Method for tandem mass spectrometry analysis in ion trap mass analyzer

Patent metadata

Field	Value
Publication number	US-9640377-B2
Application number	US-201414905912-A
Country	US
Kind code	B2
Filing date	Jul 4, 2014
Priority date	Jul 18, 2013
Publication date	May 2, 2017
Grant date	May 2, 2017

Abstract

This invention is related to a tandem mass spectrometric analysis method in ion trap mass analyzer. Such method comprise three stages as represented by selective isolation, collision induced disassociation and mass scanning of ion. At the collision induced isolation stage, this invention is expected to endow parent ion of certain mass-charge ratio with energy through resonance excitation by changing cycle of radio frequency signals, namely frequency of radio frequency voltage imposed on the ion trap; such high-energy ions produced through resonance excitation are to be disassociated through collision with neutral molecules in the ion trap, which will further generate product ion to realize tandem mass spectrometric analysis. Advantage of this method lies in the fact that it can realize collision induced disassociation by changing scanning cycle at the stage of collision induced disassociation stage through software configuration, which can significantly simplify experimental devices and methods for tandem mass spectrometric analysis.

First claim

The invention claimed is:

1. A tandem mass spectrometric analysis method in an ion trap mass analyzer, comprising three stages as represented by
selective isolation, collision induced disassociation and mass scanning of ion in proper sequence, wherein:
selected parent ion is to be isolated at said stage of selective isolation of ion; whereas parent ion isolated is to be confined in the ion trap through collision with neutral gas molecules and cooling under the action of electric field produced by working voltage in ion trap;
at said collision induced disassociation stage, cycle of ion excited radio frequency voltage signals imposed on the ion trap pole is changed, to further change cycle of radio frequency voltage produced by resonance excitation of ion; as a result of it, ion of certain mass-charge ratio is to be provided with higher energy, subjecting to resonance excitation by ion excited radio frequency voltage of certain cycle or frequency; ion subjecting to resonance excitation is to be disassociated to generate fragment ion through collision with neutral molecules in ion trap; fragment ion subjecting to cooling in ion trap is to be confined for follow-up mass analysis;
at said mass scanning and analysis stage, ion in ion trap is to subject to resonance excitation under the action of dipolar excitation voltage as imposed on the electrode of ion trap: eventually, it is to be discharged from lead-out bole or groove of ion extraction electrode to capture mass spectrometry signals, subjecting to detection on ion detector outside ion trap,
wherein voltage amplitude and duty ratio of digital bound radio voltage remain unchanged at said stage of collision induced disassociation; cycle of digital radio voltage is to be selected while its initial and final cycle value remain unchanged; further select a certain frequency division number n, namely frequency relation β between cycle of ion excited radio voltage and digital bound radio voltage (n=β/2); in view of relation with value β, cycle of ion resonance excited radio voltage is to be changed while duty ratio remains unchanged; accompanied by variation to ion resonance excited radio voltage, collision energy is to be produced through resonance motion among ions.

2. The tandem mass spectrometric analysis method according to claim 1 , wherein mass-to-charge ratio is to subject to linear scanning at said mass scanning and analysis stage.

3. The tandem mass spectrometric analysis method according to claim 1 , wherein wave form of ion excited radio voltage signals imposed is digital square wave or sine wave at said stage of collision induced disassociation.

4. The tandem mass spectrometric analysis method according to claim 1 , wherein neutral cooling gas delivered to ion trap is to be supplemented at the said stage of collision induced disassociation.

5. The tandem mass spectrometric analysis method according to claim 1 , wherein frequency and amplitude of digital bound radio voltage are in constant value at said stage of collision induced disassociation.

6. The said tandem mass spectrometric analysis method according to claim 1 , wherein the frequency ratio between ion excited radio voltage and digital bound radio voltage is random at the said stage of collision, induced disassociation.

7. The tandem mass spectrometric analysis method according to claim 1 , wherein said ion trap is a 3D or 2D linear ion trap.

8. The tandem mass spectrometric analysis method according to claim 1 , wherein said ion trap is ion trap array or field regulated ion trap.

Assignees

• Univ Fudan

Inventors

• Xu Fuxing
• Wang Liang
• Ding Chuanfan

Classifications

• H01J49/0031

  Step by step routines describing the use of the apparatus (H01J49/0081 takes precedence) · CPC title

• H01J49/0081 Primary

  Tandem in time, i.e. using a single spectrometer · CPC title

• H01J49/0063

  by applying a resonant excitation voltage · CPC title

• H01J49/427

  Ejection and selection methods · CPC title