Electrokinetic migration across artificial liquid membranes - New concept for rapid sample preparation of biological fluids

被引:606
作者
Pedersen-Bjergaard, S [1 ]
Rasmussen, KE [1 ]
机构
[1] Univ Oslo, Sch Pharm, N-0316 Oslo, Norway
关键词
electrokinetic migration; artificial liquid membranes; sample preparation; biological fluids; drugs;
D O I
10.1016/j.chroma.2006.01.025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Basic drug substances were transported across a thin artificial organic liquid membrane by the application of 300 V d.c. From a 300 mu l aqueous donor compartment (containing 10 mM HCl), the drugs migrated through a 200 mu m artificial liquid membrane of 2-nitrophenyl octyl ether immobilized in the pores of a polypropylene hollow fiber, and into a 30 mu l aqueous acceptor solution of 10 mM HCl inside the lumen of the hollow fiber. The transport was forced by an electrical potential difference sustained over the liquid membrane, resulting in electrokinetic migration of drug substances from the donor compartment to the acceptor solution. Within 5 min of operation at 300 V, pethidine, nortriptyline, methadone, haloperidol. and loperamide were extracted with recoveries in the range 70-79%, which corresponded to enrichments in the range 7.0-7.9. The chemical composition of the organic liquid membrane strongly affected the permeability, and may serve as an efficient tool for controlling the transport selectivity. Water samples, human plasma, and human urine were successfully processed, and in light of the present report, electrokinetic migration across thin artificial liquid membranes may be an interesting tool for future isolation within chemical analysis. (c) 2006 Elsevier B.V All rights reserved.
引用
收藏
页码:183 / 190
页数:8
相关论文
共 27 条
[1]   Three-compartment electrodialysis device for on-line sample cleanup and enrichment prior to capillary electrophoresis [J].
Buscher, BAP ;
Tjaden, UR ;
vanderGreef, J .
JOURNAL OF CHROMATOGRAPHY A, 1997, 788 (1-2) :165-172
[2]   On-line electrodialysis capillary zone electrophoresis of adenosine triphosphate and inositol phosphates [J].
Buscher, BAP ;
Tjaden, UR ;
vanderGreef, J .
JOURNAL OF CHROMATOGRAPHY A, 1997, 764 (01) :135-142
[3]  
CLARK WM, 1992, CHEMTECH, V22, P425
[4]   QUANTITATIVE ENRICHMENT OF TRACE LEVELS OF IONS BY ELECTRODIALYSIS [J].
COX, JA ;
CARLSON, R .
ANALYTICA CHIMICA ACTA, 1981, 130 (02) :313-321
[5]   ELECTRODIALYTIC SAMPLE TREATMENT COUPLED ONLINE WITH HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
DEBETS, AJJ ;
KOK, WT ;
HUPE, KP ;
BRINKMAN, UAT .
CHROMATOGRAPHIA, 1990, 30 (7-8) :361-366
[6]   Back extraction of platinum metals from liquid membranes in an electric field [J].
Kulikova, L ;
Petrichenko, O ;
Serga, V ;
Jansone, A .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2004, 34 (01) :103-109
[7]   ELECTROPHORETIC TRANSPORT OF SOLUTES IN AQUEOUS 2-PHASE SYSTEMS [J].
LEVINE, ML ;
BIER, M .
ELECTROPHORESIS, 1990, 11 (08) :605-611
[8]   Two-phase electro-electrodialysis for recovery and concentration of citric acid [J].
Luo, GS ;
Shan, XY ;
Qi, X ;
Lu, YC .
SEPARATION AND PURIFICATION TECHNOLOGY, 2004, 38 (03) :265-271
[9]   Two-phase electro-electrodialysis with an emulsion as anolyte [J].
Luo, GS ;
Liu, JG ;
Lu, YC ;
Pan, S ;
Wang, JD .
SEPARATION SCIENCE AND TECHNOLOGY, 2004, 39 (06) :1267-1278
[10]   Concentration of formic acid solution by electro-electrodialysis [J].
Luo, GS ;
Wu, FY .
SEPARATION SCIENCE AND TECHNOLOGY, 2000, 35 (15) :2485-2496