IP Library Granted Patent US 9,957,472
Granted Patent B2
US 9,957,472 · App. 13/625,836 · Granted May 1, 2018

Deterministic high-density single-cell trap array

Inventors: Kwanghun Chung (Menlo Park, CA); Catherine Rivet (Atlanta, GA); Hang Lu (Atlanta, GA); Melissa Kemp (Atlanta, GA)
Assignee: Georgia Tech Research Corporation
C12M21/06C12M23/16
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Quick Facts
Patent No.
US 9,957,472
App. No.
13/625,836
Granted
May 1, 2018
Kind
B2
Abstract

A microfluidic platform for single-cell capture, stimulation, and imaging. It passively traps 4,000 single cells on a 4.5 mm 2 footprint in 30 seconds, with a single-cell loading efficiency of 95%. The array format and optimized geometry allows for easy, robust and efficient single-cell loading, while maintaining captured cells in a low shear stress environment for long-term studies. Because cells are captured sequentially, the system is adequate for rare cell samples. Trapped cells can be exposed to various environmental conditions and chemical stimulus and their dynamic response can be monitored over time. The information gained from high-throughput, single-cell time lapsed imaging presents new opportunities in quantifying cellular responses, as averaged information by other measurement methods eliminates sub-population phenotypes.

Claims (31)

1. A microfluidic cell trap array comprising:

a cell-delivery channel defined between channel walls, the channel having an inlet and an outlet; and

cell traps formed in at least a portion of the channel walls such that each cell traps comprise a cavity to trap a cell therein;

wherein the cell trap array has a density of greater than 800 traps/mm 2 .

2. The microfluidic cell trap array of claim 1 , wherein the cell trap array has a loading efficiency of greater than 70%.

3. The microfluidic cell trap array of claim 1 , wherein the cell trap array has a loading efficiency of greater than 90%.

4. The microfluidic cell trap array of claim 1 , wherein the cell-delivery channel comprises a generally serpentine channel.

5. The microfluidic cell trap array of claim 4 , wherein the generally serpentine channel comprises a plurality of generally parallel subchannels connected to one another via subchannel end portions.

6. The microfluidic cell trap array of claim 5 , wherein the subchannel end portions have an appropriate curvature such that the generally serpentine channel with a plurality of generally parallel subchannels provides for a generally uniform medium flow rate therethrough.

7. The microfluidic cell trap array of claim 1 , wherein:

the cell-delivery channel forms a serpentine channel including a plurality of switchback subchannels connected to one another via subchannel end portions;

wherein at least a portion of the total number of subchannels have a cell trapping zone along the length of a subchannel, the cell trapping zone bounded by a leading cell focusing zone and a trailing cell focusing zone;

wherein in each cell trapping zone, the cell traps comprise a plurality of single-cell traps sized to capture a single cell; and

wherein each cell focusing zone comprises a plurality of flowthrough apertures sized so as not to capture a cell flowing therethrough, such that media having cells traveling through a subchannel having a cell trapping zone will experience both a flow parallel to the length of the subchannel to carry cells through the array, and a normal flow moving travelling cells closer to the traps in the cell trapping zone after passing the leading cell focusing zone.

8. The microfluidic single-cell trap array of claim 7 , wherein at least a portion of the single-cell traps have a geometry engineered so that traps experience similar flow rates near one another in order to provide a generally uniform trapping condition for each trap.

9. The microfluidic single-cell trap array of claim 7 , wherein at least a portion of the single-cell traps have a geometry engineered so that once a cell occupies a trap, it physically excludes another cell from being trapped in the same trap.

10. The microfluidic single-cell trap array of claim 7 , wherein at least a portion of the single-cell traps have a geometry engineered so that once a cell occupies a trap, neither the media flow through the single-cell trap array nor another cell can dislodge a trapped cell.

11. The microfluidic single-cell trap array of claim 7 , wherein after passing a cell focusing zone, travelling cells in proximity to a single-cell trap experience two flows, a main stream (Q) flowing in the direction of the cell-delivery channel, and a directing stream (q) directing the cell into a single-cell trap; and

wherein the ratio Q/q is engineered to guide cells into non-occupied traps, and once all traps in a subchannel having a cell trapping zone contain trapped cells, travelling cells pass a downstream cell focusing zone, and travel to a next subchannel.

12. The microfluidic cell trap array of claim 1 , wherein at least a portion of the cell traps comprise a non-reactive surface that form a cavity to capture a cell within the cavity without biochemical interaction between a cell and the non-reactive surface.

13. The microfluidic cell trap array of claim 1 , wherein at least a portion of the cell traps comprise traps formed by walls separated by a gap so each such trap forms a cavity that is sized to provide a surface area that can only trap a single cell.

14. The microfluidic cell trap array of claim 1 , wherein at least a portion of the cell traps comprise traps formed by walls separated by a gap so each such trap forms a cavity that is shaped to provide a surface area that can only trap a single cell.

15. A microfluidic cell trap array comprising:

a cell-delivery channel having an inlet and an outlet, the cell-delivery channel forming a serpentine channel including a plurality of switchback subchannels connected to one another via subchannel end portions; and

cell traps formed in a wall of the channel;

wherein the cell traps formed in a wall of the channel comprise a plurality of single-cell traps formed in at least a portion of the total number of subchannels, such that single-cell traps each comprise a cavity to trap a cell therein;

wherein the cell trap array comprises a single-cell trap array having the density of greater than 800 traps/mm 2 ; and

wherein the single-cell trap array has a loading efficiency of greater than 70%.

16. The microfluidic cell trap array of claim 15 , wherein in at least a portion of the total number of subchannels having single-cell traps, such subchannels have a cell trapping zone along the length of the subchannel, and a cell focusing zone on at least one side of the cell trapping zone.

17. The microfluidic cell trap array of claim 16 , wherein the subchannels having a cell trapping zone have a cell focusing zone on both sides of the cell trapping zone.

18. The microfluidic cell trap array of claim 16 , the cell trapping zone comprising at least a portion of the single-cell traps, the single-cell traps sized to capture a single cell, and the cell focusing zone comprising flowthrough apertures sized so as not to capture a cell flowing therethrough.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jun 17, 2021
From: GEORGIA INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 056615/0816 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2014
From: CHUNG, KWANGHUN; RIVET, CATHERINE; LU, HANG; KEMP, MELISSA
To: GEORGIA TECH RESEARCH CORPORATION
Reel/Frame 033340/0342 →
Continuity (2)
Provisional Application 61537895 · Sep 22, 2011
Related Publication 20130078163A1 · Mar 28, 2013