COAGULATION ASSAY APPARATUS AND METHODS THEREOF

1 . A disposable bioassay diagnostic cartridge for monitoring anticoagulant activity, the disposable cartridge comprising:

a first well holding an amount of matrix, the matrix being either a drying matrix or a liquid matrix;

a second well holding a plurality of microparticles, wherein the plurality of microparticles are uncoated latex with at least one surface type, and the at least one surface type being chosen from a group consisting of unreacted plain, sulfate, carboxylate, and amidine; and

a third well comprising an amount of an activation agent, the activation agent being chosen from a group consisting of thromboplastin, thrombin, ellagic acid, activated partial thromboplastin, Factor II, Factor VII, Factor I, Factor X, Factor XII, activated protein C, snake venom, negatively charged phospholipids, calcium ions, tissue factor, silica, koalin, and celite.

2 . The disposable cartridge according to claim 1 , wherein the matrix further comprises at least one of NaCl, PEG, TWEEN, carbohydrate, and CaCl2.

3 . The disposable cartridge according to claim 1 , the disposable cartridge further comprising an integrated cuvette capable of facilitating at least two optical detection readings.

4 . The disposable cartridge according to claim 1 , the disposable cartridge further comprising an integrated cuvette having a first wall capable of facilitating a first optical detection reading via a first LED at 530 nm; and a second wall capable of facilitating a second optical detection reading via a second LED at 660 nm.

5 . The disposable cartridge according to claim 1 , the disposable cartridge further comprising an integrated cuvette having first and second walls capable of facilitating a first optical detection reading via a first LED at 530 nm, and a second optical detection reading via a second LED at 660 nm.

6 . (canceled)

7 . A coagulation bioassay comprising:

a matrix, the matrix comprising at least one of glycine, sodium chloride, and 1% simethicone;

a plurality of microparticles suspended within the matrix, and wherein the plurality of microparticles are uncoated latex having at least one surface type; and

an amount of activation agent, the activation agent being chosen from a group consisting of thromboplastin, thrombin, ellagic acid, activated partial thromboplastin, Factor II, Factor VII, Factor I, Factor X, Factor XII, activated protein C, snake venom, negatively charged phospholipids, calcium ions, tissue factor, silica, koalin, and celite.

8 . The coagulation bioassay according to claim 7 , wherein the at least one surface type is selected from a group consisting of plain, sulfate, amidine, and carboxylate.

9 . The coagulation bioassay according to claim 7 , wherein the matrix is one of a drying matrix and a liquid matrix.

10 . The coagulation bioassay according to claim 7 , wherein each of the plurality of microparticles have a diameter of from about 10 nm to 150 nm.

11 . The coagulation bioassay according to claim 7 , wherein each of the plurality microparticles have a diameter in a range of from 90 nm to 110 nm.

12 . The coagulation bioassay according to claim 7 , wherein the plurality of microparticles are in a percent weight per volume solution selected from a group consisting of 0.006% weight per volume solution; 0.01% weight per volume solution; and 0.08% weight per volume solution.

13 . A method of obtaining clotting time measurements using one of dilute, lysed whole blood, or plasma, the method comprising the steps of:

selecting a microparticle matrix having a matrix and a plurality of microparticles within the matrix, wherein the plurality of microparticles are uncoated latex with at least one surface type, and the at least one surface type chosen from a group consisting of unreacted plain, sulfate; carboxylate, and amidine chemical structures retaining activity;

using the microparticle matrix as a reagent with the one of dilute, lysed whole blood, or plasma; and

obtaining clotting time measurements of the one of dilute, lysed whole blood, or plasma; and

determining a hemoglobin level of the one of dilute, lysed whole blood, or plasma; and

correcting the clotting time measurements by adjusting for the hemoglobin level of the one of dilute, lysed whole blood, or plasma.

14 . The method according to claim 13 further comprising: adding a separate activation agent to the reaction mixture to further activate natural clotting substrates in the one of dilute, lysed whole blood, or plasma.

15 . The method according to claim 14 wherein the activation agent is selected from a group consisting of thromboplastin, thrombin, ellagic acid, activated partial thromboplastin, Factor II, Factor VII, Factor I, Factor X, Factor XII, activated protein C, snake venom, negatively charged phospholipids, calcium ions, tissue factor, silica, koalin, and celite.

16 . The method according to claim 13 wherein obtaining the clotting time measurements of the one of dilute; lysed whole blood, or plasma further comprises repeatedly measuring an optical density of the one of dilute, lysed whole blood, or plasma, at a first wavelength over a period of time.

17 . The method according to claim 16 wherein determining the hemoglobin level of the one of dilute, lysed whole blood, or plasma, comprises measuring an optical density of the one of dilute, lysed whole blood, or plasma, at a second wavelength.

18 . The method according to claim 17 wherein the first wavelength is in a range of between 620 nm to 700 nm, and the second wavelength is in a range of between 500 nm to 550 nm.

19 . The method according to claim 13 wherein the step of obtaining clotting time measurements of the one of dilute, lysed whole blood, or plasma further comprising obtaining an optical density value difference of at least 0.08.

20 . The method according to claim 13 wherein the matrix is a liquid matrix and further comprises 0.17M glycine at pH 10.0, 1.29M NaCl, and 1% simethicone diluted with injection grade purified water.