IP Library Granted Patent US 8,785,848
Granted Patent B2
US 8,785,848 · App. 13/792,043 · Granted Jul 22, 2014

Parallel ion mass and ion mobility analysis

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Quick Facts
Patent No.
US 8,785,848
App. No.
13/792,043
Granted
Jul 22, 2014
Kind
B2
Abstract

The present invention relates to a parallel IMS and MS measurement method where a sample flow is split and delivered to an IMS and a MS in parallel. A parallel acquisition MS/IMS method is used to supplement LC-MS and or MS data by using a synchronized MS/IMS acquisition.

Claims (24)

1. A method for identifying components of a sample in mass spectral data comprising:

a. splitting a sample flow into a mass analyzer and an ion mobility based separator for independent parallel ion mass and ion mobility analysis;

b. acquiring mass spectral data of the sample using the mass analyzer while synchronously acquiring ion mobility data using the ion mobility based separator;

c. performing a normalization between corresponding peaks of the mass spectral data and that of the peaks in the ion mobility data; and

d. displaying which ion mobility peaks correspond to the mass spectra peaks.

2. The method in claim 1 , wherein the normalization is accomplished by using a timing index and/or a calibrant.

3. The method in claim 2 , wherein the timing index is created based on the timing of each flow component's arrival at one or more analytical instrument.

4. The method in claim 3 , wherein the analytical instrument can be, but not limited to: IMS, MS, conductivity detector, UV detector, diode-array or a detector.

5. The method in claim 2 , further comprises a LC separation prior to splitting the sample flow into the mass analyzer and the ion mobility based separator.

6. The method in claim 2 , wherein the timing index is created based on the components of the sample's chromatography properties whereby the resolution obtained using the LC separation is used as a reference to determine the timing index resolution.

7. The method in claim 2 , wherein the calibrant is added to the sample flow or as one of the components of the sample.

8. The method in claim 1 , wherein the sample flow comprises isomers.

9. The method in claim 8 , wherein the isomers are constitutional isomers.

10. The method in claim 9 , wherein the constitutional isomers are skeletal isomers.

11. The method in claim 9 , wherein the constitutional isomers are regioisomers.

12. The method in claim 9 , wherein the constitutional isomers are functional group isomers.

13. The method in claim 9 , wherein the constitutional isomers are topoisomers.

14. The method in claim 8 , wherein the isomers are stereoisomers.

15. The method in claim 14 , wherein the stereoisomers are diastereomers.

16. The method in claim 14 , wherein the stereoisomers are enantiomers.

17. The method in claim 14 , wherein the stereoisomers are cis-trans isomers.

18. The method in claim 14 , wherein the stereoisomers are conformers.

19. The method in claim 14 , wherein the stereoisomers are rotamers.

20. The method in claim 14 , wherein the stereoisomers are atropisomers.

Assignments (1)
NUNC PRO TUNC ASSIGNMENT Recorded Apr 10, 2015
From: WU, CHING; KRUEGER, CLINTON ALAWN; MIDEY, ANTHONY JOSEPH; OSGOOD, MARK A.
To: EXCELLIMS CORPORATION
Reel/Frame 035411/0589 →