JPH0134350B2 - - Google Patents

Info

Publication number: JPH0134350B2
Authority: JP; Japan
Prior art keywords: reagent; bilirubin; present; ferrocyanide; composition
Prior art date: 1982-08-11
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Expired

Application number

JP57139499A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5928664A (ja

Inventor

Shinichi Tejima

Noboru Mitsuhida

Yoshitaka Nakagiri

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Toyobo Co Ltd

Original Assignee

Toyobo Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1982-08-11

Filing date

1982-08-11

Publication date

1989-07-19

1982-08-11 Application filed by Toyobo Co Ltd filed Critical Toyobo Co Ltd

1982-08-11 Priority to JP13949982A priority Critical patent/JPS5928664A/ja

1984-02-15 Publication of JPS5928664A publication Critical patent/JPS5928664A/ja

1989-07-19 Publication of JPH0134350B2 publication Critical patent/JPH0134350B2/ja

Status Granted legal-status Critical Current

Links

239000003153 chemical reaction reagent Substances 0.000 claims description 42
239000000203 mixture Substances 0.000 claims description 15
238000005259 measurement Methods 0.000 claims description 9
108010013563 Lipoprotein Lipase Proteins 0.000 claims description 8
102000003992 Peroxidases Human genes 0.000 claims description 8
108040007629 peroxidase activity proteins Proteins 0.000 claims description 8
102000057621 Glycerol kinases Human genes 0.000 claims description 7
102000000587 Glycerolphosphate Dehydrogenase Human genes 0.000 claims description 7
108010041921 Glycerolphosphate Dehydrogenase Proteins 0.000 claims description 7
UETZVSHORCDDTH-UHFFFAOYSA-N iron(2+);hexacyanide Chemical compound [Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] UETZVSHORCDDTH-UHFFFAOYSA-N 0.000 claims description 7
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 7
108010090622 glycerol oxidase Proteins 0.000 claims description 3
108700016170 Glycerol kinases Proteins 0.000 claims description 2
102100022119 Lipoprotein lipase Human genes 0.000 claims 1
125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
BPYKTIZUTYGOLE-IFADSCNNSA-N Bilirubin Chemical compound N1C(=O)C(C)=C(C=C)\C1=C\C1=C(C)C(CCC(O)=O)=C(CC2=C(C(C)=C(\C=C/3C(=C(C=C)C(=O)N\3)C)N2)CCC(O)=O)N1 BPYKTIZUTYGOLE-IFADSCNNSA-N 0.000 description 36
RLFWWDJHLFCNIJ-UHFFFAOYSA-N 4-aminoantipyrine Chemical compound CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 description 19
239000000276 potassium ferrocyanide Substances 0.000 description 14
XOGGUFAVLNCTRS-UHFFFAOYSA-N tetrapotassium;iron(2+);hexacyanide Chemical compound [K+].[K+].[K+].[K+].[Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] XOGGUFAVLNCTRS-UHFFFAOYSA-N 0.000 description 14
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
210000002966 serum Anatomy 0.000 description 9
102000043296 Lipoprotein lipases Human genes 0.000 description 7
150000001448 anilines Chemical class 0.000 description 7
150000003626 triacylglycerols Chemical class 0.000 description 7
102000004190 Enzymes Human genes 0.000 description 6
108090000790 Enzymes Proteins 0.000 description 6
210000001124 body fluid Anatomy 0.000 description 6
239000010839 body fluid Substances 0.000 description 6
101710163410 Probable glycerol kinase Proteins 0.000 description 5
150000002500 ions Chemical class 0.000 description 5
238000000034 method Methods 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
238000002835 absorbance Methods 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
230000000694 effects Effects 0.000 description 4
239000007983 Tris buffer Substances 0.000 description 3
238000004040 coloring Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000000691 measurement method Methods 0.000 description 3
CIPVVROJHKLHJI-UHFFFAOYSA-N n,n-diethyl-3-methylaniline Chemical compound CCN(CC)C1=CC=CC(C)=C1 CIPVVROJHKLHJI-UHFFFAOYSA-N 0.000 description 3
