Heart-cutting 2D-CE with on-line preconcentration for the chiral analysis of native amino acids

被引:32
作者
Anouti, Suzanne [1 ]
Vandenabeele-Trambouze, Odile [1 ]
Cottet, Herve [1 ]
机构
[1] Univ Montpellier, Inst Biomol Max Mousseron, F-34059 Montpellier, France
关键词
Contactless conductivity detection; Heart-cutting 2D separations; Moving chemical reaction boundary; Native amino acids; On-line sample preconcentration; CHEMICAL-REACTION BOUNDARY; CAPILLARY-ZONE-ELECTROPHORESIS; SAMPLE STACKING; SEPARATION; ANALYTES;
D O I
10.1002/elps.200900639
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The use of transient moving chemical reaction boundary (tMCRB) was investigated for the on-line preconcentration of native amino acids in heart-cutting 2D-CE with multiple detection points using contactless conductivity detection The tMCRB focusing was obtained by using ammonium formate (pH 8 56) as sample matrix and acetic acid (pH 2.3) as a BCE in the first dimension of the heart-cutting 2D-CE Different experimental parameters such as the injected volume and the concentration in ammonium formate were optimized for improving the sensitivity of detection A stacked fraction from the first dimension was selected, Isolated in the capillary, and then separated in the second dimension in the presence of a chiral selector ((+)-(18-crown-6)-2,3,11,12-tetra-carboxylic acid). This on-line tMCRB preconcentration coupled with heart-cutting 2D-CE was applied with success to the chiral separation of D,L-phenylalanine, and h,L-threonine in a mixture of 22 native ammo acids. The sample mixture was diluted in 0 8 M of ammonium formate, and injected at a concentration of 2 5 mu M for each enantiomer with a volume corresponding to 10% of the total capillary volume An LOD (S/N = 3) of 2 mu M was determined for L-threonine
引用
收藏
页码:1029 / 1035
页数:7
相关论文
共 36 条
[21]   Stacking and quantitative analysis of lovastatin in urine samples by the transient moving chemical reaction boundary method in capillary electrophoresis [J].
Li, Min ;
Fan, Liu-Yin ;
Zhang, Wei ;
Cao, Cheng-Xi .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2007, 387 (08) :2719-2725
[22]   On-line sample concentration techniques in capillary electrophoresis: Velocity gradient techniques and sample concentration techniques for biomolecules [J].
Lin, CH ;
Kaneta, T .
ELECTROPHORESIS, 2004, 25 (23-24) :4058-4073
[23]   Recent advances in amino acid analysis by capillary electrophoresis [J].
Poinsot, V ;
Bayle, C ;
Couderc, F .
ELECTROPHORESIS, 2003, 24 (22-23) :4047-4062
[24]  
Prata C, 2001, ELECTROPHORESIS, V22, P4129, DOI 10.1002/1522-2683(200111)22:19<4129::AID-ELPS4129>3.0.CO
[25]  
2-I
[26]   Exceeding 5000-fold concentration of dilute analytes in micellar electrokinetic chromatography [J].
Quirino, JP ;
Terabe, S .
SCIENCE, 1998, 282 (5388) :465-468
[27]   Determination of proteinogenic amino acids in human plasma by capillary electrophoresis with contactless conductivity detection [J].
Samcová, E ;
Tuma, P .
ELECTROANALYSIS, 2006, 18 (02) :152-157
[28]  
Shihabi ZK, 2002, ELECTROPHORESIS, V23, P1612, DOI 10.1002/1522-2683(200206)23:11<1612::AID-ELPS1612>3.0.CO
[29]  
2-3
[30]   On-line sample preconcentration in capillary electrophoresis Fundamentals and applications [J].
Simpson, Steven L., Jr. ;
Quirino, Joselito P. ;
Terabe, Shigeru .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1184 (1-2) :504-541