Liquid chromatography/mass spectrometry methods for the analysis of polar molecules

Abstract

A mixed-mode chromatography method for the determination of phosphorylated sugars in a sample is provided. The mixed-mode chromatography method includes obtaining a sample comprising at least one phosphorylated sugar. The sample is introduced onto a chromatography system. The chromatography system includes a column having a stationary phase material contained inside the column. The stationary phase material has a surface comprising a hydrophobic surface group and at least one ionizable modifier. The sample with a mobile phase eluent is flowed through the column, where the at least one phosphorylated sugar is substantially resolved and retained within seven minutes. The mobile phase eluent includes water with an additive and acetonitrile with the additive. The mobile phase eluent has a pH less than 6. The at least one phosphorylated sugar is detected using a detector.

Claims

1. A mixed-mode chromatography method for the determination of phosphorylated sugars in a sample, the mixed-mode chromatography method comprising: obtaining a sample comprising at least one phosphorylated sugar; introducing the sample onto a chromatography system comprising a column having a stationary phase material contained inside the column, the stationary phase material having a surface comprising a hydrophobic surface group and at least one ionizable modifier; flowing the sample with a mobile phase eluent through the column, wherein the at least one phosphorylated sugar is substantially resolved and retained within seven minutes, the mobile phase eluent comprising water with an additive and acetonitrile with the additive, the mobile phase eluent having a pH less than 6; and detecting the at least one phosphorylated sugar using a detector.

2. The mixed-mode chromatography method of claim 1, wherein the pH of the mobile phase eluent is less than 3.

3. The mixed-mode chromatography method of claim 2, wherein the pH of the mobile phase eluent is about 2.7.

4. The mixed-mode chromatography method of claim 1, wherein the additive is 0.1% formic acid.

5. The mixed-mode chromatography method of claim 1, wherein the mobile phase eluent comprises a mobile phase A consisting essentially of 0.1% formic acid in water and a mobile phase B consisting essentially of 0.1% formic acid in acetonitrile.

6. The mixed-mode chromatography method of claim 5, wherein the mobile phase eluent has a linear or step gradient elution comprising a. 100% mobile phase A, 0% mobile phase B at an initial time; b. 70% mobile phase A, 30% mobile phase B at a time of 3 minutes; c. 5% mobile phase A, 95% mobile phase B at a time of 3.5 minutes; d. 5% mobile phase A, 95% mobile phase B at a time of 6.5 minutes e. 100% mobile phase A, 0% mobile phase B at a time of 7 minutes.

7. The mixed-mode chromatography method of claim 1, wherein the sample with the mobile phase eluent is flowed through the column at a rate from 0.2-1.0 mL/min.

8. The mixed-mode chromatography method of claim 1, wherein the hydrophobic surface group comprises a fluoro-phenyl functional group.

9. The mixed-mode chromatography method of claim 1, wherein the hydrophobic surface group comprises a phenyl-hexyl functional group.

10. The mixed-mode chromatography method of claim 1, wherein the hydrophobic surface group comprises a C.sub.18 functional group.

11. The mixed-mode chromatography method of claim 1, wherein the detector is a mass spectrometer.

12. A mixed-mode chromatography method for the determination of amino acids in a sample, the mixed mode chromatography method comprising: obtaining a sample comprising at least one amino acid; introducing the sample onto a chromatography system comprising a column having a stationary phase material contained inside the column, the stationary phase material having a surface comprising a hydrophobic surface group and at least one ionizable modifier; flowing the sample with a mobile phase eluent through the column, wherein the at least one amino acid is substantially resolved and retained within seven minutes, the mobile phase eluent comprising water with an additive and acetonitrile with the additive, the mobile phase eluent having a pH less than 6; and detecting the at least one amino acid using a detector.

13. The mixed-mode chromatography method of claim 12, wherein the pH of the mobile phase eluent is less than 3.

14. The mixed-mode chromatography method of claim 13, wherein the pH of the mobile phase eluent is about 2.7.

15. The mixed-mode chromatography method of claim 12, wherein the additive is 0.1% formic acid.

16. The mixed-mode chromatography method of claim 12, wherein the mobile phase eluent comprises a mobile phase A consisting essentially of 0.1% formic acid in water and a mobile phase B consisting essentially of 0.1% formic acid in acetonitrile.

17. The mixed-mode chromatography method of claim 16, wherein the mobile phase eluent has a linear or step gradient elution comprising a. 100% mobile phase A, 0% mobile phase B at an initial time; b. 70% mobile phase A, 30% mobile phase B at a time of 3 minutes; c. 5% mobile phase A, 95% mobile phase B at a time of 3.5 minutes; d. 5% mobile phase A, 95% mobile phase B at a time of 6.5 minutes e. 100% mobile phase A, 0% mobile phase B at a time of 7 minutes.

18. The mixed-mode chromatography method of claim 12, wherein the sample with the mobile phase eluent is flowed through the mixed-mode column at a rate of about 0.2-1.0-mL/min.

19. The mixed-mode chromatography method of claim 12, wherein the hydrophobic surface group comprises a fluoro-phenyl functional group.

20. The mixed-mode chromatography method of claim 12, wherein the hydrophobic surface group comprises a phenyl-hexyl functional group.

21. The mixed-mode chromatography method of claim 12, wherein the hydrophobic surface group comprises a C.sub.18 functional group.

22. The mixed-mode chromatography method of claim 12, wherein the detector is a mass spectrometer.

23. The mixed-mode chromatography method of claim 12, wherein the at least one amino acid is glutamate, glutamine, isoleucine, or leucine.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The technology will be more fully understood from the following detailed description taken in conjunction with the accompanying drawings, in which:

(2) FIG. 1 is a flow chart of a mixed-mode chromatography method for the determination of a phosphorylated sugar, an amino acid and/or an organic acid in a sample, according to an illustrative embodiment of the technology.

