MICROFLUIDIC CHIP
    7.
    发明申请
    MICROFLUIDIC CHIP 审中-公开

    公开(公告)号:WO2022211637A1

    公开(公告)日:2022-10-06

    申请号:PCT/NL2022/050186

    申请日:2022-04-02

    Applicant: EMULTECH B.V.

    Abstract: The invention relates to a microfluidic chip comprising at least two units for droplet formation, each unit comprising a first supply channel for supplying a first phase, a second supply channel for supplying a second phase and a discharge channel for discharging a product phase, wherein the first and second supply channel converge at a junction to the discharge channel. The hydraulic resistance of the supply channels is higher than that of the discharge channel, so that there is a better flow at the junction, yielding droplets of higher uniformity. In a preferred embodiment, there is a manifold that feeds all the units for droplet formation in a parallel fashion, wherein the manifold has at least a ten times lower hydraulic resistance than the supply channels in the units for droplet formation. This results in droplets that have an even higher uniformity. Another advantage, especially with higher numbers of units for droplet formation in the chip, is that there is less disturbance of liquid flow by gas bubbles and less inactivity of channels when starting a process in the microfluidic chip.

    IN VITRO DIAGNOSTIC DEVICE
    10.
    发明申请

    公开(公告)号:WO2021252810A1

    公开(公告)日:2021-12-16

    申请号:PCT/US2021/036885

    申请日:2021-06-10

    Inventor: VAINIKKA, Caleb

    Abstract: A method of identifying the presence of an analyte may include providing an in vitro test device and a test swab; obtaining a sample using the test swab; transitioning the locking member from the first configuration to the second configuration; advancing the plunger into the housing to pierce the one or more reagent pouches in the reagent region to cause reagent therein to be released and mix; inserting the test swab with obtained sample into the interior of the plunger; rotating the in vitro test device and disposing it on its plunger base; and determining whether the analyte is present. The in vitro test device may include a plunger, a housing, one or more reagent pouches disposed in the housing, a lateral flow test strip, and a locking member having configurations that either allow or prevent reagent in the one or more reagent pouches from being released.

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