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Electrochemiluminescence (ECL) immunosensor for detection of Francisella tularensis on screen-printed gold electrode array

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Abstract

An electrochemiluminescence (ECL) immunosensor for the rapid detection of the Francisella tularensis pathogen using whole antibodies or antibody fragments as capture biomolecule is described. A sandwich immunoassay was used with either lipopolysaccharide (LPS) or the whole inactivated bacterial cell (LVS) as a target, while Ru(bpy)3 2+-encapsulated silicate nanoparticles were linked to the secondary antibody and used as ECL labels. The assay was performed in a fluidic chip housed in a custom-built black box incorporating electronics, optics and fluidics. The obtained limit of detection for LPS was 0.4 ng/mL, while for the LVS it was 70 and 45 bacteria/mL when the capturing molecule was the whole antibody and the antibody F(ab) fragment, respectively.

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Acknowledgments

This work has been carried out with financial support from the Commission of the European Communities, RTD programme “The lab-free CBRN detection device for the identification of biological pathogens on nucleic acid and immunological level as lab-on-a-chip system applying multisensor technologies”, MultisenseChip [FP7-SEC-2010-1]. The authors thank microfluidic ChipShop (http://www.microfluidic-chipshop.com/) for provision of the microfluidics.

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Correspondence to Anna-Maria Spehar-Délèze or Ciara K. O’Sullivan.

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The authors declare that they have no conflicts of interest.

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Published in the topical collection Analytical Electrochemiluminescence with guest editors Hua Cui, Francesco Paolucci, Neso Sojic, and Guobao Xu.

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Spehar-Délèze, AM., Julich, S., Gransee, R. et al. Electrochemiluminescence (ECL) immunosensor for detection of Francisella tularensis on screen-printed gold electrode array. Anal Bioanal Chem 408, 7147–7153 (2016). https://doi.org/10.1007/s00216-016-9658-x

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  • DOI: https://doi.org/10.1007/s00216-016-9658-x

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