(3) FIG. 2 is a schematic of a mixed-mode chromatography system, according to an illustrative embodiment of the technology.

(4) FIG. 3A is an MRM chromatogram for the separation of isocitric acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(5) FIG. 3B is an MRM chromatogram for the separation of citric acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(6) FIG. 3C is an MRM chromatogram for the separation of aconitic acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(7) FIG. 3D is an MRM chromatogram for the separation of alpha ketoglutaric acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(8) FIG. 3E is an MRM chromatogram for the separation of succinic acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(9) FIG. 3F is an MRM chromatogram for the separation of malic acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(10) FIG. 3G is an MRM chromatogram for the separation of fumaric acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(11) FIG. 3H is an MRM chromatogram for the separation of lactic acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(12) FIG. 3I is an MRM chromatogram for the separation of pyruvate acid, a TCA cycle analyte, on CSH C.sub.18 100 μM STD, according to an illustrative embodiment of the technology.

(13) FIG. 4A is an MRM chromatogram for the separation of isocitric acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(14) FIG. 4B is an MRM chromatogram for the separation of citric acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(15) FIG. 4C is an MRM chromatogram for the separation of aconitic acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(16) FIG. 4D is an MRM chromatogram for the separation of alpha ketoglutaric acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(17) FIG. 4E is an MRM chromatogram for the separation of succinic acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(18) FIG. 4F is an MRM chromatogram for the separation of malic acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(19) FIG. 4G is an MRM chromatogram for the separation of fumaric acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(20) FIG. 4H is an MRM chromatogram for the separation of lactic acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(21) FIG. 4I is an MRM chromatogram for the separation of pyruvate acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(22) FIG. 5A is an MRM chromatogram for the separation of isocitric acid, a TCA cycle analyte, on CSH phenyl hexyl 100 μM STD, according to an illustrative embodiment of the technology.

(23) FIG. 5B is an MRM chromatogram for the separation of citric acid, a TCA cycle analyte, on CSH fluoro phenyl 100 μM STD, according to an illustrative embodiment of the technology.

(24) FIG. 5C is an MRM chromatogram for the separation of aconitic acid, a TCA cycle analyte, on CSH fluoro phenyl 100 μM STD, according to an illustrative embodiment of the technology.

(25) FIG. 5D is an MRM chromatogram for the separation of alpha ketoglutaric acid, a TCA cycle analyte, on CSH fluoro phenyl 100 μM STD, according to an illustrative embodiment of the technology.

(26) FIG. 5E is an MRM chromatogram for the separation of succinic acid, a TCA cycle analyte, on CSH fluoro phenyl 100 μM STD, according to an illustrative embodiment of the technology.

(27) FIG. 5F is an MRM chromatogram for the separation of malic acid, a TCA cycle analyte, on CSH fluoro phenyl 100 μM STD, according to an illustrative embodiment of the technology.

(28) FIG. 5G is an MRM chromatogram for the separation of fumaric acid, a TCA cycle analyte, on CSH fluoro phenyl 100 μM STD, according to an illustrative embodiment of the technology.

(29) FIG. 5H is an MRM chromatogram for the separation of lactic acid, a TCA cycle analyte, on CSH fluoro phenyl 100 μM STD, according to an illustrative embodiment of the technology.

(30) FIG. 5I is an MRM chromatogram for the separation of pyruvate acid, a TCA cycle analyte, on CSH fluoro phenyl 100 μM STD, according to an illustrative embodiment of the technology.

(31) FIG. 6A is a chromatogram for the separation of TCA cycle metabolites using a BEH C.sub.18 column, according to an illustrative embodiment of the technology.

(32) FIG. 6B is a chromatogram for the separation of TCA cycle metabolites using a CSH C.sub.18 column, according to an illustrative embodiment of the technology.

(33) FIG. 6C is a chromatogram for the separation of TCA cycle metabolites using a CSH phenyl-hexyl column, according to an illustrative embodiment of the technology.

(34) FIG. 7A is a chromatogram for the separation of glutamate acid using a CSH C.sub.18 STD column, according to an illustrative embodiment of the technology.

(35) FIG. 7B is a chromatogram for the separation of glutamine acid using a CSH C.sub.18 STD column, according to an illustrative embodiment of the technology.

(36) FIG. 7C is a chromatogram for the separation of isoleucine acid using a CSH C.sub.18 STD column, according to an illustrative embodiment of the technology.

(37) FIG. 7D is a chromatogram for the separation of leucine acid using a CSH C.sub.18 STD column, according to an illustrative embodiment of the technology.

(38) FIG. 8A is a chromatogram for the separation of glutamate acid using a CSH phenyl hexyl STD column, according to an illustrative embodiment of the technology.

(39) FIG. 8B is a chromatogram for the separation of glutamine acid using a CSH phenyl hexyl STD column, according to an illustrative embodiment of the technology.

(40) FIG. 8C is a chromatogram for the separation of isoleucine acid using a CSH phenyl hexyl STD column, according to an illustrative embodiment of the technology.

(41) FIG. 8D is a chromatogram for the separation of leucine acid using a CSH phenyl hexyl STD column, according to an illustrative embodiment of the technology.

(42) FIG. 9A is a chromatogram for the separation of glutamate acid using a CSH fluoro phenyl STD column, according to an illustrative embodiment of the technology.

(43) FIG. 9B is a chromatogram for the separation of glutamine acid using a CSH fluoro phenyl STD column, according to an illustrative embodiment of the technology.

(44) FIG. 9C is a chromatogram for the separation of isoleucine acid using a CSH fluoro phenyl STD column, according to an illustrative embodiment of the technology.

(45) FIG. 9D is a chromatogram for the separation of leucine acid using a CSH fluoro phenyl STD column, according to an illustrative embodiment of the technology.

