Not merely a drop in the ocean: The integration of capillary electrophoresis (CE) with droplet generation driven by electroosmotic flow enabled the compartimentalization of molecular components separated by CE in a series of droplets (see picture; the green bars represent the separated analytes). The droplet-confined bands can be docked and studied on a chip.
Spatially periodic optical fields can be used to sort dielectric microscopic particles as a function of size, shape or refractive index. In this paper we elucidate through both theory and experiment the behavior of silica microspheres moving under the influence of the periodic optical field provided by a Bessel beam. We compare two different computational models, one based on Mie scattering, the other on geometrical ray optics and find good qualitative agreement, with both models predicting the existence of distinct size-dependent phases of particle behavior. We verify these predictions by providing experimental observations of the individual behavioral phases.
The motion of colloidal particles on a periodic optical potential energy landscape in the presence of an external driving force may result in particle separation. In contrast to recent methods of holographic or interferometric generation of such landscapes, we use an acousto-optic deflector to create two-dimensional landscapes. We present what is believed to be the first experimental realization of fractionation with simultaneous sorting of four different sizes of colloidal microparticle into laterally separated parallel laminar streams.
We demonstrate passive optical sorting of cell populations in the absence of any externally driven fluid flow. Specifically, we report the movement of erythrocytes and lymphocytes in an optical landscape, consisting of a circularly symmetric light pattern created by a Bessel light beam. These distinct cell populations move, spontaneously and differentially, across the underlying periodic optical landscape. Thus, we were able to separate lymphocytes from a mixed population of cells containing erythrocytes and then collect the lymphocytes in a microcapillary reservoir. We also demonstrate an enhanced form of this separation that exploits the polarizability of silica microspheres by attaching spheres coated with antibodies to cell surface markers to a subpopulation of lymphocytes. These techniques may be applied using standard laboratory apparatus.
We demonstrate the use of a spatial light modulator (SLM) to facilitate the trapping of particles in three-dimensional structures through time-sharing. This method allows particles to be held in complex, three-dimensional configurations using cycling of simple holograms. Importantly, we discuss limiting factors inherent in current phase only SLM design for applications in both optical tweezing and atom trapping.
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