Issue 5, 2013

Micro-organism extraction from biological samples using DEP forces enhanced by osmotic shock

Abstract

On the road towards efficient diagnostics of infectious diseases, sample preparation is considered as the key step and remains a real technical challenge. Finding new methods for extraction of micro-organisms from a complex biological sample remains a major challenge prior to pathogen detection and analysis. This paper reports a new technique for capturing and isolating micro-organisms from a complex sample. To achieve the segregation of pathogens and blood cells, dielectrophoretic forces applied to bioparticles previously subjected to an osmotic shock are successfully implemented within a dedicated microfluidic device. Our device involves an electrode array of interdigitated electrodes, coated with an insulating layer, to minimize electrochemical reactions with the electrolyte and to enable long-time use. The electric field intensity inside the device is optimized, considering the insulating layer, for a given frequency bandwidth, enabling the separation of bioparticles by dielectrophoretic forces. Our predictions are based on analytical models, consistent with numerical simulations (using COMSOL Multiphysics) and correlated to experimental results. The method and device have been shown to extract different types of micro-organisms spiked in a blood cell sample. We strongly believe that this new separation approach may open the way towards a simple device for pathogen extraction from blood and more generally complex samples, with potential advantages of genericness and simplicity.

Graphical abstract: Micro-organism extraction from biological samples using DEP forces enhanced by osmotic shock

Article information

Article type
Paper
Submitted
08 Oct 2012
Accepted
05 Dec 2012
First published
06 Dec 2012

Lab Chip, 2013,13, 901-909

Micro-organism extraction from biological samples using DEP forces enhanced by osmotic shock

E. Bisceglia, M. Cubizolles, F. Mallard, F. Vinet, O. Français and B. Le Pioufle, Lab Chip, 2013, 13, 901 DOI: 10.1039/C2LC41128H

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