Performance control strategies of one-step immuno-chromatographic assay system for Salmonella typhimurium

被引:18
作者
Paek, SH [1 ]
Lee, CW
Yook, SH
Kwon, OH
Park, YN
机构
[1] Korea Univ, Grad Sch Biotechnol, Seoul 136701, South Korea
[2] Doosan Training & Technol Ctr, Prod Dev Grp, Yongin 449840, Kyonggi Do, South Korea
[3] Yeondong Pharmaceut Corp, R&D Ctr, Yongin 449830, Kyonggi Do, South Korea
关键词
immuno-chromatographic assay; sensitivity; signal-to-noise ratio; optimization;
D O I
10.1080/00032719908542824
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
To attain optimum sensitivity (defined as the minimum detection limit) in an assay, an immuno-chromatographic assay system for Salmonella typhimurium (see Figure 1) were arranged at three different stages of: preparation of the respective system components, integration of the analytical parts, and trial test after fabrication. Primary approaches focused on the manufacture of two major components. In preparing the gold-antibody conjugate as tracer, important steps that may eventually affect the system performance were an appropriate blocking of residual surfaces of gold particles after conjugation and the subsequent separation of excess antibody used. The immobilized antibody on nitrocellulose membrane brought about variable results according to the storage time of the antibody solution before addition and also incubation conditions of the added solution onto the membrane. In the second stage, analytical elements were adapted for the construction of the system. Chemical composition of a medium used for elution as well as for the component production significantly altered the signal intensity. The concentrations of the both antibodies (conjugated and immobilized) as well as the time for antigen-antibody reaction (reflected by the volume of sample absorption pad) were the critical parameters that regulated the relative magnitude of the signal to the background obtained at zero dose of analyte. As the final step of control, the system fabricated was adjusted to a signal-to-noise ratio by two methods. Thermal treatment of the NC membrane with the immobilized antibody was effective to eliminate the background signal, while a detergent addition into the sample solution could be used to increase the signal density within a limited concentration range of analyte. Under the conditions optimized for sensitivity, the chromatographic system detected 2.5x10(5) cells/mL, or higher after an assay time of approximately 15 min.
引用
收藏
页码:335 / 360
页数:26
相关论文
共 20 条
[1]  
ALBRECHT RM, 1993, IMMUNOCYTOCHEMISTRY, P151
[2]  
Baudhuin P., 1989, COLLOIDAL GOLD, P1
[3]   LATEX-BASED THIN-LAYER IMMUNOAFFINITY CHROMATOGRAPHY FOR QUANTITATION OF PROTEIN ANALYTES [J].
BIRNBAUM, S ;
UDEN, C ;
MAGNUSSON, CGM ;
NILSSON, S .
ANALYTICAL BIOCHEMISTRY, 1992, 206 (01) :168-171
[4]   Immunoelectrochemical assays for bacteria: Use of epifluorescence microscopy and rapid-scan electrochemical techniques in development of an assay for Salmonella [J].
Brewster, JD ;
Gehring, AG ;
Mazenko, RS ;
VanHouten, LJ ;
Crawford, CJ .
ANALYTICAL CHEMISTRY, 1996, 68 (23) :4153-4159
[5]  
CHARD T, 1987, INTRO RADIOIMMUNOASS, P274
[6]  
CHEN R, 1987, CLIN CHEM, V33, P1521
[7]   REMOVAL OF FALSE-POSITIVE REACTIONS FROM PLASMA IN AN ENZYME-IMMUNOASSAY FOR BOVINE INTERFERON-GAMMA [J].
JONES, SL ;
COX, JC ;
SHEPHERD, JM ;
ROTHEL, JS ;
WOOD, PR ;
RADFORD, AJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1992, 155 (02) :233-240
[8]  
KENNA JG, 1985, J IMMUNOL METH
[9]  
KUEN LS, 1993, J IMMUNOL METHODS, V163, P277
[10]   Affinity immunosensor for milk progesterone: Identification of critical parameters [J].
Laitinen, MPA ;
Vuento, M .
BIOSENSORS & BIOELECTRONICS, 1996, 11 (12) :1207-1214