Electrokinetic stacking injection of neutral analytes under continuous conductivity conditions

被引:42
作者
Palmer, J
Burgi, DS
Landers, JP
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22901 USA
[2] Univ Virginia, Dept Pathol, Charlottesville, VA 22901 USA
关键词
D O I
10.1021/ac010522c
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In capillary electrokinetic chromatography, neutral analytes can be injected by electroosmotic flow directly from a sample matrix into a separation buffer containing an electrokinetic vector with an opposite mobility. Analytes are injected at the velocity of electroosmotic flow but are retained at the interface of the sample matrix co-ion and separation buffer micelle zones as analyte/micelle complexes. A simple electrokinetic chromatography system containing sodium dodecyl sulfate as the micellar agent with borate as the buffering electrolyte included in the separation buffer and in the sample matrix to provide continuous conductivity was investigated. Concentrations of the micelle, methanol, and borate in the separation buffer were explored to increase maximum injection length of neutral analytes. Reducing the analyte velocity in the separation buffer without substantially decreasing the velocity of the analyte during injection from the sample vial allowed greatly extended sample plug injection lengths. It is presently possible to inject sample solvent volumes equivalent to similar to7 effective capillary lengths (180 cm) with a 50-mum-i.d. capillary (24.5 cm effective capillary length), total volume of sample injection similar to3.5 muL Equations describing the injection process and maximum injection lengths for this mode of stacking in electrokinetic capillary chromatography are introduced. The result of this work leads to a postulated generalization of electrokinetic stacking injection maximums for electrophoretic processes, and the concept of orthogonal analyte stacking/ injection systems is discussed.
引用
收藏
页码:632 / 638
页数:7
相关论文
共 15 条
[1]  
Beckers JL, 2000, ELECTROPHORESIS, V21, P2747, DOI 10.1002/1522-2683(20000801)21:14<2747::AID-ELPS2747>3.0.CO
[2]  
2-Z
[3]   OPTIMIZATION IN SAMPLE STACKING FOR HIGH-PERFORMANCE CAPILLARY ELECTROPHORESIS [J].
BURGI, DS ;
CHIEN, RL .
ANALYTICAL CHEMISTRY, 1991, 63 (18) :2042-2047
[4]   EFFECT OF ORGANIC MODIFIER CONCENTRATIONS ON ELECTROKINETIC MIGRATIONS IN MICELLAR ELECTROKINETIC CHROMATOGRAPHY [J].
CHEN, N ;
TERABE, S ;
NAKAGAWA, T .
ELECTROPHORESIS, 1995, 16 (08) :1457-1462
[5]   EFFECTS OF ORGANIC MOBILE PHASE MODIFIERS IN MICELLAR ELECTROKINETIC CAPILLARY CHROMATOGRAPHY [J].
GORSE, J ;
BALCHUNAS, AT ;
SWAILE, DF ;
SEPANIAK, MJ .
JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY & CHROMATOGRAPHY COMMUNICATIONS, 1988, 11 (08) :554-559
[6]  
HJERTON S, 1990, ELECTROPHORESIS, V11, P685
[7]  
HUANG X, 1988, ANAL CHEM, V60, P377
[8]   ZONE ELECTROPHORESIS IN OPEN-TUBULAR GLASS-CAPILLARIES [J].
JORGENSON, JW ;
LUKACS, KD .
ANALYTICAL CHEMISTRY, 1981, 53 (08) :1298-1302
[9]   Charged chelate capillary electrophoresis of endogenous corticosteroids [J].
Palmer, J ;
Atkinson, S ;
Yoshida, WY ;
Stalcup, AM ;
Landers, JP .
ELECTROPHORESIS, 1998, 19 (16-17) :3045-3051
[10]   Stacking neutral analytes in capillary electrokinetic chromatography with high-salt sample matrixes [J].
Palmer, J ;
Landers, JP .
ANALYTICAL CHEMISTRY, 2000, 72 (08) :1941-1943