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EP-3869192-B1 - METHOD FOR QUANTITATIVE DETECTION OF VARIOUS METABOLITES IN BIOLOGICAL SAMPLE

EP3869192B1EP 3869192 B1EP3869192 B1EP 3869192B1EP-3869192-B1

Inventors

  • JIA, WEI
  • XIE, Guoxiang
  • WANG, LU

Dates

Publication Date
20260513
Application Date
20191021

Claims (11)

  1. A quantitative detection method of multiple metabolic components in a biological sample, comprising performing derivatization treatment on the biological sample and then detecting the derivatized biological sample by liquid chromatography-mass spectrometry, wherein during derivatization treatment, 3-nitrophenylhydrazine is used as a derivatization reagent, and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide is used as a derivatization reaction catalyst; the biological sample is selected from urine, blood, cerebrospinal fluid, tissue, cells, saliva and fecal samples of a mammal; the multiple metabolic components in the biological sample are selected from one or more of amino acid, phenol, phenyl or benzyl derivative, indole, organic acid, fatty acid, sugar, and bile acid and have different magnitudes in content; wherein the method comprises the following steps: a) collecting a biological sample; b) extracting the biological sample with a mixed solvent of methanol, chloroform, and water, performing centrifugation, and then taking a supernatant, namely a biological sample extract; c) adding the same volume of a 3-nitrophenylhydrazine methanol solution and a 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide pyridine solution into the biological sample extract obtained in b), and performing uniform vortex mixing and heating for derivatization, wherein the concentration of used 3-nitrophenylhydrazine is 100-320 mmol/L, the concentration of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide is 50-200 mmol/L, the reaction temperature is 20-60°C, and the reaction time is 10-120 minutes; d) adding a carbon-13 labeled isotope internal standard solution obtained from the reaction of 3-nitrophenylhydrazine and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide into the derivatized biological sample extract obtained in c); and e) adding a methanol-water mixed solution into the sample in d) for dilution, and determining amino acid, phenol, phenyl or benzyl derivative, indole, organic acid, fatty acid, sugar, and bile acid by liquid chromatography-mass spectrometry.
  2. The detection method according to claim 1, wherein in step c), the concentration of used 3-nitrophenylhydrazine is 150-220 mmol/L, the concentration of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide is 80-120 mmol/L, the reaction temperature is 20-40°C, and the reaction time is 30-60 minutes.
  3. The detection method according to claim 1, wherein when the biological sample is urine, blood, saliva or cerebrospinal fluid, a treatment method of the biological sample in step b) comprises: taking an appropriate amount of the biological sample, extracting the biological sample with a mixed solvent of cold methanol, chloroform and water at a volume ratio of 3:1:1, shaking the mixture for a few seconds, performing centrifugation on the sample at a rotation speed of 10000-20000 rpm at a low temperature for 5-15 minutes, and transferring a supernatant into an autosampler glass vial for subsequent derivatization treatment.
  4. The detection method according to claim 1, wherein when the biological sample is a fecal sample, a treatment method of the biological sample in step b) comprises: freeze-drying the fecal sample; homogenizing an appropriate amount of the freeze-dried fecal sample with an appropriate amount of a mixed solvent of cold methanol, chloroform and water at a volume ratio of 3:1:1, performing centrifugation on the sample at a rotation speed of 10000-20000 rpm at a low temperature for 15-30 minutes, and transferring a supernatant into an autosampler glass vial for subsequent derivatization treatment.
  5. The detection method according to claim 1, wherein when the biological sample is a tissue or cell sample, a treatment method of the biological sample in step b) comprises: adding an appropriate amount of a mixed solvent of cold methanol, chloroform and water at a volume ratio of 3:1:1 into the sample for homogenization, performing centrifugation on the sample at a rotation speed of 10000-20000 rpm at 4°C for 15-30 minutes, and transferring a supernatant into an autosampler glass vial for subsequent derivatization treatment.
