Electrokinetic migration of acidic drugs across a supported liquid membrane

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Standard

Electrokinetic migration of acidic drugs across a supported liquid membrane. / Balchen, Marte; Gjelstad, Astrid; Rasmussen, Knut Einar; Pedersen-Bjergaard, Stig.

I: Journal of Chromatography A, Bind 1152, Nr. 1-2, 08.06.2007, s. 220-225.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Balchen, M, Gjelstad, A, Rasmussen, KE & Pedersen-Bjergaard, S 2007, 'Electrokinetic migration of acidic drugs across a supported liquid membrane', Journal of Chromatography A, bind 1152, nr. 1-2, s. 220-225. https://doi.org/10.1016/j.chroma.2006.10.096

APA

Balchen, M., Gjelstad, A., Rasmussen, K. E., & Pedersen-Bjergaard, S. (2007). Electrokinetic migration of acidic drugs across a supported liquid membrane. Journal of Chromatography A, 1152(1-2), 220-225. https://doi.org/10.1016/j.chroma.2006.10.096

Vancouver

Balchen M, Gjelstad A, Rasmussen KE, Pedersen-Bjergaard S. Electrokinetic migration of acidic drugs across a supported liquid membrane. Journal of Chromatography A. 2007 jun. 8;1152(1-2):220-225. https://doi.org/10.1016/j.chroma.2006.10.096

Author

Balchen, Marte ; Gjelstad, Astrid ; Rasmussen, Knut Einar ; Pedersen-Bjergaard, Stig. / Electrokinetic migration of acidic drugs across a supported liquid membrane. I: Journal of Chromatography A. 2007 ; Bind 1152, Nr. 1-2. s. 220-225.

Bibtex

@article{68eceb6cbae94daf9a5316329b90872b,
title = "Electrokinetic migration of acidic drugs across a supported liquid membrane",
abstract = "Electrokinetic cross membrane extraction of acidic drugs was demonstrated for the first time. The acidic drugs were extracted from an alkaline aqueous donor solution (300 μl), through a thin supported liquid membrane of 1-heptanol sustained in the pores of the wall of a porous hollow fiber, and into an aqueous alkaline acceptor solution (30 μl) present inside the lumen of the hollow fiber by the application of a d.c. electrical potential. The negative electrode was placed in the donor solution, and the positive electrode was placed in the acceptor solution. Optimal extractions were accomplished with 1-heptanol as the supported liquid membrane, with 50 V as the driving force, and with pH 12.0 in both the donor and acceptor solutions, respectively (NaOH). Equilibrium extraction conditions were obtained after 5 min of operation with the whole assembly agitated at 1200 rpm. Eleven different acidic drugs were extracted with recovery values between 8 and 100%, and initial data supported that electrokinetic cross membrane extraction provided repeatable data and linear response between original donor concentration and final acceptor concentration of the acidic model compounds.",
keywords = "Acidic drugs, Electrokinetic migration, Sample preparation, Supported liquid membranes",
author = "Marte Balchen and Astrid Gjelstad and Rasmussen, {Knut Einar} and Stig Pedersen-Bjergaard",
year = "2007",
month = jun,
day = "8",
doi = "10.1016/j.chroma.2006.10.096",
language = "English",
volume = "1152",
pages = "220--225",
journal = "Journal of Chromatography",
issn = "0301-4770",
publisher = "Elsevier",
number = "1-2",

}

RIS

TY - JOUR

T1 - Electrokinetic migration of acidic drugs across a supported liquid membrane

AU - Balchen, Marte

AU - Gjelstad, Astrid

AU - Rasmussen, Knut Einar

AU - Pedersen-Bjergaard, Stig

PY - 2007/6/8

Y1 - 2007/6/8

N2 - Electrokinetic cross membrane extraction of acidic drugs was demonstrated for the first time. The acidic drugs were extracted from an alkaline aqueous donor solution (300 μl), through a thin supported liquid membrane of 1-heptanol sustained in the pores of the wall of a porous hollow fiber, and into an aqueous alkaline acceptor solution (30 μl) present inside the lumen of the hollow fiber by the application of a d.c. electrical potential. The negative electrode was placed in the donor solution, and the positive electrode was placed in the acceptor solution. Optimal extractions were accomplished with 1-heptanol as the supported liquid membrane, with 50 V as the driving force, and with pH 12.0 in both the donor and acceptor solutions, respectively (NaOH). Equilibrium extraction conditions were obtained after 5 min of operation with the whole assembly agitated at 1200 rpm. Eleven different acidic drugs were extracted with recovery values between 8 and 100%, and initial data supported that electrokinetic cross membrane extraction provided repeatable data and linear response between original donor concentration and final acceptor concentration of the acidic model compounds.

AB - Electrokinetic cross membrane extraction of acidic drugs was demonstrated for the first time. The acidic drugs were extracted from an alkaline aqueous donor solution (300 μl), through a thin supported liquid membrane of 1-heptanol sustained in the pores of the wall of a porous hollow fiber, and into an aqueous alkaline acceptor solution (30 μl) present inside the lumen of the hollow fiber by the application of a d.c. electrical potential. The negative electrode was placed in the donor solution, and the positive electrode was placed in the acceptor solution. Optimal extractions were accomplished with 1-heptanol as the supported liquid membrane, with 50 V as the driving force, and with pH 12.0 in both the donor and acceptor solutions, respectively (NaOH). Equilibrium extraction conditions were obtained after 5 min of operation with the whole assembly agitated at 1200 rpm. Eleven different acidic drugs were extracted with recovery values between 8 and 100%, and initial data supported that electrokinetic cross membrane extraction provided repeatable data and linear response between original donor concentration and final acceptor concentration of the acidic model compounds.

KW - Acidic drugs

KW - Electrokinetic migration

KW - Sample preparation

KW - Supported liquid membranes

UR - http://www.scopus.com/inward/record.url?scp=34248598187&partnerID=8YFLogxK

U2 - 10.1016/j.chroma.2006.10.096

DO - 10.1016/j.chroma.2006.10.096

M3 - Journal article

C2 - 17126351

AN - SCOPUS:34248598187

VL - 1152

SP - 220

EP - 225

JO - Journal of Chromatography

JF - Journal of Chromatography

SN - 0301-4770

IS - 1-2

ER -

ID: 231651117