Fabrication of vascularized tissue using microfabricated two-dimensional molds

Patent metadata

Field	Value
Publication number	US-9738860-B2
Application number	US-201414153591-A
Country	US
Kind code	B2
Filing date	Jan 13, 2014
Priority date	Apr 28, 2000
Publication date	Aug 22, 2017
Grant date	Aug 22, 2017

Abstract

Methods and materials for making complex, living, vascularized tissues for organ and tissue replacement, especially complex and/or thick, structures, such as liver tissue is provided. Tissue lamina is made in a system comprising an apparatus having (a) a first mold or polymer scaffold, a semi-permeable membrane, and a second mold or polymer scaffold, wherein the semi-permeable membrane is disposed between the first and second molds or polymer scaffolds, wherein the first and second molds or polymer scaffolds have means defining microchannels positioned toward the semi-permeable membrane, wherein the first and second molds or polymer scaffolds are fastened together; and (b) animal cells. Methods for producing complex, three-dimensional tissues or organs from tissue lamina are also provided.

First claim

We claim:

1. A tissue lamina assembly comprising:
a lower mold having an upper side defining lower mold microchannels;
an upper mold having a lower side defining upper mold microchannels that oppose the lower mold microchannels;
a semi-permeable membrane disposed between the lower and upper molds to separate the respective microchannels; and
cells cultured on at least one side of the semi-permeable membrane.

2. A tissue lamina assembly as recited in claim 1 , wherein the lower and upper molds are fastened together.

3. A tissue lamina assembly as recited in claim 1 , wherein each of the first and second molds and the semi-permeable membrane are comprised of material that is suitable for attachment and culturing of animal cells and the cells are animal cells.

4. A tissue lamina assembly as recited in claim 1 , wherein the cells are cultured on both sides of the semi-permeable membrane.

5. A tissue lamina assembly as recited in claim 1 , wherein the lower mold microchannels form an inlet in fluid communication with an outlet through a plurality of branching microchannels.

6. A tissue lamina assembly as recited in claim 5 , further comprising a nutrient supply connected to the inlet and an excretion removal line connected to the outlet.

7. A tissue lamina assembly as recited in claim 5 , further comprising a pump connected to the inlet for circulating fluid through the tissue lamina assembly.

8. A tissue lamina assembly as recited in claim 5 , wherein the upper mold microchannels form a branching pattern identical to a branching pattern in the lower mold.

9. A tissue lamina assembly as recited in claim 5 , wherein the inlet is directly connected to blood vessels of an animal.

10. A tissue lamina assembly as recited in claim 1 , wherein the lower and upper molds are fabricated from a material that is biodegradable.

11. A tissue lamina assembly as recited in claim 1 , wherein the upper mold has an upper side defining upper mold microchannels, and
further comprising: a second upper mold having a lower side defining second upper mold microchannels that oppose the upper mold microchannels of the upper side; and a second semi-permeable membrane disposed between the upper and second upper molds to separate the respective microchannels; and
cells cultured on at least one side of the second semi-permeable membrane.

12. A tissue lamina assembly as recited in claim 11 , wherein the second upper mold has an upper side defining second upper mold microchannels, and
further comprising: a third upper mold having a lower side defining third upper mold microchannels that oppose the second upper mold microchannels of the upper side; and a third semi-permeable membrane disposed between the second and third upper molds to separate the respective microchannels; and
cells cultured on at least one side of the third semi-permeable membrane.

13. A tissue lamina assembly as recited in claim 1 , wherein the lower mold microchannels are open-faced channels and open portions of the lower mold microchannels are adjacent to the semi-permeable membrane.

14. A tissue lamina assembly as recited in claim 1 , wherein the microchannels have a diameter from about 1 um to about 500 um.

15. A tissue lamina assembly as recited in claim 1 , further comprising a second tissue lamina assembly attached to the upper mold, the second tissue lamina assembly including: a third mold having a side defining third mold microchannels; a fourth mold having a side defining fourth mold microchannels that oppose the third mold microchannels; a second semi-permeable membrane disposed between the third and fourth molds to separate the respective microchannels; and cells cultured on at least one side of the semi-permeable membrane.

16. A lamina assembly capable of supplementing or replacing at least one organ function, comprising:
a lower mold having an upper side defining a plurality of branched microchannels;
an upper mold having a lower side defining at least one channel that opposes at least a portion of the branched microchannels; and
a semi-permeable membrane disposed between the branched microchannels and the at least one channel.

17. A lamina assembly as recited in claim 16 , wherein the plurality of branched microchannels have endothelial cells seeded therein and the at least one channel has parenchymal cells therein.

18. A lamina assembly as recited in claim 16 , further comprising cells cultured on at least one side of the semi-permeable membrane, wherein the semi-permeable membrane allows exchange of oxygen, nutrients and waste between fluid circulating in the plurality of branched microchannels and the at least one channel.

19. A lamina assembly as recited in claim 16 , wherein each of the first and second molds and the semi-permeable membrane are comprised of material that is suitable for attachment and culturing of animals cells and the cells are animal cells and the cells are cultured on both sides of the semi-permeable membrane.

20. A lamina assembly as recited in claim 16 , wherein the lower and upper molds are fastened together and the plurality of branched microchannels form at least one inlet in communication with at least one outlet.

Assignees

• Charles Stark Draper Laboratory Inc
• Massachusetts Gen Hospital

Inventors

• Vacanti Joseph P
• Shin Young-Moon M
• Ogilvie Jennifer
• Sevy Alexander
• Maemura Tomoyuki
• Ishii Osamu
• Kaazempur-Mofrad Mohammad R
• Borenstein Jeffrey T
• King Kevin R
• Wang Chiao-Chun
• Weinberg Eli

Classifications

• A61L27/3604 Primary

  characterised by the human or animal origin of the biological material, e.g. hair, fascia, fish scales, silk, shellac, pericardium, pleura, renal tissue, amniotic membrane, parenchymal tissue, fetal tissue, muscle tissue, fat tissue, enamel · CPC title

• C12M25/02

  Membranes; Filters (filters or filtration in general B01D24/00-B01D41/00) · CPC title

• C12N2533/12

  Glass · CPC title

• C12M21/08 Primary

  for producing artificial tissue or for ex-vivo cultivation of tissue (prostheses A61F2/00, grafts A61L27/00) · CPC title

• C12N5/0062

  General methods for three-dimensional culture · CPC title