  6. The detection method according to claim 1, wherein the volume ratio of methanol to water in step e) is 1:1.
  7. The detection method according to any one of claims 1 to 6, wherein the multiple metabolic components of the biological sample may be selected from the following multiple metabolites: fructose 1,6-diphosphate, 10Z-nonadecenoic acid, trans-11-octadecenoic acid, cis-11-octadecenoic acid, 12-dehydrocholic acid, 12-hydroxystearic acid, 12-ketolithocholic acid, 1-methylhistidine, 2,2-dimethylsuccinic acid, 2,3-diaminopropionic acid, glucoside 24-chenodeoxycholic acid, 2-butenoic acid, 2-oxoadipic acid, 2-methyl-4-pentenoic acid, 2-methyl-β-alanine, 2-methylbutyric acid, 2-methylhexanoic acid, 2-methylglutaric acid, 2-methylglutamic acid, 2-furoic acid, 2-hydroxy-2-methylbutyric acid, 2-hydroxy-3-methylbutyric acid, 2-hydroxybutyric acid, 2-hydroxycaproic acid, 2-hydroxycinnamic acid, 2-hydroxyphenylacetic acid, 2-hydroxyhippuric acid, 2-phenylpropionic acid, 2-phenylglycine, 3-(3-hydroxyphenyl)-3-hydroxypropionic acid, 3-(4-hydroxyphenyl)lactic acid, 3,4-dihydroxymandelic acid, 3,4-dihydroxyphenylpropionic acid, 3,4 -dehydro-DL-proline, 3,5-diiodo-L-thyroxine, 3β-cholic acid, 3-pyridineacetic acid, 3-indoleacrylic acid, 3-indolepropionic acid, 3-indoleacetamide, 3-oxyalanine, 3-aminosalicylic acid, 3-chloro-L-tyrosine, 3-methyl-2-oxobutyric acid, 3-methyl-2-oxovaleric acid, 3-methylindole, 3-methyladipic acid, 3-methylglutamic acid, 3-nitrotyrosine, sulfate 3-taurolithocholic acid, sulfate 3-lithocholic acid, 3-hydroxy-2-aminobenzoic acid, 3-hydroxybutyric acid, 3-hydroxypropionic acid, 3-hydroxyisovaleric acid, 3-hydroxyphenylacetic acid, 3-hydroxyhippuric acid, 3-dehydrocholic acid, 3-phenylbutyric acid, 4-methyl-2-oxovaleric acid, 4-methylhexanoic acid, 4-methoxyphenylacetic acid, 4-hydroxy-3-methoxymandelic acid, 4-hydroxycinnamic acid, 4-hydroxybenzoic acid, 4-hydroxyhippuric acid, 4-hydroxyphenyllactic acid, 4-hydroxyphenylpyruvic acid, 4-phenylbutyric acid, 5-aminolevulinic acid, 5-hydroxytryptophan, 5-hydroxytryptamine, 5-hydroxylysine, 6,7-diketolithocholic acid, 6-phosphogluconic acid, 6-ketolithocholic acid, 7,12-diketolithocholic acid, 7-ketolithocholic acid, 7-ketodeoxycholic acid, 9,11-conjugated linoleic acid, D-2-hydroxyglutaric acid, D-galactose, D-xylose, D-xylulose, D-fructose, D-ribose, D-ribose-5-phosphate, D-ribulose, D-ribulose-5-phosphate, D-mannose, D-glucose, D-maltose, L-2-aminobutyric acid, L-3-phenyllactic acid, L-alanine, L-serine, L-acetylcamitine, L-lactic acid, L-allothreonine, L-cysteine, L-homoserine, L-homocysteine, L-homocitrulline, L-pipecolic acid, L-aspartic acid, L-asparagine, L-sorbose, L-lignic acid, L-norleucine, L-kynurenine, L-thyronine, L-arginine, L-histidine, L-valine, L-cystine, L-cystathionine, L-proline, L-tryptophan, L-threonine, L-phenylalanine, L-malic acid, L-methionine, L-glutamine, L-glutamic acid, L-lysine, L-tyrosine, L-arabinose, N-(3-phenylpropionyl)glycine, N-acetyl-L-alanine, N-acetyl-L-aspartic acid, N-acetyl-L-phenylalanine, N-acetyl-L-methionine, N-acetyl-L-tyrosine, N-acetylserine, N-acetyl-D-glucosamine, N-acetyl-L-phenylalanine, N-acetylmannosamine, N-acetylneuraminic