Počet záznamů: 1  

Determination of binding constants of multiple charged cyclodextrin complexes by ACE using uncorrected and ionic strength corrected actual mobilities of the species involved

  1. 1.
    SYSNO ASEP0517791
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevDetermination of binding constants of multiple charged cyclodextrin complexes by ACE using uncorrected and ionic strength corrected actual mobilities of the species involved
    Tvůrce(i) Sázelová, Petra (UOCHB-X) RID, ORCID
    Koval, Dušan (UOCHB-X) RID, ORCID
    Severa, Lukáš (UOCHB-X) RID, ORCID
    Teplý, Filip (UOCHB-X) RID, ORCID
    Vigh, G. (US)
    Kašička, Václav (UOCHB-X) RID, ORCID
    Zdroj.dok.Electrophoresis. - : Wiley - ISSN 0173-0835
    Roč. 41, 7/8 (2020), s. 523-535
    Poč.str.13 s.
    Jazyk dok.eng - angličtina
    Země vyd.DE - Německo
    Klíč. slovaaffinity capillary electrophoresis ; binding constant ; cyclodextrins ; electrophoretic mobility ; ionic strength
    Vědní obor RIVCB - Analytická chemie, separace
    Obor OECDAnalytical chemistry
    CEPGA17-10832S GA ČR - Grantová agentura ČR
    GA18-02597S GA ČR - Grantová agentura ČR
    Způsob publikováníOmezený přístup
    Institucionální podporaUOCHB-X - RVO:61388963
    UT WOS000500308100001
    EID SCOPUS85076163030
    DOI10.1002/elps.201900352
    AnotaceIn this study, the apparent binding constants and limiting mobilities of the multiply charged complexes of the Δ− and Λ−enantiomers of Ru(II)‐ and Fe(II)‐polypyridyl associates ([Ru(2,2′‐bipyridine)3]2+, [Ru(1,10‐phenanthroline)3]2+, and [Fe(1,10‐phenanthroline)3]2+) with single‐isomer 2,3‐diacetylated‐6‐sulfated‐cyclodextrins (CDs) (12Ac‐6S‐α‐CD, 14Ac‐7S‐β‐CD, and 16Ac‐8S‐γ‐CD) were determined by ACE using uncorrected and ionic strength corrected actual mobilities of the species involved. Two limiting models were tested for the ionic strength correction of the actual mobilities based on an empirical relation for the ionic strength correction of multivalent ionic species. In model 1, the nominal values of the charge numbers (zS,nom) and analytical concentrations (cS,nom) of the above CD selectors in the BGEs were applied for calculation of the BGE ionic strength, as usual. In model 2, the CD selectors were considered as singly charged species (zS = −1) with |zS,nom|‐times higher concentrations in the BGE than their analytical concentrations (cS = |zS,nom| × cS,nom) in the calculation of the BGE ionic strength. In all three cases–with uncorrected actual mobilities as well as with actual mobilities corrected according to the two limiting models–the measured effective mobilities of the above enantiomers fit well the theoretical curves of their mobility dependences on the CD selectors concentrations in the BGE, with high average coefficients of determination (R2 = 0.9890–0.9995). Nevertheless, the best physico‐chemically meaningful values of the apparent binding constants and the limiting mobilities of the enantiomer‐CDs complexes with low RSDs were obtained using the actual mobilities of the species involved corrected according to model 2.
    PracovištěÚstav organické chemie a biochemie
    Kontaktasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Viktorie Chládková, Tel.: 232 002 434
    Rok sběru2021
    Elektronická adresahttps://onlinelibrary.wiley.com/doi/full/10.1002/elps.201900352
Počet záznamů: 1  

  Tyto stránky využívají soubory cookies, které usnadňují jejich prohlížení. Další informace o tom jak používáme cookies.