Abstract: Various methods and systems are provided for reducing elasto-capillary coalescence of nanostructures. In one embodiment, a method includes providing a plurality of wet nanostructures on an electrode with a counter electrode positioned in air opposite the wet nanostructures. An electric field is applied between the counter electrode and the wet nanostructures using a voltage source, thereby reducing aggregation of the nanostructures. In another embodiment, an elasto-capillary coalescence reduction apparatus includes an electrode configured to receive a plurality of wet nanostructures, a counter electrode positioned in air opposite the wet nanostructures, and a voltage source coupled to the electrode and the counter electrode. The voltage source is configured to apply an electric field across the electrode and the nanostructures, which causes each of the nanostructures to repel a neighboring nanostructure.

Abstract: A method of forming a phosphor coating layer on a light emitting diode (LED) chip using electrophoresis includes separating phosphor particles in a suspension according to a particle size, and coating the phosphor particles on a surface of the LED chip by sequentially depositing the separated phosphor particles on the surface of the LED chip according to the particle size. An apparatus to form a phosphor coating layer on an LED chip includes an electrophoresis bath to accommodate a suspension containing phosphor particles separated into layers according to a particle size, and electrodes disposed inside the electrophoresis bath. The electrodes may include a cathode electrode on which the LED chip may be arranged, and an anode electrode.

Abstract: Methods are provided for manipulating droplets. The methods include providing the droplet on a surface comprising an array of electrodes and a substantially co-planer array of reference elements, wherein the droplet is disposed on a first one of the electrodes, and the droplet at least partially overlaps a second one of the electrodes and an intervening one of the reference elements disposed between the first and second electrodes. The methods further include activating the first and second electrodes to spread at least a portion of the droplet across the second electrode and deactivating the first electrode to move the droplet from the first electrode to the second electrode.

Abstract: Sensing device and sensing method are disclosed. The multi-dimensional force sensing device includes a soft laminose dielectric structure, a conductive sheet, at least one first electrode sheet, at least one second electrode sheet, a measuring unit and an analysis unit. The soft laminose dielectric structure has a first surface and a second surface opposite to each other. The conductive sheet is disposed on the first surface and has a vertical projection area. The first electrode sheet is disposed on the second surface and totally in the range of the vertical projection area. The second electrode sheet is disposed on the second surface and partially in the range of the vertical projection area. The analysis unit analyzes the magnitude and direction of a force applied on the conductive sheet according to the capacitance between the at least one first electrode sheet and between the first and the second electrode sheets.

Abstract: Apparatuses and methods for manipulating droplets are disclosed. In one embodiment, an apparatus for manipulating droplets is provided, the apparatus including a substrate, multiple arrays of electrodes disposed on the substrate, wherein corresponding electrodes in each array are connected to a common electrical signal, and a dielectric layer disposed on the substrate first side surface and patterned to cover the electrodes.

Abstract: A sample testing vessel may include a flexible plastic tube and a self-sealing injection channel. The flexible plastic tube may have a seal defining a first compartment and a second compartment, wherein the seal comprises a pressure gate providing a fluid-tight seal between first and second compartments and opening upon application of a threshold pressure. The injection channel may be normally substantially free of fluid and capable of fluid communication with the tubule.

Abstract: A sample processing apparatus includes a sample carrier receiving region configured to receive a sample carrier. The sample carrier includes at least one sample channel carrying at least one sample, at least one agent chamber carrying at least one agent to be moved to the at least one sample channel to facilitate processing of the at least one sample, and the at least one agent chamber includes at least one chamber cover covering at least one opening of the at least one agent chamber, inhibiting flow of the at least one agent from the at least one agent chamber to the at least one sample channel. The sample processing apparatus further includes a chamber opener configured to facilitate opening the at least one chamber cover. The sample processing apparatus further includes a fluid mover that moves the agent out of the at least one agent chamber after the at least one chamber cover is opened and into the at least one sample channel.

