IP Library › Granted Patent US 12,252,675
Granted Patent B2
US 12,252,675 · App. 17/309,061 · Granted Mar 18, 2025

Tissue culture platform having multiple well chambers fluidically coupled via microfluidic channels and selector valves

Inventors: Hunter B. Rogers (Chicago, IL); Teresa K. Woodruff (Chicago, IL); Ji-Yong Julie Kim (Evanston, IL); Hannes Marcus Campo (Evanston, IL)
Assignee: Northwestern University
C12M21/08C12M23/12C12M23/16C12M23/26C12M23/34C12M23/48C12M23/58C12M27/00C12M29/00C12M41/40
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,252,675
App. No.
17/309,061
Granted
Mar 18, 2025
Kind
B2
Abstract

Tissue culture platforms that may be configured for tissue culture or biological cell culture, and methods for use thereof, are described. In general, the tissue culture platforms include multiple well chambers that are fluidically coupled by one or more channels Flow between the different well chambers is controlled via one or more selector valves, enabling a single tissue culture platform that can provide multiple integrated culture subsystems, multiple non-interacting culture subsystems, or combinations thereof.

Claims (60)

1. A tissue culture assembly, comprising:

a base plate;

a plurality of culture subsystems coupled to the base plate, each culture subsystem comprising:

a plurality of well chambers;

a plurality of channels;

a selector valve fluidically coupling the plurality of well chambers via the plurality of channels;

wherein the selector valve is operable to modify a fluid path to facilitate exchange of media within a given culture subsystem or between culture subsystems of the plurality of culture subsystems;

a base station comprising:

an enclosure;

a plurality of motors housed in the enclosure; and

wherein, the base plate is removably coupled to the base station;

wherein each selector valve is a pneumatically actuated selector valve, and further comprising a pump source housed in the enclosure of the base station, the pump source being operable to pneumatically actuate each selector valve.

2. The tissue culture assembly of claim 1 , wherein the plurality of well chambers comprises at least one culture well, at least one donor well, and at least one acceptor well.

3. The tissue culture assembly of claim 1 , wherein the selector valve is a pneumatically actuated selector valve comprising a reservoir and a flexible membrane, wherein the selector valve is operable to modify the fluid path by modifying a pressure in the reservoir to deflect the flexible membrane.

4. The tissue culture assembly of claim 1 , wherein the first well chamber is in a first culture subsystem and the second well chamber is in a second culture subsystem.

5. The tissue culture assembly of claim 1 , wherein the first well chamber and the second well chamber are in a single culture subsystem.

6. The tissue culture assembly of claim 1 , wherein the selector valve is operable to modify the fluid path to recirculate within a selected well chamber.

7. The tissue culture assembly of claim 1 , wherein the selector valve in each of the plurality of culture subsystems is operable to facilitate exchange of media between the culture subsystems to define a plurality of integrated culture subsystems.

8. The tissue culture assembly of claim 1 , wherein the selector valve in each of the plurality of culture subsystems is operable to facilitate exchange of media within each culture subsystem while preventing exchange of media between the culture subsystems in order to define a plurality of non-interacting culture subsystems.

9. The tissue culture assembly of claim 1 , wherein the selector valve in each of the plurality of culture subsystems is operable to facilitate exchange of media between the culture subsystems to define a plurality of integrated culture subsystems.

10. The tissue culture assembly of claim 1 , wherein the selector valve is a rotary valve that is operable to change the fluid path between well chambers by rotating the rotary valve.

11. The tissue culture assembly of claim 1 , further comprising a base station comprising:

an enclosure;

a plurality of motors housed in the enclosure; and

wherein, the base plate is removably coupled to the base station.

12. The tissue culture assembly of claim 11 , wherein each of the plurality of motors operatively engages one of the selector valves when the base plate is removably coupled to the base station.

13. The tissue culture assembly of claim 12 , further comprising a controller that controls an operation of the plurality of motors to adjust the fluid path defined by each selector valve.

14. The tissue culture assembly of claim 13 , wherein each selector valve is a rotary valve that is operable to change the fluid path between well chambers by rotating the rotary valve through operation of each respective one of the plurality of motors.

15. The tissue culture assembly of claim 11 , wherein each selector valve is a pneumatically actuated selector valve, and further comprising a pump source housed in the enclosure of the base station, the pump source being operable to pneumatically actuate each selector valve.

