CA1079615A - Compose pour la determination enzymatique du glucose - Google Patents

Compose pour la determination enzymatique du glucose

Info

Publication number: CA1079615A
Authority: CA; Canada
Prior art keywords: liter; glucose; millimol; group; enolic
Prior art date: 1976-11-08
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

CA289,446A

Other languages

English (en)

Inventor

Franco Meiattini

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.)

ISTITUTO SIEROTERAPICO E VACCINOGENO TOSCANO "SCLAVO" SpA

Original Assignee

ISTITUTO SIEROTERAPICO E VACCINOGENO TOSCANO "SCLAVO" SpA

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.)

1976-11-08

Filing date

1977-10-25

Publication date

1980-06-17

1977-10-25 Application filed by ISTITUTO SIEROTERAPICO E VACCINOGENO TOSCANO "SCLAVO" SpA filed Critical ISTITUTO SIEROTERAPICO E VACCINOGENO TOSCANO "SCLAVO" SpA

1980-06-17 Application granted granted Critical

1980-06-17 Publication of CA1079615A publication Critical patent/CA1079615A/fr

Status Expired legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 15
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 title claims abstract description 10
239000008103 glucose Substances 0.000 title claims abstract description 10
239000000376 reactant Substances 0.000 claims abstract description 18
150000001875 compounds Chemical class 0.000 claims abstract description 10
102000003992 Peroxidases Human genes 0.000 claims abstract description 5
235000019420 glucose oxidase Nutrition 0.000 claims abstract description 4
239000000872 buffer Substances 0.000 claims description 7
239000000306 component Substances 0.000 claims description 5
239000000843 powder Substances 0.000 abstract description 4
210000004369 blood Anatomy 0.000 abstract description 3
239000008280 blood Substances 0.000 abstract description 3
108040007629 peroxidase activity proteins Proteins 0.000 abstract description 3
210000002700 urine Anatomy 0.000 abstract description 3
239000012472 biological sample Substances 0.000 abstract 1
239000000126 substance Substances 0.000 description 7
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
238000009472 formulation Methods 0.000 description 5
102100033121 Transcription factor 21 Human genes 0.000 description 4
101710119687 Transcription factor 21 Proteins 0.000 description 4
238000000034 method Methods 0.000 description 4
239000008363 phosphate buffer Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
239000002253 acid Substances 0.000 description 3
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
210000002966 serum Anatomy 0.000 description 2
GTOQWWQKBBZILU-UHFFFAOYSA-N 2-hydroxypropane-1,2,3-tricarboxylic acid;quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1.OC(=O)CC(O)(C(O)=O)CC(O)=O GTOQWWQKBBZILU-UHFFFAOYSA-N 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-M 4-hydroxybenzoate Chemical compound OC1=CC=C(C([O-])=O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-M 0.000 description 1
101100451301 Caenorhabditis elegans mls-2 gene Proteins 0.000 description 1
108010015776 Glucose oxidase Proteins 0.000 description 1
239000004366 Glucose oxidase Substances 0.000 description 1
102000004316 Oxidoreductases Human genes 0.000 description 1
108090000854 Oxidoreductases Proteins 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical compound NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 description 1
UTKBLLDLHPDWDU-ODZAUARKSA-N acetic acid;(z)-but-2-enedioic acid Chemical compound CC(O)=O.OC(=O)\C=C/C(O)=O UTKBLLDLHPDWDU-ODZAUARKSA-N 0.000 description 1
GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
230000007547 defect Effects 0.000 description 1
229940116332 glucose oxidase Drugs 0.000 description 1
238000011534 incubation Methods 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
238000005259 measurement Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 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
210000002381 plasma Anatomy 0.000 description 1
102000004169 proteins and genes Human genes 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
YQUVCSBJEUQKSH-UHFFFAOYSA-N protochatechuic acid Natural products OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 description 1
239000012088 reference solution Substances 0.000 description 1
229960000581 salicylamide Drugs 0.000 description 1
229960001860 salicylate Drugs 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000012086 standard solution Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
230000009466 transformation Effects 0.000 description 1
238000000844 transformation Methods 0.000 description 1
POSZUTFLHGNLHX-KSBRXOFISA-N tris maleate Chemical compound OCC(N)(CO)CO.OCC(N)(CO)CO.OC(=O)\C=C/C(O)=O POSZUTFLHGNLHX-KSBRXOFISA-N 0.000 description 1
WKOLLVMJNQIZCI-UHFFFAOYSA-N vanillic acid Chemical compound COC1=CC(C(O)=O)=CC=C1O WKOLLVMJNQIZCI-UHFFFAOYSA-N 0.000 description 1
TUUBOHWZSQXCSW-UHFFFAOYSA-N vanillic acid Natural products COC1=CC(O)=CC(C(O)=O)=C1 TUUBOHWZSQXCSW-UHFFFAOYSA-N 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
- C12Q1/54—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving glucose or galactose