Abstract: A digital microfluidic platform utilizes dual active matrix circuitry to actuate and heat liquid droplets on a biochip. Liquid droplets are introduced into a droplet handling area of the biochip where they can be actuated by electrodes residing in pixels of an actuating active matrix array according to the electrowetting on dielectric phenomenon and heated by heating elements residing in pixels of a heating active matrix array. Pixels of the actuating active matrix array and the heating active matrix array are independently addressable such that droplets in the droplet handling area can be selectively heated and actuated according to their location. The actuating active matrix array and heating active matrix array can be formed on the same or different substrates with the droplet handling area disposed above or between the substrates.

Abstract: The present invention provides modified droplet actuator systems, software, and software-executed methods for use in droplet actuator operation and droplet actuator systems that are configured and programmed to execute such software. An aspect of the software components of the invention is an interface description file for each hardware component of a microfluidics system that allows hardware components to be changed without modifying the program for performing droplet operations protocols. Another aspect of the software components of the invention is the establishment of electrode-to-electrode relationships and other aspects of droplet actuator configurations, which may be used when programming droplet operations protocols. Another aspect of the software components of the invention is a physical design library of predefined electrode elements that may be used by a droplet actuator designer when constructing a layout of electrodes.

Abstract: The invention provides an electrophoresis cassette, methods for making the electrophoresis cassette, and method of fractionating analytes from a sample based upon electrophoretic mobility in a single application of the sample to an electrophoretic system.

Abstract: The invention provides an electrophoresis cassette, methods for making the electrophoresis cassette, and method of fractionating analytes from a sample based upon electrophoretic mobility in a single application of the sample to an electrophoretic system.

Abstract: The invention relates to a novel sealing composition for the manufacture of an electrophoretic or liquid crystal display, and a sealing process using the composition. The composition allows electrophoretic or liquid crystal cells to be seamlessly sealed and the sealing layer free of any defects.

Abstract: A cartridge (1) comprises a working film (10) for manipulating samples in liquid droplets with an electrode array (20) when the working film (10) of the cartridge (1) is placed on said electrode array (20).

Abstract: A control device for a sample separation apparatus, the sample separation apparatus including a first separation unit and a second separation unit downstream of the first separation unit and supplied with the fluidic sample after treatment by the first separation unit. A control device is configured for controlling the first separation unit to execute a primary separation sequence within a time interval for separating the fluidic sample into fractions, and for controlling the second separation unit to execute secondary separation sequences within the time interval for further separating the separated fractions into sub-fractions, wherein the secondary separation sequences form part of a common sample separation method defined by a common specification of the sample separation involving a set of parameters, and adjusting, over a progress of the primary separation sequence, at least one parameter according to which at least one of the plurality of secondary separation sequences is executed.

Abstract: To provide an anode which can prevent scale from being deposited on the contact surface of the anode with materials to be processed, an apparatus including the anode for electrical treatment, and a method for electrical treatment using the apparatus. An endless conveyor belt 1 formed using filter cloth is provided between rollers 2 and 3 so as to be able to rotate over a cathode plate 4 formed using a porous plate. Anode units 21 to 25 are arranged in the carrying direction of the conveyor belt 1. A coating 7 is provided on the lower surface of an anode plate 33 of each of the anode units and is in the form of a porous synthetic resin plate or a porous glass filter having at least any one of water permeability and electric conductivity.

Abstract: A method for pumping through an orifice of a first substrate, a first volume of liquid in contact with a first hydrophobic surface of said substrate, wherein a pressure variation between the first volume of liquid and a second volume of liquid, located in contact with said orifice and a second hydrophobic surface of said substrate, is achieved by electrowetting.

