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  • 1.
    Boija, Susanne
    et al.
    Mid Sweden University, Faculty of Science, Technology and Media, Department of Chemical Engineering.
    Almesåker, Ann
    Mid Sweden University, Faculty of Science, Technology and Media, Department of Chemical Engineering.
    Hedenström, Erik
    Mid Sweden University, Faculty of Science, Technology and Media, Department of Chemical Engineering.
    Bylund, Dan
    Mid Sweden University, Faculty of Science, Technology and Media, Department of Natural Sciences.
    Edlund, Håkan
    Mid Sweden University, Faculty of Science, Technology and Media, Department of Chemical Engineering.
    Norgren, Magnus
    Mid Sweden University, Faculty of Science, Technology and Media, Department of Chemical Engineering.
    Determination of conditional stability constants for some divalent transition metal ion-EDTA complexes by electrospray ionization mass spectrometry2014In: Journal of Mass Spectrometry, ISSN 1076-5174, E-ISSN 1096-9888, Vol. 49, no 7, p. 550-556Article in journal (Refereed)
    Abstract [en]

    Conditional stability constants of coordination complexes comprising divalent transition metals, Cu2+, Ni2+, Zn2+, Co2+, and ethylenediaminetetraacetic acid (EDTA) were determined utilizing electrospray ionization mass spectrometry. The deviation of signal response of a reference complex was monitored at addition of a second metal ion. The conditional stability constant for the competing metal was then determined through solution equilibria equations. The method showed to be applicable to a system where Co2+ and Zn2+ competed for EDTA at pH 5. When Cu2+ and Ni2+ competed for EDTA, the equilibrium changed over time. This change was shown to be affected in rate and size by the type of organic solvent added. In this work, 30% of either methanol or acetonitrile was used. It was found that if calibration curves are prepared for both metal complexes in solution and the measurements are repeated with sufficient time space, any change in equilibrium of sample solutions will be discovered. Copyright © 2014 John Wiley & Sons, Ltd. Copyright © 2014 John Wiley & Sons, Ltd.

  • 2.
    Moberg, My
    et al.
    Uppsala University.
    Bergquist, Jonas
    Uppsala University.
    Bylund, Dan
    Mid Sweden University, Faculty of Science, Technology and Media, Department of Natural Sciences.
    A generic stepwise optimization strategy for liquid chromatography electrospray ionization tandem mass spectrometry methods2006In: Journal of Mass Spectrometry, ISSN 1076-5174, E-ISSN 1096-9888, Vol. 41, no 10, p. 1334-1345Article in journal (Refereed)
    Abstract [en]

    The feasibility and advantages of using sophisticated chemometric tools in combination with the execution of thoroughly planned experiments to determine experimental conditions for optimal performance of an LC-ESI-MS/MS analysis is demonstrated. A stepwise strategy is proposed, which provides a controlled optimization procedure of the chromatographic quality (in terms of separation among the sample constituents) and maximizes the mass spectrometric signal of the selected product ions. Design of experiments (DOE) and response surface methodology are applied throughout the procedure. The stepwise approach has the advantage of dealing with the different optimization criteria separately, i.e. first ensuring sufficient chromatographic separation, then maximizing the amount of precursor ion entering the mass spectrometer, and finally generating high amounts of selected product ions. The experiments are performed on a linear ion trap mass spectrometer. Retention mapping using the band-tracking model is applied during LC development, which facilitates the optimization of segmented gradients. A set of different siderophores, strong iron chelates, is used as the model substances.

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