Landscapes

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

CA289,446A 1976-11-08 1977-10-25 Compose pour la determination enzymatique du glucose Expired CA1079615A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT2911776A IT1123670B (it)	1976-11-08	1976-11-08	Composizione adatta alla determinazione enzimatica del glugosio

Publications (1)

Publication Number	Publication Date
CA1079615A true CA1079615A (fr)	1980-06-17

Family

ID=11226323

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA289,446A Expired CA1079615A (fr)	1976-11-08	1977-10-25	Compose pour la determination enzymatique du glucose

Country Status (13)

Country	Link
JP (1)	JPS5358293A (fr)
AR (1)	AR217266A1 (fr)
AU (1)	AU503975B2 (fr)
BE (1)	BE860607A (fr)
BR (1)	BR7707498A (fr)
CA (1)	CA1079615A (fr)
DE (1)	DE2749991A1 (fr)
ES (1)	ES464038A1 (fr)
FR (1)	FR2370282A1 (fr)
GB (1)	GB1593735A (fr)
GR (1)	GR63608B (fr)
IT (1)	IT1123670B (fr)
NL (1)	NL7712310A (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5520471A (en) *	1978-08-01	1980-02-13	Kyowa Hakko Kogyo Co Ltd	Hydrogen peroxide quantifying method
US4460684A (en) *	1982-08-02	1984-07-17	Miles Laboratories, Inc.	Ascorbate-resistant broad range glucose test composition, test device and method
US4935346A (en) *	1986-08-13	1990-06-19	Lifescan, Inc.	Minimum procedure system for the determination of analytes
RU2123701C1 (ru) *	1998-05-26	1998-12-20	Общество с ограниченной ответственностью "Импакт"	Набор для ферментного анализа и способ его получения
DE102004050209A1 (de) *	2004-10-15	2006-04-20	Merck Patent Gmbh	Mittel und Verfahren zum Nachweis von Furfuralen
CN114609129B (zh) *	2022-03-09	2026-02-06	杭州布布主宠物科技有限公司	一种猫用葡萄糖检测颗粒及葡萄糖指示猫砂和制备方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT986838B (it) *	1972-05-12	1975-01-30	Sclavo Inst Sieroterapeut	Complesso di reagenti per la deter minazione enzimatica del glucosio sistema glucosio ossidasi perossi dasi con metodo manuale e automati co con lettura a termine o in cinetica

1976
- 1976-11-08 IT IT2911776A patent/IT1123670B/it active
1977
- 1977-10-25 CA CA289,446A patent/CA1079615A/fr not_active Expired
- 1977-10-27 AU AU30103/77A patent/AU503975B2/en not_active Expired
- 1977-11-02 GR GR54695A patent/GR63608B/el unknown
- 1977-11-03 ES ES464038A patent/ES464038A1/es not_active Expired
- 1977-11-04 GB GB4605777A patent/GB1593735A/en not_active Expired
- 1977-11-07 FR FR7733450A patent/FR2370282A1/fr not_active Withdrawn
- 1977-11-07 BR BR7707498A patent/BR7707498A/pt unknown
- 1977-11-08 JP JP13314377A patent/JPS5358293A/ja active Pending
- 1977-11-08 NL NL7712310A patent/NL7712310A/xx not_active Application Discontinuation
- 1977-11-08 DE DE19772749991 patent/DE2749991A1/de not_active Withdrawn
- 1977-11-08 BE BE182448A patent/BE860607A/fr not_active IP Right Cessation
- 1977-11-08 AR AR26987877A patent/AR217266A1/es active

