IP Library Granted Patent US 10,416,070
Granted Patent B1
US 10,416,070 · App. 16/426,322 · Granted Sep 17, 2019

Cell capture system and method of use

Inventor: Kalyan Handique (Plymouth, MI)
Assignee: Celsee Diagnostics, Inc.
G01N15/1484B01L3/502715B01L3/502746B01L3/502761C12M47/04G01N1/20G01N1/28G01N1/40G01N1/405B01L3/021B01L2200/0652B01L2200/0668B01L2300/0636B01L2300/0654B01L2300/0672B01L2300/0816B01L2300/0819B01L2300/0848B01L2300/0877B01L2300/168B01L2400/086G01N1/4077G01N2015/0065G01N2015/1006G01N2015/149G01N2035/00158G06K9/00127
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Quick Facts
Patent No.
US 10,416,070
App. No.
16/426,322
Filed
May 30, 2019
Granted
Sep 17, 2019
Kind
B1
Art Unit
1797
USPC
436/63
Abstract

A cell capture system including an array, an inlet manifold, and an outlet manifold. The array includes a plurality of parallel pores, each pore including a chamber and a pore channel, an inlet channel fluidly connected to the chambers of the pores; an outlet channel fluidly connected to the pore channels of the pores. The inlet manifold is fluidly connected to the inlet channel, and the outlet channel is fluidly connected to the outlet channel. A cell removal tool is also disclosed, wherein the cell removal tool is configured to remove a captured cell from a pore chamber.

Claims (38)

1. A method for automatically processing target particles in single-particle format, the method comprising:

at a workstation, receiving a substrate comprising a network having an input channel at an upstream end, one or more output channels at a downstream end, and a set of structures in communication with the input channel and the one or more output channels, wherein flow from the input channel is configured to reach at least one of the one or more output channels only by way of the set of structures;

at the workstation, retaining a container comprising a set of target particles; from a controller in communication with a handling subsystem of the workstation, receiving a set of instructions for automatic processing of the set of target particles, in single-particle format; and based upon the set of instructions:

with the handling subsystem, transmitting the set of target particles into the network;

isolating each of the set of target particles in single-particle format with an isolation material, within the network of the substrate, and

delivering, by way of the handling subsystem, a reagent material from a reagent container into the input channel of the substrate.

2. The method of claim 1 , wherein isolating each of the set of target particles in single-particle format comprises isolating a set of target cells of a sample by way of a set of structures of the network.

3. The method of claim 2 , wherein isolating each of the set of target cells comprises separating each target cell from adjacent target cells with a set of barriers configured to fluidly isolate each target cell from adjacent target cells within the network, wherein the set of barriers block fluid flow between adjacent target cells.

4. The method of claim 3 , wherein isolating comprises segregating each of the set of target cells in single-cell format in a spatially arranged array within the network.

5. The method of claim 4 , wherein the network comprises a plurality of pores, each pore in the plurality of pores displaced from at least one other pore in the plurality of pores and comprising: a chamber having an upstream end, and a pore channel, fluidly coupled to the chamber at a downstream end of the chamber, having a pore channel width configured to block egress of a particle,

wherein the input channel is directly fluidly coupled to the upstream end of each chamber of the plurality of pores,

wherein the output channel is directly fluidly coupled to each pore channel of the plurality of pores,

wherein flow from the input channel is configured to reach the output channel only by way of the plurality of parallel pores, and

wherein isolating each of the set of target cells in single-cell format comprises isolating the set of target cells in single-cell format at the plurality of pores.

6. The method of claim 1 , wherein the reagent material is configured for performing at least one of: a molecular reaction, immunostaining, a single cell proteomic analysis, nucleic acid analysis, and genomic sequencing individually for each target particle of the set of target particles.

7. The method of claim 1 , wherein the reagent material is configured for performing a polymerase chain reaction (PCR) process, and wherein the method further comprises performing the PCR process individually for each of the set of target particle in single-particle format.

8. The method of claim 1 , further comprising receiving instructions for performing at least one of: pipetting, aliquoting, mixing, pumping, and monitoring fluid delivery; and executing the set of instructions with the handling subsystem.