Abstract: A display apparatus (1) comprises a matrix display device (DD) with pixels (10) wherein particles (14) move in a fluid (13) between electrodes (6, 6?, 7). An optical state of the pixels (10) is defined by a value of a drive voltage (VDi) and a duration (Di) of a drive period (TDi) during which the drive voltage (VDi) is present across the pixel (10). A DC-balancing circuit (3) controls the amplitudes of the drive voltages (VDi) and/or durations (Di) of drive periods (TDi) to obtain a substantially zero time-average value (N) across each pixel (10) or across each sub-group of pixels. This control of the amplitude of the drive voltages (VDi) and/or the duration (Di) of the drive periods (TDi) allows minimizing the image retention, without requiring reset pulses causing all pixels (10) to become temporarily white or black.

Abstract: Apparatuses and methods for manipulating droplets on a printed circuit board (PCB) are disclosed. Droplets are actuated upon a printed circuit board substrate surface by the application of electrical potentials to electrodes defined on the PCB. The use of soldermask as an electrode insulator for droplet manipulation as well techniques for adapting other traditional PCB layers and materials for droplet-based microfluidics are also disclosed.

Abstract: The present invention relates to a method and system for determining particle properties. Such properties may for example be charge, size, drift, etc. The method comprises determining (110) an electric mobility distribution based on detection of individual particles. The latter may be performed for a single particle over time, for a plurality of particles at the same time or in a combination thereof. The method also comprises deriving a particle property based on a periodicity in the electric mobility distribution.

Abstract: A method for dispensing charged particles includes applying a bias voltage to promote motion of charged molecules through a nanopore, detecting passage of at least one charged molecule through the nanopore, and manipulating an electrostatic potential barrier inside the nanopore, so as to prevent movement of additional charged molecules through the nanopore.

Abstract: A pump includes a flow passage through which a liquid containing an electrolytic solution is conveyed, a pair of electrodes in the flow passage to apply an electric field along the direction in which the liquid is conveyed, and a conductive member connected to one of the pair of electrodes and in contact with the liquid in the flow passage. The conductive member includes a sidewall portion that locally divides a flow of the liquid in the flow passage. The conductive member connected to one of the pair of electrodes may be a polyhedron or a column that is convex toward the electrode to which the conductive member is not connected.

Abstract: A liquid transporting device using electrowetting on dielectric technique is provided. A sampling liquid is accurately transported on a substrate in a channel-free manner. The sampling liquid is spun off the substrate by a centrifugal force after the sampling liquid has been detected. The liquid transporting device can be applied to a biochemical detecting apparatus and a biochemical detecting method, thereby fulfilling requirements of accurate sample transportation in the biomedical field. The liquid transporting device is simplified to reduce overall costs, thus being helpful for decreasing high prices of biomedical detecting systems.

Abstract: An osmotic pump comprises a first chamber (8) comprising an osmotically active substance (18), a second chamber (15) arranged to be filled with a solvent (17), and a semi-permeable barrier (14) separating the first chamber (8) from the second chamber (15). The semi-permeable barrier (14) is impermeable to the osmotic active substance and permeable to the solvent (17). The osmotic pump further comprises a pressure device (60) in fluid communication with the second chamber (15), wherein the pressure device (60) is arranged for pressurizing the solvent in the second chamber.

Abstract: A droplet actuator and method of providing a droplet comprising an target substance on the droplet actuator, and including discrete flow and continuous flow functionality. Discrete flow function is controlled by electrodes arranged for conducting droplet operations on a substrate surface. The continuous flow function includes a fluid path arranged for flowing a fluid therethrough. The discrete flow and continuous flow functions may be by a barrier, including a second fluid path through the barrier. The continuous flow function may include a capture surface comprising a component having an affinity for the target substance. Methods of the invention may include flowing a fluid comprising the target substance through the fluid path; capturing the target substance on the capture surface; and forming a droplet in the discrete flow region via the second fluid path and the electrodes comprising the captured target substance.

Abstract: The present invention relates to a droplet-based nucleic acid amplification apparatus and system. According to one embodiment, a droplet microactuator is provided made using a first substrate including a fluorescing material and including a detection region for detecting a fluorescence signal from a droplet, which detection region is coated with a light absorbing, low fluorescence or non-fluorescing material.