acid, N-acetylhistidine, N-acetylhydroxytryptamine, N-acetyltryptophan, N-acetylglutamine, N-acetyllysine, N-acetylornithine, N-methylnicotinamide, N-phenylacetyl-glutamine, N-phenylacetylphenylalanine, S-adenosine homocysteine, α-D-glucose, α-lactose, α-linolenic acid, α-hydroxyisobutyric acid, α-ketoglutaric acid, α-muricholic acid, β-D-trehalose, β-alanine, β-ursocholic acid, β-muricholic acid, γ-L-glutamyl-L-alanine, γ-linolenic acid, γ-aminobutyric acid, ω-muricholic acid, butyric acid, trimethylamine nitroxide, adenosine triphosphate, malonic acid, propionic acid, acetoacetic acid, acetylcysteine, acetylglycine, acetylornithine, acetic acid, guanidine acetate, glycolic acid, lactulose, lactoylglutathione, heneicosanoic acid, cis-12-heneicosenoic acid, heptacosanoic acid, tricosanoic acid, cis-14-tricosenoic acid, docosanoic acid, docosatrienoic acid, cis-13,16-docosadienoic acid, docosapentaenoic acid, docosahexaenoic acid, docosatetraenoic acid, trans-13-docosaenoic acid, cis-13-docosaenoic acid, pentacosanoic acid, octacosanoic acid, hexacosanoic acid, tetracosanoic acid, eicosanoic acid, eicosatrienoic acid, eicosadienoic acid, eicosapentaenoic acid, trans-11-eicosenoic acid, cis-11-eicosenoic acid, cis-5-eicosenoic acid, cis-8-eicosenoic acid, dimethylglycine, adenosine diphosphate, linoleic acid, leucine, alloisoleucine, allolithocholic acid, allocholic acid, undecenoic acid, heptadecanoic acid, tridecanoic acid, nonadecanoic acid, nonadecadienoic acid, pentadecanoic acid, galactonic acid, galactitol, mecysteine, protocatechuic acid, apocholic acid, dehydrolithocholic acid, nordeoxycholic acid, trans-9-tetradecenoic acid, trans-aconitic acid, trans-4-hydroxyproline, trans-9-heptadecenoic acid, trans-9-pentadecenoic acid, trans-9-hexadecenoic acid, trans-linolenic acid, trans-cinnamic acid, elaidic acid, homocysteine, pyrrole-2-carboxylic acid, picolinic acid, indole, indole-3-methyl acetate, indole-3-carboxylic acid, indoleacetic acid, purine, azelaic acid, nonanoic acid, dopa, dopamine, melibiose, fumaric acid, acetaminophen, p-aminohippuric acid, p-cresol sulfate, symmetrical dimethylarginine, p-hydroxymandelic acid, p-hydroxyphenylacetic acid, homogentisic acid, adipic acid, pimelic acid, isobutyric acid, isoleucine, isovaleric acid, citric acid, isoursodeoxycholic acid, isohyodeoxycholic acid, isolithocholic acid, isocholic acid, isodeoxycholic acid, glutaric acid, glutaconic acid, valeric acid, mandelic acid, lauric acid, fructose-6-phosphate, citraconic acid, citric acid, citramalic acid, ribonolactone, ribonic acid, raffinose, palmitoleic acid, palmitic acid, norvaline, n-hydroxyphenylacetic acid, oxidized glutathione, aminoadipic acid, aminocaproic acid, salicyluric acid, oleic acid, trehalose, nicotinic acid, pyroglutamic acid, ursocholic acid, ursodeoxycholic acid, tauro-α-muricholic acid, tauro-b-muricholic acid, tauro-w-muricholic acid, tauroursodeoxycholic acid, taurohyocholic acid, taurohyodeoxycholic acid, taurolithocholic acid, taurocholic acid, taurodehydrocholic acid, taurochenodeoxycholic acid, hyocholic