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Electrophoretic Determination of Symmetric and Asymmetric Dimethylarginine in Human Blood Plasma with Whole Capillary Sample Injection

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    SYSNO ASEP0541396
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleElectrophoretic Determination of Symmetric and Asymmetric Dimethylarginine in Human Blood Plasma with Whole Capillary Sample Injection
    Author(s) Tůma, P. (CZ)
    Sommerová, B. (CZ)
    Koval, Dušan (UOCHB-X) RID, ORCID
    Couderc, F. (FR)
    Article number2970
    Source TitleInternational Journal of Molecular Sciences. - : MDPI
    Roč. 22, č. 6 (2021)
    Number of pages14 s.
    Languageeng - English
    CountryCH - Switzerland
    Keywordsamino acid ; capillary coating ; capillary electrophoresis ; clinical analysis ; contactless conductivity detection ; dimethylarginines ; sample treatment ; stacking
    OECD categoryAnalytical chemistry
    Method of publishingOpen access
    Institutional supportUOCHB-X - RVO:61388963
    UT WOS000645825400001
    EID SCOPUS85102454435
    DOI10.3390/ijms22062970
    AnnotationAsymmetric and symmetric dimethylarginines are toxic non-coded amino acids. They are formed by post-translational modifications and play multifunctional roles in some human diseases. Their determination in human blood plasma is performed using capillary electrophoresis with contactless conductivity detection. The separations are performed in a capillary covered with covalently bonded PAMAPTAC polymer, which generates anionic electroosmotic flow and the separation takes place in the counter-current regime. The background electrolyte is a 750 mM aqueous solution of acetic acid with pH 2.45. The plasma samples for analysis are treated by the addition of acetonitrile and injected into the capillary in a large volume, reaching 94.5% of the total volume of the capillary, and subsequently subjected to electrophoretic stacking. The attained LODs are 16 nm for ADMA and 22 nM for SDMA. The electrophoretic resolution of both isomers has a value of 5.3. The developed method is sufficiently sensitive for the determination of plasmatic levels of ADMA and SDMA. The determination does not require derivatization and the individual steps in the electrophoretic stacking are fully automated. The determined plasmatic levels for healthy individuals vary in the range 0.36–0.62 µM for ADMA and 0.32–0.70 µM for SDMA.
    WorkplaceInstitute of Organic Chemistry and Biochemistry
    Contactasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Year of Publishing2022
    Electronic addresshttps://doi.org/10.3390/ijms22062970
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