(46) FIG. 10A is a chromatogram for the separation of methylmalonic acid using a CSH C.sub.18 column, according to an illustrative embodiment of the technology.

(47) FIG. 10B is a chromatogram for the separation of succinic acid using a CSH C.sub.18 column, according to an illustrative embodiment of the technology.

(48) FIG. 10C is a chromatogram for the separation of aconitic acid using a CSH C.sub.18 column, according to an illustrative embodiment of the technology.

(49) FIG. 10D is a chromatogram for the separation of itaconic acid using a CSH C.sub.18 column, according to an illustrative embodiment of the technology.

(50) FIG. 11A is a chromatogram for the separation of methylmalonic acid using a CSH phenyl hexyl column, according to an illustrative embodiment of the technology.

(51) FIG. 11B is a chromatogram for the separation of succinic acid using a CSH phenyl hexyl column, according to an illustrative embodiment of the technology.

(52) FIG. 11C is a chromatogram for the separation of aconitic acid using a CSH phenyl hexyl column, according to an illustrative embodiment of the technology.

(53) FIG. 11D is a chromatogram for the separation of itaconic acid using a CSH phenyl hexyl column, according to an illustrative embodiment of the technology.

(54) FIG. 12A is a chromatogram for the separation of methylmalonic acid using a CSH fluoro phenyl column, according to an illustrative embodiment of the technology.

(55) FIG. 12B is a chromatogram for the separation of succinic acid using a CSH fluoro phenyl column, according to an illustrative embodiment of the technology.

(56) FIG. 12C is a chromatogram for the separation of aconitic acid using a CSH fluoro phenyl column, according to an illustrative embodiment of the technology.

(57) FIG. 12D is a chromatogram for the separation of itaconic acid using a CSH fluoro phenyl column, according to an illustrative embodiment of the technology.

(58) FIG. 13A is a chromatogram for the separation of glucose 6 phosphate using a CSH C.sub.18 column, according to an illustrative embodiment of the technology.

(59) FIG. 13B is a chromatogram for the separation of glucose 6 phosphate using a CSH phenyl hexyl column, according to an illustrative embodiment of the technology.

(60) FIG. 13C is a chromatogram for the separation of glucose 6 phosphate using a CSH fluoro phenyl column, according to an illustrative embodiment of the technology.

DETAILED DESCRIPTION

(61) The technology provides methods for chromatography separation and detection of polar molecules, for example, phosphorylated sugars, amino acids, organic acids, and/or nucleotides using a mixed-mode or reversed-phase chromatography column that includes a stationary phase material having a surface comprising a hydrophobic surface group and at least one ionizable modifier.

Definitions

(62) As used herein, the term “about” means that the numerical value is approximate and small variations would not significantly affect the practice of the disclosed embodiments. Where a numerical limitation is used, unless indicated otherwise by the context, “about” means the numerical value can vary by ±10% and remain within the scope of the disclosed embodiments.

(63) As used herein, the term “high purity” or “high purity chromatographic material” includes a material which is prepared form high purity precursors. In certain aspects, high purity materials have reduced metal contamination and/or non-diminished chromatographic properties including, but not limited to, the acidity of surface silanols and the heterogeneity of the surface.

(64) As used herein, the term “chromatographic surface” includes a surface which provides for chromatographic separation of a sample. In certain aspects, the chromatographic surface is porous. In some aspects, a chromatographic surface can be the surface of a particle, a superficially porous material or a monolith. In certain aspects, the chromatographic surface is composed of the surface of one or more particles, superficially porous materials or monoliths used in combination during a chromatographic separation. In certain other aspects, the chromatographic surface is non-porous.

(65) As used herein, the term “ionizable modifier” includes a functional group which bears an electron donating or electron withdrawing group. In certain aspects, the ionizable modifier contains one or more carboxylic acid groups, amino groups, imido groups, amido groups, pyridyl groups, imidazolyl groups, ureido groups, thionyl-ureido groups or aminosilane groups, or a combination thereof. In other aspects, the ionizable modifier contains a group bearing a nitrogen or phosphorous atom having a free electron lone pair. In certain aspects, the ionizable modifier is covalently attached to the material surface and has an ionizable group. In some instances it is attached to the chromatographic material by chemical modification of a surface hybrid group.

(66) As used herein, the term “hydrophobic surface group” includes a surface group on the chromatographic surface which exhibits hydrophobicity. In certain aspects, a hydrophobic group can be a carbon bonded phase such as a C.sub.4 to C.sub.18 bonded phase. In other aspects, a hydrophobic surface group can contain an embedded polar group such that the external portion of the hydrophobic surface maintains hydrophobicity. In some instances it is attached to the chromatographic material by chemical modification of a surface hybrid group. In other instances the hydrophobic group can be C.sub.4-C.sub.30, embedded polar, chiral, phenylalkyl, or pentafluorophenyl bonding and coatings.

(67) As used herein, the term “hybrid”, including “hybrid inorganic/organic material,” includes inorganic-based structures wherein an organic functionality is integral to both the internal or “skeletal” inorganic structure as well as the hybrid material surface. The inorganic portion of the hybrid material may be, e.g., alumina, silica, titanium, cerium, or zirconium or oxides thereof, or ceramic material.

(68) “Hybrid” includes inorganic-based structures wherein an organic functionality is integral to both the internal or “skeletal” inorganic structure as well as the hybrid material surface. As noted above, exemplary hybrid materials are shown in U.S. Pat. Nos. 4,017,528, 6,528,167, 6,686,035 and 7,175,913, the contents of each of which are incorporated hereby by reference.

(69) As used herein, the term “surface modifiers” include (typically) organic functional groups which impart a certain chromatographic functionality to a chromatographic stationary phase. The porous inorganic/organic hybrid materials possess both organic groups and silanol groups which may additionally be substituted or derivatized with a surface modifier.

