Abstract: Under one aspect, a device is provided for use in luminescent imaging. The device can include a photonic superlattice including a first material, the first material having a first refractive index. The first material can include first and second major surfaces and first and second pluralities of features defined through at least one of the first and second major surfaces, the features of the first plurality differing in at least one characteristic from the features of the second plurality. The photonic superlattice can support propagation of a first wavelength and a second wavelength approximately at a first angle out of the photonic superlattice, the first and second wavelengths being separated from one another by a first non-propagating wavelength that does not selectively propagate at the first angle out of the photonic superlattice.

Abstract: Electrophoresis device including: a first flow passage extending in a first direction and through which a sample and a buffer solution flow; a sample collecting part provided at an end portion of the first flow passage and configured to collect the sample; electrodes disposed at both sides of the first flow passage in a second direction perpendicular to the first direction and configured to apply a voltage to the first flow passage in the second direction; second flow passages communicating with both sides of the first flow passage in the second direction, configured to accommodate the electrodes, and through which a second buffer solution flows; and partition walls fixed to communicating portions between the first and second flow passages with a predetermined bonding strength and configured to block movement of substances between the first and second flow passages. The partition walls are formed of a gel material having ion permeability.

Abstract: A continuous flow particle separation system for separating metallic and nonmetallic particles from a mixed-particle suspension includes a fluid channeling component defining an input channel and first and second output channels fluidly connected to the input channel at a bifurcated junction, a first electrode and a second electrode arranged proximate the input channel at least partially prior to the bifurcated junction, and an alternating current (AC) electric power source electrically connected to the first and second electrodes.

Abstract: The present invention relates to bead incubating and washing on a droplet actuator. Methods for incubating magnetically responsive beads that are labeled with primary antibody, a sample (i.e., analyte), and secondary reporter antibodies on a magnet, on and off a magnet, and completely off a magnet are provided. Also provided are methods for washing magnetically responsive beads using shape-assisted merging of droplets. Also provided are methods for shape-mediated splitting, transporting, and dispensing of a sample droplet that contains magnetically responsive beads. The apparatuses and methods of the invention provide for rapid time to result and optimum detection of an analyte in an immunoassay.

Abstract: Contemplated methods and devices are drawn to preparation and analysis of analytes from biological samples. In a preferred embodiment the analytes are nucleic acids that are both released from biological compartment present in the sample and fragmented through the use of a voltage potential applied to a pair of electrodes. The nucleic acids thus prepared are subsequently characterized.

Abstract: Herein is described a process method and device used for nonporous, or porous media, that is metallic, ceramic, or of rock based compositions, such as geologic materials which may house inclusions such that under electromigration, thermophoresis, electrophoresis, magnetophoresis, electromagnetics, leads to combined advection, convection, electro-magnetic kinetics, osmosis, and diffusion. Meaning that under the influence of a solvent, cell, enclosure, contacts, and second enclosure material, yields the expulsion of trapped housed matter such as kerogen, oil, gas condensates, water-oil mixtures, hydrocarbons, terpenes, organic compounds, methane, inorganic material, solvent, or other organic material(s), or oil-gas-water type natural resource material. This is a simple environmental friendly method by which to expel housed and/or trapped media that is then released for collection, storage, and removal.

Abstract: This method for disposing fine objects, in a substrate preparing step, prepares a substrate having specified positions where fine objects (120) are to be disposed in an area where a first electrode (111) and a second electrode (112) face each other, and in a fluid introducing step, a fluid (121) is introduced on the substrate (110). The fluid (121) contains a plurality of the fine objects (120). The fine objects (120) are diode elements, each of which has, as an alignment structure, a front side layer (130) composed of a dielectric material, and a rear side layer (131) composed of a semiconductor. In the fine object disposing step, by applying an AC voltage to between the first electrode (111) and the second electrode (112), the fine objects (120) are disposed by dielectrophoresis with the front side layer (130) facing up at the predetermined positions in the area (A) where the first electrode (111) and the second electrode (112) face each other.

