Apparatus and method for generating chemical signatures using differential desorption
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.
1. A device comprising:
a desorption ionization source adapted to generate a first stream of energetic particles at a first temperature and a second stream of energetic particles at a second temperature, where the desorption ionization source is adapted to direct the first stream of energetic particles towards a target area on the sorbent coated fiber, where the sorbent coated fiber has a length and a diameter, where the sorbent coated fiber has been in contact with a sample, where the first stream of energetic particles forms a plurality of first sample ions, where the desorption ionization source is adapted to direct the second stream of energetic particles towards the target area on the sorbent coated fiber, where the second stream of energetic particles forms a plurality of second sample ions; and
an analyzer, adapted to analyze one or both one or more of the plurality of first sample ions and one or more of the plurality of second sample ions.
2. The device of claim 1 , where the length of the sorbent coated fiber is between:
a lower limit of approximately 4 mm; and
an upper limit of approximately 150 mm.
3. The device of claim 1 , where the diameter of the sorbent coated fiber is between:
a lower limit of approximately 0.05 mm; and
an upper limit of approximately 2 mm.
4. The device of claim 1 , further comprising a holder adapted to hold the sorbent coated fiber while one or both the first stream of energetic particles and the second stream of energetic particles impacts the sorbent coated fiber.
5. The device of claim 1 , where the desorption ionization source is an electrospray ionization source.
6. The device of claim 1 , where the desorption ionization source is a DART ionization source.
7. The device of claim 1 , where the desorption ionization source utilizes a stream of carrier gas molecules to direct one or both the first energetic particles and the second energetic particles at the target area.
8. The device of claim 7 , where the carrier gas is selected from the group consisting of helium, nitrogen, oxygen, neon, argon, krypton, and xenon.
9. The device of claim 7 , where the temperature of the stream of carrier gas molecules is between:
a lower limit of approximately 270° K; and
an upper limit of approximately 600° K.
10. The device of claim 1 , where the step of analyzing comprises analyzing molecule ions with a mass spectrometer in one or both positive and negative ionization modes.
11. A device comprising:
a desorption ionization source adapted to generate a plurality of first sample ions and a plurality of second sample ions, where the plurality of first sample ions are formed from a first stream of energetic particles with a first temperature impacted a sorbent coated fiber and the plurality of second sample ions are formed from a second stream of energetic particles with a second temperature impacted the sorbent coated fiber; and
an analyzer, adapted to analyze one or more of the plurality of first sample ions and the plurality of second sample ions.
12. The device of claim 11 , where the sorbent coated fiber has a length between:
a lower limit of approximately 4 mm; and
an upper limit of approximately 150 mm.
13. The device of claim 11 , where the sorbent coated fiber has a diameter between:
a lower limit of approximately 0.05 mm; and
an upper limit of approximately 2 mm.
14. The device of claim 11 , further comprising a holder adapted to hold the sorbent coated fiber while one or both the first stream of energetic particles and the second stream of energetic particles impacts the sorbent coated fiber.
15. The device of claim 11 , 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 device of claim 11 , where the desorption ionization source utilizes a stream of carrier gas molecules to direct one or both the first energetic particles and the second energetic particles at the sorbent coated fiber.
17. The device of claim 16 , where the carrier gas is selected from the group consisting of helium, nitrogen, oxygen, neon, argon, krypton, and xenon.
18. The device of claim 16 , where the temperature of the stream of carrier gas molecules is between:
a lower limit of approximately 270° K; and
an upper limit of approximately 600° K.
19. A device comprising:
a first desorption ionization source adapted to generate a plurality of first sample ions formed from a first stream of energetic particles with a first temperature impacting a sorbent coated fiber;
a second desorption ionization source adapted to generate a plurality of second sample ions formed from a second stream of energetic particles with a second temperature impacting the sorbent coated fiber; and
an analyzer, adapted to analyze one or more of the plurality of first sample ions and the plurality of second sample ions.
20. The device of claim 19 , where one or both the first desorption ionization source and the second desorption ionization source are 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.