Automated amplified flow immunoassay for cocaine

被引:55
作者
Bauer, CG
Eremenko, AV
Kühn, A
Kürzinger, K
Makower, A
Scheller, FW
机构
[1] Univ Potsdam, Inst Biochem & Mol Physiol, D-14943 Luckenwalde, Germany
[2] Boehringer Mannheim GmbH, Diagnost Lab, D-82377 Penzberg, Germany
关键词
D O I
10.1021/ac971388s
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An amplified now immunoassay (AFIA) was developed for cocaine, which combines a noncompetitive immunoenzymometric assay (IEMA) with an on-line detection of the enzyme label alkaline phosphatase (ALP) by a substratere-cycling biosensor. In the IEMA, the analyte cocaine first binds to a labeled polyclonal anti-cocaine antibody. Then, the excess labeled antibody is separated on an affinity column that contains a perfusion chromatography carrier modified by immobilized cocaine. The unbound complexes of the analyte cocaine with the ALP-labeled antibody are detected postcolumn, The detector senses phenol produced by ALP from phenyl phosphate. As detector, an amperometric substrate-recycling biosensor was used, which consists of a Clark-type oxygen electrode covered by tyrosinase and pyrroloquinoline quinone-dependent glucose dehydrogenase. The lower limit of detection is 380 pM (38 fmol) for cocaine. The sampling rate is 26/h. Cocaine could be detected from "real samples" with an imprecision of +/-10% (it = 3) and with a recovery of 49 +/- 3% for various concentrations. AFIA is generally important as a new approach for the fast detection of picomolar concentrations of haptens.
引用
收藏
页码:4624 / 4630
页数:7
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