Literature DB >> 22592983

Investigation of absolute and relative response for three different liquid chromatography/tandem mass spectrometry systems; the impact of ionization and detection saturation.

Lars B Nilsson1, Patrik Skansen.   

Abstract

RATIONALE: The investigations in this article were triggered by two observations in the laboratory; for some liquid chromatography/tandem mass spectrometry (LC/MS/MS) systems it was possible to obtain linear calibration curves for extreme concentration ranges and for some systems seemingly linear calibration curves gave good accuracy at low concentrations only when using a quadratic regression function.
METHODS: The absolute and relative responses were tested for three different LC/MS/MS systems by injecting solutions of a model compound and a stable isotope labeled internal standard. The analyte concentration range for the solutions was 0.00391 to 500 μM (128,000×), giving overload of the chromatographic column at the highest concentrations. The stable isotope labeled internal standard concentration was 0.667 μM in all samples.
RESULTS: The absolute response per concentration unit decreased rapidly as higher concentrations were injected. The relative response, the ratio for the analyte peak area to the internal standard peak area, per concentration unit was calculated. For system 1, the ionization process was found to limit the response and the relative response per concentration unit was constant. For systems 2 and 3, the ion detection process was the limiting factor resulting in decreasing relative response at increasing concentrations.
CONCLUSIONS: For systems behaving like system 1, simple linear regression can be used for any concentration range while, for systems behaving like systems 2 and 3, non-linear regression is recommended for all concentration ranges. Another consequence is that the ionization capacity limited systems will be insensitive to matrix ion suppression when an ideal internal standard is used while the detection capacity limited systems are at risk of giving erroneous results at high concentrations if the matrix ion suppression varies for different samples in a run.
Copyright © 2012 John Wiley & Sons, Ltd.

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Year:  2012        PMID: 22592983     DOI: 10.1002/rcm.6239

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  2 in total

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Authors:  Matthew T Olson; Autumn Breaud; Robert Harlan; Nkechinyere Emezienna; Sabitha Schools; Alfred L Yergey; William Clarke
Journal:  Clin Chem       Date:  2013-02-20       Impact factor: 8.327

2.  High-throughput extraction and quantification method for targeted metabolomics in murine tissues.

Authors:  Sven Zukunft; Cornelia Prehn; Cornelia Röhring; Gabriele Möller; Martin Hrabě de Angelis; Jerzy Adamski; Janina Tokarz
Journal:  Metabolomics       Date:  2017-12-30       Impact factor: 4.290

  2 in total

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