IP Library Granted Patent US 11,414,635
Granted Patent B2
US 11,414,635 · App. 16/094,086 · Granted Aug 16, 2022

Integration of three dimensional cell culture scaffolds in microfluidic devices by direct fiber spinning

Inventors: Robert Scott Martin (Kirkwood, MO); Chengpeng Chen (St. Louis, MO); Scott Allen Sell (St. Louis, MO)
Assignee: Saint Louis University
C12M23/16C12M25/14D01D5/0985D01D7/00
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Quick Facts
Patent No.
US 11,414,635
App. No.
16/094,086
Granted
Aug 16, 2022
Kind
B2
Abstract

Disclosed are fluidic devices and methods for preparing fluidic devices. More particularly, disclosed are fluidic devices having fiber scaffolds and methods for their preparation. Also disclosed are methods for culturing cells using the fluidic devices having fiber scaffolds.

Claims (17)

1. A method for preparing a fluidic device comprising an electrospun fiber scaffold on an inner wall surface of the fluidic device, the method comprising:

providing a fluidic device, the fluidic device comprising: an inlet end, an outlet end, an outer wall, an inner wall, and a channel, the channel defined therethrough by the inner wall and extending between the inlet end and the outlet end; and

selectively coating an inner surface of the inner wall of the fluidic device by placing one of the inlet end or outlet end of the fluidic device proximate to a cannula of an electrospun fiber spinning apparatus, wherein the electrospun fiber spinning apparatus comprises a gas sheath device;

applying gas flow to the gas sheath device;

pumping a polymer solution through the cannula of the electrospun fiber spinning apparatus to prepare a plurality of electrospun fibers;

directing the plurality of electrospun fibers into the fluidic device, wherein the plurality of electrospun fibers form an electrospun fiber scaffold on the inner wall surface of the fluidic device.

2. The method of claim 1 , wherein all of the inner wall surface comprises the plurality of electrospun fiber scaffolds.

3. The method of claim 1 , wherein the inlet end further comprises threads.

4. The method of claim 1 , wherein the outlet end further comprises threads.

5. The method of claim 1 , further comprising contacting the fluidic device with a cell suspension.

6. The method of claim 1 , wherein the electrospun fiber diameter ranges from 10 nm to 2.5 μm.

7. The method of claim 1 , wherein the distance from the cannula to the fluidic device inlet is 2 millimeters.

8. The method of claim 1 , wherein the inner wall of the fluidic device is selectively coated from 1 time to 10 times.

9. The method of claim 1 , wherein the inner wall of the fluidic device is selectively coated for a time ranging from 1 second to 20 seconds.

10. The method of claim 1 , further comprising a drying step after the coating step.

11. The method of claim 1 , wherein the electrospun fiber scaffold comprises a pore size ranging from 90 μm 2 to 135 μm 2 .

12. The method of claim 1 , wherein the polymer solution comprises a synthetic polymer, a natural protein and combinations thereof.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 2, 2023
From: SAINT LOUIS UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 064467/0156 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2018
From: MARTIN, ROBERT SCOTT; CHEN, CHENGPENG; SELL, SCOTT ALLEN
To: SAINT LOUIS UNIVERSITY
Reel/Frame 047182/0317 →
Continuity (2)
Provisional Application 62324073 · Apr 18, 2016
Related Publication 20210222104A1 · Jul 22, 2021