; National Research Council Canada
Peer reviewedYes
NPARC number23002370
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Record identifier0adc83b4-98e1-4ae6-85a7-8f1e4d51dec0
Record created2017-10-24
Record modified2017-10-24
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