Microfluidic device and method of using same

• US 8,124,032 B2
• Filed: 07/15/2005
• Issued: 02/28/2012
• Est. Priority Date: 07/16/2004
• Status: Expired due to Fees

• Current Assignee: Simon Fraser University
• Original Assignee: Simon Fraser University
• Inventors: Li, Paul Chi Hang, Peng, Xing Yue
• Primary Examiner(s): Sines, Brian J
• Assistant Examiner(s): Wecker, Jennifer
• Application Number:
  US11/572,134
• Publication Number:
  US 20080138848A1
• Time in Patent Office: 2,419 Days
• Field of Search: None
• US Class Current: 422/527
• CPC Class Codes: B01L 2200/0668 Trapping microscopic beads
• CPC Class Codes: B01L 2400/0415 electrical forces, e.g. electrokinetic
• CPC Class Codes: B01L 2400/0487 fluid pressure, pneumatics
• CPC Class Codes: B01L 2400/086 using baffles or other fixed flow obstructions
• CPC Class Codes: B01L 3/502761 specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules investigating characteristics of particles G01N15/00
• CPC Class Codes: C12M 23/16 Microfluidic devices; Capillary tubes integrated microfluidic structures B01L3/5027; microreactors B01J19/0093
• CPC Class Codes: G01N 1/40 Concentrating samples

Abstract

The invention relates to a microfluidic device comprising one or more fluid channels, one or more fluid ports, and a V-shaped particle retention structure. The fluid channel is generally opposite the particle retention structure, fluid ports are located between the fluid channel and the particle retention structure, and the particle retention structure has sloped side walls. Fluid, including reagents, can be delivered to the microfluidic device through the one or more fluid channels or the fluid ports. The invention also relates to methods of using the microfluidic device to monitor, observe, measure, or record a biological parameter of a particle, to separate a single particle from a group of particles, to culture a cell, to treat a particle, and to move a particle back and forth in the device.

Claims

1. A microfluidic device comprising:

a. at least one first channel for introducing a first fluid into the device;

b. a particle retention structure spaced-apart from the first channel for retaining a particle therein, wherein said particle retention structure is generally V-shaped in a top plan view, the particle retention structure having opposed wall portions and a central wall portion disposed between and joining the opposed wall portions, wherein the particle retention structure is located generally opposite the first channel, and wherein the opposed and central wall portions have sloped side walls extending from an upper portion thereof to a lower portion of said microfluidic device; and

c. one or more fluid ports disposed between the first channel and the particle retention structure for introducing a second fluid into the microfluidic device, and for allowing one or more of the first and second fluids to flow out of the microfluidic device.

2. A microfluidic device according to claim 1, wherein the sloped side walls are inclined downwardly.

3. A microfluidic device according to claim 1, wherein the sloped side walls are curved.

4. A microfluidic device according to claim 3, wherein the sloped side walls are arcuately curved.

5. A microfluidic device according to claim 4, wherein said arcuately curved side walls have an arc with a radius of curvature which is two or more times the width of the particle to be retained in the microfluidic device.

6. A microfluidic device according to claim 1, wherein the first channel has a width greater than the width of the particle to be retained in the microfluidic device.

7. A microfluidic device according to claim 1, wherein the central wall portion has a width 2 or more times the width of the particle to be retained in the microfluidic device.

8. A microfluidic device according to claim 1, wherein the particle retention structure has a height 2 or more times the width of the particle to be retained in the microfluidic device.

9. A microfluidic device according to claim 1, wherein the width of the one or more fluid ports is 2 or more times the width of the particle to be retained in the microfluidic device.

10. A microfluidic device according to claim 9, wherein the width of the one or more fluid ports is 4 times the width of the particle to be retained in the microfluidic device.

11. A microfluidic device according to claim 1, wherein the opposed wall portions are angled between 0°

and 180°

relative to lateral end portions of the particle retention structure.

12. A microfluidic device according to claim 11, wherein the opposed wall portions are angled 135°

relative to the lateral end portions of the particle retention structure.

13. A microfluidic device according to claim 1, wherein a first fluid is delivered through the first channel, and the first fluid forms a zero speed point against the particle retention structure.

14. A microfluidic device according to claim 13, wherein the zero speed point is laterally shifted by an increase in delivery of the second fluid from one of the one or more fluid ports.

15. A microfluidic device according to claim 13, wherein the zero speed point is laterally shifted by an increase in electric potential or fluid potential in one of the one or more fluid ports.

