Microfluidics and Miniaturization
A new gravity-driven microfluidic-based electrochemical assay coupled to magnetic beads for nucleic acid detection
Article first published online: 21 OCT 2010
DOI: 10.1002/elps.201000288
Copyright © 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

ELECTROPHORESIS
Special Issue: Miniaturization
Volume 31, Issue 22, pages 3727–3736, November 2010
Additional Information
How to Cite
Laschi, S., Miranda-Castro, R., González-Fernández, E., Palchetti, I., Reymond, F., Rossier, J. S. and Marrazza, G. (2010), A new gravity-driven microfluidic-based electrochemical assay coupled to magnetic beads for nucleic acid detection. ELECTROPHORESIS, 31: 3727–3736. doi: 10.1002/elps.201000288
Publication History
- Issue published online: 15 NOV 2010
- Article first published online: 21 OCT 2010
- Manuscript Accepted: 17 JUL 2010
- Manuscript Revised: 12 JUL 2010
- Manuscript Received: 24 MAY 2010
Funded by
- Spanish Government, projects FICYT. Grant Numbers: IB08-087, CTQ 2008-02429
- European Social Fund (ESF)
- Spanish Ministerio de Educación y Ciencia
- Abstract
- Article
- References
- Cited By
Keywords:
- Biosensors;
- Hybridisation;
- Magnetic particles;
- Microfluidics;
- Nucleic acids
Abstract
In this work, the characterisation and the optimisation of hybridisation assays based on a novel, rapid and sensitive micro-analytical, gravity-driven, flow device is reported. This device combines a special chip containing eight polymer microchannels, with a portable, computer-controlled instrument. The device is used as a platform for affinity experiments using oligonucleotide-modified paramagnetic particles. In our approach, both hybridisation and labelling events are performed on streptavidin-coated paramagnetic microparticles functionalised with a biotinylated capture probe. Modified particles, introduced in the microchannel inlet of the chip, accumulate near the electrode surface by virtue of a magnetic holder. After hybridisation with the complementary sequence, the hybrid is labelled with an alkaline phosphatase conjugate. The electrochemical substrate for alkaline phosphatase revelation is p-aminophenyl phosphate. Solutions and reagents are sequentially passed through the microchannels, until enzyme substrate is added for in situ signal detection. Upon readout, the magnet array is flipped away, beads are removed by addition of regeneration buffer, and the so-regenerated chip is ready for further analysis. This protocol has been applied to the analytical detection of specific DNA sequences of Legionella pneumophila, with an RSD=8.5% and a detection limit of 0.33 nM.

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