Abstract: Axially fed fluid is sheared during long residence time in a radial workspace between counter-rotating coaxial disk-shaped centrifugal impellers. Gases evolve in the fractal turbulence of a shear layer, which is forced between laminar boundary layers, and an axial suction pump axially extracts evolved noncondensables and volatiles through cores of radial vortices in the shear layer. Cavitation due to shear between the impellers kills pathogens by shock waves, microjets, OH radicals, and nearby UV light pulses. Oppositely charged electrodes bounding the workspace cause electroporesis and electrohydraulic cavitation. The electrodes are counter-rotating ridged armatures of disk dynamos, forming a dynamic capacitor having audio frequency pulsed electric fields. Electrode erosion by arcing is prevented by shear between the electrodes.

Abstract: Methods and devices for the separation of particles (20, 21, 22) in a compartment (30) of a fluidic microsystem (100) are described, in which the movement of a liquid (10) in which particles (20, 21, 22) are suspended with a predetermined direction of flow through the compartment (30), and the generation of a deflecting potential in which at least a part of the particles (20, 21, 22) is moved relative to the liquid in a direction of deflection are envisaged, whereby further at least one focusing potential is generated, so that at least a part of the particles is moved opposite to the direction of deflection relative to the liquid by dielectrophoresis under the effect of high-frequency electrical fields, and guiding of particles with different electrical, magnetic or geometric properties into different flow areas (11, 12) in the liquid takes place.

Abstract: In a particle focusing apparatus and a method for focusing particles, the particle focusing apparatus includes a channel, a fixing member, a fluid feeding portion and a power supply. The channel has first and second ends and extends substantially in a line. The fixing member includes a first fixing portion connected to and fixing the first end, and a second fixing portion connected to and fixing the second end. The fluid feeding portion feeds fluid having particles into the channel. The power supply has first and second terminals. The first terminal passes through the first fixing portion and is electrically connected to an anode of the power supply. The second terminal passes through the second fixing portion and is electrically connected to a cathode of the power supply. Thus, particles fed into the channel may be more easily and efficiently focused to a central region inside the channel.

Abstract: A system providing selective spin modification and reaction in an electrolytic cell. An electrolytic cell is coupled to a magnet that provides a level-splitting magnetic field in a region of electrolyte adjacent to a working electrode, thus establishing a spin resonance for an unpaired electron associated with a chemical species in the region of electrolyte adjacent to the working electrode. The working electrode carries an excitation current produced by a switching source or amplifier. The excitation current produces an alternating magnetic field adjacent to the working electrode that alters the spin state population density for the unpaired electron associated with a chemical species within the electrolyte, thereby enhancing or inhibiting the reaction of the chemical species during subsequent electrolysis.

Abstract: The invention provides a method of redistributing magnetically responsive beads in a droplet. The method may include providing a droplet including magnetically responsive beads. The droplet may be provided within a region of a magnetic field having sufficient strength to attract the magnetically responsive beads to an edge of the droplet or towards an edge of the droplet, or otherwise regionalize or aggregate beads within the droplet. The method may also include conducting on a droplet operations surface one or more droplet operations using the droplet without removing the magnetically responsive beads from the region of the magnetic field. The droplet operations may in some cases be electrode-mediated. The droplet operations may redistribute and/or circulate the magnetically responsive beads within the droplet. In some cases, the droplet may include a sample droplet may include a target analyte.

Abstract: The present invention relates a use of the electrocapture-based separation technology combined with mass spectrometry (e.g. sequence of polypeptides by collision-induce dissociation mass spectrometry, for the identification and/or characterization molecules of interest). In addition, it relates physical interfaces between electrocapture-based separations and different types mass spectrometers for on-line analysis, as well as the coupling of electrocapture-based separations, liquid chromatography and different types of mass spectrometrometers. It also relates the combination of the electrocapture-base separation technology with other liquid separation methods, as e.g. liquid chromatography, in order to achieve multidimensional separations prior mass spectrometrical analysis. The invention also relates to a separation device comprising a capture device, a fluidic connector e.g. an electrospray source, an electrospray interface-source and a mass spectrometer.

