Abstract: A microparticle sorting microchip for a flow cytometer is provided to enable sorting of microparticles at higher speed, higher purity, and higher acquisition rate. The microparticle sorting microchip includes a main channel through which a microparticle-containing fluid flows, a trap channel coaxially communicating with the main channel, a trap chamber communicating with the trap channel, and a gate channel intersecting the trap channel. The trap channel has an opening intersecting the gate channel. The trap channel has a smaller cross-sectional area upstream of the opening than downstream of the opening along a direction in which the microparticle-containing fluid flows.

Abstract: A well plate assembly with an interior channel system in the well plate lid provides a more efficient and uniform distribution of fluid into a receptacle positioned below the well plate lid. The channel system in the lid allows air, or other fluid, to pass through with the use of a pump to each of a plurality of channels in the receptacle. Inlet and outlet valves in the lid prevent a gasket positioned between the lid and the receptacle from releasing contact with the receptacle due to high pressure experienced during the injection of fluid into the assembly. Specifically, pressure under a specified tolerance passes through the inlet valves, and if the pressure within the channel system exceeds the limit of the outlet valve, the outlet valve opens and allows air to escape the lid safely without disturbing the fluid flow into the channels below.

Abstract: An electroporation device is disclosed, which includes a first tubular electrode including a first inlet and a first outlet; an aqueous solution supply connected to the first tubular electrode and configured for supplying an aqueous solution to the first tubular electrode and for allowing a droplet of the aqueous solution to be discharged from the first outlet of the first tubular electrode, the aqueous solution contains a cell and a delivery target substance; a second tubular electrode including a second inlet and a second outlet, wherein the second inlet is spaced away from the first outlet at a spacing corresponding to a size of a portion of the droplet; a power supply for applying a voltage to the electrodes for electroporation of the cell in the droplet; and a droplet sucking unit connected to the second electrode and configured for allowing the droplet to be sucked into the second electrode.

Abstract: A microfluidic device for detection of an analyte in a fluid is described. The microfluidic device comprises a substrate having a first surface defining entrances to one or more chambers defined in the substrate, surfaces of the chambers defining a second surface of the substrate, the first surface being modified for selective targeting and capture of at least one analyte to operably effect a blocking of the entrance to at least one of the chambers, and wherein a response characteristic of the microfluidic device is operably varied by the blocking of the entrance to the at least one of the chambers, thereby providing an indication of the presence of the analyte within the fluid.

Abstract: The present invention generally relates to systems and techniques for manipulating fluids and/or making droplets. In certain aspects, the present invention generally relates to droplet production. The droplets may be formed from fluids from different sources. In one set of embodiments, the present invention is directed to a microfluidic device comprising a plurality of droplet-making units, and/or other fluidic units, which may be substantially identical in some cases. Substantially each of the fluidic units may be in fluidic communication with a different source of a first fluid and a common source of a second fluid, in certain embodiments. In one aspect, substantially the same pressure may be applied to substantially all of the different sources of fluid, which may be used to cause fluid to move from the different sources into the microfluidic device. In some cases, the fluids may interact within the fluidic units, e.g., by reacting, or for the production of droplets within the microfluidic device.

Abstract: A method for providing a solution of a substance in a microfluidic device includes providing a dispersion of a first medium and of a lyophilizate of the substance, the lyophilizate being insoluble in the first medium, and adding a second medium to the dispersion, the lyophilizate being soluble in the second medium. The method further includes dissolving the lyophilizate in the second medium such that the solution of the substance in the second medium is obtained, and separating the solution obtained by the dissolving of the lyophilizate from the first medium.

Abstract: A microfluidic injection and manifold assembly includes a microfluidic chip having at least a first fluid port and a second fluid port, and a fluid pathway between the first fluid port and the second fluid port. A manifold has a seat on which the microfluidic chip is received, and at least a first fluid channel. The fluid channel has an external fluid port spaced from the seat and an internal fluid port in the seat and connected in fluid communication with the first fluid port of the microfluidic chip. At least a first injector is secured to the manifold and has a plunger and a drive assembly. The drive assembly is activatable to force the plunger into the external fluid port of the manifold to force fluid from the first fluid channel of the manifold into the fluid pathway of the microfluidic chip.

Abstract: The present invention discloses a flow path structure of a cartridge for nucleic acid extraction comprising: a plurality of elongated grooves formed on the surface of the cartridge body; and a shaft hole formed in the center of the body, wherein the plurality of grooves have a starting point formed around the shaft hole and an ending point extending from the starting point toward the outer region of the body.

Abstract: A method and filtering system are described. The filtering system comprises a vacuuming plate having a base with a plurality of outlet openings extending therethrough, a plurality of walls extending from the base to define a cavity, and a vacuum port in fluid communication with the cavity; and a filtering unit mounted to the vacuuming plate and enclosing the cavity. The filtering unit comprises a filter plate with a plurality of filter openings extending therethrough and aligned with the outlet openings; a filtering membrane extending across the filter plate and covering the plurality of filter openings; and a piercing plate on the filter plate maintaining the filtering membrane therebetween, the piercing plate having a plurality of vessel piercing members extending away from the filtering membrane, the vessel piercing members having conduits extending through the piercing plate, the conduits aligned with the filter openings to allow fluid flow therebetween.

