Surface plasmon resonance sensor for domoic acid based on grafted imprinted polymer
2004 (English)In: Biosensors & bioelectronics, ISSN 0956-5663, E-ISSN 1873-4235, Vol. 20, no 2, 145-152 p.Article in journal (Refereed) Published
A molecularly imprinted polymer (MIP) film for domoic acid (DA) was synthesised by direct photo-grafting onto a gold chip suitable for a surface plasmon resonance (SPR) based bioanalytical instrument system, the BlAcore 3000(TM). The gold surface was first functionalised with a self-assembled monolayer of 2-mercaptoethylamine and subsequent carbodiimide chemistry was performed for covalent attachment of the photoinitiator, 4,4-azobis(cyanovaleric acid). This ensured that the formation of the MIP thin film, comprising 2-(diethyl amino) ethyl methacrylate as functional monomer and ethylene glycol dimethacrylate as cross-linker, occurred only at the surface level. Optimisation and control over the grafting procedure were achieved using contact angle measurements and atomic force microscope (AFM) imaging. The surface grafting resulted in the formation of thin and homogeneous MIP film with thickness of 40 nm. A competitive binding assay was performed with free DA and its conjugate with horseradish peroxidase, which was used as a refractive label. The sensor was evaluated for its sensitivity, cross-reactivity, and robustness by using a BlAcore 3000(TM). Likewise, monoclonal antibodies acting as natural receptors for the toxin were studied with the same BlAcore system. Results of a comparison between the artificial and natural receptors are reported. In contrast to monoclonal antibodies, the regeneration of MIP chip did not affect its recognition properties and continuous measurement was possible over a period of at least 2 months. (C) 2004 Elsevier B.V. All rights reserved.
Place, publisher, year, edition, pages
Elsevier Science B.V., Amsterdam. , 2004. Vol. 20, no 2, 145-152 p.
domoic acid; MIP; thin films; SPR; AFM
Engineering and Technology
IdentifiersURN: urn:nbn:se:liu:diva-65196DOI: 10.1016/j.bios.2004.01.032ISI: 000224034400002OAI: oai:DiVA.org:liu-65196DiVA: diva2:395038