A microfluidic apparatus for delivering droplets of a first fluid to droplets of a second fluid, comprising a main channel, with a carrier fluid carrying droplets of the second fluid, an auxiliary channel, fluidly coupled to the main channel at a first intersection via a first orifice with a first fluid interface, and at a second intersection downstream to the first intersection via a second orifice with a second fluid interface, wherein a flow of the carrier fluid induces a difference of pressure between the first and second orifice generating a balance condition such that a meniscus of the second fluid interface is maintained in the auxiliary channel, at the vicinity of the second orifice, wherein a balance deviation triggers a release of a volume of the first fluid from the second fluid interface into the main channel.

A system for continuous high-throughput treatment, in particular electroporation or transfection, of a population of cells or selected cells in a population of cells, is described. The system comprises a fluidic device comprising a microfluidic channel, a pump fluidically coupled to the fluidic device and configured to pump the population of cells in a carrier liquid unidirectionally along the microfluidic channel, and a processor. The microfluidic channel has an upstream detection zone comprising a detection electrode module configured to detect a change in electrical impedance across the microfluidic channel at the upstream detection zone corresponding to a cell passing the upstream detection zone and a cell treatment zone located downstream of the upstream detection zone and comprising a cell treatment module configured to treat the cell passing the cell treatment zone. The processor is operatively coupled to the detection electrode module and configured to calculate the velocity V of the cell passing the upstream detection zone based on the change in electrical impedance, and transiently actuate the cell treatment module when the cell reaches the cell treatment module based on the calculated velocity V of the cell and a distance D1 between the detection electrode module and the cell treatment module. A method for electroporation of cells is also described.

In one example in accordance with the present disclosure, a particle dispensing system is described. The particle dispensing system includes a port to receive a number of fluid cartridges. Each fluid cartridge is to hold an amount of fluid to be ejected. The particle dispensing system also includes an optical verification system to determine, following ejection, a count of a number of particles ejected during an ejection event. The particle dispensing system also includes a controller to selectively activate a number of fluid ejectors to eject the amount of fluid.

The present invention relates to droplet-based surface modification and washing. According to one embodiment, a method of splitting a droplet is provided, the method including providing a droplet microactuator including a droplet including one or more beads and immobilizing at least one of the one or more beads. The method further includes conducting one or more droplet operations to divide the droplet to yield a set of droplets including a droplet including the one or more immobilized beads and a droplet substantially lacking the one or more immobilized beads.

A method and system are provided for extracting a target analyte from a sample using acoustic ejection technology. The method involves applying focused acoustic energy to a fluid reservoir housing a fluid composition that contains a target analyte and comprises an upper region and a lower region, where the concentration of the target analyte in the upper region differs from that in the lower region. The focused acoustic energy is applied in a manner that is effective to result in the ejection of a fluid droplet from from the fluid composition into a droplet receiver, wherein the concentration of the analyte in the droplet corresponds to either the concentration of the analyte in the upper region or the concentration of the analyte in the lower region, and wherein the concentration of the analyte is substantially uniform throughout the droplet. The fluid composition may comprise an ionic liquid, used in the extraction of ionic target analytes. Related methods and an acoustic extraction system are also provided.

A digital dispense system for preparing and analyzing a plurality of samples. The system includes two or more fluid droplet ejection devices. Each fluid droplet ejection device contains a fluid droplet ejection cartridge containing at least one fluid to be dispensed. The fluid droplet ejection cartridge is attached to a translation mechanism for moving the fluid droplet ejection cartridge back and forth over a sample holder in an x direction. A sample tray translation mechanism is provided for moving a sample tray along a production path in a y direction orthogonal to the x direction through the two or more fluid droplet ejection devices.

Provided herein is generally tubular container, preferably including a plurality of reservoirs defined therein. The container can be adapted for acoustic ejection of a fluid disposed within at least one of the reservoirs of the plurality of reservoirs. Alternatively, the container can be adapted for extraction of a fluid disposed within at least one of the reservoirs of the plurality of reservoirs using a non-acoustic liquid handling method.

A physical quantity detection device including a container that is formed with an accommodation space accommodating a detection object formed of a dielectric, a first electrode and at least one second electrode that face with each other via the accommodation space, and an electrostatic capacitance detector that detects an electrostatic capacitance between the first electrode and the second electrode by applying an alternating current voltage between the first electrode and the second electrode. A frequency of the alternating current voltage applied between the first electrode and the second electrode is 1 kHz or higher.

Disclosed herein is a system to detect and characterize individual particles and cells using at least either optic or electric detection as the particle or cell flows through a microfluidic channel. The system also provides for sorting particles and cells or isolating individual particles and cells.

A matrix droplet extruder includes a casing; one or a plurality of reagent containers; a plurality of pneumatic connectors on the casing that are each configured to be connected to a pneumatic actuator to provide controlled pneumatic pressure to one or more of said plurality of the pneumatic connectors; a droplet matrix extrusion surface with one or a plurality of printing zones, each printing zone comprising an array of perforations; and a liquid management chip for dispensing one or more reagents from said one or a plurality of reagent containers through the array of perforations of said one or a plurality of printing zones, so as to repeatedly generate a matrix of droplets when applying the pneumatic pressure to said one or more reagents.