A screening device for testing saliva for the presence of certain constituents. The device has a D-shaped profile when viewed from above and includes a first wall with planar front face through which all of the test strips are viewed and a curved rear second wall. The device also includes a floor surface with an uppermost portion extending from the rear wall to a lowermost portion at the first wall such that saliva squeezed from a sampler at a location between the upper most portion and the lowermost portion flows downwardly to the test strips.

A fluid transfer device includes a syringe barrel having a chamber, a first plunger slidably movable inside the chamber, and a second plunger slidably movable inside the chamber. The distal end portion of the first plunger is engageable with the proximal end portion of the second plunger such that when the distal end portion of the first plunger and the proximal end portion of the second plunger are engaged, the second plunger is movable by the first plunger. A check valve may be incorporated into the distal end portion of the second plunger to allow a fluid to pass therethrough in a direction towards the proximal end portion of the second plunger and prevent a fluid to pass therethrough in a reverse direction. A fluid transfer assembly and a sampling method are also described.

Provided is a micro-fluid chip that enables reducing contamination between branch channels, has a relatively simple channel structure and facilitates miniaturization. A micro-fluid chip 1 having a channel structure 3 through which a fluid is delivered, wherein the channel structure 3 includes: a main channel 4 having an inflow port 5 and an outflow port 6; a plurality of branch channels 11 to 13 connected to the main channel 4, each branch channel having an inflow end on a side connected to the main channel 4 and an outflow end that is an end portion on an opposite side to the inflow end; and a sub-branch channel 14 connected to the main channel 4 between at least one pair of adjacent branch channels 11 and 12 among the plurality of branch channels 11 to 13, the sub-branch channel 14 having an inflow end on a side connected to the main channel 4.

A particle manipulation device includes a substrate and a microchannel included in the substrate and configured to receive a fluid including particles therein. A biasing structure is formed on the substrate adjacent to, but outside the microchannel. The biasing structure is configured to dispense radiation at a frequency to bias movement of the particles within the microchannel from outside the microchannel.

The present invention relates to a system and method for cell separation. The system includes: a cartridge having a polygonal shape in cross section and including an injection part, a separation chip separating a flow channel of a sample injected through the injection part, and a discharge part; and a base plate coupled to the cartridge through its upper surface and including a magnetic chip for cancer cell capture, liquid sensors, and valves. The method includes: coupling a cut plane of one side of the cell separation cartridge to one side of the base plate; engaging a recess formed at the other end of the cell separation cartridge with a pin formed at the other end of the base plate; fixing holes of the separation chip of the cell separation cartridge and holes of the magnetic chip of the base plate using a fixing member to match the holes of the separation chip of the cell separation cartridge and the holes of the magnetic chip of the base plate; and determining whether a pattern of the separation chip of the cell separation cartridge matches a pattern of the magnetic chip of the base plate.

Provided is a multi-flux micro-fluidic chip including a chip body. The chip body includes a fluid inflow cavity communicated with an external air path, reaction-quantification cavities, waste liquid cavities, and a fluid path distribution cavity disposed at a middle position of the chip body. The two or more reaction-quantification cavities are distributed on two sides of the fluid path distribution cavity in rows to form the first and second row of reaction-quantification cavities respectively; and they are communicated with a fluid outlet of the fluid path distribution cavity through fluid path branches, and a fluid inlet of the fluid path distribution cavity through fluid path branches, and a fluid inlet of the fluid path distribution cavity is communicated with a fluid outlet of the fluid inflow cavity and an external fluid path, which making it possible to detect multiple items simultaneously and greatly improving the flux of the micro-fluidic chip.

The present invention relates to the use of acoustic waves for the manipulation and sorting of particles and cells. In an embodiment, there is provided a microfluidic device for manipulating a particle in a fluid suspension, the device comprising: (a) a substrate; (b) a channel defined in the substrate, the channel having an inlet for receiving the fluid suspension and an outlet for discharging the fluid suspension; and (c) an acoustic source configured to deliver a travelling surface acoustic wave transverse the flow of the fluid suspension in the channel, wherein the acoustic source is an interdigital transducer (IDT), the IDT comprises a plurality of concentric circular arcs having a tapered end directed at the channel, and the tapered end has an aperture of between 4 m and 150 m. In an alternative embodiment, the device comprises a second channel disposed intermediate the first channel and the acoustic source wherein the first and second channels are connected by a pumping channel.

Provided herein are devices, systems, and methods for analysis of objects, such as cells. The devices, systems, and methods organize a plurality of objects in a plurality of partitions by trapping an object in a trap and transferring the object to an adjacent partition. The devices, systems, and methods provide for parallel analysis of a plurality of objects.

Microfluidic structures and methods for manipulating fluids and reactions are provided. Such structures and methods may involve positioning fluid samples, e.g., in the form of droplets, in a carrier fluid (e.g., an oil, which may be immiscible with the fluid sample) in predetermined regions in a microfluidic network. In some embodiments, positioning of the droplets can take place in the order in which they are introduced into the microfluidic network (e.g., sequentially) without significant physical contact between the droplets. Because of the little or no contact between the droplets, there may be little or no coalescence between the droplets. Accordingly, in some such embodiments, surfactants are not required in either the fluid sample or the carrier fluid to prevent coalescence of the droplets. Structures and methods described herein also enable droplets to be removed sequentially from the predetermined regions.

Provided are a chip for separating or aligning fine particles, a device for separating or aligning fine particles including two or more chips for separating or aligning fine particles, and a method for separating or aligning fine particles using the chip for separating or aligning fine particles or the device for separating or aligning fine particles. The chip for separating or aligning fine particles includes: (i) a passage part in which a space where a fluid including fine particles which are capable of flowing is integrally formed and which has an inclined groove formed on one surface thereof; (ii) an inlet part which is positioned on one end of the passage part and into which the fluid is introduced; and (iii) a fine particle discharge part which is positioned on one side surface of the passage part, wherein one or more inclined grooves are formed to be inclined at an angle greater than 0 and less than 90 with respect to a line which is perpendicular to both side surfaces of the passage part.