Integrated microfluidic system, method and kit for performing assays

Patent metadata

Field	Value
Publication number	US-9821312-B2
Application number	US-201314427404-A
Country	US
Kind code	B2
Filing date	Sep 12, 2013
Priority date	Sep 12, 2012
Publication date	Nov 21, 2017
Grant date	Nov 21, 2017

Abstract

The present invention provides a microfluidic system, method and kit for performing assays. The system may comprise a microfluidic device and a detector, wherein the assay yields results that may be read by a detector and analyzed by the system. The assay may comprise one or more chemical or biological reaction against, or performed on, a sample or multiple samples. The sample(s) may become larger and/or smaller during the performance of the assay. The sample(s) may be present within a vehicle, or on a carrier within a vehicle, in the microfluidic device, and wherein the vehicle may become larger and/or smaller during the performance of the assay. The assay may be a cascading assay comprising a series of multiple assays, wherein each assay may be the same or different, and wherein each assay in the series of multiple assays may further comprise one or more process or step.

First claim

What is claimed is:

1. A method for forming assay droplets comprising the steps of:
providing a microfluidic device comprising a first plurality of reagent droplets, the first plurality of reagent droplets comprising a first reagent set, and a second plurality of reagent droplets, the second plurality of droplets comprising a second reagent set;
forming, from a sample and the first plurality of reagent droplets, a first plurality of assay droplets in the microfluidic device, wherein the forming comprises injecting in the microfluidic device at least a portion of a sample into some or all of the first plurality of reagent droplets; and
forming, from the first plurality of assay droplets and the second plurality of reagent droplets, a second plurality of assay droplets, wherein the forming comprises injecting in the microfluidic device different portions of an assay droplet from the first plurality of assay droplets into multiple droplets from the second plurality of reagent droplets, thereby creating a second plurality of assay droplets in the microfluidic device.

2. The method of claim 1 , further comprising detecting the product of a chemical reaction in the second plurality of assay droplets.

3. The method of claim 1 , further comprising injecting a reagent into the first plurality of reagent droplets or the first plurality of assay droplets.

4. The method of claim 3 , wherein the reagent is a polymerase.

5. The method of claim 4 , further comprising thermocycling the first plurality of assay droplets.

6. The method of claim 2 , wherein the detecting occurs within the microfluidic device.

7. The method of claim 3 , wherein the first plurality of reagent droplets comprises a primer library.

8. The method of claim 7 , wherein the first plurality of reagent droplets comprise labels.

9. The method of claim 7 , wherein the reagent is a DNA polymerase.

10. The method of claim 9 , wherein the second reagent set comprises a library of nucleic acid probes.

11. The method of claim 10 , wherein the nucleic acid probes are random hexamers.

12. The method of claim 10 , wherein the detecting comprises detecting the hybridization of one or more of the nucleic acid probes to a product of a chemical reaction in the second plurality of assay droplets.

13. The method of claim 1 , further comprising conducting a first chemical reaction in the first plurality of assay droplets.

14. The method of claim 13 , wherein the first chemical reaction is conducted in the microfluidic device.

15. The method of claim 14 , further comprising conducting a second chemical reaction in the second plurality of assay droplets.

16. The method of claim 15 , wherein the first chemical reaction is conducted in the microfluidic device.

17. The method of claim 1 , wherein one or more of (a) the first plurality of reagent droplets, (b) the first plurality of assay droplets, (c) the second plurality of reagent droplets, or (d) the second plurality of assay droplets are the aqueous phase of an emulsion.

18. The method of claim 15 , wherein the second chemical reaction comprises contacting one or more probe to an amplified nucleic acid in the assay droplets.

19. The method of claim 18 , wherein the one or more probe is 6-8 nucleotides long.

20. The method of claim 18 , wherein the one or more probe queries a locus to detect the presence or absence of a particular nucleic acid sequence variance.

21. The method of claim 18 , wherein hybridization of the probes determines the sequence of the nucleic acid.

Assignees

• Bio Rad Laboratories Inc

Inventors

• Esmail Adnan
• Healy John
• Hung Tony
• Kiani Sepehr
• Mary Pascaline
• Raz Tal

Classifications

• B01L2400/0415

  electrical forces, e.g. electrokinetic · CPC title

• B01L2300/0816

  Cards, e.g. flat sample carriers usually with flow in two horizontal directions · CPC title

• B01L2300/0864

  comprising only one inlet and multiple receiving wells, e.g. for separation, splitting · CPC title

• B01L2300/0636

  Integrated biosensor, microarrays · CPC title

• B01L2400/0433

  vibrational forces · CPC title