A fluid preparation device can include a fluid-receiving vessel and a fluid loader with multiple fluid chambers including a first fluid chamber and a second fluid chamber. The multiple fluid chambers can partially be defined by actuator seals that are positioned on an actuator. The actuator can be moveable among a plurality of positions and the actuator seals can be positioned on the actuator to fluidically separate the first fluid chamber from the second fluid chamber when the actuator is in a closed position from the plurality of positions, allow fluidic communication between the second fluid chamber and the fluid-receiving vessel when the actuator is in a first open position from the plurality of positions, and allow fluidic communication between the first fluid chamber and the second fluid chamber when the actuator is in a second open position from the plurality of positions.

A biological component separator can include a vertically layered fluid column with a plurality of fluids positioned in fluid layers and a density-differential interface along which two fluids from the plurality of fluids are positioned. The biological component separator can also include a magnetic field generator positioned about the vertically layered fluid column and having multiple magnetic field profiles appliable across the vertically layered fluid column. The multiple magnetic field profiles can include a particle aggregating profile to concentrate magnetizing particles when present in the vertically layered fluid column and a particle sweeping profile to re-suspend and sweep the magnetizing particles when present across the vertically layered fluid column.

A vertically layered fluid column can include a plurality of fluids positioned in fluid layers, a density-differential interface along which two fluids from the plurality of fluids are positioned, and a capillary force-supported interface along which two fluids from the plurality of the fluids are positioned.

The disclosure is related to a liquid processing module, a liquid testing system and a testing method. The liquid processing module includes a base, a first valve and at least one negative pressure generator. The base has a first groove and at least one first opening. The first opening is connected to the first groove. The first valve is slidably located in the first groove. The negative pressure generator is configured to generate or remove negative pressure at the first opening in response to the first opening and the first groove being connected with each other.

The present invention provides a method for generating a droplet array on a microfluidic chip, comprising the following steps: assembling an upper chip and a lower chip to an initial position, a fluid channel of the upper chip partially or completely covering a microporous array of the lower chip; injecting a solution into a chip, the solution being partially or fully filled in the microporous array of the lower chip; and relatively moving the upper chip and the lower chip to a liquid dividing position, the fluid channel of the upper chip and the microporous array of the lower chip being overlapped no longer, and the solution being dispersed into the microporous array to form a droplet array. A contact surface between the upper chip and the lower chip is hydrophobic, and the microporous array sufficiently separates the generated droplets physically, thereby avoiding cross-contamination. The present invention can effectively control the size and shape of the generated droplet.

A lateral flow test strip reader for reading an output of a lateral flow assay to determine a presence or absence of a target in a sample includes: a housing having a lateral flow test strip receptacle for receiving a lateral flow test strip therein, the lateral flow test strip receptacle defining a test region and a control region for a lateral flow test strip; a light source that generates an excitation light beam; at least one lens for optically expanding the excitation light beam in a direction across the test region and the control region such that the excitation light beam is configured to simultaneously impinge and excite both the test region and the control region; and an optical detector configured to simultaneously detect an image comprising emission signals from the test region and the control region, wherein the detected emission signals indicate a presence or absence of a target in the sample.

A manually actuated chromatography device comprising a chamber for receiving a liquid sample, a pump with a metering valve, and a chromatography element, wherein the pump moves a predetermined volume of liquid from the sample chamber to the chromatography element.

Phase separating tubes for the separation of multiphase systems and/or for separate extraction of immiscible liquids, for example by the use centrifugation. The invention extends to methods of extracting liquids from multi-phase systems.

Instrument free “plasticware” is provided that enables multi-step molecular reactions in a diagnostics context. A hollow plunger that is movable within a surrounding tube defines a reaction chamber inside the plunger. By moving the plunger to different positions in the tube, a sample can be collected, then the sample can be washed, and finally the reaction chamber can be sealed to perform diagnostic reactions on the sample. The juxtaposition of large sample collection/washing volume with small reaction volume allows one to conduct a wide range of diagnostic assays including a LAMP (Loop mediated isothermal amplification) based saliva test in a small, portable self-contained device. Applications include Molecular diagnostics for health applications (including COVID19 test), Environmental Monitoring, Disease surveillance, and Veterinary health.

A device including a housing, a zone and a means for testing a fluid sample within the housing is disclosed. The housing is constructed of a fluid impermeable material, and defines a first fluid port, and a second fluid port. The first fluid port is configured to connect to a fluid collection device to receive a fluid sample from the fluid collection device into the housing. The second port is configured to pass the fluid sample from the housing into a testing instrument. The zone is formed in the housing. The zone is constructed of a material that allows an analysis of the fluid sample positioned within the housing, and located adjacent to the zone.