Abstract: The conventional micropump and the conventional micromixer have the following problems. In a mechanical or hydrodynamic method, the structure of the inside of a flow path is complex so as to easily cause clogging, and manufacturing cost is high, and dead volume is large. Additionally, in an electrical method, the conventional micropump or the conventional micromixer was incapable of operating with a liquid having the concentration of a physiological saline that is important in the medical or biological field although the structure of the flow path is simple. These problems are solved by applying an AC voltage to a pair of electrodes in which an electrode-to-electrode gap between the pair of electrodes is vertically arranged and by generating the flow of a fluid in the direction opposite to gravity along the electrode-to-electrode gap.

Abstract: Various embodiments provide an exemplary lab-on-a-chip (LOC) system that serves as an analytical tool and/or as a separation medium for an electrolyte solution including various charged molecular species. The LOC system can include an integrated nanofluidic FET device in combination with suitable analysis systems. By applying and controlling a longitudinal electric field and a transverse electric potential, the flow and the pH of the electrolyte solution in the nanofluidic channels can be controlled.

Abstract: A fluid-application mechanism is to cause fluid to be applied onto media. An electrowetting mechanism is to generate an electric field to affect the fluid applied onto the media.

Abstract: The invention provides a method of inhibiting biological damage to a cellulosic structural element exposed to environmental moisture, said method comprising applying a pulsed asymmetric electrical voltage to a decay-prone region of a said element over a prolonged time period.

Abstract: An instrument for electrophoresis includes a sample-separating portion in which a slab sample-separating medium that separates a sample is provided. The instrument for electrophoresis includes a sample-transporting portion that transports a sample-containing medium containing the sample to the sample-separating portion. The instrument for electrophoresis includes a positioning portion that is provided to the sample-separating portion and/or the sample-transporting portion and used for connecting the sample-transporting portion to a predetermined position of the sample-separating portion.

Abstract: The invention provides methods and systems for ruggedizing a nucleic acid analyzing apparatus. The ruggedized apparatus can be used reliably and effectively in uncontrolled environments, such as, for example at a crime scene to collect and analyze forensic data, as well as in semi-controlled environments, such as, for example at a point of care location.

Abstract: Methods and systems for sequencing a biological molecule or polymer, e.g., a nucleic acid, are provided. One or more donor labels, which are attached to a pore or nanopore, may be illuminated or otherwise excited. A polymer having a monomer labeled with one or more acceptor labels, may be translocated through the pore. Either before, after or while the labeled monomer of the polymer passes through, exits or enters the pore, energy may be transferred from the excited donor label to the acceptor label of the monomer. As a result of the energy transfer, the acceptor label emits energy, and the emitted energy is detected in order to identify the labeled monomer of the translocated polymer and to thereby sequence the polymer.

Abstract: An apparatus for manipulating droplets is provided. In one embodiment, the apparatus includes a substrate having a set of electrical leads for connecting electrodes to a controller, a first set of electrodes, each connected to a separate one of the electrical leads, and a second set of electrodes, all connected to a single one of the electrical leads. In another embodiment, the apparatus includes a substrate having a set of X electrodes, and a set of Y electrical leads, each connected to one or more electrodes, wherein X is greater than Y.

Abstract: A microfluidic system for creating encapsulated droplets whose shells can be further removed comprises: two electrode plates and a spacing structure disposed between the two electrode plates. One of the electrode plates has three reservoir electrodes and a plurality of channel electrodes. The three electrodes are respectively used for accommodating a shell liquid, a core liquid, and a removing liquid which is able to remove the shell liquid. The channel electrodes are used for communicating droplets among the three reservoir electrodes. Via these arrangements, the microfluidic system can create a quantitative shell droplet and a quantitative core droplet, and then merge the shell and core droplets to form an encapsulated droplet. Moreover, the shell of the encapsulated droplet can be removed by mixing it with the removing liquid. This invention is further provided with a method for creating an encapsulated droplet with a removable shell.