acid, hyodeoxycholic acid, succinylacetone, succinic acid, citrulline, glycodehydrocholic acid, glycolithocholic acid, glycodeoxycholic acid, glycine, glycochenodeoxycholic acid, glyceraldehyde, glyceraldehyde-3-phosphate, choline glycerophosphate, glycoursodeoxycholic acid, glycohyocholic acid, glycohyodeoxycholic acid, glycocholic acid, glyproline, glycyl-L-leucine, mannose-6-phosphoric acid, mannitol, methylmalonic acid, methylsuccinic acid, formic acid, capric acid, lithocholic acid, selenomethionine, thiamine, glycolithocholic sulfate, stearic acid, liothyronine, dihydroxyacetone phosphate, phosphoribosyl pyrophosphate, creatine phosphate, hydroxypyruvic acid, glycine hydroxyphenylacetate, cinnamic acid, sarcosine, carnosine, creatine, inositol, epinephrine, choline, cholic acid, dehydrocholic acid, demethylcholic acid, adenosine monophosphate, arachidonic acid, phenylpyruvic acid, phenethylamine, phenylpropionic acid, phenyllactic acid, benzamide, benzoic acid, oxalic acid, shikimic acid, glucaric acid, glucose-6-phosphate, glucose lactone, sebacic acid, ricinoleic acid, sucrose, methionine sulfoxide, itaconic acid, melatonin, glutathione, myristic acid, erythronic acid, erythrose, suberic acid, caprylic acid, phthalic acid, tartaric acid, tyramine, quinic acid, m-aminobenzoic acid, asymmetric dimethylarginine, tannic acid, cis-10,12-octadecadienoic acid, cis-12,15-heneicosadienoic acid, cis-12-tridecenoic acid, cis-15-tetracosenic acid, cis-2-hydroxycinnamic acid, cis-9-tetradecenoic acid, cis-10-heptadecenoic acid, cis-11-dodecenoic acid, cis-4-hydroxyproline, cis-5-dodecenoic acid, cis-7-hexadecenoic acid, cis-9-heptadecenoic acid, cis-aconitic acid, vanillic acid, hippuric acid, maleic acid, homovanillic acid, ornithine, guanosine monophosphate, guanosine triphosphate, anserine, chenodeoxycholic acid, maltotriose, maltitol, rhamnose and murideoxycholic acid.
  8. Use of a metabolic chip in the detection method according to any one of claims 1 to 7, the metabolic chip comprising a chip carrier, a filter device and dry solid powder of a standard product and a quality control product, wherein the chip carrier is a microtiter plate, each well of the microtiter plate is provided with an independent filter device, and the powder obtained by dehydrating or freeze-drying solutions of the standard product and the quality control product is placed on the filter device in each well of the microtiter plate; the standard product is selected from one or more of amino acid, phenol, phenyl or benzyl derivative, indole, organic acid, fatty acid, sugar, and bile acid standard products; the quality control product is selected from one or more of amino acid, phenol, phenyl or benzyl derivative, indole, organic acid, fatty acid, sugar, and bile acid standard products corresponding to the standard products above.
  9. Use of the metabolic chip according to claim 8, wherein the microtiter plate is selected from a 48-well plate, a 96-well plate and a 384-well plate, and the filter device is a filter membrane made of polyvinylidene fluoride, cellulose acetate, or nylon with a pore size of 0.20-0.45 micron.
