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Selenium speciation in paired serum and cerebrospinal fluid samples. / Solovyev, Nikolay; Berthele, Achim; Michalke, Bernhard.

в: Analytical and Bioanalytical Chemistry, Том 405, 2013, стр. 1875-1884.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Solovyev, N, Berthele, A & Michalke, B 2013, 'Selenium speciation in paired serum and cerebrospinal fluid samples', Analytical and Bioanalytical Chemistry, Том. 405, стр. 1875-1884. https://doi.org/10.1007/s00216-012-6294-y

APA

Solovyev, N., Berthele, A., & Michalke, B. (2013). Selenium speciation in paired serum and cerebrospinal fluid samples. Analytical and Bioanalytical Chemistry, 405, 1875-1884. https://doi.org/10.1007/s00216-012-6294-y

Vancouver

Solovyev N, Berthele A, Michalke B. Selenium speciation in paired serum and cerebrospinal fluid samples. Analytical and Bioanalytical Chemistry. 2013;405:1875-1884. https://doi.org/10.1007/s00216-012-6294-y

Author

Solovyev, Nikolay ; Berthele, Achim ; Michalke, Bernhard. / Selenium speciation in paired serum and cerebrospinal fluid samples. в: Analytical and Bioanalytical Chemistry. 2013 ; Том 405. стр. 1875-1884.

BibTeX

@article{9e3ec1ba1fc242d59016f435f960f6fd,
title = "Selenium speciation in paired serum and cerebrospinal fluid samples",
abstract = "Se speciation was performed in 24 individual paired serum and cerebrospinal fluid (CSF) samples from neurologically healthy persons. Strong anion exchange (SAX) separation, coupled to inductively coupled plasma–dynamic reaction cell–mass spectrometry (ICP-DRC-MS),was employed. Species identification was done by standard matched retention time, standard addition and by size exclusion chromatography followed from SAX (2-D SECSAX-ICP-DRC-MS) and by SAX followed from CE-ICPDRC-MS (2-D SAX-CE-ICP-DRC-MS). Limit of detection (LoD, 3×standard deviation (SD) of noise) was in the range of 0.026–0.031 μg/L for all investigated species and thus was set uniformly to 0.032 μg/L. Quality control for total Se determination was performed by analysing control materials “human serum” and “urine”, where determined values met target values. Several Se species were found in both sample types having following median values (sequence: serum/ CSF, each in μg Se/L): total Se, 58.39/0.86; selenoprotein P (SePP), 5.19/0.47; Se-methioni",
keywords = "Selenium speciation, Cerebrospinal fluid, Serum, Thioredoxin reductase, Glutathione peroxidase",
author = "Nikolay Solovyev and Achim Berthele and Bernhard Michalke",
year = "2013",
doi = "10.1007/s00216-012-6294-y",
language = "English",
volume = "405",
pages = "1875--1884",
journal = "Analytical and Bioanalytical Chemistry",
issn = "1618-2642",
publisher = "Springer Nature",

}

RIS

TY - JOUR

T1 - Selenium speciation in paired serum and cerebrospinal fluid samples

AU - Solovyev, Nikolay

AU - Berthele, Achim

AU - Michalke, Bernhard

PY - 2013

Y1 - 2013

N2 - Se speciation was performed in 24 individual paired serum and cerebrospinal fluid (CSF) samples from neurologically healthy persons. Strong anion exchange (SAX) separation, coupled to inductively coupled plasma–dynamic reaction cell–mass spectrometry (ICP-DRC-MS),was employed. Species identification was done by standard matched retention time, standard addition and by size exclusion chromatography followed from SAX (2-D SECSAX-ICP-DRC-MS) and by SAX followed from CE-ICPDRC-MS (2-D SAX-CE-ICP-DRC-MS). Limit of detection (LoD, 3×standard deviation (SD) of noise) was in the range of 0.026–0.031 μg/L for all investigated species and thus was set uniformly to 0.032 μg/L. Quality control for total Se determination was performed by analysing control materials “human serum” and “urine”, where determined values met target values. Several Se species were found in both sample types having following median values (sequence: serum/ CSF, each in μg Se/L): total Se, 58.39/0.86; selenoprotein P (SePP), 5.19/0.47; Se-methioni

AB - Se speciation was performed in 24 individual paired serum and cerebrospinal fluid (CSF) samples from neurologically healthy persons. Strong anion exchange (SAX) separation, coupled to inductively coupled plasma–dynamic reaction cell–mass spectrometry (ICP-DRC-MS),was employed. Species identification was done by standard matched retention time, standard addition and by size exclusion chromatography followed from SAX (2-D SECSAX-ICP-DRC-MS) and by SAX followed from CE-ICPDRC-MS (2-D SAX-CE-ICP-DRC-MS). Limit of detection (LoD, 3×standard deviation (SD) of noise) was in the range of 0.026–0.031 μg/L for all investigated species and thus was set uniformly to 0.032 μg/L. Quality control for total Se determination was performed by analysing control materials “human serum” and “urine”, where determined values met target values. Several Se species were found in both sample types having following median values (sequence: serum/ CSF, each in μg Se/L): total Se, 58.39/0.86; selenoprotein P (SePP), 5.19/0.47; Se-methioni

KW - Selenium speciation

KW - Cerebrospinal fluid

KW - Serum

KW - Thioredoxin reductase

KW - Glutathione peroxidase

U2 - 10.1007/s00216-012-6294-y

DO - 10.1007/s00216-012-6294-y

M3 - Article

VL - 405

SP - 1875

EP - 1884

JO - Analytical and Bioanalytical Chemistry

JF - Analytical and Bioanalytical Chemistry

SN - 1618-2642

ER -

ID: 5627276