Liquid-phase microextraction combined with capillary electrophoresis, a promising tool for the determination of chiral drugs in biological matrices

被引:86
作者
Andersen, S [1 ]
Halvorsen, TG [1 ]
Pedersen-Bjergaard, S [1 ]
Rasmussen, KE [1 ]
机构
[1] Univ Oslo, Sch Pharm, N-0316 Oslo, Norway
关键词
liquid-phase microextraction; extraction methods; enantiomer separations; hollow fibres; antidepressants; mianserin;
D O I
10.1016/S0021-9673(02)00223-6
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A disposable device for liquid-phase microextraction (LPME) based on porous polypropylene hollow fibres has recently been introduced. In the present paper, LPME was combined with capillary electrophoresis (CE) and the combination was for the first time evaluated for chiral determination of drugs in biological matrices. The chiral antidepressant drug mianserin was selected as model compound. The mianserin enantiomers were extracted from 0.5 ml of plasma added internal standard and made alkaline with 0.25 ml of 2 M NaOH. The unionised analytes were extracted into di-n-hexyl ether impregnated in the pores of the hollow fibre, and into an acidic solution inside the hollow fibre. This resulted in a three-phase system where the extracts were aqueous, and hence directly compatible with the CE system. Efficient sample clean-up was seen and the extraction recovery was 80% for both enantiomers. Discrimination between the enantiomers in the extraction system was not observed. The limit of quantitation (S/N=10; 12.5 ng/ml for both enantiomers) and the limit of detection (S/N=3; 4 ng/ml for both enantiomers) were below the therapeutic range for mianserin. The method was validated and successfully applied to determine R- and S-mianserin in plasma samples from seven patients treated with mianserin, indicating that LPME-CE is a promising combination for analysis of racemic drugs present in low concentrations in biological matrices. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:303 / 312
页数:10
相关论文
共 44 条
[1]   Enantiomer separation of drugs by capillary electromigration techniques [J].
Blaschke, G ;
Chankvetadze, B .
JOURNAL OF CHROMATOGRAPHY A, 2000, 875 (1-2) :3-25
[2]   MIANSERIN - REVIEW OF ITS PHARMACOLOGICAL PROPERTIES AND THERAPEUTIC EFFICACY IN DEPRESSIVE-ILLNESS [J].
BROGDEN, RN ;
HEEL, RC ;
SPEIGHT, TM ;
AVERY, GS .
DRUGS, 1978, 16 (04) :273-301
[3]   Recent trends in enantioseparations using capillary electromigration techniques [J].
Chankvetadze, B .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 1999, 18 (07) :485-498
[4]   Enantioseparations in capillary electromigration techniques: recent developments and future trends [J].
Chankvetadze, B ;
Blaschke, G .
JOURNAL OF CHROMATOGRAPHY A, 2001, 906 (1-2) :309-363
[5]   STEREOSPECIFIC REVERSAL OF STRESS-INDUCED ANHEDONIA BY MIANSERIN AND ITS (+)-ENANTIOMER [J].
CHEETA, S ;
BROEKKAMP, C ;
WILLNER, P .
PSYCHOPHARMACOLOGY, 1994, 116 (04) :523-528
[6]   STEREOSELECTIVE DISPOSITION OF MIANSERIN IS RELATED TO DEBRISOQUIN HYDROXYLATION POLYMORPHISM [J].
DAHL, ML ;
TYBRING, G ;
ELWIN, CE ;
ALM, C ;
ANDREASSON, K ;
GYLLENPALM, M ;
BERTILSSON, L .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1994, 56 (02) :176-183
[7]   PLASMA-CONCENTRATIONS OF MIANSERIN AFTER SINGLE DOSE AND AT STEADY-STATE IN DEPRESSED ELDERLY PATIENTS [J].
DAWLING, S ;
FORD, S ;
ARIYANAYAGAM, P ;
ONEAL, H ;
LEWIS, RR .
CLINICAL PHARMACOKINETICS, 1987, 12 (01) :73-78
[8]   DETERMINATION OF THE ENANTIOMERS OF MIANSERIN, DESMETHYLMIANSERIN, AND 8-HYDROXYMIANSERIN IN THE PLASMA AND URINE OF MIANSERIN-TREATED PATIENTS [J].
EAP, CB ;
POWELL, K ;
CAMPUSSOUCHE, D ;
MONNEY, C ;
BAETTIG, D ;
TAESCHNER, W ;
BAUMANN, P .
CHIRALITY, 1994, 6 (07) :555-563
[9]   Determination of the enantiomers of mianserin and its metabolites in plasma by capillary electrophoresis after liquid-liquid extraction and on-column sample preconcentration [J].
Eap, CB ;
Powell, K ;
Baumann, P .
JOURNAL OF CHROMATOGRAPHIC SCIENCE, 1997, 35 (07) :315-320
[10]   Enantioselective determination by capillary electrophoresis with cyclodextrins as chiral selectors [J].
Fanali, S .
JOURNAL OF CHROMATOGRAPHY A, 2000, 875 (1-2) :89-122