초록 ▼

A device (6) to sample molecules of biological interest is described. The device (6) includes capture zones (10) whose developed surface area is much greater than the surface so that sampling by contact allows a sufficient quantity of molecules to be obtained to achieve reliable analysis, whilst bei

A device (6) to sample molecules of biological interest is described. The device (6) includes capture zones (10) whose developed surface area is much greater than the surface so that sampling by contact allows a sufficient quantity of molecules to be obtained to achieve reliable analysis, whilst being sized so that the device (6) is neither invasive nor aggressive. In particular, the device comprises tiered capture zones (10) located on a support (12) fabricated using microtechnology techniques; the capture zones (10) may advantageously be functionalised.

대표청구항 ▼

1. A microtechnological sampling device for sampling molecules of biological interest by contact in an in vivo biopsy operation, the device comprising: a support having a first face opposite a second face,at least one first capture zone on the first face, wherein the developed surface area of the at

1. A microtechnological sampling device for sampling molecules of biological interest by contact in an in vivo biopsy operation, the device comprising: a support having a first face opposite a second face,at least one first capture zone on the first face, wherein the developed surface area of the at least one first capture zone is at least three times greater than its surface, anda manipulating rod, wherein a one end part of the manipulating rod comprises the support so that the sampling is conducted by said first capture zone. 2. The device according to claim 1, comprising at least one second capture zone on the second face such that the developed surface area of the second capture zone is greater than its surface. 3. The device according to claim 2, wherein the developed surface area of the at least one second capture zone is at least three times greater than its surface. 4. The device according to claim 1, comprising a plurality of first capture zones on the first face separated by first interval zones. 5. The device according to claim 4, comprising a plurality of second capture zones on the second face separated by second interval zones, wherein each first zone being opposite a second zone. 6. The device according to claim 4, comprising separators of the capture zones in the interval zones. 7. The device according to claim 6, wherein the separators are notches on the first and/or second face. 8. The device according to claim 1, wherein the support is in a wafer form. 9. The device according to claim 8, wherein the first and second faces of the support are planar with the exception of the capture zones and, optionally, notches on the first and/or second face. 10. The device according to claim 1, wherein the at least one first capture zone comprises a bottom wall provided with a plurality of protuberances. 11. The device according to claim 10, wherein the support is in plastic. 12. The device according to claim 10, wherein the support is a microtechnological substrate. 13. The device according to claim 12, wherein the substrate is silicon. 14. The device according to claim 10, wherein the height of the protuberances lies between 10 μm and 400 μm, and the surface of the protuberances is between 3×3 μm and 80×80 μm. 15. The device according to claim 10, wherein the protuberances are separated by spaces having a width of less than 50 μm. 16. The device according to claim 10, wherein the protuberances have a hexagonal or octagonal section. 17. The device according to claim 10, wherein the bottom wall and/or protuberances are functionalised. 18. The device according to claim 1, further comprising a guide sleeve for defining a pathway of the sampling device tissue subjected to the biopsy, wherein the manipulating rod is slidable within the guide sleeve. 19. The device according to claim 17, wherein the functionalisation comprises the presence of ligands secured to the surface by a silylated function. 20. The device according to claim 10, comprising microbeads in the spaces between the protuberances. 21. The device according to claim 20, wherein the microbeads are functionalised. 22. The device according to claim 1, wherein the at least one first capture zone comprises a cavity and microbeads arranged in the cavity. 23. The device according to claim 22, comprising a membrane which holds the microbeads in the capture zone. 24. The device according to claim 21, wherein the functionalisation of the microbeads comprises at least two different ligands specific to a majority protein and a minority protein. 25. The device according to claim 18, wherein a diameter of the manipulating rod and the guide sleeve is from a millimeter range to 100 μm. 26. The device according to claim 18, wherein the guide sleeve comprises means for providing a contact of the at least one capture zone and the molecules of biological interest only when the device is in contact with the molecules of biological interest. 27. The device according to claim 18, wherein the guide sleeve comprises means for providing a contact of the at least one capture zone and the molecules of biological interest only when the device is inside tissue to be analyzed. 28. The device according to claim 18, wherein the at least one first capture zone contacts the molecules of biological interest through a rotating or sliding window only when the device is inside tissue to be analyzed. 29. The device according to claim 18, wherein the at least one first capture zone contacts the molecules of biological interest only when the device is inside tissue to be analyzed, through a fixed window in the guide sleeve which is at a distance such that the at least one first capture zone faces the window when the manipulating rod longitudinally abuts the closed end of the guide sleeve. 30. The device according to claim 18, wherein the manipulating rod and the guide sleeve are made of a surgical stainless steel material. 31. The device according to claim 1, wherein the manipulating rod is made of a surgical stainless steel material. 32. A microtechnological sampling device for sampling molecules of biological interest by contact in an in vivo biopsy operation, the device comprising: a support having a first face opposite a second face, andat least one first capture zone on the first face such that the developed surface area of the at least one first capture zone is at least three times greater than its surface,wherein the at least one first capture zone captures the molecules of biological interest during the in vivo biopsy operation. 33. The device according to claim 32, wherein (i) the at least one first capture zone comprises at least one structural feature selected from the group consisting of a protruding structure, a cavity, and a combination thereof, and (ii) the developed surface of the at least one first capture zone includes the bottom surface of the capture zone and a surface area of each of the side walls of the at least one structural feature. 34. The device according to claim 32, comprising at least one second capture zone on the second face such that the developed surface area of the at least one second capture zone is greater than its surface, wherein (iii) the at least one second capture zone comprises at least one structural feature selected from the group consisting of a protruding structure, a cavity, and a combination thereof, and (iv) the developed surface of the at least one second capture zone includes the bottom surface of the capture zone and a surface area of each of the side walls of the at least one structural feature. 35. The device according to claim 32, wherein the developed surface area of the at least one second capture zone is at least three times greater than its surface. 36. The device according to claim 32, wherein the at least one structural feature is a protruding structure. 37. A mapping method for a tissue comprising: providing the microtechnological device of claim 1,placing the microtechnological device in the tissue,contacting the tissue with the capture zones, andanalysing a sample comprising the tissue. 38. The method according to claim 37, further comprising sectioning the device so as to separate the capture zones.