Parallel single cell analysis on an integrated microfluidic platform for cell trapping, lysis and analysis

We report here a novel and easily scalable microfluidic platform for the parallel analysis of hundreds of individual cells, with controlled single cell trapping, followed by their lysis and subsequent retrieval of the cellular content for on-chip analysis. The device consists of a main channel and an array of shallow side channels connected to the main channel via trapping structures. Cells are individually captured in dam structures by application of a negative pressure from an outlet reservoir, lyzed on site and the cellular content controllably extracted and transported in the individual side channels for on-chip analysis.\u

Radiative properties of desert aerosols by optical ground-based measurements at solar wavelengths

Les caractéristiques radiatives des poussières atmosphériques ont été mesurées d'avril à mai 1986 à la station de Mbour (16,9°W; 14,3°N) située à 80 km au sud de Dakar (Sénégal). Couplée avec des mesures satellitaires cette étude présente les premières conclusions des observatoires au sol pendant 15 journées consécutives. L'épaisseur optique varie fortement d'un évènement à l'autre (0,4-2 dans la bande spectrale de 450 mm). Les propriétés radiatives des aérosols sont en accord avec les modèles proposés notamment par SHETTLE's (1984) sur l'impact des brumes sèches sur le bilan énergétique de la planète (Résumé d'auteur

Characterisation of spin-incoherent transport in one dimension

Spin-incoherent transport in quantum wires, whereby exchange coupling between neighbouring electrons is overcome by thermal energy, leading to the suppression of spin modes of transport expected in a Luttinger liquid, has been observed in the form of a conductance plateau at e(2)/h in the absence of a magnetic field. We present here further characterisation of this spin-incoherent plateau in a source-drain bias, which causes it to evolves to 0.85 x 2e(2)/h. Laterally shifting the channel and illuminating the sample allows us to verify its origin

Energy-dependent tunneling from few-electron dynamic quantum dots

We measure the electron escape rate from surface-acoustic-wave dynamic quantum dots (QDs) through a tunnel barrier. Rate equations are used to extract the tunneling rates, which change by an order of magnitude with tunnel-barrier-gate voltage. We find that the tunneling rates depend on the number of electrons in each dynamic QD because of Coulomb energy. By comparing this dependence to a saddle-point-potential model, the addition energies of the second and third electron in each dynamic QD are estimated. The scale (similar to a few meV) is comparable to those in static QDs as expected

Single-electron population and depopulation of an isolated quantum dot using a surface-acoustic-wave pulse

We use a pulse of surface acoustic waves (SAWs) to control the electron population and depopulation of a quantum dot. The barriers between the dot and reservoirs are set high to isolate the dot. Within a time scale of similar to 100 s the dot can be set to a nonequilibrium charge state, where an empty (occupied) level stays below (above) the Fermi energy. A pulse containing a fixed number of SAW periods is sent through the dot, controllably changing the potential, and hence the tunneling probability, to add (remove) an electron to (from) the dot

Experimental results and first 22Na source image reconstruction by two prototype modules in coincidence of a liquid xenon positron emission tomograph for small animal imaging

International audienceA detector with a very specific design using liquid Xenon (LXe) in the scintillation mode is studied for Positron Emission Tomography (PET) of small animals. Two prototype modules equipped with Position Sensitive Photo Multiplier Tubes (PSPMTs) operating in the VUV range (178 nm) and at 165 K were built and studied in coincidence. This paper reports on energy, time and spatial resolution capabilities of this experimental test bench. Furthermore, these experimental results were used to perform the first image reconstruction of a 22Na source placed in the experimental setup

Wetting films on chemically heterogeneous substrates

Based on a microscopic density functional theory we investigate the morphology of thin liquidlike wetting films adsorbed on substrates endowed with well-defined chemical heterogeneities. As paradigmatic cases we focus on a single chemical step and on a single stripe. In view of applications in microfluidics the accuracy of guiding liquids by chemical microchannels is discussed. Finally we give a general prescription of how to investigate theoretically the wetting properties of substrates with arbitrary chemical structures.Comment: 56 pages, RevTeX, 20 Figure

Sonoprinting liposomes on tumor spheroids by microbubbles and ultrasound

Ultrasound-triggered drug-loaded microbubbles have great potential for drug delivery due to their ability to locally release drugs and simultaneously enhance their delivery into the target tissue. We have recently shown that upon applying ultrasound, nanoparticle-loaded microbubbles can deposit nanoparticles onto cells grown in 2D monolayers, through a process that we termed "sonoprinting". However, the rigid surfaces on which cell monolayers are typically growing might be a source of acoustic reflections and aspherical microbubble oscillations, which can influence microbubble-cell interactions. In the present study, we aim to reveal whether sonoprinting can also occur in more complex and physiologically relevant tissues, by using free-floating 3D tumor spheroids as a tissue model. We show that both monospheroids (consisting of tumor cells alone) and cospheroids (consisting of tumor cells and fibroblasts, which produce an extracellular matrix) can be sonoprinted. Using doxorubicin-liposome-loaded microbubbles, we show that sonoprinting allows to deposit large amounts of doxorubicin-containing liposomes to the outer cell layers of the spheroids, followed by doxorubicin release into the deeper layers of the spheroids, resulting in a significant reduction in cell viability. Sonoprinting may become an attractive approach to deposit drug patches at the surface of tissues, thereby promoting the delivery of drugs into target tissues