Apparatus and method for trapping bead based reagents within microfluidic analysis systems

• US 6,432,290 B1
• Filed: 11/26/1999
• Issued: 08/13/2002
• Est. Priority Date: 11/26/1999
• Status: Expired due to Term

• Current Assignee: The Governors of the University of Alberta (University of Alberta)
• Original Assignee: The Governors of the University of Alberta (University of Alberta)
• Inventors: Oleschuk, Richard, Shultz-Lockyear, Loranelle, Skinner, Cameron, Harrison, D. Jed, Li, Paul
• Primary Examiner(s): Tung, T.
• Assistant Examiner(s): NOGUEROLA, ALEXANDER STEPHAN
• Application Number:
  US09/450,272
• Time in Patent Office: 991 Days
• Field of Search: 204/450, 204/451, 204/455, 204/453, 204/600, 204/601, 204/604, 204/605, 210/656, 210/661, 422/70, 422/90, 422/100, 422/68.1
• US Class Current: 204/453
• CPC Class Codes: B01L 2200/0668 Trapping microscopic beads
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2300/087 Multiple sequential chambers
• CPC Class Codes: B01L 2400/0415 electrical forces, e.g. electrokinetic
• CPC Class Codes: B01L 2400/0487 fluid pressure, pneumatics
• CPC Class Codes: B01L 3/0241 Drop counters; Drop formers making arrays for combinatorial libraries B01J19/0046; automation of dispensing for analysis G01N35/10
• CPC Class Codes: B01L 3/5027 by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip B01L3/5023 takes precedence; micromixers B01F33/30; microreactors for synthesis B01J19/0093; microcapillary devices in general B81B1/00
• CPC Class Codes: B01L 3/502753 characterised by bulk separation arrangements on lab-on-a-chip devices, e.g. for filtration or centrifugation separation in general B01D; microapparatus for analysis using electrophoresis G01N27/44791; sample preparation G01N1/28
• CPC Class Codes: G01N 2030/009 Extraction
• CPC Class Codes: G01N 2030/285 electrically driven carrier
• CPC Class Codes: G01N 2030/565 slurry packing
• CPC Class Codes: G01N 27/44704 Details; Accessories
• CPC Class Codes: G01N 27/44791 Microapparatus sample containers with integrated microfluidic structures B01L3/5027
• CPC Class Codes: G01N 30/56 Packing methods or coating methods
• CPC Class Codes: G01N 30/6095 Micromachined or nanomachined, e.g. micro- or nanosize

Abstract

The present invention provides an on-chip packed reactor bed design that allows for an effective exchange of packing materials such as beads at a miniaturized level. The present invention extends the function of microfluidic analysis systems to new applications including on-chip solid phase extraction (SPE) and on-chip capillary electrochromatography (CEC). The design can be further extended to include integrated packed bed immuno- or enzyme reactors.

Claims

1. A microfluidic analysis system, comprising:

(a) a substantially planar substrate having an upper surface;

(b) at least one main channel formed into said upper surface, said main channel having first and second ends and a defined direction of flow in use;

(c) a cover plate arranged over said planar substrate, said cover plate closing off said channel from above;

(d) a first weir formed across said main channel and between said first and second ends of said channel, said first weir providing at least one flow gap to allow, in use, at least some fluid to flow past said first weir while trapping packing material having constituent particles that are generally larger than said flow gap; and

(e) a second weir located upstream from said connected first end of said side channel, said first and second weirs forming a chamber therebetween, said second weir providing at least one flow gap to allow, in use, at least some fluid to flow past said second weir while trapping said packing material within said chamber.

2. The microfluidic analysis system claimed in claim 1, further comprising at least one side channel formed into said planar substrate, said side channel being connected at a first end to said main channel at a location upstream from said first weir, and at a second end to a reservoir, said side channel providing a higher flow resistance than said main channel.

3. The microfluidic analysis system claimed in claim 2, wherein, each side channel connection to said main channel is provided with a hook structure whereby, in use, packing material is sprayed into said chamber to facilitate even packing.

4. The microfluidic analysis system claimed in claim 3, wherein, said hook structure at least partially obstructs direct line-of-sight entry of packing material from said side channel into said chamber and forms a chamber mouth to one side of said hook structure.

5. The microfluidic analysis system claimed in claim 1, wherein, said flow gaps comprise a generally uniform gap between said cover plate and the top of said weirs.

6. The microfluidic analysis system claimed in claim 1, wherein, said flow gaps comprise a plurality of substantially vertical gaps in said weirs.

7. The microfluidic analysis system claimed in any previous claim, wherein, said system is formed entirely on a single microfluidic chip.

8. A method of creating a packed reactor bed in the microfluidic analysis system claimed in claim 2, said method comprising, effecting a pressure driven flow by providing a relatively high pressure at said second end of said main channel and at said reservoir, said reservoir containing packing material, and providing a relatively low pressure at said first end of said main channel, whereby, packing material flows from said reservoir into said main channel and is trapped against said first weir.

9. The method as claimed in claim 8, wherein, packing material is removed from the said main channel by providing relatively high pressure at said first and second ends of said main channel while providing relatively low pressure at said reservoir.

10. A method of packing the chamber in the microfluidic analysis system claimed in claim 2, said method comprising, providing a non-conductive substrate and effecting an electrokinetic flow by applying a relatively high voltage at said reservoir, said reservoir containing packing material, and providing relatively low voltages at said first and second ends of said main channel, whereby, packing material flows from said reservoir into said chamber and is trapped by said first and second weirs.

