DK2682476T3 - Fremgangsmåde til kvantificering af kolesterol i højdensitetslipoprotein 2 og anvendelse af et reagenskit til fremgangsmåden - Google Patents
Fremgangsmåde til kvantificering af kolesterol i højdensitetslipoprotein 2 og anvendelse af et reagenskit til fremgangsmåden Download PDFInfo
- Publication number
- DK2682476T3 DK2682476T3 DK12752957.6T DK12752957T DK2682476T3 DK 2682476 T3 DK2682476 T3 DK 2682476T3 DK 12752957 T DK12752957 T DK 12752957T DK 2682476 T3 DK2682476 T3 DK 2682476T3
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- Prior art keywords
- cholesterol
- phospholipase
- hdl2
- hdl
- reagent
- Prior art date
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- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 title claims description 112
- 238000000034 method Methods 0.000 title claims description 70
- 235000012000 cholesterol Nutrition 0.000 title claims description 52
- 108010021075 HDL2 Lipoproteins Proteins 0.000 title claims description 9
- 239000003153 chemical reaction reagent Substances 0.000 title description 106
- 108010010234 HDL Lipoproteins Proteins 0.000 claims description 105
- 102000015779 HDL Lipoproteins Human genes 0.000 claims description 105
- 238000006243 chemical reaction Methods 0.000 claims description 45
- 108090000553 Phospholipase D Proteins 0.000 claims description 35
- 102000011420 Phospholipase D Human genes 0.000 claims description 33
- 238000012360 testing method Methods 0.000 claims description 33
- 102000015439 Phospholipases Human genes 0.000 claims description 29
- 108010064785 Phospholipases Proteins 0.000 claims description 29
- ZIIUUSVHCHPIQD-UHFFFAOYSA-N 2,4,6-trimethyl-N-[3-(trifluoromethyl)phenyl]benzenesulfonamide Chemical compound CC1=CC(C)=CC(C)=C1S(=O)(=O)NC1=CC=CC(C(F)(F)F)=C1 ZIIUUSVHCHPIQD-UHFFFAOYSA-N 0.000 claims description 28
- 102000014384 Type C Phospholipases Human genes 0.000 claims description 22
- 108010079194 Type C Phospholipases Proteins 0.000 claims description 22
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 claims description 3
- 208000010152 Huntington disease-like 3 Diseases 0.000 description 55
- 102000000019 Sterol Esterase Human genes 0.000 description 30
- 108010055297 Sterol Esterase Proteins 0.000 description 30
- 108010089254 Cholesterol oxidase Proteins 0.000 description 28
- 102000004895 Lipoproteins Human genes 0.000 description 26
- 108090001030 Lipoproteins Proteins 0.000 description 26
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 26
- 238000002835 absorbance Methods 0.000 description 24
- 239000007992 BES buffer Substances 0.000 description 21
- RLFWWDJHLFCNIJ-UHFFFAOYSA-N 4-aminoantipyrine Chemical compound CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 description 20
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 20
- 238000005259 measurement Methods 0.000 description 20
- 108010023302 HDL Cholesterol Proteins 0.000 description 17
- 108010061312 Sphingomyelin Phosphodiesterase Proteins 0.000 description 17
- 102000011971 Sphingomyelin Phosphodiesterase Human genes 0.000 description 17
- 108010013563 Lipoprotein Lipase Proteins 0.000 description 16
- 102000043296 Lipoprotein lipases Human genes 0.000 description 16
- 238000005199 ultracentrifugation Methods 0.000 description 16
- 239000004094 surface-active agent Substances 0.000 description 15
- 102000016938 Catalase Human genes 0.000 description 14
- 108010053835 Catalase Proteins 0.000 description 14
- 102000003992 Peroxidases Human genes 0.000 description 14
- 108040007629 peroxidase activity proteins Proteins 0.000 description 14