9. The method of claim 8 , wherein the set of target particles comprises a set of target cells, the method further comprising: automatically transmitting a subportion of the set of target cells from the network in a viable state, with the handling subsystem.

10. The method of claim 1 , wherein transmitting the sample with the set of target particles into the network comprises transmitting a cell suspension comprising a set of target cells into the network.

11. The method of claim 1 , wherein isolating with the isolation material comprises delivering the isolation material, comprising at least one of an oil and a hydrogel, into an isolation inlet of the substrate in communication with the network.

12. The method of claim 1 , further comprising co-capturing a set of target cells with a set of functionalized magnetic particles as the set of target particles, thereby forming a set of complexes, wherein isolating the set of target particles in single-particle format comprises isolating the set of complexes in single-complex format.

13. The method of claim 12 , further comprising magnetically separating the set of target cells from the sample, by way of the set of functionalized magnetic particles.

14. A method for automatically processing target particles in single-particle format, the method comprising:

at a workstation, receiving a substrate comprising a network having an input channel at an upstream end, an output channel at a downstream end, and a set of structures in communication with the input channel and the output channel;

at the workstation, retaining a sample comprising a set of target cells;

at the workstation, retaining a volume comprising a set of functionalized particles;

from a controller in communication with a handling subsystem of the workstation, receiving a set of instructions for automatic processing of the set of target cells, in single cell format; and

based upon the set of instructions:

with the handling subsystem, transmitting the sample and the volume into the network;

co-capturing the set of target cells with the set of functionalized particles within the network in single-particle format;

isolating the set of target cells with an isolation material, within the network, and

delivering, by way of the handling subsystem, a reagent material from a reagent container into the input channel of the substrate.

15. The method of claim 14 , wherein the set of functionalized particles comprise functionalized magnetic particles configured to couple with the set of target cells.

16. The method of claim 15 , further comprising magnetically separating the set of target cells from the sample, by way of the set of functionalized magnetic particles.

17. The method of claim 16 , further comprising isolating the set of target cells and the set of functionalized particles as a set of complexes within the network, in single-complex format.

18. The method of claim 17 , further comprising: based on the set of instructions automatically delivering the isolation material, comprising an oil, into an isolation inlet of the substrate, and automatically isolating the set of complexes in single-complex format, as a spaced array, with the oil.

19. The method of claim 18 , further comprising automatically transmitting a subportion of the set of target cells from the network in a viable state, with the handling subsystem.

20. The method of claim 19 , wherein the reagent material is configured for performing a polymerase chain reaction (PCR) process, and wherein the method further comprises, based upon the set of instructions, performing the PCR process individually for each of the set of target cells in single-cell format.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 5, 2020
From: CELSEE, INC.
To: BIO-RAD LABORATORIES, INC.
Reel/Frame 054269/0742 →
CHANGE OF NAME Recorded Sep 24, 2020
From: CELSEE DIAGNOSTICS, INC.
To: CELSEE, INC.
Reel/Frame 053881/0555 →
CHANGE OF NAME Recorded Jun 3, 2019
From: DENOVO SCIENCES, INC.
To: CELSEE DIAGNOSTICS, INC.
Reel/Frame 049354/0340 →
CHANGE OF NAME Recorded May 30, 2019
From: DENOVO SCIENCES, INC.
To: CELSEE DIAGNOSTICS, INC.
Reel/Frame 050305/0486 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 30, 2019
From: HANDIQUE, KALYAN
To: DENOVO SCIENCES, INC.
Reel/Frame 049319/0113 →
Continuity (7)
Continuation 16419254 · May 22, 2019
Continuation 16048104 · Jul 27, 2018
Continuation 15657553 · Jul 24, 2017
Continuation 15333420 · Oct 25, 2016
Continuation 14607918 · Jan 28, 2015
Continuation 13557510 · Jul 25, 2012
Provisional Application 61513785 · Aug 1, 2011
Cited By (11)
US 12,196,661 US 12,228,492 US 12,276,659 US 12,312,595 US 12,332,241 US 12,352,679 US 12,379,387 US 12,434,242 US 12,461,007 US 12,551,886 US 12,669,427