IP Library Granted Patent US 7,101,467
Granted Patent B2
US 7,101,467 · App. 10/744,915 · Granted Sep 5, 2006

Mixed mode microfluidic systems

Assignee: Caliper Life Sciences, Inc.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,101,467
App. No.
10/744,915
Granted
Sep 5, 2006
Kind
B2
Abstract

Methods and systems that employ hybrid fluid flow profiles for optimized movement of materials through channel networks. These systems employ hybrid pressure-based and electrokinetic based flow systems for moving materials through interconnected channel networks while maintaining interconnection among the various channel segments. In particular, the invention is generally directed to channel networks where flow in a first channel segment is driven by pressure flow with its consequent parabolic flow profile, while flow in an interconnected channel segment is dominated by electrokinetic flow with its consequent plug flow profile. The invention also provides channel networks wherein fluid flow in channel segments is driven by both pressure and electric field and the multiple species contained in a fluid plug are separated (and can be concentrated) by altering the applied pressure and electric fields in the various channel segments of the channel networks.

Claims (22)

1. A method of extracting a charged species from a sample and concentrating it, comprising:

providing an interconnected channel network comprising a first, second and third channel segment which intersect at a first fluid junction, the second channel segment terminating in a first fluid reservoir at one end and intersecting the first fluid junction at its other end, and a fourth channel segment intersecting the third channel segment at a second fluid junction at one end and terminating in a second fluid reservoir at its other end, the second fluid reservoir comprising a first buffer;

flowing the charged species in the sample in a second buffer through the interconnected channel network by applying a first pressure differential across the first and second channel segments and a second pressure differential across the third and fourth channel segments, wherein the first pressure differential is larger than the second pressure differential and the first buffer has a different ionic strength than the second buffer; and

applying a voltage differential across the first and second reservoirs which is sufficient to cause a substantial portion of the charged species in the sample in the first fluid junction to flow into the third channel segment.

2. The method of claim 1 , wherein the first, second, third and fourth channel segments are disposed in a body structure of a microfluidic device.

3. The method of claim 1 , wherein the first pressure differential is generated by applying a vacuum to the first fluid reservoir.

4. The method of claim 1 , wherein the second pressure differential is generated at least in part by applying a positive pressure to the second fluid reservoir.

5. The method of claim 1 , wherein the first buffer has a higher ionic strength than the second buffer.

6. The method of claim 1 , wherein the difference between the first pressure differential and the second pressure differential is such that a pressure driven flow rate or velocity in the first channel segment is at least about two times greater than a pressure driven flow rate or velocity in the third channel segment.

7. The method of claim 1 , wherein the difference between the first pressure differential and the second pressure differential is such that a pressure driven flow rate or velocity in the first channel segment is at least about five times greater than a pressure driven flow rate or velocity in the third channel segment.

8. The method of claim 1 , wherein the difference between the first pressure differential and the second pressure differential is such that a pressure driven flow rate or velocity in the first channel segment is at least about ten times greater than a pressure driven flow rate or velocity in the third channel segment.

9. The method of claim 1 , wherein the difference between the first pressure differential and the second pressure differential is such that a pressure driven flow rate or velocity in the first channel segment is at least about twenty times greater than a pressure driven flow rate or velocity in the third channel segment.

10. The method of claim 1 , wherein an electrokinetic velocity of the charged species in the second channel segment is greater than its pressure driven velocity.

11. The method of claim 1 , wherein an electrokinetic velocity of the charged species in the fourth channel segment is less than its pressure driven velocity.

12. The method of claim 1 , further comprising a fifth channel segment fluidly coupled to the second fluid junction, wherein a total flow rate or velocity of the charged species in the fifth channel segment is about five times less than a total flow rate or velocity of the charged species in the third channel segment.

13. The method of claim 1 , further comprising a fifth channel segment fluidly coupled to the second fluid junction, wherein a total flow rate or velocity of the charged species in the fifth channel segment is about ten times less than a total flow rate or velocity of the charged species in the third channel segment.

14. The method of claim 1 , wherein the charged species is DNA or RNA.

15. The method of claim 14 , further comprising amplifying the DNA or RNA one or more times in a fifth channel segment of the interconnected channel network.

16. The method of claim 1 , wherein the first buffer forms a fluid boundary with the second buffer in the second fluid junction sufficient to concentrate the charged species in or near the second fluid junction.

17. The method of claim 16 , wherein the charged species is concentrated at least about five times in or near the second fluid junction.

18. The method of claim 16 , wherein the charged species is concentrated at least about ten times in or near the second fluid junction.

19. The method of claim 1 , wherein a substantial portion of the sample in the second buffer other than the charged species flows into the second channel segment.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2004
From: SPAID, MICHAEL A.
To: CALIPER LIFE SCIENCES, INC.
Reel/Frame 015430/0968 →
CHANGE OF NAME Recorded May 17, 2004
From: CALIPER TECHNOLOGIES CORP.
To: CALIPER LIFE SCIENCES, INC.
Reel/Frame 015333/0787 →
Continuity (4)
Continuation In Part 1038690000 · Mar 4, 2003
Provisional Application 6038130600 · May 17, 2002
Provisional Application 6036195700 · Mar 5, 2002
Related Publication 20040188254A1 · Sep 30, 2004