(70) The language “surface modified” is used herein to describe the composite material of the present technology that possess both organic groups and silanol groups which may additionally be substituted or derivatized with a surface modifier. “Surface modifiers” include (typically) organic functional groups which impart a certain chromatographic functionality to a chromatographic stationary phase. Surface modifiers such as disclosed herein are attached to the base material, e.g., via derivatization or coating and later crosslinking, imparting the chemical character of the surface modifier to the base material. In one embodiment, the organic groups of a hybrid material, react to form an organic covalent bond with a surface modifier. The modifiers can form an organic covalent bond to the material's organic group via a number of mechanisms well known in organic and polymer chemistry including but not limited to nucleophilic, electrophilic, cycloaddition, free-radical, carbene, nitrene, and carbocation reactions. Organic covalent bonds are defined to involve the formation of a covalent bond between the common elements of organic chemistry including but not limited to hydrogen, boron, carbon, nitrogen, oxygen, silicon, phosphorus, sulfur, and the halogens. In addition, carbon-silicon and carbon-oxygen-silicon bonds are defined as organic covalent bonds, whereas silicon-oxygen-silicon bonds that are not defined as organic covalent bonds. A variety of synthetic transformations are well known in the literature, see, e.g., March, J. Advanced Organic Chemistry, 3rd Edition, Wiley, New York, 1985.

(71) Methods

(72) FIG. 1 is a flow chart of a reversed phase or mixed-mode chromatography method 100 for the determination of phosphorylated sugars, amino acids, and/or organic acids in a sample. In some embodiments, the amino acid is glutamate, glutamine, isoleucine, or leucine. In some embodiments, the organic acid is a metabolite or intermediate of the tricarboxylic acid (TCA) cycle, for example, isocitric, citric, aconitic, a-ketoglutaric, succinic, malic, fumaric, lactic, pyruvic acid.

(73) The reversed-phase/mixed mode chromatography method 100 includes obtaining a sample that includes the phosphorylated sugars, amino acids, and/or organic acids 105. In some embodiments, the sample includes phosphorylated sugars, amino acids, and organic acids. The sample can include one of a phosphorylated sugar, amino acid or organic acid, or any combination thereof. In some embodiments, the sample includes multiple different types or sugars, amino acids, and/or organic acids. In other embodiments, the sample can also include a nucleotide.

(74) The sample is introduced 110 to a reversed-phase/mixed-mode chromatography system. FIG. 2 is a schematic of an exemplary reversed-phase or mixed-mode chromatography system 200. The reversed-phase or mixed-mode chromatography system 200 includes a mobile phase reservoir 205 that stores a mobile phase eluent or multiple mobile phase eluents. A pump 210, pumps the mobile phase eluent(s) from the mobile phase reservoir 205 to the reversed-phase or mixed-mode chromatography column 215. A sample 220 is introduced into the mobile phase eluent flow stream prior to the reversed-phase or mixed-mode chromatography column 215. The sample 220 and the mobile phase combine prior to entering the reversed-phase or mixed-mode chromatography column 215, and form a combined flow stream.

(75) The mobile phase eluent includes water with an additive and acetonitrile with an additive. The additive can be formic acid. In some embodiments, the additive is 0.1% formic acid. The additive can be a buffer that is compatible with mass spectrometry. The mobile phase eluent can consist of two separate mobile phases, mobile phase A and mobile phase B. Mobile phase A can consist essentially of 0.1% formic acid in water and mobile phase B can consist essentially of 0.1% formic acid in acetonitrile.

(76) The mobile phase eluent can have a linear or step gradient elution. The linear or step gradient elution can be a. 100% mobile phase A, 0% mobile phase B at an initial time; b. 70% mobile phase A, 30% mobile phase B at a time of 3 minutes; c. 5% mobile phase A, 95% mobile phase B at a time of 3.5 minutes; d. 5% mobile phase A, 95% mobile phase B at a time of 6.5 minutes; and e. 100% mobile phase A, 0% mobile phase B at a time of 7 minutes.

(77) The mobile phase eluent can have a flow rate between about 0.2 to about 1.0 mL/min. The mobile phase eluent flow rate can be about 0.2 mL/min, 0.3 mL/min, 0.4 mL/min, 0.5 mL/min, 0.6 mL/min, 0.7 mL/min, 0.8 mL/min, 0.9 mL/min, or 1.0 mL/min. These values can be used to define a range. In some embodiments the flow rate of the mobile phase eluent is about 0.40 mL/min.

(78) The mobile phase eluent has a pH less than 6. In some embodiments the pH of the mobile phase eluent is less than 5. In other embodiments, the pH of the mobile phase eluent is less than 3. The pH of the mobile phase eluent can be 2.7. The pH of the mobile phase eluent can be 2.0, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, 3.0, 3.1, 3.2, 3.3, 3.4, 3.5, 3.6, 3.7, 3.8, 3.9, 4.0, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, 5.0, 5.1, 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, 5.8, 5.9, or 6.0. These values can be used to define a range.

