Microfluidic devices for measuring platelet coagulation and associated systems and methods
The present technology relates generally to microfluidic devices for measuring platelet coagulation, and associated systems and methods. In some embodiments, a fluidics device includes an array of microstructures including pairs of generally rigid blocks and generally flexible posts. The fluidics device further includes at least one fluid channel configured to accept the array. The fluid channel is configured to induce fluid flow of a biological sample, such as whole blood, through the array. The fluidics device can further include a detection component configured to measure a degree of deflection of one or more of the flexible posts in the array. In some embodiments, the fluidics device comprises a handheld device and usable for point of care testing of platelet forces and coagulation.
1. A fluidics device, comprising:
an array of microstructures including generally rigid blocks and generally flexible structures;
at least one fluid channel sized to accept the array, wherein the fluid channel is configured to induce fluid flow of a biological sample over and through the array; and
a detection component configured to detect a degree of deflection of one or more of the flexible structures in the array,
wherein the generally rigid blocks and the generally flexible structures are positioned within the fluid channel, and wherein the generally rigid blocks are spaced apart from the generally flexible structures along the fluid channel.
2. The device of claim 1 wherein the array comprises pairs of the generally rigid blocks and the generally flexible structures.
3. The device of claim 1 wherein the microstructures are made from at least one of silicon, polymers, metal, or ceramics.
4. The device of claim 1 wherein the detection component comprises a magnetic detection component.
5. The device of claim 4 wherein the magnetic detection component comprises a spin valve, Hall probe, or fluxgate magnetometer.
6. The device of claim 4 wherein at least one of the generally flexible structures includes a magnetic material.
7. The device of claim 4 wherein:
one or more of the generally flexile structures includes a magnetic material; and
the magnetic detection component comprises spin valves,
wherein at least one of the spin valves is positioned between at least one of the generally rigid blocks and at least one of the generally flexible structures, and further wherein the magnetic detection components is configured to detect changes in a magnetic field in the array caused by deflection of the one or more generally flexible structures including the magnetic material.
8. The device of claim 1 wherein the detection component comprises an optical detection component, and wherein the optical detection component is a phase contrast microscope, a fluorescence microscope, a confocal microscope, or a photodiode.
9. The device of claim 1 wherein at least some of the microstructures are at least partially coated with at least one binding element selected from a group consisting of proteins, enzymes, bioactive minerals, glycans, polyglycans, glycoproteins, collagen, von Willebrand factor, vitronectin, laminin, monoclonal antibodies, polyclonal antibodies, plasmin, agonists, matrix proteins, inhibitors of actin-myosin activity, and fragments thereof.
10. The device of claim 1 wherein the fluidics device comprises a handheld-size device.
11. The device of claim 1 , further comprising a display configured to display a characteristic of the biological sample based on the degree of deflection of the one or more generally flexible structures.
12. A fluidics device, comprising:
an array of microstructures including generally rigid blocks and generally flexible structures;
at least one fluid channel sized to accept the array, wherein the fluid channel is configured to induce fluid flow of a biological sample over and through the array; and
a detection component configured to detect a degree of deflection of one or more of the flexible structures in the array,
wherein the generally rigid blocks and the generally flexible structures are positioned within the fluid channel, and wherein the generally rigid blocks are positioned along the fluid channel upstream of the generally flexible structures.
13. The device of claim 12 wherein the array comprises pairs of the generally rigid blocks and the generally flexible structures.
14. The device of claim 12 wherein the microstructures are made from at least one of silicon, polymers, metal, or ceramics.
15. The device of claim 12 wherein the detection component comprises a magnetic detection component, and wherein the magnetic detection component comprises a spin valve, Hall probe, or fluxgate magnetometer.
16. The device of claim 12 wherein at least one of the generally flexible structures include a magnetic material.
17. The device of claim 12 wherein the magnetic detection component comprises spin valves, and wherein at least one of the spin valves is positioned between at least one of the generally rigid blocks and at least one of the generally flexible structures, and further wherein the magnetic detection component is configured to detect changes in a magnetic field in the array caused by deflection of the generally flexible structures including the magnetic material.
18. The device of claim 12 wherein the detection component comprises an optical detection component, and wherein the optical detection component is one of a phase contrast microscope, a fluorescence microscope, a confocal microscope, or a photodiode.
19. The device of claim 12 wherein at least some of the microstructures are at least partially coated with at least one binding element selected from a group consisting of proteins, enzymes, bioactive minerals, glycans, polyglycans, glycoproteins, collagen, von Willebrand factor, vitronectin, laminin, monoclonal antibodies, polyclonal antibodies, plasmin, agonists, matrix proteins, inhibitors of actin-myosin activity, and fragments thereof.
20. The device of claim 12 wherein the fluidics device comprises a handheld-size device.
21. The device of claim 12 , further comprising a display configured to display a characteristic of the biological sample based on the degree of deflection of the one or more generally flexible structures.