  10. Use of the metabolic chip according to claim 8, wherein the standard product and the quality control product may be selected from the following multiple metabolites: fructose 1,6-diphosphate, 10Z-nonadecenoic acid, trans-11-octadecenoic acid, cis-11-octadecenoic acid, 12-dehydrocholic acid, 12-hydroxystearic acid, 12-ketolithocholic acid, 1-methylhistidine, 2,2-dimethylsuccinic acid, 2,3-diaminopropionic acid, glucoside 24-chenodeoxycholic acid, 2-butenoic acid, 2-oxoadipic acid, 2-methyl-4-pentenoic acid, 2-methyl-β-alanine, 2-methylbutyric acid, 2-methylhexanoic acid, 2-methylglutaric acid, 2-methylglutamic acid, 2-furoic acid, 2-hydroxy-2-methylbutyric acid, 2-hydroxy-3-methylbutyric acid, 2-hydroxybutyric acid, 2-hydroxycaproic acid, 2-hydroxycinnamic acid, 2-hydroxyphenylacetic acid, 2-hydroxyhippuric acid, 2-phenylpropionic acid, 2-phenylglycine, 3-(3-hydroxyphenyl)-3-hydroxypropionic acid, 3-(4-hydroxyphenyl)lactic acid, 3,4-dihydroxymandelic acid, 3,4-dihydroxyphenylpropionic acid, 3,4-dehydro-DL-proline, 3,5-diiodo-L-thyroxine, 3β-cholic acid, 3-pyridineacetic acid, 3-indoleacrylic acid, 3-indolepropionic acid, 3-indoleacetamide, 3-oxyalanine, 3-aminosalicylic acid, 3-chloro-L-tyrosine, 3-methyl-2-oxobutyric acid, 3-methyl-2-oxovaleric acid, 3-methylindole, 3-methyladipic acid, 3-methylglutamic acid, 3-nitrotyrosine, sulfate 3-taurolithocholic acid, sulfate 3-lithocholic acid, 3-hydroxy-2-aminobenzoic acid, 3-hydroxybutyric acid, 3-hydroxypropionic acid, 3-hydroxyisovaleric acid, 3-hydroxyphenylacetic acid, 3-hydroxyhippuric acid, 3-dehydrocholic acid, 3-phenylbutyric acid, 4-methyl-2-oxyvaleric acid, 4-methylhexanoic acid, 4-methoxyphenylacetic acid, 4-hydroxy-3-methoxymandelic acid, 4-hydroxycinnamic acid, 4-hydroxybenzoic acid, 4-hydroxyhippuric acid, 4-hydroxyphenyllactic acid, 4-hydroxyphenylpyruvic acid, 4-phenylbutyric acid, 5-aminolevulinic acid, 5-hydroxytryptophan, 5-hydroxytryptamine, 5-hydroxylysine, 6,7-diketolithocholic acid, 6-phosphogluconic acid, 6-ketolithocholic acid, 7,12-diketolithocholic acid, 7-ketolithocholic acid, 7-ketodeoxycholic acid, 9,11-conjugated linoleic acid, D-2-hydroxyglutaric acid, D-galactose, D-xylose, D-xylulose, D-fructose, D-ribose, D-ribose-5-phosphate, D-ribulose, D-ribulose-5-phosphate, D-mannose, D-glucose, D-maltose, L-2-aminobutyric acid, L-3-phenyllactic acid, L-alanine, L-serine, L-acetylcarnitine, L-lactic acid, L-allothreonine, L-cysteine, L-homoserine, L-homocysteine, L-homocitrulline, L-pipecolic acid, L-aspartic acid, L-asparagine, L-sorbose, L-lignic acid, L-norleucine, L-kynurenine, L-thyronine, L-arginine, L-histidine, L-valine, L-cystine, L-cystathionine, L-proline, L-tryptophan, L-threonine, L-phenylalanine, L-malic acid, L-methionine, L-glutamine, L-glutamic acid, L-lysine, L-tyrosine, L-arabinose, N-(3-phenylpropionyl)glycine, N-acetyl-L-alanine, N-acetyl-L-aspartic acid, N-acetyl-L-phenylalanine, N-acetyl-L-methionine, N-acetyl-L-tyrosine, N-acetylserine, N-acetyl-D-glucosamine, N-acetyl-L-phenylalanine, N-acetylmannosamine, N-acetylneuraminic acid, N-acetylhistidine, N-acetylhydroxytryptamine, N-acetyltryptophan, N-acetylglutamine, N-acetyllysine, N-acetylornithine, N-methylnicotinamide, N-phenylacetyl-glutamine, N-phenylacetylphenylalanine, S-adenosine