16. The tissue culture assembly of claim 11 , wherein the base station further comprises a slot that receives the base plate.

17. The tissue culture assembly of claim 16 , wherein the slot comprises a tray.

18. The tissue culture assembly of claim 16 , wherein the base station further comprises a stage that is moveable between a lowered position and a raised position, such that when in the raised position the stage engages the base plate when the base plate is positioned in the slot.

19. The tissue culture assembly of claim 18 , wherein the stage includes an interface that extends from an upper surface of the stage to engage a recess formed in a lower surface of the base plate.

20. The tissue culture assembly of claim 19 , wherein the interface is a actuatable interface such that actuation of the interface when the stage is engaged with the base plate causes the selector valve to modify the fluid path to facilitate exchange of media within the given culture subsystem or between culture subsystems.

21. The tissue culture assembly of claim 20 , wherein the actuatable interface is a rotatable interface and actuation of the interface comprises rotation of the interface.

22. The tissue culture assembly of claim 19 , wherein the interface includes a first aperture coupled to a pump source, and the recess includes a second aperture coupled to the selector valve, such that when the stage is engaged with the base plate that first aperture and the second aperture are coupled such that operation of the pump source causes the selector value to open and close the fluid path.

23. The tissue culture assembly of claim 1 , wherein the plurality of channels comprises a plurality of microfluidic channels.

24. The tissue culture assembly of claim 23 , wherein the plurality of microfluidic channels are formed in the base plate.

25. The tissue culture assembly of claim 1 , wherein at least the plurality of well chambers and the plurality of channels are composed of a hydrophobic material.

26. The tissue culture assembly of claim 25 , wherein the hydrophobic material is polystyrene.

27. The tissue culture assembly of claim 25 , wherein the hydrophobic material is treated to reduce its hydrophobicity.

28. The tissue culture assembly of claim 27 , wherein the hydrophobic material is treated using a plasma treating to reduce its hydrophobicity.

29. The tissue culture assembly of claim 1 , wherein at least the plurality of well chambers and the plurality of channels are composed of hydrophilic acrylic.

30. A tissue culture assembly, comprising:

a base plate;

a plurality of culture subsystems coupled to the base plate, each culture subsystem comprising:

a plurality of well chambers;

a plurality of channels;

a selector valve fluidically coupling the plurality of well chambers via the plurality of channels;

a base station comprising:

an enclosure;

a plurality of motors housed in the enclosure;

wherein, the base plate is removably coupled to the base station;

wherein the selector valve is operable to modify a fluid path to facilitate exchange of media within a given culture subsystem or between culture subsystems of the plurality of culture subsystems;

wherein the base station further comprises a slot that receives the base plate;

wherein the base station further comprises a stage that is moveable between a lowered position and a raised position, such that when in the raised position the stage engages the base plate when the base plate is positioned in the slot;

wherein the stage includes an interface that extends from an upper surface of the stage to engage a recess formed in a lower surface of the base plate; and

wherein the interface includes a first aperture coupled to a pump source, and the recess includes a second aperture coupled to the selector valve, such that when the stage is engaged with the base plate that first aperture and the second aperture are coupled such that operation of the pump source causes the selector value to open and close the fluid path.

31. The tissue culture assembly of claim 1 , wherein the selector valve is operable between an open state and a closed state, such that when in the open state the selector valve modifies the fluid path to fluidically couple a first well chamber to a second well chamber of the plurality of well chambers via ones of the plurality of channels in fluid communication with the selector valve, the first well chamber, and the second well chamber.

