Počet záznamů: 1  

Electrochemical sensor based on phospholipid modified glassy carbon electrode - determination of paraquat

  1. 1.
    SYSNO ASEP0490129
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevElectrochemical sensor based on phospholipid modified glassy carbon electrode - determination of paraquat
    Tvůrce(i) Tomková, H. (CZ)
    Sokolová, Romana (UFCH-W) RID, ORCID, SAI
    Opletal, T. (CZ)
    Kučerová, P. (CZ)
    Kučera, L. (CZ)
    Součková, J. (CZ)
    Skopalová, J. (CZ)
    Barták, P. (CZ)
    Zdroj.dok.Journal of Electroanalytical Chemistry. - : Elsevier - ISSN 1572-6657
    Roč. 821, JUL 2018 (2018), s. 33-39
    Poč.str.7 s.
    Jazyk dok.eng - angličtina
    Země vyd.CH - Švýcarsko
    Klíč. slovaasolectin ; phospholipid ; paraquat ; sensor
    Vědní obor RIVCG - Elektrochemie
    Obor OECDAnalytical chemistry
    CEPGA17-05387S GA ČR - Grantová agentura ČR
    Institucionální podporaUFCH-W - RVO:61388955
    UT WOS000437818600006
    EID SCOPUS85039704657
    DOI10.1016/j.jelechem.2017.12.048
    AnotaceElectrochemical sensor based on glassy carbon electrode modified with asolectin (mixture of soybean phospholipids) was developed. Properties of phospholipid layer, such as thickness and compactness, were investigated using atomic force microscopy and X-ray photoelectron spectroscopy. Phospholipids completely cover whole surface and the thickness of the layer 7.1 ± 1.2 nm corresponds to the value of the phospholipid bilayer of cell membranes. Due to the accumulation of paraquat in the phospholipid layer, square wave voltammetry with asolectin modified electrode exhibits three times higher sensitivity, measured as a slope of calibration dependence, and better linearity in comparison to unmodified glassy carbon electrode. Limit of detection 2.2 nmol L−1 and recoveries higher than 88% were achieved in model samples of water. The method was used for determination of paraquat in real sample of river water and results were compared with high performance liquid chromatography and differential pulse voltammetry on hanging mercury drop electrode giving 0.071 ± 0.010, 0.050 ± 0.010 and 0.061 ± 0.008 μmol L−1, respectively.
    PracovištěÚstav fyzikální chemie J.Heyrovského
    KontaktMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Rok sběru2019
Počet záznamů: 1  

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