Determination of selenoprotein P in human plasma by solid phase extraction and inductively coupled plasma mass spectrometry

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Determination of selenoprotein P in human plasma by solid phase extraction and inductively coupled plasma mass spectrometry. / Bendahl, L.; Sidenius, U.; Gammelgaard, Bente.

In: Analytica Chimica Acta, Vol. 411, No. 1-2, 2000, p. 103-108.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Bendahl, L, Sidenius, U & Gammelgaard, B 2000, 'Determination of selenoprotein P in human plasma by solid phase extraction and inductively coupled plasma mass spectrometry', Analytica Chimica Acta, vol. 411, no. 1-2, pp. 103-108.

APA

Bendahl, L., Sidenius, U., & Gammelgaard, B. (2000). Determination of selenoprotein P in human plasma by solid phase extraction and inductively coupled plasma mass spectrometry. Analytica Chimica Acta, 411(1-2), 103-108.

Vancouver

Bendahl L, Sidenius U, Gammelgaard B. Determination of selenoprotein P in human plasma by solid phase extraction and inductively coupled plasma mass spectrometry. Analytica Chimica Acta. 2000;411(1-2):103-108.

Author

Bendahl, L. ; Sidenius, U. ; Gammelgaard, Bente. / Determination of selenoprotein P in human plasma by solid phase extraction and inductively coupled plasma mass spectrometry. In: Analytica Chimica Acta. 2000 ; Vol. 411, No. 1-2. pp. 103-108.

Bibtex

@article{555f2b9ec02e4c488ebaab27e86e5c4e,
title = "Determination of selenoprotein P in human plasma by solid phase extraction and inductively coupled plasma mass spectrometry",
abstract = "A method based on solid phase extraction was developed for the determination of selenoprotein P as selenium in human plasma. Separation of selenoprotein P from other selenium-containing proteins was accomplished by immobilized metal-ion affinity chromatography. The selenium content was subsequently measured by inductively coupled plasma mass spectrometry (ICP-MS) monitoring the Se-82 isotope. Linear response was observed in the concentration range 0.3-70.8 mu g/l selenium as selenoprotein P with a correlation coefficient of 0.9994. The precision expressed as relative standard deviation was better than 2% in this range. The estimated limit of detection was 2 mu g/l and the experimentally verified quantification limit was 5 mu g/l, giving a relative standard deviation less than 2%. (C) 2000 Elsevier Science B.V. All rights reserved",
author = "L. Bendahl and U. Sidenius and Bente Gammelgaard",
year = "2000",
language = "English",
volume = "411",
pages = "103--108",
journal = "Analytica Chimica Acta",
issn = "0003-2670",
publisher = "Elsevier",
number = "1-2",

}

RIS

TY - JOUR

T1 - Determination of selenoprotein P in human plasma by solid phase extraction and inductively coupled plasma mass spectrometry

AU - Bendahl, L.

AU - Sidenius, U.

AU - Gammelgaard, Bente

PY - 2000

Y1 - 2000

N2 - A method based on solid phase extraction was developed for the determination of selenoprotein P as selenium in human plasma. Separation of selenoprotein P from other selenium-containing proteins was accomplished by immobilized metal-ion affinity chromatography. The selenium content was subsequently measured by inductively coupled plasma mass spectrometry (ICP-MS) monitoring the Se-82 isotope. Linear response was observed in the concentration range 0.3-70.8 mu g/l selenium as selenoprotein P with a correlation coefficient of 0.9994. The precision expressed as relative standard deviation was better than 2% in this range. The estimated limit of detection was 2 mu g/l and the experimentally verified quantification limit was 5 mu g/l, giving a relative standard deviation less than 2%. (C) 2000 Elsevier Science B.V. All rights reserved

AB - A method based on solid phase extraction was developed for the determination of selenoprotein P as selenium in human plasma. Separation of selenoprotein P from other selenium-containing proteins was accomplished by immobilized metal-ion affinity chromatography. The selenium content was subsequently measured by inductively coupled plasma mass spectrometry (ICP-MS) monitoring the Se-82 isotope. Linear response was observed in the concentration range 0.3-70.8 mu g/l selenium as selenoprotein P with a correlation coefficient of 0.9994. The precision expressed as relative standard deviation was better than 2% in this range. The estimated limit of detection was 2 mu g/l and the experimentally verified quantification limit was 5 mu g/l, giving a relative standard deviation less than 2%. (C) 2000 Elsevier Science B.V. All rights reserved

M3 - Journal article

VL - 411

SP - 103

EP - 108

JO - Analytica Chimica Acta

JF - Analytica Chimica Acta

SN - 0003-2670

IS - 1-2

ER -

ID: 44288145