High-sensitive capillary zone electrophoresis analysis by electrokinetic injection with transient isotachophoretic preconcentration: Electrokinetic supercharging

被引:123
作者
Hirokawa, T
Okamoto, H
Gas, B
机构
[1] Hiroshima Univ, Grad Sch Engn, Dept Appl Chem, Higashihiroshima 7398527, Japan
[2] Charles Univ Prague, Fac Sci, Dept Phys Chem, Prague, Czech Republic
关键词
capillary zone electrophoresis; computer simulation; electrokinetic supercharging; transient isotachophoresis preconcentration;
D O I
10.1002/elps.200390058
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The principle of an on-line preconcentration method,for capillary zone electrophoresis (CZE) named electrokinetic supercharging (EKS), is described and based on computer 2 simulation the preconcentration behavior of the method is discussed. EKS is an electrokinetic injection method with transient isotachophoretic process, is a powerful preconcentration technique for the analysis of dilute samples. After filling the separation capillary with supporting electrolyte, an appropriate amount of a leading electrolyte was filled and the electrokinetic injection was started. After a while, terminating electrolyte was filled subsequently and migration current was applied. This procedure enabled the introduction of a large amount of sample components from a dilute sample without deteriorating separation. Computer simulation of the electrokinetic injection revealed that EKS was effective for the preconcentration of analytes with wide mobility ranges by proper choice of transient isotachophoresis (ITP) system and electroosmotic flow (EOF) should be suppressed to increase injectable amount of analytes under constant voltage mode. A test mixture of rare-earth chlorides was used to demonstrate the uses of EKS-CZE. When a 100 muL sample was used, the low limit of detectable concentration was 0.3 mug/L (1.8 nm for Er), which was comparable or even better than that of ion chromatography and inductively coupled plasma-atomic emission spectrometry (ICP-AES).
引用
收藏
页码:498 / 504
页数:7
相关论文
共 20 条
[1]   ISOTACHOPHORESIS WITH 2 LEADING IONS AND MIGRATION BEHAVIOR IN CAPILLARY ZONE ELECTROPHORESIS .2. MIGRATION BEHAVIOR IN CAPILLARY ZONE ELECTROPHORESIS [J].
BECKERS, JL ;
EVERAERTS, FM .
JOURNAL OF CHROMATOGRAPHY, 1990, 508 (01) :19-26
[2]  
Beckers JL, 2000, ELECTROPHORESIS, V21, P2747, DOI 10.1002/1522-2683(20000801)21:14<2747::AID-ELPS2747>3.0.CO
[3]  
2-Z
[4]   ON-COLUMN SAMPLE CONCENTRATION USING FIELD AMPLIFICATION IN CZE [J].
CHIEN, RL ;
BURGI, DS .
ANALYTICAL CHEMISTRY, 1992, 64 (08) :A489-A496
[5]   ON-COLUMN TRANSIENT AND COUPLED COLUMN ISOTACHOPHORETIC PRECONCENTRATION OF PROTEIN SAMPLES IN CAPILLARY ZONE ELECTROPHORESIS [J].
FORET, F ;
SZOKO, E ;
KARGER, BL .
JOURNAL OF CHROMATOGRAPHY, 1992, 608 (1-2) :3-12
[6]   SAMPLE SELF-STACKING IN ZONE ELECTROPHORESIS - THEORETICAL DESCRIPTION OF THE ZONE ELECTROPHORETIC SEPARATION OF MINOR COMPOUNDS IN THE PRESENCE OF BULK AMOUNTS OF A SAMPLE COMPONENT WITH HIGH MOBILITY AND LIKE CHARGE [J].
GEBAUER, P ;
THORMANN, W ;
BOCEK, P .
JOURNAL OF CHROMATOGRAPHY, 1992, 608 (1-2) :47-57
[7]   SAMPLE SELF-STACKING AND SAMPLE STACKING IN ZONE ELECTROPHORESIS WITH MAJOR SAMPLE COMPONENTS OF LIKE CHARGE - GENERAL-MODEL AND SCHEME OF POSSIBLE MODES [J].
GEBAUER, P ;
THORMANN, W ;
BOCEK, P .
ELECTROPHORESIS, 1995, 16 (11) :2039-2050
[8]  
Hirokawa T, 2001, ELECTROPHORESIS, V22, P3483, DOI 10.1002/1522-2683(200109)22:16<3483::AID-ELPS3483>3.0.CO
[9]  
2-O
[10]  
Hirokawa T, 2001, ELECTROPHORESIS, V22, P3444, DOI 10.1002/1522-2683(200109)22:16<3444::AID-ELPS3444>3.0.CO