Device For Carrying Out A Biological Assay

• US 20080248590A1
• Filed: 11/25/2005
• Published: 10/09/2008
• Est. Priority Date: 11/26/2004
• Status: Abandoned Application

• Current Assignee: NorChip AS
• Original Assignee: NorChip AS
• Inventors: Karlsen, Frank, Gulliksen, Anja, Solli, Lars Anders
• Application Number:
  US11/791,401
• Publication Number:
  US 20080248590A1
• Time in Patent Office: Days
• US Class Current: 436/518
• CPC Class Codes: B01L 2200/0621 Control of the sequence of chambers filled or emptied
• CPC Class Codes: B01L 2200/0673 Handling of plugs of fluid surrounded by immiscible fluid
• CPC Class Codes: B01L 2200/16 Reagents, handling or storing thereof
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2300/087 Multiple sequential chambers
• CPC Class Codes: B01L 2400/0427 Electrowetting
• CPC Class Codes: B01L 2400/0487 fluid pressure, pneumatics
• CPC Class Codes: B01L 3/502784 specially adapted for droplet or plug flow, e.g. digital microfluidics automatic analysis using a stream of discrete samples in a tube system G01N35/08
• CPC Class Codes: Y10T 156/10 Methods of surface bonding and/or assembly therefor

Abstract

An integrated lab-on-a-chip device for carrying out an assay to detect the presence of a biological molecule in a fluid sample, the device comprising: (a) an inlet for a fluid sample; (b) one or more reaction sites each in fluid communication with the inlet; (c) one or more reagent reservoir systems each containing reagents required for an assay to detect a biological molecule, the reagents being arranged sequentially in each reservoir system in the order in which they are required for the assay and separated from one another by a fluid.

Claims

1. An integrated lab-on-a-chip device for carrying out an assay to detect the presence of a biological molecule in a fluid sample, the device comprising:

(a) an inlet for a fluid sample;

(b) one or more reaction sites each in fluid communication with the inlet;

(c) one or more reagent reservoir systems each containing reagents required for an assay to detect a biological molecule, the reagents being arranged sequentially in each reservoir system in the order in which they are required for the assay and separated from one another by a fluid;

wherein each of the one or more reaction sites is in fluid communication with a separate reagent reservoir system, whereby the reagents in each reagent reservoir system can be sequentially introduced into the reaction site in fluid communication therewith when the device is in use.

2. A device according to claim 1 which further includes (d) means for sequentially introducing the reagents in each reagent reservoir into the reaction site in fluid communication therewith.

3. A device according to claim 2 wherein the means for sequentially introducing the reagents in each reagent reservoir into the reaction site in fluid communication therewith is a micropump.

4. A device according to claim 2 wherein the means for sequentially introducing the reagents in each reagent reservoir into the reaction site in fluid communication therewith is a variable volume chamber.

5. A device according to claim 2 wherein the means for sequentially introducing the reagents in each reagent reservoir into the reaction site in fluid communication therewith is electrowetting.

6. A device according to claim 1, further comprising (e) a waste unit in fluid communication with each of the reaction sites.

7. A device according to claim 1, wherein at least one reagent reservoir system is pre-loaded with two or more different liquid reagents, each reagent being separated by a fluid.

8. A device according to claim 7 which further comprises (f) a mixing unit in fluid communication with at least one reagent reservoir system pre-loaded with two or more liquid reagents.

9. A device according to claim 1 wherein the fluid separating the reagents in at least one reservoir system is air.

10. A device according to claim 1 wherein each reagent reservoir system comprises a channel or conduit in fluid communication with a reaction site.

11. A device according to claim 10 wherein the channel or conduit is curved, arcuate, convoluted or sinuate.

12. A device according to claim 1 wherein at least one reagent reservoir system is pre-loaded with one or more reagents in solid form.

13. A device according to claim 1, wherein liquid sample introduced at the inlet is communicated to the reaction site(s) by electrowetting when the device is in use.

14. A device according to claim 1 wherein the assay is a biological binding assay.

15. A device according to claim 14, wherein at least one reaction site contains a capture binding receptor capable of specifically binding to a biological molecule to be detected.

16. A device according to claim 15, wherein the capture binding receptor is immobilised in the reaction site.

17. A device according to claim 15 wherein the capture binding receptor comprises an antibody, an F(ab′

)₂ fragment, a single chain antibody fragment, an Fv fragment, a single chain Fv fragment, a nucleic acid, a lectin, a ligand-binding receptor, a hormone receptor, a cytokine receptor, a nucleic acid binding protein or an aptamer.

18. A device according to claim 15 wherein the reagent reservoir is pre-loaded with, in order of proximity to the reaction site, a reagent comprising secondary receptors capable of binding to the molecule to be detected, optionally a wash buffer, and one or more reagents which permit detection of the secondary receptors when bound to the molecule to be detected.

19. A device according to claim 18 wherein the reagents which permit detection of the secondary receptors comprise, in order of proximity to the reaction site, reagents capable of forming a reagent complex when added to the reaction site, which reagent complex comprises the secondary receptor linked to a nucleic acid label molecule, and reagents which permit detection of the nucleic acid label by amplifying a region of the nucleic acid and simultaneously detecting products of the amplification reaction in real-time.

20. A device according to claim 19, wherein the reagent reservoir is pre-loaded with, in order of proximity to the reaction site, a wash buffer, secondary receptors, a wash buffer, a conjugate comprising a nucleic acid label linked to a component capable of specifically binding to the secondary receptors, a wash buffer, reaction buffer for real-time NASBA detection of the nucleic acid label and enzymes for real-time NASBA detection of the nucleic acid label.

21. An apparatus for use in carrying out an assay to detect the presence of a biological molecule, the apparatus comprising a device according to claim 1.

22. An apparatus according to claim 21 which includes separate means for sequentially introducing the reagents in each reagent reservoir into the reaction site in fluid communication therewith.

23. A method for the manufacture of an integrated lab-on-a-chip device for carrying out an assay to detect the presence of a biological molecule as described in claim 1, which method comprises:

A) providing a substrate having an inlet recess, one or more reaction site recesses and one or more reagent reservoir system recesses in a surface thereof;

B) providing a cover; and

C) bonding the cover to the substrate to create (a) the inlet, (b) one or more reaction sites and (c) one or more reagent reservoir systems, each being defined by the respective recess in said surface and the adjacent surface of the cover.

24. A method according to claim 23, further comprising the step of introducing reagents required for an assay to detect the presence of a biological molecule into at least one reagent reservoir system either before or after bonding the cover to the substrate.

25. A method according to claim 24 which comprises introducing two or more different liquid reagents into at least one reagent reservoir system either before or after bonding the cover to the substrate, wherein the liquid reagents are separated by a fluid.

26. A method according to claim 23, further comprising the step of introducing capture binding receptors into at least one reaction site either before or after bonding the cover to the substrate.

27. A method of carrying out an assay for detection of a biological molecule using a device according to claim 1, the method comprising loading a fluid sample to be tested into the device via the inlet, communicating the sample to the one or more reaction sites and sequentially adding the reagents pre-loaded in at least one reagent reservoir system to the reaction site in fluid communication therewith in the order in which they are stored in the reagent reservoir system.