IP Library Granted Patent US 11,376,591
Granted Patent B2
US 11,376,591 · App. 16/893,885 · Granted Jul 5, 2022

Light sequencing and patterns for dielectrophoretic transport

Inventors: Troy A. Lionberger (Berkeley, CA); Brandon R. Bruhn (San Francisco, CA); John A. Tenney (Piedmont, CA); Eric D. Hobbs (Livermore, CA)
Assignee: Berkeley Lights, Inc.
B01L3/50273B01L3/502715B01L3/502761B03C5/005B03C5/024B03C5/026G01N27/44791B01L2200/0647B01L2400/0424B01L2400/0454B03C2201/26
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Quick Facts
Patent No.
US 11,376,591
App. No.
16/893,885
Granted
Jul 5, 2022
Kind
B2
Abstract

Optically-actuated microfluidic devices permit the use of spatially-modulated light to manipulate micro-objects such as biological cells. Systems and methods are described for providing sequences of light patterns to move and direct a plurality of micro-objects within the environment of a microfluidic device. The sequenced light patterns provide improved efficiency in directing the transport of the plurality of micro-objects. Other embodiments are described.

Claims (26)

1. A method of disposing a selected micro-object of a plurality of micro-objects within a chamber of a microfluidic device, the method comprising:

introducing the plurality of micro-objects into a flow path of a microfluidic device, wherein the chamber comprises an opening to the flow path;

projecting a first light sequence into the microfluidic device, the first light sequence comprising a light bar having a starting position within the chamber, wherein, during the projection of the first light sequence, the light bar moves from the starting position to an ending position in the flow path, thereby excluding micro-objects of the plurality of micro-objects from a chamber portion proximal to the flow path; and

projecting a second light sequence into the microfluidic device, the second light sequence comprising one or more shapes configured to at least partially surround the selected micro-object, wherein, during the projection of the second light sequence, the one or more shapes move into the chamber, thereby disposing the selected micro-object therein.

2. The method of claim 1 , wherein projecting the first light sequence and/or the second light sequence comprises activating dielectrophoresis forces within the microfluidic device.

3. The method of claim 2 , wherein the light bar is projected across the chamber, thereby activating DEP electrodes across the chamber.

4. The method of claim 3 , wherein the light bar is projected across the chamber in a direction parallel to a width of the opening of the chamber to the flow path.

5. The method of claim 1 , wherein the light bar is a single contiguous light bar.

6. The method of claim 1 , wherein the chamber opens laterally from the flow path.

7. The method of claim 1 , wherein the chamber is a sequestration pen having a single opening to the flow path, the sequestration pen comprising an isolation region and a connection region fluidically connecting the isolation region to the flow path.

8. The method of claim 1 , wherein the second light sequence comprises one or more light cages.

9. The method of claim 8 , wherein the one or more light cages comprises a shape including an angled leading edge.

10. The method of claim 1 , wherein the flow path comprises a channel.

11. A method of disposing a set of selected micro-objects of a plurality of micro-objects within corresponding chambers of a plurality of chambers of a microfluidic device, the method comprising:

introducing the plurality of micro-objects into a flow path of a microfluidic device, wherein each of the plurality of chambers comprises an opening to the flow path;

projecting a first light sequence into the microfluidic device, the first light sequence comprising a light bar having a starting position within each of the plurality of chambers, wherein, during the projection of the first light sequence, the light bar moves from the starting position to an ending position in the flow path, thereby excluding micro-objects of the plurality of micro-objects from a chamber portion proximal to the flow path of each chamber of the plurality of chambers; and

projecting a plurality of second light sequences into the microfluidic device, each second light sequence comprising one or more shapes configured to at least partially surround a selected micro-object of the set of selected micro-objects, wherein, during the projection of the plurality of second light sequences, the one or more shapes of each second light sequence move into a corresponding chamber of the plurality of chambers, thereby disposing the selected micro-object of the set of selected micro-objects therein.

12. The method of claim 11 , wherein projecting the first light sequence and/or the plurality of second light sequences comprises activating dielectrophoresis forces within the enclosure of the microfluidic device.

13. The method of claim 12 , wherein the light bar is projected across each of the plurality of chambers, thereby activating DEP electrodes across each of the plurality of chambers.

14. The method of claim 13 , wherein the light bar is projected across each of the plurality of chambers in a direction parallel to a width of the opening of each of the plurality of chambers to the flow path.

15. The method of claim 11 , wherein the light bar is a single contiguous light bar.

16. The method of claim 11 , wherein each of the plurality of chambers opens laterally from the flow path.

17. The method of claim 11 , wherein each of the plurality of chambers is a sequestration pen having a single opening to the flow region, wherein each sequestration pen has an isolation region and a connection region fluidically connecting the isolation region to the flow path.

18. The method of claim 11 , wherein each second light sequence of the plurality of second light sequences comprises one or more light cages.

19. The method of claim 18 , wherein each of the one or more light cages comprises a shape including an angled leading edge.

20. The method of claim 11 , wherein the flow path comprises a channel.

Assignments (4)
MERGER Recorded Apr 9, 2026
From: BRUKER CELLULAR ANALYSIS, INC.
To: BRUKER SPATIAL BIOLOGY, INC.
Reel/Frame 075375/0517 →
MERGER AND CHANGE OF NAME Recorded Nov 30, 2023
From: PHENOMEX INC.; BIRD MERGERSUB CORPORATION
To: BRUKER CELLULAR ANALYSIS, INC.
Reel/Frame 065726/0624 →
CHANGE OF NAME Recorded Sep 20, 2023
From: BERKELEY LIGHTS, INC.
To: PHENOMEX INC.
Reel/Frame 064961/0794 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2020
From: LIONBERGER, TROY A.; BRUHN, BRANDON R.; TENNEY, JOHN A.; HOBBS, ERIC D.
To: BERKELEY LIGHTS, INC.
Reel/Frame 052879/0348 →