Separation of neutral substances by non-aqueous capillary electrophoresis through interactions with cationic additives

被引:29
作者
Tjornelund, J [1 ]
Hansen, SH [1 ]
机构
[1] Royal Danish Sch Pharm, Dept Analyt & Pharmaceut Chem, DK-2100 Copenhagen, Denmark
关键词
pharmaceutical analysis; buffer composition; vitamins; parabens; hydroxybenzoates; quaternary ammonium compounds; non-aqueous capillary electrophoresis;
D O I
10.1016/S0021-9673(97)01011-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The electrophoretic behaviour of neutral substances in non-aqueous capillary electrophoresis systems with tetraalkylammonium ions or long-chain trimethylammonium ions accompanied by different counter ions added have been investigated. Separation of neutral substances was only achieved in the highly dipolar aprotic solvents acetonitrile or propylene carbonate. The long-chain trimethylammonium ions were, however, not sufficiently soluble in acetonitrile. Thus, the studies comparing various types of ammonium ions were performed using propylene carbonate. The separation of the test solutes was improved with increasing concentrations of additives in the solvent. The type of ammonium ion as well as the counter ion were found to be important for the size of the separation window obtained. The separation principle was used for the determination of the water insoluble vitamin K-1 as well as the preservatives methylparaben and propylparaben in a pharmaceutical product. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:475 / 482
页数:8
相关论文
共 17 条
[1]   CAPILLARY ELECTROKINETIC CHROMATOGRAPHY WITH A SUSPENSION OF CHROMATOGRAPHIC PARTICLES [J].
BACHMANN, K ;
GOTTLICHER, B ;
HAAG, I ;
HAN, KY ;
HENSEL, W ;
MAINKA, A .
JOURNAL OF CHROMATOGRAPHY A, 1994, 688 (1-2) :283-292
[2]   GRADIENT ELUTION FOR MICELLAR ELECTROKINETIC CAPILLARY CHROMATOGRAPHY [J].
BALCHUNAS, AT ;
SEPANIAK, MJ .
ANALYTICAL CHEMISTRY, 1988, 60 (07) :617-621
[3]   MICELLAR ELECTROKINETIC CAPILLARY CHROMATOGRAPHY OF NEUTRAL SOLUTES WITH MICELLES OF ADJUSTABLE SURFACE-CHARGE DENSITY [J].
CAI, J ;
ELRASSI, Z .
JOURNAL OF CHROMATOGRAPHY, 1992, 608 (1-2) :31-45
[4]   REVERSED-PHASE ION-PAIR HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY OF DRUGS AND RELATED-COMPOUNDS USING UNDERIVATIZED SILICA AS THE STATIONARY PHASE [J].
CROMMEN, J .
JOURNAL OF CHROMATOGRAPHY, 1979, 186 (DEC) :705-724
[5]   ENANTIOSELECTIVE HYDROPHOBIC ENTANGLEMENT OF ENANTIOMERIC SOLUTES WITH CHIRAL FUNCTIONALIZED MICELLES BY ELECTROKINETIC CHROMATOGRAPHY [J].
DOBASHI, A ;
ONO, T ;
HARA, S ;
YAMAGUCHI, J .
JOURNAL OF CHROMATOGRAPHY, 1989, 480 :413-420
[6]   BARE SILICA, DYNAMICALLY MODIFIED WITH LONG-CHAIN QUATERNARY AMMONIUM-IONS - THE TECHNIQUE OF CHOICE FOR MORE REPRODUCIBLE SELECTIVITY IN REVERSED-PHASE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY [J].
HANSEN, SH ;
HELBOE, P ;
THOMSEN, M .
JOURNAL OF CHROMATOGRAPHY, 1991, 544 (1-2) :53-76
[7]   ACID-BASE EQUILIBRIA IN DIPOLAR APROTIC-SOLVENTS [J].
KOLTHOFF, IM .
ANALYTICAL CHEMISTRY, 1974, 46 (13) :1992-2003
[8]   CHIRAL SEPARATIONS BY HOST-GUEST COMPLEXATION WITH CYCLODEXTRIN AND CROWN-ETHER IN CAPILLARY ZONE ELECTROPHORESIS [J].
KUHN, R ;
STOECKLIN, F ;
ERNI, F .
CHROMATOGRAPHIA, 1992, 33 (1-2) :32-36
[10]   Separation of polycyclic aromatic hydrocarbons by nonaqueous capillary electrophoresis using charge-transfer complexation with planar organic cations [J].
Miller, JL ;
Khaledi, MG ;
Shea, D .
ANALYTICAL CHEMISTRY, 1997, 69 (06) :1223-1229