- 235000002639 sodium chloride Nutrition 0.000 description 14
- SVLRFMQGKVFRTB-UHFFFAOYSA-M sodium;3-(3,5-dimethoxyanilino)-2-hydroxypropane-1-sulfonate Chemical compound [Na+].COC1=CC(NCC(O)CS([O-])(=O)=O)=CC(OC)=C1 SVLRFMQGKVFRTB-UHFFFAOYSA-M 0.000 description 14
- 102000004190 Enzymes Human genes 0.000 description 13
- 108090000790 Enzymes Proteins 0.000 description 13
- 239000011780 sodium chloride Substances 0.000 description 13
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 12
- HQPMKSGTIOYHJT-UHFFFAOYSA-N ethane-1,2-diol;propane-1,2-diol Chemical compound OCCO.CC(O)CO HQPMKSGTIOYHJT-UHFFFAOYSA-N 0.000 description 11
- 229920001993 poloxamer 188 Polymers 0.000 description 11
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- IHPYMWDTONKSCO-UHFFFAOYSA-N 2,2'-piperazine-1,4-diylbisethanesulfonic acid Chemical compound OS(=O)(=O)CCN1CCN(CCS(O)(=O)=O)CC1 IHPYMWDTONKSCO-UHFFFAOYSA-N 0.000 description 4
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- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 2
- AJTVSSFTXWNIRG-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanesulfonic acid Chemical compound OCC[NH+](CCO)CCS([O-])(=O)=O AJTVSSFTXWNIRG-UHFFFAOYSA-N 0.000 description 2
- NUFBIAUZAMHTSP-UHFFFAOYSA-N 3-(n-morpholino)-2-hydroxypropanesulfonic acid Chemical compound OS(=O)(=O)CC(O)CN1CCOCC1 NUFBIAUZAMHTSP-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 102000006410 Apoproteins Human genes 0.000 description 2
- 108010083590 Apoproteins Proteins 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 102100031415 Hepatic triacylglycerol lipase Human genes 0.000 description 2
- 208000031226 Hyperlipidaemia Diseases 0.000 description 2
- 102100037611 Lysophospholipase Human genes 0.000 description 2
- 108020002496 Lysophospholipase Proteins 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 241000047703 Nonion Species 0.000 description 2
- 108010058864 Phospholipases A2 Proteins 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 239000012295 chemical reaction liquid Substances 0.000 description 2
- 150000001841 cholesterols Chemical class 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 238000006911 enzymatic reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002327 glycerophospholipids Chemical class 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 239000000852 hydrogen donor Substances 0.000 description 2
- 108010022197 lipoprotein cholesterol Proteins 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- BGXNGARHYXNGPK-UHFFFAOYSA-N 2-[1-[(4-methoxyphenyl)methylsulfanyl]cyclohexyl]acetic acid Chemical compound C1=CC(OC)=CC=C1CSC1(CC(O)=O)CCCCC1 BGXNGARHYXNGPK-UHFFFAOYSA-N 0.000 description 1
- LVQFQZZGTZFUNF-UHFFFAOYSA-N 2-hydroxy-3-[4-(2-hydroxy-3-sulfonatopropyl)piperazine-1,4-diium-1-yl]propane-1-sulfonate Chemical compound OS(=O)(=O)CC(O)CN1CCN(CC(O)CS(O)(=O)=O)CC1 LVQFQZZGTZFUNF-UHFFFAOYSA-N 0.000 description 1
- HSXUNHYXJWDLDK-UHFFFAOYSA-N 2-hydroxypropane-1-sulfonic acid Chemical compound CC(O)CS(O)(=O)=O HSXUNHYXJWDLDK-UHFFFAOYSA-N 0.000 description 1
- AOTXQRRUWFSXCN-UHFFFAOYSA-N 3-(3,5-dimethoxyanilino)-2-hydroxypropane-1-sulfonic acid Chemical compound COC1=CC(NCC(O)CS(O)(=O)=O)=CC(OC)=C1 AOTXQRRUWFSXCN-UHFFFAOYSA-N 0.000 description 1
- BTIDJAQNJLWPTI-UHFFFAOYSA-N 3-(n-ethyl-3,5-dimethoxyanilino)-2-hydroxypropane-1-sulfonic acid Chemical compound OS(=O)(=O)CC(O)CN(CC)C1=CC(OC)=CC(OC)=C1 BTIDJAQNJLWPTI-UHFFFAOYSA-N 0.000 description 1
- KEWSCDNULKOKTG-UHFFFAOYSA-N 4-cyano-4-ethylsulfanylcarbothioylsulfanylpentanoic acid Chemical compound CCSC(=S)SC(C)(C#N)CCC(O)=O KEWSCDNULKOKTG-UHFFFAOYSA-N 0.000 description 1
