Method and apparatus for maintaining multiple planar fluid flows

• US 7,314,718 B1
• Filed: 04/03/2002
• Issued: 01/01/2008
• Est. Priority Date: 04/03/2001
• Status: Active Grant

• Current Assignee: Texas Tech University System
• Original Assignee: BioArray Solutions Limited (Werfen SA)
• Inventors: Dasgupta, Purnendu Kumar, Surowiec, Kazimierz, Berg, Jordan Mitchell
• Primary Examiner(s): Lam; Ann Y
• Application Number:
  US10/115,417
• Time in Patent Office: 2,099 Days
• Field of Search: 435/4, 435/7.1, 435 5- 75, 435/7.8, 435 791- 795, 422 55- 63, 422 681- 73, 436514-519, 436/523
• US Class Current: 435/7.1
• CPC Class Codes: B01L 2200/0636 Focussing flows, e.g. to laminate flows
• CPC Class Codes: B01L 2200/16 Reagents, handling or storing thereof
• CPC Class Codes: B01L 2300/0645 Electrodes
• CPC Class Codes: B01L 2300/0874 Three dimensional network
• CPC Class Codes: B01L 2300/089 Virtual walls for guiding liquids
• CPC Class Codes: B01L 2400/0415 electrical forces, e.g. electrokinetic
• CPC Class Codes: B01L 2400/0487 fluid pressure, pneumatics
• CPC Class Codes: B01L 3/5025 for parallel transport of multiple samples
• CPC Class Codes: B01L 3/502776 specially adapted for focusing or laminating flows
• CPC Class Codes: G01N 33/54366 Apparatus specially adapted for solid-phase testing

Abstract

The present invention provides a method of performing analyses and assays involving multiple interactions of reagent-containing fluid flows with liquid and solid target substances. The methods of the invention allow the simultaneous manipulation of different fluids on a small planar surface. The invention also provides a flow cell and method of use thereof for analyzing fluid-fluid and fluid-solid interactions in a substantially planar system. The flow cell contains at least one chamber and a plurality of inlets thereto allowing the introduction of a plurality of fluids in fluidic contact. The cell depth is the smallest dimension of the flow cell, and is of a magnitude, from about 50 to about 1000 microns such that any mixing of adjacent fluids in the chamber is substantially limited to mixing by passive diffusion. Interactions between reagents in fluids and target substances maintained in the fluid cell, or interactions between diffusion-mixed reagents in adjacent fluids, may be analyzed by standard analysis methods.

Claims

1. A method for analyzing interactions between reagents and target substances, comprising:

(a) providing at least three primary fluid flows in substantially the same plane, said primary fluid flows all being adjacent simultaneous substantially parallel fluid flows, wherein said primary fluid flows are contained in a chamber having at least one internal cross-sectional dimension of less than 1000 microns, and wherein at least one of said primary fluid flows comprises a target substance and is flanked on each side by a primary fluid flow, and wherein the primary fluid flows flanking said target-comprising primary fluid flow comprise, respectively, a first reagent and a second reagent capable of reacting with the target substance;

(b) providing one or more secondary fluid flows, said secondary fluid flow(s) located in a plane that is substantially orthogonal to the plane of said primary fluid flows, wherein each of said secondary fluid flows is introduced into one of said primary fluid flows comprising a target substance, and wherein at least one secondary fluid flow comprises a third reagent capable of reacting with the target substance; and

(c) monitoring reactions between reagents and target substances.

2. The method of claim 1, wherein at least one primary fluid flow comprising a target substance is contacted with one or more of said primary fluid flows comprising a reagent (a) prior to providing said one or more secondary fluid flows, (b) after providing said one or more secondary fluid flows, or (c) before and after providing said one or more secondary fluid flows.

3. The method of claim 1, wherein the target substance is selected from the group consisting of cells;

isolated cell fractions;

beads displaying on their surfaces chemical functional groups, biological molecules, or cells; and

combinations thereof.

4. The method of claim 1 wherein the target substance is monitored before and after contact with the first reagent, the second reagent or the third reagent.

5. The method of claim 1 wherein said primary fluid flow comprising a target substance is contacted with said first and second reagents, said primary fluid flows having flow rates tuned to provide contact between said target substance and said first and second reagents in a flow zone containing only target substance and said first reagent, a flow zone containing only said target substance and said second reagent, and a flow zone containing said target substance and said first and second reagents wherein interactions at each of the flow zones are monitored.

6. The method of claim 1, wherein a cell culture comprising motile cells is contacted with two or more of said primary fluid flows and analysis is performed on movement of said motile cells between said fluid flows.

7. The method of claim 1, wherein flow rates of one or more of any of the fluid flows are varied so as to vary at least one of (i) the reaction time of the reagent with the target substance or (ii) the amount of diffusion-based intermixing occurring between adjacent fluid flows.

8. The method of claim 1 wherein two or more of said primary fluid flows contain different reagents and contact the same target substance.

9. The method of claim 1 wherein said secondary fluid flows are either constant or pulsatile, such that pulsatile fluid flows result in mechanical intermixing of said secondary fluid flows and said primary fluid flows.

