Development of a simple in-vial liquid-phase microextraction device for drug analysis compatible with capillary gas chromatography, capillary electrophoresis and high-performance liquid chromatography

Research output: Contribution to journalConference articleResearchpeer-review

Standard

Development of a simple in-vial liquid-phase microextraction device for drug analysis compatible with capillary gas chromatography, capillary electrophoresis and high-performance liquid chromatography. / Rasmussen, Knut Einar; Pedersen-Bjergaard, Stig; Krogh, Mette; Grefslie Ugland, Hege; Grønhaug, Trine.

In: Journal of Chromatography A, Vol. 873, No. 1, 17.03.2000, p. 3-11.

Research output: Contribution to journalConference articleResearchpeer-review

Harvard

Rasmussen, KE, Pedersen-Bjergaard, S, Krogh, M, Grefslie Ugland, H & Grønhaug, T 2000, 'Development of a simple in-vial liquid-phase microextraction device for drug analysis compatible with capillary gas chromatography, capillary electrophoresis and high-performance liquid chromatography', Journal of Chromatography A, vol. 873, no. 1, pp. 3-11. https://doi.org/10.1016/S0021-9673(99)01163-2

APA

Rasmussen, K. E., Pedersen-Bjergaard, S., Krogh, M., Grefslie Ugland, H., & Grønhaug, T. (2000). Development of a simple in-vial liquid-phase microextraction device for drug analysis compatible with capillary gas chromatography, capillary electrophoresis and high-performance liquid chromatography. Journal of Chromatography A, 873(1), 3-11. https://doi.org/10.1016/S0021-9673(99)01163-2

Vancouver

Rasmussen KE, Pedersen-Bjergaard S, Krogh M, Grefslie Ugland H, Grønhaug T. Development of a simple in-vial liquid-phase microextraction device for drug analysis compatible with capillary gas chromatography, capillary electrophoresis and high-performance liquid chromatography. Journal of Chromatography A. 2000 Mar 17;873(1):3-11. https://doi.org/10.1016/S0021-9673(99)01163-2

Author

Rasmussen, Knut Einar ; Pedersen-Bjergaard, Stig ; Krogh, Mette ; Grefslie Ugland, Hege ; Grønhaug, Trine. / Development of a simple in-vial liquid-phase microextraction device for drug analysis compatible with capillary gas chromatography, capillary electrophoresis and high-performance liquid chromatography. In: Journal of Chromatography A. 2000 ; Vol. 873, No. 1. pp. 3-11.

Bibtex

@inproceedings{8250c7f068184b4c9caa9da52339a478,
title = "Development of a simple in-vial liquid-phase microextraction device for drug analysis compatible with capillary gas chromatography, capillary electrophoresis and high-performance liquid chromatography",
abstract = "A simple, inexpensive and disposable device for liquid-phase microextraction (LPME) is presented for use in combination with capillary gas chromatography (GC), capillary electrophoresis (CE) and high-performance liquid chromatography (HPLC). 1-4 ml samples of human urine or plasma were filled into conventional 4-ml vials, whereafter 15-25 μl of the extraction medium (acceptor solution) was filled into a short piece of a porous hollow fiber and placed into the sample vial. The drugs of interest were extracted from the sample solutions and into the small volumes of acceptor solution based on high partition coefficients and were preconcentrated by a factor of 30-125. For LPME in combination with GC, the porous hollow fiber was filled with 15 μl n-octanol as the acceptor solution. Following 30 min of extraction, the organic acceptor solution was injected directly into the GC system. For LPME in combination with CE and HPLC, n-octanol was immobilized within the pores of the hollow fiber, while the internal volume of the fiber was filled with either 25 μl of 0.1 M HCl (for extraction of basic compounds) or 25 μl 0.02 M NaOH (for acidic compounds). Following 45 min extraction, the aqueous acceptor solution was injected directly into the CE or HPLC system. Owing to the low cost, the extraction devices were disposed after a single extraction which eliminated the possibility of carry over effects. In addition, because no expensive instrumentation was required for LPME, 10-30 samples were extracted in parallel to provide a high number of samples per unit time capacity. (C) 2000 Elsevier Science B.V.",
keywords = "Amphetamines, Benzodiazepines, Extraction methods, Hollow fibers, Liquid-phase microextraction, Nonsteroidal anti-inflammatory drugs",
author = "Rasmussen, {Knut Einar} and Stig Pedersen-Bjergaard and Mette Krogh and {Grefslie Ugland}, Hege and Trine Gr{\o}nhaug",
year = "2000",
month = mar,
day = "17",
doi = "10.1016/S0021-9673(99)01163-2",
language = "English",
volume = "873",
pages = "3--11",
journal = "Journal of Chromatography",
issn = "0301-4770",
publisher = "Elsevier",
number = "1",
note = "ExTech Symposium: Advances in Extraction Technologies ; Conference date: 26-04-1999 Through 30-04-1999",

