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Autor(en) / Beteiligte
Titel
Simultaneous analysis of 16 metal ions by ion‐pairing high‐performance liquid chromatography‐electrospray ionization tandem mass spectrometry
Ist Teil von
  • Journal of the Chinese Chemical Society (Taipei), 2022-10, Vol.69 (10), p.1754-1764
Ort / Verlag
Weinheim: Wiley‐VCH Verlag GmbH & Co. KGaA
Erscheinungsjahr
2022
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Metal ions can be analyzed by ESI‐MS with chelating agents. However, matrix effect and the marginal difference in atomic weight of the isotopes of some metal ions make the analysis of a metal ion mixture not feasible. In this paper, we present the use of IP‐HPLC in conjunction with a metal ion chelating agent to analyze the metal ion mixtures. Hydrophobic (±)‐trans‐1,2‐cyclohexylenedinitrilotetraacetic acid (CDTA) was used to chelate 16 metal ions. The chelates were then separated by IP‐HPLC followed by ESI‐MS analysis. For IP‐HPLC, different combinations of primary amines and their salts were employed as the ion‐pairing reagent in eluent on a high‐pH resistant C‐18 column under basic conditions. For ESI‐MS, Q‐Exactive Focus system was used. Among the metal ions, the results indicated that Al3+ showed the lowest LOD (3.88 × 10−3 μM) while Zn2+ showed the highest (0.227 μM). The sensitivity was close to that of ICP‐AES. The coefficients of determination (R2) were greater than 0.995 except for Sr2+ (R2 = 0.9899), indicating the high accuracy of the method. Finally, this method was used to analyze the black soybean samples from two different sources. Eight metal ions were successfully identified with simultaneous detection of sugars, organic acids, and nucleotides. We present the use of IP‐HPLC in conjunction with a metal ion chelating agent to analyze the metal ion mixtures. Hydrophobic CDTA was used to chelate 16 metal ions. The chelates were then separated by IP‐HPLC followed by ESI‐MS analysis. Primary amines and their salts were employed as the ion‐pairing reagent.
Sprache
Englisch
Identifikatoren
ISSN: 0009-4536
eISSN: 2192-6549
DOI: 10.1002/jccs.202200303
Titel-ID: cdi_proquest_journals_2727568121

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