10. The method of claim 1 wherein interactions are monitored through spectrophotometry, electrochemistry or microscopy.

11. The method of claim 1 wherein one or more of said fluid flows are driven by mechanical pumping, gravity, pneumatic pressure, electrostatic force, or a combination thereof.

12. The method of claim 1 wherein the target substance(s) are chosen from the group consisting of peptides, polypeptides, antigens, antibodies, oligonucleotides, polynucleotides, carbohydrates and polysaccharides.

13. The method of claim 1 wherein the spatial relationship of the fluid flows is determined by a pattern of inlets and outlets from the chamber.

14. The method of claim 13 wherein, relative to the fluid flow direction, the inlets are offset from the outlets.

15. The method of claim 13 wherein the inlets are located at substantially the center of the chamber and the primary fluid flows radially outward from the center.

16. The method of claim 1 wherein the spatial relationship of the fluid flows is determined by the relative velocities of the fluid flows.

17. The method of claim 1 wherein the spatial relationship of the fluid flows is determined by electrodes which attract electrolytes in the fluids.

18. The method of claim 1 wherein all of said secondary fluid flows comprise different reagents.

19. The method of claim 1 wherein said one or more secondary fluid flows are introduced into the chamber at its smallest dimension.

20. A method for analyzing interactions between reagents and target substances, comprising:

(a) providing three or more adjacent simultaneous substantially parallel fluid flows in substantially the same plane, wherein said three or more adjacent simultaneous fluid flows are contained in a chamber having at least one internal cross-sectional dimension of less than 1000 microns, at least one of said fluid flows comprising a reagent capable of reacting with a target substance and at least one other of said fluid flows comprising a target substance;

(b) adjusting one or more of flow rate, length of the flow path, and internal cross-sectional dimension to thereby control the desired quantity and rate of intermixing by passive diffusion such that said intermixing by passive diffusion creates three flow zones in any middle flow that is between two other adjacent simultaneous flanking fluid flows, a first flow zone containing the middle fluid flow and only one of said flanking fluid flows, a second flow zone containing the middle fluid flow and only the other of said flanking fluid flows, and third flow zone containing the middle fluid flow and both of said flanking fluid flows; and

(c) monitoring reactions between reagents and target substances at each of the flow zones.

21. A method for analyzing interactions between reagents and target substances, comprising:

(a) providing two or more primary fluid flows in substantially the same plane, said primary fluid flows being adjacent simultaneous substantially parallel fluid flows, wherein said two or more primary fluid flows are contained in a chamber having at least one internal cross-sectional dimension of less than 1000 microns, said chamber having a pair of ports that are capable of providing a secondary fluid flow in a direction nonparallel to that of said adjacent simultaneous fluid flows to thereby induce intermixing of said primary fluid flows, said ports being located on substantially opposite sides of said chamber, and wherein at least one of said primary fluid flows comprises a reagent capable of reacting with a target substance and at least one other of said primary fluid flows comprises the target substance;

(b) contacting with a target substance one or more of said primary fluid flows comprising a reagent; and

(c) monitoring reactions between reagents and target substances.

22. A method for analyzing interactions between reagents and target substances comprising:

(a) providing two or more adjacent simultaneous fluid flows in substantially a single plane wherein said two or more adjacent simultaneous fluid flows are contained in a chamber having at least one internal cross-sectional dimension of less than 1000 microns, said chamber having at least one electrically grounded fluid inlet and a plurality of ports located substantially at the perimeter of the chamber, wherein said ports independently function as either fluid inlets or fluid outlets, wherein there is one fluid inlet for each of said adjacent simultaneous fluid flows and at least one fluid outlet, said chamber additionally having one or more electrodes around its perimeter such that the applying voltage to said electrodes will result in electrophoretically driven fluid flow, and wherein at least one of said fluid flows comprises a reagent;

(b) contacting one or more of said adjacent simultaneous fluid flows with a target substance; and

(c) monitoring reactions between reagents and target substances.

23. The method of claim 22 wherein said secondary fluid flow is a pulsating fluid flow.

24. The method of claim 22 wherein said inlets and outlets are substantially orthogonal to the substantially single same plane of said adjacent simultaneous fluid flows of step (a).

25. The method of claim 22 wherein said chamber additionally has one or more ports located substantially at the center of the chamber and extending substantially orthogonally to the internal cross-sectional dimension of less than 1000 microns and wherein a single electrode is connected around the perimeter of the chamber and to said ports, said fluid outlets having counter electrodes along the edges thereof.

26. The method or claim 22 wherein a plurality of independent electrodes not connected to one another are placed around the perimeter of the chamber.

27. The method of claim 26 wherein a different voltage is applied to different electrodes.

28. The method of claim 22 wherein one port is a grounded fluid inlet, one port is a positively charged fluid outlet, and one port is a negatively charged fluid outlet.

29. The method of claim 28 wherein at least one fluid flow comprises a mixture of at least one positively charged species and one negatively charged species.