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Speciation analysis of mercury employing volatile species generation: Approaches to reliable determination in blood and hair

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22340%2F21%3A43926681" target="_blank" >RIV/60461373:22340/21:43926681 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/68081715:_____/21:00544232 RIV/00216208:11310/21:10436731

  • Výsledek na webu

    <a href="https://www.sciencedirect.com/science/article/pii/S0026265X21006925#ak005" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0026265X21006925#ak005</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.microc.2021.106606" target="_blank" >10.1016/j.microc.2021.106606</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Speciation analysis of mercury employing volatile species generation: Approaches to reliable determination in blood and hair

  • Popis výsledku v původním jazyce

    Two approaches to Hg speciation analysis, both employing volatile species generation (VSG) were optimized and subsequently applied to biological sample analysis. The first one employs post-column VSG after HPLC separation of Hg species (Hg2+, MeHg+, EtHg+ and PhHg+) prior to their ICP-MS detection (HPLC-VSG-ICP-MS). The optimized post-column VSG step enhances sensitivity 30–40 times and improves limits of detection (LOD) by a factor of five in comparison with the setup without VSG step (HPLC-ICP-MS). LODs between 3 and 6 ng L−1 have been reached by HPLC-VCG-ICP-MS while those reached by HPLC-ICP-MS ranged significantly higher (15–26 ng L−1). Additionally, the VSG step reduces significantly the effect of organic mobile phase on ICP plasma during gradient elution required for PhHg+ determination. Moreover, a simple and short (7 min) two-stage extraction procedure was proposed for simultaneous determination of Hg2+, MeHg+ and EtHg+ in human blood. Acceptable extraction efficiency of Hg species without their inter-conversions was confirmed by Hg speciation analysis in human blood certified reference materials (Seronorm Trace Elements Whole Blood L-1 and L-2) resulting in recoveries better than 90% (Hg2+, MeHg+) and 80% for EtHg+, respectively. The second approach to Hg speciation analysis is based on selective extraction of MeHg+ from hair samples with 2 mol L−1 HCl. Extraction selectivity was verified by HPLC-ICP-MS employing the IAEA-086 certified reference material of human hair. Three spectrometric detectors were compared for subsequent Hg determination in the extracts from hair including single purpose mercury analyzer AMA-254, VSG-AAS and ICP-MS resulting in MeHg+ recovery of 100 ± 10%. © 2021 Elsevier B.V.

  • Název v anglickém jazyce

    Speciation analysis of mercury employing volatile species generation: Approaches to reliable determination in blood and hair

  • Popis výsledku anglicky

    Two approaches to Hg speciation analysis, both employing volatile species generation (VSG) were optimized and subsequently applied to biological sample analysis. The first one employs post-column VSG after HPLC separation of Hg species (Hg2+, MeHg+, EtHg+ and PhHg+) prior to their ICP-MS detection (HPLC-VSG-ICP-MS). The optimized post-column VSG step enhances sensitivity 30–40 times and improves limits of detection (LOD) by a factor of five in comparison with the setup without VSG step (HPLC-ICP-MS). LODs between 3 and 6 ng L−1 have been reached by HPLC-VCG-ICP-MS while those reached by HPLC-ICP-MS ranged significantly higher (15–26 ng L−1). Additionally, the VSG step reduces significantly the effect of organic mobile phase on ICP plasma during gradient elution required for PhHg+ determination. Moreover, a simple and short (7 min) two-stage extraction procedure was proposed for simultaneous determination of Hg2+, MeHg+ and EtHg+ in human blood. Acceptable extraction efficiency of Hg species without their inter-conversions was confirmed by Hg speciation analysis in human blood certified reference materials (Seronorm Trace Elements Whole Blood L-1 and L-2) resulting in recoveries better than 90% (Hg2+, MeHg+) and 80% for EtHg+, respectively. The second approach to Hg speciation analysis is based on selective extraction of MeHg+ from hair samples with 2 mol L−1 HCl. Extraction selectivity was verified by HPLC-ICP-MS employing the IAEA-086 certified reference material of human hair. Three spectrometric detectors were compared for subsequent Hg determination in the extracts from hair including single purpose mercury analyzer AMA-254, VSG-AAS and ICP-MS resulting in MeHg+ recovery of 100 ± 10%. © 2021 Elsevier B.V.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10406 - Analytical chemistry

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2021

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    MICROCHEMICAL JOURNAL

  • ISSN

    0026-265X

  • e-ISSN

    1095-9149

  • Svazek periodika

    170

  • Číslo periodika v rámci svazku

    7

  • Stát vydavatele periodika

    NL - Nizozemsko

  • Počet stran výsledku

    11

  • Strana od-do

    nestránkováno

  • Kód UT WoS článku

    000696315700003

  • EID výsledku v databázi Scopus

    2-s2.0-85111008172