DD201733A5 - Verfahren und reagenz zur bestimmung von cholestrin - Google Patents
Verfahren und reagenz zur bestimmung von cholestrin Download PDFInfo
- Publication number
- DD201733A5 DD201733A5 DD81235411A DD23541181A DD201733A5 DD 201733 A5 DD201733 A5 DD 201733A5 DD 81235411 A DD81235411 A DD 81235411A DD 23541181 A DD23541181 A DD 23541181A DD 201733 A5 DD201733 A5 DD 201733A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- cholesterol
- mmol
- reagent
- determination
- buffer
- Prior art date
Links
- 239000003153 chemical reaction reagent Substances 0.000 title claims abstract description 34
- 238000000034 method Methods 0.000 title claims abstract description 24
- 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 claims abstract description 61
- 235000012000 cholesterol Nutrition 0.000 claims abstract description 29
- 108010089254 Cholesterol oxidase Proteins 0.000 claims abstract description 25
- WDNBURPWRNALGP-UHFFFAOYSA-N 3,4-Dichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1 WDNBURPWRNALGP-UHFFFAOYSA-N 0.000 claims abstract description 20
- 241000187747 Streptomyces Species 0.000 claims abstract description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 10
- 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 claims abstract description 10
- 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 claims abstract description 10
- 108010055297 Sterol Esterase Proteins 0.000 claims abstract description 9
- 102000000019 Sterol Esterase Human genes 0.000 claims abstract description 9
- 244000005700 microbiome Species 0.000 claims abstract description 8
- 230000036284 oxygen consumption Effects 0.000 claims abstract description 5
- RLFWWDJHLFCNIJ-UHFFFAOYSA-N 4-aminoantipyrine Chemical compound CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 239000003599 detergent Substances 0.000 claims description 15
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 9
- 102000003992 Peroxidases Human genes 0.000 claims description 8
- 108040007629 peroxidase activity proteins Proteins 0.000 claims description 8
- 239000007983 Tris buffer Substances 0.000 claims description 7
- 238000005259 measurement Methods 0.000 claims description 7
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims description 7
- 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 claims description 6
- 125000003716 cholic acid group Chemical group 0.000 claims description 6
- 101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 5
- 239000000872 buffer Substances 0.000 claims description 5
- 150000002989 phenols Chemical class 0.000 claims description 5
- 239000008363 phosphate buffer Substances 0.000 claims description 5
- 102000004316 Oxidoreductases Human genes 0.000 claims description 2
- 108090000854 Oxidoreductases Proteins 0.000 claims description 2
- 239000008366 buffered solution Substances 0.000 claims description 2
- 239000007787 solid Substances 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 description 5
- 108090000790 Enzymes Proteins 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 238000001514 detection method Methods 0.000 description 4
- 230000002255 enzymatic effect Effects 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- ITRHZTGVVSWIDC-UHFFFAOYSA-N 11-methyl-1-(11-methyldodecoxy)dodecane Chemical compound CC(C)CCCCCCCCCCOCCCCCCCCCCC(C)C ITRHZTGVVSWIDC-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- UMPSXRYVXUPCOS-UHFFFAOYSA-N 2,3-dichlorophenol Chemical class OC1=CC=CC(Cl)=C1Cl UMPSXRYVXUPCOS-UHFFFAOYSA-N 0.000 description 2
- 241000187654 Nocardia Species 0.000 description 2
- 241001312733 Streptomyces griseofuscus Species 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- -1 azide Chemical compound 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- 239000012928 buffer substance Substances 0.000 description 2
- 230000002860 competitive effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- CKFGINPQOCXMAZ-UHFFFAOYSA-N methanediol Chemical compound OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- NRHMKIHPTBHXPF-TUJRSCDTSA-M sodium cholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 NRHMKIHPTBHXPF-TUJRSCDTSA-M 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- CFFZDZCDUFSOFZ-UHFFFAOYSA-N 3,4-Dihydroxy-phenylacetic acid Chemical compound OC(=O)CC1=CC=C(O)C(O)=C1 CFFZDZCDUFSOFZ-UHFFFAOYSA-N 0.000 description 1