(79) The reversed-phase or mixed-mode chromatography column 215 contains a stationary phase inside the column 215. The stationary phase material has a surface that includes a hydrophobic surface group and an ionizable modifier. In some embodiment, the hydrophobic surface group contains a phenyl functional group. The phenyl functional group can include unsubstituted and substituted phenyl groups. The stationary phase can include a fluoro-phenyl functional group or a phenyl-hexyl functional group. The stationary phase material can include inorganic/organic hybrid particles or ethylene bridged hybrid particles. The mean particle size can measure about 0.1 μm, 0.2 μm, 0.3 μm, 0.4 μm, 0.5 μm, 0.6 μm, 0.7 μm, 0.8 μm, 0.9 μm, 1.0 μm, 1.1 μm, 1.2 μm, 1.3 μm, 1.4 μm, 1.5 μm, 1.6 μm, 1.7 μm, 1.8 μm, 1.9 μm, 2.0 μm, 2.1 am, 2.2 μm, 2.3 μm, 2.4 μm, 2.5 μm, 2.6 μm, 2.7 μm, 2.8 μm, 2.9 μm, 3.0 μm, 3.1 μm, 3.2 μm, 3.3 μm, 3.4 μm, 3.5 μm, 3.6 μm, 3.7 μm, 3.8 μm, 3.9 μm, 4.0 μm, 4.1 μm, 4.2 μm, 4.3 μm, 4.4 μm, 4.5 μm, 4.6 μm, 4.7 μm, 4.8 μm, 4.9 μm, 5.0 μm, 5.1 μm, 5.2 μm, 5.3 μm, 5.4 μm, 5.5 μm, 5.6 μm, 5.7 μm, 5.8 μm, 5.9 μm, 6.0 μm, 6.5 μm, 7.0 μm, 7.5 μm, 8.0 μm, 8.5 μm, 9.0 μm, 9.5 μm, 10.0 μm, 10.5 μm, 11.0 μm, 11.5 μm, 12.0 μm, 12.5 μm, 13.0 μm, 13.5 μm, 14.0 μm, 14.5 am, or 15 μm. These values can define a range. In one embodiment, the particle size is about 1.7 μm.

(80) The functional group imparts a certain chromatographic functionality to a chromatographic stationary phase material. The hydrophobic surface group is attached to the base material (particle), for example, via derivatization or coating and later crosslinking, imparting the chemical character of the hydrophobic surface group or functional group to the base material (e.g., the inorganic/organic hybrid particles or ethylene bridged hybrid particles described above).

(81) The ionizable modifiers and hydrophobic surface groups can be applied to a base particle using a variety of methods. For example, starting with an unbonded based particle (e.g., ethylene bridged hybrid particle (BEH)), a small controlled charge can be applied to the BEH particle surface. The resulting charged surface hybrid (CSH) particle can be then bonded and sometimes endcapped with the functional group, for example, a fluoro-phenyl functional group, a phenyl-hexyl functional group or a C.sub.18 functional group.

(82) The inorganic/organic hybrid particles possess both organic groups and silanol groups which can additionally be substituted or derivatized with a surface modifier. “Surface modifiers” include (typically) organic functional groups which impart a certain chromatographic functionality to a chromatographic stationary phase. The surface modifier can be, for example, a C.sub.18 group, unsubstituted and substituted phenyl groups, a fluoro-phenyl, or phenyl-hexyl functional group. Examples of these functional groups are shown below.

(83) ##STR00001## Example of a stationary phase having a C.sub.18 functional group.

(84) ##STR00002## Example of a stationary phase having a fluoro-phenyl functional group.

(85) ##STR00003## Example of a stationary phase having a phenyl-hexyl functional group.

(86) Table 1 shows the properties of charged surface hybrid (CSH) bonded with C.sub.18, fluoro-phenyl or phenyl-hexyl functional groups.

(87) TABLE-US-00001 TABLE 1 Properties of CSH Bonded Phases Surface Concentration pH (μmol/m.sup.2) Endcapping % C Range CSH C.sub.18 2.3 yes 15.5 1-11 CSH Phenyl-Hexyl 2.3 yes 13.5 1-11 CSH Fluoro-Phenyl 2.3 no 10.2 1-8 

(88) The anion-exchange characteristics of CSH bonded phases make them useful for separating polar acidic compounds (e.g., phosphorylated sugars, amino acids, organic acids, and/or nucleotides), which are typically poorly retained on reversed-phase columns. This is demonstrated for a number of different types of analytes in the Examples.

(89) Referring back to FIG. 2, the reversed-phase chromatography column 215 can have any inner diameter that allows for the efficient separation of acidic polar compounds, e.g., phosphorylated sugars, amino acids, organic acids, and/or nucleotides. The inner diameter of the chromatography column 215 can be, for example, 0.05 mm, 0.075 mm, 0.1 mm, 0.2 mm, 0.3 mm, 0.4 mm, 0.5 mm, 0.6 mm, 0.7 mm, 0.8 mm. 0.9 mm, 1.0 mm, 1.1 mm, 1.2 mm, 1.3 mm, 1.4 mm, 1.5 mm, 1.6 mm, 1.7 mm, 1.8 mm, 1.9 mm, 2.0 mm, 2.1 mm, 2.2 mm, 2.3 mm, 2.4 mm, 2.5 mm, 2.6 mm, 2.7 mm, 2.8 mm, 2.9 mm, or 3 mm. These values can be used to define a range. In some embodiments, the inner diameter of the reversed-phase chromatography column 215 is 2.1 mm.

(90) Similarly, the reversed-phase chromatography column 215 can have any length that allows for the separation of acidic polar compounds, e.g., phosphorylated sugars, amino acids, organic acids, and/or nucleotides. The length can be, for example, about 5 mm, 10 mm, 20 mm, 25 mm, 30 mm, 35 mm, 40 mm, 45 mm, 50 mm, 55 mm, 60 mm, 65 mm, 70 mm, 75 mm, 80 mm, 85 mm, 90 mm, 95 mm, 100 mm, 105 mm, 110 mm, 115 mm, 120 mm, 125 mm 150 mm, 200 mm, 250 mm, or 300 mm. These values can be used to define a range. In some embodiments, the length of the reversed-phase chromatography column 215 is 100 mm.

(91) The reversed-phase chromatography system 200 can have a detector 222 positioned downstream of the column 215. The detector 222 can be used to detect the acidic polar compounds, e.g., phosphorylated sugars, amino acids, organic acids, and/or nucleotides eluting from the reversed-phase or mixed-mode chromatography column 215. The detector 222 can be a mass spectrometer. In some embodiments, the detector 222 is a tandem mass spectrometer (MS/MS). The detector can be a tandem quadrupole mass spectrometer.

