Apparatus and method for generating chemical signatures using differential desorption

• US 10,283,340 B2
• Filed: 08/17/2018
• Issued: 05/07/2019
• Est. Priority Date: 06/15/2014
• Status: Active Grant

• Current Assignee: Bruker Scientific LLC (Bruker Corporation)
• Original Assignee: IonSense, Inc. (Bruker Corporation)
• Inventors: Musselman, Brian D
• Primary Examiner(s): Maskell, Michael
• Application Number:
  US16/104,479
• Publication Number:
  US 20190006166A1
• Time in Patent Office: 263 Days
• Field of Search: 250281, 250282, 250288
• CPC Class Codes: G01N 1/4022 by thermal techniques; Phase changes
• CPC Class Codes: G01N 2001/028 Sampling from a surface, swabbing, vaporising
• CPC Class Codes: G01N 2030/009 Extraction
• CPC Class Codes: G01N 2030/062 extracting sample from raw material
• CPC Class Codes: H01J 49/0031 Step by step routines describing the use of the apparatus H01J49/0081 takes precedence
• CPC Class Codes: H01J 49/045 with means for using a nebulising gas, i.e. pneumatically assisted
• CPC Class Codes: H01J 49/16 using surface ionisation, e.g. field-, thermionic- or photo-emission
• CPC Class Codes: H01J 49/165 Electrospray ionisation

Abstract

The present invention is directed to a method and device to generate a chemical signature for a mixture of analytes. The present invention involves using a SPME surface to one or both absorb and adsorb the mixture of analytes. In an embodiment of the invention, the surface is then exposed to different temperature ionizing species chosen with appropriate spatial resolution to desorb a chemical signature for the mixture of analytes.

Claims

1. A method of analyzing a sample, the method comprising the steps:

contacting a sorbent coated screen with a sample, where the sorbent coated mesh is of sufficient size to permit multiple exposure of the sorbent coated mesh to a plurality of different temperature gasses from a desorption ionization source;

directing a carrier gas with a first temperature from the desorption ionization source at a first target area on the sorbent coated mesh to generate a plurality of first sample ions;

directing the carrier gas with a second temperature from the desorption ionization source at a second target area on the sorbent coated mesh to generate a plurality of second sample ions, where the second target area is not exposed to the carrier gas with the first temperature;

directing one or both the plurality of first sample ions and the plurality of second sample ions into an analysis instrument; and

analyzing one or both the plurality of first sample ions and the plurality of second sample ions, thereby analyzing the sample.

2. The method of claim 1, where the sorbent coated mesh comprises one or more materials selected from the group consisting of wire mesh screen, paper screen, plastic screen, fiber screen, cloth screen, polymer screen, silica screen, Teflon screen, polymer impregnated Teflon screen, cellulose screen, and hydrophobic support material coated and impregnated mesh screen.

3. The method of claim 1, where the sorbent coated mesh comprises a sorbent coating of one or more materials selected from the group consisting of C-18, PDMS/divinyl-benzene, PDMS, cation exchange, C-8, C-4, carbon, functionalized carbon, tenax and inorganic materials.

4. The method of claim 1, where the carrier gas is selected from the group consisting of helium, nitrogen, oxygen, neon, argon, krypton, and xenon.

5. The method of claim 1, where the temperature of one or both the carrier gas at the first temperature and the carrier gas at the second temperature is between:

a lower limit of approximately 270°

K; and

an upper limit of approximately 600°

K.

6. The method of claim 1, where the analysis instrument is a mass spectrometer in one or both positive and negative ionization modes.

7. The method of claim 1, where the desorption ionization source is selected from the group consisting of DART, DESI, MALDI, UV laser, IR laser, APCI, directed electrospray, electrospray, dielectric barrier discharge, and flowing after-glow plasma.

8. The method of claim 1, where a holder positions the sorbent coated mesh while one or both the carrier gas with the first temperature and the carrier gas with the second temperature impacts the sorbent coated screen.

9. The method of claim 1, where the sorbent coated mesh is contacted with the sample in a plurality of locations on the sorbent coated screen.

10. A method of analyzing a sample, the method comprising the steps:

contacting a sorbent coated fiber with a sample, where the sorbent coated fiber is of sufficient size to permit multiple exposure of the sorbent coated fiber to a plurality of different temperature gasses from a desorption ionization source;

directing a carrier gas with a first temperature from the desorption ionization source at a first target area on the sorbent coated fiber to generate a plurality of first sample ions;

directing the carrier gas with a second temperature from the desorption ionization source at a second target area on the sorbent coated fiber to generate a plurality of second sample ions, where the second temperature is substantially constant;

directing one or both the plurality of first sample ions and the plurality of second sample ions into an analysis instrument; and

analyzing one or both the plurality of first sample ions and the plurality of second sample ions, thereby analyzing the sample.

11. The method of claim 10, where the sorbent coated fiber comprises one or more of a loop of wire, a segment of wire, a metal ribbon, a metal strand or an un-insulated wire, animal string, paper, perforated paper, silica, fused silica, plastic, plastic foam, polymer, Teflon, polymer impregnated Teflon, cellulose, and hydrophobic support material coated fiber and impregnated fiber.

12. The method of claim 10, where the sorbent coated fiber comprises a sorbent coating of one or more materials selected from the group consisting of C-18, PDMS/divinyl-benzene, PDMS, cation exchange, C-8, C-4, carbon, functionalized carbon, tenax and inorganic materials.

13. The method of claim 10, where the carrier gas is selected from the group consisting of helium, nitrogen, oxygen, neon, argon, krypton, and xenon.

14. The method of claim 10, where the temperature of one or both the carrier gas at the first temperature and the carrier gas at the second temperature is between:

a lower limit of approximately 270°

K; and

an upper limit of approximately 600°

K.

15. The method of claim 10, where the desorption ionization source is selected from the group consisting of DART, DESI, MALDI, UV laser, IR laser, APCI, directed electrospray, electrospray, dielectric barrier discharge, and flowing after-glow plasma.

16. The method of claim 10, where a holder positions the sorbent coated fiber while one or both the carrier gas with the first temperature and the carrier gas with the second temperature impacts the sorbent coated fiber.

17. The method of claim 10, where the sorbent coated fiber is contacted with the sample in a plurality of locations on the sorbent coated fiber.

18. A method of analyzing a sample, the method comprising the steps:

contacting a sorbent coated filament with a sample, where the sorbent coated filament is of sufficient size to permit multiple exposure of the sorbent coated filament to a plurality of different temperature gasses from a desorption ionization source;

directing a carrier gas with a first temperature from the desorption ionization source at a first target area on the sorbent coated filament to generate a plurality of first sample ions;

directing the carrier gas with a second temperature from the desorption ionization source at a second target area on the sorbent coated filament to generate a plurality of second sample ions, where the second target area is not exposed to the carrier gas with the first temperature;

directing one or both the plurality of first sample ions and the plurality of second sample ions into an analysis instrument; and

analyzing one or both the plurality of first sample ions and the plurality of second sample ions, thereby analyzing the sample.

19. The method of claim 18, where the sorbent coated fiber comprises a sorbent coating of one or more materials selected from the group consisting of C-18, PDMS/divinyl-benzene, PDMS, cation exchange, C-8, C-4, carbon, functionalized carbon, tenax and inorganic materials.

20. The method of claim 18, where one or both the carrier gas at the first temperature and the carrier gas at the second temperature is between:

a lower limit of approximately 270°

K; and

an upper limit of approximately 600°

K.