Microfluidic siphoning array for nucleic acid quantification
A microfluidic device can have a plurality of microchambers connected to a microchannel via siphon apertures. The microfluidic device may be formed from a thermoplastic and capped by a thermoplastic thin film. The microfluidic device may be used for digital polymerase chain reactions by forcing reagent into the microchambers at low pressure via an inlet, forcing any gas trapped in the microfluidic device to outgas through the thin film by applying high pressure to the microfluidic device via inlets and outlets of the microfluidic device, and applying air at low pressure to the inlets in order to digitize the chambers such that the reagent in each chamber is isolated from the reagent in other chambers by an air gap. After digitization, the device may be used to run a digital polymerase chain reaction process.
1. A method for using a microfluidic device comprising:
providing said microfluidic device comprising a microchannel, wherein said microchannel comprises at least one inlet and at least one outlet, and wherein said microfluidic device further comprises a plurality of microchambers connected to said microchannel by a plurality of siphon apertures, and a thermoplastic thin film disposed adjacent to a surface of said microfluidic device such that said thermoplastic thin film caps said microchannel, said plurality of microchambers, and said plurality of siphon apertures;
filling said plurality of microchambers of said microfluidic device with a reagent by applying said reagent at a first pressure to said at least one inlet;
applying a high pressure gas at a second pressure at said at least one inlet or at said at least one outlet to force gas within the plurality of microchambers to pass through said thermoplastic thin film capping said plurality of microchambers, said plurality of siphon apertures, and said microchannel, wherein said second pressure is greater than said first pressure; and
applying a low pressure gas at a third pressure at said at least one inlet to introduce said low pressure gas into the microchannel without introducing said low pressure gas into said plurality of microchambers, wherein said third pressure is less than said second pressure.
2. The method of claim 1 , wherein the method is performed using a single integrated machine.
3. The method of claim 1 , further comprising providing a polymerase chain reaction (PCR) reagent comprising nucleic acid molecules to each of the plurality of microchambers.
4. The method of claim 3 , further comprising performing PCR by thermal cycling said plurality of microchambers.
5. The method of claim 3 , further comprising acquiring images of said plurality of microchambers.
6. The method of claim 4 , further comprising counting a number of said plurality of microchambers within which said PCR successfully amplifies said nucleic acid molecules.
7. The method of claim 6 , further comprising applying Poison statistics to said number of said plurality of microchambers within which said PCR successfully amplifies said PCR reagent to quantify nucleic acids within said PCR reagent.
8. The method of claim 1 , wherein said microchannel comprises a plurality of sub-channels connected via a cross-channel and wherein said plurality of microchambers are connected to said plurality of sub-channels.
9. The method of claim 8 , wherein the plurality of sub-channels are substantially parallel to one another such that said plurality of microchambers are in a grid configuration.
10. The method of claim 1 , wherein said third pressure is between about 1 pound per square inch (psi) and 4 psi.
11. The method of claim 1 , wherein said second pressure is between about 8 psi and 16 psi.
12. The method of claim 1 , wherein said high pressure gas comprises air, nitrogen, carbon dioxide, a noble gas, or any combination thereof.
13. The method of claim 1 , wherein said thermoplastic thin film comprises a cyclo-olefin polymer.
14. The method of claim 1 , further comprising a pneumatic pump in fluid communication with said at least one inlet or said at least one outlet.
15. The method of claim 1 , wherein said plurality of microchambers comprises between 1,000 and 20,000 microchambers.
16. The method of claim 1 , wherein said plurality of microchambers are cylindrical in shape.
17. The method of claim 1 , wherein said microfluidic device is formed by injection molding.
18. The method of claim 1 , wherein said thermoplastic thin film is formed by injection molding.