}

RIS

TY - GEN

T1 - Development of a simple in-vial liquid-phase microextraction device for drug analysis compatible with capillary gas chromatography, capillary electrophoresis and high-performance liquid chromatography

AU - Rasmussen, Knut Einar

AU - Pedersen-Bjergaard, Stig

AU - Krogh, Mette

AU - Grefslie Ugland, Hege

AU - Grønhaug, Trine

PY - 2000/3/17

Y1 - 2000/3/17

N2 - A simple, inexpensive and disposable device for liquid-phase microextraction (LPME) is presented for use in combination with capillary gas chromatography (GC), capillary electrophoresis (CE) and high-performance liquid chromatography (HPLC). 1-4 ml samples of human urine or plasma were filled into conventional 4-ml vials, whereafter 15-25 μl of the extraction medium (acceptor solution) was filled into a short piece of a porous hollow fiber and placed into the sample vial. The drugs of interest were extracted from the sample solutions and into the small volumes of acceptor solution based on high partition coefficients and were preconcentrated by a factor of 30-125. For LPME in combination with GC, the porous hollow fiber was filled with 15 μl n-octanol as the acceptor solution. Following 30 min of extraction, the organic acceptor solution was injected directly into the GC system. For LPME in combination with CE and HPLC, n-octanol was immobilized within the pores of the hollow fiber, while the internal volume of the fiber was filled with either 25 μl of 0.1 M HCl (for extraction of basic compounds) or 25 μl 0.02 M NaOH (for acidic compounds). Following 45 min extraction, the aqueous acceptor solution was injected directly into the CE or HPLC system. Owing to the low cost, the extraction devices were disposed after a single extraction which eliminated the possibility of carry over effects. In addition, because no expensive instrumentation was required for LPME, 10-30 samples were extracted in parallel to provide a high number of samples per unit time capacity. (C) 2000 Elsevier Science B.V.

AB - A simple, inexpensive and disposable device for liquid-phase microextraction (LPME) is presented for use in combination with capillary gas chromatography (GC), capillary electrophoresis (CE) and high-performance liquid chromatography (HPLC). 1-4 ml samples of human urine or plasma were filled into conventional 4-ml vials, whereafter 15-25 μl of the extraction medium (acceptor solution) was filled into a short piece of a porous hollow fiber and placed into the sample vial. The drugs of interest were extracted from the sample solutions and into the small volumes of acceptor solution based on high partition coefficients and were preconcentrated by a factor of 30-125. For LPME in combination with GC, the porous hollow fiber was filled with 15 μl n-octanol as the acceptor solution. Following 30 min of extraction, the organic acceptor solution was injected directly into the GC system. For LPME in combination with CE and HPLC, n-octanol was immobilized within the pores of the hollow fiber, while the internal volume of the fiber was filled with either 25 μl of 0.1 M HCl (for extraction of basic compounds) or 25 μl 0.02 M NaOH (for acidic compounds). Following 45 min extraction, the aqueous acceptor solution was injected directly into the CE or HPLC system. Owing to the low cost, the extraction devices were disposed after a single extraction which eliminated the possibility of carry over effects. In addition, because no expensive instrumentation was required for LPME, 10-30 samples were extracted in parallel to provide a high number of samples per unit time capacity. (C) 2000 Elsevier Science B.V.

KW - Amphetamines

KW - Benzodiazepines

KW - Extraction methods

KW - Hollow fibers

KW - Liquid-phase microextraction

KW - Nonsteroidal anti-inflammatory drugs

UR - http://www.scopus.com/inward/record.url?scp=0034002699&partnerID=8YFLogxK

U2 - 10.1016/S0021-9673(99)01163-2

DO - 10.1016/S0021-9673(99)01163-2

M3 - Conference article

C2 - 10757280

AN - SCOPUS:0034002699

VL - 873

SP - 3

EP - 11

JO - Journal of Chromatography

JF - Journal of Chromatography

SN - 0301-4770

IS - 1

T2 - ExTech Symposium: Advances in Extraction Technologies

Y2 - 26 April 1999 through 30 April 1999

ER -

ID: 231654033