Tuned synthetic dendrimer calibrants for mass spectrometry

Patent metadata

Field	Value
Publication number	US-12087564-B2
Application number	US-202117557879-A
Country	US
Kind code	B2
Filing date	Dec 21, 2021
Priority date	May 21, 2012
Publication date	Sep 10, 2024
Grant date	Sep 10, 2024

Abstract

Provided are synthetic dendrimer calibrants for mass spectrometry. The calibrants are distinguished by their relative case and rapidity of synthesis, comparatively low cost, long shelf life, high purity, and amenability to batch synthesis as mixtures. The latter characteristic enables parallel preparation of higher molecular weight compounds displaying useful distributions of discrete molecular weights, thereby providing multi-point mass spectrometry calibration standards. Methods of making, tuning and using said calibrants are provided.

First claim

What is claimed is:

1. A composition comprising:
a first dendrimer comprising a first core molecule, wherein said first core molecule is selected from the group consisting of: a molecule comprising between 1 and 8 alcohol functionalities, a molecule comprising between 1 and 8 amine functionalities, and a molecule comprising at least one amine functionality and at least one alcohol functionality wherein the combined number of amine and alcohol functionalities of said first core molecule is at least 2 but no greater than 8; and
a second dendrimer comprising a second core molecule, wherein said second core molecule is selected from the group consisting of: a molecule comprising between 1 and 8 alcohol functionalities, a molecule comprising between 1 and 8 amine functionalities, and a molecule comprising at least one amine functionality and at least one alcohol functionality wherein the combined number of amine and alcohol functionalities of said second core molecule is at least 2 but no greater than 8;
wherein said first core molecule has a different number of total alcohol functionalities and amine functionalities than said second core molecule;
wherein the first dendrimer and the second dendrimer each have a mass defect falling within a scarcine valley of an average amino acid; and
wherein the first core molecule and the second core molecule each comprise a mass defect marker selected from the group consisting of phosphorous, iodine, bromine, and combinations thereof.

2. A method of calibrating a mass spectrometer, the method comprising:
providing a composition comprising
a first dendrimer comprising a first core molecule, wherein said first core molecule is selected from the group consisting of: a molecule comprising between 1 and 8 alcohol functionalities, a molecule comprising between 1 and 8 amine functionalities, and a molecule comprising at least one amine functionality and at least one alcohol functionality, wherein the combined number of amine and alcohol functionalities of said first core molecule is at least 2 but no greater than 8, and the first core molecule comprises three iodine atoms; and
a second dendrimer comprising a second core molecule, wherein said second core molecule is selected from the group consisting of: a molecule comprising between 1 and 8 alcohol functionalities, a molecule comprising between 1 and 8 amine functionalities, and a molecule comprising at least one amine functionality and at least one alcohol functionality wherein the combined number of amine and alcohol functionalities of said second core molecule is at least 2 but no greater than 8;
wherein said first core molecule has a different number of total alcohol functionalities and amine functionalities than said second core molecule; and
wherein said composition has physical properties;

ionizing at least a portion of said composition;
collecting data from said ionized portion of said composition; and
relating said data to said physical properties.

3. A method of calibrating a mass spectrometer, the method comprising:
providing a composition comprising a first dendrimer comprising a first core molecule, wherein said first core molecule is selected from the group consisting of: a molecule comprising between 1 and 8 alcohol functionalities, a molecule comprising between 1 and 8 amine functionalities, and a molecule comprising at least one amine functionality and at least one alcohol functionality wherein the combined number of amine and alcohol functionalities of said first core molecule is at least 2 but no greater than 8; and a second dendrimer comprising a second core molecule, wherein;
said second core molecule comprises a subsequent generation dendrimer of said first core molecule;
the first dendrimer and the second dendrimer each have a mass defect falling within a scarcine valley of an average amino acid;
the first core molecule and the second core molecule each comprise a mass defect marker selected from the group consisting of phosphorous, iodine, bromine, and combinations thereof; and
said composition has physical properties;

ionizing at least a portion of said composition;
collecting data from said ionized portion of said composition; and
relating said data to said physical properties.

4. The method of claim 3 , wherein said first core molecule comprises three iodine atoms.

5. The method of claim 3 , wherein the first core molecule comprises a tertiary amine functionality.

6. The method of claim 3 , wherein the mass defect marker for the first core molecule and for the second core molecule is iodine.

7. The method of claim 3 , wherein the first dendrimer and the second dendrimer each have a mass defect distinct from an averagine ridge of an average amino acid.

8. The method of claim 7 , wherein the average amino acid has an average chemical formula of C 4.9384 H 7.7583 N 1.3577 O 1.4773 S 0.0417 with a molecular weight of 111.05431.

9. The method of claim 7 , wherein the first dendrimer and the second dendrimer each have a mass difference of about 0.2 amu about 0.5 amu relative to the averagine ridge.

10. The method of claim 7 , wherein the first dendrimer and the second dendrimer each have a mass difference of about 0.3 amu to about 0.5 amu relative to the averagine ridge.

11. The method of claim 7 , wherein the first dendrimer and the second dendrimer each have a mass difference of about 0.4 amu to about 0.5 amu relative to the averagine ridge.

12. The method of claim 7 , wherein the first dendrimer and the second dendrimer each have a mass difference of about 0.5 amu relative to the averagine ridge.

13. The composition of claim 1 , wherein at least one of the first core molecule and the second core molecule comprises a tertiary amine functionality.

14. The composition of claim 1 , wherein the mass defect marker for the first core molecule and for the second core molecule is iodine.

15. The composition of claim 1 , wherein the first dendrimer and the second dendrimer each have a mass defect distinct from an averagine ridge of an average amino acid.

16. The composition of claim 15 , wherein the average amino acid has an average chemical formula of C 4.9384 H 7.7583 N 1.3577 O 1.4773 S 0.0417 with a molecular weight of 111.05431.

17. The composition of claim 15 , wherein the first dendrimer and the second dendrimer each have a mass difference of about 0.2 amu about 0.5 amu relative to the averagine ridge.

18. The composition of claim 15 , wherein the first dendrimer and the second dendrimer each have a mass difference of about 0.3 amu to about 0.5 amu relative to the averagine ridge.

19. The composition of claim 15 , wherein the first dendrimer and the second dendrimer each have a mass difference of about 0.4 amu to about 0.5 amu relative to the averagine ridge.

20. The composition of claim 15 , wherein the first dendrimer and the second dendrimer each have a mass difference of about 0.5 amu relative to the averagine ridge.

Assignees

• The Administrators Of The Tulane Educational Fund

Inventors

• Grayson Scott

Classifications

• C07D319/06 Primary

  not condensed with other rings · CPC title

• C07D493/22

  in which the condensed system contains four or more hetero rings · CPC title

• H01J49/004

  Combinations of spectrometers, tandem spectrometers, e.g. MS/MS, MSn · CPC title

• Y10T436/10

  Composition for standardization, calibration, simulation, stabilization, preparation or preservation; processes of use in preparation for chemical testing · CPC title

• G01N30/72

  Mass spectrometers {(mass spectrometers per se H01J49/00)} · CPC title