FLUIDIC CARTRIDGES FOR ELECTROCHEMICAL DETECTION OF DNA

• US 20090042280A1
• Filed: 12/06/2005
• Published: 02/12/2009
• Est. Priority Date: 12/13/2004
• Status: Abandoned Application

• Current Assignee: Geneohm Sciences Incorporated (Becton Dickinson & Co)
• Original Assignee: Geneohm Sciences Incorporated (Becton Dickinson & Co)
• Inventors: Holmlin, Robert Erik, Yang, Xing
• Application Number:
  US11/721,533
• Publication Number:
  US 20090042280A1
• Time in Patent Office: Days
• US Class Current: 435/287.200
• CPC Class Codes: B01L 2200/10 Integrating sample preparation and analysis in single entity, e.g. lab-on-a-chip concept
• CPC Class Codes: B01L 2200/16 Reagents, handling or storing thereof
• CPC Class Codes: B01L 2300/0636 Integrated biosensor, microarrays
• CPC Class Codes: B01L 2300/0645 Electrodes
• CPC Class Codes: B01L 2300/0877 Flow chambers
• CPC Class Codes: B01L 2300/1822 using Peltier elements
• CPC Class Codes: B01L 2300/1827 using resistive heater
• CPC Class Codes: B01L 2400/049 vacuum
• 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: B01L 7/52 with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples amplification or hybridisation processes per se C12Q1/68; controlling sequential reactions for synthesis B01J19/0046

Abstract

A flow cell cartridge for the detection of differences in nucleic acid sequences is disclosed. The flow cell cartridge has an electrode array and two openings, in which one opening is for the entry and exit of sample, and the other opening is for the control of the entry and exit of sample through the exertion of negative and positive pressure. The entire flow cell cartridge can be moved from sample to sample to allow different samples to be drawn into the cartridge into contact with an electrochemical electrode array, thus allowing reactions to occur in the chamber itself.

Claims

1. A flow cell cartridge, said flow cell cartridge comprising:

a housing forming a chamber, wherein the housing has a first opening adapted for the flow of a liquid and a second opening adapted for the flow of a gas, wherein said openings open to the inside of the chamber and movement of a gas out of said second opening is adapted to move a gas or a liquid into said first opening; and

an electrode array positioned inside said chamber such that a probe on the electrode array is exposed to the inside of the chamber, wherein the electrode array has an electrically conductive connection to a point external to the chamber, and wherein at least a portion of the electrode array has probe nucleic acid bound thereto.

2. The flow cell cartridge of claim 1, wherein the probe nucleic acid comprises peptide nucleic acid segments.

3. The flow cell cartridge of claim 2, wherein the chamber is shaped in two dimensions in a diamond shape.

4. The flow cell cartridge of claim 1, wherein the housing is configured to accept a pipette tip over a portion of the housing section creating the first opening.

5. The flow cell cartridge of claim 4, wherein the chamber has a first opening that is gas permeable and liquid permeable, and has a second opening that is gas permeable but not significantly liquid permeable.

6. The flow cell cartridge of claim 1, wherein the electrically conductive connection to the exterior of the chamber is configured to contact spring loaded pins.

7. The flow cell cartridge of claim 1, wherein the electrically conductive connections to the electrode array comprise pre-deformed metal bumps.

8. The flow cell cartridge of claim 1, further comprising a Peltier device.

9. The flow cell cartridge of claim 1, further comprising a temperature sensor.

10. The flow cell cartridge of claim 9, wherein the temperature sensor is positioned within the chamber.

11. The flow cell cartridge of claim 1, further comprising a resistive heater and a temperature sensor.

12. A flow cell cartridge, said flow cell cartridge comprising:

a housing, said housing comprising

     1) a front half and

     2) a back half, wherein the front half when joined with the back half forms

     3) a chamber, and wherein said housing has a first opening that is both liquid and gas permeable and a second opening that is gas permeable but is not significantly liquid permeable;

at least a working electrode and a reference electrode, wherein said electrodes are in said chamber; and

an electrical connection located on an external surface of the housing, wherein said electrical connection is in electrical contact with one or more of said electrodes.

13. The flow cell cartridge of claim 12, further comprising a Peltier device thermally coupled to said chamber.

14. The flow cell cartridge of claim 13, further comprising a temperature sensor thermally coupled to said chamber.

15. The flow cell cartridge of claim 14, further comprising a nucleic acid probe attached to said working electrode.

16. The flow cell cartridge of claim 15, further comprising a peptide nucleic acid segment attached to said working electrode.

17. The flow cell cartridge of claim 12, further comprising a counter ion.

18. The flow cell cartridge of claim 17, wherein the counter ion is a ruthenium ion.

19. The flow cell cartridge of claim 12, wherein the back half of the housing comprises a substrate for an electrode.

20. The flow cell cartridge of claim 12, wherein the second opening is connected to a vacuum source.

21. The flow cell cartridge of claim 20, wherein the first opening is connected to a pipette tip.

22. A method of applying a sample to an electrode array, the method comprising:

contacting a first opening of a flow cell cartridge (FCC) to a sample to be tested, wherein said FCC comprises a housing, said housing comprising a chamber, said chamber having a first opening and a second opening, and an electrode array contained within said chamber; and

applying a negative pressure to the second opening for a period of time to move the sample through the first opening and into the chamber, thus promoting contact between the sample and the electrode array.

23. The method of claim 22, further comprising incubating a sample or reagent solution in said chamber for a time sufficient for polynucleotide indicative of the presence of analyte in a sample to bind to a probe nucleic acid attached to said electrode, and then expelling said sample or reagent solution from the chamber by exerting a positive pressure through said second opening.

24. The method of claim 22 or 23, further comprising applying a negative pressure to the second opening to bring into the FCC a set of reagents for performing a rolling circle amplification;

and performing a rolling circle amplification inside of said chamber.

25. The method of claim 24, further comprising waiting for a period of time sufficient to allow a target nucleotide segment in said chamber that is indicative of the presence of analyte in said sample to bind to a probe nucleic acid attached to said electrode, and determining an electrical signal at said electrode that is indicative of the presence of said target polynucleotide segment.

26. (canceled)

27. A method for performing an assay, comprising:

providing a housing having a first opening, a second opening, a chamber interposed between said first and second opening, wherein said chamber includes at least one binding moiety for indicating a positive assay;

providing at least first, second, and third wells containing liquids or reagents useful in performing an assay;

positioning the first opening in liquid contact with the first well;

moving liquid from the first well through the first opening and into the chamber by removing gas from the second opening;

positioning the first opening in liquid contact with the second well;

moving liquid from the second well through the first opening and into the chamber by removing gas from the second opening;

positioning the first opening in liquid contact with the third well;

moving liquid from the third well through the first opening and into the chamber by removing gas from the second opening; and

ascertaining whether said binding moiety has participated in binding indicative of a positive assay.

28-51. -51. (canceled)