Integration of nanocapillary arrays into microfluidic devices for use as analyte concentrators

被引:52
作者
Zhang, Y [1 ]
Timperman, AT [1 ]
机构
[1] W Virginia Univ, Dept Chem, Morgantown, WV 26506 USA
关键词
D O I
10.1039/b300102d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A nanocapillary array was integrated into a microfluidic device and its ability to concentrate analytes was characterized. Through the application of an electric field across the channel, large molecules were concentrated in front of the nanocapillary array, and a concentrated analyte band was ejected from the channel by reversing the polarity of the electric field. The effects of nanocapillary diameter, analyte charge, analyte concentration, analyte plug length, and analyte relative mobility were investigated. Concentration factors up to 300-fold were measured for fluorescein. By concentrating anionic FITC-labeled peptides, it was demonstrated that the magnitude of the electrophoretic mobility did not have a measurable effect on the concentration factor. Therefore, multiple analytes can be concentrated in front of the same nanocapillary array without adjusting the conditions, provided the analytes have the same net charge. In the presence of an electric field, a charge trapping effect was observed; small anionic molecules can be concentrated in front of nanocapillary array with channel diameters which are orders of magnitude above the molecular weight cut-offs for hydrodynamically driven systems. The concentrating process was found to be very efficient for fluorescein, as no leakage through the nanocapillary array or sorption of fluorescein to the nanocapillary array was observed. Due to their flexibility and efficiency, it is anticipated that nanocapillary arrays will find increased utility in electrokinetically driven microfluidic systems.
引用
收藏
页码:537 / 542
页数:6
相关论文
共 46 条
[1]   Micro total analysis systems. 2. Analytical standard operations and applications [J].
Auroux, PA ;
Iossifidis, D ;
Reyes, DR ;
Manz, A .
ANALYTICAL CHEMISTRY, 2002, 74 (12) :2637-2652
[2]  
Bonneil E, 1999, J Capill Electrophor Microchip Technol, V6, P61
[3]   OPTIMIZATION IN SAMPLE STACKING FOR HIGH-PERFORMANCE CAPILLARY ELECTROPHORESIS [J].
BURGI, DS ;
CHIEN, RL .
ANALYTICAL CHEMISTRY, 1991, 63 (18) :2042-2047
[4]   ON-COLUMN SAMPLE CONCENTRATION USING FIELD AMPLIFICATION IN CZE [J].
CHIEN, RL ;
BURGI, DS .
ANALYTICAL CHEMISTRY, 1992, 64 (08) :A489-A496
[5]   POROUS CERAMIC BED SUPPORTS FOR FUSED-SILICA PACKED CAPILLARY COLUMNS USED IN LIQUID-CHROMATOGRAPHY [J].
CORTES, HJ ;
PFEIFFER, CD ;
RICHTER, BE ;
STEVENS, TS .
JOURNAL OF HIGH RESOLUTION CHROMATOGRAPHY & CHROMATOGRAPHY COMMUNICATIONS, 1987, 10 (08) :446-448
[6]   Protein concentration and enzyme digestion on microbeads for MALDI-TOF peptide mass mapping of proteins from dilute solutions [J].
Doucette, A ;
Craft, D ;
Li, L .
ANALYTICAL CHEMISTRY, 2000, 72 (14) :3355-3362
[7]   GLASS CHIPS FOR HIGH-SPEED CAPILLARY ELECTROPHORESIS SEPARATIONS WITH SUBMICROMETER PLATE HEIGHTS [J].
EFFENHAUSER, CS ;
MANZ, A ;
WIDMER, HM .
ANALYTICAL CHEMISTRY, 1993, 65 (19) :2637-2642
[8]   Identification of proteins by capillary electrophoresis tandem mass spectrometry - Evaluation of an on-line solid-phase extraction device [J].
Figeys, D ;
Ducret, A ;
Aebersold, R .
JOURNAL OF CHROMATOGRAPHY A, 1997, 763 (1-2) :295-306
[9]   Optimization of solid phase microextraction capillary zone electrophoresis mass spectrometry for high sensitivity protein identification [J].
Figeys, D ;
Zhang, Y ;
Aebersold, R .
ELECTROPHORESIS, 1998, 19 (13) :2338-2347
[10]  
FINTSCHENKO Y, 1999, SPIE, P202