초록 ▼

The present invention relates to a method for presenting an analyte of a liquid sample as an MS-analyte to a mass spectrometer. More particularly, the method comprises the steps of applying a liquid sample containing the analyte to a sample inlet port of a microchannel structure of a microfluidic de

The present invention relates to a method for presenting an analyte of a liquid sample as an MS-analyte to a mass spectrometer. More particularly, the method comprises the steps of applying a liquid sample containing the analyte to a sample inlet port of a microchannel structure of a microfluidic device, said structure also comprising an outlet port (MS-port) that is capable of being interfaced with a mass spectrometer, passing the analyte to the MS-port thereby transforming it to an MS-analyte, and presenting the MS-analyte to mass spectrometer via the MS-port.

대표청구항 ▼

The invention claimed is: 1. A method for presenting an analyte of a liquid sample as an MS-analyte to a mass spectrometer comprising the steps of: (i) applying the liquid sample containing the analyte to a sample inlet port of a microchannel structure of a microfluidic device, said microchannel st

The invention claimed is: 1. A method for presenting an analyte of a liquid sample as an MS-analyte to a mass spectrometer comprising the steps of: (i) applying the liquid sample containing the analyte to a sample inlet port of a microchannel structure of a microfluidic device, said microchannel structure comprises an outlet port (MS-port) that is interfaced with a mass spectrometer and inertia force is used for liquid transportation within at least a part of said microchannel structure; (ii) passing the analyte to the MS-port thereby transforming the analyte to an MS-analyte, and (iii) presenting the MS-analyte to the mass spectrometer via the MS-port. 2. The method of claim 1, wherein the analyte is a biopolymer comprising a carbohydrate structure, a nucleic acid structure or a peptide structure. 3. The method of claim 1, wherein the analyte comprises a peptide structure. 4. The method of claim 1, wherein transformation of said analyte to an MS-analyte comprises digestion of the analyte into fragments. 5. The method of claim 4, wherein said digestion is a chemical digestion or an enzymatic digestion. 6. The method of claim 1, wherein transformation of said analyte to an MS-analyte comprises chemical derivatization of the analyte. 7. The method of claim 1, wherein transformation of said analyte to an MS-analyte comprises mass tagging of said analyte or of a derivative formed during the transformation. 8. The method of to claim 7, wherein said derivative to be mass tagged is a fragment of the analyte. 9. The method of claim 1, wherein the inertia force is centrifugal force. 10. The method of claim 1, wherein said MS-port comprises an opening permitting release of the MS-analytes into the mass spectrometer. 11. The method of claim 1, wherein said microfluidic device comprises a planar substrate having at least one microchannel structure that extends radially in the plane of the substrate with said MS-pen being located at an outer position and said sample inlet port at an inner position. 12. The method of claim 11, wherein said planar substrate alter or simultaneously with the application of the sample is spun around its central axis which is perpendicular to said plane thereby forcing liquids present in the microchannel structure to move outwards. 13. The method of claim 11 wherein said microfluidic device comprises a plurality of said microchannel structures. 14. The method of claim 11, wherein the plurality of microchannel structures are annularly arranged around a central axis. 15. The method of claim 14, wherein each EDI area comprises a conducting layer (layer I) with a conductive connection. 16. The method of claim 15, wherein said separation zone comprises a separation medium which is capable of selectively capturing said derivative when a liquid containing said derivative is allowed to pass through the zone. 17. The method of claim 15, wherein transformation of an analyte to said MS-analyte occurs in a reaction zone in said microchannel. 18. The method of 15, wherein said separation zone separates, concentrates, or purifies the analyte, MS-analyte or derivative thereof. 19. The method of claim 15, wherein said separation zone comprises separation medium which exhibits ligand structures that are capable of binding to said analyte or said MS-analyte or derivative by affinity or reversible covalent bonds. 20. The method of claim 15, wherein the separation zone is located downstream the sample inlet port and upstream the MS port. 21. The method of claim 15, wherein the separation zone is located within the MS-port. 22. The method of claim 1, wherein the MS-port comprises an electro spray arrangement. 23. The method of claim 22, wherein there are two or more EDI areas on the microfluidic device and that layer I in at least two of said EDI areas are present in a common continuous conducting layer comprising the connection for electricity. 24. The method of claim 1, wherein the MS-port comprises an EDI arrangement with an EDI area. 25. The method of claim 1, wherein the microchannel structure further comprises a separation zone. 26. The method of claim 25, wherein said separation zone and said reaction zone coincide. 27. The method of claim 1, wherein the MS-analyte is a derivative of the analyte.