DEVICES AND METHODS FOR PLASMA SEPARATION AND STORAGE

    公开(公告)号:WO2020014190A1

    公开(公告)日:2020-01-16

    申请号:PCT/US2019/040945

    申请日:2019-07-09

    Abstract: A centrifugal cartridge or disk used for extraction of light supernatant fractions from fluid samples is described, particularly for non-homogenous fluid biological samples such as whole blood. The device may be used to collect cell-free blood plasma or a fraction of whole blood containing target cells such as leukocytes. Single or multiple channels are described, including channels with passive valves, gaskets, receiving cavities, inlet holes, capillary wicking ridges, distal cavities for cell retention, separator gel, and density medium. Centrifugal action causes whole blood in a receiving cavity to pass into one or more channels where it separates into blood cells, plasma and optionally fractions of an intermediate density. After spin, the plasma returns to the receiving cavity by way of the one or more channels for extraction through the inlet hole or other inwardly located hole. Disposable cartridges are constructed of monolithic top and bottom plates, which may be joined together by an elastomeric outer seal.

    DEVICE AND METHOD OF IMAGING FLUIDIC SAMPLES

    公开(公告)号:WO2019240959A1

    公开(公告)日:2019-12-19

    申请号:PCT/US2019/034663

    申请日:2019-05-30

    Abstract: A device and method for automated imaging of samples are described, particularly for non-homogeneous fluid biological samples. One purpose is particle quantification and other analysis. A device comprises a fluidic disk, a monolithic optical subsystem comprising a camera, imaging optics, rotational and focus motors, controller, and user interface. In a method, the fluidic disk receives a biological sample containing particles of interest and distributes them into multiple channels of defined thickness. Spatially distinct portions of the sample are drawn into each channel. The fluidic disk is then rotated by a motor such that a portion of each channel comes into alignment with the imaging optics and then each portion is imaged sequentially, thereby compensating for sample non-homogeneity. Embodiments include monochromatic LED illumination and image processing and particle counting in the channel images.

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