Microfluidic assay apparatus and methods of use

Patent metadata

Field	Value
Publication number	US-9518977-B2
Application number	US-201314058225-A
Country	US
Kind code	B2
Filing date	Oct 19, 2013
Priority date	Oct 19, 2012
Publication date	Dec 13, 2016
Grant date	Dec 13, 2016

Abstract

Methods and microfluidic apparatus are disclosed for drug prediction. A microfluidic apparatus has (a) a plate, (b) a plurality of wells defined in the plate, (c) a plurality of closed microchannels defined in the plate, and (d) a sample platform defining a plurality of open microchannels, where the plurality of closed microchannels are each in communication with one of the plurality of wells and one of the plurality of open microchannels of the sample platform.

First claim

The invention claimed is:

1. A microfluidic apparatus, comprising:
a plate;
a plurality of wells defined in the plate;
a plurality of closed microchannels defined in the plate, wherein each closed microchannel of the plurality of closed microchannels comprises a first portion and a second portion, wherein the first portion of each closed microchannel is defined at a higher level in the plate than the second portion of each closed microchannel; and
a sample platform defining a plurality of open microchannels, wherein the plurality of closed microchannels are each in communication with one of the plurality of wells and one of the plurality of open microchannels of the sample platform.

2. The microfluidic apparatus of claim 1 , wherein a top surface of the first portion of each closed microchannel is positioned above or even with a top surface of the sample platform.

3. The microfluidic apparatus of claim 1 , wherein a bottom surface of the second portion of each closed microchannel is positioned even with a bottom surface of the plurality of open microchannels.

4. The microfluidic apparatus of claim 1 , wherein the first portion of each closed microchannel is coupled to the plurality of wells and the second portion of each closed microchannel is coupled to the plurality of open microchannels.

5. The microfluidic apparatus of claim 1 , wherein the first portion of each closed microchannel is arranged horizontally within the plate and the second portion of each closed microchannel is arranged vertically within the plate.

6. The microfluidic apparatus of claim 1 , wherein the plurality of open microchannels have a width that ranges from about 10 μm to about 1 mm.

7. The microfluidic apparatus claim 1 , wherein the plurality of open microchannels have a height that ranges from about 10 μm to about 1 mm.

8. The microfluidic apparatus of claim 1 , wherein the plurality of wells comprises 10 to 100 wells.

9. The microfluidic apparatus of claim 1 , wherein the plurality of open microchannels are arranged parallel to one another in a close but spaced apart configuration.

10. A microfluidic apparatus, comprising:
a plate;
a plurality of wells defined in the plate;
a plurality of closed microchannels defined in the plate;
a sample platform defining a plurality of open microchannels, wherein the plurality of closed microchannels are each in communication with one of the plurality of wells and one of the plurality of open microchannels of the sample platform; and
a removable porous membrane disposed on a top surface of the sample platform.

11. The microfluidic apparatus of claim 10 , wherein the membrane comprises vertical pores.

12. The microfluidic apparatus of claim 10 , wherein the membrane has a high porosity ranging from about 50% to about 90%.

13. The microfluidic apparatus of claim 10 , wherein the membrane comprises polyethylene terephthalate or polytetrafluoroethylene, or combinations thereof.

14. The microfluidic apparatus of claim 1 , further comprising an incubator configured to receive the plate.

15. A method for use of the microfluidic apparatus of claim 1 , the method comprising:
providing a first plurality of reagents in a first set of the plurality of open microchannels in the sample platform;
providing a control media in a second set of the plurality of open microchannels in the sample platform;
providing a tissue sample disposed on a porous membrane, wherein the porous membrane is disposed on the sample platform;
providing, via an incubator, humid air in communication with the tissue sample and the porous membrane; and
perfusing the first plurality of reagents in the first set of the plurality of open microchannels and the control media in the second set of the plurality of open microchannels through the porous membrane and into the tissue sample via evaporative pumping.

16. The method of claim 15 , further comprising rotating the membrane on the sample platform and perfusing a second plurality of reagents into the tissue sample.

17. The method of claim 15 , wherein the first set and the second set of the plurality of open microchannels are arranged parallel to each other, wherein each microchannel of the second set of the plurality of open microchannels is arranged in between two microchannels of the first set of the plurality of open microchannels.

18. The method of claim 15 , wherein the method is performed for a period of time ranging from about twenty-four hours to about seventy-two hours.

Assignees

• Univ Washington Through Its Center For Commercialization

Inventors

• Folch Albert
• Monnat Raymond J
• Chang Chi-Ting
• Horowitz Lisa
• Sip Christopher G
• Rostomily Robert C

Classifications

• B01L2300/0867

  Multiple inlets and one sample wells, e.g. mixing, dilution · CPC title

• B01L3/502715

  characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces · CPC title

• B01L2200/027

  for microfluidic devices · CPC title

• B01L2300/0816

  Cards, e.g. flat sample carriers usually with flow in two horizontal directions · CPC title

• B01L2400/0487

  fluid pressure, pneumatics · CPC title