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J S Rossier

Publications and source records attributed to J S Rossier.

3 recordsLinked to original sources

Enzyme linked immunosorbent assay on a microchip with electrochemical detection.

This paper presents the development of a sandwich immunoassay in disposable plastic microchips. Photoablated microchannels with integrated electrodes have been used for the development of enzyme-linked-immunosorbent-assay (ELISA). The presence of the electrode inside the 40 nL microchannel enables the detection of the redox active enzyme substrate directly inside the reaction channel. Furthermore, due to the small diffusion distances, each incubation time can be reduced to five minutes instead of a few hours in standard microtiterplates. The initial characterisation of this immunoassay has been performed with a large protein complex D-Dimer-alkaline phosphatase. This system was used for the detection of immobilised antibodies on the surface of the photoablated microchannel. In a second step, a sandwich immunoassay with a horseradish peroxidase-secondary antibody conjugate (HRP-conjugate) was used to detect D-Dimer between 0.1 and 100 nM, which is the relevant concentration range of the clinical tests.

Adsorption↗

Polymer microspray with an integrated thick-film microelectrode.

A microfabrication process leading to a sheathless electrospray interface for mass spectrometry analysis is described. Photoablation is performed on a polymer substrate, allowing the integration of a thick-film conductive track in a sealed microchannel. High voltage is supplied close to the outlet, through an embedded microelectrode. The microspray is generated directly from the edge of the substrate without any tip addition. The flexibility of this technology provides a wide range of dimensions for the probe and the microelectrode design, including location, shape, and conductive material used. Thanks to the thick-film microelectrode and the hydrophobicity of the polymer, which avoids solution spreading at the outlet, the device has been found to be an efficient ionization source providing a stable MS signal through time. Moreover, the same device can be used several times without failure. The performance of the microspray has been studied in simple infusion mode for proteins and reserpine MS analyses. The detection limit of reserpine was found to be at the picomolar level in full-scan MS mode. It implies also that approximately 500 zmol was read consumed during 3 min of infusion. A dynamic range from pico- to millimolar level is also underlined.

Microelectrodes↗

Microchannel networks for electrophoretic separations.

UV excimer laser photoablation was used to micro-machine polymer substrates not only to drill microchannel structures but also to change the surface physical properties of the substrates. We first describe how UV laser photoablation can be used for the patterning of biomolecules on a polymer and discuss parameters such as surface coverage of active antibodies and equilibration time. Secondly, we show how to design a single-use capillary electrophoresis system comprising an on-chip injector, column and electrochemical detector. The potential of this disposable plastic device is discussed and briefly compared to classical systems. Finally, preliminary results on protein separation by isoelectric focusing on a disposable microchip are presented.

Adsorption↗