Low shear microfluidic devices and methods of use and manufacturing thereof

Patent metadata

Field	Value
Publication number	US-11940441-B2
Application number	US-202017019102-A
Country	US
Kind code	B2
Filing date	Sep 11, 2020
Priority date	Dec 20, 2013
Publication date	Mar 26, 2024
Grant date	Mar 26, 2024

Abstract

Provided herein relates to systems and methods for producing and using a body having a central channel separated by one or more membranes. The membrane(s) are configured to divide the central channel into at least one mesochannel and at least one microchannel. The height of the mesochannel is substantially greater than the height of the microchannel. A gaseous fluid can be applied through the mesochannel while a liquid fluid flowing through the microchannel. The systems and methods described herein can be used for various applications, including, e.g., growth and differentiation of primary cells such as human lung cells, as well as any other cells requiring low shear and/also stratified structures, or simulation of a microenvironment in living tissues and/or organs (to model physiology or disease states, and/or to identify therapeutic agents and/or vaccines). The systems and methods can also permit co-culture with one or more different cell types.

First claim

What is claimed is:

1. A method for culturing cells comprising:
1) providing a microfluidic device comprising:
a. a body comprising a central channel therein; and
b. an at least partially porous membrane positioned within the central channel, the membrane configured to separate the central channel to format at least one microchannel and at least one mesochannel, wherein a height ratio of the at least one mesochannel to the at least one microchannel ranges from 10:1 to about 50:1;

2) seeding human epithelial cells from a patient on said membrane facing the at least one mesochannel; and
3) culturing the seeded human cells from step 2) on said membrane submerged within a first liquid.

2. The method of claim 1 , wherein the method further comprises:
4) removing the first liquid from the at least one mesochannel, such that a gas-liquid interface is established, whereby said human cells are induced to differentiate into pseudostratified epithelial cells.

3. The method of claim 1 , wherein the human epithelial cells are primary cells.

4. The method of claim 1 , wherein the epithelial cells are selected from the group consisting of airway cells, bronchial cells, and nasal epithelial cells.

5. The method of claim 1 , wherein the cells are from a patient with a disease.

6. The method of claim 5 , wherein said disease is selected from the group consisting of asthma, cystic fibrosis, sarcoidosis, and idiopathic lung fibrosis.

7. The method of claim 1 , wherein the at least partially porous membrane is positioned along a plane and is configured to separate the central channel to form a first channel and a second channel, and at least the first channel has a height sufficient to form a stratified structure.

Assignees

• Harvard College

Inventors

• Ingber Donald E
• Hajipouran Benam Kambez
• Villenave Remi
• Hamilton Geraldine A
• Hassell Bryan
• Hinojosa Christopher D
• Lucchesi Carolina

Classifications

• G01N33/5044 Primary

  involving specific cell types · CPC title

• C12M21/08 Primary

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

• C12M23/16

  Microfluidic devices; Capillary tubes (integrated microfluidic structures B01L3/5027; microreactors B01J19/0093) · CPC title

• C12M25/02

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

• C12M35/04

  Mechanical means, e.g. sonic waves, stretching forces, pressure or shear stimuli · CPC title