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 3
STBWJPWQQLXSCK-UHFFFAOYSA-N 3-(n-ethyl-3-methoxyanilino)propane-1-sulfonic acid Chemical compound OS(=O)(=O)CCCN(CC)C1=CC=CC(OC)=C1 STBWJPWQQLXSCK-UHFFFAOYSA-N 0.000 description 2
JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
AWUCVROLDVIAJX-UHFFFAOYSA-N alpha-glycerophosphate Natural products OCC(O)COP(O)(O)=O AWUCVROLDVIAJX-UHFFFAOYSA-N 0.000 description 2
VEQOALNAAJBPNY-UHFFFAOYSA-N antipyrine Chemical compound CN1C(C)=CC(=O)N1C1=CC=CC=C1 VEQOALNAAJBPNY-UHFFFAOYSA-N 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 2
GNGACRATGGDKBX-UHFFFAOYSA-N dihydroxyacetone phosphate Chemical compound OCC(=O)COP(O)(O)=O GNGACRATGGDKBX-UHFFFAOYSA-N 0.000 description 2
238000005691 oxidative coupling reaction Methods 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
229960005222 phenazone Drugs 0.000 description 2
AWUCVROLDVIAJX-GSVOUGTGSA-N sn-glycerol 3-phosphate Chemical compound OC[C@@H](O)COP(O)(O)=O AWUCVROLDVIAJX-GSVOUGTGSA-N 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
KRNUKKZDGDAWBF-UHFFFAOYSA-N 2-(n-ethyl-n-m-toluidino)ethanol Chemical compound OCCN(CC)C1=CC=CC(C)=C1 KRNUKKZDGDAWBF-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
ZTQGWROHRVYSPW-UHFFFAOYSA-N 3-(n-ethyl-3-methylanilino)-2-hydroxypropane-1-sulfonic acid Chemical compound OS(=O)(=O)CC(O)CN(CC)C1=CC=CC(C)=C1 ZTQGWROHRVYSPW-UHFFFAOYSA-N 0.000 description 1
IBSUMVZKDLDAEK-UHFFFAOYSA-N 3-(n-ethyl-3-methylanilino)propane-1-sulfonic acid Chemical compound OS(=O)(=O)CCCN(CC)C1=CC=CC(C)=C1 IBSUMVZKDLDAEK-UHFFFAOYSA-N 0.000 description 1
MOYHVSKDHLMMPS-UHFFFAOYSA-N 3-methoxy-n,n-dimethylaniline Chemical compound COC1=CC=CC(N(C)C)=C1 MOYHVSKDHLMMPS-UHFFFAOYSA-N 0.000 description 1
241000193798 Aerococcus Species 0.000 description 1
235000011330 Armoracia rusticana Nutrition 0.000 description 1
240000003291 Armoracia rusticana Species 0.000 description 1
241000228212 Aspergillus Species 0.000 description 1
241000222120 Candida <Saccharomycetales> Species 0.000 description 1
241000186321 Cellulomonas Species 0.000 description 1
241000146387 Chromobacterium viscosum Species 0.000 description 1
MNQZXJOMYWMBOU-VKHMYHEASA-N D-glyceraldehyde Chemical compound OC[C@@H](O)C=O MNQZXJOMYWMBOU-VKHMYHEASA-N 0.000 description 1
102000004895 Lipoproteins Human genes 0.000 description 1
108090001030 Lipoproteins Proteins 0.000 description 1
JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
102000004316 Oxidoreductases Human genes 0.000 description 1
108090000854 Oxidoreductases Proteins 0.000 description 1
241000192001 Pediococcus Species 0.000 description 1
241000589516 Pseudomonas Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
-1 dichloceride Chemical compound 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
229910001425 magnesium ion Inorganic materials 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
239000000049 pigment Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
239000000264 sodium ferrocyanide Substances 0.000 description 1
GTSHREYGKSITGK-UHFFFAOYSA-N sodium ferrocyanide Chemical compound [Na+].[Na+].[Na+].[Na+].[Fe+2].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] GTSHREYGKSITGK-UHFFFAOYSA-N 0.000 description 1
235000012247 sodium ferrocyanide Nutrition 0.000 description 1

Classifications

- 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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
Proteomics, Peptides & Aminoacids (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Microbiology (AREA)
Biochemistry (AREA)
Physics & Mathematics (AREA)
Molecular Biology (AREA)
Biotechnology (AREA)
Biophysics (AREA)
Analytical Chemistry (AREA)
Immunology (AREA)
Bioinformatics & Cheminformatics (AREA)
General Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Investigating Or Analysing Biological Materials (AREA)
Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