(92) A data acquisition module 225 can be in communication with the detector 222. The data acquisition module 225 can be used, for example, to gather/collect and analyze data received from the detector 222. The data acquisition module 225 can be a computer having software installed to collect and analyze the data.

(93) Referring back to FIG. 1, the sample and mobile phase eluent (combined flow stream) are flowed 115 through the reversed-phase/mixed-mode chromatography column (e.g., column 215 of FIG. 2). The acidic polar compounds, e.g., phosphorylated sugars, amino acids, organic acids, and/or nucleotides are substantially resolved and retained on the column. In some embodiments, the phosphorylated sugars, amino acids, organic acids, and/or nucleotides are separated in about 7 minutes.

(94) The retention time, resolution from other analytes in the sample and selectivity of analytes in a chromatography separation can be influenced by a number of factors. These factors can include the strong eluent or mobile phase, the pH of the sample and mobile phase as well as the profile and duration of the gradient. For example, a positively charged sorbent (e.g., a CSH sorbent) will attract negatively charged molecules (e.g., organic acids, phosphorylated sugars, amino acids and nucleotides). Therefore, these negatively charged analytes will be attracted to and retained on a positively charged sorbent. The mobile phase gradient can then be manipulated or changed to selectively release the negatively charged analytes to elute from the column. For example, decreasing the pH of the mobile phase eluent over time will result in the negatively charged analytes being released from the stationary phase material and will elute from the column.

(95) The phosphorylated sugars, amino acids, organic acids, and/or nucleotides are detected 120 using a detector or multiple detectors, for example, detector 222 of FIG. 2. The detector can be used to detect the phosphorylated sugars, amino acids, organic acids, and/or nucleotides eluting from the reversed-phase/mixed mode chromatography column. The detector can be a mass spectrometer.

EXAMPLES

Example 1: Metabolites and Intermediates of the Tricarboxylic Acid (TCA) Cycle

(96) Standards were prepared in water and diluted with water to make a solution of 100 μmolar for metabolites and intermediates of the tricarboxylic acid (TCA) cycle, for example, isocitric, citric, aconitic, a-ketoglutaric, succinic, malic, fumaric, lactic and pyruvic organic acids. The structures of these metabolites and intermediates of the tricarboxylic acid (TCA) cycle are shown below.

(97) ##STR00004##

(98) Samples were injected onto an LC/MS system in neat solution and spiked into human plasma treated with dipotassium ethylenediaminotetraacetic acid (K2EDTA). These analytes were then separated using an ACQUITY® UPLC® I-Class LC system (commercially available from Waters Technologies Corporation, Milford, Mass. USA) coupled with a Xevo® TQ S tandem quadrupole mass spectrometer operated in ESI negative mode and in MRM acquisition mode (commercially available from Waters Technologies Corporation, Milford, Mass. USA). Details of the method are described in Tables 2 and 3.

(99) TABLE-US-00002 TABLE 2 Liquid Chromatography Conditions Columns ACQUITY ® UPLC ® CSH C.sub.18 column; 130 Å 1.7 μm 2.1 × 100 mm ACQUITY ® UPLC ® CSH Phenyl-Hexyl column; 130 Å 1.7 μm 2.1 × 100 mm ACQUITY ® UPLC ® CSH Fluoro-Phenyl column; 130 Å 1.7 μm 2.1 × 100 mm (commercially available from Waters Technologies Corporation, Milford, MA USA) Mobile Phase A 100% water, 0.1% formic acid (v/v) Mobile Phase B 100% acetonitrile, 0.1% formic acid (v/v) Column 50° C. Temperature Injection Volume 3 μL Sample Diluent Water Detection Tandem quadrupole MS MRM mode ESI negative mode

(100) TABLE-US-00003 TABLE 3 Gradient Table Time Flow Rate (min) (mL/min) % A % B Curve Initial 0.40 100.0 0.00 Initial 3.00 0.40 70 30.0 6 3.50 0.40 5.0 95.0 6 6.50 0.40 5.0 95.0 6 7.00 0.40 100.0 0.0 6

(101) FIGS. 3A-3I present MRM chromatograms of various TCA cycle metabolites and intermediates and the effectiveness of a mixed mode separations using a CSH C.sub.18 column at 100 μM STD. FIG. 3A shows the MRM chromatogram for isocitric acid. FIG. 3B shows the MRM chromatogram for citric acid. FIG. 3C shows the MRM chromatogram for aconitic acid. FIG. 3D shows the MRM chromatogram for alpha ketoglutaric acid. FIG. 3E shows the MRM chromatogram for succinic acid. FIG. 3F shows the MRM chromatogram for malic acid. FIG. 3G shows the MRM chromatogram for fumaric acid. FIG. 3H shows the MRM chromatogram for lactic acid. FIG. 3I shows the MRM chromatogram for pyruvate acid.

(102) FIGS. 4A-4I present MRM chromatograms of various TCA cycle metabolites and intermediates and the effectiveness of a mixed mode separations using a CSH phenyl hexyl column at 100 μM STD. FIG. 4A shows the MRM chromatogram for isocitric acid. FIG. 4B shows the MRM chromatogram for citric acid. FIG. 4C shows the MRM chromatogram for aconitic acid. FIG. 4D shows the MRM chromatogram for alpha ketoglutaric acid. FIG. 4E shows the MRM chromatogram for succinic acid. FIG. 4F shows the MRM chromatogram for malic acid. FIG. 4G shows the MRM chromatogram for fumaric acid. FIG. 4H shows the MRM chromatogram for lactic acid. FIG. 4I shows the MRM chromatogram for pyruvate acid.

