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Trimethylselenonium ion determination in human urine by high-performance liquid chromatography–hydride generation–atomic fluorescence spectrometry optimization of the hydride generation step

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F22%3A43924393" target="_blank" >RIV/60461373:22340/22:43924393 - isvavai.cz</a>

  • Result on the web

    <a href="https://link.springer.com/article/10.1007/s00216-022-04408-6" target="_blank" >https://link.springer.com/article/10.1007/s00216-022-04408-6</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00216-022-04408-6" target="_blank" >10.1007/s00216-022-04408-6</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Trimethylselenonium ion determination in human urine by high-performance liquid chromatography–hydride generation–atomic fluorescence spectrometry optimization of the hydride generation step

  • Original language description

    This work describes the intricacies of the determination of the trimethylselenonium ion (TMSe) in human urine via high-performance liquid chromatography–hydride generation–atomic fluorescence spectrometry (HPLC-HG-AFS). By definition, this technique requires that the separated TMSe can be online converted into a volatile compound. Literature data for the determination of TMSe via the hydride generation technique are contradictory; i.e., some authors claim that direct formation of volatile compounds is possible under reduction with NaBH4, whereas others reported that a digestion step is mandatory prior to conversion. We studied and optimized the conditions for online conversion by varying the mobile phase composition (pyridine, phosphate, and acetate), testing different reaction coils, and optimizing the hydride generation conditions, although technically no hydride (H2Se) is formed but a dimethylselenide (DMSe). The optimized conditions were used for the analysis of 64 urine samples of 16 (unexposed) volunteers and the determination of low amounts of TMSe (LOD = 0.2 ng mL−1). Total (specific gravity–corrected) selenium concentrations in the urine samples ranged from 7.9 ± 0.7 to 29.7 ± 5.0 ng mL−1 for individual volunteers. Four volunteers were characterized as TMSe producers (hINMT genotype GA) and 12 were non-producers (hINMT genotype GG). Urine of TMSe producers contained 2.5 ± 1.7 ng mL−1 of TMSe, compared to 0.2 ± 0.2 ng mL−1 for non-producers. © 2022, Springer-Verlag GmbH Germany, part of Springer Nature.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10406 - Analytical chemistry

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Analytical and Bioanalytical Chemistry

  • ISSN

    1618-2642

  • e-ISSN

    1618-2650

  • Volume of the periodical

    415

  • Issue of the periodical within the volume

    09 November 2022

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    10

  • Pages from-to

    "317–326"

  • UT code for WoS article

    000880277600001

  • EID of the result in the Scopus database

    2-s2.0-85141500072