- 241000186146 Brevibacterium Species 0.000 description 1
- 102000016938 Catalase Human genes 0.000 description 1
- 108010053835 Catalase Proteins 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 239000007995 HEPES buffer Substances 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 241000482007 Streptomyces acidomyceticus Species 0.000 description 1
- 241000187391 Streptomyces hygroscopicus Species 0.000 description 1
- 241001655322 Streptomycetales Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229940058934 aminoquinoline antimalarials Drugs 0.000 description 1
- 150000005010 aminoquinolines Chemical class 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000003613 bile acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229940099352 cholate Drugs 0.000 description 1
- BHQCQFFYRZLCQQ-OELDTZBJSA-N cholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-OELDTZBJSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 229960003964 deoxycholic acid Drugs 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- SIOLDWZBFABPJU-UHFFFAOYSA-M isotridecanoate Chemical compound CC(C)CCCCCCCCCC([O-])=O SIOLDWZBFABPJU-UHFFFAOYSA-M 0.000 description 1
- 238000002796 luminescence method Methods 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- HWYHZTIRURJOHG-UHFFFAOYSA-N luminol Chemical compound O=C1NNC(=O)C2=C1C(N)=CC=C2 HWYHZTIRURJOHG-UHFFFAOYSA-N 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- CQRYARSYNCAZFO-UHFFFAOYSA-N salicyl alcohol Chemical compound OCC1=CC=CC=C1O CQRYARSYNCAZFO-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- FHHPUSMSKHSNKW-SMOYURAASA-M sodium deoxycholate Chemical compound [Na+].C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC([O-])=O)C)[C@@]2(C)[C@@H](O)C1 FHHPUSMSKHSNKW-SMOYURAASA-M 0.000 description 1
- FNXKBSAUKFCXIK-UHFFFAOYSA-M sodium;hydrogen carbonate;8-hydroxy-7-iodoquinoline-5-sulfonic acid Chemical class [Na+].OC([O-])=O.C1=CN=C2C(O)=C(I)C=C(S(O)(=O)=O)C2=C1 FNXKBSAUKFCXIK-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000003431 steroids Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-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
- C12Q1/60—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving cholesterol
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/805—Test papers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/81—Packaged device or kit
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/886—Streptomyces
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)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19803046241 DE3046241A1 (de) | 1980-12-08 | 1980-12-08 | Verfahren und reagenz zur bestimmung von cholesterin |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD201733A5 true DD201733A5 (de) | 1983-08-03 |
Family
ID=6118631
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD81235411A DD201733A5 (de) | 1980-12-08 | 1981-12-04 | Verfahren und reagenz zur bestimmung von cholestrin |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4503144A (fr) |
| EP (1) | EP0053692B1 (fr) |
| JP (1) | JPS5818080B2 (fr) |
| AR (1) | AR227209A1 (fr) |
| AT (1) | ATE5002T1 (fr) |
| AU (1) | AU528296B2 (fr) |
| CA (1) | CA1179243A (fr) |
| DD (1) | DD201733A5 (fr) |
| DE (2) | DE3046241A1 (fr) |
| ES (1) | ES8300136A1 (fr) |
| YU (1) | YU44105B (fr) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59230161A (ja) * | 1983-06-13 | 1984-12-24 | Wako Pure Chem Ind Ltd | 還元性物質の分解方法及び分解用試薬 |
| DE3329387A1 (de) * | 1983-08-13 | 1985-02-21 | Flemming GmbH, 6204 Taunusstein | Verfahren und reagenz zur bestimmung von cholesterin |
| US4680259A (en) * | 1984-09-26 | 1987-07-14 | Eastman Kodak Company | Analytical element and method for colorimetric determination of total cholesterol |
| JPS61108400A (ja) * | 1984-10-31 | 1986-05-27 | Amano Pharmaceut Co Ltd | コレステロ−ルの定量法 |
| DE3509238A1 (de) * | 1985-03-14 | 1986-09-18 | Boehringer Mannheim Gmbh, 6800 Mannheim | Stabilisierung der aktivitaet von peroxidase in loesung |
| EP0223977B1 (fr) * | 1985-11-25 | 1990-10-10 | Wako Pure Chemical Industries, Ltd. | Méthode pour le développement des couleurs dans des examens cliniques |
