Quantitative Determination of Iron-Siderophore Complexes in Peat by Isotope-Exchange Size-Exclusion UPLC-Electrospray Ionization High-Resolution Accurate Mass (HRAM) Mass Spectrometry.
Luluil MaknunKatarzyna KińskaIván González-ÁlvarezLaurent OuerdaneBéatrice LaugaAtitaya SiripinyanondJoanna SzpunarRyszard ŁobińskiPublished in: Analytical chemistry (2023)
A method was developed for the quantification of iron-siderophore complexes by electrospray high-resolution accurate mass (HRAM) mass spectrometry (MS) without the need for authentic standards. The bulk of iron-siderophore complexes was purified by solid-phase extraction (SPE) and concentrated by evaporation. The individual complexes were identified by fast size-exclusion chromatography (FastSEC)-Orbitrap MS n on the basis of the exact molecular mass (±1 ppm) and MS 2 or MS 3 fragmentation. Their capability to readily exchange the natural 56 Fe for the added 58 Fe was demonstrated by SEC with ICP MS and ESI MS detection. The method was applied to the analysis of peat sampled in the eastern part of the French Pyrenean mountains. Nineteen siderophores belonging to four different classes were identified and quantified. The results were validated using ICP MS detection of iron by matching the sum of iron complexes determined by isotope exchange-ESI MS within each peak observed by FastSEC-ICP MS.
Keyphrases
- mass spectrometry
- high resolution
- liquid chromatography
- gas chromatography
- ms ms
- high performance liquid chromatography
- solid phase extraction
- tandem mass spectrometry
- capillary electrophoresis
- high resolution mass spectrometry
- multiple sclerosis
- simultaneous determination
- ultra high performance liquid chromatography
- liquid chromatography tandem mass spectrometry
- molecular dynamics
- iron deficiency
- molecularly imprinted
- loop mediated isothermal amplification