Sample introduction systems for reversed phase LC-ICP-MS of selenium using large amounts of methanol - comparison of systems based on membrane desolvation, a spray chamber and direct injection

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Sample introduction systems for reversed phase LC-ICP-MS of selenium using large amounts of methanol - comparison of systems based on membrane desolvation, a spray chamber and direct injection. / Bendahl, L.; Gammelgaard, Bente.

I: Journal of Analytical Atomic Spectrometry, Bind 20, Nr. 5, 2005, s. 410-416.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bendahl, L & Gammelgaard, B 2005, 'Sample introduction systems for reversed phase LC-ICP-MS of selenium using large amounts of methanol - comparison of systems based on membrane desolvation, a spray chamber and direct injection', Journal of Analytical Atomic Spectrometry, bind 20, nr. 5, s. 410-416.

APA

Bendahl, L., & Gammelgaard, B. (2005). Sample introduction systems for reversed phase LC-ICP-MS of selenium using large amounts of methanol - comparison of systems based on membrane desolvation, a spray chamber and direct injection. Journal of Analytical Atomic Spectrometry, 20(5), 410-416.

Vancouver

Bendahl L, Gammelgaard B. Sample introduction systems for reversed phase LC-ICP-MS of selenium using large amounts of methanol - comparison of systems based on membrane desolvation, a spray chamber and direct injection. Journal of Analytical Atomic Spectrometry. 2005;20(5):410-416.

Author

Bendahl, L. ; Gammelgaard, Bente. / Sample introduction systems for reversed phase LC-ICP-MS of selenium using large amounts of methanol - comparison of systems based on membrane desolvation, a spray chamber and direct injection. I: Journal of Analytical Atomic Spectrometry. 2005 ; Bind 20, Nr. 5. s. 410-416.

Bibtex

@article{8479fb0214ab418b98f2d2ef36c58eb6,
title = "Sample introduction systems for reversed phase LC-ICP-MS of selenium using large amounts of methanol - comparison of systems based on membrane desolvation, a spray chamber and direct injection",
abstract = "Three sample introduction systems were compared for their efficiency in introducing a variety of biologically relevant selenium species in organic solutions with the purpose of mimicking the effluent from a chromatographic system. The sample introduction systems consisted of a microconcentric nebuliser (MCN) in combination with a membrane desolvator ( MD), a MCN in combination with a cyclonic spray chamber ( CS) and a direct injection nebuliser ( DIN), respectively. Thirteen selenium standards diluted in 50% methanol were introduced in each system at a flow rate of 50 mu l min(-1). Except for the selenite and methaneseleninic acid standards that were lost in the MCN-MD system, similar normalized response factors were achieved for the standards regardless of the sample introduction system. When trimethylselenonium and selenate standards were continuously infused in a linear methanol gradient from 10 to 90%, the signal was almost unaffected when the MCN-MD was used as interface. The signals from the MCN-CS introduction system were almost unaffected in methanol concentrations between 10 and 40%, after which they slowly declined. The signal from the DIN showed a plateau in signal intensity at methanol concentrations between 35 and 70%. Detection limits in flow injection analysis, expressed as the concentration that would result in a signal equivalent to three times the peak to peak noise of the baseline, were estimated to be 200, 150 and 100 ng Se L-1 for the MCN-CS, MCN-MD and DIN, respectively. The independence of the signal from the methanol concentration in the eluent allowed quanti. cation of human selenoprotein P isoforms by gradient microbore reversed phase chromatography (mu RPC) on the basis of an internal trimethylselenonium standard. The MCN-MD system was applied for mu RPC analysis of Se-77 enriched yeast samples and more than 30 selenium containing compounds were separated using a linear gradient from 5% to 95% methanol, some of the selenium species eluting in 85% methanol",
author = "L. Bendahl and Bente Gammelgaard",
year = "2005",
language = "English",
volume = "20",
pages = "410--416",
journal = "Journal of Analytical Atomic Spectrometry",
issn = "0267-9477",
publisher = "Royal Society of Chemistry",
number = "5",

}

RIS

TY - JOUR

T1 - Sample introduction systems for reversed phase LC-ICP-MS of selenium using large amounts of methanol - comparison of systems based on membrane desolvation, a spray chamber and direct injection

AU - Bendahl, L.