| DE3636851A1 (de) * | 1986-10-29 | 1988-05-11 | Boehringer Mannheim Gmbh | Verfahren und reagenz zur spezifischen bestimmung des cholesterins der hdl-fraktion |
| US5171688A (en) * | 1988-08-30 | 1992-12-15 | Cholestech Corporation | Self-corrected assay device |
| US5156954A (en) * | 1989-03-08 | 1992-10-20 | Cholestech Corporation | Assay device and method using a signal-modulating compound |
| US5487978A (en) * | 1988-11-03 | 1996-01-30 | Gds Technology, Inc. | Method, composition and device for the determination of cholesterol using cholesterol oxidase obtained from bacterial strain NRRL B-18713 |
| US5114350A (en) * | 1989-03-08 | 1992-05-19 | Cholestech Corporation | Controlled-volume assay apparatus |
| JPH0359460A (ja) * | 1989-07-28 | 1991-03-14 | Tohoku Denshi Sangyo Kk | 過酸化脂質の高感度検出方法および検出用組成物 |
| US5110724A (en) * | 1990-04-02 | 1992-05-05 | Cholestech Corporation | Multi-analyte assay device |
| GB9416002D0 (en) * | 1994-08-08 | 1994-09-28 | Univ Cranfield | Fluid transport device |
| EP1357383B1 (fr) * | 2002-04-09 | 2005-11-09 | Cholestech Corporation | Méthode et dispositif de test permettant de doser le cholesterol HDL (lipoproteine à haute densité) |
| JP4343574B2 (ja) | 2003-04-15 | 2009-10-14 | 株式会社放電精密加工研究所 | プレス成形機 |
| ATE483165T1 (de) * | 2007-01-09 | 2010-10-15 | Cholestech Corp | Vorrichtung und verfahren zur messung des ldl- assoziierten cholesterols |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR195000A1 (es) * | 1972-05-17 | 1973-08-30 | Boehringer Mannheim Gmbh | Procedimiento para la determinacion de colesterol |
| GB1479994A (en) * | 1974-03-04 | 1977-07-13 | Abbott Lab | Single reagent for the enzymatic determination of cholesterol and method therefor |
| US3983005A (en) * | 1974-03-25 | 1976-09-28 | Eastman Kodak Company | Integral element for the analysis of cholesterol |
| DE2558536B2 (de) * | 1975-12-24 | 1979-07-12 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren zur kinetischen Substratbestimmung und Reagens zu seiner Durchführung |
| DE2816229C2 (de) * | 1978-04-14 | 1983-11-10 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und Mittel zur Beseitigung von Trübungen |
| US4226713A (en) * | 1978-04-24 | 1980-10-07 | Goldberg Jack M | Diagnostic agents |
| DE2911284C2 (de) * | 1979-03-22 | 1982-01-28 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und Reagenz zur Aktivierung der Cholesterinesterase |
| DE2924875A1 (de) * | 1979-06-20 | 1981-01-29 | Boehringer Mannheim Gmbh | Verfahren zur gewinnung von cholesterinoxidase |
| IT1130252B (it) * | 1980-02-04 | 1986-06-11 | Elvi Spa | Metodo per l'eliminazione dell'interferenza da biliribuna nel dosaggio di perossido di idrigeno mediante una reazione di trinder modificata |
-
1980
- 1980-12-08 DE DE19803046241 patent/DE3046241A1/de not_active Withdrawn
-
1981
- 1981-10-22 EP EP81108753A patent/EP0053692B1/fr not_active Expired
- 1981-10-22 AT AT81108753T patent/ATE5002T1/de not_active IP Right Cessation
- 1981-10-22 DE DE8181108753T patent/DE3161188D1/de not_active Expired
- 1981-10-29 AR AR287278A patent/AR227209A1/es active
- 1981-11-18 CA CA000390371A patent/CA1179243A/fr not_active Expired
- 1981-11-20 ES ES507307A patent/ES8300136A1/es not_active Expired
- 1981-12-04 DD DD81235411A patent/DD201733A5/de not_active IP Right Cessation
- 1981-12-07 YU YU2859/81A patent/YU44105B/xx unknown
- 1981-12-07 US US06/328,350 patent/US4503144A/en not_active Expired - Lifetime
- 1981-12-07 AU AU78331/81A patent/AU528296B2/en not_active Expired
- 1981-12-08 JP JP56196400A patent/JPS5818080B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AU528296B2 (en) | 1983-04-21 |
| ES507307A0 (es) | 1982-11-01 |
| EP0053692B1 (fr) | 1983-10-12 |
| YU44105B (en) | 1990-02-28 |
| EP0053692A1 (fr) | 1982-06-16 |
| JPS5818080B2 (ja) | 1983-04-11 |
| DE3161188D1 (en) | 1983-11-17 |
| YU285981A (en) | 1984-04-30 |
| JPS57122800A (en) | 1982-07-30 |
| US4503144A (en) | 1985-03-05 |
| DE3046241A1 (de) | 1982-07-15 |
| ES8300136A1 (es) | 1982-11-01 |
| AR227209A1 (es) | 1982-09-30 |
| CA1179243A (fr) | 1984-12-11 |
| ATE5002T1 (de) | 1983-10-15 |
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