- 102100029470 Apolipoprotein E Human genes 0.000 description 1
- 101710095339 Apolipoprotein E Proteins 0.000 description 1
- 102000013918 Apolipoproteins E Human genes 0.000 description 1
- 108010025628 Apolipoproteins E Proteins 0.000 description 1
- YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 description 1
- 102100034808 CCAAT/enhancer-binding protein alpha Human genes 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 229940123748 Catalase inhibitor Drugs 0.000 description 1
- 102100037637 Cholesteryl ester transfer protein Human genes 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 239000006173 Good's buffer Substances 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- 102000019267 Hepatic lipases Human genes 0.000 description 1
- 108050006747 Hepatic lipases Proteins 0.000 description 1
- 101000945515 Homo sapiens CCAAT/enhancer-binding protein alpha Proteins 0.000 description 1
- 101000880514 Homo sapiens Cholesteryl ester transfer protein Proteins 0.000 description 1
- 238000008214 LDL Cholesterol Methods 0.000 description 1
- 229910021380 Manganese Chloride Inorganic materials 0.000 description 1
- GLFNIEUTAYBVOC-UHFFFAOYSA-L Manganese chloride Chemical compound Cl[Mn]Cl GLFNIEUTAYBVOC-UHFFFAOYSA-L 0.000 description 1
- CRJGESKKUOMBCT-VQTJNVASSA-N N-acetylsphinganine Chemical compound CCCCCCCCCCCCCCC[C@@H](O)[C@H](CO)NC(C)=O CRJGESKKUOMBCT-VQTJNVASSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920002415 Pluronic P-123 Polymers 0.000 description 1
- 229920002025 Pluronic® F 88 Polymers 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000000489 anti-atherogenic effect Effects 0.000 description 1
- 230000000702 anti-platelet effect Effects 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000005842 biochemical reaction Methods 0.000 description 1
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- 229910001628 calcium chloride Inorganic materials 0.000 description 1
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- 229940106189 ceramide Drugs 0.000 description 1
- ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 description 1
- GGCLNOIGPMGLDB-GYKMGIIDSA-N cholest-5-en-3-one Chemical compound C1C=C2CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 GGCLNOIGPMGLDB-GYKMGIIDSA-N 0.000 description 1
- NYOXRYYXRWJDKP-UHFFFAOYSA-N cholestenone Natural products C1CC2=CC(=O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 NYOXRYYXRWJDKP-UHFFFAOYSA-N 0.000 description 1
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- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 238000010494 dissociation reaction Methods 0.000 description 1
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- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 235000019626 lipase activity Nutrition 0.000 description 1
- INHCSSUBVCNVSK-UHFFFAOYSA-L lithium sulfate Inorganic materials [Li+].[Li+].[O-]S([O-])(=O)=O INHCSSUBVCNVSK-UHFFFAOYSA-L 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000011565 manganese chloride Substances 0.000 description 1
- 235000002867 manganese chloride Nutrition 0.000 description 1
- 229940099607 manganese chloride Drugs 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003905 phosphatidylinositols Chemical class 0.000 description 1
- 210000002381 plasma Anatomy 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000004141 reverse cholesterol transport Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- HDARHUHTZKLJET-UHFFFAOYSA-M sodium;3-(n-ethyl-3,5-dimethoxyanilino)-2-hydroxypropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN(CC)C1=CC(OC)=CC(OC)=C1 HDARHUHTZKLJET-UHFFFAOYSA-M 0.000 description 1
