Method of delivering PCR solution to microfluidic PCR chamber

Patent metadata

Field	Value
Publication number	US-9630158-B2
Application number	US-201013263464-A
Country	US
Kind code	B2
Filing date	Apr 12, 2010
Priority date	Apr 10, 2009
Publication date	Apr 25, 2017
Grant date	Apr 25, 2017

Abstract

The present invention relates to systems and methods of performing in-line mixing of assay components and delivery of such mixed components into microfluidic channels. In one aspect, a method of delivering mixed assay components is provided which comprises causing an unmixed primer solution to flow into a first mixing channel, the unmixed primer solution comprising a common reagent and a primer, holding the unmixed primer solution in the first mixing channel for at least a threshold amount of time to allow the unmixed primer solution to transition into a mixed primer solution, causing a buffer to flow into a second mixing channel, the buffer comprising the common reagent but not including a primer, and, after holding the unmixed primer solution in the first mixing channel for at least the threshold amount of time, drawing, from the first mixing channel, the mixed primer solution into a common exit channel.

First claim

The invention claimed is:

1. A method of delivering a solution flow, comprising:
causing a reagent and a primer to flow into a first mixing channel;
stopping the reagent and the primer in the first mixing channel by keeping both ends of the first mixing channel at the same pressure for at least a threshold amount of time so as to allow the reagent and the primer to mix, thereby forming a reagent/primer mixture;
causing a buffer to flow into a second mixing channel, the first and second mixing channels being located on a mixing chip, wherein the mixing chip is separate and in fluid communication with a PCR chip through an interface chip, wherein the PCR chip is configured for performing an amplification reaction;
after holding the reagent and the primer in the first mixing channel for at least the threshold amount of time, drawing, from the first mixing channel, the reagent/primer mixture into a common exit channel located on the mixing chip; and
adding DNA samples to the reagent/primer mixture while the reagent/primer mixture is in the interface chip.

2. The method of claim 1 , wherein the threshold amount of time is the amount of time it takes for the reagent and the primer to mix by diffusion.

3. The method of claim 1 , wherein the threshold amount of time is greater than 10 seconds.

4. The method of claim 1 , wherein the first and second mixing channels are microfluidic channels and the common exit channel is a microfluidic channel.

5. The method of claim 4 , wherein the microfluidic channels are formed on the mixing chip.

6. The method of claim 5 , further comprising: configuring the mixing chip such that the common exit channel is in fluid communication with an input well of the interface chip.

7. The method of claim 6 , wherein the interface chip is configured such that the input well located on the interface chip is in fluid communication with a plurality of DNA sample wells located on the interface chip.

8. The method of claim 7 , further comprising connecting the interface chip with the PCR chip such that each of the plurality of the DNA sample wells located on the interface chip and input well of the interface chip are in fluid communication with an input well of the PCR chip.

9. The method of claim 1 , further comprising: causing a buffer to flow into the first mixing channel after a least a portion of the reagent/primer mixture has been drawn out of the first mixing channel and into the common exit channel, the buffer comprising the reagent but not including a primer.

10. The method of claim 1 , further comprising:
while holding at least a portion of the reagent and the primer in the first mixing channel, holding the buffer in the second mixing channel;
while holding at least a portion of the buffer in the second mixing channel, causing a reagent and a second primer to flow into a third mixing channel;
holding the reagent and the second primer in the third mixing channel for at least a second threshold amount of time so as to allow the reagent and the second primer to mix, thereby forming a second reagent/primer mixture;
after drawing the reagent/primer mixture into the common exit channel, drawing, from the second mixing channel, the buffer into the common exit channel; and
after drawing, from the second mixing channel, the buffer into the common exit channel, drawing, from the third mixing channel, the second reagent/primer mixture into the common exit channel;
wherein the buffer separates the first reagent/primer mixture from the second reagent/primer mixture within the common exit channel.

11. The method of claim 10 , wherein the step of drawing the buffer into the common exit channel occurs substantially immediately after substantially all of the reagent/primer mixture exits the first mixing channel.

12. The method of claim 10 , wherein the step of drawing the second reagent/primer mixture into the common exit channel occurs substantially immediately after substantially all of the buffer exits the second mixing channel.

13. The method of claim 10 , wherein the first threshold amount of time and the second threshold amount are the same amount of time.

14. The method of claim 10 , wherein the first threshold amount of time and the second threshold amount are different amounts of time.

15. A system for analyzing DNA, comprising:
an apparatus for mixing a primer with a reagent, comprising:
a reagent container;
a primer container;
an input channel in fluid communication with the reagent container and the primer container;
a first mixing channel in fluid communication with the input channel;
a second mixing channel in fluid communication with the input channel, the first and second mixing channels being located on a mixing chip, wherein the mixing chip is separate and in fluid communication with a PCR chip through an interface chip, wherein the PCR chip is configured for performing an amplification reaction; and
a controller, wherein the controller is configured such that the controller is operable to put the apparatus in a state in which a reagent and primer are stopped in the first mixing channel by keeping both ends of the first mixing channel at the same pressure for a threshold amount of time so as to allow the reagent and the primer to mix, thereby forming a reagent/primer mixture, and a buffer is held in the second mixing channel, and the controller is further configured such that the controller (i) causes the reagent/primer mixture to be drawn out of the first mixing channel and into a common exit channel located on the mixing chip after the reagent and the primer has been held in the first mixing channel for at least a threshold amount of time, and (ii) causes DNA samples to be added to the reagent/primer mixture while the reagent/primer mixture is in the interface chip.

16. The system of claim 15 , wherein the threshold amount of time is the amount of time it takes for the reagent and the primer to mix by diffusion.

17. The system of claim 15 , wherein the threshold amount of time is greater than about 10 seconds.

18. The system of claim 15 , wherein the first and second mixing channels are microfluidic channels and the common exit channel is a microfluidic channel.

19. The system of claim 18 , wherein the microfluidic channels are formed on the mixing chip.

20. The system of claim 19 , wherein the mixing chip is configured such that the common exit channel is in fluid communication with an input well of the interface chip.

21. The system of claim 20 , wherein the interface chip is configured such that the input well located on the interface chip is in fluid communication with a plurality of DNA sample wells located on the interface chip.

22. The system of claim 21 , wherein the interface chip is connected to the PCR chip such that each of the plurality of DNA sample wells located on the interface chip and input well of the interface chip are in fluid communication with an input well of the PCR chip.

23. The system of claim 15 , wherein the controller is further configured such that the controller causes a buffer to enter the first mixing channel after the reagent/primer mixture exits the first mixing channel and before any other primer enters the first mixing channel.

24. The system of claim 15 , wherein the apparatus further comprises a third mixing channel.

25. The system of claim 15 , wherein the common exit channel is in fluid communication with one or more DNA sample wells of

Assignees

• Inoue Hiroshi
• Canon Us Life Sciences Inc

Inventors

• Inoue Hiroshi

Classifications

• B01L2300/0867

  Multiple inlets and one sample wells, e.g. mixing, dilution · CPC title

• B01F13/0093 Primary

  Operations & Transport · mapped topic

• B01L2300/0864

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

• B01L2300/0816

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

• B01L7/52

  with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples · CPC title