Literature DB >> 25619987

Analysis of paralytic shellfish toxins using high-field asymmetric waveform ion mobility spectrometry with liquid chromatography-mass spectrometry.

Daniel G Beach1, Jeremy E Melanson, Randy W Purves.   

Abstract

The analysis of paralytic shellfish toxins (PSTs) by liquid chromatography-mass spectrometry remains a challenge because of their high polarity, large number of analogues and the complex matrix in which they occur. Here we investigate the potential utility of high-field asymmetric waveform ion mobility spectrometry (FAIMS) as a gas-phase ion separation tool for analysis of PSTs by mass spectrometry. We investigate the separation of PSTs using FAIMS with two divergent goals: using FAIMS as a primary separation tool for rapid screening by electrospray ionization (ESI)-FAIMS-MS or combined with LC in a multidimensional LC-ESI-FAIMS-MS separation. First, a survey of the parameters that affect the sensitivity and selectivity of PST analysis by FAIMS was carried out using ESI-FAIMS-MS. In particular, the use of acetonitrile as a gas additive in the carrier gas flow offered good separation of all PST epimeric pairs. A second set of FAIMS conditions was also identified, which focussed PSTs to a relatively narrow CV range allowing development of an LC-ESI-FAIMS-MS method for analysis of PST toxins in complex mussel tissue extracts. The quantitative capabilities of this method were evaluated by analysing a PST containing mussel tissue matrix material. Results compared favourably with analysis by an established LC-post-column oxidation-fluorescence method with recoveries ranging from 70 to 106%, although sensitivity was somewhat reduced. The current work represents the first successful separation of PST isomers using ion mobility and shows the promise of FAIMS as a tool for analysis of algal biotoxins in complex samples and outlines some critical requirements for its future improvement.

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Year:  2015        PMID: 25619987     DOI: 10.1007/s00216-015-8488-6

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  5 in total

1.  Differential Mobility Spectrometry for Improved Selectivity in Hydrophilic Interaction Liquid Chromatography-Tandem Mass Spectrometry Analysis of Paralytic Shellfish Toxins.

Authors:  Daniel G Beach
Journal:  J Am Soc Mass Spectrom       Date:  2017-04-03       Impact factor: 3.109

2.  Differential mobility spectrometry (DMS) reveals the elevation of urinary acetylcarnitine in non-human primates (NHPs) exposed to radiation.

Authors:  Nicholas B Vera; Zhidan Chen; Evan Pannkuk; Evagelia C Laiakis; Albert J Fornace; Derek M Erion; Stephen L Coy; Jeffrey A Pfefferkorn; Paul Vouros
Journal:  J Mass Spectrom       Date:  2018-07       Impact factor: 1.982

3.  DMS as an orthogonal separation to LC/ESI/MS/MS for quantifying isomeric cerebrosides in plasma and cerebrospinal fluid.

Authors:  Hongbin Xu; Frederic R Boucher; Thao T Nguyen; Graeme P Taylor; Julianna J Tomlinson; Roberto A Ortega; Brigitte Simons; Michael G Schlossmacher; Rachel Saunders-Pullman; Walt Shaw; Steffany A L Bennett
Journal:  J Lipid Res       Date:  2018-11-09       Impact factor: 5.922

Review 4.  Recent Advances and Future Challenges in Modified Mycotoxin Analysis: Why HRMS Has Become a Key Instrument in Food Contaminant Research.

Authors:  Laura Righetti; Giuseppe Paglia; Gianni Galaverna; Chiara Dall'Asta
Journal:  Toxins (Basel)       Date:  2016-12-02       Impact factor: 4.546

5.  Differential Mobility-Mass Spectrometry Double Spike Isotope Dilution Study of Release of β-Methylaminoalanine and Proteinogenic Amino Acids during Biological Sample Hydrolysis.

Authors:  Daniel G Beach; Elliott S Kerrin; Sabrina D Giddings; Michael A Quilliam; Pearse McCarron
Journal:  Sci Rep       Date:  2018-01-08       Impact factor: 4.379

  5 in total

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