- IRQRBVOQGUPTLG-UHFFFAOYSA-M sodium;3-(n-ethyl-3-methylanilino)-2-hydroxypropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN(CC)C1=CC=CC(C)=C1 IRQRBVOQGUPTLG-UHFFFAOYSA-M 0.000 description 1
- ZPCAZHPYLUKSMY-UHFFFAOYSA-M sodium;3-(n-ethyl-3-methylanilino)-2-hydroxypropane-1-sulfonate;dihydrate Chemical compound O.O.[Na+].[O-]S(=O)(=O)CC(O)CN(CC)C1=CC=CC(C)=C1 ZPCAZHPYLUKSMY-UHFFFAOYSA-M 0.000 description 1
- NASFKTWZWDYFER-UHFFFAOYSA-N sodium;hydrate Chemical compound O.[Na] NASFKTWZWDYFER-UHFFFAOYSA-N 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- RBTVSNLYYIMMKS-UHFFFAOYSA-N tert-butyl 3-aminoazetidine-1-carboxylate;hydrochloride Chemical compound Cl.CC(C)(C)OC(=O)N1CC(N)C1 RBTVSNLYYIMMKS-UHFFFAOYSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/92—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving lipids, e.g. cholesterol, lipoproteins, or their receptors
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/34—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase
- C12Q1/44—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving hydrolase involving esterase
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/60—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving cholesterol
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/90—Enzymes; Proenzymes
- G01N2333/914—Hydrolases (3)
- G01N2333/916—Hydrolases (3) acting on ester bonds (3.1), e.g. phosphatases (3.1.3), phospholipases C or phospholipases D (3.1.4)
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Immunology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- Analytical Chemistry (AREA)
- Microbiology (AREA)
- Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Hematology (AREA)
- Biomedical Technology (AREA)
- Urology & Nephrology (AREA)
- General Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Endocrinology (AREA)
- Cell Biology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Claims (5)
1. Fremgangsmåde til kvantificering af kolesterol i højdensitetslipoprotein 2, hvilken fremgangsmåde omfatter at lade phospholipase indvirke på højdensitetslipoprotein og at kvantificere kolesterol, hvor phospholipasen er phospholipase C og/eller phospholipase D.
2. Fremgangsmåde ifølge krav 1, hvor phospholipasen er reaktiv med mindst phosphatidylcholin.
3. Fremgangsmåde ifølge krav 1 eller 2, hvor koncentrationen af phospholipasen er 0,1 til 200 U/ml.
4. Anvendelse af et kit omfattende phospholipase C og/eller phospholipase D til kvantificering af kolesterol i højdensitetslipoprotein 2 ved hjælp af fremgangsmåden ifølge et hvilket som helst af kravene 1 til 3.
5. Fremgangsmåde til kvantificering af højdensitetslipoprotein 2 kolesterol i en testprøve, hvilken fremgangsmåde omfatter: et første trin med at overføre kolesteroler, som ikke er højdensitetslipoproteiner, i en testprøve til ydersiden af reaktionssystemet; og et andet trin med at kvantificere højdensitetslipoprotein 2 kolesterol blandt de højdensitetslipoproteiner, der er tilbage i reaktionssystemet; hvor det andet trin udføres ved hjælp af fremgangsmåden ifølge et hvilket som helst af kravene 1 til 3.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011042374 | 2011-02-28 | ||
| PCT/JP2012/054797 WO2012118017A1 (ja) | 2011-02-28 | 2012-02-27 | 高密度リポタンパク質2中のコレステロールの定量方法およびそのための試薬キット |
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| DK2682476T3 true DK2682476T3 (da) | 2017-04-24 |
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| DK12752957.6T DK2682476T3 (da) | 2011-02-28 | 2012-02-27 | Fremgangsmåde til kvantificering af kolesterol i højdensitetslipoprotein 2 og anvendelse af et reagenskit til fremgangsmåden |
