The present disclosure relates to a microfluidic immunoassay chip and a microfluidic line immunoassay method. The microfluidic immunoassay chip includes a loading cell, a reaction and detection cell, a washing cell, an enzyme storing cell, a substrate cell, and a termination cell, and a waste liquid cell. A detection membrane strip is disposed in the reaction and detection cell and coated with a capture antigen or a capture antibody.

A fluidic storage device capable of long-term storage of biological, chemical, and biochemical substances, including fluids and solids of a corrosive nature or generally incompatible with traditional reagent storage methods like blister packs. The fluidic device employs a fiber-based substrate which allows the substance to be stored long-term within the structure of the fiber-based substrate through capillary action. The stored substance can be released from the fiber-based substrate and used as needed as a result of active or passive forces incurred on the fluidic device. The storage as described herein will assist in minimizing the hazards associated with performing POI and POC testing by scaling down the required reagent volumes as well as facilitating long-term reagent storage and analysis on a single integrated, portable fluidic device.

A device for separating blood plasma from whole blood includes a first reservoir and a second reservoir. The first reservoir is configured to receive a sample of whole blood including red blood cells and includes a collection region and a constricted region. The second reservoir is fluidically connected to the constricted region of the first reservoir, such that, responsive to centrifugal force applied to the device, the sample of whole blood disposed within the first reservoir separates into a first fraction and a second fraction. The first fraction is located in the collection region and includes blood plasma from which substantially all red blood cells have been removed. The second fraction is located in the second reservoir and includes blood plasma and red blood cells that have been removed from the first fraction by the centrifugal force. The constricted region inhibits the second fraction from entering the collection region.

A device for separation and/or preservation of non-cellular components from a biofluid sample includes at least one separation member to separate the non-cellular components from the sample and to retain cellular components, at least one extraction member to permit extraction of the non-cellular components from the separation member, at least one flow assay to analyze the non-cellular components extracted, and a housing in which the separation member, the extraction member and the flow assay are arranged. The housing is configured to be shifted from a first configuration to a second configuration In the first configuration, the separation member and the extraction member are fluidly coupled so that the device is configured to extract the non-cellular components In the second configuration, the separation member and the extraction member are fluidly uncoupled to prevent a preservative added to the separation member from reaching the extraction member and/or the flow assay.

A droplet microfluidic chip and a method for producing microdroplets are disclosed. The droplet microfluidic chip includes at least one droplet-producing unit. The droplet-producing unit includes a dispersion phase chamber, a quantitation chamber, a capillary nozzle, and a continuous phase chamber. The droplet microfluidic chip has a rotation center. The dispersion phase chamber is provided with a loading hole configured to introduce a dispersion phase liquid. The quantitation chamber is in communication with the dispersion phase chamber and further away from the rotation center than the dispersion phase chamber. The capillary nozzle is further away from the rotation center than the quantitation chamber. One end of the capillary nozzle is in communication with the quantitation chamber, and the capillary nozzle is extended from the joining end in a direction away from the rotation center. The continuous phase chamber is in communication with the other end of the capillary nozzle away from the quantitation chamber, and the continuous phase chamber is further away from the rotation center than the capillary nozzle. The continuous phase chamber accommodates a continuous phase liquid.

A cartridge for detecting one or more characteristics of a fluid in a diagnostic assay system includes a plurality of chambers. At least one of the plurality of chambers includes a wall. The wall includes an intermediate portion disposed between an exterior surface and an interior surface of the wall. The intermediate portion can include a hygroscopic element configured to extend an active period of detection of a reagent. The intermediate portion can include a dummy material configured to slow a wetting of a reagent by the fluid. The intermediate portion can include an air gap configured to reduce internal stress and/or strain in the cartridge. A reagent can be enclosed by the wall of the at least one of the plurality of chambers. The reagent can be a lyophilized reagent.

In one embodiment, a cartridge includes at least one compartment and a reagent in the at least one compartment. The reagent is a chemical composition for testing at least one of soil and vegetation for a chemical contained in the soil or vegetation. The reagent can be used in a soil and/or vegetation analysis test. The cartridge can contain an authentication chip to ensure that the reagent is the correct reagent for the analysis test.

An automated laboratory system includes a storage system including a frame and a platform slidably mounted to the frame such that the platform is slidable relative to the frame between a docked position and an undocked position, the platform being configured to carry an instrument. The system also includes a robotic device proximate the storage system and being configured to access the instrument carried by the platform. Another automated laboratory system includes a storage system including a table and a tabletop having a central axis and being rotatably positioned on the table such that the tabletop is rotatable about the central axis between a docked position and an undocked position, the tabletop being configured to carry an instrument. The system also includes a robotic device proximate the storage system and being configured to access the instrument carried by the tabletop.

A biological detection system includes a control module, a bearing rotatable plate, a first driving module, rotatable sub-plates, second driving modules, and test cassettes. The bearing rotatable plate has a main rotating shaft. The first driving module is electrically connected to the control module and connected to the main rotating shaft, so that the bearing rotatable plate rotates about the main rotating shaft. The rotatable sub-plates each has a respective independent rotating shaft. The rotatable sub-plates are rotatably disposed on the bearing rotatable plate about the respective independent rotating shaft. The independent rotating shafts and the main rotating shaft may have different rotating directions and rotating speeds. The second driving modules are electrically connected to the control module, so that the rotatable sub-plates independently rotate about the respective independent rotating shaft. The test cassettes are detachably disposed on the rotatable sub-plates, and each of the test cassettes includes a micro-channel structure.

A method according to one or more aspects may be a method of measuring a detection material contained in a sample by using a cartridge including: chambers each capable of housing at least one of the detection material and a reagent; and a path through which the detection material is transferred between the chambers. The method may include: moving at least one of the chambers and the path to a measurement position and an image capturing range by rotating the cartridge about a rotational shaft; measuring the detection material in the measurement position; and capturing an image of a monitoring target comprising at least one of the chambers and the path in the image capturing range.