The disclosure provides devices, systems and methods for the generation of encapsulated reagents and the partitioning of encapsulated reagents for use in subsequent analyses and/or processing, such as in the field of biological analyses and characterization.

Devices, systems, and their methods of use, for generating droplets are provided. One or more geometric parameters of a microfluidic channel can be selected to generate droplets of a desired and predictable droplet size.

Device (145) for dispensing drops of liquid, characterised in that it comprises: —at least one container (100) for a liquid, comprising at least one internal chamber and an upper opening, each chamber having a lower aperture and a seal sealing the upper opening, the seal having a substantially planar resiliently deformabie flexible portion, —at least one mechanical actuation means (146) configured to deform a flexible portion of a seal of at least one container, —a means (147) for selecting the volume of a drop to be dispensed from a plurality of drop volumes, a means (148) for determining the volume of liquid present in at least one container, and—a means (149) for controlling the actuation means, which means controls the movement from at least one point of the flexible portion of a container seal, as a non-constant function of the drop volume to be dispensed and the volume of liquid present in the container.

A dosing device is proposed which is designed for dosed output of a fluid. The dosing device has a block-shaped channel body, through which a dosing channel system passes. The dosing channel system has a fluid infeed opening and a plurality of fluid output openings. The fluid output openings are formed by the channel apertures of narrowed output sections of a plurality of output channels of the dosing channel system. The entire dosing channel system, including the output channels, is formed in the block-shaped channel body. The dosing channel system is preferably structured such that the flow velocity of the fluid channelled through during operation is at least substantially the same throughout with the exception of in the output sections of the output channels.

A perforate element for use in a print head for non-contact liquid printing comprises: at least one ejection element including an outlet, configured to eject a bulk flow of printing liquid out of the print head; and a liquid residence element, arranged to provide a layer of liquid over the outlet which extends laterally of the outlet and through which the bulk flow is ejected.

Systems and methods for positive dispense verification are disclosed. In one embodiment, a system has a plurality of light emitters. The light from the emitters is directed toward a plurality of light detectors across a proximately horizontal plane. The liquid dispense device is positioned above the horizontal plane of light emission from the plurality of light emitters to the plurality of light detectors such that the dispensed liquid will travel through the horizontal plane defined by the emitted light and onto the container being inoculated. Each of the plurality of detectors is coupled to an amplifier. The amplifier generates a signal in response to an interrupt in the transmission of light from the light emitters to the light detectors when the light path is disrupted by the dispense of liquid confirming the liquid was dispensed onto the container.

Embodiments include microfluidic devices and related methods. A microfluidic device for producing microbubbles may include a first microfluidic channel for supplying a continuous phase fluid, the first microfluidic channel including a convergent section and a constant-width section downstream from the convergent section, wherein the constant-width section discharges into a junction; a second microfluidic channel for supplying a dispersed phase fluid, the second microfluidic channel including an orthogonal section oriented orthogonal to the constant-width section, wherein the orthogonal section discharges into the junction; and a third microfluidic channel for conveying produced microbubbles, the third microfluidic channel including a divergent section, wherein the junction discharges into the divergent section.

Systems and methods for positive dispense verification. In one aspect, a system has a plurality of light emitters. The light from the emitters is directed toward a plurality of light detectors across a proximately horizontal plane. The liquid dispense device is positioned above the horizontal plane of light emission from the plurality of light emitters to the plurality of light detectors such that the dispensed liquid will travel through the horizontal plane defined by the emitted light and onto the container being inoculated. Each of the plurality of detectors is coupled to an amplifier. The amplifier generates a signal in response to an interrupt in the transmission of light from the light emitters to the light detectors when the light path is disrupted by the dispense of liquid confirming the liquid was dispensed onto the container.

Method of analysis. In the method, a first emulsion and a second emulsion substantially separated from one another by a spacer fluid may be formed. The first emulsion, the spacer fluid, and the second emulsion may be flowed in a channel from a fluid inlet to a fluid outlet of a heating and cooling station having two or more temperature-controlled zones, such that each emulsion is thermally cycled to promote amplification of a nucleic acid target in droplets of the emulsion. Amplification data may be collected from individual droplets of each emulsion downstream of the heating and cooling station. A level of the nucleic acid target present in each emulsion may be determined based on the amplification data collected from the individual droplets of the emulsion.

The present invention discloses a method for preparing a micro-channel array plate, comprising the steps of : (1) arranging a first optical fiber glass rod and a second optical fiber glass rod closely, melting the two glass rods into a whole at a high temperature to obtain a melted glass rod, drawing the melted glass rod at least one time into a longer and thinner glass rod than the melted glass rod, and cutting the drawn glass rod into small pieces to obtain a micro-channel array plate blank, wherein the corrosion resistance of the first optical fiber glass rod and the second optical fiber glass rod to the same corrosive liquid is different; (2) corroding the micro-channel array plate blank by a corrosive liquid to obtain a micro-channel array plate crude product with through holes; and (3) conducting hydrophobic treatment on the micro-channel array plate crude product to obtain the micro-channel array plate.