The present disclosure describes systems and methods for versatile acoustic tweezer trapping and transport configurations. Examples can use ultrasound for contact-free, biocompatible, and precise manipulation of particles from millimeter to sub-micrometer scale along a narrow and complex path. Examples include spatially complex particle trapping and manipulation inside a boundary-free chamber using a single pair of sources and a shadow waveguide. The shadow waveguide structure can be disposed just outside a microfluidic chamber to guide and control the acoustic wave fields inside the chamber. The shadow waveguide can create a tightly confined, spatially complex acoustic field inside the chamber without an interior structure that could interfere with net flow or transport.

A microfluidic device capable of trapping contents in a manner suitable for high-throughput imaging is described herein. The microfluidic device may include one or more trapping devices, with each trapping device having a plurality of trapping channels. The trapping channels may be configured to receive contents via an inlet channel that connects a sample reservoir to the trapping channels via fluid communication. The trapping channels are shaped such that contents within the trapping channels are positioned for optimal imaging purposes. The trapping channels are also connect to at least one exit channel via fluid communication. The fluid, and contents within the fluid, may be controlled via hydraulic pressure.

A technique relates to a machine for sorting. A removable cartridge includes a nanofluidic module. The removable cartridge includes an input port and at least two output ports. The nanofluidic module is configured to sort particles in a sample fluid. A holder is configured to receive the removable cartridge. A pressurization system is configured to couple to the input port of the removable cartridge. The pressurization system is configured to drive the sample fluid into the nanofluidic module for separation to the at least two output ports.

A fluid delivery device includes at least one area onto which at least one support element having at least one well may be placed in a defined position. The fluid delivery device further includes at least one pipetting device having a connector configured to releasably connect the at least one pipetting device with a disposable tip and with a fluid displacement element which enables aspiration and ejection of a defined volume of liquid to or from the disposable tip. The at least one pipetting element is movable in a vertical and preferably in at least one horizontal direction. The fluid delivery device also includes a blowing element that has at least one aperture coupled to a source of pressurized gas and is movable in a vertical and preferably at least one horizontal direction. A system includes such a fluid delivery device and the at least one support element.

A method for analyzing biological samples is disclosed herein. In an embodiment, the method includes receiving a fluid sample into a cartridge device, which comprises: a fluidic chamber; at least one microfluidic channel in fluid communication with the fluidic chamber; and a venting port configured to apply a pneumatic force to the fluidic chamber; and inserting the cartridge device into a reader device to perform measurements, wherein the cartridge device is positioned in a vertical or tilted position such that at least a portion of the fluid sample inside the fluidic chamber is pulled by gravity in a direction away from the venting port or towards the bottom of the fluidic chamber.

The present disclosure relates to a nucleic acid analysis apparatus using a cartridge which can simplify the nucleic acid extraction and applicable to a molecular diagnostic POCT equipment. The nucleic acid analysis device includes a stage on which a cartridge is mountable, a nucleic acid extraction unit, and a control unit. The nucleic acid extraction unit performs a nucleic acid extraction through crushing of the sample, the cell disruption, and the nucleic acid purification as well as a nucleic acid amplification. The control unit controls the stage and the nucleic acid extraction unit so that the nucleic acid extraction through the crushing of the sample, the cell disruption, and the nucleic acid purification as well as the nucleic acid amplification are collectively performed.

A microchip controlling system comprises a microchip which is configured by adhesion of an elastic sheet and a plate/sheet member, and on which a flow path is provided as an inadhesive section between the elastic sheet and the plate/sheet member; and a microchip controlling apparatus comprising a valve mechanism which is inflated or deflated so as to control the flow path to be opened or closed.

A fluid control device includes an inlet configured to be placed directly or indirectly in fluid communication with a bodily fluid source and an outlet configured to be placed in fluid communication with a fluid collection device. The fluid control device has a first state in which a negative pressure differential produced from an external source such as the fluid collection device is applied to the fluid control device to draw an initial volume of bodily fluid from the bodily fluid source, through the inlet, and into a sequestration portion of the fluid control device. The fluid control device has a second state in which (1) the sequestration portion sequesters the initial volume, and (2) the negative pressure differential draws a subsequent volume of bodily fluid, being substantially free of contaminants, from the bodily fluid source, through the fluid control device, and into the fluid collection device.

The invention relates to a method for setting a cell concentration and/or a particle concentration in a dispensing device that has a fluid chamber into which a liquid sample is introduced that has a liquid and cells and/or particles, wherein the cell concentration and/or the particle concentration is determined, in particular in one region of the dispensing device, and the cell concentration and/or particle concentration that has been determined is compared with a target value and the cells and/or particles, in particular one or the other, that are present in the fluid chamber are moved or not moved as a function of the result of the comparison.

The present disclosure relates to systems and methods for quantifying mechanical properties of a cell containing a nucleus and cytoplasm. The system comprises a microfluidic comprises a varying width configured to deform the cell to multiple deformation levels, an imaging device configured to obtain image data of the cell received by the microfluidic channel and a processor in communication with the imaging device. The processor is configured to receive, from the imaging device, image data of the cell deformed within the microfluidic channel at a first deformation level and a second deformation level different from the first deformation level and to determine, based on the image data, one or more parameters associated with the deformed cell at the first deformation level and the second deformation level.