Creation of cell aggregates by dielectrophoresis for the in vitro study of electrochemotherapy

International audienc

A reproducible method for μm precision alignment of PDMS microchannels with on-chip electrodes using a mask aligner

This paper describes a reproducible method for μm precision alignment of polydimethylsiloxane (PDMS) microchannels with coplanar electrodes using a conventional mask aligner for lab-on-a-chip applications. It is based on the use of a silicon mold in combination with a PMMA sarcophagus for precise control of the parallelism between the top and bottom surfaces of molded PDMS. The alignment of the fabricated PDMS slab with electrodes patterned on a glass chip is then performed using a conventional mask aligner with a custom-made steel chuck and magnets. This technique allows to bond and align chips with a resolution of less than 2 μm

Performance improvement of a plasmonic sensor using a combination of AC electrokinetic effects

International audienc

Magnetic microfluidic device as a complementary tool for investigating microbial diversity

National audienc

Selective micro-patterning of microbial cells onto micro-magnet arrays for single cell analysis

International audienc

Selective micro-patterning of microbial cells onto micro-magnet arrays for single cell analysis

International audienc

Microfluidic immunomagnetic cell separation using integrated permanent micromagnets

International audienceIn this paper, we demonstrate the possibility to trap and sort labeled cells under flow conditions using a microfluidic device with an integrated flat micro-patterned hard magnetic film. The proposed technique is illustrated using a cell suspension containing a mixture of Jurkat cells and HEK (Human Embryonic Kidney) 293 cells. Prior to sorting experiments, the Jurkat cells were specifically labeled with immunomagnetic nanoparticles, while the HEK 293 cells were unlabeled. Droplet-based experiments demonstrated that the Jurkat cells were attracted to regions of maximum stray field flux density while the HEK 293 cells settled in random positions. When the mixture was passed through a polydimethylsiloxane (PDMS) microfluidic channel containing integrated micromagnets, the labeled Jurkat cells were selectively trapped under fluid flow, while the HEK cells were eluted towards the device outlet. Increasing the flow rate produced a second eluate much enriched in Jurkat cells, as revealed by flow cytometry. The separation efficiency of this biocompatible, compact micro-fluidic separation chamber was compared with that obtained using two commercial magnetic cell separation kit