Abstract: The present invention provides a membrane carrier 3 comprising a flow path 2 and a detection zone 3y, wherein a microstructure is provided at the bottom of the flow path 2 and a mean surface roughness of the microstructure is 0.005 to 10.0 ?m.

Abstract: Disclosed herein are methods and devices for antigen-specific T cell identification or neoantigen identification. Also disclosed herein are devices for separating and isolating antigen-specific T cells or other particles of a certain size from a population of particles of different sizes. Also describe herein are methods and devices for the separation and isolation of barcoded T cells from other nanoparticles containing barcodes for subsequent analysis and further processing of a viable T cell.

Abstract: Methods and systems for optofluidic device fabrication and design are herein disclosed. In examples, a user may manufacture the optofluidic device using stereolithography (SLA) three-dimensional (3D) printing, in which photosensitive resin is exposed to a focused laser, solidifying specific areas of resin. The optofluidic device may guide light for a broad wavelength range from a liquid or gas channel comprised within and may be used to guide the emission of light and particles of interest to a detector to identify the particles.

Abstract: A sensor cassette insertable into an analysis module for carrying out electrochemical measurement processes in sample fluids, including a sensor carrier which is essentially planar and carries electrochemical sensor elements for determining chemical and/or physical parameters of the sample fluids. The sensor elements are connected to conductor tracks formed on the sensor carrier. A cover part is arranged on the sensor carrier, in which at least one groove-shaped measuring channel that is intended for the flow of the sample fluid and opens towards the sensor carrier is formed, which measuring channel is connected to at least one electrochemical sensor element and is fluidly connected to at least one fluid connector arranged on the side facing away from the sensor carrier. The cover part is a two-component injection molded part having a hard component and a soft, component. The measuring channel is formed in the soft component over its entire length.

Abstract: The present invention aims at providing a fluidic device that can hold a large amount of solutions in a reservoir without depending on an attitude. The reservoir includes a meandering flow path including: a plurality of first flow paths that extend linearly along a first direction and that are arranged to be spaced in a second direction crossing the first direction; and a second flow path that extends linearly along the second direction such that a connection between first end sides of the adjacent first flow paths and a connection between second end sides of the adjacent first flow paths are alternately switched along the second direction for each first flow path, wherein the meandering flow path meanders along the second direction.

Abstract: Provided are a cell screening device and a cell screening method, for use in performing screening on different cells. The cell screening device is provided with: at least two flowing channels, used for allowing a solution containing cells to flow through; a communicating path, used for allowing the adjacent flowing channels to communicate with each other; a detection unit, used for detecting the types of cells in the solution flowing in the flowing channels; and a screening actuator, generating push force according to the detection result of the detection unit, so as to push cells in the solution flowing in the flowing channel to flow into the adjacent flowing channel through the communicating path.

Abstract: The invention is a novel and non-obvious design and implementation of an inductive sensor for quantifying magnetic particles. The invention parts way from the conventional methods of using wounded coils to a design that is compatible with an integrated circuit (IC) chip fabrication processes and/or printed circuit board (PCB) manufacturing. The increased accuracy from these fabrication methods provides a significant improvement to sensor sensitivity. In addition, the design of the inductive sensor enables easy integration with lateral flow assay (LFA) technology. The sensor can be applied to detect and quantify molecules to provide information on health, hazard or safety.

Abstract: A single electron transistor conjugated to a bacteriophage form a detectable probe where an RF signal identify the location of such probe at the site of specific biological matrix and provide a unique electronic signal such as a Coulomb Staircase and where such signal act as a diagnostic beacon and where such probe and a detector form a mesoscopic detector. The detector uses: a bioprobe containing the phage with its conjugated SET and the properties of the phage specificity; phage mobility within the biological environment and the phage ability to act as a carrier for the SET; and the SET's ultimate use as a beacon for the detection.

Abstract: Microfluidic cartridge (10) comprising a sampling device (30) having a sealing ring (32) arranged to form a microfluidic chamber (31) when a support containing a biological sample is brought into contact with the sealing ring, and a microfluidic network device (13) configured to supply reagents to the microfluidic chamber. The sampling device further comprises inlet and outlet distribution networks (33a, 33b) in fluid communication with the microfluidic chamber and a slide holder (35) to guide and position said support containing a biological sample on the sampling device. The microfluidic network device comprises a plurality of reagent inlet channels (18) fluidly connectable to reagent sources, at least one reagent outlet channel (22) fluidly connected to the sampling device inlet distribution network (33a), and a plurality of valves (25) operable to selectively connect the inlet channels to the at least one outlet channel.

Abstract: The present invention provides a membrane carrier 3 comprising a flow path 2 and a detection zone 3y, wherein a microstructure is provided at the bottom of the flow path 2 and a mean surface roughness of the microstructure is 0.005 to 10.0 ?m.

Abstract: The invention provides a device, method, and system for high throughput detection of nucleic acid expression in individual cells. Cells are encapsulated in aqueous microdroplets which are merged with a biocompatible matrix, allowing on-chip fluorescence in situ hybridization on both adherent and non-adherent cells. The invention also provides multiplexed detection of nucleic acids, proteins, and cellular activity. The device and methods can be used to assess cellular interactions and to test the effects of antitumor agents.