ARTIFICIAL MICROVASCULAR DEVICE AND METHODS FOR MANUFACTURING AND USING THE SAME

• US 20090234332A1
• Filed: 03/05/2009
• Published: 09/17/2009
• Est. Priority Date: 03/17/2008
• Status: Abandoned Application

• Current Assignee: Charles Stark Draper Laboratory Incorporated
• Original Assignee: Charles Stark Draper Laboratory Incorporated
• Inventors: Borenstein, Jeffrey T., Kim, Ernest S., Keegan, Mark E., Hsiao, James C.
• Application Number:
  US12/398,311
• Publication Number:
  US 20090234332A1
• Time in Patent Office: Days
• US Class Current: 604/891.100
• CPC Class Codes: A61M 37/00 Other apparatus for introducing media into the body for reproduction or fertilisation A61B17/425; apparatus for iontophoresis or cataphoresis A61N1/30; Percutany, i.e. introducing medicines into the body by diffusion through the skin salt baths A61H33/04
• CPC Class Codes: B29C 33/3857 by making impressions of one or more parts of models, e.g. shaped articles and including possible subsequent assembly of the parts
• CPC Class Codes: C12M 23/16 Microfluidic devices; Capillary tubes integrated microfluidic structures B01L3/5027; microreactors B01J19/0093
• CPC Class Codes: C12M 23/40 Manifolds; Distribution pieces fluid transfer means B01L3/563
• CPC Class Codes: C12M 25/02 Membranes; Filters filters or filtration in general B01D24/00-B01D41/00
• CPC Class Codes: C12M 25/06 Plates; Walls; Drawers; Multilayer plates
• CPC Class Codes: C12M 41/40 of pressure
• CPC Class Codes: C12N 2527/00 Culture process characterised by the use of mechanical forces, e.g. strain, vibration
• CPC Class Codes: C12N 5/0691 Vascular smooth muscle cells; 3D culture thereof, e.g. models of blood vessels
• CPC Class Codes: G01N 33/5005 involving human or animal cells immunoassay G01N33/56966; immunoassays of protozoa G01N33/56905; protozoa in screening assays C12Q1/025

Abstract

Artificial microvascular devices may include a polymer scaffold that defines a channel with a distensible wall.

Claims

1. An artificial microvascular device, comprising:

a polymer scaffold defining a first channel therein, said first channel having at least one distensible wall.

2. The device of claim 1 wherein the distensible wall has both a thickness and an elastic modulus associated therewith, the product of the thickness and the elastic modulus being less than about 100 Pascal-meters.

3. The device of claim 2 wherein the product of the thickness and the elastic modulus is less than about 50 Pascal-meters.

4. The device of claim 1 wherein the distensible wall comprises polydimethylsiloxane and has a thickness of less than about 40 micrometers.

5. The device of claim 1 wherein the polymer scaffold is transparent.

6. The device of claim 1 wherein the polymer scaffold comprises a material selected from the group consisting of polystyrene, polyesteramide, polyglycerol sebacate, polydimethylsiloxane, polycarbonate, silk fibroin, polyurethane, polyoctanediol citrate, polydiol citrate, and polycaprolactone.

7. The device of claim 1 wherein the distensible wall comprises an elastomeric polymer.

8. The device of claim 7 wherein the elastomeric polymer comprises a material selected form the group consisting of polyesteramide, polyglycerol sebacate, polydimethylsiloxane, silk fibroin, polyurethane, polyoctanediol citrate, polydiol citrate, and polycaprolactone.

9. The device of claim 1 wherein cells are seeded within the first channel.

10. The device of claim 9 wherein the cells induce distension of the distensible wall.

11. The device of claim 1 wherein the distensible wall forms an outer boundary of the device.

12. The device of claim 1 wherein the distensible wall separates the first channel from a second channel defined by the polymer scaffold, at least part of the second channel being axially parallel to at least part of the first channel.

13. The device of claim 12 wherein the second channel is in pressure balance with an environment within which the device is located.

14. The device of claim 12 wherein the second channel is in fluidic communication with a pressurizing device.

15. The device of claim 12 wherein a difference in pressures in the first and the second channels induces distension of the distensible wall.

16. The device of claim 12 wherein cells are seeded within the second channel.

17. The device of claim 1 wherein the distensible wall is fenestrated.

18. An artificial microvascular device, comprising:

a polymer scaffold defining first and second channels therein, at least part of the first channel being axially parallel to at least part of the second channel, and wherein the first and second channels are separated by a fenestrated wall.

19. The device of claim 18 wherein cells of a first type are seeded in the first channel and cells of a second type are seeded in the second channel.

20. The device of claim 19 wherein the cells of the first type comprise endothelial cells and the cells of the second type comprise vascular cells.

21. The device of claim 20 wherein the vascular cells are selected from the group consisting of smooth muscle cells, pericytes, and fibroblasts.

22. The device of claim 19 wherein the cells of the first type comprise endothelial cells and the cells of the second type are selected from the group consisting of smooth muscle cells, pericytes, fibroblasts, neurons, adipocytes, dermal cells, epithelial cells, skeletal muscle cells, bone cells, and hepatocytes.

23. The device of claim 19 wherein the cells of the first type chemically communicate with the cells of the second type through the fenestrated wall.

24. The device of claim 18 wherein the polymer scaffold defines a third channel that is separated from the first channel by a distensible wall.

25. A method of manufacturing an artificial microvascular device, comprising:

(a) applying a moldable polymer to a master mold that comprises at least one inverse channel;

(b) curing and removing the polymer, thereby creating a stamp having an open channel; and

(c) coupling a polymer sheet to the stamp such as to cover the open side of the channel,

wherein the polymer sheet is sufficiently thin so as to render a channel wall that it forms distensible.

26. The method of claim 25 wherein the master mold comprises a first inverse channel and a second inverse channel substantially parallel thereto, the first channel and the second channel being separated by less than 40 micrometers.

27. The method of claim 25 further comprising repeating steps (a) and (b) to create a second stamp, and coupling the second stamp to the thin polymer sheet such as to cover the open side of the channel contained in the second stamp and such as to align the channel contained in the second stamp with the channel contained in the first stamp.

28. The method of claim 25 further comprising inserting tubing into inlet and outlet holes in fluid communication with the channel.

29. The method of claim 25 further comprising seeding cells in the channel.

30. A method of testing a response of an artificial microvascular device to a mechanical stimulus, the method comprising:

(a) providing an artificial microvascular device comprising a polymer scaffold that defines a first channel therein, said first channel having at least one distensible wall and further having cells plated therein; and

(b) observing a response of the distensible wall to a mechanical stimulus.

31. The method of claim 30 further comprising applying the mechanical stimulus.

32. The method of claim 31 wherein the mechanical stimulus comprises a pressure applied to the distensible wall.

33. The method of claim 32 wherein the pressure is applied through pressurizing a second channel separated from the first channel by the distensible wall.

34. The method of claim 30 wherein the cells provide the mechanical stimulus.

35. The method of claim 30 further comprising integrating the device with an optical apparatus.