Sample stacking in laboratory-on-a-chip devices

被引:66
作者
Yang, H [1 ]
Chien, RL [1 ]
机构
[1] Caliper Technol Corp, Mt View, CA 94043 USA
关键词
sample stacking; chip technology;
D O I
10.1016/S0021-9673(01)00856-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sample stacking is a very important sample concentration technique. It has been used widely in capillary electrophoresis (CE). There are many different stacking techniques. One of the most popular techniques is called "field-amplified sample stacking" where an electric field discontinuity is set up across a concentration boundary. Charged analytes will then automatically stacked due to velocity changes after they cross the concentration boundary. There are several different strategies to perform sample stacking in microfluidic laboratory-on-a-chip devices. One could simply inject a plug of low concentration buffer containing sample into a channel surrounded by high concentration buffer. The electric field is then applied to stack the sample and move the whole plug into the separation channel. One could also stack the sample in a side channel adjacent to the separation channel. The disadvantage of this sample stacking technique is the difficulty in control of the precise location of stacked sample. We present a new sample stacking technique applied specifically to microfluidic laboratory -on -a-chip devices. Up to hundreds of fold increases in sample concentration can be achieved. We have also combined this stacking with electrophoretic separation in the same device. (C) 2001 Elsevier Science BV All rights reserved.
引用
收藏
页码:155 / 163
页数:9
相关论文
共 15 条
[1]  
[Anonymous], HDB CAPILLARY ELECTR
[2]   FIELD AMPLIFIED SAMPLE INJECTION IN HIGH-PERFORMANCE CAPILLARY ELECTROPHORESIS [J].
CHIEN, RL ;
BURGI, DS .
JOURNAL OF CHROMATOGRAPHY, 1991, 559 (1-2) :141-152
[3]   ELECTROOSMOTIC PROPERTIES AND PEAK BROADENING IN FIELD-AMPLIFIED CAPILLARY ELECTROPHORESIS [J].
CHIEN, RL ;
HELMER, JC .
ANALYTICAL CHEMISTRY, 1991, 63 (14) :1354-1361
[4]   TRACE ANALYSIS OF PROTEINS BY CAPILLARY ZONE ELECTROPHORESIS WITH ON-COLUMN TRANSIENT ISOTACHOPHORETIC PRECONCENTRATION [J].
FORET, F ;
SZOKO, E ;
KARGER, BL .
ELECTROPHORESIS, 1993, 14 (5-6) :417-428
[5]   THE USE OF A CONCENTRATION STEP TO COLLECT URINARY COMPONENTS SEPARATED BY CAPILLARY ELECTROPHORESIS AND FURTHER CHARACTERIZATION OF COLLECTED ANALYTES BY MASS-SPECTROMETRY [J].
GUZMAN, NA ;
TREBILCOCK, MA ;
ADVIS, JP .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1991, 14 (05) :997-1015
[6]   CAPILLARY ELECTROPHORESIS AND SAMPLE INJECTION SYSTEMS INTEGRATED ON A PLANAR GLASS CHIP [J].
HARRISON, DJ ;
MANZ, A ;
FAN, ZH ;
LUDI, H ;
WIDMER, HM .
ANALYTICAL CHEMISTRY, 1992, 64 (17) :1926-1932
[7]  
HARRISON DJ, 1998, MICRO TOTAL ANAL SYS
[8]   MICROCHIP ELECTROPHORESIS WITH SAMPLE STACKING [J].
JACOBSON, SC ;
RAMSEY, JM .
ELECTROPHORESIS, 1995, 16 (04) :481-486
[9]   EFFECTS OF INJECTION SCHEMES AND COLUMN GEOMETRY ON THE PERFORMANCE OF MICROCHIP ELECTROPHORESIS DEVICES [J].
JACOBSON, SC ;
HERGENRODER, R ;
KOUTNY, LB ;
WARMACK, RJ ;
RAMSEY, JM .
ANALYTICAL CHEMISTRY, 1994, 66 (07) :1107-1113
[10]  
KRIVANKOVA L, 1995, J CHROMATOGR A, V716, P35