Surface plasmon resonance-based trace detection of small molecules by competitive and signal enhancement immunoreaction

被引:26
作者
Aizawa, Hidenobu
Tozuka, Mitsuhiro
Kurosawa, Shigeru
Kobayashi, Koichi
Reddy, Subrayal M.
Higuchi, Masahiro
机构
[1] Natl Inst Adv Ind Sci & Technol, Tsukuba, Ibaraki 3058565, Japan
[2] Musashi Inst Technol, Inst Mat Sci, Tokyo 1588557, Japan
[3] Univ Surrey, Sch Biomed & Mol Sci, Guildford GU2 7XH, Surrey, England
[4] Mie Univ, Fac Engn, Tsu, Mie 5148507, Japan
关键词
surface plasmon resonance (SPR); SPR-immunosensor; 2,4-dinitrophenol (DNP); DNP-protein conjugate; anti-DNP-protein monoclonal antibody; signal enhancement immunoreaction;
D O I
10.1016/j.aca.2007.03.074
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A surface plasmon resonance (SPR)-immunosensor for detection of the low molecular weight compound 2,4-dinitorophenol (DNP) at ultra-low concentration has been developed. The sensor strategy is based on a competitive immunoreaction between DNP and a DNP-protein conjugate, namely DNP-bovine serum albumin conjugate (DNP-BSA). Anti-DNP monoclonal antibody was immobilized on a gold thin-film coated SPR-sensor chip by means of a chemical coupling process. DNP-BSA, on contact with the anti-DNP antibody immobilized SPR-immunosensor chip causes an increase in the resonance angle of the sensor chip. The optimum concentration of immobilized antibody on the SPR-sensor chip is 100 mu g mL(-1). The SPR-immunosensor response for free DNP determination using the competitive immunoreaction had a response time of ca. 15 min. Using this method, DNP could be determined in the concentration range 1 ppt to 1 ppb. The SPR signal for ppt levels of DNP was enhanced by a factor of three by subsequently treating immuno-bound DNP-BSA with a secondary anti-DNP antibody. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:191 / 194
页数:4
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