homocysteine, α-D-glucose, α-lactose, α-linolenic acid, α-hydroxyisobutyric acid, α-ketoglutaric acid, α-muricholic acid, β-D-trehalose, β-alanine, β-ursocholic acid, β-muricholic acid, γ-L-glutamyl-L-alanine, γ-linolenic acid, γ-aminobutyric acid, ω-muricholic acid, butyric acid, trimethylamine nitroxides, adenosine triphosphate, malonic acid, propionic acid, acetoacetic acid, acetylcysteine, acetylglycine, acetylornithine, acetic acid, guanidine acetate, glycolic acid, lactulose, lactoylglutathione, heneicosanoic acid, cis-12-heneicosenoic acid, heptacosanoic acid, tricosanoic acid, cis-14-tricosenoic acid, docosanoic acid, docosatrienoic acid, cis-13,16-docosadienoic acid, docosapentaenoic acid, docosahexaenoic acid, docosatetraenoic acid, trans-13-docosaenoic acid, cis-13-docosaenoic acid, pentacosanoic acid, octacosanoic acid, hexacosanoic acid, tetracosanoic acid, eicosanoic acid, eicosatrienoic acid, eicosadienoic acid, eicosapentaenoic acid, trans-11-eicosenoic acid, cis-11-eicosenoic acid, cis-5-eicosenoic acid, cis-8-eicosenoic acid, dimethylglycine, adenosine diphosphate, linoleic acid, leucine, alloisoleucine, allolithocholic acid, allocholic acid, undecenoic acid, heptadecanoic acid, tridecanoic acid, nonadecanoic acid, nonadecadienoic acid, pentadecanoic acid, galactonic acid, galactitol, mecysteine, protocatechuic acid, apocholic acid, dehydrolithocholic acid, nordeoxycholic acid, trans-9-tetradecenoic acid, trans-aconitic acid, trans-4-hydroxyproline, trans-9-heptadecenoic acid, trans-9-pentadecenoic acid, trans-9-hexadecenoic acid, trans-linolenic acid, trans-cinnamic acid, elaidic acid, homocysteine, pyrrole-2-carboxylic acid, picolinic acid, indole, indole-3-methyl acetate, indole-3-carboxylic acid, indoleacetic acid, purine, azelaic acid, nonanoic acid, dopa, dopamine, melibiose, fumaric acid, acetaminophen, p-aminohippuric acid, p-cresol sulfate, symmetrical dimethylarginine, p-hydroxymandelic acid, p-hydroxyphenylacetic acid, homogentisic acid, adipic acid, pimelic acid, isobutyric acid, isoleucine, isovaleric acid, citric acid, isoursodeoxycholic acid, isohyodeoxycholic acid, isolithocholic acid, isocholic acid, isodeoxycholic acid, glutaric acid, glutaconic acid, valeric acid, mandelic acid, lauric acid, fructose-6-phosphate, citraconic acid, citric acid, citramalic acid, ribonolactone, ribonic acid, raffinose, palmitoleic acid, palmitic acid, norvaline, n-hydroxyphenylacetic acid, oxidized glutathione, aminoadipic acid, aminocaproic acid, salicyluric acid, oleic acid, trehalose, nicotinic acid, pyroglutamic acid, ursocholic acid, ursodeoxycholic acid, tauro-α-muricholic acid, tauro-b-muricholic acid, tauro-w-muricholic acid, tauroursodeoxycholic acid, taurohyocholic acid, taurohyodeoxycholic acid, taurolithocholic acid, taurocholic acid, taurodehydrocholic acid, taurochenodeoxycholic acid, hyocholic acid, hyodeoxycholic acid, succinylacetone, succinic acid, citrulline, glycodehydrocholic acid, glycolithocholic acid, glycodeoxycholic acid, glycine, glycochenodeoxycholic acid, glyceraldehyde, glyceraldehyde-3-phosphate, choline