AU - Gammelgaard, Bente

PY - 2005

Y1 - 2005

N2 - Three sample introduction systems were compared for their efficiency in introducing a variety of biologically relevant selenium species in organic solutions with the purpose of mimicking the effluent from a chromatographic system. The sample introduction systems consisted of a microconcentric nebuliser (MCN) in combination with a membrane desolvator ( MD), a MCN in combination with a cyclonic spray chamber ( CS) and a direct injection nebuliser ( DIN), respectively. Thirteen selenium standards diluted in 50% methanol were introduced in each system at a flow rate of 50 mu l min(-1). Except for the selenite and methaneseleninic acid standards that were lost in the MCN-MD system, similar normalized response factors were achieved for the standards regardless of the sample introduction system. When trimethylselenonium and selenate standards were continuously infused in a linear methanol gradient from 10 to 90%, the signal was almost unaffected when the MCN-MD was used as interface. The signals from the MCN-CS introduction system were almost unaffected in methanol concentrations between 10 and 40%, after which they slowly declined. The signal from the DIN showed a plateau in signal intensity at methanol concentrations between 35 and 70%. Detection limits in flow injection analysis, expressed as the concentration that would result in a signal equivalent to three times the peak to peak noise of the baseline, were estimated to be 200, 150 and 100 ng Se L-1 for the MCN-CS, MCN-MD and DIN, respectively. The independence of the signal from the methanol concentration in the eluent allowed quanti. cation of human selenoprotein P isoforms by gradient microbore reversed phase chromatography (mu RPC) on the basis of an internal trimethylselenonium standard. The MCN-MD system was applied for mu RPC analysis of Se-77 enriched yeast samples and more than 30 selenium containing compounds were separated using a linear gradient from 5% to 95% methanol, some of the selenium species eluting in 85% methanol

AB - Three sample introduction systems were compared for their efficiency in introducing a variety of biologically relevant selenium species in organic solutions with the purpose of mimicking the effluent from a chromatographic system. The sample introduction systems consisted of a microconcentric nebuliser (MCN) in combination with a membrane desolvator ( MD), a MCN in combination with a cyclonic spray chamber ( CS) and a direct injection nebuliser ( DIN), respectively. Thirteen selenium standards diluted in 50% methanol were introduced in each system at a flow rate of 50 mu l min(-1). Except for the selenite and methaneseleninic acid standards that were lost in the MCN-MD system, similar normalized response factors were achieved for the standards regardless of the sample introduction system. When trimethylselenonium and selenate standards were continuously infused in a linear methanol gradient from 10 to 90%, the signal was almost unaffected when the MCN-MD was used as interface. The signals from the MCN-CS introduction system were almost unaffected in methanol concentrations between 10 and 40%, after which they slowly declined. The signal from the DIN showed a plateau in signal intensity at methanol concentrations between 35 and 70%. Detection limits in flow injection analysis, expressed as the concentration that would result in a signal equivalent to three times the peak to peak noise of the baseline, were estimated to be 200, 150 and 100 ng Se L-1 for the MCN-CS, MCN-MD and DIN, respectively. The independence of the signal from the methanol concentration in the eluent allowed quanti. cation of human selenoprotein P isoforms by gradient microbore reversed phase chromatography (mu RPC) on the basis of an internal trimethylselenonium standard. The MCN-MD system was applied for mu RPC analysis of Se-77 enriched yeast samples and more than 30 selenium containing compounds were separated using a linear gradient from 5% to 95% methanol, some of the selenium species eluting in 85% methanol

M3 - Journal article

VL - 20

SP - 410

EP - 416

JO - Journal of Analytical Atomic Spectrometry

JF - Journal of Analytical Atomic Spectrometry

SN - 0267-9477

IS - 5

ER -

ID: 44288277