32. The tissue culture assembly of claim 31 , wherein the selector valve is further operable to modify a flow rate through the fluid path when the selector valve is in the open state.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 1, 2022
From: KIM, JI-YONG JULIE; CAMPO, HANNES MARCUS
To: NORTHWESTERN UNIVERSITY
Reel/Frame 061943/0358 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2022
From: WOODRUFF, TERESA K.; ROGERS, HUNTER
To: NORTHWESTERN UNIVERSITY
Reel/Frame 060709/0333 →
Continuity (2)
Provisional Application 62746967 · Oct 17, 2018
Related Publication 20220025308A1 · Jan 27, 2022
References Cited (43)
US 8906685B2 · Takayama · 2014 [cited by applicant]
US 9222932B2 · Shepherd · 2015 [cited by applicant]
US 9243221B2 · Yarmush · 2016 [cited by applicant]
US 9273276B2 · Shuler · 2016 [cited by applicant]
US 9512393B2 · Kasuto · 2016 [cited by applicant]
US 9575055B2 · Gevaert · 2017 [cited by applicant]
US 9695399B2 · Woodruff · 2017 [cited by applicant]
US 9777252B2 · Cuiffi · 2017 [cited by applicant]
US 9791433B2 · Marx · 2017 [cited by applicant]
US 10023832B2 · Wikswo · 2018 [cited by applicant]
US 20020133072A1 · Wang · 2002 [cited by applicant]
US 20050266582A1 · Modlin · 2005 [cited by applicant]
US 20080145924A1 · Kobayashi · 2008 [cited by applicant]
US 20110207209A1 · Hammons · 2011 [cited by examiner]
US 20130108801A1 · Naessens · 2013 [cited by applicant]
US 20140030752A1 · Cuiffi · 2014 [cited by applicant]
US 20140302549A1 · Marx · 2014 [cited by applicant]
US 20150298123A1 · Block · 2015 [cited by applicant]
US 20160145554A1 · Ingber · 2016 [cited by applicant]
US 20160145555A1 · Ingber · 2016 [cited by applicant]
US 20160264918A1 · Shimase · 2016 [cited by examiner]
US 20160274085A1 · Nair · 2016 [cited by applicant]
US 20170081625A1 · Wikswo · 2017 [cited by applicant]
US 20170227525A1 · Griffith · 2017 [cited by examiner]
US 20170252701A1 · Nosrati · 2017 [cited by applicant]
US 20180057796A1 · Woodruff · 2018 [cited by applicant]
US 20200190479A1 · Woodruff · 2020 [cited by applicant]
US 20200224147A1 · Rogers · 2020 [cited by applicant]
WO 2000017624A2 · 2000 [cited by applicant]
WO 2010031194A1 · 2010 [cited by applicant]
WO 2014081840A1 · 2014 [cited by applicant]
WO 2017059436A1 · 2017 [cited by applicant]
WO 2017096282A1 · 2017 [cited by applicant]
International Searching Authority. International Search Report and Written Opinion for application PCT/US2019/056615. Mailed on Jan. 9, 2020. 11 pages. [cited by applicant]
Lee, P. J., et al. “Microfluidic system for automated cell-based assays.” JALA: Journal of the Association for Laboratory Automation 12.6 (2007): 363-367. [cited by applicant]
Maschmeyer, I., et al. “A four-organ-chip for interconnected long-term co-culture of human intestine, liver, skin and kidney equivalents.” Lab on a Chip 15.12 (2015): 2688-2699. [cited by applicant]
Puccinelli, J. P., et al. “Automated high-throughput microchannel assays for cell biology: Operational optimization and characterization.” JALA: Journal of the Association for Laboratory Automation 15.1 (2010): 25-32. [cited by applicant]
Renggli. 2017. Microfluidic Multi-Tissue Platform for Use with Spherical Microtissues. Analytical Science Magazine. Available online at https://analyticalscience.wiley.com/do/10.1002/gitlab.15455/full/. [cited by applicant]
Tsuda, S., et al. “Customizable 3D printed ‘plug and play’ millifluidic devices for programmable fluidics.” PLoS One 10.11 (2015): e0141640. [cited by applicant]
Vereshchagina, E., et al. “Plate reader compatible membrane-integrated microfluidic platform for high-throughput cellular assays.” 2013 Transducers & Eurosensors XXVII: The 17th International Conference on Solid-State S… [cited by applicant]
Virumbrales-Munoz, M., et al. “Multiwell capillarity-based microfluidic device for the study of 3D tumour tissue-2D endothelium interactions and drug screening in co-culture models.” Scientific reports 7.1 (2017): 1-15. [cited by applicant]
Wagner, I., et al. “A dynamic multi-organ-chip for long-term cultivation and substance testing proven by 3D human liver and skin tissue co-culture.” Lab on a Chip 13.18 (2013): 3538-3547. [cited by applicant]
Xiao, S., et al. “A Microfluidic Culture Model of the Human Reproductive Tract and 28-Day Menstrual Cycle.” Nature Communications, vol. 8, 2017, p. 14584. [cited by applicant]