Integrated active flux microfluidic devices and methods
The invention relates to a microfabricated device for the rapid detection of DNA, proteins or other molecules associated with a particular disease. The devices and methods of the invention can be used for the simultaneous diagnosis of multiple diseases by detecting molecules (e.g. amounts of molecules), such as polynucleotides (e.g., DNA) or proteins (e.g., antibodies), by measuring the signal of a detectable reporter associated with hybridized polynucleotides or antigen/antibody complex. In the microfabricated device according to the invention, detection of the presence of molecules (i.e., polynucleotides, proteins, or antigen/antibody complexes) are correlated to a hybridization signal from an optically-detectable (e.g. fluorescent) reporter associated with the bound molecules. These hybridization signals can be detected by any suitable means, for example optical, and can be stored for example in a computer as a representation of the presence of a particular gene. Hybridization probes can be immobilized on a substrate that forms part of or is exposed to a channel or channels of the device that form a closed loop, for circulation of sample to actively contact complementary probes. Universal chips according to the invention can be fabricated not only with DNA but also with other molecules such as RNA, proteins, peptide nucleic acid (PNA) and polyamide molecules.
1. A method for effectively mixing two or more different fluids in a microfluidic device, which method comprises:
(a) introducing the different fluids to a microfluidic device, the microfluidic device having:
(i) a loop channel communicating with at least one service channel, and
(ii) a pump associated with the loop channel, so that each of the different fluids is loaded into the loop channel; and
(b) circulating the different fluids using the pump associated with the loop channel to mix the different fluids, wherein the pump is a peristaltic pump comprising at least three cooperating microvalves acting within the loop channel.
2. A method according to claim 1 , wherein the microfluidic device has at least one inlet channel and at least one outlet channel, the different fluids being loaded into the loop channel through at least one inlet channel.
3. A method according to claim 2 , wherein:
the microfluidic device has two or more inlet channels; and
each of the two or more different fluids is loaded into the loop channel through a different inlet channel.
4. A method according to claim 2 , wherein each inlet channel and each outlet channel is separated from the loop channel by a microvalve.
5. A method according to claim 4 , wherein the microvalves separating the inlet and outlet channels from the loop channel are closed while the pump is activated.
6. A method according to claim 4 , wherein the microvalves separating the inlet and outlet channels from the loop channel remain open while the pump is activated.
7. A method according to claim 1 , wherein at least one of the different fluids comprises a solution of molecules.
8. A method according to claim 7 , wherein the solution of molecules contains molecules selected from a group consisting of: nucleic acid molecules, polypeptide molecules, antibody molecules.
9. A method according to claim 1 , wherein at least one of the different fluids comprises a suspension of particles.
10. A method according to claim 9 , wherein the suspension of particles contains particles selected from a group consisting of: cells, virions, and microscopic beads.
11. A method according to claim 1 , wherein the microfluidic device further comprises a microvalve separating the loop channel from the service channel.
12. A method for binding a sample to a target, which method comprises:
(a) introducing a fluid containing the sample to a microfluidic device, the microfluidic device having:
(i) a loop channel communicating with at least one service channel and having molecules of the target disposed therein, and
(ii) a pump associated with the loop channel, so that the fluid containing the sample is loaded into the loop channel; and
(b) circulating the fluid through the loop channel using the pump, wherein the sample binds to the target molecules disposed in the loop as the fluid circulates therethrough, and wherein the pump is a peristaltic pump comprising at least three cooperating microvalves acting within the loop channel.
13. A method according to claim 12 , wherein the target molecules are selected from a group consisting of polynucleotide probes, protein probes, antibody probes, biotin and avidin.
14. A method according to claim 12 , wherein the sample comprises nucleic acid molecules, protein molecules, cells or virions.
15. A method according to claim 14 , wherein
the sample comprises nucleic acid molecules, and
the target comprises polynucleotide probes specific for nucleic acid molecules in the sample.
16. A method according to claim 14 , wherein:
the target comprises biotin molecules, and
the sample comprises particles or molecules having a biotin specific label.
17. A method according to claim 12 , wherein the loop channel resides in a layer of elastomeric material.
18. A method according to claim 12 , wherein the microfluidic device further comprises a microvalve separating the loop channel from the service channel.