Therapeutic cell washing, concentration, and separation utilizing acoustophoresis

Patent metadata

Field	Value
Publication number	US-10640760-B2
Application number	US-201715586116-A
Country	US
Kind code	B2
Filing date	May 3, 2017
Priority date	May 3, 2016
Publication date	May 5, 2020
Grant date	May 5, 2020

Abstract

Multi-stage acoustophoretic devices for continuously separating a second fluid or a particulate from a host fluid are disclosed. Methods of operating the multi-stage acoustophoretic devices are also disclosed. The systems may include multiple acoustophoretic devices fluidly connected to one another in series, each acoustophoretic device comprising a flow chamber, an ultrasonic transducer capable of creating a multi-dimensional acoustic standing wave, and a reflector. The systems can further include pumps and flowmeters.

First claim

The invention claimed is:

1. A method of washing particles, the method comprising:
providing an initial mixture of a first media and particles to a chamber of an acoustophoretic device, the acoustophoretic device also comprising at least one ultrasonic transducer that includes a piezoelectric material;
driving the at least one ultrasonic transducer to create an acoustic standing wave in the chamber, such that at least a portion of the particles are trapped and held against fluid flow in the acoustic standing wave;
forming clusters of the trapped particles to grow in size to exit the acoustic standing wave; and
mixing the trapped particles and clusters with a second media to wash the trapped particles and clusters.

2. The method of claim 1 , further comprising:
providing the initial mixture to the chamber to obtain an intermediate mixture of the trapped particles in a reduced volume of the first media;
collecting the intermediate mixture;
mixing the intermediate mixture with the second media to form a secondary mixture; and
providing the secondary mixture to the chamber to obtain a final mixture of the trapped particles in a reduced volume of the second media.

3. The method of claim 1 , wherein the second media is provided to the chamber after the initial mixture is provided to the chamber.

4. The method of claim 1 , wherein the acoustophoretic device further comprises a collector for collecting the trapped particles and clustered particles therein, the collector located below the at least one ultrasonic transducer; and
wherein the collector leads to a collection container that contains the second media.

5. The method of claim 1 , wherein the second media is a biocompatible wash or a buffer solution.

6. The method of claim 1 , wherein the particles are cells.

7. The method of claim 6 , wherein the cells are Chinese hamster ovary (CHO) cells, NSO hybridoma cells, baby hamster kidney (BHK) cells, human cells, regulatory T-cells, Jurkat T-cells, CAR-T cells, B cells, or NK cells, peripheral blood mononuclear cells (PBMCs), algae, plant cells, bacteria, or viruses.

8. The method of claim 6 , wherein the cells are attached to microcarriers.

9. The method of claim 1 , wherein the piezoelectric material of the at least one ultrasonic transducer is in the form of a piezoelectric array formed from a plurality of piezoelectric elements.

10. The method of claim 9 , wherein the piezoelectric elements are operated out of phase with each other.

11. The method of claim 1 , wherein the acoustophoretic device further comprises a cooling unit for cooling the at least one ultrasonic transducer.

12. The method of claim 1 , wherein the acoustic standing wave is a multi-dimensional acoustic standing wave.

13. The method of claim 1 , wherein, over time, the second media gradually displaces the first media in the flow chamber of the acoustophoretic device.

14. A method of separating microcarriers from cells, comprising:
feeding an initial mixture of a first media and microcarriers with attached cells thereon through a flow chamber of an acoustophoretic device, the acoustophoretic device comprising at least one ultrasonic transducer including a piezoelectric material that is configured to be driven to create an acoustic standing wave in the flow chamber;
driving the at least one ultrasonic transducer to create an acoustic standing wave in the flow chamber, and to trap and hold against fluid flow at least a portion of the microcarriers with attached cells in the acoustic standing wave;
forming clusters of the at least portion of the microcarriers with attached cells in the acoustic standing wave to grow in size to exit the acoustic standing wave;
washing the trapped microcarriers with attached cells and clusters by flowing a second media through the flow chamber to remove the first media; and
flowing a third media containing an enzyme through the flow chamber to separate the cells from the microcarriers.

15. The method of claim 14 , wherein the microcarriers remain trapped in the acoustic standing wave or clusters, and further comprising recovering a mixture of the cells and the third media.

16. The method of claim 14 , wherein the enzyme is trypsin.

17. A culture bag, comprising:
a sidewall that surrounds an internal volume, the internal volume including an upper portion and a lower portion;
a fill port at an upper end of the culture bag in the upper portion;
a drain port at a lower end of the culture bag in the lower portion; and
a wash outlet located at a bottom end of the upper portion between the fill port and the drain port;
wherein the upper portion has a larger diameter than the lower portion.

18. The culture bag of claim 17 , wherein the wash outlet is connected to a wash inlet located in the lower portion of the culture bag.

19. The culture bag of claim 17 , wherein the lower portion comprises from about 1% to about 5% of the internal volume.

20. An acoustophoretic system, comprising:
the culture bag of claim 17 ;
at least one ultrasonic transducer including a piezoelectric material that is configured to be driven to create a multi-dimensional acoustic standing wave in the culture bag; and
means for moving the at least one ultrasonic transducer relative to the culture bag between the upper end and the lower end thereof.

21. The acoustophoretic system of claim 20 , further comprising a tank into which the culture bag can be placed, and wherein the means for moving the at least one ultrasonic transducer is a conveyor system located outside of the tank.

22. The acoustophoretic system of claim 20 , further comprising means for sealing the culture bag between the upper portion and the lower portion thereof.

23. An acoustophoretic system, comprising:
an acoustophoretic device comprising a feed port, a drain port located below the feed port and configured to operate as (i) a wash inlet and (ii) a concentrate outlet, a waste outlet, and at least one ultrasonic transducer including a piezoelectric material that is configured to be driven to create an acoustic standing wave; and
a selector valve connected to the feed port and to the drain port of the acoustophoretic device.

24. The acoustophoretic system of claim 23 , further comprising the selector valve coupled to a feed input or a wash input.

25. The acoustophoretic system of claim 24 , further comprising a feed selector valve coupled to the feed input and the wash input and the selector valve.

26. The acoustophoretic system of claim 25 , further comprising the feed selector valve being upstream of the selector valve.

27. The acoustophoretic system of claim 25 , further comprising an outflow selector valve connected to the drain port and the waste outlet.

Assignees

• Flodesign Sonics Inc

Inventors

• Lipkens Bart
• Presz Jr Walter M
• Dutra Brian
• Gilmanshin Rudolf
• Dionne Jason
• Leidel Chris
• Masi Louis
• Ghoshal Goutam
• Chitale Kedar

Classifications

• C12M23/14

  Bags · CPC title

• C12M25/14

  Scaffolds; Matrices (in general C12N5/0068) · CPC title

• C12M47/04

  Cell isolation or sorting (purging biological preparations of unwanted cells C12N5/0081, determining the presence or kind of microorganism C12Q1/04) · CPC title

• C12N1/02 Primary

  Separating microorganisms from their culture media · CPC title

• C12M47/02

  Separating microorganisms from the culture medium; Concentration of biomass (separating microorganisms from their culture media C12N1/02) · CPC title