Fluid handling methods for use in mesoscale analytical devices

• US 5,635,358 A
• Filed: 02/14/1994
• Issued: 06/03/1997
• Est. Priority Date: 05/01/1992
• Status: Expired due to Term

• Current Assignee: Trustees Of The University Of Pennsylvania (University of Pennsylvania)
• Original Assignee: Trustees Of The University Of Pennsylvania (University of Pennsylvania)
• Inventors: Kricka, Larry J., Wilding, Peter, Zemel, Jay N.
• Primary Examiner(s): Chin, Christopher L.
• Application Number:
  US08/196,021
• Time in Patent Office: 1,205 Days
• Field of Search: 422/55, 422/58, 422/61, 422/101, 435/7.2, 435/7.21, 435/259, 435/287, 435/291, 435/810, 435/287.1, 435/287.2, 435/288.2, 435/288.4, 435/288.5, 435/288.7, 436/164, 436/165, 436/514, 436/518, 436/524, 436/527, 436/805-807, 436/809, 436/824
• US Class Current: 435/7.2
• CPC Class Codes: B01F 25/41 Mixers of the fractal type
• CPC Class Codes: B01F 35/7182 with means for feeding the material with a fractal or tree-type distribution in a surface
• CPC Class Codes: B01J 19/0093 Microreactors, e.g. miniaturised or microfabricated reactors laboratory containers with capillary fluid transport in microfabricated channels or chambers B01L3/5027
• CPC Class Codes: B01J 2219/0059 Sequential processes
• CPC Class Codes: B01J 2219/00722 Nucleotides
• CPC Class Codes: B01L 2300/0645 Electrodes
• CPC Class Codes: B01L 2300/0681 Filter
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2400/0406 capillary forces
• CPC Class Codes: B01L 2400/0487 fluid pressure, pneumatics
• 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: B01L 9/527 for microfluidic devices, e.g. used for lab-on-a-chip
• CPC Class Codes: C40B 40/06 Libraries containing nucleotides or polynucleotides, or derivatives thereof
• CPC Class Codes: Y10S 366/03 Micromixers: variable geometry from the pathway influences mixing/agitation of non-laminar fluid flow
• CPC Class Codes: Y10S 435/81 Packaged device or kit
• CPC Class Codes: Y10S 436/805 Optical property
• CPC Class Codes: Y10S 436/806 Electrical property or magnetic property
• CPC Class Codes: Y10S 436/807 Apparatus included in process claim, e.g. physical support structures
• CPC Class Codes: Y10S 436/809 Multifield plates or multicontainer arrays
• CPC Class Codes: Y10S 436/824 Immunological separation techniques

Abstract

Disclosed are devices and methods for analyzing a fluid cell containing sample. The devices are composed of a solid substrate, microfabricated to define at least one sample inlet port and a mesoscale flow system. The mesoscale flow system includes a sample flow channel, extending from the inlet port, and a cell handling region for treating cells disposed in fluid communication with the flow channel. The devices may further include a component for inducing flow of cells in the sample through the flow system. In one embodiment, the cell-handling region may include a cell lysis component to enable the lysis of cells in the sample, prior to, e.g., the detection of an intracellular component in the cell sample. In another embodiment, the cell handling region may have a cell capture region, with binding sites which reversibly bind to a specific population of cells in the cell sample, to permit the isolation of the specific cell population from the sample. The devices can be utilized in a wide range of automated sensitive and rapid tests for the analysis of a fluid cell containing sample.

Claims

1. A method of separating a target subpopulation of cells in a cell-containing liquid sample comprising the steps of:

(A) providing a mesoscale sample flow passage comprising a solid wall having immobilized thereon a binding protein specific for a cell membrane-bound protein characteristic of said target population;

(B) passing a cell-containing liquid sample through said passage under conditions to permit capture of members of the cell target subpopulation by reversible cell surface protein-immobilized protein binding, while permitting other cells to pass therethrough; and

(C) changing the conditions in said flow passage to release said target subpopulation of cells.

2. The method of claim 1 wherein said conditions to permit capture comprise a flow rate of fluid in said flow passage that permits said capture and wherein said flow rate is increased in step C to shear cells off said solid wall.

3. The method of claim 1 wherein step C is conducted by introducing a solvent in said flow channel which desorbs said cells from said solid wall.

4. A method for detecting an analyte in a fluid, cell-containing sample, the method comprising the steps of:

(i) providing a device comprising;

a solid substrate microfabricated to define;

a sample inlet port; and

a mesoscale flow system comprising;

a sample flow channel extending from said inlet port; and

a cell handling region for treating cells disposed in fluid communication with said flow channel, said cell handling region comprising a cell lysing structure; and

means for detecting an analyte in a fluid sample in said flow system;

(ii) delivering a cell-containing fluid sample to the inlet port and through the flow system to the cell lysing structure in the cell handling region thereby to lyse cells in the sample producing a lysed cell sample; and

(iii) detecting an analyte in the fluid sample in the flow system with the detection means.

5. The method of claim 4 wherein the device, provided in step (i), further comprises means for inducing flow of cells in a sample through the mesoscale flow channel and the cell handling region to force cells in the sample into contact with the cell lysing structure, thereby to lyse cells in the sample;

and

wherein step (ii) comprises delivering a cell-containing fluid sample to the inlet port and through the flow system to the cell lysing structure in the cell handling region with the flow inducing means.