11. The method as claimed in claim 10, wherein, packing material may be removed from the chamber by reversing said electrokinetic flow.

12. A method of packing the chamber in the microfluidic analysis system claimed in claim 2, said method comprising, effecting a pressure driven flow by providing a relatively high pressure at said reservoir, said reservoir containing packing material, and providing relatively low pressure at said first and second main reservoirs, whereby, packing material flows from said packing material reservoir into said chamber and is trapped by said first and second weirs.

13. The method as claimed in claim 12, wherein, packing material may be removed from the chamber by reversing said pressure driven flow.

14. A method of packing the chamber in the microfluidic analysis system claimed in claim 13, said method comprising, providing magnetically charged packing material, and effecting a magnetically driven flow by providing a magnetically attractive force in the chamber, whereby, the packing material enters the chamber and is trapped by said first and second weirs.

15. The method as claimed in claim 14, wherein, packing material may be removed from the chamber by reversing said magnetic force in said chamber.

16. A method of creating a packed reactor bed in a microfluidic analysis system comprising:

(a) a substantially planar substrate having an upper surface;

(b) at least one main channel formed into said upper surface, said main channel having first and second ends and a defined direction of flow in use;

(c) a cover plate arranged over said planar substrate, said cover plate closing off said channel from above;

(d) a first weir formed across said main channel and between said first and second ends of said channel, said first weir providing at least one flow gap to allow, in use, at least some fluid to flow past said first weir while trapping packing material having constituent particles that are generally larger than said flow gap; and

(e) at least one side channel formed into said planar substrate, said side channel being connected at a first end to said main channel at a location upstream from said first weir, and at a second end to a reservoir, said side channel providing a higher flow resistance than said main channel,

said method comprising, providing a non-conductive substrate and effecting an electrokinetic flow by applying a relatively high voltage at said second end of said main channel and at said reservoir, said reservoir containing packing material, and providing a relatively low voltage at said first end of said main channel, whereby, packing material flows from said reservoir into said main channel and is trapped against said first weir.

17. The method as claimed in claim 16, wherein, packing material is removed from said main channel by providing a relatively high voltage at said first and second ends of said main channel while providing a relatively low voltage at said reservoir.

18. A method of treating a sample within a microfluidic analysis system, comprising the steps of:

(a) providing a main channel having a trapping zone suitable for trapping packing material;

(b) providing a first weir positioned at a first end of said trapping zone, wherein said first weir has at least one flow gap to allow, in use, at least some fluid to flow past said first weir while trapping said packing material within said zone;

(c) providing a second weir positioned at a second end of said trapping zone, wherein said second weir has at least one flow gap to allow, in use, at least some fluid to flow past said second weir while trapping said packing material within said zone;

(d) providing a slurry of a reagent treated packing material prepared in a solution having a predetermined composition of a solvent;

(e) providing a flow channel having a first end connected to said trapping zone, wherein said first end is positioned between said first weir and said second weir;

(f) inducing a flow of said packing material into said trapping zone through said flow channel so as to load said trapping zone and form a packed bed of said packing material; and

(g) flowing a sample containing analytes through said packed bed, said reagent treating the sample, whereby the sample leaving the trapping zone has an altered analyte composition.

19. The method claimed in claim 18, further comprising the step of:

(h) adjusting the composition of the solvent, so as to affect the aggregation of said packing material and the stabilization of the packed bed.

20. The method claimed in claim 18 wherein, step (d) comprises providing packing material comprising porous beads.

21. The method claimed in claim 20, wherein said porous beads are selected to have a diameter in the range from about 0.7 to about 10.0 μ

m.

22. The method claimed in claim 21, wherein said solvent is acetonitrile, and step (h) comprises adjusting the concentration level to less than about 50% to stabilize the packed bed.

23. The method claimed in claim 22 further including the steps of adjusting the concentration level to above 50% to destabilize the packed bed, and reversing the flow in step (f) so as to unload said trapping zone.

24. The method claimed in claim 23, further including the step of repeating step (f) so as to reload said trapping zone, and readjusting the concentration level to restabilize the packed bed.

25. The method claimed in claim 21, wherein said solvent is acetonitrile, and step (h) comprises adjusting the concentration level to less than about 30% to stabilize the packed bed.

26. The method claimed in claim 20, wherein said porous beads are selected to have a diameter in the range from about 1.5 to about 4.0 μ

m.

27. The method claimed in claim 18, further comprising the steps of:

before step (f), adding a neutral surfactant to said packing material so as to inhibit aggregation; and

after step (f), removing the neutral surfactant to promote aggregation.

28. The method claimed in claim 18, wherein step (f) comprises applying a fluid force to induce the flow of said packing material.

29. The method claimed in claim 18, wherein said packing material comprises at least some electrically charged particles and step (f) comprises applying a voltage potential to induce the flow of said packing material.

30. The method claimed in claim 18, wherein said packing material comprises at least some particles susceptible to a magnetic field and step (f) comprises applying a magnetic field to induce the flow of said packing material.

31. The method claimed in any one of claims 18, 19, 20, 21, 2623, 24, 27, 28, 29 and 30, including the step of providing a hook structure at the connection point between said flow channel and said trapping zone, so as to prevent direct line-of-sight entry of said packing material, thereby to promote even packing.