16. A microfluidic device according to claim 1 further comprising a detection window for detecting a particle retained in the particle retention structure.

17. A microfluidic device according to claim 16, wherein the detection window is located proximate the central wall portion.

18. A microfluidic device according to claim 1, wherein the central wall portion comprises one or more grooves.

19. A microfluidic device according to claim 1, wherein the device comprises two or more particle retention structures.

20. A microfluidic device according to claim 1, wherein the device comprises two or more first channels.

21. A microfluidic device according to claim 1, wherein the device comprises two or more fluid ports located on opposite lateral sides of the particle retention structure.

23. A method of monitoring, observing, measuring, or recording a biological parameter of a particle comprising:

introducing a particle into a microfluidic device according to claim 1; and

monitoring, observing, measuring, or recording a biological parameter of the particle in the microfluidic device.

24. A method according to claim 23, wherein the biological parameter is monitored, observed, measured, or recorded through a detection window in the microfluidic device.

25. A method according to claim 23 further comprising measuring the background levels of the parameter to be monitored, observed, measured, or recorded and subtracting the background levels from the levels of the parameter being monitored, observed, measured, or recorded.

26. A method according to claim 25, wherein measuring the background levels of the parameter comprises adjusting the background levels for photobleaching.

27. A method according to claim 12, wherein the biological parameter is selected from a group consisting of size, morphology, growth rate, biomarkers, influx of a substance, efflux of a substance, reaction of the particle to one or more stimuli, and reaction of the particle to changes in environment of the particle.

28. A method according to claim 27, wherein the substance that is influxed or effluxed is selected from the group consisting of a coloured substance, a chromogenic substance, a fluorescent substance, a fluorescent-labelled substance, and a radio-labeled substance.

29. A method according to claim 23, wherein monitoring, observing, measuring, or recording a biological parameter of the particle comprises measuring a level of fluorescence, colour, or radiation.

30. A method according to claim 23, wherein kinetic or thermodynamic parameters are mathematically extracted from the biological parameter of the particle.

31. A method according to claim 23, wherein the biological parameter is monitored, observed, measured, or recorded through a detection window in the microfluidic device in real-time and over extended periods of time.

32. A method of culturing a cell comprising:

introducing a cell into a microfluidic device according to claim 1;

providing the cell in the microfluidic device with a suitable cell culture fluid; and

growing the cell in the microfluidic device,

wherein the cell culture fluid is continuously delivered into the microfluidic device to form a zero speed point, and the cell is retained in the zero speed point.

33. A method of treating a particle with a fluid comprising:

introducing a particle into a microfluidic device according to claim 1,

delivering a fluid comprising a compound into the microfluidic device; and

allowing the compound in the fluid to react with, or be adsorbed on, or be absorbed into the particle.

34. A method according to claim 23, wherein the particle is selected from the group consisting of cells, beads, viral particles, proteins, protein crystals, and nanoparticles.

35. A method according to claim 23, wherein the particle is a yeast cell.

36. A method of separating a particle from a group of particles comprising injecting the group of particles into a microfluidic device according to claim 1, continuously injecting fluid into the microfluidic device through the first channel to form a zero speed point, and retaining only one particle in the zero speed point, and allowing other particles in the group of particles to move away from the zero speed point.

37. A method of moving a particle comprising:

introducing a particle into a microfluidic device according to claim 1;

subjecting the particle in the microfluidic device to a fluid flow comprising a first fluid from the first channel and a second fluid from the one or more fluid ports;

isolating the particle in a zero speed point; and

moving the zero speed point in the microfluidic device by increasing delivery of the second fluid from one of the one or more fluid ports.

38. A method according to claim 23, wherein the particle is a cell.

39. A method according to claim 26, wherein adjusting the background levels for photobleaching comprises adjusting decreased fluorescent levels caused by photobleaching.

22. A microfluidic device comprising:

a. one or more first channels for introducing a first fluid into the device;

b. a particle retention structure spaced-apart from the first channel for retaining a particle therein, wherein said particle retention structure is generally V-shaped in a top plan view, the particle retention structure having opposed wall portions and a central wall portion disposed between and joining the opposed wall portions, wherein the particle retention structure is located generally opposite the first channel, and wherein the opposed and central wall portions have sloped side walls extending from an upper portion thereof to a lower portion of said microfluidic device; and

c. fluid ports disposed between the first channel and the particle retention structure for introducing a second fluid into the microfluidic device, and for allowing one or more of the first and second fluids to flow out of the microfluidic device.