(103) FIGS. 5A-5I present MRM chromatograms of various TCA cycle metabolites and intermediates and the effectiveness of a mixed mode separations using a CSH fluoro phenyl column at 100 μM STD. FIG. 5A shows the MRM chromatogram for isocitric acid. FIG. 5B shows the MRM chromatogram for citric acid. FIG. 5C shows the MRM chromatogram for aconitic acid. FIG. 5D shows the MRM chromatogram for alpha ketoglutaric acid. FIG. 5E shows the MRM chromatogram for succinic acid. FIG. 5F shows the MRM chromatogram for malic acid. FIG. 5G shows the MRM chromatogram for fumaric acid. FIG. 5H shows the MRM chromatogram for lactic acid. FIG. 5I shows the MRM chromatogram for pyruvate acid.

(104) The metabolites in the TCA cycle are highly polar, most containing two or three carboxylic acid groups (see structures above). The pK.sub.a values of the most acidic groups in these molecules range from approximately 2.8 to 3.8. They are poorly retained on conventional reversed-phase columns. It was determined that these compounds were retained on the three CSH materials, using a mobile phase containing 0.1% formic acid in water and in acetonitrile. As shown by comparing FIGS. 3A-I, 4A-I and 5A-I, the most promising results were obtained using the CSH phenyl hexyl column. While the CSH fluoro-phenyl column showed greater retention of these analytes, several exhibited poor peak shapes under these conditions.

(105) FIGS. 6A-C show chromatograms of the separation of TCA cycle metabolites using a BEH C.sub.18 column (FIG. 6A), a CSH C.sub.18 column (FIG. 6B) and a CSH phenyl-hexyl column (FIG. 6C). The columns were all 1.7 am 2.1×100 mm columns. In each of these figures, 1 is isocitric acid, 2 is malic acid, 3 is alpha-ketoglutaric acid, 4 is lactic acid, 5 is citric acid, 6 is fumaric acid, 7 is aconitric acid, and 8 is succinic acid.

(106) The CSH columns have significant retention for anions when the mobile pH is less than 5, with retention increasing as the pH is decreased. The relative retention of anions increases from CSH C.sub.18<CSH phenyl-hexyl<CSH fluoro-phenyl. The ability to retain anions makes CSH columns useful for the separation of polar acids such as the TCA cycle metabolites.

Example 2: Amino Acids

(107) Standards were prepared in water and diluted with water to make a solution of 100 μMolar for glutamine and glutamate and 10 μg/mL for leucine and isoleucine. These analytes were then separated using an ACQUITY® UPLC® I-Class LC system (commercially available from Waters Technologies Corporation, Milford, Mass. USA) coupled with a Xevo® TQ S tandem quadrupole mass spectrometer operated in ESI negative mode and in MRM acquisition mode (commercially available from Waters Technologies Corporation, Milford, Mass. USA). Details of the method are described in Tables 4 and 5.

(108) TABLE-US-00004 TABLE 4 Liquid Chromatography Conditions Columns ACQUITY ® UPLC ® CSH C.sub.18 column; 130 Å 1.7 μm 2.1 × 100 mm ACQUITY ® UPLC ® CSH Phenyl-Hexyl column; 130 Å 1.7 μm 2.1 × 100 mm ACQUITY ® UPLC ® CSH Fluoro-Phenyl column; 130 Å 1.7 μm 2.1 × 100 mm (commercially available from Waters Technologies Corporation, Milford, MA USA) Mobile Phase A 100% water, 0.1% formic acid (v/v) Mobile Phase B 100% acetonitrile, 0.1% formic acid (v/v) Column 50° C. Temperature Injection Volume 3 μL Sample Diluent Water Detection Tandem quadrupole MS MRM mode ESI negative mode

(109) TABLE-US-00005 TABLE 5 Gradient Table Time Flow Rate (min) (mL/min) % A % B Curve Initial 0.40 100.0 0.00 Initial 3.00 0.40 70 30.0 6 3.50 0.40 5.0 95.0 6 6.50 0.40 5.0 95.0 6 7.00 0.40 100.0 0.0 6

(110) FIGS. 7A-7D show the analysis of amino acids using a CSH C.sub.18 STD sorbent in a reversed phase column. FIG. 7A shows the MRM chromatogram for glutamic acid. FIG. 7B shows the MRM chromatogram for glutimine acid. FIG. 7C shows the MRM chromatogram for isoleucine acid. FIG. 7D shows the MRM chromatogram for leucine acid.

(111) FIGS. 8A-8D show the analysis of amino acids using a CSH phenyl hexyl STD sorbent in a reversed phase column. FIG. 8A shows the MRM chromatogram for glutamic acid. FIG. 8B shows the MRM chromatogram for glutimine acid. FIG. 8C shows the MRM chromatogram for isoleucine acid. FIG. 8D shows the MRM chromatogram for leucine acid.

(112) FIGS. 9A-9D show the analysis of amino acids using a CSH fluoro phenyl STD sorbent in a reversed phase column. FIG. 9A shows the MRM chromatogram for glutamic acid. FIG. 9B shows the MRM chromatogram for glutimine acid. FIG. 9C shows the MRM chromatogram for isoleucine acid. FIG. 9D shows the MRM chromatogram for leucine acid.

(113) As can be seen from a comparison of FIGS. 7-9, the CSH phenyl hexyl column showed increased separation and retention for glutamate and glutamine compared to the CSH C.sub.18 column. Moreover, the CSH fluoro phenyl column showed increased separation and retention for glutamate and glutamine compared to both the CSH CSH C.sub.18 column and the CSH phenyl hexyl column.

(114) In contrast, the opposite result can be seen for isoleucine and leucine where the CSH phenyl hexyl column showed decreased separation and retention for glutamate and glutamine compared to the CSH C.sub.18 column. Moreover, the CSH fluoro phenyl column showed decreased separation and retention for glutamate and glutamine compared to both the CSH CSH C.sub.18 column and the CSH phenyl hexyl column.