Abstract: Components of a mixture are separated by feeding charged molecules of the components into a end surface of a suitable medium, for example a gel. The molecules are drawn in a first direction through the medium by means of an DC electric field, while at the same time being subjected to an alternating voltage with a strongly asymmetric profile in a direction transverse to the first direction. The nonlinear behavior of the electrically-generated migration causes a large number of molecules to migrate transversely out of the medium while only a small number of molecules reach the opposite end surface of the medium. A superimposed DC voltage in the transverse direction selects which of the mixture components migrate all the way through the medium in the first direction. The separated components can be sampled from the opposite end surface and from points on the upper and lower medium surfaces.

Abstract: The invention provides a device, system, and method for isolating one or more sample components of a sample material following separation of the sample material into a plurality of sample components. The device includes first and second pinching channels, a separation channel extending between the first and second pinching channels, a collection leg that includes a collection well between first and second ends of the collection leg, and a waste leg, all of which are in fluid communication with a switching region. In the method, a sample material is separated into a plurality of separated components in the device and one or more of the separated components are isolated in the collection well. The separated components are constrained and elongated in the switching region by first and second buffer streams.

Abstract: Disclosed are a method and apparatus that use an electric field for improved biological assays. The electric field is applied across a device having wells, which receive reactants, which carry a charge. The device thus uses a controllable voltage source between the first and second electrodes, which is controllable to provide a positive charge and a negative charge to a given electrode. By controlled use of the electric field charged species in a fluid in a fluid channel are directed into or out of the well by an electric field between the electrodes. The present method involves the transport of fluids, as in a microfluidic device, and the electric field-induced movement of reactive species according to various assay procedures, such as DNA sequencing, synthesis or the like.

Abstract: A liquid driver system having a flow channel for delivering a liquid, includes a conductor member placed in the flow channel, electrodes for applying an electric field to the conductor member and delivering the liquid by application of a driving force to the liquid by electroosmotic flow produced around the conductor member by the electric field, and a first flow limiter at a position displaced from the conductor member to limit a liquid flow in a reverse direction of liquid flowing in forward and reverse directions relative to the conductor member, wherein a maximum length of the flow limiter is smaller than a length of the conductor member in the forward flow direction, and the flow limiter is placed relative to the conductor member, having a thickness (2c), such that a gap (?) between the conductor member and the flow limiter satisfies the relation of ?<c.

Abstract: A component separating device includes a flow channel, an acoustic wave generator for generating an acoustic wave in the flow channel, a first inlet channel for introducing a fist solution containing solid particles into the flow channel, a second inlet channel for introducing a second solution, and outlet channels for discharging a solution from the flow channel. A density grade generator is provided at the first inlet channel for forming a density grade of the solid particles. This component separating device extracts the solid particles into a high-purity solution at a high collecting rate.

Abstract: A particle transporter based on travelling-wave dielectrophoresis is provided. The particle transporter includes a plurality of turn-around electrodes. The turn-around electrodes are disposed on a substrate and arranged in a fan shape. The turn-around electrodes provide an arc channel for transporting a plurality of particles. Wherein, the turn-around electrodes are not connected to each other, and neighboring sides of any two adjacent electrodes of the turn-around electrodes are approximately parallel.

Abstract: The present invention provides a mechanism for separating or isolating charged particles under the influence of an electric field without metal electrodes being in direct contact with the sample solution. The metal electrodes normally in contact with the sample are replaced with high conductivity fluid electrodes situated parallel and adjacent to the sample. When the fluid electrodes transmit the electric field across the sample, particles within the sample migrate according to their electrophoretic mobility.

