A novel biochip technology for detection of explosives -: TNT:: Synthesis, characterisation and application

被引:56
作者
Larsson, A
Angbrant, J
Ekeroth, J
Månsson, P
Liedberg, B [1 ]
机构
[1] Linkoping Univ, Div Sensor Sci & Mol Phys, IFM, SE-58183 Linkoping, Sweden
[2] Linkoping Univ, Div Chem, IFM, SE-58183 Linkoping, Sweden
[3] Biosensor Applicat Sweden AB, SE-17446 Sundbyberg, Sweden
关键词
explosives; competitive immunoassay; self-assembled monolayers; quartz crystal microbalance; surface plasmon resonance;
D O I
10.1016/j.snb.2005.07.025
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This contribution describes the synthesis, characterisation and evaluation of a novel biochip technology for the detection of the explosive substance 2,4,6-trinitrotoluene (TNT). Two types of thiols are self-assembled to produce the biochip on gold, namely oligo(ethylene glycol) (OEG)-alkyl thiols terminated with a hydroxyl group and a TNT-analogue (2,4-dinitrobenzene), respectively. Three different TNT-analogues are mixed in various proportions with hydroxyl-terminated OEG-thiols to obtain highly selective and sensitive biochips with a low non-specific binding. The produced self-assembled monolayers (SAMs) are thoroughly characterised with null ellipsometry, contact angle goniometry, infrared reflection absorption spectroscopy (IRAs) and X-ray photoelectron spectroscopy (XPS) and they all meet high standards in terms of molecular conformation, packing and orientation. The biochip, is designed to function as a platform for a competitive label-free immunoassay and two real-time transducers-surface plasmon resonance (SPR) and quartz crystal microbalance (QCM)-are used to monitor the dissociation of on-line immobilised monoclonal antibodies produced against TNT. The three TNT-analogues are all potential candidates for the development of a functional biochip, though one of them displayed superior properties in terms of shorter recovery/stabilisation time after antibody immobilisation and a better response/loading capacity ratio. This is particularly evident when using low antigen (TNT-analogue) content in the mixed SAM. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:730 / 748
页数:19
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