Apparatus and method for trapping bead based reagents within microfluidic analysis systems
Abstract
An on-chip packed reactor bed design is disclosed that allows for an effective exchange of packing materials such as beads at a miniaturized level. Also disclosed is a method of treating a sample within a microfluidic analysis system, comprising: providing a main channel having a trapping zone; providing a slurry of a reagent treated packing material; inducing a flow of said packing material into said trapping zone through a flow channel connected to said trapping zone to load said trapping zone and form a packed bed of said packing material; and flowing a sample containing analytes through said packed bed, said reagent treating the sample. 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
exact text as granted — not AI-modified1 . 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 slurry of a reagent treated packing material prepared in a solution having a predetermined composition of a solvent; c) inducing a flow of said packing” material into said trapping zone through a flow channel connected to said trapping zone so as to load said trapping zone and form a packed bed of said packing material; d) 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.
2 . The method claimed in claim 1 , further comprising the step of:
e) adjusting the composition of the solvent, so as to affect the aggregation of said packing material and the stabilization of the packed bed.
3 . The method claimed in claim 1 , wherein, step b) comprises providing packing material comprising porous beads.
4 . The method claimed in claim 3 , wherein said porous beads are selected to have a diameter in the range from about 0.7 to about 10.0 μm.
5 . (canceled)
6 . The method claimed in claim 4 , wherein said solvent is acetonitrile, and step e) comprises adjusting the concentration level to less than about 50% to stabilize the packed bed.
7 . (canceled)
8 . The method claimed in claim 6 , further including the steps of adjusting the concentration level to above 50% to destabilize the packed bed, and reversing the flow in step c) so as to unload said trapping zone.
9 . (canceled)
10 . The method claimed in claim 1 , further comprising the steps of:
before step c), adding a neutral surfactant to said packing material so as to inhibit aggregation; and after step c), removing the neutral surfactant to promote aggregation.
11 . The method claimed in claim 1 , further comprising the steps of:
after step c) introducing a polymerizable agent into the flow channel and polymerizing said agent, so as to stabilize the packed bed.
12 . The method claimed in claim 1 , wherein step d) comprises applying a fluid force to induce the flow of said packing material.
13 . The method claimed in claim 1 , wherein said packing material comprises at least some electrically charged particles and step d) comprises applying a voltage potential to induce the flow of said packing material.
14 . (canceled)
15 . (canceled)
16 . A method of trapping bead based reagents within a microfluidic analysis system, comprising the steps of:
a) providing a main channel having a trapping zone suitable for trapping bead based packing material; b) providing a slurry of a reagent treated beads prepared in a solution having a predetermined composition of a solvent; c) inducing a flow of said beads into said, trapping zone through a flow channel connected to said trapping zone so as to load said trapping zone and form a packed bed of said beads; and d) adjusting the composition of the solvent, so as to affect the aggregation of. said packing material and the stabilization of the packed bed.
17 . 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; and 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.
18 . The microfluidic analysis system claimed in claim 17 , further comprising at least one side channel formed into the upper surface of 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.
19 . The microfluidic analysis system claimed in claim 18 , further comprising 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.
20 . The microfluidic analysis system claimed in claim 19 , wherein, each side channel connection to said main channel is provided with a hook structure curved to one side whereby, in use, packing material is sprayed into said chamber to facilitate even packing.
21 .- 28 . (canceled)
29 . A method of packing the chamber in the microfluidic analysis system claimed in claim 19 , said method comprising, providing a nonconductive 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, so that packing material flows from said reservoir into said chamber and is trapped by said first and second weirs.
30 . (canceled)
31 . A method of packing the chamber in the microfluidic analysis system claimed in claim 19 , 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.
32 . The method as claimed in claim 31 , wherein, packing material may be removed from the chamber by reversing said pressure driven flow.
33 . A method of packing the chamber in the microfluidic analysis system claimed in claim 32 , 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.
34 . (canceled)
35 . The method claimed in anyone of claims 25 - 34 , wherein, said packing material comprises porous beads.
36 .- 39 . (canceled)Join the waitlist — get patent alerts
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