G01N2001/4088

Flow cell for the selective enrichment of target particles or cells

The present invention relates to the field of micro fluidics. Specifically, the present invention relates to a novel flow cell for the selective enrichment of target particles or cells from a fluid. The flow cell exhibits a novel design which greatly improves the target particle or cell yield. The invention also provides a micro fluidic device, comprising the flow cell according to the invention. In another aspect, the invention relates to the use of a flow cell or a micro fluidic device of the invention for the isolation of target particles or cells from a fluid sample. Finally, the invention relates to a method for the selective enrichment of target particles or cells from a fluid using the flow cell of the invention.

INTEGRATED DUAL-MODE CHROMATOGRAPHY TO ENRICH EXTRACELLULAR VESICLES FROM PLASMA
20230070693 · 2023-03-09 ·

The present disclosure provides, in some embodiments, devices, methods, and kits for purifying extracellular vesicles (EVs) using size exclusion chromatography in tandem with cation exchange chromatography, which can be referred to as dual-mode chromatography (DMC).

PREPROCESSING DEVICE, PREPROCESSING METHOD, AND NON-TRANSITORY COMPUTER READABLE MEDIUM STORING PROGRAM
20220331793 · 2022-10-20 ·

In a recovery device, a removing target such as a blood cell is removed from a liquid sample in a sample container using a first filter unit, and a microorganism is filtered from the liquid sample using a second filter unit. A controller causes a first switch to block a flow channel in response to a sensor detecting a bubble. A medium flows from a second connection unit of the second filter unit toward a first connection unit. Thus, the microorganism filtered by the second filter unit is recovered by a recovery container together with the medium.

System, apparatus and method for material preparation and/or handling

Oscillating angularly rotating a container containing a material may cause the material to be separate. Denser or heavier material may unexpectedly tend to collected relatively close to the axis of rotation, while less dense or light material may tend to collect relatively away from the axis of rotation. Oscillation along an arcuate path provides high lysing efficiency. Alternatively, a micromotor may drive an impeller removably received in a container. Lysing may be implemented in batch mode, flow-through stop or semi-batch mode, or flow-through continuous mode. Lysing particulate material may exceed material to be lysed or lysed material and/or air may be essentially eliminated from a chamber to increase lysing efficiency.

Systems and Methods for Biological Sample Collection
20230074519 · 2023-03-09 ·

A container for collecting a sample is provided that can include a housing, an enclosure pivotally coupled to and slidably engaged with the housing, and a sample holder slidably engaged with and received within the enclosure. The sample holder can include a substrate configured to receive the sample. The container in a first configuration can include the enclosure being engaged with the housing to enclose and seal the substrate within an interior volume of the container. The container in a second configuration can include the enclosure exposing the substrate to the ambient environment.

AUTOMATED SOLID PHASE EXTRACTION USING FILTER TIPS

Devices and methods for performing pre-analysis sample processing of biological and chemical samples using robotic liquid handlers are disclosed. Methods for solid phase extraction, protein precipitation and filtration of biological and chemical samples using automation and the devices in a rapid and convenient way are described.

WATER QUALITY SAMPLER

A water quality sampler includes a membrane receptacle and at least 7 sample membranes. The membrane receptacle comprises at least 7 membrane cavities disposed on a top surface of the membrane receptacle. Each membrane cavity is configured to hold a sample membrane and the sample membranes are each removably positioned within the membrane cavities and extend at least 1 cm out from the top surface of the membrane receptacle. A bottom of the membrane receptacle comprises a protruding lip that traces a bottom edge of the membrane receptacle in a downward direction, where the protruding lip encompasses a stacking chamber capable of receiving a top end of a second water quality sampler to allow stacking of multiple water quality samplers.

Method and apparatus for the filtration of biological solutions
11633698 · 2023-04-25 · ·

A system, method and device are disclosed for bio-processing a feed stream and providing a constant output by operating a continuous single-pass tangential-flow process. The single-pass process provides high conversion concentration while operating at relatively low feed flow rates, and the process can also be used to provide constant output diafiltration.

Device for detecting the quality of a liquid in a supply pipe

The invention relates to a device for detecting the quality of a liquid in a supply pipe, in particular for detecting the water quality in a water pipe, comprising a flow cell, which has an inlet opening, an outlet opening and at least one receiving device for the arrangement of at least one sensor. The inlet opening and the outlet opening are provided on a base surface of the flow cell intended for connection to the supply pipe, the inlet opening of the flow cell is connected to an intake pipe, the free end of which is intended for arrangement in the supply pipe, said intake pipe being received displaceably in its longitudinal direction in the flow cell or having an adjustable length, and a liquid pump of a flow of the liquid in the supply pipe is connected to the intake pipe.

Extracellular vesicle isolation by nanomembranes

Provided are methods, devices, and kits for the isolation of extracellular vesicles using silicon nanomembranes. A method for EV isolation includes the steps of collecting a biofluid sample, contacting the biofluid sample with a pre-filtration membrane, thereby forming a first filtrate and a first retentate, optionally, washing the first retentate of the pre-filtration membrane, contacting the first filtrate from the pre-filtration membrane with a capture membrane, thereby forming a second filtrate and a second retentate, optionally, washing the second retentate, and eluting the second retentate from the capture membrane or lysing the second retentate to recover the contents.