Abstract: Techniques are generally described that include electrokinetic pumping an emulsion comprising an ionic fluid and a nonpolar fluid to promote flow of the ionic fluid by electro-osmotic flow and drag the nonpolar fluid by viscous drag forces. In some examples, the electrokinetic pump may be utilized to deliver one or more reagents within a fluidic reactor system, such as a micro-scale reactor system. In some additional examples, a reagent may be dissolved in the nonpolar fluid of a first emulsion and pumped through the electrokinetic pump to a mixing channel to allow the reagent of the first emulsion to react with a reagent of second emulsion to form a reactive product.

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: Devices and methods for detecting the length of analytes and/or sequencing analytes are provided in which two or more electrical signals are obtained as an analyte traverses a fluidic channel. Detection of the relative position of probes hybridized to a biopolymer and/or the length of the analyte (e.g., a biopolymer) does not rely on the absolute time between detection events of a given electrical signal to determine a distance associated with the biopolymer. Instead, multiple signals are obtained (e.g., as functions of time) corresponding to a plurality of detector volumes at known locations along a fluidic channel through which the biopolymer passes, and the distances are determined from the multiple signals.

Abstract: The present invention relates to a wettability switch that comprises an electrochemically active element having a wetting surface with switchable wetting properties. The electrochemically active element comprises an electrochemically active polymer, and surface active molecules each having a lyophobic portion and a lyophilic portion. In the wettability switch, each of said surface active molecules exposes one of said lyophobic portion and said lyophilic portion towards said wetting surface, and the identity of said portion depends on an electrochemical state of said polymer.

Abstract: Disclosed is a reaction kit for preventing the entry of foreign matter into a reaction plate from the outside and the pollution of a surrounding environment. The reaction kit includes: a reaction plate (2) having, on the top surface side thereof, a reaction container (4) for carrying out the reaction of a sample and a reagent container (12) containing a reagent used for the reaction of a sample and sealed with a film (14); a dispensation tip (20) arranged on the top surface side of the reaction plate (2); a cover (24) covering a space above the top surface of the reaction plate (2) and movably supporting the dispensation tip (20) so that a distal end thereof is located inside the space covered with the cover (4) and a proximal end thereof is located outside the space; and a sample container (32) for introducing a sample into the space covered with the cover (24) from the outside through a sealable opening (31) provided in a part of the cover (24).

Abstract: An apparatus, a method and a process to achieve manipulation of particles and/or solutions through the use of electrokinetic properties are disclosed. The manipulation is performed using a disposable device positioned on top of a stage for purposes of powering the electrodes. The fluidic solution is brought into contact with the active part of the device and then manipulated.

Abstract: Provided is a method of producing an electrophoretic display sheet having a substrate and a microcapsule-containing layer disposed on one surface side of the substrate and including microcapsules and a binder holding the microcapsules, the microcapsules each composed of a shell and an electrophoretic dispersion liquid sealed in the shell and containing at least one type of electrophoretic particles. The method includes the step of forming the microcapsule-containing layer where the microcapsules are arranged in a single layer without overlapping in the thickness direction of the substrate by supplying a microcapsule dispersion containing the microcapsules and the binder onto the substrate and then pressurizing the microcapsule dispersion in the thickness direction of the substrate.

Abstract: Disclosed herein is a gas sensitive apparatus that is useful in view of its applicability to the detection or quantitative determination of individual gases present in a gas mixture, and is advantageous in view of its compact size, and its low power consumption.

Abstract: An electrokinetic actuator for fluid flow titration including two chambers separated from one another by a porous dielectric disposed therebetween. A plurality of electrodes are disposed about a perimeter of the first and second chambers. Polar electrolyte disposed within the actuator is able to pass through the porous dielectric between the first and second chambers upon the application of an electric field or electric potential to the plural electrodes. A mechanical valve actuation mechanism connected to the second chamber allows for fine titration of fluid flow using electro-osmosis, including full-flow and/or complete cut-off. The polar electrolyte is isolated to prohibit intermixing with a fluid being titrated (such as cerebrospinal fluid).