High resolution sampling system for use with surface ionization technology

• US 7,777,181 B2
• Filed: 05/25/2007
• Issued: 08/17/2010
• 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 I
• Assistant Examiner(s): Sahu; Meenakshi S
• Application Number:
  US11/754,115
• Publication Number:
  US 20080067348A1
• Time in Patent Office: 1,180 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: 250/288
• 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 method for analyzing an analyte comprising:

directing a plurality of ionizing species at an analyte; and

orienting a tube relative to the analyte and the plurality of ionizing species;

wherein the analyte is at approximately atmospheric pressure, wherein ions formed from the analyte are transferred through the tube into a mass spectrometer.

2. The method of claim 1, wherein the plurality of ionizing species is formed from a DART source.

3. A system for analyzing an analyte comprising:

a spectrometer;

an apparatus for positioning the analyte, wherein the analyte is at approximately atmospheric pressure;

an apparatus for orienting one or more tubes around the analyte, wherein the one or more tubes have a proximal end and a distal end, wherein the proximal end of the one or more tubes is directed toward the analyte and the distal end of the one or more tubes is directed toward the spectrometer; and

an apparatus for generating a plurality of ionizing species, wherein the apparatus directs the plurality of ionizing species at the analyte, wherein the plurality of ionizing species form analyte ions, wherein the analyte ions enter the proximal end and exit the distal end of the one or more tubes, wherein the analyte ions enter the spectrometer and are analyzed.

4. The system of claim 3, wherein:

one or more of the tubes are one or more of flexible, curved and coiled.

5. The system of claim 3, wherein:

one or more of the tubes is a length of between;

a lower limit of approximately 10<sup>−

2</sup> m; and

an upper limit of approximately 3 m.

6. The system of claim 3, wherein:

one or more of the tubes is positioned a distance away from the analyte of between;

a lower limit of approximately 10<sup>−

5</sup> m; and

an upper limit of approximately 2×

10<sup>−

1</sup> m.

7. The system of claim 3, wherein the apparatus for generating a plurality of ionizing species is selected from the group consisting of a direct analysis real time (DART) source, a desorption electrospray ionization (DESI) source, an atmospheric laser desorption ionization source, a Corona discharge source, an inductively coupled plasma (ICP) source and a glow discharge source, wherein the spectrometer is a mass spectrometer.

8. The system of claim 3, wherein the diameter of one or more of the tubes is between:

a lower limit of approximately 10<sup>−

4</sup> m; and

an upper limit of approximately 10<sup>−

1</sup> m.

9. The system of claim 3, further comprising:

an apparatus to accurately adjust the position of one or more of the tubes relative to one or both the analyte and the plurality of ionizing species.

10. The system of claim 3, wherein:

one or more of the tubes 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.

11. The system of claim 3, wherein:

the proximal end of one or more of the one or more tubes is positioned relative to one or both the analyte and the plurality of ionizing species at an angle between;

a lower limit of approximately 10 degrees; and

an upper limit of approximately 90 degrees.

12. The system of claim 3, further comprising:

an inner conductive surface applied to one or more of the one or more tubes, wherein one or more potentials are applied to the inner conductive surface of one or more of the one or more tubes.

13. The system of claim 12, wherein one or more analyte ions are attracted to the potential applied to the inner conductive surface of the one or more tubes.

14. The system of claim 12, wherein the inner conductive surface inside diameter is between:

a lower limit of approximately 10<sup>−

4</sup> m; and

an upper limit of approximately 10<sup>−

1</sup> m.

15. The system of claim 12, wherein:

the inner tube conductive surface is positioned relative to one or both the analyte and the plurality of ionizing species at an angle between;

a lower limit of approximately 10 degrees; and

an upper limit of approximately 90 degrees.

16. The system of claim 12, wherein:

the inner tube conductive surface protrudes from the proximal end of one or more of the tubes 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 system of claim 12, wherein:

the inner tube conductive surface is positioned a distance away from the analyte of between;

a lower limit of approximately 10<sup>−

5</sup> m; and

an upper limit of approximately 10<sup>−

1</sup> m.

18. The system of claim 12, further comprising:

an apparatus to accurately adjust the position of the inner tube conductive surface relative to one or both the analyte and the plurality of ionizing species.

19. The system of claim 12, wherein:

the inner tube conductive surface extends inside the tube from the proximal end of the tube by a distance of between;

a lower limit of approximately 10<sup>−

4</sup> m; and

an upper limit of approximately 10<sup>−

1</sup> m.

20. The system of claim 12, further comprising:

locating the analyte on a reference position; and

an apparatus for locating the reference position and positioning the inner conductive surface relative to the reference position to analyze the analyte.

21. The system of claim 3, further comprising:

an outer conductive surface of one or more of the tubes, wherein one or more potentials are applied to the outer conductive surface of one or more of the tubes.

22. A system for analyzing an analyte comprising:

a spectrometer;

an apparatus for positioning the analyte, wherein the analyte is at approximately atmospheric pressure;

an apparatus for orienting one or more tubes around the analyte, wherein the one or more tubes have a proximal end and a distal end, wherein the proximal end of the one or more tubes is directed toward the analyte and the distal end of the one or more tubes is directed toward the spectrometer, wherein one or more of the tubes is comprised of two or more segments;

wherein the segment which constitutes the proximal end of the tube is the proximal segment and the segment which constitutes the distal end of the tube is the distal segment;

wherein the proximal segment of the tube has a smaller inner diameter than the distal segment of between;

a lower limit of 1% of the inside diameter of the distal segment; and

an upper limit of approximately 50% of the inside diameter of the distal segment; and

an apparatus for generating a plurality of ionizing species, wherein the apparatus directs the plurality of ionizing species at the analyte, wherein the plurality of ionizing species form analyte ions, wherein the analyte ions enter the proximal segment and exit the distal segment of the one or more tubes, wherein the analyte ions enter the spectrometer and are analyzed.