The development of a non-competitive immunoenzymometric assay of cocaine

被引:27
作者
Eremenko, AV
Bauer, CG
Makower, A
Kanne, B
Baumgarten, H
Scheller, FW
机构
[1] Univ Potsdam, Inst Biochem & Mol Physiol, Dept Anat & Biochem, MDC Mol Med, D-13122 Berlin, Germany
[2] Boehringer Mannheim GmbH, D-82377 Penzberg, Germany
关键词
non-competitive immunoenzymometric assay; cocaine; POROS; 50; OH; perfusion chromatography; biosensor; flow injection;
D O I
10.1016/S0003-2670(97)00590-4
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A non-competitive immunoenzymometric assay (IEMA) of cocaine has been developed. An excess of alkaline phosphatase (ALP) labelled polyclonal antibody (pAb) is added to cocaine in solution. After short-time incubation, the free antibody-ALP conjugate is separated from the cocaine-pAb-ALP complex by passing an affinity column POROS 50 OH derivatized with an immobilized cocaine derivative (benzoylecgonine-1,8-diamino-3,4-dioxaoctane or ecgonine-l,8-diamino-3,4-dioxaoctane). The cocaine-pAb-ALP complex is collected after passing the column. The cocaine concentration is quantified spectrophotometrically by measuring the ALP activity using p-nitrophenyl phosphate as substrate. The analytical response was proportional to the cocaine concentration in the sample with a detection limit of 0.5 nM (0.15 ng ml(-1)) cocaine. The combined approach developed with an amperometric bienzyme electrode, and the potential for on line cocaine monitoring are discussed. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:5 / 13
页数:9
相关论文
共 22 条
[1]  
AFEYAN NB, 1963, SCIENCE, V358, P603
[2]   A SIMPLE METHOD FOR THE ESTIMATION OF AMINO-GROUPS ON INSOLUBLE MATRIX BEADS [J].
ANTONI, G ;
PRESENTINI, R ;
NERI, P .
ANALYTICAL BIOCHEMISTRY, 1983, 129 (01) :60-63
[3]   CELLULOSE BEADS - A WEAK LEAKING AFFINITY SUPPORT [J].
BAESELER, M ;
BOEDEN, HF ;
KOELSCH, R ;
LASCH, J .
JOURNAL OF CHROMATOGRAPHY, 1992, 589 (1-2) :93-100
[4]   Zeptomole-detecting biosensor for alkaline phosphatase in an electrochemical immunoassay for 2,4-dichlorophenoxyacetic acid [J].
Bauer, CG ;
Eremenko, AV ;
EhrentreichForster, E ;
Bier, FF ;
Makower, A ;
Halsall, HB ;
Heineman, WR ;
Scheller, FW .
ANALYTICAL CHEMISTRY, 1996, 68 (15) :2453-2458
[5]   DETERMINATION OF COCAINE IN BIOLOGICAL MATRICES USING REVERSED-PHASE HPLC - APPLICATION TO PLASMA AND BRAIN-TISSUE [J].
BONATE, PL ;
DAVIS, CM ;
SILVERMAN, PB ;
SWANN, A .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1995, 18 (17) :3473-3494
[6]   A NOVEL CARBONOCHLORIDATE FOR ACTIVATION OF SUPPORTS CONTAINING HYDROXYL-GROUPS [J].
BUTTNER, W ;
BECKER, M ;
RUPPRICH, C ;
BOEDEN, HF ;
HENKLEIN, P ;
LOTH, F ;
DAUTZENBERG, H .
BIOTECHNOLOGY AND BIOENGINEERING, 1989, 33 (01) :26-31
[7]   A FIBEROPTIC COCAINE BIOSENSOR [J].
DEVINE, PJ ;
ANIS, NA ;
WRIGHT, J ;
KIM, S ;
ELDEFRAWI, AT ;
ELDEFRAWI, ME .
ANALYTICAL BIOCHEMISTRY, 1995, 227 (01) :216-224
[8]   IN-UTERO EXPOSURE TO COCAINE - A REVIEW [J].
ELLIS, JE ;
BYRD, LD ;
SEXSON, WR ;
PATTERSONBARNETT, CA .
SOUTHERN MEDICAL JOURNAL, 1993, 86 (07) :725-731
[9]  
GOERLACHGRAW A, 1994, TIAFT SOFT JOINT C
[10]  
GUILBAULT GG, 1991, BIOTECHNOL APPL BIOC, V14, P133