glycerophosphate, glycoursodeoxycholic acid, glycohyocholic acid, glycohyodeoxycholic acid, glycocholic acid, glyproline, glycyl-L-leucine, mannose-6-phosphoric acid, mannitol, methylmalonic acid, methylsuccinic acid, formic acid, capric acid, lithocholic acid, selenomethionine, thiamine, glycolithocholic sulfate, stearic acid, liothyronine, dihydroxyacetone phosphate, phosphoribosyl pyrophosphate, creatine phosphate, hydroxypyruvic acid, glycine hydroxyphenylacetate, cinnamic acid, sarcosine, carnosine, creatine, inositol, epinephrine, choline, cholic acid, dehydrocholic acid, demethylcholic acid, adenosine monophosphate, arachidonic acid, phenylpyruvic acid, phenethylamine, phenylpropionic acid, phenyllactic acid, benzamide, benzoic acid, oxalic acid, shikimic acid, glucaric acid, glucose-6-phosphate, glucose lactone, sebacic acid, ricinoleic acid, sucrose, methionine sulfoxide, itaconic acid, melatonin, glutathione, myristic acid, erythronic acid, erythrose, suberic acid, caprylic acid, phthalic acid, tartaric acid, tyramine, quinic acid, m-aminobenzoic acid, asymmetric dimethylarginine, tannic acid, cis-10,12-octadecadienoic acid, cis-12,15-heneicosadienoic acid, cis-12-tridecenoic acid, cis-15-tetracosenic acid, cis-2-hydroxycinnamic acid, cis-9-tetradecenoic acid, cis-10-heptadecenoic acid, cis-11-dodecenoic acid, cis-4-hydroxyproline, cis-5-dodecenoic acid, cis-7-hexadecenoic acid, cis-9-heptadecenoic acid, cis-aconitic acid, vanillic acid, hippuric acid, maleic acid, homovanillic acid, ornithine, guanosine monophosphate, guanosine triphosphate, anserine, chenodeoxycholic acid, maltotriose, maltitol, rhamnose and murideoxycholic acid.
  11. The use of the metabolic chip according to any one of claims 8 to 10, comprising the following steps: a) collecting a biological sample; b) according to the sample type, preparing a corresponding biological sample extract by using the corresponding method according to claim 3 or 4 or 5; c) adding the prepared biological sample extract into each well of the metabolic chip in an equal amount, adding the same volume of a 3-nitrophenylhydrazine methanol solution and a 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide pyridine solution into each well, and performing uniform vortex mixing and heating for derivatization, wherein the concentration of used 3-nitrophenylhydrazine is 100-320 mmol/L, the concentration of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide is 50-200 mmol/L, the reaction temperature is 20-60°C, and the reaction time is 10-120 minutes; d) adding a carbon-13 labeled isotope internal standard solution obtained from the reaction of 3-nitrophenylhydrazine and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide into the derivatized biological sample extract obtained in c); and e) adding a methanol-water mixed solution into each well in the metabolic chip in d) for dilution, placing the metabolic chip in a tandem mass spectrometer for determination of amino acid, phenol, phenyl or benzyl derivative, indole, organic acid, fatty acid, sugar, and bile acid by liquid chromatography-mass spectrometry, and calculating concentrations of target metabolites in the sample based on results.

