Development of sandwich HPLC microcolumns for analyte adsorption on the millisecond time scale

被引:18
作者
Clarke, W [1 ]
Hage, DS [1 ]
机构
[1] Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
关键词
D O I
10.1021/ac000870z
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new class of columns is reported that uses only microgram quantities of active support and that provides for the retention of biological compounds and other analytes on the millisecond time scale. This was accomplished by packing standard HPLC supports into layers as;small as 60 mum in length and using only 90 mug of support material. This provided columns with effective residence times in the millisecond time range when routine HPLC flow rates and pressures were used. The retention of analytes by such columns was examined under both adsorption- and diffusion-limited conditions. The RPLC adsorption of hemoglobin (a system with diffusion-limited retention) was found to give 95% binding in as little as 4 ms. The adsorption of fluorescein by an anti-fluorescein antibody column (an adsorption-limited system) gave 95% retention in 100-120 ms. One application examined for these columns was their use in a chromatographic-based competitive binding immunoassay. This used bovine serum albumin (BSA) as the model analyte and fluorescein-labelled BSA was used for detection. The resulting approach had a contact time of 180 ms between the sample and an anti-BSA immunoaffinity microcolumn and provided a signal within 5-25 s after sample injection. The columns developed in this work should also be useful in other situations that involve a small amount of a stationary phase or that require short column residence times.
引用
收藏
页码:1366 / 1373
页数:8
相关论文
共 37 条
[1]   FLOW-THROUGH PARTICLES FOR THE HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHIC SEPARATION OF BIOMOLECULES - PERFUSION CHROMATOGRAPHY [J].
AFEYAN, NB ;
GORDON, NF ;
MAZSAROFF, I ;
VARADY, L ;
FULTON, SP ;
YANG, YB ;
REGNIER, FE .
JOURNAL OF CHROMATOGRAPHY, 1990, 519 (01) :1-29
[2]   BOVINE SERUM-ALBUMIN ADSORPTION AND DESORPTION RATES ON SOLID-SURFACES WITH VARYING SURFACE-PROPERTIES [J].
CHENG, YL ;
DARST, SA ;
ROBERTSON, CR .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1987, 118 (01) :212-223
[3]   Antibody immobilization to high-performance liquid chromatography supports - Characterization of maximum loading capacity for intact immunoglobulin G and Fab fragments [J].
Clarke, W ;
Beckwith, JD ;
Jackson, A ;
Reynolds, B ;
Karle, EM ;
Hage, DS .
JOURNAL OF CHROMATOGRAPHY A, 2000, 888 (1-2) :13-22
[4]   RAPID HETEROGENEOUS COMPETITIVE ELECTROCHEMICAL IMMUNOASSAY FOR IGG IN THE PICOMOLE RANGE [J].
DEALWIS, U ;
WILSON, GS .
ANALYTICAL CHEMISTRY, 1987, 59 (23) :2786-2789
[5]   Investigation of anion-exchange and immunoaffinity particle-loaded membranes for the isolation of charged organic analytes from water [J].
Dombrowski, TR ;
Wilson, GS ;
Thurman, EM .
ANALYTICAL CHEMISTRY, 1998, 70 (09) :1969-1978
[6]   INVESTIGATION OF THE KINETIC-PROPERTIES OF PARTICLE-LOADED MEMBRANES FOR SOLID-PHASE EXTRACTION BY FORCED FLOW PLANAR CHROMATOGRAPHY [J].
FERNANDO, WPN ;
LARRIVEE, ML ;
POOLE, CF .
ANALYTICAL CHEMISTRY, 1993, 65 (05) :588-595
[7]   Development of a theoretical model for chromatographic-based competitive binding immunoassays with simultaneous injection of sample and label [J].
Hage, DS ;
Thomas, DH ;
Chowdhuri, AR ;
Clarke, W .
ANALYTICAL CHEMISTRY, 1999, 71 (15) :2965-2975
[8]   SPLIT-PEAK AFFINITY CHROMATOGRAPHIC STUDIES OF THE IMMOBILIZATION-DEPENDENT ADSORPTION-KINETICS OF PROTEIN-A [J].
HAGE, DS ;
WALTERS, RR ;
HETHCOTE, HW .
ANALYTICAL CHEMISTRY, 1986, 58 (02) :274-279
[9]   HIGH-PERFORMANCE IMMUNOAFFINITY CHROMATOGRAPHY AND CHEMILUMINESCENT DETECTION IN THE AUTOMATION OF A PARATHYROID-HORMONE SANDWICH IMMUNOASSAY [J].
HAGE, DS ;
KAO, PC .
ANALYTICAL CHEMISTRY, 1991, 63 (06) :586-595
[10]   THEORY OF A SEQUENTIAL ADDITION COMPETITIVE-BINDING IMMUNOASSAY BASED ON HIGH-PERFORMANCE IMMUNOAFFINITY CHROMATOGRAPHY [J].
HAGE, DS ;
THOMAS, DH ;
BECK, MS .
ANALYTICAL CHEMISTRY, 1993, 65 (11) :1622-1630