US2004031917A1PendingUtilityA1

Method for improving signal-to-noise ratios for atmospheric pressure ionization mass spectrometry

Priority: Nov 30, 2000Filed: Nov 28, 2001Published: Feb 19, 2004
Est. expiryNov 30, 2020(expired)· nominal 20-yr term from priority
Inventors:James Hager
H01J 49/0031H01J 49/0045
42
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Claims

Abstract

A method of improving the signal to noise ratio of an ion beam, utilizing a tandem mass spectrometer comprising two mass filters separated by a collision cell. The first mass filter is operated in a resolving mode such that only a narrow mass-to-charge range of precursor ions are stable and accelerated towards the collision cell which contains neutral gas to promote collisional activation and subsequent fragmentation of unwanted fragile ions while minimizing fragmentation of desired analyte ions. The second mass filter is scanned synchronously with the first mass filter such that only ions that do not fragment are recorded by the ion detector. Thus, analyte ions that have fragmentation values higher than unwanted background ions are preferentially detected thereby increasing the signal-to-noise ratio of the ion beam.

Claims

exact text as granted — not AI-modified
1 . A method of improving the signal to noise ratio of an ion beam, the method comprising: 
 (1) subjecting the ion beam to a first mass resolving step, to select precursor ions;    (2) colliding said precursor ions with a gas, to promote at least one of fragmentation and reaction of unwanted ions, whereby the unwanted ions generate secondary ions having a mass-tocharge ratio different from the mass-to-charge ratio of the precursor ions; and    (3) subjecting the ion beam including the secondary ions to a second mass resolving step, to reject ions with a mass-to-charge ratio different from the mass-to-charge ratio of the precursor ions, thereby increasing the signal-to-noise ratio of the ion beam.    
     
     
         2 . A method as claimed in  claim 1 , which includes effecting step (1) in a first mass spectrometer, step (2) in a collision cell, and step (3) in a second mass spectrometer.  
     
     
         3 . A method as claimed in  claim 2 , which includes scanning the first mass spectrometer through a range of mass-to-charge ratios and synchronously scanning the second mass spectrometer to select ions with the mass-to-charge ratio of the precursor ions.  
     
     
         4 . A method as claimed in  claim 3 , which includes operating the second mass spectrometer to reject ions having a mass-to-charge ratio less than the mass-to-charge ratio of the precursor ions.  
     
     
         5 . A method as claimed in  claim 3 , which includes operating the second mass spectrometer to reject both ions with a mass-to-charge ratio greater than the mass-to-charge ratio of the precursors ions and ions with a mass-to-charge ratio less than the mass-to-charge ratio of the precursor ions.  
     
     
         6 . A method as claimed in  claim 1 , which includes effecting step (1) in a first mass spectrometer and effecting steps (2) and (3) in a collision cell.  
     
     
         7 . A method as claimed in  claim 6 , which includes scanning the first mass spectrometer through a range of mass-to-charge ratios and synchronously scanning the collision cell through a range of mass-to-charge ratios including the mass-to-charge ratio of the precursor ions.  
     
     
         8 . A method as claimed in  claim 7 , which includes operating the collision cell to reject ions having a mass-to-charge ratio less than the mass-to-charge ratio of the precursor ions.  
     
     
         9 . A method as claimed in  claim 7 , which includes providing a pass band for the collision cell around the mass-to-charge ratio of the precursor ions, thereby to reject both ions with a mass-to-charge ratio greater than the mass-to-charge ratio of the precursor ions and ions with a mass-to-charge ratio less than the mass-to-charge ratio of the precursor ions.  
     
     
         10 . A method as claimed in  claim 5 , which includes providing each of the first and second mass spectrometers as a quadrupole mass filter and providing the second mass spectrometer with a detector.  
     
     
         11 . A method as claimed in  claim 10 , which includes providing the collision cell with a quadrupole rod set.  
     
     
         12 . A method as claimed in  claim 9 , which includes providing the first mass spectrometer as a quadrupole mass filter.  
     
     
         13 . A method as claimed in  claim 12 , which includes providing the collision cell with a quadrupole rod set and a detector.  
     
     
         14 . A method as claimed in  claim 3 , which includes providing the first mass spectrometer as a 3-dimensional ion trap mass spectrometer.  
     
     
         15 . A method as claimed in  claim 3 , which includes providing the first mass spectrometer as a 2-dimensional ion trap mass spectrometer.  
     
     
         16 . A method as claimed in  claim 3 , which includes providing the first mass spectrometer as a time-of-flight mass spectrometer.  
     
     
         17 . A method as claimed in  claim 10 ,  11 ,  12  or  13 , which includes operating the second mass spectrometer in an RF-only mode with a q value between 0.6 and 0.907 for selecting said precursor ions.  
     
     
         18 . A method as claimed in  claim 17  which includes operating the second mass spectrometer with a q value near 0.706 and with a DC value such that the second mass spectrometer operates near the tip of the first stability region.  
     
     
         19 . A method as claimed in  claim 11  or  13 , which includes operating the quadrupole rod set of the collision cell with a q value in the range of 0.6 to 0.907 for the mass-to-charge ratio of the precursor ions.  
     
     
         20 . A method as claimed in  claim 19 , which includes providing a DC signal to the second mass spectrometer and operating the second mass spectrometer with a q value near 0.76 to provide a passband around the tip of the first stability region.  
     
     
         21 . A method as claimed in  claim 3 ,  14 ,  15  or  16 , which includes providing th second mass spectrometer as a time-of-flight mass spectrometer.  
     
     
         22 . A method as claimed in  claim 3 ,  14 ,  15  or  16 , which includes providing the second mass spectrometer as a 3-dimensional ion trap mass spectrometer.  
     
     
         23 . A method as claimed in  claim 3 ,  14 ,  15  or  16 , which includes providing the second mass spectrometer as a 2-dimensional ion trap mass spectrometer.  
     
     
         24 . A method as claimed in  claim 3 , which includes providing said collision cell with an RF multipole rod set, supplying an RF voltage to the multipole rod set, and adjusting the RF voltage such that only said precursor ions of interest from the first mass spectrometer are transmitted through the collision cell.  
     
     
         25 . A method as claimed in  claim 3 , which includes supplying said collision cell with a neutral gas to maintain a desired pressure therein, to promote at least one of fragmentation and reaction of unwanted ions.  
     
     
         26 . A method as claimed in  claim 1 ,  3  or  7 , which includes subsequently subjecting the ion beam to at least one further stage of colliding the precursor ions with a gas to effect one of reaction and fragmentation to produce product ions and mass analyzing the product ions, thereby to effect multiple steps of mass spectroscopy.

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