A system for operating an electrokinetic device includes a support configured to hold and operatively couple with the electrokinetic device, an integrated electrical signal generation subsystem configured to apply a biasing voltage across a pair of electrodes in the electrokinetic device, and a light modulating subsystem configured to emit structured light onto the electrokinetic device. The system can further include a thermally controlled flow controller, and/or be configured to measure impedance across the electrokinetic device. The system can be a light microscope, including an optical train. The system can further include a light pipe, which can be part of the light modulating system, and which can be configured to supply light of substantially uniform intensity to the light modulating system or directly to the optical train.

An electronic driving circuit for a microfluidic device, having a number of synchronized driving stages to generate a respective driving signal for each electrode or group of electrodes of the microfluidic device, the driving signals having a desired amplitude, frequency and phase-shift. Each driving stage has a switching-mode amplifier stage to receive a clock signal and a target signal and to generate, at an output thereof, an output signal defining a respective driving signal. The amplifier stage has: a switching module, coupled to a first internal node and controlled by the clock signal for selectively bringing the first internal node to a control signal; a filter module, coupled between the first internal node and the output, to provide the output signal; and a feedback module.

Disclosed herein are example embodiments of a transformative sensor apparatus that is capable of detecting and quantifying the presence of a substance of interest such as a specified bacteria within a sample via changes in impedance exhibited by a detection electrode array. In an example embodiment, sensitivity is improved by including a focusing electrode array in a rampdown channel to focus a concentration of the substance of interest into a detection region. The focusing electrodes include an opposing pair of electrodes in a rampdown orientation. The focusing electrode may also include tilted thin film finger electrodes extending from the rampdown electrodes. In another example embodiment, trapping electrodes are positioned to trap a concentration of the substance of interest onto the detection electrode array.

A driving method for a digital microfluidic chip, the digital microfluidic chip including a first electrode and a second electrode that are adjacent, the driving method including: applying a first driving signal to the first electrode and a second driving signal to the second electrode, wherein an applying period of the first driving signal and an applying period of the second driving signal are mutually staggered, and a total time length of the applying period of the first driving signal is less than a total time length of the applying period of the second driving signal.

An apparatus for immobilizing a particle in a fluid and a method for operating the apparatus are disclosed. The apparatus includes a membrane for separating a fluid from a compartment, one or more electrodes disposed proximate to the membrane, a counter-electrode, wherein the one or more electrodes and the counter-electrode are configured to generate a non-linear electric field across the one or more electrodes and the counter-electrode, and a power source for providing an alternating current (AC) across the one or more electrodes and the counter-electrode, thereby generating an oscillating non-linear electric field for immobilizing a particle suspended in the fluid that flows between the one or more electrodes and the counter-electrode. The membrane can have an opening to allow for mechanical manipulation of the particle that is immobilized with a sharp member configured to enter across the membrane from the compartment.

A cell capture apparatus includes a cell separation unit having a flat plate shape and a cell capture unit having a flat plate shape located therebelow. A liquid sample and a carrier liquid flow in a cell-separation flow passage of the cell separation unit. The liquid sample contains multiple large cells, multiple small cells, and a sample liquid component. The cell-separation flow passage separates a set of large cells and the carrier liquid from a set of small cells and the sample liquid component. The cell capture unit includes a large-cell flow passage in which the set of large cells and the carrier liquid flows, and multiple electrode wires for attracting the large cells by means of dielectrophoresis. Multiple cell capturing wells are formed in the large-cell flow passage. Each of the multiple cell capturing wells has a size that can capture one of the large cells attracted by the electrode wires.

An apparatus and method for isolating bacterial particles in a sample using a container with material in temporary fluid blocking position to lower orifice in the container, a separation medium having an electrical conductivity lower than and physical density greater than that of the sample above the material that supports a sample concentrate after passing through the separation medium when exposed to centrifugal force, a heating element for liquefying the material to permit flow into a chamber past an electrode array that attracts and holds subject particles. The system allows rapid detection and isolation of particles from samples from animal, human, environmental sites, a bio-industrial reactor or a food or beverage production facility requiring relatively small volumes, short incubation times resulting in structurally intact particles for further analysis. Testing may be completed in a single unit that requires decreased technician manipulation, fewer steps and a decrease in cross-contamination.

Provided are methods and systems useful for screening large libraries of effector molecules. Such methods and systems are particularly useful in microfluidic systems and devices. The methods and systems provided herein utilize encoded effectors to screen large libraries of effectors.

Provided are methods and systems useful for screening large libraries of effector molecules. Such methods and systems are particularly useful in microfluidic systems and devices. The methods and systems provided herein utilize encoded effectors to screen large libraries of effectors.

Devices, techniques, and processes are disclosed that use electrical impedance to detect of the presence and contents of droplets including cells, nucleic acids, proteins, or solute concentrations in an array of retrievable, trackable, trapped droplets in a fluidic system. Electrodes may be positioned underneath individual droplet traps in a microchannel to assay droplet contents and/or actuating droplets for the release of the droplets from corresponding traps. The disclosed technology may be used for detection of the results of solvent extraction processes including time-dependent quantification of metal ion concentration in the aqueous and organic phases, for wastewater treatment, heavy metal detection, pharmaceutical industry, and/or biotechnology, or for environmental monitoring of wastewater for toxic metal, monitoring of biological cell viability and proliferation, monitoring of extraction processes used in heavy metal mining, monitoring of extraction processes used in nuclear fuel processing, monitoring kinetics of enzyme processes, and/or assessing pharmacodynamics and drug efficacy.