Engineered nanoscale multicomponent particles are introduced and are called “quants.” Methods and apparatuses for producing such multicomponent nanoparticles are provided. A single quant can be manufactured to contain a variety of different internal component molecules. Likewise, a plurality of such quants may be manufactured wherein the plurality of quants are suspended in an aqueous solution. Typically, quants are produced in quantity and concentration adequate to support human scale therapeutics. In some embodiments, millions or billions of quants are suspended in a volume of aqueous solution for delivery to a patient. When manufactured to the same specification, the plurality of quants are uniform in size, uniform in chemical composition, and therefore uniform in functionality. Functional uniformity is an essential aspect of quants, manifested in design and production. By controlling the variables of manufacture, such as particle size and composition, and by redefining a drug dose as the measured number of quants delivered (as opposed to measuring a drug dose by the mass of its active ingredient), the performance of these nanoparticle-based drugs introduce significant efficiencies and much higher value products to the expanding therapeutics market.

Cartridges and related systems and methods are disclosed. In accordance with an implementation, a method includes securing a sample container in a sample container receptacle of a cartridge using a sample container lock and coupling the cartridge to a cartridge receptacle of a system. The method also includes depositing a sample from the sample container within a sample well of the cartridge and determining a presence of a target molecule within the sample using the system. In response to the target molecule being present within the sample, the method includes releasing the sample container lock of the cartridge to allow the sample container to be removed from the sample container receptacle and for the cartridge to remain coupled to the system.

A method includes mounting an integrated electro-microfluidic probe card to a device area on a bio-sensor device wafer, wherein the electro-microfluidic probe card has a first major surface and a second major surface opposite the first major surface. The method further includes electrically connecting at least one electronic probe tip extending from the first major surface to a corresponding conductive area of the device area. The method further includes stamping a test fluid onto the device area. The method further includes measuring via the at least one electronic probe tip a first electrical property of one or more bio-FETs of the device area based on the test fluid.

Described herein are digital microfluidic (DMF) devices and corresponding methods for managing reagent solution evaporation during a reaction. Reactions on the DMF devices described here are performed in an air or gas matrix. The DMF devices include a means for performing reactions at different temperatures. To address the issue of evaporation of the reaction droplet especially when the reaction is performed at higher temperatures, a means for introducing a replenishing droplet has been incorporated into the DMF device. A replenishing droplet is introduced every time when it has been determined that the reaction droplet has fallen below a threshold volume. Detection and monitoring of the reaction droplet may be through visual, optical, fluorescence, colorimetric, and/or electrical means.

Devices and methods for characterization of analyte mixtures are provided. Some methods described herein include performing enrichment steps on a device before expelling enriched analyte fractions from the device for subsequent analysis. Also included are devices for performing these enrichment steps.

The technology described herein generally relates to systems for extracting polynucleotides from multiple samples, particularly from biological samples, and additionally to systems that subsequently amplify and detect the extracted polynucleotides. The technology more particularly relates to microfluidic systems that carry out PCR on multiple samples of nucleotides of interest within microfluidic channels, and detect those nucleotides. The technology still more particularly relates to automated devices for carrying out pipetting operations, particularly on samples in parallel, consistent with sample preparation and delivery of PCR-ready nucleotide extracts to a cartridge wherein PCR is run.

A dispenser for receiving and dispensing volumes of fluid, on which a piston/cylinder unit having a piston and a cylinder, can be fitted in a releasable manner by means of a movement running at least substantially in an axial direction of the dispenser. The dispenser has a piston actuator for moving the piston relative to the cylinder. The piston actuator is arranged in a movable manner in the dispenser and is driven by means of a drive. The dispenser has a locking element which is arranged in a movable manner in the dispenser and is driven by a further drive. Also disclosed is a system for receiving and dispensing volumes of fluid, to a method for fitting a piston/cylinder unit in a releasable manner on a dispenser, and to a method for releasing a piston/cylinder unit which has been fitted on a dispenser.

A droplet discharge device for discharging a droplet into one or more droplet storage parts of a storage vessel; the droplet discharge device including: a droplet discharge part configured to discharge the droplet in a predetermined amount from a nozzle hole of the droplet discharge part; a storage vessel holding part configured to hold the storage vessel; a mover part configured to move the droplet discharge part relative to the storage vessel that is held by the storage vessel holding part; and a detecting part configured to detect a shape of a surface of the storage vessel that is held by the storage vessel holding part.

There is provided an assembly, useable to screen sample fluids for predefined molecules, the comprising, a needle unit comprising n hollow needles, wherein n is greater than one; a flow cell unit comprising m flow cells, wherein m is greater than one, each flow cell having an input and an output, and a test surface on which ligands can be provided; a first selector valve unit which is fluidly connected between the needle unit and flow cell unit, which is operable to selectively fluidly connect any one of the n hollow needles with the m flow cells in the flow cell unit; a pumping means which is selectively operable to provide negative pressure; a second selector valve unit which is fluidly connected between the pumping means and the output of each flow cell. There are further provided methods of screening sample fluids for predefined molecule.

A manual-electronic pipetting device for pipetting a medium. The pipetting device includes a controller, a manually displaceable actuating element, at least one piston for aspirating and discharging the medium, a motor for driving the at least one piston in response to an actuation and/or displacement of the actuating element, at least one sensor for determining a displacement of the actuating element, and a data storage. The controller determines a pipetting protocol based on at least one sensor signal of the at least one sensor during a displacement of the actuating element, the controller further storing the pipetting protocol in the data storage, the pipetting protocol including data records indicative of a position and a speed of the at least one piston during the displacement of the actuating element.