IP Library Granted Patent US 7,553,647
Granted Patent B2
US 7,553,647 · App. 11/351,843 · Granted Jun 30, 2009

Microfluidic differential extraction cartridge

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Quick Facts
Patent No.
US 7,553,647
App. No.
11/351,843
Granted
Jun 30, 2009
Kind
B2
Abstract

A differential extraction system is directed to a microfluidic-based integrated cartridge to automate differential extraction of specific cell types within a mixed sample. The integrated cartridge includes a sonication module for selective cell lysis, separating means to eliminate centrifugation, high surface area pillar chip modules to purify DNA from a cell lysate, and microfluidic circuitry to integrate the steps in an automated platform.

Claims (28)

1. A method of selectively lysing a specific cell type, the method comprising:

a. providing a sample to an integrated cartridge, the sample including at least two different cell types;

b. lysing a first cell type using a lysing means within the integrated cartridge to form a first lysate while at least one non-lysed cell type remains intact;

c. separating the first lysate from the sample using separating means within the integrated cartridge, thereby forming a separated sample including the intact at least one non-lysed cell type; and

d. moving the separated sample from the separating means to the lysing means using microfluidic circuitry and a back-flow capability.

2. The method of claim 1 wherein the first cell type is lysed at a first sonication energy and the lysing the first cell type comprises applying the first sonication energy to the sample.

3. The method of claim 1 wherein lysing the first cell type comprises applying a first chemical treatment to the sample.

4. The method of claim 1 further comprising lysing the second cell type to form a second lysate.

5. The method of claim 4 wherein lysing the second cell type comprises applying a second chemical treatment to the sample.

6. The method of claim 4 wherein the second cell type is lysed at a second sonication energy and lysing the second cell type comprises applying the second sonication energy to the sample.

7. The method of claim 4 wherein the second cell type is included within the at least one remaining intact cell type.

8. The method of claim 4 wherein the first cell type comprises an epithelial cell and the second cell type comprises a sperm cell.

9. The method of claim 4 wherein the second cell type comprises a virus, a microbe, or a spore.

10. The method of claim 1 wherein the first cell type comprises a virus, a microbe, or a spore.

11. A method to automate the selective lysing of a specific cell type, the method comprising:

a. providing a sample to an integrated cartridge, the sample including at least two different cell types;

b. automatically lysing a first cell type using a lysing means within the integrated cartridge to form a first lysate while at least one non-lysed cell type remains intact;

c. automatically separating the first lysate from the sample using separating means within the integrated cartridge, thereby forming a separated sample including the intact at least one non-lysed cell type; and

d. automatically moving the separated sample from the separating means to the lysing means using microfluidic circuitry and a back-flow capability.

12. The method of claim 11 wherein the first cell type is lysed at a first sonication energy and automatically lysing the first cell type comprises automatically applying the first sonication energy to the sample.

13. The method of claim 11 wherein automatically lysing the first cell type comprises automatically applying a first chemical treatment to the sample.

14. The method of claim 11 further comprising automatically lysing the second cell type to form a second lysate.

15. The method of claim 14 wherein automatically lysing the second cell type comprises automatically applying a second chemical treatment to the sample.

16. The method of claim 14 wherein the second cell type is lysed at a second sonication energy and automatically lysing the second cell type comprises automatically applying the second sonication energy to the sample.

17. The method of claim 14 wherein the second cell type is included within the at least one remaining intact cell type.

18. The method of claim 14 wherein the first cell type comprises an epithelial cell and the second cell type comprises a sperm cell.

19. The method of claim 14 wherein the second cell type comprises a virus, a microbe, or a spore.

20. The method of claim 11 wherein the first cell type comprises a virus, a microbe, or a spore.

Assignments (3)
SECURITY AGREEMENT Recorded Feb 8, 2013
From: MICROFLUIDIC SYSTEMS
To: TCA GLOBAL CREDIT MASTER FUND, LP
Reel/Frame 029778/0430 →
SECURITY AGREEMENT Recorded Jan 21, 2013
From: POSITIVEID CORPORATION; MICROFLUIDIC SYSTEMS
To: THE BOEING COMPANY
Reel/Frame 029665/0880 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2006
From: YUAN, BOB; AFLATOONI, NIMA
To: MICROFLUIDIC SYSTEMS, INC.
Reel/Frame 017566/0688 →