IP Library Granted Patent US 11,130,935
Granted Patent B2
US 11,130,935 · App. 15/121,553 · Granted Sep 28, 2021

Microfluid device and three-dimensional microculture method for cell

Inventors: Kenichiro Kamei (Kyoto, JP); Yong Chen (Kyoto, JP)
Assignees: KYOTO UNIVERSITY; Ushio Denki Kabushiki Kaisha
C12M25/14C12M23/16C12M35/08C12N5/0062C12N2501/999
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Quick Facts
Patent No.
US 11,130,935
App. No.
15/121,553
Granted
Sep 28, 2021
Kind
B2
Abstract

The invention provides a microfluidic device comprising at least one cell culture chamber, the at least one cell culture chamber being connected to at least two openings, the device being configured to supply at least one physiologically active substance from at least one of the openings to the at least one cell culture chamber in such a manner as to form a concentration gradient or concentration gradients in the at least one cell culture chamber when cells and a hydrogel are introduced into the at least one cell culture chamber to culture the cells in a 3D-gel medium.

Claims (22)

1. A microfluidic device consisting of a first part being formed by a mold and a second part that differs from the first part,

wherein the first part and the second part are plate members that are adhered together,

wherein the first part and second part comprise at least one cell culture chamber, the at least one cell culture chamber being connected to two or more openings, the device being configured to supply at least one physiologically active substance from at least one of the openings to the at least one cell culture chamber in such a manner as to form a concentration gradient or concentration gradients in the at least one cell culture chamber when cells and a hydrogel are introduced into the at least one cell culture chamber to culture the cells in a 3D gel medium,

wherein the diameter of each of the two or more openings is larger than the diameter of the at least one cell culture chamber,

wherein the height of each of the two or more openings is greater than the height of the at least one cell culture chamber,

wherein the at least one cell culture chamber forms a closed space except for the connection to the two or more openings, and

wherein a first opening of the two or more openings is for providing a fresh culture solution to the at least one cell culture chamber, and a second opening of the two or more openings is for discharging used culture solution from the at least one cell culture chamber,

wherein the first opening is directly connected to the at least one cell culture chamber, and the second opening is connected to the at least one cell culture chamber through a microchannel.

2. The microfluidic device according to claim 1 , wherein the hydrogel is formed inside the at least one cell culture chamber.

3. The microfluidic device according to claim 1 , being configured for use in a high-throughput fashion and comprising from 10 to 400 cell culture chambers.

4. A 3D cell microculture method comprising the steps of introducing cells and a fluidized hydrogel into the at least one cell culture chamber of the microfluidic device according to claim 1 ;

converting the hydrogel into a gel; and

supplying at least one physiologically active substance from the at least one of the openings in such a manner as to form a concentration gradient or concentration gradients inside the at least one cell culture chamber to culture the cells in the presence of the at least one physiologically active substance.

5. The 3D cell microculture method according to claim 4 , wherein the cells are pluripotent stem cells.

6. The 3D cell microculture method according to claim 4 , wherein the cells are human pluripotent stem cells.

7. The 3D microculture method according to claim 4 , wherein multiple physiologically active substances are supplied into the at least one cell culture chamber in such a manner as to form concentration gradients.

8. The microfluidic device according to claim 1 , wherein a flow in a channel connecting one of the two or more openings to the at least one cell culture chamber is coincident with the direction in which the gradient or gradients are formed and the direction in which the cells are introduced.

9. The microfluidic device according to claim 1 , comprising 16, 48, 96, or 384 cell culture chambers.

10. The microfluidic device according to claim 1 , wherein the at least one cell culture chamber has a height of about 100 to 1,000 μm, a width of about 100 to 1,000 μm, and a depth of about 1,000 to 10,000 μm, and wherein the microchannel that connects the at least one cell culture chamber to the two or more openings has a length of about 1,000 to 10,000 μm and a diameter of about 100 to 1,000 μm.

11. The microfluidic device according to claim 1 , wherein the at least one cell culture chamber has a volume of 100 to 2,000 μL.

12. The microfluidic device according to claim 1 , wherein the shape of space for culture in the at least one cell culture chamber is a cylindrical shape, a square tube shape, or an elliptic cylindrical shape.

13. The microfluidic device according to claim 1 , wherein the two or more openings are positioned within the microfluidic device so as to correspond to the wells of a conventional 16-well, 48-well, 96-well, or 384-well plate.

Assignments (3)
NUNC PRO TUNC ASSIGNMENT Recorded May 22, 2026
From: USHIO DENKI KABUSHIKI KAISHA
To: ZEON CORPORATION
Reel/Frame 074736/0684 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 29, 2021
From: KYOTO UNIVERSITY
To: KYOTO UNIVERSITY; USHIO DENKI KABUSHIKI KAISHA
Reel/Frame 057026/0148 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 25, 2016
From: KAMEI, KENICHIRO; CHEN, YONG
To: KYOTO UNIVERSITY
Reel/Frame 039542/0499 →
Priority Claims (1)
JP JP2014-034166 · Feb 25, 2014 · national
Continuity (1)
Related Publication 20160369218A1 · Dec 22, 2016