Also Published As

Publication number	Publication date
IT1123670B (it)	1986-04-30
FR2370282A1 (fr)	1978-06-02
NL7712310A (nl)	1978-05-10
BR7707498A (pt)	1978-07-18
AU503975B2 (en)	1979-09-27
ES464038A1 (es)	1978-07-16
AR217266A1 (es)	1980-03-14
AU3010377A (en)	1979-05-03
GB1593735A (en)	1981-07-22
DE2749991A1 (de)	1978-05-11
GR63608B (en)	1979-11-26
BE860607A (fr)	1978-05-08
JPS5358293A (en)	1978-05-26

Legal Events

Date	Code	Title	Description
1997-06-17	MKEX	Expiry

Publication	Publication Date	Title
EP0230229B1 (fr)	1991-09-25	Composition stable pour la détermination des substances avec une activité péroxidique
Akimoto et al.	1990	Luminol chemiluminescence reaction catalyzed by a microbial peroxidase
US4517287A (en)	1985-05-14	Method and reagent for the enzymatic determination of enzyme substrates
EP0240849B1 (fr)	1993-11-24	Dispositif de teinte contrôlée
NL8500181A (nl)	1985-08-16	Voor gebruik gereed vloeibaar reagens ter bepaling van het glucosegehalte in bloed.
GB2043891A (en)	1980-10-08	Determination of hydrogen peroxide
US3997470A (en)	1976-12-14	Surfactant containing reagent formulations for assaying biological specimens and methods of preparing same
JP2539225B2 (ja)	1996-10-02	グルコ−ス定量用安定化液体酵素組成物、それを用いる試薬キット及び定量方法
EP0575515B1 (fr)	1999-07-21	Stabilisation d'un reactif contenant une enzyme pour la determination d'un analyte
US3816262A (en)	1974-06-11	Reagent formulations for assaying biological specimens amd methods of preparing and using same
CA1154366A (fr)	1983-09-27	Methode de dosage enzymatique et solutions stabilisees pour le dosage du cholesterol total dans le serum humain
CA1079615A (fr)	1980-06-17	Compose pour la determination enzymatique du glucose
JPH06510905A (ja)	1994-12-08	フェナジン含有指示薬を含む試薬および検定法
US3876502A (en)	1975-04-08	Reagent formulations for assaying urea nitrogen in biological specimens and methods of preparing and using same
EP0463755A1 (fr)	1992-01-02	Réactif NADH aqueux et stable, et trousse
EP0603831B1 (fr)	1999-11-10	Réactif combiné liquide et stable pour la determination de dioxyde de carbone dans le serum
JPH01108997A (ja)	1989-04-26	血液又は血液から導出した試料中の血清のフルクトスアミン含量を特異的に測定する方法及び試薬、及び非特異的還元作用を有するか、又は／及び溷濁を惹起する試料成分を除去する方法
JP2619222B2 (ja)	1997-06-11	血液試料または血液由来の試料中のフルクトサミン含量を測定するための試薬と方法
JP2009106182A (ja)	2009-05-21	被検成分の定量方法、分析用デバイス、及び分析装置
US5266472A (en)	1993-11-30	Stabilization of the enzyme urate oxidase in liquid form
WO1998031829A1 (fr)	1998-07-23	Procedes et reactifs permettant d'evaluer la teneur en acide ascorbique
JP2994831B2 (ja)	1999-12-27	コレステロールの定量法および定量用試薬
EP1083235A2 (fr)	2001-03-14	Solution d'un coenzyme réduit
Kovar et al.	1983	Determination of cholesterol in sera
JP3674450B2 (ja)	2005-07-20	Ｇｐｔ測定用試薬