Description

BACKGROUND Technical Field The present invention relates to the field of detection of biological samples, specifically relates to a quantitative determination method of multiple metabolic components such as amino acid, phenol, phenyl or benzyl derivative, indole, organic acid, fatty acid, sugar, and bile acid in a biological sample, and more specifically relates to a detection method of a biological sample by using chemical derivatization and tandem mass spectrometry and use of a a metabolic chip in the method. Related Art Metabolomics involves unbiased analysis of all metabolites (metabolomes) in cells, body fluids and tissues. At present, with a metabolomics platform based on nuclear magnetic resonance (NMR) or mass spectrometry (MS), many small molecule (MW<1500) metabolites are detected, but only relative (non-absolute) concentrations of the metabolites in biological fluids (serum/plasma or urine) and tissues of subjects suffering from metabolic diseases are provided to determine that the concentrations are different from those of a control group. Due to high chemical diversity of the metabolomes, there is a great challenge to full-spectrum quantitative detection of these metabolites. Since a quantitative metabolomics platform for large-scale biological sample analysis is in deficiency, clinical practicality and application of metabolomics have not yet been realized. Quantitative metabolomics is used for identifying and quantifying as many metabolites as possible in a biological sample. Compared with traditional targeted and non-targeted methods, quantitative metabolomics has many advantages, including lowest cross-platform variability, improved stability and maintenance of full-spectrum metabolic characteristics and more detailed information about the identity and concentration of specific metabolites. With regard to quantification of metabolite concentration, reliable analytical data is a prerequisite for development of metabolic-based clinical trials or a thorough understanding of functions of organisms and biological systems in translational researches. One of the technical challenges is that concentrations of metabolites are in a range of more than a dozen of magnitudes. For example, glucose in blood is in some compounds such as eicosanoids in a millimolar range and a femtomolar range. There are also different platform challenges in size and polarity differences of compounds. In order to overcome these challenges, gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS) have been applied to a maximum coverage. However, the difficulty in quantitative detection of multiple indexes at the same time has not yet been solved. There are only a few major metabolic pathways, such as glycolysis, aerobic respiration, tricarboxylic acid (TCA) cycle, fatty acid oxidation (β-oxidation) and gluconeogenesis. Cells are used to transfer energy and maintain metabolic homeostasis, and due to defects in these key pathways in storage and disposal of major classes of molecules (such as amino acid, carbohydrate, and lipid), metabolic disorders are caused. Therefore, unique characteristics of metabolites in biological systems can be reflected in quantitative detection of these metabolites. As important substances involved in physiological metabolism of the human body, amino acid, phenol, phenyl or benzyl derivative, indole, organic acid, fatty acid, sugar, and bile acid are maintained at a certain level in normal metabolism in the human body. Generally, the changes of concentrations of these substances indicate that there are abnormalities in metabolic pathways of the human body. Based on detection of concentrations of these substances and clinical manifestations, judgment of clinical diseases is facilitated. Han Jun et al. (Isotope-labeling derivatization with 3-nitrophenyhydrazine for LC/multiple-reaction monitoring-mass-spectrometry-based quantitation of carnitines in dried blood spots: Analytica Chimica Acta, vol 1037, 5. February 2018, pages 177-187) and Han Jun et al. (An isotope-labeled chemical derivatization method for the quantitation of short-chain fatty acids in human feces by liquid chromatography-tandem mass spectrometry: Analytica Chimica Acta, Vol 854, 1 January 2015, pages 86-94) disclose a quantitative detection method of multiple metabolic components in a biological sample. In view of the shortcomings of the prior art, an objective of the present invention is to provide a detection method for quantitatively detecting multiple components in a biological sample at the same time. SUMMARY An objective of the present invention is to provide a quantitative detection method capable of quantitatively detecting multiple metabolic components in a biological sample at the same time and the use of a metabolic chip in the method. The multiple metabolic components include, but are not limited to, multiple amino acids, phenols, phenyl or benzyl derivatives, indoles, organic acids