Abstract: The invention comprises a method of treating sludges which includes the steps of applying an electric field to the sludge to effect dewatering prior to further dewatering of the sludge. Typically the sludge comprises dilute phase sludge, and the electric field is a DC electric field. The pH of the sludge may be adjusted to between substantially 5 and substantially 6 prior to applying the electric field.

Abstract: A disease detection system which includes an electrophoresis apparatus and a biomarker detector. The apparatus includes: (a) a transport passage; (b) a plurality of separation passages, each of the separation passages having an overlapping portion that overlaps the transport passage; and (c) a different biomarker concentrator in each of the overlapping portions and which concentrates at least one different biomarker from a specimen from an animal introduced into the transport passage. A plurality of the different biomarkers is associated with at least one predetermined disease, such as diabetes, heart disease or cancer. The detector detects the presence of the different biomarkers which were concentrated by the biomarker concentrators and delivered to the biomarker detector via the separation passages. First and second sets of the biomarker concentrators can be associated with respective first and second predetermined diseases and the user can determine which set will be used in each procedure.

Abstract: The invention describes detection methods and devices that comprise nanostructures and which detection mechanism is based on the quantum confinement effects. The nanostructures are built to have specific energy levels designed to match the energy levels of the targeted analyte that is to be detected. The analyte species are sensed by measuring charge or/and energy transfer between the species and the nanostructures, which will be proportional to the overlap between the density of states distribution in the nanostructures and the density of states distribution in the targeted analyte species. Different molecular species have different electronic density of states, so the charge or/and energy transfer between the targeted analyte and detector nanostructures will occur only for specific analyte which has the same electronic density of states as the detectors nanostructure.

Abstract: A microbe testing device 10 comprises a measurement cell 1 for holding a sample liquid X, and a rotor 3 that is rotated, by magnetic force imparted from outside the measurement cell 1, along a bottom face 11b in the sample liquid X held in the measurement cell 1. The sample liquid X is stirred by rotating the rotor 3 so that only its end portions are in contact with the bottom face 11b of the measurement cell 1.

Abstract: The present invention relates to a free flow electrophoresis microchip for the electrophoretic separation of charged components, a free flow electrophoresis separation system incorporating the same, and a free flow electrophoresis method of separating charged components, the microchip comprising: a separation chamber in which charged components are in use separated; a plurality of separation medium inlet channels having outlets fluidly connected to one, inlet side of the separation chamber through which flows of a separation medium are in use introduced into the separation chamber such as to develop a laminar flow having a flow direction through the separation chamber; a sample inlet channel having an outlet fluidly connected to the inlet side of the separation chamber through which a flow of a sample containing charged components is in use introduced into the separation chamber; a plurality of outlet channels having inlets fluidly connected to another, outlet side of the separation chamber opposite the inlet

Abstract: Exemplary electrophoretic ink capsules for electrophoretic displays, and methods for making the exemplary electrophoretic ink capsules are disclosed. In various embodiments, the electrophoretic ink capsules can include triboelectrically charged electrophoretic particles having higher electrical conductivity than conventionally charged electrophoretic particles allowing fabrication of electrophoretic displays with lower switching fields and faster response times.

Abstract: A particle separator for separating different types of particles with different properties includes a channel unit including a flow channel through which a first fluid having particles with at least one physical characteristic and a second fluid that flows near the first fluid, and a plurality of outflow channels that are connected to the flow channel and that separate the fluid having passed the flow channel; and a field forming unit, installed adjacent to the flow channel, for separating the particles included in the first fluid from the first fluid and generating a non-uniform field so that the particles may flow together with the second fluid.

Abstract: A centrifugal spectrometer has a solid rotor (10) formed within which there are cavities or blades (12). In use, each blade is filled with a buffer solution, and a sample to be separated is placed in a sample well (32) at the end of a separation channel (24). The rotor is spun at a controlled velocity and, at the same time, a controlled potential difference is applied along the length of the blade. The blade shape causes the resultant electric field to vary as a function of radial distance. The sample separates out into bands, which move along the channel (24) under the combined influence of the centrifugal force and the varying electric field. The bands focus at differing equilibrium points according to their charge/mass ratios. The band positions are determined by a readout head (36). The dynamic range of the device may be controlled by altering the rotational velocity and the voltages that are applied.

