IP Library Granted Patent US 8,585,971
Granted Patent B2
US 8,585,971 · App. 13/452,054 · Granted Nov 19, 2013

Devices and method for enrichment and alteration of cells and other particles

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Quick Facts
Patent No.
US 8,585,971
App. No.
13/452,054
Granted
Nov 19, 2013
Kind
B2
Abstract

The invention features devices and methods for the deterministic separation of particles. Exemplary methods include the enrichment of a sample in a desired particle or the alteration of a desired particle in the device. The devices and methods are advantageously employed to enrich for rare cells, e.g., fetal cells, present in a sample, e.g., maternal blood and rare cell components, e.g., fetal cell nuclei. The invention further provides a method for preferentially lysing cells of interest in a sample, e.g., to extract clinical information from a cellular component, e.g., a nucleus, of the cells of interest. In general, the method employs differential lysis between the cells of interest and other cells (e.g., other nucleated cells) in the sample.

Claims (32)

1. A system to manipulate particles in a fluid, the system comprising:

a first channel through which particles and magnetic beads in a fluid are flowed, wherein a portion of the particles bind to the magnetic beads; and

a device to manipulate the particles and the magnetic beads, the device comprising:

a second channel extending from one or more inlets to one or more outlets, wherein the second channel is bounded by a first wall, and a second wall located opposite from the first wall;

a first array of obstacles disposed within the second channel and bounded by the first wall and a first array boundary;

a second array of obstacles disposed within the second channel and bounded by the second wall and a second array boundary, and

a bypass channel defined by a region within the second channel devoid of obstacles between the first array boundary and the second array boundary, wherein the first array and the second array are configured to deflect the portion of the particles that bind to the magnetic beads in the fluid flowed through the first array and the second array, respectively, toward the bypass channel.

2. The system of claim 1 , wherein the portion of the particles that bind to the magnetic beads have respective hydrodynamic sizes that are greater than hydrodynamic sizes of remaining particles that do not bind to the magnetic beads.

3. The system of claim 2 , wherein the device further comprises:

a first outlet located closer to the first wall than to the bypass channel to receive a portion of the remaining particles not deflected by the first array;

a second outlet located closer to the second wall than to the bypass channel to receive another portion of the remaining particles not deflected by the second array; and

a third outlet located at an end of the bypass channel to receive the portion of the particles that bind to the magnetic beads, and are deflected by the first array and the second array and collected in the bypass channel.

4. The system of claim 1 , wherein the first array of obstacles comprises a plurality of first obstacles that form a network of gaps and comprises at least first and second rows of the obstacles, wherein the second row is displaced laterally relative to the first row so that a fluid passing through a gap in the first row is divided unequally when flowing around an obstacle and into two gaps on either side of the obstacle in the second row.

5. The system of claim 4 , wherein the second array of obstacles comprises a plurality of second obstacles that form a network of gaps and comprises at least first and second rows of the obstacles, wherein the second row is displaced laterally relative to the first row so that fluid passing through a gap in the first row is divided unequally when flowing around an obstacle and into two gaps in the second row.

6. The system of claim 1 , wherein the one or more inlets further comprise:

a first inlet located closer to the first wall than to the bypass channel to receive the fluid for flowing through the first array of obstacles; and

a second inlet located closer to the second wall than to the bypass channel to receive the fluid for flowing through the second array of obstacles.

7. The system of claim 1 , wherein the bypass channel is disposed along a longitudinal axis of the channel.

8. The system of claim 1 , further comprising:

a third array of obstacles disposed within the second channel in series with the first array of obstacles, and bounded by the first wall and a third array boundary; and

a fourth array of obstacles disposed within the second channel in series with the second array of obstacles, and bounded by the second wall and a fourth array boundary,

wherein the bypass channel extends to a region between the third array boundary and the fourth array boundary.

9. The system of claim 8 , further comprising:

a second bypass channel defined by a region between the third array boundary and the bypass channel; and

a third bypass channel defined by a region between the fourth array boundary and the bypass channel.

10. The system of claim 1 , wherein the first array of obstacles form a network of gaps of a substantially constant width of 10-30 μm.

11. The system of claim 10 , wherein the width of the gaps is 18-24 μm.

12. The system of claim 1 , wherein obstacles in the second array are shaped with a maximum dimension in an average flow direction of the array that is less than a maximum dimension orthogonal to the average flow direction of the array.

13. The system of claim 1 , wherein the first array and the second array are disposed on either side of a longitudinal axis of the channel.

14. The system of claim 1 , wherein the first array is a mirror image of the second array.

15. The system of claim 1 , further comprising fin structures arranged adjacent to the bypass channel and the first array to inhibit fluid that has flowed into the bypass channel from re-entering the first array.

16. The system of claim 1 , wherein the fluid is a biological sample and the particles include cells in the biological sample.

Assignments (9)
CERTIFICATE OF CONVERSION FROM A LIMITED LIABILITY COMPANY TO A CORPORATION Recorded Jun 14, 2024
From: GPB SCIENTIFIC, LLC
To: GPB SCIENTIFIC, INC.
Reel/Frame 067737/0606 →
RELEASE OF SECURITY INTEREST Recorded Jun 14, 2024
From: SILICON VALLEY BANK, A DIVISION OF FIRST-CITIZENS BANK & TRUST COMPANY
To: GPB SCIENTIFIC, INC.
Reel/Frame 067732/0146 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2024
From: GPB SCIENTIFIC, INC. (D/B/A CURATE BIOSCIENCES)
To: CURATE (ABC), LLC
Reel/Frame 067737/0738 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2024
From: CURATE (ABC), LLC
To: ZEON CORPORATION
Reel/Frame 067737/0769 →
SECURITY INTEREST Recorded Sep 28, 2023
From: GPB SCIENTIFIC, INC.
To: FIRST-CITIZENS BANK & TRUST COMPANY
Reel/Frame 065082/0354 →
QUIT CLAIM ASSIGNMENT Recorded Jun 28, 2012
From: THE GENERAL HOSPITAL CORPORATION
To: TONER, MEHMET
Reel/Frame 028466/0138 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2012
From: HUANG, LOTIEN RICHARD; BARBER, THOMAS; CARVALHO, BRUCE L.; KAPUR, RAVI; VERNUCCI, PAUL; WANG, ZIHUA
To: VERINATA HEALTH, INC
Reel/Frame 028462/0662 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2012
From: VERINATA HEALTH, INC
To: THE GENERAL HOSPITAL CORPORATION
Reel/Frame 028462/0872 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 28, 2012
From: TONER, MEHMET
To: THE GENERAL HOSPITAL CORPORATION; GPB SCIENTIFIC, LLC
Reel/Frame 028463/0208 →