IP Library › Granted Patent US 10,857,260
Granted Patent B2
US 10,857,260 · App. 15/864,387 · Granted Dec 8, 2020

Coaxial needle for fabricating a multi scale, multi layer blood vessel or vascular network employing 3D bioprinting

Inventors: Haitao Cui (Arlington, VA); Wei Zhu (Washington, DC); Lijie Grace Zhang (Washington, DC)
Assignee: The George Washington University
A61L27/16A61L27/18A61L27/222A61L27/3808A61L27/3826A61L27/507A61L27/52B29C64/118B29C64/209B33Y10/00B33Y30/00A61F2/062A61L2430/22B29C64/135B33Y70/00
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 10,857,260
App. No.
15/864,387
Granted
Dec 8, 2020
Kind
B2
Abstract

A coaxial needle having two or more passageways for forming a biomimetic bioprinted blood vessel tubular construct. The coaxial needle has an external needle passageway and an internal needle passageway separated by an internal barrier, and having a nozzle at an end thereof. A bioink is provided flowable through the external needle passageway and a crosslinking solution is provided flowable through the internal needle passageway. The crosslinking solution contacts the bioink as the crosslinking solution and bioink exit the nozzle thereby forming a tubular blood vessel construct.

Claims (44)

1. A method of forming a biomimetic blood vessel comprising:

flowing a bioink through an external needle passageway of a coaxial needle and out through a nozzle of the coaxial needle, the nozzle being at one end of the coaxial needle;

flowing a crosslinking solution through an internal needle passageway of the coaxial needle and out through the nozzle of the coaxial needle, the external needle passageway and internal needle passageway being separated by a barrier; and

contacting the crosslinking solution with the bioink as the crosslinking solution and the bioink exit the nozzle thereby forming a tubular blood vessel construct,

wherein the bioink comprises a gelatin methacrylate functionalized with a catechol.

2. The method of claim 1 , wherein the bioink is cell-laden.

3. The method of claim 2 , wherein the bioink is cell-laden with smooth muscle cells.

4. The method of claim 1 , wherein the crosslinking solution comprises a crosslinking agent.

5. The method of claim 4 , wherein the crosslinking agent is an oxidant.

6. The method of claim 5 , wherein the oxidant is a periodate salt or a derivative thereof.

7. The method of claim 1 , wherein the crosslinking solution comprises a removable fugitive ink.

8. The method of claim 7 , wherein the fugitive ink comprises a block copolymer of ethylene oxide and propylene oxide.

9. The method of claim 1 , wherein the crosslinking solution is cell-laden.

10. The method of claim 1 , wherein the crosslinking solution is cell-laden with endothelial cells.

11. The method of claim 1 , further comprising flowing a cell-laden fluid in a passageway between the external needle passageway and the internal needle passageway.

12. A system comprising:

a coaxial needle having an external needle passageway and an internal needle passageway separated by an internal barrier, and having a nozzle at an end thereof;

a bioink flowable through the external needle passageway; and

a crosslinking solution flowable through the internal needle passageway,

the crosslinking solution contacting the bioink as the crosslinking solution and bioink exit the nozzle thereby forming a tubular blood vessel construct,

wherein the bioink comprises a gelatin methacrylate functionalized with a crosslinkable group, and

the crosslinking solution comprises a crosslinking agent, wherein the crosslinking agent is a periodate salt or a derivative thereof.

13. The system of claim 12 , wherein the crosslinking solution comprises a removable fugitive ink.

14. The system of claim 13 , wherein the fugitive ink comprises a block copolymer of ethylene oxide and propylene oxide.

15. The system of claim 12 , wherein

the bioink is cell-laden with smooth muscle cells, and

the crosslinking solution is cell-laden with endothelial cells,

wherein the tubular blood vessel construct comprises a bilayer of cells having an outer layer containing smooth muscle cells and an inner layer containing endothelial cells.

16. The system of claim 12 , further comprising the tubular blood vessel construct being embedded in a scaffold.

17. A method of forming a biomimetic blood vessel comprising:

flowing a bioink through an external needle passageway of a coaxial needle and out through a nozzle of the coaxial needle, the nozzle being at one end of the coaxial needle;

flowing a crosslinking solution through an internal needle passageway of the coaxial needle and out through the nozzle of the coaxial needle, the external needle passageway and internal needle passageway being separated by a barrier;

flowing a cell-laden fluid in a passageway between the external needle passageway and the internal needle passageway; and

contacting the crosslinking solution with the bioink as the crosslinking solution and the bioink exit the nozzle thereby forming a tubular blood vessel construct.

18. The method of claim 17 , wherein the crosslinking solution comprises an oxidant and a removable fugitive ink, wherein the oxidant is a periodate salt or a derivative thereof, and the removable fugitive ink comprises a block copolymer of ethylene oxide and propylene oxide.

19. The method of claim 17 , wherein the bioink is cell-laden with smooth muscle cells.

20. The method of claim 17 , wherein the crosslinking solution is cell-laden with endothelial cells.

21. A system comprising:

a coaxial needle having an external needle passageway and an internal needle passageway separated by an internal barrier, and having a nozzle at an end thereof;

a bioink flowable through the external needle passageway, wherein the bioink comprises a gelatin methacrylate functionalized with a catechol; and

a crosslinking solution flowable through the internal needle passageway, wherein the crosslinking solution comprises an oxidant or a derivative thereof,

the crosslinking solution contacting the bioink as the crosslinking solution and bioink exit the nozzle thereby forming a tubular blood vessel construct.

22. The system of claim 21 , wherein the crosslinking solution comprises a removable fugitive ink, the fugitive ink comprising a block copolymer of ethylene oxide and propylene oxide.

23. The system of claim 22 , wherein the crosslinking solution comprises endothelial cells.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 29, 2018
From: CUI, HAITAO; ZHU, WEI; ZHANG, LIJIE GRACE
To: THE GEORGE WASHINGTON UNIVERSITY
Reel/Frame 045920/0270 →
Continuity (2)
Provisional Application 62445599 · Jan 12, 2017
Related Publication 20190008998A1 · Jan 10, 2019
Cited By (1)
US 12,734,026