Protein and nucleic acid detection for microfluidic devices

1. A method for detecting a nucleic acid target and a polypeptide target in a fluid sample, the method comprising:

introducing the fluid sample to a system comprising:

a microfluidic disc comprising a substrate, a first assay area, and a second assay area, in which each of the first and second assay areas is disposed, at least in part, within or on the substrate; and

a non-contact temperature control system for the microfluidic device, wherein the temperature control system comprising an infrared emitter configured to emit at a wavelength of from about 1 μm to about 5 μm and positioned to direct radiation to a first surface of the microfluidic device, and wherein a focal point of the emitter configured to be positioned on or within the first assay area, or a portion thereof, of the microfluidic device;

generating a plurality of first complexes on a plurality of first particles in the first assay area, wherein at least one first complex comprises the nucleic acid target and a first label agent;

generating a plurality of second complexes on a plurality of second particles in the second assay area, wherein at least one second complex comprises the polypeptide target and a second label agent, in which the plurality of first complexes and the plurality of second complexes can be generated sequentially in any order or simultaneously;

transporting the plurality of first particles through a first density medium in the first assay area and the plurality of second particles through a second density medium in the second assay area; and

detecting a signal from the first label agent of the first complex bound to the first particle and/or the second label agent of the second complex bound to the second particle.

2. The method of claim 1 , wherein the temperature control system further comprises a reflector configured to reflect radiation that is collected from a second surface of the microfluidic device, wherein the second surface opposes the first surface, and wherein the focal point of the emitter and a vertex of the reflector are aligned along a central axis.

3. The method of claim 1 , wherein the system further comprises:

a mask configured to be disposed between the emitter and the microfluidic device, wherein the mask comprises an opening to provide selective heating of the first assay area of the microfluidic device and a shielded region to provide selective masking of the second assay area of the microfluidic device.

4. The method of claim 1 , wherein the temperature control system further comprises a cooling fan configured to be in proximity to the emitter.

5. The method of claim 4 , wherein the emitter and the cooling fan are configured to be positioned above the microfluidic device, and wherein the reflector and the detection module are configured to be positioned below the microfluidic device.

6. The method of claim 1 , wherein the focal point is configured to be positioned on or within the first assay area containing a density medium.

7. The method of claim 6 , wherein the first assay area includes a narrowed region and the focal point is configured to be positioned on or within the narrowed region.

8. The method of claim 1 , wherein the generating a plurality of first complexes step comprises heating the first assay area with the emitter.

9. The method of claim 1 , wherein transporting step comprises spinning the microfluidic disc.

10. The method of claim 1 , wherein the detecting step comprises detecting a signal from the first and/or second label agents present in the first and/or second assay area by employing a detection module, and wherein the detection module is configured to generate an electronic detection signal based, at least in part, on the signal from the first and/or second label agents.

11. The method of claim 1 , wherein the first density medium has a density lower than a density of the plurality of first particles and higher than a density of the fluid sample within the first assay area.

12. The method of claim 11 , wherein the first assay area further comprises a further density medium, a plurality of cells, a plurality of sedimentation particles, and/or a separation layer fluid.

13. The method of claim 1 , wherein the second density medium has a density lower than a density of the plurality of second particles and higher than a density of the fluid sample within the second assay area.

14. The method of claim 13 , wherein the second assay area further comprises a further density medium, a plurality of cells, a plurality of sedimentation particles, and/or a separation layer fluid.

15. The method of claim 1 , wherein the at least one first complex comprises the nucleic acid target hybridized to the first label agent, in which the first label agent is bound to at least one first particle.

16. The method of claim 15 , wherein the first label agent comprises a nucleic acid portion configured to hybridize to a sequence of the nucleic acid agent and a detectable label.

17. The method of claim 1 , wherein the at least one first complex comprises the nucleic acid target bound to a cationic surface of at least one first particle and wherein the first label agent is bound to the nucleic acid target.

18. The method of claim 1 , wherein the at least one second complex comprises the polypeptide target bound to a capture agent disposed on a surface of at least one second particle and wherein the second label agent is bound to the polypeptide target.

19. A method for detecting a nucleic acid target in a fluid sample, the method comprising:

introducing the fluid sample to a system comprising:

a microfluidic disc comprising a substrate and a first assay area, which is disposed, at least in part, within or on the substrate; and

a non-contact temperature control system for the microfluidic device, wherein the temperature control system comprising an infrared emitter configured to emit at a wavelength of from about 1 μm to about 5 μm and positioned to direct radiation to a first surface of the microfluidic device, and wherein a focal point of the emitter configured to be positioned on or within the first assay area, or a portion thereof, of the microfluidic device;

generating a plurality of first complexes on a plurality of first particles in the first assay area, wherein at least one first complex comprises the nucleic acid target and a first label agent;

transporting the plurality of first particles through a first density medium in the first assay area; and

detecting a signal from the first label agent of the first complex bound to the first particle.

20. A method for detecting a nucleic acid target and a polypeptide target in a fluid sample, the method comprising:

introducing the fluid sample to a system comprising:

a microfluidic disc comprising a substrate, a first assay area, and a second assay area, in which each of the first and second assay areas is disposed, at least in part, within or on the substrate;

a non-contact temperature control system for the microfluidic device, wherein the temperature control system comprising an infrared emitter configured to emit at a wavelength of from about 1 μm to about 5 μm and positioned to direct radiation to a first surface of the microfluidic device, and wherein a focal point of the emitter configured to be positioned on or within the first assay area, or a portion thereof, of the microfluidic device; and

a mask configured to be disposed between the emitter and the microfluidic device, wherein the mask comprises an opening to provide selective heating of the first assay area of the microfluidic device and a shielded region to provide selective masking of the second assay area of the microfluidic device;

generating a plurality of first complexes on a plurality of first particles in the first assay area, wherein at least one first complex comprises the nucleic acid target and a first label agent, wherein the generating comprises selectively heating the first assay area by employing the mask and the emitter;

generating a plurality of second complexes on a plurality of second particles in the second assay area, wherein at least one second complex comprises the polypeptide target and a second label agent, in which the plurality of first complexes and the plurality of second complexes can be generated sequentially in any order or simultaneously;

transporting the plurality of first particles through a first density medium in the first assay area and the plurality of second particles through a second density medium in the second assay area; and

detecting a signal from the first label agent of the first complex bound to the first particle and/or the second label agent of the second complex bound to the second particle.