Apparatus and method for thermal assisted desorption ionization systems

• US 8,822,949 B2
• Filed: 02/02/2012
• Issued: 09/02/2014
• Est. Priority Date: 02/05/2011
• Status: Active Grant

• Current Assignee: Bruker Scientific LLC (Bruker Corporation)
• Original Assignee: IonSense, Inc. (Bruker Corporation)
• Inventors: Krechmer, Jordan, Musselman, Brian D.
• Primary Examiner(s): Vanore, David A
• Application Number:
  US13/364,322
• Publication Number:
  US 20120199735A1
• Time in Patent Office: 943 Days
• Field of Search: 250/423.R, 250/425, 250/426, 250/493.1
• US Class Current: 250/426
• CPC Class Codes: G01N 27/626 using heat to ionise a gas
• CPC Class Codes: G01N 27/64 using wave or particle radiation to ionise a gas, e.g. in an ionisation chamber
• CPC Class Codes: H01J 27/26 using surface ionisation, e.g. field effect ion sources, thermionic ion sources H01J27/20, H01J27/24 take precedence
• CPC Class Codes: H01J 49/004 Combinations of spectrometers, tandem spectrometers, e.g. MS/MS, MSn
• CPC Class Codes: H01J 49/04 Arrangements for introducing or extracting samples to be analysed, e.g. vacuum locks; Arrangements for external adjustment of electron- or ion-optical components
• CPC Class Codes: H01J 49/0431 for liquid samples interfaces to liquid chromatographs G01N30/7233
• CPC Class Codes: H01J 49/049 with means for applying heat to desorb the sample; Evaporation
• CPC Class Codes: H01J 49/10 Ion sources; Ion guns
• CPC Class Codes: H01J 49/126 Other arc discharge ion sources using an applied magnetic field
• CPC Class Codes: H01J 49/14 using particle bombardment, e.g. ionisation chambers
• CPC Class Codes: H01J 49/24 Vacuum systems, e.g. maintaining desired pressures
• CPC Class Codes: Y10T 436/24 Nuclear magnetic resonance, electron spin resonance or other spin effects or mass spectrometry

Abstract

The present invention is directed to a method and device to desorb an analyte using heat to allow desorption of the analyte molecules, where the desorbed analyte molecules are ionized with ambient temperature ionizing species. In various embodiments of the invention a current is passed through a mesh upon which the analyte molecules are present. The current heats the mesh and results in desorption of the analyte molecules which then interact with gas phase metastable neutral molecules or atoms to form analyte ions characteristic of the analyte molecules.

Claims

1. A device for analyzing an analyte comprising:

a spectrometer configured for analyzing the analyte, with an entrance for accepting analyte ions and a detector for detecting analyzed analyte ions;

an atmospheric pressure source configured for generating ionizing species;

a supply adapted to one or more of generate heat, transfer heat, conduct heat and radiate heat; and

one or more mesh positioned between the source and the spectrometer, where the analyte is introduced on or near the one or more mesh, where the supply can one or more of generate heat, transfer heat, conduct heat and radiate heat to the analyte, where analyte molecules desorbed from the one or more mesh interact with the ionizing species generated by the source to form a plurality of analyte ions which enter the spectrometer and are analyzed.

2. The device of claim 1, further comprising a gas ion separator positioned between the one or more mesh and the spectrometer entrance.

3. The device of claim 1, wherein the atmospheric pressure source is selected from the group of sources consisting of a direct analysis real time (DART), Plasma Assisted Desorption/Ionization (PADI), Dielectric Barrier Discharge ionization source (DBDI or DCBI), Desorption Atmospheric Pressure Chemical Ionization (DAPCI), Desorption Sonic Spray Ionization (DeSSI), Desorption Atmospheric Pressure Photoionization (DAPPI), and Flowing Atmospheric-Pressure Afterglow (FAPA) and a desorption electrospray ionization (DESI), an atmospheric laser desorption ionization, a Corona discharge, an inductively coupled plasma (ICP) and a glow discharge source.

4. The device of claim 1, where the supply is adapted to deliver a power to one of the one or more mesh of between:

a lower limit of approximately 10² Watts; and

an upper limit of approximately 10³ Watts.

5. The device of claim 1, where the region between the entrance and the detector of the spectrometer is at approximately atmospheric pressure.

6. The device of claim 1, where the supply can be configured to apply a first potential to a first mesh containing the analyte.

7. The device of claim 6, where the first potential is approximately the same potential as a potential applied to the entrance to the spectrometer.

8. The device of claim 6, where the supply can be configured to apply a second potential to a second mesh, where the second potential is different from the first potential.

9. The device of claim 8, where the kinetic energy of the analyte ions desorbed from the first mesh can be adjusted by adjusting the second potential.

10. The device of claim 1, where the supply is configured to independently heat a first and a second location on at least one of the one or more mesh, where the first location is different than the second location.

11. The device of claim 1, where a first mesh is orientated relative to a second mesh, where the ionizing species contact the first mesh before the ionizing species contact the second mesh.

12. The device of claim 11, where a tube is used to deliver a solution containing the analyte on or near the first wire mesh.

13. A device for derivatizing and analyzing an analyte comprising:

a spectrometer for analyzing the analyte, where the spectrometer has an entrance;

a source configured for generating ionizing species, where the source has a proximal end and a distal end, where the distal end is proximal to the spectrometer entrance; and

one or more mesh positioned in the atmospheric pressure region, where the analyte and a derivatizing reagent are applied on a mesh, where the ionizing species generated by the source are directed at the mesh, where analyte molecules are desorbed from the mesh and form a plurality of analyte ions which enter the spectrometer.

14. The device of claim 13, where the region between the distal end of the source and the entrance of the spectrometer is at approximately atmospheric pressure.

15. The device of claim 13, where the ionizing species are generated at least in part by heating an ionizing gas.

16. The device of claim 13, where the mesh comprises two or more connected filaments, where one or more of the filaments are selected from the group consisting of a metal, an animal string, paper, perforated paper, fiber, cloth, silica, plastic, plastic foam, polymer, teflon, polymer impregnated teflon, cellulose, hydrophobic support material coated filament and hydrophobic support material impregnated filament.

17. A device for analyzing an analyte comprising:

an ion mobility spectrometer including an entrance and a detector;

a source configured for generating ionizing species;

a supply adapted to one or more of generate heat, transfer heat, conduct heat, radiate heat and apply an electric potential; and

two or more mesh positioned between the source and the spectrometer, where the analyte is applied on or near a first mesh, where the supply can one or more of generate heat, transfer heat, conduct heat and radiate heat to the analyte to desorb molecules of the analyte, where molecules desorbed from the first mesh interact with the ionizing species generated by the source to form analyte ions.

18. The device of claim 17, where the ion mobility spectrometer is operated at approximately atmospheric pressure.

19. The device of claim 17, where at least one of the two or more mesh have a potential equal to the potential applied to the ion mobility spectrometer.

20. The device of claim 17, where an electric potential is applied to a second mesh, where the kinetic energy of the analyte ions are altered by the potential applied to the second mesh.