Method and Apparatus for Assaying Blood Clotting

• US 20090104637A1
• Filed: 01/31/2007
• Published: 04/23/2009
• Est. Priority Date: 01/31/2006
• Status: Abandoned Application

• Current Assignee: University of Chicago
• Original Assignee: University of Chicago
• Inventors: Kastrup, Christian J., Song, Helen, Shen, Feng, Ismagilov, Rustem F., Runyon, Matthew K.
• Application Number:
  US12/162,763
• Publication Number:
  US 20090104637A1
• Time in Patent Office: Days
• US Class Current: 435/13
• CPC Class Codes: G01N 33/86 involving blood coagulating time or factors, or their receptors

Abstract

This invention provides an apparatus for assaying clotting activity. The apparatus includes an inlet for a blood fluid and two or more patches of material in the vessel. The material is capable of initiating a clotting pathway in a blood fluid. This invention also provides an apparatus for measuring clot propagation, which includes a region with material capable of initiating a clotting pathway, and a region where the clot propagation is monitored. Also provided are methods for assaying clotting activity, assaying the integrity of a blood clotting pathway, assaying the effect of a substance on the integrity of a blood clotting pathway, monitoring clot propagation, and preventing clot propagation from one vessel to another.

Claims

1. An apparatus for assaying clotting activity comprising:

an inlet for a blood fluid;

a vessel in fluid communication with the inlet; and

at least a first and a second patch in the vessel, wherein

(a) the patches each comprise stimulus material which is capable of initiating a clotting pathway when contacted with a blood fluid from a subject; and

(b)(i) the stimulus material in the first patch differs from the second patch;

or

(b)(ii) the concentration of stimulus material in the first patch differs from the second patch;

or

(b)(iii) the first patch has a surface area different from the second patch;

or

(b)(iv) the first patch has a shape different from the second patch;

or

(b)(v) the first patch has a size different from the second patch.

2. The apparatus of claim 1, comprising a plurality of patches.

3. The apparatus of claim 2, wherein the distance between the members of a first set of two patches is different from the distance between the members of a second set of two patches.

4. The apparatus of claim 2, wherein a first set of patches is at a first location and a second set of patches is at a second location;

and wherein the number of patches in the first set is different from the number of patches in the second set.

5. The apparatus of claim 1, wherein the stimulus material comprises at least one clotting stimulus selected from the group of tissue factor, factor II, factor XII, factor X, glass, glasslike substances, kaolin, dextran sulfate, amyloid beta, ellagic acid, bacteria, and bacterial components.

6. The apparatus of claim 1, wherein the patches are beads.

7. The apparatus of claim 1, further comprising beads, wherein the patches are associated with the beads.

8. The method of claim 1, wherein the patch further comprises inert material.

9. The apparatus of claim 1, wherein the vessel comprises two intersecting microchannels, and wherein the channels are in fluid communication with each other.

10. A method of assaying blood clotting, comprising

contacting blood fluid from a subject with at least a first and second patch, wherein

(a) the patches each comprise stimulus material which is capable of initiating a clotting pathway when contacted with a blood fluid from a subject;

and

(b)(i) the stimulus material in the first patch differs from the second patch;

or

(b)(ii) the concentration of stimulus material in the first patch differs from the second patch;

or

(b)(iii) the first patch has a surface area different from the second patch;

or

(b)(iv) the first patch has a shape different from the second patch;

or

(b)(v) the first patch has a size different from the second patch; and

determining which patches initiate clotting of the blood fluid from the subject.

11. The method of claim 10, wherein the stimulus material is capable of initiating a clotting pathway in blood fluid from a healthy subject.

12. The method of claim 10, wherein the contacting is for a time sufficient for at least the largest patch to initiate the clotting pathway in a blood fluid from a healthy subject.

13. The method of claim 10, further comprising a surface in which the patches are associated.

14. The method of claim 13, further comprising contacting blood fluid from the subject with a third patch associated with the surface, and wherein the distance between the first and second patches differs from the distance between the second and third patches.

15. The method of claim 13, wherein the surface is a microfluidic channel.

16. The method of claim 15, wherein the blood fluid is contacted with the patches in plugs separated by an immiscible fluid.

17. The method of claim 15, wherein the blood fluid is contacted with the patches as a continuous stream.

18. The method of claim 10, wherein the patches are each independently a bead.

19. The method of claim 10, wherein the patches are each independently associated with a bead.

20. The method of claim 18, wherein either the size or the shape of each beads differ.

21. The method of claim 10, wherein the clotting pathway is a platelet aggregation pathway.

22. The method of claim 10, wherein contacting comprises first contacting a first amount of blood fluid with a first concentration of beads and second contacting a second amount of blood fluid with a second concentration of beads;

wherein each bead independently is associated with a patch comprising a stimulus material and an inert material.

23. The method of claim 21, wherein aliquots of blood fluid are titrated with beads of increasing size.

24. The method of claim 10, wherein determining comprises observing optically.

25. The method of claim 10, wherein determining comprises measuring scattering of light.

26. The method of claim 10, wherein the blood fluid is selected from the group consisting of whole blood, blood constituents, plasma, a solution of plasma proteins, and a solution of cells from blood.

27. The method of claim 10, further comprising first adding an excess of a clotting factor to the blood fluid before contacting the blood fluid with the patches.

28. The method of claim 10, further comprising adding a test substance to a blood fluid before contacting the blood fluid with the patches.

29. The method of claim 10, further comprising monitoring the rate of propagation of a blood clot.

30. The method of claim 10, further comprising adding a blood fluid from a different subject to the blood fluid before contacting the blood fluid with the patches.

31. An apparatus for measuring clot propagation comprising:

a first region comprising a stimulus material; and

a second region in communication with the first region suitable for monitoring the propagation of a clot;

wherein when a blood fluid is placed in the first region, a clot forms and propagates to the second region.

32. The apparatus of claim 31, further comprising a patch comprising the stimulus material.

33. The apparatus of claim 31, wherein the apparatus comprises a microchannel comprising the first and second regions.

34. The apparatus of claim 31, wherein the apparatus comprises a plurality of microchannels, each microchannel comprising separate first and second regions.

35. The apparatus of claim 31, comprising at least one set of intersecting microchannels, wherein the second region is at the intersection of the first set of the microchannels.

36. The apparatus of claim 35, comprising a plurality of microchannels and at least two intersections of the microchannels, wherein the second region is at one of the intersections and wherein the sizes of the two intersections are different.

37. A method of monitoring clot propagation, comprising the steps of:

contacting a blood fluid with a first region of an apparatus, the first region comprising a stimulus material, and

monitoring clot propagation in a second region of the apparatus, the second region in communication with the first region.