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
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