초록 ▼

The present invention is directed to a variety of microfluidic devices with configurations including the use of biochannels or microchannels comprising arrays of capture binding ligands to capture target analytes in samples. The invention provides microfluidic cassettes or devices that can be used t

The present invention is directed to a variety of microfluidic devices with configurations including the use of biochannels or microchannels comprising arrays of capture binding ligands to capture target analytes in samples. The invention provides microfluidic cassettes or devices that can be used to effect a number of manipulations on a sample to ultimately result in target analyte detection or quantification.

대표청구항 ▼

1. A method of detecting a target analyte in a plurality of samples, said method comprising:introducing at least a first sample to a first microchannel; introducing at least a second sample to a second microchannel; wherein said first and second microchannel each comprise a plurality of spatially di

1. A method of detecting a target analyte in a plurality of samples, said method comprising:introducing at least a first sample to a first microchannel; introducing at least a second sample to a second microchannel; wherein said first and second microchannel each comprise a plurality of spatially distinct regions upon which capture binding ligands are immobilized; flowing said first and second sample through said first and second microchannels to form at least one assay complex comprising the target analyte; recirculating the flow of at least one sample in at least one microchannel and detecting said target analyte. 2. A method according to claim 1, wherein said capture binding ligands are nucleic acids.3. A method according to claim 1, wherein said capture binding ligands are proteins.4. A method according to claim 1, wherein said spatially distinct regions comprise porous polymer with said capture binding ligands bound to the porous polymer.5. A method according to claim 1, wherein said spatially distinct regions comprise beads with said capture binding ligands bound to the bead.6. A method according to claim 1, further comprisingforming said spatially distinct regions by introducing hydrogels into at least said first or second microchannel. 7. A method according to claim 1, further comprising:selectively dispensing said capture binding ligands on spatially distinct portions of hydrogel. 8. A method according to claim 1, further comprising:selectively dispensing said capture binding ligands on spatially distinct portions of polyacrylamide. 9. A method according to claim 1, wherein said method further comprises:generating an optical signal indicative of the assay complex; and wherein said detecting comprises detecting the optical signal. 10. A method according to claim 1, wherein said method further comprises:generatin a fluorescent signal indicative of the assay complex, and wherein said detecting comprises detecting the fluorescenet signale. 11. A method according to claim 1, wherein said method further comprisesgenerating an electronic signal indicative of the assay complex; and wherein said detecting comprises detecting the electronic signal. 12. A method according to claim 1, wherein said first or second microchannel is at least partially formed from a substrate comprising glass.13. A method according to claim 1, wherein said first or second microchannel is at least partially formed from a substrate comprising plastic.14. A method according to claim 1, wherein said first or second microchannel is at least partially formed from a substrate comprising polymer.15. A method of detecting a target analyte in a plurality of samples, said method comprising:introducing at least a first sample to a first microchannel; introducing at least a second sample to a second microchannel; wherein said first and second microchannel each comprise a plurality of spatially distinct regions comprising electrodes upon which capture binding ligands are immobilized; flowing said first and second sample through said first and second microchannels to form at least one assay complex comprising the target analyte; recirculating the flow of at least one sample in least one microchannel; and detecting said target analyte. 16. A method according to claim 15, wherein said capture binding ligands are nucleic acids.17. A method according to claim 15, wherein said capture binding ligands are proteins.18. A method according to claim 15, wherein said method further comprises:generating an optical signal indicative of the assay complex; and wherein said detecting comprises detecting the optical signal. 19. A method according to claim 15, wherein said method further comprises:generating a fluorescent signal indicative of the assay complex, and wherein said detecting comprises detecting the fluorescent signal. 20. A method according to claim 15, wherein said method further comprisesgenerating an electronic signal indicative of the assay complex; and wherein said detecting comprises detecting the electronic signal. 21. A method according to claim 15, wherein said first or second microchannel is at least partially formed from a substrate comprising glass.22. A method according to claim 15, wherein said first or second microchannel is at least partially formed from a substrate comprising plastic.23. A method according to claim 15, wherein said first or second microchannel is at least partially formed from a substrate comprising polymer.24. A method according to claim 15, wherein said detecting occurs on at least one of said electrodes.25. A method according to claim 15, further comprising pumping said first or second sample.