JP13949982A 1982-08-11 1982-08-11 トリグリセライド測定用試薬組成物 Granted JPS5928664A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP13949982A JPS5928664A (ja)	1982-08-11	1982-08-11	トリグリセライド測定用試薬組成物

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP13949982A JPS5928664A (ja)	1982-08-11	1982-08-11	トリグリセライド測定用試薬組成物

Publications (2)

Publication Number	Publication Date
JPS5928664A JPS5928664A (ja)	1984-02-15
JPH0134350B2 true JPH0134350B2 (fr)	1989-07-19

Family

ID=15246695

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP13949982A Granted JPS5928664A (ja)	1982-08-11	1982-08-11	トリグリセライド測定用試薬組成物

Country Status (1)

Country	Link
JP (1)	JPS5928664A (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4547461A (en) *	1983-01-18	1985-10-15	Eastman Kodak Company	Composition, analytical element and method for the quantification of creatine kinase
JPH0614879B2 (ja) *	1984-04-27	1994-03-02	株式会社ヤトロン	ビリルビンの干渉を回避して行なう生体成分の測定方法
CN106399460B (zh) *	2016-09-29	2020-03-17	中国医学科学院北京协和医院	用于测定甘油三酯的试剂盒和方法

Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS4950991A (fr) *	1972-05-12	1974-05-17
JPS5324893A (en) *	1976-08-19	1978-03-08	Eastman Kodak Co	Unitary element for detection of glycerine or glyceride

1982
- 1982-08-11 JP JP13949982A patent/JPS5928664A/ja active Granted

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS4950991A (fr) *	1972-05-12	1974-05-17
JPS5324893A (en) *	1976-08-19	1978-03-08	Eastman Kodak Co	Unitary element for detection of glycerine or glyceride

Also Published As

Publication number	Publication date
JPS5928664A (ja)	1984-02-15

Publication	Publication Date	Title
US4251629A (en)	1981-02-17	Determination of hydrogen peroxide
CA1155737A (fr)	1983-10-25	Procede et agents de diagnostic pour la detection de reactions d'oxydo-reduction
Nägele et al.	1984	Reagent for the enzymatic determination of serum total triglycerides with improved lipolytic efficiency
Bruss et al.	1978	Enzymatic microdetermination of glycogen
Deacon et al.	1979	Enzymic assay of total cholesterol involving chemical or enzymic hydrolysis--a comparison of methods.
EP0355864A2 (fr)	1990-02-28	Méthode de mesure quantitative de substances oxydantes utilisant des composés leuco du triarylméthane comme matière colorante
Rautela et al.	1978	Automated enzymic measurement of total cholesterol in serum.
US4247631A (en)	1981-01-27	Reagent and method for the analytic determination of hydrogen peroxide
JPH0577399B2 (fr)	1993-10-26
JPH0464592B2 (fr)	1992-10-15
JPH0452120B2 (fr)	1992-08-20
USRE32016E (en)	1985-10-29	Analysis of lactic acid or lactate using lactate oxidase
JPS6134799B2 (fr)	1986-08-09
US4160696A (en)	1979-07-10	Ascorbic acid determination
US3630847A (en)	1971-12-28	Diagnostic agent for use in the determination of hydroperoxides and of peroxidate-active substances
US4166763A (en)	1979-09-04	Analysis of lactic acid or lactate using lactate oxidase
JPH0319505B2 (fr)	1991-03-15
US4291121A (en)	1981-09-22	Bilirubin-resistant determination of uric acid and cholesterol
US4547461A (en)	1985-10-15	Composition, analytical element and method for the quantification of creatine kinase
US4910134A (en)	1990-03-20	Ascorbic acid decomposing method
EP0306803B1 (fr)	1993-10-20	Composition de test, dispositif et procédé pour la détection visuelle du péroxyde d'hydrogène
JPH0134350B2 (fr)	1989-07-19
US5196314A (en)	1993-03-23	Process and reagent for the determination of substrates or enzyme activities
US4778757A (en)	1988-10-18	Method for the determination of substrates or enzyme activities
JPH0369520B2 (fr)	1991-11-01