Design and implementation of an automated liquid-phase microextraction-chip system coupled on-line with high performance liquid chromatography

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Design and implementation of an automated liquid-phase microextraction-chip system coupled on-line with high performance liquid chromatography. / Li, Bin; Petersen, Nickolaj J.; Payán, María D Ramos; Hansen, Steen Honoré; Pedersen-Bjergaard, Stig.

In: Talanta, Vol. 120, 03.2014, p. 224-9.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Li, B, Petersen, NJ, Payán, MDR, Hansen, SH & Pedersen-Bjergaard, S 2014, 'Design and implementation of an automated liquid-phase microextraction-chip system coupled on-line with high performance liquid chromatography', Talanta, vol. 120, pp. 224-9. https://doi.org/10.1016/j.talanta.2013.12.016

APA

Li, B., Petersen, N. J., Payán, M. D. R., Hansen, S. H., & Pedersen-Bjergaard, S. (2014). Design and implementation of an automated liquid-phase microextraction-chip system coupled on-line with high performance liquid chromatography. Talanta, 120, 224-9. https://doi.org/10.1016/j.talanta.2013.12.016

Vancouver

Li B, Petersen NJ, Payán MDR, Hansen SH, Pedersen-Bjergaard S. Design and implementation of an automated liquid-phase microextraction-chip system coupled on-line with high performance liquid chromatography. Talanta. 2014 Mar;120:224-9. https://doi.org/10.1016/j.talanta.2013.12.016

Author

Li, Bin ; Petersen, Nickolaj J. ; Payán, María D Ramos ; Hansen, Steen Honoré ; Pedersen-Bjergaard, Stig. / Design and implementation of an automated liquid-phase microextraction-chip system coupled on-line with high performance liquid chromatography. In: Talanta. 2014 ; Vol. 120. pp. 224-9.

Bibtex

@article{b1e64947a41a4daba7e3ce2fa09e940c,
title = "Design and implementation of an automated liquid-phase microextraction-chip system coupled on-line with high performance liquid chromatography",
abstract = "An automated liquid-phase microextraction (LPME) device in a chip format has been developed and coupled directly to high performance liquid chromatography (HPLC). A 10-port 2-position switching valve was used to hyphenate the LPME-chip with the HPLC autosampler, and to collect the extracted analytes, which then were delivered to the HPLC column. The LPME-chip-HPLC system was completely automated and controlled by the software of the HPLC instrument. The performance of this system was demonstrated with five alkaloids i.e. morphine, codeine, thebaine, papaverine, and noscapine as model analytes. The composition of the supported liquid membrane (SLM) and carrier was optimized in order to achieve reasonable extraction performance of all the five alkaloids. With 1-octanol as SLM solvent and with 25mM sodium octanoate as anionic carrier, extraction recoveries for the different opium alkaloids ranged between 17% and 45%. The extraction provided high selectivity, and no interfering peaks in the chromatograms were observed when applied to human urine samples spiked with alkaloids. The detection limits using UV-detection were in the range of 1-21ng/mL for the five opium alkaloids presented in water samples. The repeatability was within 5.0-10.8% (RSD). The membrane liquid in the LPME-chip was regenerated automatically between every third injection. With this procedure the liquid membrane in the LPME-chip was stable in 3-7 days depending on the complexity of sample solutions with continuous operation. With this LPME-chip-HPLC system, series of samples were automatically injected, extracted, separated, and detected without any operator interaction.",
author = "Bin Li and Petersen, {Nickolaj J.} and Pay{\'a}n, {Mar{\'i}a D Ramos} and Hansen, {Steen Honor{\'e}} and Stig Pedersen-Bjergaard",
note = "Copyright {\textcopyright} 2013 Elsevier B.V. All rights reserved.",
year = "2014",
month = mar,
doi = "10.1016/j.talanta.2013.12.016",
language = "English",
volume = "120",
pages = "224--9",
journal = "Talanta",
issn = "0039-9140",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Design and implementation of an automated liquid-phase microextraction-chip system coupled on-line with high performance liquid chromatography

AU - Li, Bin

AU - Petersen, Nickolaj J.

AU - Payán, María D Ramos

AU - Hansen, Steen Honoré

AU - Pedersen-Bjergaard, Stig

N1 - Copyright © 2013 Elsevier B.V. All rights reserved.

PY - 2014/3

Y1 - 2014/3

N2 - An automated liquid-phase microextraction (LPME) device in a chip format has been developed and coupled directly to high performance liquid chromatography (HPLC). A 10-port 2-position switching valve was used to hyphenate the LPME-chip with the HPLC autosampler, and to collect the extracted analytes, which then were delivered to the HPLC column. The LPME-chip-HPLC system was completely automated and controlled by the software of the HPLC instrument. The performance of this system was demonstrated with five alkaloids i.e. morphine, codeine, thebaine, papaverine, and noscapine as model analytes. The composition of the supported liquid membrane (SLM) and carrier was optimized in order to achieve reasonable extraction performance of all the five alkaloids. With 1-octanol as SLM solvent and with 25mM sodium octanoate as anionic carrier, extraction recoveries for the different opium alkaloids ranged between 17% and 45%. The extraction provided high selectivity, and no interfering peaks in the chromatograms were observed when applied to human urine samples spiked with alkaloids. The detection limits using UV-detection were in the range of 1-21ng/mL for the five opium alkaloids presented in water samples. The repeatability was within 5.0-10.8% (RSD). The membrane liquid in the LPME-chip was regenerated automatically between every third injection. With this procedure the liquid membrane in the LPME-chip was stable in 3-7 days depending on the complexity of sample solutions with continuous operation. With this LPME-chip-HPLC system, series of samples were automatically injected, extracted, separated, and detected without any operator interaction.

AB - An automated liquid-phase microextraction (LPME) device in a chip format has been developed and coupled directly to high performance liquid chromatography (HPLC). A 10-port 2-position switching valve was used to hyphenate the LPME-chip with the HPLC autosampler, and to collect the extracted analytes, which then were delivered to the HPLC column. The LPME-chip-HPLC system was completely automated and controlled by the software of the HPLC instrument. The performance of this system was demonstrated with five alkaloids i.e. morphine, codeine, thebaine, papaverine, and noscapine as model analytes. The composition of the supported liquid membrane (SLM) and carrier was optimized in order to achieve reasonable extraction performance of all the five alkaloids. With 1-octanol as SLM solvent and with 25mM sodium octanoate as anionic carrier, extraction recoveries for the different opium alkaloids ranged between 17% and 45%. The extraction provided high selectivity, and no interfering peaks in the chromatograms were observed when applied to human urine samples spiked with alkaloids. The detection limits using UV-detection were in the range of 1-21ng/mL for the five opium alkaloids presented in water samples. The repeatability was within 5.0-10.8% (RSD). The membrane liquid in the LPME-chip was regenerated automatically between every third injection. With this procedure the liquid membrane in the LPME-chip was stable in 3-7 days depending on the complexity of sample solutions with continuous operation. With this LPME-chip-HPLC system, series of samples were automatically injected, extracted, separated, and detected without any operator interaction.

U2 - 10.1016/j.talanta.2013.12.016

DO - 10.1016/j.talanta.2013.12.016

M3 - Journal article

C2 - 24468363

VL - 120

SP - 224

EP - 229

JO - Talanta

JF - Talanta

SN - 0039-9140

ER -

ID: 97870742