Device for the analysis of chemical or biochemical specimens, comparative analysis, and associated analysis process

• US 20030027354A1
• Filed: 06/10/2002
• Published: 02/06/2003
• Est. Priority Date: 06/08/2001
• Status: Abandoned Application

• Current Assignee: Francois Geli
• Original Assignee: Francois Geli
• Inventors: Geli, Francois
• Application Number:
  US10/164,423
• Publication Number:
  US 20030027354A1
• Time in Patent Office: Days
• US Class Current: 436/178
• CPC Class Codes: G01N 2030/165 retention gaps
• CPC Class Codes: G01N 27/44704 Details; Accessories
• CPC Class Codes: G01N 27/44717 Arrangements for investigating the separated zones, e.g. localising zones
• CPC Class Codes: G01N 27/44773 Multi-stage electrophoresis, e.g. two-dimensional electrophoresis
• CPC Class Codes: G01N 30/461 with serial coupling of separation columns
• CPC Class Codes: G01N 30/466 with separation columns in parallel
• CPC Class Codes: G01N 30/6043 in parallel
• CPC Class Codes: G01N 30/6095 Micromachined or nanomachined, e.g. micro- or nanosize
• CPC Class Codes: G01N 30/76 Acoustical detectors measurement of mechanical vibrations or ultrasonic, sonic or infrasonic waves G01H
• CPC Class Codes: Y10T 436/25375 Liberation or purification of sample or separation of material from a sample [e.g., filtering, centrifuging, etc.]
• CPC Class Codes: Y10T 436/255 including use of a solid sorbent, semipermeable membrane, or liquid extraction

Abstract

A device for the chemical or biochemical analysis of biological or chemical samples, notably for a comparative analysis of at least two samples, comprises multiple fractionation micro-columns 2 for the fractionation of sample components, each fractionation micro-column 2 comprising at least a micro-channel 3 segment fitted with intermediate separation means, the micro-channel 3 segment comprising an inlet 3a for the introduction of a sample-enriched mobile phase and an outlet 3b for the evacuation of the fluids and situated at a teminal extremity. The device comprises also capture fluidic means 7 of the fractionated products which are located at a terminal element 9 of each fractionation micro-columns 2 and upstream from the evacuation outlet 3b, capture micro-channels 8 which are used to collect the captured fractionation products and groups of selective micro-cantilevers 13 which are associated with the fractionation micro-columns 2 and situated downstream from the capture micro-channels 8, a micro-cantilever 13 being fitted with detection means which are associated with analytical means.

Claims

1. Device for the chemical or biochemical analysis of biological or chemical samples, notably for a comparative analysis of at least two samples, comprising multiple fractionation micro-columns (2) for the fractionation of sample components, each fractionation micro-column (2) comprising at least a micro-channel segment fitted with intermediate separation means, the microchannel segment comprising an inlet for the introduction of a sample-enriched mobile phase and an outlet for the evacuation of the fluids and situated at a teminal extremity, characterized by the fact that it comprises capture fluidic means (7), for the capture of the fractionated products, which are situated at the level of a terminal element of each fractionation micro-columns (2) and upstream from the evacuation outlet, by capture micro-channels which are used to collect the fractionation products and by groups of selective micro-cantilevers (13) which are associated with the fractionation micro-columns (2), are situated downstream from the capture micro-channels, a micro-cantilever (13) being fitted with detection means which are associated with analytical means.

2. Device according to the claim 1 and characterized by the fact that a fractionation micro-column (2) or a group (3) of fractionation micro-columns is different from another micro-column (2) or another group (3) of fractionation micro-columns by an element of length, the terminal element being situated on each fractionation micro-column (2) at a given distance from the terminal extremity of the fractionation micro-column (2).

3. Device according to any of the claims 1 or 2 and characterized by the fact that each fractionation micro-column (2) is different from the next longer fractionation micro-column (2) by a given element of length.

4. Device designed according to any of the previous claims and characterized by the fact that it comprises secondary fractionation micro-columns (20) which are situated downstream from the capture fluidic means (7) and upstream from the group of micro-cantilevers (13) which is associated with a fractionation micro-column (2) and used for the secondary fractionation of the captured fractionation products.

5. Device designed according to any of the previous claims, characterized by the fact that it comprises several groups of fractionation micro-columns (2), each group of fractionation micro-columns (2) having a selectivity which is determined by the separation means of in the fractionation microcolumns (2) comprising a stationary phase, coated or not coated, and/or associated with separation electrical means.

6. Device designed according to claim 5 and characterized by the fact that it comprises a support (1) equipped with multiple groups of fractionation micro-columns (2), capture means (7), associated groups of micro-cantilevers (13) and a feeding channel for all of the fractionation micro-columns.

7. Device designed according to any of the previous claims and characterized by the fact that the selective micro-cantilevers (13) comprise detection means which are based on their surface status or coating status of their surface or their chemical nature or the chemical nature of the coating on their surface.

