Microfluidic assay devices

• US 7,682,817 B2
• Filed: 12/23/2004
• Issued: 03/23/2010
• Est. Priority Date: 12/23/2004
• Status: Active Grant

• Current Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Original Assignee: Kimberly-Clark Worldwide Incorporated (Kimberly-Clark Corporation)
• Inventors: Cohen, David Samuel, Feaster, Shawn Ray
• Primary Examiner(s): Yang; N.
• Application Number:
  US11/021,545
• Publication Number:
  US 20060137434A1
• Time in Patent Office: 1,916 Days
• Field of Search: None
• US Class Current: 435/287.1
• CPC Class Codes: B01L 2300/069 Absorbents; Gels to retain a fluid
• CPC Class Codes: B01L 2300/0803 Disc shape
• CPC Class Codes: B01L 2300/0816 Cards, e.g. flat sample carriers usually with flow in two horizontal directions
• CPC Class Codes: B01L 2300/0864 comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
• CPC Class Codes: B01L 2400/0406 capillary forces
• CPC Class Codes: B01L 3/502746 characterised by the means for controlling flow resistance, e.g. flow controllers, baffles B01L3/502738 takes precedence

Abstract

A microfluidic assay device for determining the presence or absence of an analyte within a fluid test sample is provided. The present invention provides a technique for achieving continuous flow in a microfluidic device by using at least one input channel, an analysis zone, and a plurality of wicking channels disposed about the perimeter of the analysis zone. In one embodiment, for example, the wicking channels extend radially from the analysis zone. As a result of the particular configuration of the microfluidic device, an assay may performed in a “single step” without the need for active forces, such as a pressure source, electrokinetic force, etc., to induce flow of the fluid test sample through the device. Likewise, flow rate is controlled so that the dwell time of the fluid test sample within the analysis zone is long enough to allow for the desired reactions and/or detection.

Claims

1. An assay device for detecting the presence or concentration of an analyte within a fluid test sample, said assay comprising:

an input channel;

an analysis zone in fluid communication with said input channel, said analysis zone defining a periphery, wherein said analysis zone serves as a location for detecting the analyte;

from 3 to about 500 microfluidic wicking channels extending radially from the periphery of said analysis zone, wherein the assay device is configured so that the fluid test sample is capable of flowing through said input channel and said analysis zone primarily via capillary action, and

an absorbent material positioned within all of the wicking channels.

2. The assay device of claim 1, wherein said input channel has a cross-sectional area of less than about 20 square millimeters.

3. The assay device of claim 1, wherein said analysis zone is of a size sufficient to accommodate substantially the entire volume of the fluid test sample applied to the assay device.

4. The assay device of claim 1, wherein said analysis zone has a substantially circular shape.

5. The assay device of claim 1, wherein the fluid test sample is capable of flowing sequentially from said input channel to said analysis zone.

6. The assay device of claim 1, wherein said wicking channels taper inwardly toward said analysis zone.

7. The assay device of claim 1, wherein said wicking channels have an aspect ratio of from about 0.1 to about 10.

8. The assay device of claim 1, wherein said wicking channels have an aspect ratio of from about 0.25 to about 5.

9. The assay device of claim 1, wherein said wicking channels have an aspect ratio of from about 0.5 to about 1.5.

10. The assay device of claim 1, wherein said wicking channels have a cross-sectional area of less than about 20 square millimeters.

11. The assay device of claim 1, wherein said wicking channels have a cross-sectional area of from about 0.001 to about 10 square millimeters.

12. The assay device of claim 1, wherein said wicking channels have a cross-sectional area of from about 0.01 to about 5 square millimeters.

13. The assay device of claim 1, wherein the assay device comprises from about 15 to about 200 of said wicking channels.

14. The assay device of claim 1, further comprising an overflow zone that is in fluid communication with said wicking channels.

15. The assay device of claim 1, further comprising a substrate on or within which said input channel, said analysis zone, and said wicking channels are disposed.

16. The assay device of claim 15, wherein a separation medium is laminated to said substrate, said separation medium containing a receptive material that is capable of binding to the analyte or a complex thereof.

17. The assay device of claim 16, wherein said separation medium includes a polymer film having a metal coating.

19. The assay device of claim 1, wherein said wicking channels are spaced about equidistant from each other.

20. The assay device of claim 1, wherein the assay device comprises from about 20 to about 80 of said wicking channels.

21. The assay device of claim 1, wherein the assay device is configured so that the fluid test sample is capable of flowing through said input channel and said analysis zone without the use active forces to induce fluid flow of the fluid test sample.

23. The assay device of claim 1, wherein the absorbent material comprises nitrocellulose.

24. The assay device of claim 1, wherein the absorbent material comprises cellulosic materials.

25. The assay device of claim 1, wherein the absorbent material comprises glass fiber filter paper.

18. An assay device for detecting the presence or concentration of an analyte within a fluid test sample, said assay comprising:

an input channel;

a substantially circular analysis zone in fluid communication with said input channel, said analysis zone defining a periphery, wherein said analysis zone serves as a location for detecting the analyte;

from 3 to about 500 wicking channels extending radially from the periphery of said analysis zone, wherein said wicking channels have an aspect ratio of from about 0.1 to about 10 and a cross-sectional area of less than about 20 square millimeters;

an absorbent material positioned within one or more of the wicking channels; and

an overflow zone that is in fluid communication with and directly connected to each of the wicking channels, wherein the assay device is configured so that the fluid test sample is capable of flowing through said input channel and said analysis zone primarily via capillary action.

22. The assay device of claim 18, wherein the overflow zone is interconnected such that each wicking channel is directly connected to the same overflow zone.