IP Library Granted Patent US 9,655,993
Granted Patent B2
US 9,655,993 · App. 14/793,464 · Granted May 23, 2017

Tissue-engineered silk organs

Inventors: David L. Kaplan (Concord, MA); Fiorenzo Omenetto (Wakefield, MA); Jeffrey K. Marchant (Littleton, MA); Noorjahan Panjwani (Medford, MA); Brian Lawrence (Minneapolis, MN)
Assignee: Trustees of Tufts College
A61L27/3604A61L27/225A61L27/227A61L27/3804A61L27/3839A61L27/3891A61L27/56C12N5/0068C12N5/0621G01N33/5044A61L2300/412C12N2533/50
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 9,655,993
App. No.
14/793,464
Granted
May 23, 2017
Kind
B2
Abstract

This invention relates to a lamellae tissue layer, comprising a grooved silk fibroin substrate comprising tissue-specific cells. The silk fibroin substrates provides an excellent means of controlling and culturing cell and extracellular matrix development. A multitude of lamellae tissue layers can be used to create a tissue-engineered organ, such as a tissue-engineered cornea. The tissue-engineered organ is non-immunogenic and biocompatible.

Claims (22)

1. A lamellae tissue layer, comprising a grooved silk fibroin substrate comprising tissue-specific cells aligned thereon,

wherein the thickness of the substrate ranges from 10 nm to 1 mm, the grove width is at least 125 nm, and the groove thickness depth is at least 100 nm, such that the grooves in the substrate induce cell and extracellular matrix (ECM) alignment when said cells are cultured thereon; and

wherein the cells are selected from the group consisting of stem cells, fibroblasts, endothelial cells, epithelial cells, adipose cells capable of generating ECM on the substrate, and combinations thereof.

2. The lamellae tissue layer of claim 1 , wherein the tissue-specific cells deposit extracellular matrix on the substrate.

3. A tissue-engineered organ comprising a multitude of lamellae tissue layers, each layer comprising a grooved silk fibroin substrate of claim 2 .

4. The tissue-engineered organ of claim 3 , wherein the organ comprises micropores,

wherein spacing between the micropores is 50 μm to 100 μm and,

wherein an average diameter of the micropores ranges from 500 nm to 100 μm.

5. The tissue-engineered organ of claim 4 , wherein the micropores are created through the use of poly(ethylene oxide) phase separation chemistry, laser ablation techniques, or a combination thereof.

6. The tissue-engineered organ of claim 3 , wherein the organ is any tissue that can be formed by the assembly of the silk fibroin substrates with cultured cells and deposited extra cellular matrix.

7. The tissue-engineered organ of claim 3 , wherein the organ is a cornea.

8. The tissue-engineered organ of claim 3 , wherein the organ is optically clear, non-immunogenic and biocompatible.

9. The tissue-engineered organ of claim 3 , wherein the organ comprises an endothelial cell sheet on the bottom of the lamellae tissue layers and an epithelial cell sheet on the top of the lamellae tissue layers.

10. The tissue-engineered organ of claim 3 , wherein edges of the tissue engineered organ are sealed.

11. The tissue-engineered organ of claim 3 , comprising:

at least two lamellae tissue layers, each layer comprising a grooved silk fibroin substrate comprising fibroblast cells aligned thereon, such that the grooves in the substrate induce cell and extracellular matrix alignment when said cells are cultured thereon,

an endothelial cell sheet on the bottom of the lamellae tissue layers, and

an epithelial cell sheet on the top of the lamellae tissue layers.

12. The tissue-engineered organ of claim 3 , wherein the organ is a cornea comprising:

an endothelial cell sheet on the bottom of the lamellae tissue layers, and

an epithelial cell sheet on the top of the lamellae tissue layers, wherein a thickness of the grooved silk fibroin substrate ranges from at least about 100 nm to about 1 mm, a groove width is as least 125 nm, and a groove thickness depth is at least 100 nm, and wherein the cornea comprises micropores with a spacing of 50 μm to 100 μm.

13. The tissue engineered organ of claim 4 , wherein the average diameter of the micropores is 1 μm to 10 μm.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 9, 2016
From: TUFTS UNIVERSITY BOSTON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040579/0754 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 9, 2015
From: KAPLAN, DAVID L.; OMENETTO, FIORENZO; MARCHANT, JEFFREY K.; PANJWANI, NOORJAHAN; LAWRENCE, BRIAN
To: TRUSTEES OF TUFTS COLLEGE
Reel/Frame 036762/0411 →
Continuity (4)
Division 12528634
Provisional Application 60973023 · Sep 17, 2007
Provisional Application 60903800 · Feb 27, 2007
Related Publication 20160151538A1 · Jun 2, 2016