Systems and methods for handling microfluidic droplets

Patent metadata

Field	Value
Publication number	US-10927407-B2
Application number	US-201816022360-A
Country	US
Kind code	B2
Filing date	Jun 28, 2018
Priority date	May 11, 2006
Publication date	Feb 23, 2021
Grant date	Feb 23, 2021

Abstract

The invention generally relates to assemblies for displacing droplets from a vessel that facilitate the collection and transfer of the droplets while minimizing sample loss. In certain aspects, the assembly includes at least one droplet formation module, in which the module is configured to form droplets surrounded by an immiscible fluid. The assembly also includes at least one chamber including an outlet, in which the chamber is configured to receive droplets and an immiscible fluid, and in which the outlet is configured to receive substantially only droplets. The assembly further includes a channel, configured such that the droplet formation module and the chamber are in fluid communication with each other via the channel. In other aspects, the assembly includes a plurality of hollow members, in which the hollow members are channels and in which the members are configured to interact with a vessel.

First claim

What is claimed is:

1. A system for analyzing a haplotype of a nucleic acid, the system comprising:
a first assembly comprising
a first microfluidic channel on a microfluidic chip comprising a flow of nucleic acids and loci-specific primers in an aqueous fluid,
a second microfluidic channel on the microfluidic chip that connects to the first microfluidic channel at a junction, the second microfluidic channel comprising a stream of oil, and
a third microfluidic channel downstream of the junction comprising a plurality of aqueous droplets surrounded by the oil, wherein at least one droplet of the plurality of aqueous droplets comprises a single nucleic acid and a loci-specific primer pair specific to a segment of nucleic acid that includes two or more variant loci;

an off-chip reservoir in fluid communication with the third microfluidic channel to pool the plurality of aqueous droplets and expose the plurality of aqueous droplets to thermocycling to produce amplicons that includes the two or more variant loci in the droplet;
a second assembly comprising one or more channels operable to remove droplets from the off-chip reservoir and into a second assembly main channel; and
an analysis module connected to the second assembly main channel and operable to analyze the amplicons.

2. The system of claim 1 , wherein the first microfluidic channel is configured to combine the nucleic acids and loci-specific primers in the aqueous fluid under microfluidic control.

3. The system of claim 1 , the second assembly further comprising a module for collecting the amplicons from the plurality of aqueous droplets.

4. The system of claim 1 , wherein the analysis module analyzes the amplicons to determine a haplotype of the nucleic acid.

5. The system of claim 4 , wherein analyzing comprises detecting amplicons that originated in the same droplet.

6. The system of claim 4 , wherein analyzing comprises sequencing.

7. The system of claim 1 , wherein the nucleic acids are bound to a substrate.

8. The system of claim 7 , wherein the substrate is a bead.

9. The system of claim 1 , wherein the nucleic acids are obtained from blood, urine, cerebrospinal fluid, seminal fluid, saliva, sputum, stool, or tissue of an organism.

10. The system of claim 1 , wherein the nucleic acids comprise genomic DNA, cDNA, or RNA.

11. The system of claim 1 , wherein the aqueous fluid further comprises a polymerase and a plurality of deoxynucleotides.

12. The system of claim 1 , wherein the loci-specific primers are designed to minimize bias.

13. The system of claim 1 , wherein the oil comprises a surfactant.

14. The system of claim 4 , wherein detecting a haplotype correlates to detecting a disease.

15. The system of claim 14 , wherein the disease is cancer, and wherein the loci-specific primers are configured to hybridize to loci associated with known cancer biomarkers.

16. The system of claim 1 , wherein the off-chip reservoir comprises vessel that is pre-fitted to an output of the first assembly.

17. The system of claim 16 , wherein the vessel is connectable to the second assembly.

18. The system of claim 1 , wherein the vessel is a PCR tube, vial, or test tube.

19. The system of claim 18 , wherein the first assembly includes a device that brings a rim of the vessel into contact with the first assembly, and the second assembly includes: a second device that sealably connects the vessel to the second assembly; and a hollow member that drives oil into the vessel to displace droplets from the vessel.

Assignees

• Bio Rad Laboratories

Inventors

• Link Darren Roy

Classifications

• B01J19/0093 Primary

  Microreactors, e.g. miniaturised or microfabricated reactors (laboratory containers with capillary fluid transport in microfabricated channels or chambers B01L3/5027) · CPC title

• B01F33/3011

  using a sheathing stream of a fluid surrounding a central stream of a different fluid, e.g. for reducing the cross-section of the central stream or to produce droplets from the central stream · CPC title

• B01F23/41

  Emulsifying · CPC title

• B01L2300/0861

  Configuration of multiple channels and/or chambers in a single devices · CPC title

• C12Q1/00

  Measuring or testing processes involving enzymes, nucleic acids or microorganisms (measuring or testing apparatus with condition measuring or sensing means, e.g. colony counters, C12M1/34); Compositions therefor; Processes of preparing such compositions · CPC title