Stacking neutral analytes in capillary electrokinetic chromatography with high-salt sample matrixes

被引:59
作者
Palmer, J [1 ]
Landers, JP [1 ]
机构
[1] Univ Virginia, Dept Chem, Charlottesville, VA 22901 USA
关键词
D O I
10.1021/ac0000269
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We recently described a method to stack neutral analytes in electrokinetic chromatography dependent upon using high-salt sample matrixes (Palmer et al, Anal. Chem, 1899, 71, 1679-1687) The use of a high-mobility co-ion in the sample matrix at a higher concentration than the like-charged electrokinetic vector (e.g., charged micelle) in the separation buffer as we previously suggested induces a single-boundary, discontinuous buffer system which subsequently stacks neutral analytes, Under these conditions, it is possible to electrokinetically inject neutral analytes directly from a high-salt sample matrix via electroosmotic now, with stacking initiated simultaneously with injection. The correspondence by Quirino et al, (Anal. Chem., previous paper in this issue) suggests the effects of the high-salt sample matrix on stacking of micelles is obviated by a destacking of the micelle zone as it exits the sample zone. They reevaluate the high-salt stacking mode in terms of the gamma function. Based on the present data, it is our interpretation that the stacking efficiency is not accurately represented by the gamma function and that neither micelle zone nor neutral analyte destacking occurs under conditions we previously described. Low stacking efficiency when low-conductivity sample matrixes are used indicates that the high-salt stacking effect cannot be explained simply as a function of the k value of an analyte/micelle system.
引用
收藏
页码:1941 / 1943
页数:3
相关论文
共 5 条
[1]   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
[2]   NONUNIFORM ELECTRICAL-FIELD EFFECT CAUSED BY DIFFERENT CONCENTRATIONS OF ELECTROLYTE IN CAPILLARY ZONE ELECTROPHORESIS [J].
HUANG, XH ;
OHMS, JI .
JOURNAL OF CHROMATOGRAPHY, 1990, 516 (01) :233-240
[3]   A DISCUSSION OF THE CONSTRAINTS WHICH LEAD TO STEADY-STATE ELECTROPHORETIC BOUNDARIES [J].
MOSHER, RA ;
THORMANN, W .
ELECTROPHORESIS, 1985, 6 (10) :477-482
[4]   A universal concept for stacking neutral analytes in micellar capillary electrophoresis [J].
Palmer, J ;
Munro, NJ ;
Landers, JP .
ANALYTICAL CHEMISTRY, 1999, 71 (09) :1679-1687
[5]   Exceeding 5000-fold concentration of dilute analytes in micellar electrokinetic chromatography [J].
Quirino, JP ;
Terabe, S .
SCIENCE, 1998, 282 (5388) :465-468