Abstract: A flow controller which uses a combination of hydrostatic pressure and electroosmotic flow to control the flow of a fluid. A driving fluid (1204) whose flow rate is dependent on both hydrostatic pressures and electroosmotic flow can be used (a) directly as a working fluid in an operable device, for example a chromatograph, or (b) to displace a working fluid (1203) from a storage container (625) into an operable device (1301), or both (a) and (b). The driving fluid (1204) can be composed of one or more fluids. Part or all the driving fluid (1204) is passed through an electroosmotic device (100) so as to increase or decrease the flow rate induced by hydrostatic pressure.

Abstract: Methods and systems that employ hybrid fluid flow profiles for optimized movement of materials through channel networks. These systems employ hybrid pressure-based and electrokinetic based flow systems for moving materials through interconnected channel networks while maintaining interconnection among the various channel segments. In particular, the invention is generally directed to channel networks where flow in a first channel segment is driven by pressure flow with its consequent parabolic flow profile, while flow in an interconnected channel segment is dominated by electrokinetic flow with its consequent plug flow profile. The invention also provides channel networks wherein fluid flow in channel segments is driven by both pressure and electric field and the multiple species contained in a fluid plug are separated by altering the applied pressure and electric fields in the various channel segments of the channel networks.

Abstract: A method and apparatus are disclosed for simultaneously concentrating and separating a plurality of analytes which includes generating a continuous electric field gradient within an enclosed passageway, and where the electric field gradient is characterized by the graph of the gradient with respect to position along the length of the axis of the passageway being a non-linear, monotone, non-decreasing function with a non-increasing first derivative. Analytes entrained in a carrier fluid within the passageway are exposed simultaneously to the continuous electrical field gradient and an opposing force selected for exerting a force on the analytes. The analytes are allowed to reach equilibrium with respect to the continuous electric field gradient and the opposing force, then are released in a controlled manner to maintain separation. The unique shape of the electric field intensity curve allows for simultaneous concentration and separation of analytes.

Abstract: We have performed separation of bacterial and cancer cells from peripheral human blood in microfabricated electronic chips by dielectrophoresis. The isolated cells were examined by staining the nuclei with fluorescent dye followed by laser induced fluorescence imaging. We have also released DNA and RNA from the isolated cells electronically and detected specific marker sequences by DNA amplification followed by electronic hybridization to immobilized capture probes. Efforts towards the construction of a “laboratory-on-a-chip” system are presented which involves the selection of DNA probes, dyes, reagents and prototyping of the fully integrated portable instrument.

Abstract: An apparatus and method for electrocoriolysis, the separation of ionic substances from liquids in the electrodynamic mode. The method maximizes centrifugal forces on a fluid contained in a chamber having oppositely polarized electrodes. A feed fluid is fed into the chamber. Spacing of the electrodes can be minimized for enhancement of the process. A constant voltage can be applied. Centrifugal force and the electric potential across the chamber create enhanced separation. Concentrated solution can be removed from a location in the chamber and depleted solution from another location.

Abstract: Peak resolution in reversed-phase electrochromatography is improved in either of two alternative ways. The first is by a stepwise increase in the concentration of acetonitrile or other equivalent buffer constituent or modifier after the sample has been loaded, and the second is the inclusion of a surfactant in the mobile phase.

Abstract: Peak resolution in reversed-phase electrochromatography is improved in either of two alternative ways. The first is by a stepwise increase in the concentration of acetonitrile or other equivalent buffer constituent or modifier after the sample has been loaded, and the second is the inclusion of a surfactant in the mobile phase.

Abstract: Magnetic porous inorganic siliceous materials having a particle size of about 1 to about 200 microns useful as solid supports in various chromatography, immunoassays, synthesis and other separation and purification procedures is disclosed.