This present disclosure provides devices, systems, and methods for performing point-of-care analysis of a target analyte in a biological fluid via a binding assay. The present disclosure includes a cartridge for collecting the target analyte contained in a fluid sample and performing an assay. The cartridge includes an assay stack having a first separation layer, a second separation layer, and a detection membrane. The cartridge also includes a plurality of first complexes comprising a capture molecule and a magnetic bead and a plurality of second complexes comprising a detection molecule and a detection label. Further, the detection membrane includes a substrate that interacts with the detection label to elicit a quantifiable response in the presence of the target analyte. The quantifiable response corresponds to an amount of detection antibody present in the detection membrane, and the amount of detection antibody present corresponds to an amount of the target analyte present.

The invention relates to a method for producing at least one pattern (2) on a carrier surface (7) of a carrier (3), wherein the method comprises the following steps: a. adding a first fluid (4) to the carrier surface (7) and b. adding a second fluid (5), wherein the second fluid (5) is immiscible with the first fluid (4) and at least partially covers the first fluid (4) and c. adding at least one object (6) above the carrier surface (7), d. generating the pattern (2) by a relative movement between the object (6) and the carrier (3) in which a force is exerted on the object (6) from a force generating means (28), wherein the force transmission from the force generating means (28) on the object (6) is contactless and the pattern (2) is generated by a portion of the second fluid (15) wetting the carrier surface (7).

A microfluidic system includes a hydrophobic fluidic platform and a heater. The platform includes a plurality of electrode cells operably connected to a voltage source and a controller. The heater is configured to fuse first and second vesicles. The first and second vesicles encapsulate first and second DNA precursors, respectively. The fusing combines the first and second DNA precursors. In another embodiment, a microfluidic system includes a fluidic platform including a plurality of electrode cells, a vesicle mover, and a reaction facilitator. The vesicle mover is configured to move first and second vesicles to a selected cell of the plurality of electrode cells. The reaction facilitator is operably connected to the selected cell. A method includes providing a fluidic platform comprising a plurality of cells; moving first and second vesicles encapsulating first and second reagents, respectively, to a first cell; and fusing the first and second vesicles.

A single junction sorter for a microfluidic particle sorter, the single-junction sorter comprising: an input channel, configured to receive a fluid containing particles; an output sort channel and an output waste channel, each connected to the input channel for receiving the fluid therefrom; a bubble generator, operable to selectively displace the fluid around a particle to be sorted and thereby to create a transient flow of the fluid in the input channel; and a vortex element, configured to cause a vortex in the transient flow in order to direct the particle to be sorted into the output sort channel.

The invention relates to a particle detection device and a method for detecting particles in a fluid by means of separation. A channel structure is arranged for separating an incoming flow into a major flow comprising a minor portion of particles above the first predetermined size and a minor flow comprising a major portion of particles above the predetermined size. One or more detectors are arranged for detecting particles in the major flow and minor flow. The channel structure further comprises a choked flow restriction arranged for enabling a constant flow independent of pressure conditions.

A microfluidic device includes multiple microfluidic assay units arranged on a substrate, with each assay unit including multiple scaffold regions each containing a three-dimensional scaffold with associated cells, and a media channel surrounding a fluid-permeable boundary portion of at least a second scaffold region, wherein a fluid-permeable interface between the media channel and the second scaffold region comprises a curved shape spanning an arc of more than 90 degrees. A third scaffold region may be provided. Boundaries between different scaffold regions, and between a scaffold region and the media channel, may include microposts that may be spaced apart in a curved configuration. A method for performing an assay utilizing such a device is further provided.

Provided herein, among other aspects, are methods and apparatuses for analyzing particles in a sample. In some aspects, the particles can be analytes, cells, nucleic acids, or proteins and contacted with a tag, partitioned into aliquots, detected by a ranking device, and isolated. The methods and apparatuses provided herein may include a microfluidic chip. In some aspects, the methods and apparatuses may be used to quantify rare particles in a sample, such as cancer cells and other rare cells for disease diagnosis, prognosis, or treatment.

The invention relates to a method of performing an optical or electrical measurement in a sample of a disperse fluid, the sample comprising particles and a fluid. The method comprises the steps of: a) positioning the sample in a microfluidic cavity having a resonance frequency, b) subjecting the sample, in the cavity, to an acoustic standing wave configured for causing the particles to congregate in at least one first region of the cavity, thereby causing the fluid to occupy at least one second region of the cavity, wherein the frequency of the acoustic standing wave is varied between a frequency below the resonance frequency and a frequency above the resonance frequency, and c) performing an optical or electrical measurement in the fluid in at least one of the at least one second region of the cavity. Varying the frequency ensures reproducible results. The invention also relates to a system therefore and a method and system for measuring hematocrit.

A microfluidic component used for measuring electrical impedance across a biological object, the component including a microfluidic space including a zone referred to as measurement zone, at least two electrodes arranged facing one another on each side of the measurement zone, the component being formed by assembling, along a longitudinal junction plane, at least two superposed layers referred to as lower layer and upper layer, the two layers each having at least one cavity, the two layers being assembled with one another in such a way as to position the two cavities facing one another in order to form the microfluidic space.

A magnetic bead separation method includes: storing, in a container, a mixed liquid containing a magnetic bead and a liquid containing target molecules, and adsorbing the target molecules on the magnetic bead, the magnetic bead containing a Fe-based metal soft magnetic particle and a coating film with which the Fe-based metal soft magnetic particle is coated, and having a saturation magnetization of 50 emu/g or more and 250 emu/g or less; applying an external magnetic field to the container and magnetically attracting at least a part of the magnetic bead by the external magnetic field; and applying an acceleration to the container while the magnetic bead is magnetically attracted by the external magnetic field and desorbing the liquid adhering to the magnetic bead.