Microfluidic cell trap and assay apparatus for high-throughput analysis

Patent metadata

Field	Value
Publication number	US-10508299-B2
Application number	US-201715793681-A
Country	US
Kind code	B2
Filing date	Oct 25, 2017
Priority date	May 27, 2011
Publication date	Dec 17, 2019
Grant date	Dec 17, 2019

Abstract

Microfluidic devices are provided for trapping, isolating, and processing single cells. The microfluidic devices include a cell capture chamber having a cell funnel positioned within the cell capture chamber to direct a cell passing through the cell capture chamber towards one or more a cell traps positioned downstream of the funnel to receive a cell flowing. The devices may further include auxiliary chambers integrated with the cell capture chamber for subsequent processing and assaying of the contents of a captured cell. Methods for cell capture and preparation are also provided that include flowing cells through a chamber, funneling the cells towards a cell trap, capturing a predefined number of the cells within the trap, interrupting the flow of cells, flowing a wash solution through the chamber to remove contaminants from the chamber, and sealing the predefined number of cells in the chamber.

First claim

What is claimed is:

1. A microfluidic device comprising:
a cell capture chamber, the cell capture chamber comprising:
a first inlet for admitting flow of fluid into the cell capture chamber;
at least one mechanical cell funnel; and
a corresponding trap positioned generally downstream from each of the at least one cell funnels, wherein each or a subset of the corresponding cell traps is a mechanical cell trap,

wherein each of the at least one mechanical cell funnels is operable to direct flow of fluid at the corresponding cell trap, and wherein each cell trap is positioned to receive a cell flowing in the fluid downstream from the cell funnel while permitting the fluid and additional cells therein to flow beyond and downstream of the cell trap.

2. The microfluidic device of claim 1 , further comprising an auxiliary chamber, wherein the cell capture chamber comprises an outlet in fluid communication with the auxiliary chamber, wherein the outlet has an open and a closed position, wherein the open position allows for fluid to enter the auxiliary chamber from the cell capture chamber and the closed position prevents fluid flow into the auxiliary chamber from the cell capture chamber.

3. The microfluidic device of claim 1 , wherein each or a subset of the at least one cell funnels comprises two or more nested funnel elements.

4. The microfluidic device of claim 1 , wherein each or a subset of the at least one cell funnels is sized to permit passage of a single cell at a time.

5. The microfluidic device of claim 1 , wherein each or a subset of the corresponding cell traps is sized to receive a single cell.

6. The microfluidic device of claim 1 , further comprising a fluid injection channel in fluid communication with the cell capture chamber through a second inlet, wherein the second inlet has an open and a closed position, wherein the open position allows for fluid to enter the cell capture chamber from the fluid injection channel and in the closed position prevents fluid from flowing into the cell capture chamber from the fluid injection channel.

7. The microfluidic device of claim 1 , further comprising a fluid injection channel in fluid communication with the cell capture chamber through the first inlet.

8. The microfluidic device of claim 1 , further comprising a plurality of auxiliary chambers, wherein the plurality of auxiliary chambers comprises a first auxiliary chamber and a second auxiliary chamber,
wherein the cell capture chamber comprises an outlet in fluid communication with the first auxiliary chamber, wherein the outlet has an open and a closed position, wherein the open position allows for fluid to enter the first auxiliary chamber from the cell capture chamber and the closed position prevents fluid flow into the auxiliary chambers from the cell capture chamber, and
wherein the second auxiliary chamber is in fluid communication with the first auxiliary chamber through a first valve between the first and second auxiliary chambers, wherein the first valve has an open position to allow fluid flow from the first auxiliary chamber to the second auxiliary chamber and a closed position to prevent fluid flow from the first auxiliary chamber to the second auxiliary chamber.

9. The microfluidic device of claim 8 , further comprising a third auxiliary chamber in fluid communication with the second auxiliary chamber and a second valve between the second and third auxiliary chambers, wherein the second valve has an open position to allow fluid flow from the second auxiliary chamber to the third auxiliary chamber and a closed position to prevent fluid flow from the second auxiliary chamber to the third auxiliary chamber.

10. The microfluidic device of claim 1 , further comprising a plurality of auxiliary chambers, wherein the cell capture chamber further comprises a plurality of outlets, wherein each of the plurality of outlets is in fluid communication with a corresponding auxiliary chamber, wherein each outlet has an open and a closed position, wherein the open position allows for fluid to enter the corresponding auxiliary chamber from the cell capture chamber and the closed position prevents fluid flow into the corresponding auxiliary chamber from the cell capture chamber.

11. The microfluidic device of claim 1 , wherein each of the at least one mechanical cell funnels or a subsect thereof comprises a pair of cell deflectors each having a proximal and a distal end, wherein the proximal ends are positioned at opposite sides of the capture chamber, and wherein each distal end of the cell deflector is angled on the diagonal in a downstream direction relative to the proximal ends, whereby the distal ends of the cell deflectors provide an opening sized to permit the passage of a cell between the distal ends of the cell deflectors.

12. The microfluidic device of claim 2 , wherein the auxiliary chamber is expandable.

13. The microfluidic device of claim 8 , wherein one or more of the plurality of auxiliary chambers is expandable.

14. The microfluidic device of claim 8 , wherein the ratio between the second auxiliary chamber and the first auxiliary chamber is 5:1 by volume.

15. The microfluidic device of claim 1 , wherein each cell trap or a subset thereof comprises a perforation for permitting fluid flow through the cell trap.

16. The microfluidic device of claim 12 , wherein the ratio between the expanded auxiliary chamber and unexpanded auxiliary chamber is 5:1 by volume.

17. The microfluidic device of claim 2 , wherein, when the outlet is in the open position, the cell capture chamber and the auxiliary chamber form a compound chamber.

18. The microfluidic device of claim 17 , wherein the ratio between the cell capture chamber and the compound chamber is 1:5 by volume.

19. The microfluidic device of claim 10 , wherein, when the outlets or a subset thereof are in the open position, the cell capture chamber and the auxiliary chambers corresponding to outlets in the open position form a compound chamber.

20. The microfluidic device of claim 17 , wherein the ratio between the cell capture chamber and the compound chamber is 1:5 by volume.

21. The microfluidic device of claim 1 , wherein the cell capture chamber is expandable.

22. The microfluidic device of claim 8 , wherein, when the outlet is in the open position, and optionally the first valve is in the open position, the cell capture chamber and at least one of the plurality of auxiliary chambers form a compound chamber.

Assignees

• Univ British Columbia

Inventors

• Hansen Carl Lars Genghis
• Vanlnsberghe Michael
• White Adam
• Petriv Oleh
• Leaver Tim
• Singhal Anupam
• Bowden William
• Lecault Veronique
• Da Costa Dan
• Wu Leo
• Russell Georgia
• Sikorski Darek

Classifications

• B01L3/502761

  specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads or physically stretching molecules · CPC title

• G01N33/5005 Primary

  involving human or animal cells (immunoassay G01N33/56966; immunoassays of protozoa G01N33/56905; protozoa in screening assays C12Q1/025) · CPC title

• B01L2200/0668

  Trapping microscopic beads · CPC title

• B01L7/52

  with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples · CPC title

• B01L2300/0816

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