B01L2400/0683

THREE LAYER TEST TUBE AND ASSOCIATED METHODS
20170274373 · 2017-09-28 ·

A two layer and/or a three-layer device is disclosed that allows samples therein to remain at a warmer or a colder temperature than would be ordinarily possible without the use of the two or three-layer device. The two-layer device contains an interior layer that comprises the sample, and a middle or intermediate layer that comprises chemical species that undergoes an exothermic or endothermic reaction. The three layer device further has an outer layer that contains an insulating layer. When the three layer device is used for samples, the temperature of the sample can remain at a temperature around 11° C. or less for at least about 5.5 to 6 hours.

Multi-fluidic cartridges for sample analysis and methods for using same
09770716 · 2017-09-26 · ·

The invention is directed to multi-fluidic cartridges for sample analysis and to methods of using said cartridges. In one embodiment, the cartridge comprises: (a) a first conduit beginning at a sample entry port for receiving a fluid sample and in fluid communication with one or more sensors; (b) a plurality of rupturable fluidic pouches, each containing a different fluid and in fluid communication with a respective delivery conduit configured for delivering a respective fluid to said first conduit; and (c) at least one pneumatic pump configured to move said fluid sample to said one or more sensors and for transporting at least one of said different fluids to said first conduit.

Container and closure

A closure for dispensing one or more active agents into a container comprises a sealed or sealable chamber having a breakable wall and a hollow piston slidably mounted in a piston guide. Said hollow piston comprises an outer wall having an end in the chamber and at least one ventilation aperture. Said end has a cutting formation. Said hollow piston is slidable in the piston guide between a ventilation position in which the at least one ventilation aperture allows ventilation of the chamber and a sealed position in which the at least one ventilation aperture is sealed to prevent ventilation of the chamber and a deployed position in which the cutting formation has broken through at least a portion of the breakable wall. The outer wall has a retaining formation which engages with the piston guide to releasably resist sliding of the hollow piston between the ventilation position and the sealed position and the deployed position. The hollow piston may have an outer wall, and said outer wall has an end within the chamber, facing the breakable wall, wherein the cutting end has a first edge having a cutting formation and a gap in said cutting formation.

Fluidic cartridge for nucleic acid amplification and detection

A cartridge for assay of a target nucleic acid sequence in a liquid sample. The cartridge comprises: a fluidic portion through which the sample flows and in which nucleic acid amplification and detection takes place; a pneumatic portion which controls flow through the fluidic portion; and at least two electrodes which provide a potential difference for the detection of an amplified nucleic acid of interest.

CONTAINER AND CLOSURE
20170258683 · 2017-09-14 ·

A closure for dispensing one or more active agents into a container comprises a sealed or sealable chamber having a breakable wall and a hollow piston slidably mounted in a piston guide. Said hollow piston comprises an outer wall having an end in the chamber and at least one ventilation aperture. Said end has a cutting formation. Said hollow piston is slidable in the piston guide between a ventilation position in which the at least one ventilation aperture allows ventilation of the chamber and a sealed position in which the at least one ventilation aperture is sealed to prevent ventilation of the chamber and a deployed position in which the cutting formation has broken through at least a portion of the breakable wall. The outer wall has a retaining formation which engages with the piston guide to releasably resist sliding of the hollow piston between the ventilation position and the sealed position and the deployed position. The hollow piston may have an outer wall, and said outer wall has an end within the chamber, facing the breakable wall, wherein the cutting end has a first edge having a cutting formation and a gap in said cutting formation.

METHOD FOR COLLECTING AND PRESERVING A BIOLOGICAL SAMPLE
20220042883 · 2022-02-10 · ·

The disclosure relates to devices, solutions and methods for collecting and processing samples of bodily fluids containing cells (as well as embodiments for the collection, and processing and/or analysis of other fluids including toxic and/or hazardous substances/fluids). In addition, the disclosure relates generally to function genomic studies and to the isolation and preservation of cells from saliva and other bodily fluids (e.g., urine), for cellular analysis. With respect to devices for collection of bodily fluids, some embodiments include two mating bodies, a cap and a tube (for example), where, in some embodiments, the cap includes a closed interior space for holding a sample preservative solution and mates with the tube to constitute the (closed) sample collection device. Upon mating, the preservation solution flows into the closed interior space to preserve cells in the bodily fluid. The tube is configured to receive a donor sample of bodily fluid (e.g., saliva, urine), which can then be subjected to processing to extract a plurality of cells. The plurality of cells can be further processed to isolate one and/or another cell type therefrom. The plurality of cells, as well as the isolated cell type(s), can be analyzed for functional genomic and epigenetic studies, as well as biomarker discovery.

MECHANICAL ACTUATOR SYSTEM AND METHOD OF ACTUATION OF A DIAGNOSTIC DEVICE THEREWITH
20170259268 · 2017-09-14 ·

A mechanical actuator system for performing an assay on a disposable diagnostic cartridge having a plurality of fluid-containing blisters includes a body configured to carry the disposable diagnostic cartridge in stationary relation thereon. A lead screw is operably supported by the body and a drive motor is operably connected to the lead screw. A carriage is threadedly coupled to the lead screw, with the carriage having upper and lower wall spaced from one another. A roller is operably carried by the upper wall of the carriage. The roller is spaced from the lower wall for passage of the diagnostic cartridge between the roller and the lower wall. A driven gear is operably coupled to the roller in meshed engagement with the lead screw. Actuation of the drive motor causes the lead screw to rotate, thereby translating the carriage along the lead screw and concurrently causing the driven gear to rotate the roller.

Apparatus for hermetically sealed storage of liquids for a microfluidic system
09757724 · 2017-09-12 · ·

An apparatus for hermetically sealed storage of liquids for a microfluidic system includes at least one cavity and at least one sealing cone. A connection to the microfluidic system is established via the at least one sealing cone. Additionally, the at least one sealing cone is configured to close the at least one cavity.

Devices and methods for collecting and stabilizing biological samples

The present invention generally relates to devices and methods for collecting and stabilizing biological samples, and more particularly, for collecting and stabilizing blood or other bodily fluids from a user's fingertip, earlobe, heel or other locations. The present invention also relates to sample collection devices that simplify the process for mixing the biological samples with an additive or additives, provide for efficient storage and safe transport of the samples, and provide for easy access to the samples for subsequent processing.

NUCLEIC ACID TESTING CASSETTE

The invention provides a nucleic acid testing cassette, including a substrate, a liquid storage component, a solid-reagent storage component, and an amplification reaction region, wherein the substrate is connected to the amplification reaction region; the liquid storage component and the solid-reagent storage component are disposed on the substrate, respectively; the liquid storage component is communicated with the solid-reagent storage component through a micro flow channel; and the solid-reagent storage component is communicated with the amplification reaction region through a micro flow channel.