Fast Magnetic Field-Enhanced Linear Colloidal Agglutination Immunoassay.

We present the principle of a fast magnetic field enhanced colloidal agglutination assay, which is based on the acceleration of the recognition rate between ligands and receptors induced by magnetic forces. By applying a homogeneous magnetic field of 20 mT for only 7 s, we detect CRP (C-reactive protein) in human serum at a concentration as low as 1 pM for a total cycle time of about 1 min in a prototype analyzer. Such a short measurement time does not impair the performances of the assay when compared to longer experiments.

Numerical simulation of particle dynamics in an orifice-electrode system. Application to counting and sizing by impedance measurement.

This paper describes how to numerically tackle the problem of counting and sizing particles by impedance measurement in an orifice-electrode system. The model allows to simulate the particle dynamics submitted to strong hydrodynamic stresses through a microorifice and to compute the voltage pulses generated by the modification of the inner dielectric medium. This approach gives important information about particles size distribution and allows to quantify the role of trajectory and orientation of particles on the size measurement.

Flow cytometer based on triggered supercontinuum laser illumination.

Multiple wavelength operation in a flow cytometer is an exciting way for cell analysis based on both fluorescence and optical scattering processing. For example, this multiparametric technique is currently used to differentiate blood cells subpopulations. The choice of excitation wavelengths matching fluorochrome spectra (it is currently the opposite) and the use of a broader range of fluorochromes can be made by taking advantage of a filtered supercontinuum white light source.

Wavelength encoding technique for particle analyses in hematology analyzer.

The aim of this study is to combine multiple excitation wavelengths in order to improve accuracy of fluorescence characterization of labeled cells. The experimental demonstration is realized with a hematology analyzer based on flow cytometry and a CW laser source emitting two visible wavelengths. A given optical encoding associated to each wavelength allows fluorescence identification coming from specific fluorochromes and avoiding the use of noisy compensation method.

Automatic cytometric device using multiple wavelength excitations.

Precise identification of eosinophils, basophils, and specific subpopulations of blood cells (B lymphocytes) in an unconventional automatic hematology analyzer is demonstrated. Our specific apparatus mixes two excitation radiations by means of an acousto-optics tunable filter to properly control fluorescence emission of phycoerythrin cyanin 5 (PC5) conjugated to antibodies (anti-CD20 or anti-CRTH2) and Thiazole Orange. This way our analyzer combining techniques of hematology analysis and flow cytometry based on multiple fluorescence detection, drastically improves the signal to noise ratio and decreases the spectral overlaps impact coming from multiple fluorescence emissions.

White-light supercontinuum generation in normally dispersive optical fiber using original multi-wavelength pumping system.

We report on the experimental demonstration of a white-light supercontinuum generation in normally dispersive singlemode air-silica microstructured fiber. We demonstrate that the simultaneous excitation of the microstuctured fiber in its normal and anomalous dispersion regimes using the fundamental and second harmonic signals of a passively Q-switched microchip laser leads to a homogeneous supercontinuum in the visible range. This pumping scheme allows the suppression of the cascaded Raman effect predominance in favor of an efficient spectrum broadening induced by parametric phenomena.