Membrane for holding samples for use with surface ionization technology

• US 8,481,922 B2
• Filed: 12/23/2011
• Issued: 07/09/2013
• Est. Priority Date: 05/26/2006
• Status: Active Grant

• Current Assignee: Bruker Scientific LLC (Bruker Corporation)
• Original Assignee: IonSense, Inc. (Bruker Corporation)
• Inventors: Musselman, Brian D.
• Primary Examiner(s): Berman, Jack
• Assistant Examiner(s): SAHU, MEENAKSHI S
• Application Number:
  US13/336,984
• Publication Number:
  US 20120112057A1
• Time in Patent Office: 564 Days
• Field of Search: 250286-288, 250/281, 250/282, 250/292, 250/294, 250/295, 250/396.R, 250/423.R, 250/424
• US Class Current: 250/281
• CPC Class Codes: H01J 49/0404 Capillaries used for transferring samples or ions electrospray nozzles H01J49/167
• CPC Class Codes: H01J 49/0409 Sample holders or containers containers for retaining a material to be analyzed, B01L3/50, for DNA, C12Q1/6834, for biological materials, G01N33/543
• CPC Class Codes: H01J 49/0459 for solid samples
• CPC Class Codes: H01J 49/16 using surface ionisation, e.g. field-, thermionic- or photo-emission

Abstract

The present invention is a device to restrict the sampling of analyte ions and neutral molecules from surfaces with mass spectrometry and thereby sample from a defined area or volume. In various embodiments of the present invention, a tube is used to sample ions formed with a defined spatial resolution from desorption ionization at or near atmospheric pressures. In an embodiment of the present invention, electrostatic fields are used to direct ions to either individual tubes or a plurality of tubes positioned in close proximity to the surface of the sample being analyzed. In an embodiment of the present invention, wide diameter sampling tubes can be used in combination with a vacuum inlet to draw ions and neutrals into the spectrometer for analysis. In an embodiment of the present invention, wide diameter sampling tubes in combination with electrostatic fields improve the efficiency of ion collection.

Claims

1. A device for analyzing an analyte comprising:

a tube with a proximal end and a distal end, wherein the distal end of the tube transfers one or more analyte ions into a mass spectrometer;

a membrane positioned one or both adjacent to the tube and inside the tube, wherein the ionizing species contacts the membrane one or both before and upon entering the proximal end of the tube, wherein the membrane has been in contact with the analyte prior to being positioned relative to the tube; and

a component for generating a plurality of ionizing species, wherein the plurality of ionizing species are directed at one or both the membrane and the proximal end of the tube.

2. The device of claim 1, wherein:

the tube is made from one or more materials chosen from the group consisting of metal, glass, plastic, conductively coated plastic, conductively coated fused silica, non conductively coated plastic, non conductively coated fused silica, glass lined metal tube and resistively coated glass.

3. The device of claim 1, wherein the diameter of the tube is between:

a lower limit of approximately 10<sup>−

3</sup> m; and

an upper limit of approximately 10<sup>−

1</sup> m.

4. The device of claim 1, wherein:

the tube is positioned a distance away from the membrane between;

a lower limit of approximately 10<sup>−

5</sup> m; and

an upper limit of approximately 10<sup>−

2</sup> m.

5. The device of claim 1, wherein the ionizing species component is selected from the group consisting of a direct analysis real time (DART), a desorption electrospray ionization (DESI), an atmospheric laser desorption ionization, a Corona discharge, an inductively coupled plasma (ICP) and a glow discharge source.

6. The device of claim 1, wherein the membrane includes one or more plastic materials.

7. The device of claim 1, wherein the membrane traps molecules for analysis based on one or more interactions selected from the group consisting of affinity, non-covalent and covalent bonding.

8. The device of claim 1, further comprising:

an inner surface of the tube that is conductive, wherein a first potential is applied to the inner surface of the tube; and

an outer surface of the tube that is conductive, wherein a second potential is applied to the outer surface of the tube, wherein one or more analyte ions are attracted to the potential applied to the inner tube thereby pass through the tube into the mass spectrometer.

9. A device for analyzing an analyte comprising:

an apparatus for generating a plurality of ionizing species,

an apparatus for analyzing ions formed from the analyte;

an outer tube with a proximal and a distal end having a major axis; and

an inner tube with a proximal and a distal end having a major axis;

wherein the outer tube and the inner tube major axis are substantially co-axial, wherein the outer tube diameter is greater than the inner tube diameter;

wherein the inner tube is positioned inside the outer tube;

wherein the membrane is positioned one or both inside the inner tube and adjacent to the tube;

wherein the analyte is present on the membrane;

wherein the mass spectrometer is positioned at the distal exit of one or both the inner tube and the outer tube;

wherein the plurality of ionizing species are directed towards the proximal end of the inner tube, wherein the ionizing species interact with the analyte on the membrane, wherein a plurality of analyte ions are formed by the interaction of the ionizing species with the analyte in the membrane, wherein the ionizing species enter the inner tube in a direction parallel to the inner tube major axis and are transferred into the apparatus for analyzing the plurality of analyte ions.

10. The device of claim 9, wherein:

one or both the inner tube and the outer tube are made from one or more materials chosen from the group consisting of metal, glass, plastic, conductively coated plastic, conductively coated fused silica, non conductively coated plastic, non conductively coated fused silica, glass lined metal tube and resistively coated glass.

11. The device of claim 9, wherein:

an inner surface of the inner tube is conductive, wherein a first potential is applied to the inner surface of the inner tube, wherein an outer surface of the outer tube is conductive, wherein a second potential is applied to the outer surface of the outer tube.

12. The device of claim 9, wherein the diameter of the inner tube is between:

a lower limit of approximately 4×

10<sup>−

4</sup> m; and

an upper limit of approximately 10<sup>−

1</sup> m.

13. The device of claim 9, wherein:

the proximal end of the inner tube protrudes from the proximal end of the outer tube by a distance of between;

a lower limit of approximately 10<sup>−

4</sup> m; and

an upper limit of approximately 10<sup>−

2</sup> m.

14. The device of claim 9 wherein:

the proximal end of the inner tube is positioned a distance away from an area where the ionizing species interacts with the membrane of between;

a lower limit of approximately 10<sup>−

5</sup> m; and

an upper limit of approximately 10<sup>−

1</sup> m.

15. The device of claim 14, further comprising:

an apparatus to accurately adjust the position of the proximal end of the inner tube from the membrane.

16. The device of claim 9, wherein:

the proximal end of the outer tube protrudes from the proximal end of the inner tube by a distance of between;

a lower limit of approximately 10<sup>−

4</sup> m; and

an upper limit of approximately 10<sup>−

2</sup> m.

17. The device of claim 9, wherein:

the membrane is positioned in the inner tube at an angle between;

a lower limit of approximately 10 degrees; and

an upper limit of approximately 90 degrees.

18. The device of claim 9, wherein:

the membrane is positioned in the inner tube at a distance from the proximal end of between;

a lower limit of approximately 10<sup>−

2</sup> m; and

an upper limit of approximately 10¹ m.

19. A method for analyzing an analyte comprising:

positioning a membrane which has been in contact with the analyte one or both adjacent to a tube and inside the tube, wherein the tube has a proximal end and a distal end, wherein the distal end of the tube transfers analyte ions into a mass spectrometer; and

directing a plurality of ionizing species at one or both the membrane and the proximal end of the tube;

wherein ions formed from the analyte are transferred into the mass spectrometer.

20. The method of claim 19, wherein the membrane is a thin perforated plastic membrane.