Sensitive Method for Measuring Cis-Diol Containing Compounds in Plasma Using 2D-LC-MS/MS

• US 20150212055A1
• Filed: 01/26/2015
• Published: 07/30/2015
• Est. Priority Date: 01/27/2014
• Status: Active Grant

• Current Assignee: National Medical Services, Inc.
• Original Assignee: National Medical Services, Inc.
• Inventors: Li, Shuguang, Yue, Bingfang, Li, Wenzhe
• Granted Patent: US 9,146,219 B2
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: G01N 30/7233 interfaced to liquid or supercritical fluid chromatograph interfaces in general for introducing or extracting samples to be analysed with specially adapted mass spectrometer, see H01J49/04
• CPC Class Codes: G01N 30/7266 by electric field, e.g. electrospray
• CPC Class Codes: G01N 33/6848 Methods of protein analysis involving mass spectrometry
• CPC Class Codes: G01N 33/9406 Neurotransmitters
• CPC Class Codes: H01J 49/004 Combinations of spectrometers, tandem spectrometers, e.g. MS/MS, MSn
• CPC Class Codes: H01J 49/165 Electrospray ionisation

Abstract

The present invention provides methods for determining the amount of cis-diol containing compounds in a biological samples using mass spectrometry, particularly catecholamines (dopamine, epinephrine, norepinephrine) in a plasma sample. After a sample is mixed with an internal standard, extracted with a two-step liquid-liquid extraction process utilizing phenylboronic acid chemistry, and then derivatized with a benzoyl chloride-like agent, relevant moieties are then separated chromatographically and detected by MS/MS whereby specific ion transitions are monitored. This invention has several clinical utilities, particularly those related to measuring plasma catecholamines in patients.

Claims

1. A method for determining the amount of one or more analytes having at least one cis-diol structure in a sample, the method comprising:

a. obtaining an aliquot of a sample suspected of containing at least one analyte having at least one cis-diol structure;

b. mixing the aliquot with an internal standard;

c. extracting the analyte from the aliquot by adding a compound that binds cis-diol to form a stable cyclic borate complex wherein the extraction is completed without drying;

d. derivatizing an extract with a compound having a benzoyl moiety under room temperature;

e. separating a derivatized extract from step d by high pressure liquid chromatography (HPLC);

f. subjecting a separated and derivatized extract from step e to electrospray ionization (ESI) under conditions suitable to produce one or more ions detectable by mass spectrometry; and

g. determining an amount of one or more ions by mass spectrometry, whereby the amount of one or more ions reflects an amount of one or more analytes in the sample.

2. The method of claim 1, wherein one or more analytes are selected from a group of cis-diol containing compounds consisting of glycols, polyols, nucleic acids, glycosylated peptide/proteins, 1,2-dihydroxyalkanes, polyphenols, 2-hydroxyacids, catechols, ascorbic acid, carbohydrates, derivatives thereof and mixtures thereof.

3. The method of claim 1, wherein the compound that binds cis-diol to form a stable cyclic borate is a compound containing a phenylboronic acid moiety.

4. The method of claim 1, wherein the compound that binds cis-diol to form a stable cyclic borate is phenylboronic acid.

5. The method of claim 1, wherein the compound having a benzoyl moiety is an acyl halide.

6. The method of claim 1, wherein the compound having a benzoyl moiety is benzoyl chloride.

7. The method of claim 1, wherein one or more analytes are selected from the group consisting of epinephrine, norepinephrine, dopamine and combinations thereof.

8. The method of claim 1, wherein the amounts of two or more of the analytes selected from the group consisting of epinephrine, norepinephrine, and dopamine are determined from the same derivatized extract.

9. The method of claim 1, wherein the analytes are purified by high performance liquid chromatography (HPLC) prior to ionization.

10. The method of claim 1, wherein mass spectrometry is tandem mass spectrometry.

11. The method of claim 1, wherein separating and mass spectrometry is 2D-LC-MS/MS.

12. A method for determining the amount of catecholamines in a sample, the method comprising:

a. obtaining an aliquot of a sample suspected of containing at least one analyte having at least one catecholamine;

b. mixing the aliquot with an internal standard;

c. extracting the analyte from the sample by adding a compound that binds cis-diol to form a stable cyclic borate wherein the extraction is completed without drying;

d. derivatizing an extract with a compound having a benzoyl moiety under room temperature;

e. separating a derivatized extract from step d by high pressure liquid chromatography (HPLC);

f. subjecting a separated and derivatized extract from step e to electrospray ionization (ESI) under conditions suitable to produce one or more ions detectable by mass spectrometry; and

g. determining the amount of the one or more ions by mass spectrometry, whereby the amount of the one or more ions reflects the amount of one or more analytes in the sample.

13. The method of claim 12, wherein one or more analytes are selected from the group consisting of epinephrine, norepinephrine, dopamine and combinations thereof.

14. The method of claim 12, wherein the compound that binds cis-diol to form a stable cyclic borate is a compound containing a phenylboronic acid moiety.

15. The method of claim 12, wherein the compound that binds cis-diol to form a stable cyclic borate is phenylboronic acid.

16. The method of claim 12, wherein the compound having a benzoyl moiety is benzoyl chloride

17. The method of claim 12, wherein the amounts of two or more of the analytes selected from the group consisting of epinephrine, norepinephrine, and dopamine are determined from the same derivatized extract.

18. The method of claim 12, wherein the analytes are purified by high performance liquid chromatography (HPLC) prior to ionization.

19. The method of claim 12, wherein mass spectrometry is tandem mass spectrometry.

20. The method of claim 12, wherein separating and mass spectrometry is 2D-LC-MS/MS.