A capillary driven microfluidic system and a biosensing device including the capillary driven microfluidic system are provided. The capillary driven microfluidic system includes: a first substrate comprising at least one microfluidic channel ending in an opening, and having, adjacent to the opening, a protruding element; and a second substrate comprising at least one open cavity. The at least one protruding element and the at least one cavity include at least one hydrophilic surface. In addition, the at least one protruding element and the at least one cavity may be adapted for engaging with one another for providing transfer of a fluid between the first substrate and the second substrate. A space between the at least one hydrophilic surface of the at least one protruding element and the at least one hydrophilic surface of the at least one cavity is provided, where the separation between said surfaces is such that capillary forces are generated on the fluid upon entering inside the space.

Devices and methods for measuring analytes and target particles in a sample are disclosed. In some embodiments, the disclosure provides a cartridge device. In other embodiments, the disclosure provides a method of using a cartridge device as disclosed herein for analyzing analytes and target particles in a sample. In further embodiments, the disclosure provides an analyzer including a cartridge device and a control unit device. The control unit device is configured to receive, operate, and/or actuate the cartridge device. In some embodiments, the disclosure provides a method of using an analyzer as disclosed herein for analyzing analytes and target particles in a sample.

The present invention relates to a microfluidic system (10, 20) comprising: a sample reservoir (110, 210); a first sample channel (120, 220) connected to the sample reservoir (110, 210), branching off into a second sample channel (122, 222) ending in a first valve (130, 230), and into a third sample channel (124, 224) which branches off into a fourth sample channel (126, 226) ending in a second valve (132, 232), and into a fifth sample channel (128, 228) ending in a third valve (134, 234); a buffer reservoir (140, 240); a first trigger channel (150, 250) arranged to connect the buffer reservoir (140, 240) to the second valve (132, 232); a second trigger channel (152, 252) connecting the second valve (132, 232) and the first valve (130, 230); and an exit channel (154, 254) connected to the first valve (130, 230).

An in vitro diagnostic analyzer and a reagent card. The reagent card includes a reagent card body and a mounting body. The mounting body includes a mounting hole configured to be sleeved on receive a sample tube, a hollow needle disposed in the mounting hole, a sealing portion disposed in the mounting hole, and a gas inlet channel. An end of the hollow needle is capable of being inserted into the sample tube. The sealing portion is capable of being in sealing fit with an outer wall of the sample tube. The gas inlet channel includes a gas outlet hole, a gas inlet hole, and a first flow-stopping structure. The gas inlet hole is disposed in a surface of the reagent card body. The first flow-stopping structure is disposed between the gas outlet hole and the gas inlet hole. The gas outlet hole is configured to be in fluid communication with the sample tube mounted on the mounting hole. The reagent card body includes a sample feeding channel, a test chamber, and a venting end. The sample feeding channel is in fluid communication with a liquid outlet end of the hollow needle. The sample feeding channel and the venting end are both in fluid communication with the test chamber

A biochip for the integration of all steps in a complex process from the insertion of a sample to the generation of a result, performed without operator intervention includes microfluidic and macrofluidic features that are acted on by instrument subsystems in a series of scripted processing steps. Methods for fabricating these complex biochips of high feature density by injection molding are also provided.

A system for testing for an analyte includes a test strip. The test strip includes a first flow path. The test strip further includes a heating element in communication with a heating area of the first flow path, for heating a sample in the first flow path. The test strip further includes an e-gate, the e-gate in the first flow path, the e-gate separating the heating area from a detection area of the first flow path.

A microfluidic sealing valve 1 comprises a primary channel 2, a valve channel 4, and a geometry that permits liquid in the primary channel 2 to flow into the valve channel 4 through an inlet 5. Liquid in the primary channel 2 is inhibited from flowing through a first port 8 into the void volume 7. A meniscus 9 moved by a flow of liquid in the primary channel 2 is restrained at the first port 8. A flow of liquid through the primary channel 2 generates a capillary force that causes the flow of liquid to flow into the valve channel 4. A capillary force generated by the flow of liquid through the valve channel 4 causes the meniscus 9 to expand from the first port 8 into the primary channel, to inhibit flow of liquid in the primary channel 2 past the first port 8.

A device for detecting nucleic acids in a biological sample has a sample port, a lysis station and a sample conduit configured to mix a sample and lysis agent to form a sample-lysis mixture, pass the sample-lysis mixture across a solid-state membrane to capture nucleic acids in the biological sample therein, and receive the remainder of the sample-lysis mixture in a waste chamber. The wash station is configured to introduce the wash solution following the sample-lysis mixture, pass the wash solution across the solid-state membrane to purify nucleic acids captured therein, and receive the wash solution from the solid-state membrane in the waste chamber. The elution station is configured to pass the eluent across the solid-state membrane, elute captured nucleic acids from the solid-state membrane, and pass the captured nucleic acids into one or more reaction chambers for amplifying and detecting the captured nucleic acids.

A collection device for a biological sample to capture target compounds such as viruses or other pathogens or particles for testing from within the sample and move the captured target compound to a separate chamber for subsequent processing. The collection device can include an openable substance blister including capture particles located in a cup interior. Capture particles can attract and bind the target compounds from the sample. An extraction tube extracts any nucleic acid from the target compound for storage or subsequent amplification and testing to confirm presence of known microorganisms. The extraction tube can comprise a heat-deformable material and can be connected to a microfluidic cartridge for further processing of nucleic acid including, amplification and detection. The microfluidic cartridge includes valves and a plurality of chambers for amplification.

This disclosure pertains to a consumable product (microplate) suitable for use in assays utilizing single-molecule recognition through equilibrium Poisson sampling (SiMREPS) and in other assays employing total internal reflection fluorescence (TIRF) or HiLo microscopy. The disclosed microplate is also suitable for use in other high throughput assay systems, such as single-molecule FRET, ligand-receptor binding studies, membrane biology assays, cell-based TIRF and near-TIRF assays. The disclosure further pertains to the use of the microfluidic microplate for the detection of analytes, including nucleic acids, polypeptides, carbohydrates, lipids, post-translational modifications, amino acids, metabolites, and small molecules.