8. Device designed according to any of the previous claims and characterized by the fact that the diameter of the micro-columns (2) ranges between 1 micron (λ

m) and 100 microns (λ

m).

9. Device designed according to any of the previous claims and characterized by the fact that it comprises a fractionation support (1) equipped with fractionation micro-columns (2) and a detection support (8) equipped with micro-cantilevers (13), the supports being approximately flat and being laid out in an approximately parallel or perpendicular way.

10. Device designed according to any of the previous claims and characterized by the fact that it comprises at least one tier of preliminary fractionation micro-columns (32) which is situated upstream from the fractionation micro-columns (2) and comprises at least one preliminary fractionation micro-column (32), capture fluidic means (36, 37, 38) which are situated at the level of a terminal element of the preliminary fractionation microcolumn (32) and a collection channel that is used to collect the preliminary fractionation products to the fractionation micro-columns.

11. Device designed according to the claim 10 and characterized by the fact that the preliminary fractionation tier comprises multiple preliminary fractionation micro-columns (32), each of them being intersected by a capture channel (36), the capture micro-channel (36) being connected to a collection channel (38).

12. Device designed according to the claim 10 and characterized by the fact that the preliminary fractionation tier comprises multiple preliminary fractionation micro-columns (32) and a capture micro-channel (36) which successively intersects the preliminary fractionation micro-columns and is connected with a collection channel (38).

13. Device designed according to any of the previous claims and characterized by the fact that a fractionation micro-column comprises a terminal segment which is fitted with separation means that are different from the intermediate separation means.

14. Device designed according to any of the previous claims and characterized by the fact that the capture fluidic means which are associated with a fractionation micro-column (3, 32) comprise a capture micro-channel (8,36) which comprises an upstream portion (8a, 36a) which is connected with the downstream extremity of a capture segment (40) of the micro-column (3, 32), and a downstream segment (8b, 36b) which is connected to the upstream extremity of the capture segment (40).

15. Device designed according to any of the previous claims and characterized by the fact that it comprises a washing micro-conduit (70) for the selective micro-cantilevers and connected with capture micro-channels (8) directly upstream from the micro-cantilevers.

16. Group of chemical or biochemical comparative analyses of at least two chemical or biological which is characterized by the fact that it comprises at least two devices for the chemical or biochemical analysis of biological or chemical samples, notably for a comparative analysis of at least two samples, these devices comprising multiple fractionation micro-columns (2) for the fractionation of sample components, each fractionation micro-column (2) comprising at least a micro-channel segment fitted with intermediate separation means, the micro-channel segment comprising an inlet for the introduction of a sample-enriched mobile phase and an outlet for the evacuation of the fluids and situated at a teminal extremity, characterized by the fact that it comprises capture fluidic means (7), for the capture of the fractionated products, which are situated at the level of a terminal element of each fractionation micro-columns (2) and upstream from the evacuation outlet, by capture micro-channels which are used to collect the fractionation products and by groups of selective micro-cantilevers (13) which are associated with the fractionation micro-columns (2), are situated downstream from the capture micro-channels, a micro-cantilever (13) being fitted with detection means which are associated with analytical means.

17. Process for the chemical or biochemical analysis of chemical or biological samples characterized by the fact that the differential fractionation of a sample enriched mobile phase is performed, that different fractionation products are simultaneously captured and that each fractionation products is analyzed by a selective micro-cantilever group.

18. Process performed according to claim 17 and characterized by the fact that a captured fractionation product is fractionated before being analyzed.

19. Process performed according to any of the claims 17 or 18 and characterized by the fact that the components of a fractionation product are detected by micro-cantilevers (13), according to polarity, solvophobicity or porosity characteristics of the micro-cantilever material or of the micro-cantilever coating, or according to the polarity or solvophobicity chraracteristics or ion exchange or affinity with the functional groups which are grafted on the microcantilevers.

20. Process performed according to any of the claims 17 to 19 and characterized by the fact that a sample is fractionated by chromatography, by micro-electrophoresis or by interactions with nano-electrodes.

21. Process performed according to any of the claims 17 to 20 and characterized by the fact that the deviation or the vibration frequency of the micro-cantilevers (13) are analyzed.

22. Process performed according to any of the claims 17 to 21 and characterized by the fact that fractionation products are analyzed by mass spectrometry, before or after the analysis by micro-cantilevers (13).

23. Process performed according to any of the claims 17 to 22 and characterized by the fact that a first sample is analyzed, a second sample is analyzed and the results of both samples are compared.

24. Process performed according to the claim 23 and characterized by the fact that the first and second samples are analyzed with the intent to compare the protein patterns of the samples by selective micro-cantilevers which are able to reveal different protein patterns.

25. Process performed according to any of the claims 17 to 24 and characterized by the fact that a preliminary extraction is performed on a sample before the differential fractionation of the sample.