Desorption electrospray ionization sampling without damaging an in vivo tissue sample
US-9538945-B2 · Jan 10, 2017 · US
US9700251B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9700251-B2 |
| Application number | US-201715400358-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 6, 2017 |
| Priority date | Jun 3, 2011 |
| Publication date | Jul 11, 2017 |
| Grant date | Jul 11, 2017 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention generally relates to enclosed desorption electrospray ionization probes, systems, and methods. In certain embodiments, the invention provides a source of DESI-active spray, in which a distal portion of the source is enclosed within a transfer member such that the DESI-active spray is produced within the transfer member.
Opening claim text (preview).
What is claimed is: 1. A method for analyzing a tissue sample, the method comprising: conducting a mass spectrometry technique on a tissue sample that comprises directing a liquid droplet spray discharge from a sampling probe onto the tissue sample, wherein the liquid droplet spray discharge from the sampling probe desorbs and ionizes an analyte from the tissue sample, and wherein the mass spectrometry technique is conducted in a manner that the tissue sample can be contacted with the liquid droplet spray discharge multiple times; transferring the ions of the analyte to a mass spectrometer; and analyzing the ions of the analyte in the mass spectrometer, thereby analyzing the tissue sample. 2. The method according to claim 1 , wherein the method is repeated at least a second time on the same tissue sample. 3. The method according to claim 1 , wherein the discharge is water. 4. The method according to claim 1 , wherein the sampling probe operates without voltage. 5. The method according to claim 1 , wherein the transferring step comprises sending the ions of the analyte through a transfer member that is operably coupled to the mass spectrometer. 6. The method according to claim 5 , wherein the method further comprises generating a gas flow in the transfer member via a pump in a direction opposite that of a first direction with enough counter-flow to reduce a velocity of the discharge. 7. The method accordingly to claim 6 , wherein a distal portion of the sampling probe is sealed within the transfer member. 8. The method according to claim 7 , wherein the distal portion of the transfer member is configured to sealably interact with the tissue sample. 9. The method according to claim 1 , wherein the mass spectrometer is a bench top mass spectrometer or a handheld mass spectrometer. 10. The method according to claim 1 , wherein the tissue sample is a brain tissue sample. 11. A method for analyzing a tissue sample, the method comprising: conducting a mass spectrometry technique on a tissue sample that comprises directing a liquid droplet spray discharge from a sampling probe onto the tissue sample, wherein the liquid droplet spray discharge from the sampling probe desorbs and ionizes a lipid from the tissue sample, and wherein the mass spectrometry technique is conducted in a manner that the tissue sample can be contacted with the liquid droplet spray discharge multiple times; transferring the ions of the lipid to a mass spectrometer; and analyzing the ions of the lipid in the mass spectrometer, thereby analyzing the tissue sample. 12. The method according to claim 11 , wherein the method is repeated at least a second time on the same tissue sample. 13. The method according to claim 11 , wherein the discharge is water. 14. The method according to claim 11 , wherein the sampling probe operates without voltage. 15. The method according to claim 11 , wherein the transferring step comprises sending the ions of the analyte through a transfer member that is operably coupled to the mass spectrometer. 16. The method according to claim 15 , wherein the method further comprises generating a gas flow in the transfer member via a pump in a direction opposite that of a first direction with enough counter-flow to reduce a velocity of the discharge. 17. The method accordingly to claim 16 , wherein a distal portion of the sampling probe is sealed within the transfer member. 18. The method according to claim 17 , wherein the distal portion of the transfer member is configured to sealably interact with the tissue sample. 19. The method according to claim 11 , wherein the mass spectrometer is a bench top mass spectrometer or a handheld mass spectrometer. 20. The method according to claim 11 , wherein the tissue sample is a brain tissue sample.
Dynamic spectrometers · CPC title
Source of blood · CPC title
Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value {; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue} (non-radiation detecting or locating of foreign bodies in blood A61B5/06) · CPC title
with means for introducing as a spray, a jet or an aerosol (electrospray ion sources H01J49/165) · CPC title
Blood sampling from a fluid line external to a patient, such as a catheter line, combined with an infusion line; Blood sampling from indwelling needle sets, e.g. sealable ports, luer couplings or valves · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.