Microfluidic chip, device and system for the generation of aqueous droplets in emulsion oil for nucleic acid amplification

Patent metadata

Field	Value
Publication number	US-9790546-B2
Application number	US-201314016840-A
Country	US
Kind code	B2
Filing date	Sep 3, 2013
Priority date	Aug 31, 2012
Publication date	Oct 17, 2017
Grant date	Oct 17, 2017

Abstract

A microfluidic chip, device, system, the use thereof and method for the generation of aqueous droplets in emulsion oil for nucleic acid amplification.

First claim

What is claimed is:

1. A microfluidic chip for the generation of aqueous droplets for nucleic acid amplification, said microfluidic chip comprising:
(a) a first reservoir for uptake of a hydrophobic liquid ending in a plurality of inlets, wherein each inlet of said plurality of inlets is fluidly connected to one of a plurality of reaction vessels via one of a plurality of first microfluidic channels, wherein each inlet of said plurality of inlets is fluidly connected to a different first microfluidic channel of said plurality of first microfluidic channels, and each different first microfluidic channel is connected to a different reaction vessel, and (b) a plurality of second reservoirs for uptake of a hydrophilic solution, wherein each second reservoir of said plurality of second reservoirs ends in a vertical inlet fluidly connected to one of a plurality of second microfluidic channels connecting each second reservoir with a different first microfluidic channel via at least one T-junction, wherein said first reservoir is located within a first level and each second reservoir is located within a second level, wherein said first level is located below said second level, and wherein said at least one T-junction is characterized in that the end of each second microfluidic channel is joined to a different first microfluidic channel perpendicularly.

2. The microfluidic chip of claim 1 , comprising said hydrophilic solution and said hydrophobic liquid, wherein said hydrophilic solution is an aqueous mixture comprising a nucleic acid sample and wherein said hydrophobic liquid comprises an emulsion oil or a mixture of emulsion oils and optionally a surfactant.

3. A device for the generation of aqueous droplets for nucleic acid amplification, the device comprising a microfluidic chip according to claim 1 , wherein flow within each of said plurality of first and second microfluidic channels is provided by at least one pressure pump.

4. The device of claim 3 further comprising a stand configured to hold at least one reaction vessel for collecting the aqueous droplets, wherein the at least one reaction vessel is selected from the group consisting of a single PCR tube, a PCR strip or a 96-well plate.

5. The microfluidic chip of claim 4 , wherein the at least one reaction vessel is an 8-well strip.

6. A system for digital PCR, the system comprising:
(a) a device according to claim 3 ,
(b) a thermocycler instrument, and
(c) a read-out instrument, wherein said thermocycler instrument and said read-out instrument are operatively linked to each other.

7. The system of claim 6 , wherein said read-out instrument is a flow cytometry instrument or an imaging instrument.

8. The system of claim 6 , wherein said read-out instrument is capable of reading 1,000-100,000 droplets per second.

9. A method for the generation of aqueous droplets for nucleic acid amplification in a device comprising a microfluidic chip according to claim 1 , the method comprising the steps of:
(a) providing a hydrophobic liquid in said first reservoir,
(b) providing a hydrophilic solution in at least one second reservoir,
(c) generating a first continuous flow of said hydrophobic liquid from said first reservoir through at least one inlet of said plurality of inlets,
(d) generating a second continuous flow of said hydrophilic solution from said second reservoir through a second microfluidic channel of said plurality of second microfluidic channels, and
(e) adjusting said first continuous flow and said second continuous flow such that aqueous droplets of said hydrophilic solution are generated within said first continuous flow of hydrophobic liquid.

10. The method of claim 9 , wherein said hydrophilic solution is an aqueous mixture comprising a nucleic acid sample and said hydrophobic liquid comprises an emulsion oil or a mixture of emulsion oils and optionally a surfactant.

11. The method of claim 9 , wherein the reaction vessel is selected from the group consisting of a single PCR tube or a PCR strip.

12. A method for the generation of aqueous droplets in emulsion oil for nucleic acid amplification using the device of claim 3 or the system of claim 6 , the method comprising the steps of:
(a) providing a hydrophobic liquid in said first reservoir,
(b) providing a hydrophilic solution in at least one second reservoir,
(c) generating a first continuous flow of said hydrophobic liquid from said first reservoir through at least one inlet of said plurality of inlets,
(d) generating a second continuous flow of said hydrophilic solution from said second reservoir through a second microfluidic channel of said plurality of second microfluidic channels, and
(e) adjusting said first continuous flow and said second continuous flow such that aqueous droplets of said hydrophilic solution are generated within said first continuous flow of hydrophobic liquid.

Assignees

• Roche Molecular Systems Inc

Inventors

• Froehlich Thomas
• Bolle Jens

Classifications

• B01L3/0241

  Drop counters; Drop formers · CPC title

• B01L2400/0487

  fluid pressure, pneumatics · CPC title

• B01L2200/0673

  Handling of plugs of fluid surrounded by immiscible fluid · CPC title

• C12Q1/686 Primary

  Polymerase chain reaction [PCR] · CPC title

• B01F13/0059

  Operations & Transport · mapped topic