Example 3: Biomarkers

(115) Standards were prepared in water and diluted with water to make a solution of 100 μMolar for methylmalonic acid, aconitic acid, and succinic acid. Itaconic acid was made in a solution 10 μg/mL. These analytes were then separated using an ACQUITY® UPLC® I-Class LC system (commercially available from Waters Technologies Corporation, Milford, Mass. USA) coupled with a Xevo® TQ S tandem quadrupole mass spectrometer operated in ESI negative mode and in MRM acquisition mode (commercially available from Waters Technologies Corporation, Milford, Mass. USA). Details of the method are described in Tables 6 and 7.

(116) TABLE-US-00006 TABLE 6 Liquid Chromatography Conditions Columns ACQUITY ® UPLC ® CSH C.sub.18 column; 130 Å 1.7 μm 2.1 × 100 mm ACQUITY ® UPLC ® CSH Phenyl-Hexyl column; 130 Å 1.7 μm 2.1 × 100 mm ACQUITY ® UPLC ® CSH Fluoro-Phenyl column; 130 Å 1.7 μm 2.1 × 100 mm (commercially available from Waters Technologies Corporation, Milford, MA USA) Mobile Phase A 100% water, 0.1% formic acid (v/v) Mobile Phase B 100% acetonitrile, 0.1% formic acid (v/v) Column 50° C. Temperature Injection Volume 3 μL Sample Diluent Water Detection Tandem quadrupole MS MRM mode ESI negative mode

(117) TABLE-US-00007 TABLE 7 Gradient Table Time Flow Rate (min) (mL/min) % A % B Curve Initial 0.40 100.0 0.00 Initial 3.00 0.40 70 30.0 6 3.50 0.40 5.0 95.0 6 6.50 0.40 5.0 95.0 6 7.00 0.40 100.0 0.0 6

(118) FIGS. 10A-10D show the analysis of biomarkers using a CSH C.sub.18 sorbent in a reversed phase column. FIG. 10A shows the MRM chromatogram for methylmalonic acid. FIG. 10B shows the MRM chromatogram for succinic acid. FIG. 10C shows the MRM chromatogram for aconitic acid. FIG. 10D shows the MRM chromatogram for itaconic acid.

(119) FIGS. 11A-11D show the analysis of biomarkers using a CSH phenyl hexyl sorbent in a reversed phase column. FIG. 11A shows the MRM chromatogram for methylmalonic acid. FIG. 11B shows the MRM chromatogram for succinic acid. FIG. 11C shows the MRM chromatogram for aconitic acid. FIG. 11D shows the MRM chromatogram for itaconic acid.

(120) FIGS. 12A-12D show the analysis of biomarkers using a CSH fluoro phenyl sorbent in a reversed phase column. FIG. 12A shows the MRM chromatogram for methylmalonic acid. FIG. 12B shows the MRM chromatogram for succinic acid. FIG. 12C shows the MRM chromatogram for aconitic acid. FIG. 12D shows the MRM chromatogram for itaconic acid.

Example 4: Phosphorylated Sugars

(121) Glucose 6 phosphate standards were prepared in water and diluted with water to make a solution of 100 Molar. This analyte, structure shown below, was then separated using an ACQUITY® UPLC® I-Class LC system (commercially available from Waters Technologies Corporation, Milford, Mass. USA) coupled with a Xevo® TQ S tandem quadrupole mass spectrometer operated in ESI negative mode and in MRM acquisition mode (commercially available from Waters Technologies Corporation, Milford, Mass. USA). Details of the method are described in Tables 8 and 9.

(122) TABLE-US-00008 TABLE 8 Liquid Chromatography Conditions Columns ACQUITY ® UPLC ® CSH C.sub.18 column; 130 Å 1.7 μm 2.1 × 100 mm ACQUITY ® UPLC ® CSH Phenyl-Hexyl column; 130 Å 1.7 μm 2.1 × 100 mm ACQUITY ® UPLC ® CSH Fluoro-Phenyl column; 130 Å 1.7 μm 2.1 × 100 mm (commercially available from Waters Technologies Corporation, Milford, MA USA) Mobile Phase A 100% water, 0.1% formic acid (v/v) Mobile Phase B 100% acetonitrile, 0.1% formic acid (v/v) Column 50° C. Temperature Injection Volume 3 μL Sample Diluent Water Detection Tandem quadrupole MS MRM mode ESI negative mode

(123) TABLE-US-00009 TABLE 9 Gradient Table Time Flow Rate (min) (mL/min) % A % B Curve Initial 0.40 100.0 0.00 Initial 3.00 0.40 70 30.0 6 3.50 0.40 5.0 95.0 6 6.50 0.40 5.0 95.0 6 7.00 0.40 100.0 0.0 6

(124) ##STR00005##

(125) FIG. 13A shows the analysis of glucose 6 phosphate using a CSH C.sub.18 sorbent in a reversed phase column. FIG. 13B shows the analysis of glucose 6 phosphate using a CSH phenyl hexyl sorbent in a reversed phase column. FIG. 13C shows the analysis of glucose 6 phosphate using a CSH fluoro phenyl sorbent in a reversed phase column. As can be seen from a comparison of these three stationary phase material, the CSH fluoro phenyl sorbent showed increased separation and retention as compared to the CSH phenyl hexyl stationary phase material, which showed increased separation and retention as compared to the CSH C.sub.18 stationary phase material.

(126) From all of these examples, it is shown that the anion-exchange characteristics of CSH columns make them useful for separating polar acidic analytes, which are typically poorly retained on reversed-phase columns.

(127) Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, numerous equivalents to the specific procedures described herein. Such equivalents were considered to be within the scope of this technology and are covered by the following claims. The contents of all references, issued patents, and published patent applications cited throughout this application are hereby incorporated by reference.