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| US (2) | US10031145B2 (da) |
| EP (1) | EP2682476B1 (da) |
| JP (1) | JP5956420B2 (da) |
| KR (1) | KR101871209B1 (da) |
| CN (1) | CN103608465B (da) |
| DK (1) | DK2682476T3 (da) |
| WO (1) | WO2012118017A1 (da) |
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| KR101598597B1 (ko) * | 2014-03-14 | 2016-03-02 | 연세대학교 산학협력단 | 혈장 대사체를 이용한 고-ldl-콜레스테롤 질환 진단 장치 및 방법 |
| JP6582388B2 (ja) * | 2014-10-23 | 2019-10-02 | 東洋紡株式会社 | 高密度リポ蛋白コレステロールの測定方法 |
| US20170010290A1 (en) * | 2015-07-07 | 2017-01-12 | Mohmed E. Ashmaig | Methods of determining a high density lipoprotein phospholipid level in a sample |
| CN113528609B (zh) * | 2021-06-22 | 2024-11-01 | 美康生物科技股份有限公司 | 谷胱甘肽还原酶检测试剂盒及其制备方法和应用 |
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| JP2653755B2 (ja) * | 1994-03-08 | 1997-09-17 | 協和メデックス株式会社 | 高密度リポ蛋白中のコレステロールの定量法 |
| JP3288033B2 (ja) | 1996-12-09 | 2002-06-04 | デンカ生研株式会社 | 高密度リポ蛋白中のコレステロール定量用試薬 |
| JP4708531B2 (ja) | 2000-06-07 | 2011-06-22 | シスメックス株式会社 | Hdl亜画分中のコレステロールの測定法 |
| EP1477570B1 (en) * | 2002-01-30 | 2008-01-16 | DENKA SEIKEN Co., Ltd. | Method of quantifying cholesterol in high density lipoprotein and reagent compositions |
| US7799537B2 (en) * | 2004-11-29 | 2010-09-21 | Otsuka Pharmaceutical Co., Ltd. | Cholesterol measuring reagent containing a cholesterol esterase |
| TWI379904B (en) * | 2005-02-14 | 2012-12-21 | Kyowa Medex Co Ltd | A method for quantifying cholesterol of remnant-like particles lipoprotein, reagent and kit |
| EP1930443A4 (en) * | 2005-09-30 | 2008-10-29 | Denka Seiken Kk | METHOD FOR SELECTIVE AND SIMULTANEOUS QUANTIFICATION OF TWO SUBSTANCES IN A BIOLOGICAL SAMPLE |
| EP1959021A4 (en) * | 2005-12-09 | 2009-07-22 | Kyowa Medex Co Ltd | METHOD FOR DETERMINING CHOLESTEROLEMIA IN LIPOPROTEIN OF THE REMNANT TYPE, REAGENT AND KIT |
| KR101394802B1 (ko) * | 2007-02-28 | 2014-05-15 | 덴카 세이켄 가부시키가이샤 | 소립자 저비중 리포 단백의 정량 시약 |
| KR101586505B1 (ko) * | 2007-10-10 | 2016-01-18 | 덴카 세이켄 가부시키가이샤 | 소입자 고비중 ldl 콜레스테롤의 정량 방법 및 키트 |
| JP5500777B2 (ja) | 2008-03-06 | 2014-05-21 | デンカ生研株式会社 | Hdl3−cの測定方法及びhdl3−c測定用試薬 |
| US20130171674A1 (en) | 2010-07-23 | 2013-07-04 | Denka Seiken Co., Ltd. | Method for quantifying the amount of cholesterol in high-density lipoprotein 3 |
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2012
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- 2012-02-27 CN CN201280020681.7A patent/CN103608465B/zh active Active
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- 2012-02-27 US US14/001,766 patent/US10031145B2/en active Active
- 2012-02-27 KR KR1020137024061A patent/KR101871209B1/ko active Active
- 2012-02-27 JP JP2013502335A patent/JP5956420B2/ja active Active
- 2012-02-27 WO PCT/JP2012/054797 patent/WO2012118017A1/ja not_active Ceased
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Also Published As
| Publication number | Publication date |
|---|---|
| JPWO2012118017A1 (ja) | 2014-07-07 |
| WO2012118017A1 (ja) | 2012-09-07 |
| KR20140027108A (ko) | 2014-03-06 |
| CN103608465A (zh) | 2014-02-26 |
| CN103608465B (zh) | 2017-05-10 |
| US20180306823A1 (en) | 2018-10-25 |
| US10955426B2 (en) | 2021-03-23 |
| US10031145B2 (en) | 2018-07-24 |
| US20140045201A1 (en) | 2014-02-13 |
| EP2682476A1 (en) | 2014-01-08 |
| JP5956420B2 (ja) | 2016-07-27 |
| KR101871209B1 (ko) | 2018-06-27 |
| EP2682476B1 (en) | 2017-02-01 |
| EP2682476A4 (en) | 2015-06-17 |
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