6. The method of claim 4 wherein the cell lysing structure, in the device provided in step (i), comprises a portion of a flow channel having cell membrane piercing protrusions extending from a wall thereof;

and

wherein step (ii) comprises delivering the cell-containing fluid sample to the cell membrane piercing protrusions in the cell lysing structure, thereby to lyse cells in the sample.

7. The method of claim 4 wherein the cell lysing structure, in the device provided in step (i), comprises sharp edged particles trapped within the cell handling region;

and

wherein step (ii) comprises delivering the cell-containing fluid sample to the sharp edged particles in the cell handling region, thereby to lyse cells in the sample.

8. The method of claim 4 wherein the cell lysing structure, in the device provided in step (i), comprises a region of restricted cross-sectional dimension sufficient to permit passage of intracellular molecules while prohibiting passage of cells;

and

wherein step (ii) comprises delivering the cell-containing fluid sample to the region of restricted cross-sectional dimension, thereby to lyse cells in the sample.

9. The method of claim 4 wherein step (iii) comprises detecting the presence of an intracellular molecular component of a cell in the sample.

10. The method of claim 4, further comprising, prior to step (iii), the step of collecting insoluble cellular debris in the lysed cell sample obtained in step (ii).

11. The method of claim 4, further comprising, prior to step (iii), the step of filtering the lysed cell sample obtained in step (ii).

12. A method for analyzing a fluid, cell-containing sample, the method comprising:

(i) providing a device comprising;

a solid substrate microfabricated to define;

a sample inlet port; and

a mesoscale flow system comprising;

a sample flow channel extending from said inlet port; and

a cell handling region for treating cells disposed in fluid communication with said flow channel, said cell handling region comprising a cell capture region comprising immobilized binding sites which reversibly bind a preselected cell surface molecule of a cell population in a cell-containing fluid sample; and

means for inducing flow of cells in said sample through said mesoscale flow channel and said cell handling region; and

means for detecting an analyte in a fluid sample in said flow system;

(ii) delivering a fluid, cell containing sample to the inlet port;

(iii) inducing flow of the cell-containing sample through the flow system within the flow inducing means;

at a first flow rate sufficiently slow to permit capture of cells in a cell population in the sample by the binding sites, thereby to separate the cell population from the sample; and

at a second flow rate, higher than the first flow rate, and sufficient to release the separated cells from the capture region; and

(iv) detecting an analyte in the fluid sample in the flow system with the detection means.

13. The method of claim 12 wherein step (iv) comprises detecting the presence of an analyte comprising an extracellular component in the sample with the detection means.

14. The method of claim 12 wherein the method further comprises, prior to step (iv), the step of lysing the cells;

and

wherein step (iv) comprises detecting an analyte comprising an intracellular component of the lysed cells with the detection means.

15. The method of claim 14 further comprising filtering the lysed cell sample prior to step (iv).

17. The method of claim 5, 12 or 16 wherein the method comprises utilizing a pump to deliver the cell-containing sample to the flow system in the device.

18. The method of claim 4, 12 or 16, wherein said detecting step comprises the step of optically viewing the contents of the mesoscale flow system in the substrate.

21. The method of claim 4, 12, or 16 wherein said detecting step comprises optically or electrically gathering data within the mesoscale flow system, said data being indicative of the presence or concentration of an analyte in a sample contained within the flow system.

22. The method of claim 12 or 16 wherein said detecting step comprises detecting a particular cell type in a heterogeneous cell population in the sample.

23. The method of claim 4, 12, 16 or 20 wherein, in the device provided in step (i), within at least a portion of a channel in a said flow system, the channel width and channel depth each are between 0.1 μ

m and 500 μ

m.

24. The method of claim 23 wherein the channel width in said portion is between 2.0 and 500 μ

m.

25. The method of claim 23 wherein the channel depth in said portion is between 0.1 and 100 μ

m.

16. A method for analyzing a fluid, cell-containing sample, the method comprising:

(i) providing a device comprising;

a solid substrate microfabricated to define;

a sample inlet port; and

a mesoscale flow system comprising;

a sample flow channel extending from said inlet port; and

a cell handling structure for treating cells disposed in fluid communication with said flow channel, said cell handling structure defining;

a cell sieve comprising means defining a plurality of flow passages of restricted size allowing only cells of a sufficiently small diameter to pass therethrough; and

a cell lysing structure;

means for inducing flow of cells in a sample through said mesoscale flow channel and said cell handling structure; and

means for detecting an analyte in a fluid sample in said flow system;

(ii) delivering a fluid, cell-containing sample to the inlet port through the flow system with the flow inducing means to the cell handling structure, to permit cell sorting of the sample in the cell sieve, and cell lysis of the cell sample in the cell lysing structure; and

(iii) detecting an analyte in the sample in the flow system with the detection means.

19. The method of claim 16 wherein the method comprises detecting an analyte comprising an intracellular component of the lysed cells with the detection means.

20. A method for analyzing a cell-containing fluid sample, the method comprising:

(i) providing a device comprising;

a solid substrate microfabricated to define;

a mesoscale cell handling structure; and

at least two mesoscale flow systems, each of which comprise a flow channel and an analyte detection region, one of said flow systems being adapted to analyze a sample, the other being adapted as a control, and said flow systems being in fluid communication with said cell handling structure; and

means for inducing flow of a sample through said cell handling structure and then through both said flow systems, thereby to permit comparison of data from the detection regions of said systems;

(ii) delivering a cell-containing fluid sample to said inlet port, and through the cell handling structure and the mesoscale flow systems with the flow inducing means; and

(iii) detecting and comparing data from the detection regions of said flow systems.