PLURALITY OF REACTION CHAMBERS IN A TEST CARTRIDGE

• US 20150284773A1
• Filed: 06/18/2015
• Published: 10/08/2015
• Est. Priority Date: 05/09/2012
• Status: Active Grant

• Current Assignee: Qiagen GmbH (Qiagen NV)
• Original Assignee: Stat-Diagnostica & Innovation, S.L.
• Inventors: Bru Gibert, Rafael, Carrera Fabra, Jordi, Comengs Casas, Anna, Garcia Snchez, Jos Antonio
• Granted Patent: US 10,092,900 B2
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: B01L 2200/0605 Metering of fluids
• CPC Class Codes: B01L 2300/0627 Sensor or part of a sensor is integrated
• CPC Class Codes: B01L 2300/0848 Specific forms of parts of containers
• CPC Class Codes: B01L 2300/0861 Configuration of multiple channels and/or chambers in a single devices
• CPC Class Codes: B01L 2300/0864 comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
• CPC Class Codes: B01L 2300/087 Multiple sequential chambers
• CPC Class Codes: B01L 2300/12 Specific details about materials
• CPC Class Codes: B01L 2300/18 Means for temperature control
• CPC Class Codes: B01L 2300/1822 using Peltier elements
• CPC Class Codes: B01L 2300/1827 using resistive heater
• CPC Class Codes: B01L 2400/0475 specific mechanical means and fluid pressure
• CPC Class Codes: B01L 3/502 with fluid transport, e.g. in multi-compartment structures centrifugal-type cuvettes G01N21/07; analysis by separation into components G01N30/00; automatic analysers G01N35/00
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: C12Q 1/6806 Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay C12Q1/6804 takes precedence
• CPC Class Codes: G01N 21/75 Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated systems in which material is burnt in a flame or plasma G01N21/72, G01N21/73
• CPC Class Codes: G01N 33/50 Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing measuring or testing processes involving enzymes or microorganisms, compositions or test papers therefor; processes for forming such compositions, condition responsive control in microbiological or enzymological processes C12Q
• CPC Class Codes: G01N 33/5306 Improving reaction conditions, e.g. reduction of non-specific binding, promotion of specific binding

Abstract

A fluidic testing method is presented that includes flowing an initial amount of liquid down a first inlet channel of a single-port fluidic testing system, and splitting the initial amount of liquid from the first inlet channel into a plurality of second inlet channels. Each second inlet channel is coupled to a given test chamber of a plurality of test chambers, wherein each of the plurality of test chambers has a wall that defines a longest side of a given test chamber, and wherein each of the plurality of test chambers has only one opening through the wall of a corresponding test chamber. The method also includes filling each of the plurality of test chambers with a final amount of liquid, the final amount being substantially equal in each of the test chambers and summing from each test chamber to equal the initial amount of liquid.

Claims

1. A method comprising:

flowing an initial amount of liquid down a first inlet channel of a single-port fluidic testing system;

splitting the initial amount of liquid from the first inlet channel into a plurality of second inlet channels, each second inlet channel coupled to a given test chamber of a plurality of test chambers, wherein each of the plurality of test chambers has a wall that defines a longest side of a given test chamber, and wherein each of the plurality of test chambers has only one opening through the wall of a corresponding test chamber; and

filling each of the plurality of test chambers with a final amount of liquid, the final amount being substantially equal in each of the test chambers and summing from each test chamber to equal the initial amount of liquid.

2. The method of claim 1, wherein the wall of each test chamber is configured to be aligned substantially parallel to a gravity vector.

3. The method of claim 1, further comprising re-suspending one or more reagents disposed in one or more of the plurality of test chambers in the final amount of liquid.

4. The method of claim 1, further comprising re-suspending one or more reagents disposed in one or more of a plurality of premixing chambers in the final amount of liquid.

5. The method of claim 1, further comprising heating the contents within at least one of the plurality of test chambers.

6. The method of claim 5, wherein the heating comprises heating with a Peltier device.

7. The method of claim 5, wherein the heating comprises heating with resistive heating elements.

8. The method of claim 5, wherein the heating comprises heating with forced air.

9. The method of claim 1, further comprising detecting one or more optical properties of the contents within at least one of the plurality of test chambers.

10. The method of claim 1, wherein the flowing, splitting, and filling are performed via a single pump source.