IP Library Granted Patent US 10,967,296
Granted Patent B2
US 10,967,296 · App. 16/676,352 · Granted Apr 6, 2021

Method and device for high-throughput solution exchange for cell and particle suspensions

Inventors: Dino Di Carlo (Los Angeles, CA); Daniel R. Gossett (Los Angeles, CA); Henry T. K. Tse (San Francisco, CA)
Assignee: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
B01D12/00B01L3/502761B01L3/502776B01L3/502746B01L2200/0652B01L2300/0816B01L2400/0487B01L2400/084G01N2015/149
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Quick Facts
Patent No.
US 10,967,296
App. No.
16/676,352
Granted
Apr 6, 2021
Kind
B2
Abstract

A method of exchanging fluids with suspended particles includes providing a microfluidic device with a first inlet channel operatively coupled to a source of particles and a second inlet channel operatively coupled to an exchange fluid. A transfer channel is connected at a proximal end to the first inlet channel and the second inlet channel. First and second outlet channels are connected to a distal end of the transfer channel. The source of particles is flowed at a first flow rate into the first inlet channel while the exchange fluid is flowed at a second flow rate into the second inlet channel wherein the ratio of the second flow rate to the first flow rate is at least 1.5. Particles are collected in one of the first and second outlet channels while fluid substantially free of particles is collected in the other of the first and second outlet channels.

Claims (25)

1. A method of transferring particles across fluid streamlines comprising:

providing a microfluidic device comprising a plurality of proximal channels and a plurality of distal channels connected to a transfer channel disposed between the plurality of proximal channels and the plurality of distal channels, wherein at least one of the proximal channels is operatively coupled to a source of fluid containing particles suspended therein, at least one of the proximal channels is operatively coupled to a source of exchange fluid;

flowing the fluid containing the particles in the at least one proximal channel operatively coupled to the source of fluid containing particles suspended therein;

flowing the exchange fluid into the at least one proximal channel operatively coupled to the source of exchange fluid, wherein a co-flow state of the fluid containing the particles suspended therein and the exchange fluid is maintained along substantially all of the transfer channel, wherein at least some of the particles of the fluid containing the particles suspended therein migrate in response to inertial lift forces toward an equilibrium position (X eq ) located within the transfer channel to become migrated particles;

transferring the migrated particles into at least one of the plurality of distal channels.

2. The method of claim 1 , wherein the particles comprise cells.

3. The method of claim 1 , wherein the particles comprise red blood cells.

4. The method of claim 1 , wherein the particles comprise white blood cells.

5. The method of claim 1 , wherein the fluid containing the particles comprises blood.

6. The method of claim 1 , wherein the exchange fluid occupies a larger volume of the transfer channel as compared to the fluid containing the particles.

7. The method of claim 1 , further comprising analyzing the particles transferred into one of the plurality of distal channels with an analyzer selected from the group consisting of a flow cytometer, fluorescent-activated cell sorter (FACS), and imager.

8. The method of claim 1 , wherein the transfer channel comprises an aspect ratio (height/width) that is <1 and has a length of greater than 1 cm.

9. The method of claim 1 , further comprising directing fluid substantially free of particles into at least one of the plurality of distal channels.

10. A method of transferring particles across fluid streamlines comprising:

providing a microfluidic device comprising a plurality of solution exchange stages, wherein at least two of the plurality of solution exchange stages comprise a transfer channel having an output channel coupled to an input channel of a downstream transfer channel of a solution exchange downstream stage;

flowing a fluid containing the particles suspended therein into the plurality of solution exchange stages;

flowing an exchange fluid into the plurality of solution exchange stages, wherein the particles migrate toward an equilibrium position (X eq ) located within respective transfer channels and become migrated particles, wherein inertial lift forces in the respective transfer channels direct the particles toward the equilibrium position (X eq );

directing the migrated particles into one outlet channel in the microfluidic device; and

directing fluid substantially free of the migrated particles into one or more other outlet channels in the microfluidic device.

11. The method of claim 10 , wherein the particles comprise cells.

12. The method of claim 10 , wherein the particles comprise red blood cells.

13. The method of claim 10 , wherein the particles comprise white blood cells.

14. The method of claim 10 , wherein the fluid containing the particles comprises blood.

15. The method of claim 10 , wherein the exchange fluid occupies a larger volume of the transfer channels as compared to the fluid containing the particles.

16. The method of claim 10 , wherein a Particle Reynolds number for the migrated particles in the transfer channels is between about 0.25 and about 1.87.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2022
From: DI CARLO, DINO; GOSSETT, DANIEL R.; TSE, HENRY TK
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 059932/0301 →
Continuity (6)
Continuation 16263232 · Jan 31, 2019
Continuation 15785191 · Oct 16, 2017
Continuation 15346442 · Nov 8, 2016
Division 13884595
Provisional Application 61415067 · Nov 18, 2010
Related Publication 20200122056A1 · Apr 23, 2020
Cited By (5)
US 12,478,966 US 12,546,699 US 12,546,700 US 12,723,967 US 12,730,057