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Electrolyte system strategies for anionic isotachophoresis with electrospray-ionization mass-spectrometric detection. 2. Isotachophoresis in moving-boundary systems
P. Gebauer, Z. Malá, P. Boček,
Jazyk angličtina Země Německo
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
24123055
DOI
10.1002/elps.201300379
Knihovny.cz E-zdroje
- MeSH
- chemické modely MeSH
- hmotnostní spektrometrie s elektrosprejovou ionizací metody MeSH
- izotachoforéza metody MeSH
- koncentrace vodíkových iontů MeSH
- léčivé přípravky chemie izolace a purifikace MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
This contribution is the second part of the project on strategies used in the selection of electrolyte systems for anionic ITP with ESI-mass spectrometric detection. It presents ITP as a powerful tool for selective stacking of anionic analytes, performed in a nonconventional way in moving-boundary systems where two co-anions are present in both the leading and terminating zones. The theoretical background is given to substantiate the conditions for the existence and migration of ITP boundaries in moving-boundary systems and stacking of analytes at these boundaries. The practical aspects of the theory are shown in form of stacking-window diagrams that bring immediate information about which analytes are stacked in a given system. The presented theory and strategy are illustrated and verified on the example of analysis of a model mixture of salicylic acid, ibuprofen and diclofenac, and comparison of regular and free-acid ITP with moving-boundary ITP systems formed by formic and propionic acids and ammonium as counterion.
Citace poskytuje Crossref.org
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- $a This contribution is the second part of the project on strategies used in the selection of electrolyte systems for anionic ITP with ESI-mass spectrometric detection. It presents ITP as a powerful tool for selective stacking of anionic analytes, performed in a nonconventional way in moving-boundary systems where two co-anions are present in both the leading and terminating zones. The theoretical background is given to substantiate the conditions for the existence and migration of ITP boundaries in moving-boundary systems and stacking of analytes at these boundaries. The practical aspects of the theory are shown in form of stacking-window diagrams that bring immediate information about which analytes are stacked in a given system. The presented theory and strategy are illustrated and verified on the example of analysis of a model mixture of salicylic acid, ibuprofen and diclofenac, and comparison of regular and free-acid ITP with moving-boundary ITP systems formed by formic and propionic acids and ammonium as counterion.
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