FI63637C - Stabiliserade snabbdiagnostiska medel innehaollande oxideringsindikatorer - Google Patents

Stabiliserade snabbdiagnostiska medel innehaollande oxideringsindikatorer Download PDF

Info

Publication number: FI63637C
Authority: FI; Finland
Prior art keywords: compounds; substances; test; test strip; hydroperoxides
Prior art date: 1977-04-09

Application number

FI781015A

Other languages

English (en)

Finnish (fi)

Other versions

FI63637B (fi

FI781015A7 (fi

Inventor

Walter Rittersdorf

Hugo Tiedemann

Wolfgang Werner

Hans Wielinger

Original Assignee

Boehringer Mannheim Gmbh

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.)

1977-04-09

Filing date

1978-04-03

Publication date

1983-07-11

1978-04-03 Application filed by Boehringer Mannheim Gmbh filed Critical Boehringer Mannheim Gmbh

1978-10-10 Publication of FI781015A7 publication Critical patent/FI781015A7/fi

1983-03-31 Application granted granted Critical

1983-03-31 Publication of FI63637B publication Critical patent/FI63637B/fi

1983-07-11 Publication of FI63637C publication Critical patent/FI63637C/fi

Links

238000012360 testing method Methods 0.000 claims description 45
210000004369 blood Anatomy 0.000 claims description 20
239000008280 blood Substances 0.000 claims description 20
150000001875 compounds Chemical class 0.000 claims description 20
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 19
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 claims description 15
238000006243 chemical reaction Methods 0.000 claims description 15
239000008103 glucose Substances 0.000 claims description 15
230000003647 oxidation Effects 0.000 claims description 14
238000007254 oxidation reaction Methods 0.000 claims description 14
210000003608 fece Anatomy 0.000 claims description 12
239000000126 substance Substances 0.000 claims description 9
102000003992 Peroxidases Human genes 0.000 claims description 8
239000002253 acid Substances 0.000 claims description 8
210000001124 body fluid Anatomy 0.000 claims description 8
239000010839 body fluid Substances 0.000 claims description 8
150000002432 hydroperoxides Chemical class 0.000 claims description 8
108040007629 peroxidase activity proteins Proteins 0.000 claims description 8
239000000872 buffer Substances 0.000 claims description 7
239000003381 stabilizer Substances 0.000 claims description 6
239000013543 active substance Substances 0.000 claims description 5
125000003545 alkoxy group Chemical group 0.000 claims description 4
HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 3
125000003118 aryl group Chemical group 0.000 claims description 3
239000008139 complexing agent Substances 0.000 claims description 3
150000005840 aryl radicals Chemical class 0.000 claims description 2
230000008033 biological extinction Effects 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
239000002562 thickening agent Substances 0.000 claims description 2
239000000080 wetting agent Substances 0.000 claims description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
125000005843 halogen group Chemical group 0.000 claims 2
239000000084 colloidal system Substances 0.000 claims 1
230000001681 protective effect Effects 0.000 claims 1
239000000243 solution Substances 0.000 description 27
210000002700 urine Anatomy 0.000 description 12
238000001514 detection method Methods 0.000 description 11
230000035945 sensitivity Effects 0.000 description 8
AVKHCKXGKPAGEI-UHFFFAOYSA-N Phenicarbazide Chemical compound NC(=O)NNC1=CC=CC=C1 AVKHCKXGKPAGEI-UHFFFAOYSA-N 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
239000003963 antioxidant agent Substances 0.000 description 6
235000006708 antioxidants Nutrition 0.000 description 6
238000002474 experimental method Methods 0.000 description 6
230000001575 pathological effect Effects 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
239000004366 Glucose oxidase Substances 0.000 description 4
108010015776 Glucose oxidase Proteins 0.000 description 4
238000004820 blood count Methods 0.000 description 4
230000000694 effects Effects 0.000 description 4
235000019420 glucose oxidase Nutrition 0.000 description 4
229940116332 glucose oxidase Drugs 0.000 description 4
-1 mercapto compounds Chemical class 0.000 description 4
239000001267 polyvinylpyrrolidone Substances 0.000 description 4
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 4
229920000036 polyvinylpyrrolidone Polymers 0.000 description 4
230000000087 stabilizing effect Effects 0.000 description 4
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
239000004263 Guaiac resin Substances 0.000 description 3
229920000932 Gum guaicum Polymers 0.000 description 3
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical class C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000002250 absorbent Substances 0.000 description 3
230000002745 absorbent Effects 0.000 description 3
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 3
LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 3
235000019278 guaiac resin Nutrition 0.000 description 3
238000005470 impregnation Methods 0.000 description 3
238000000034 method Methods 0.000 description 3
230000001590 oxidative effect Effects 0.000 description 3
TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 2
JGBAASVQPMTVHO-UHFFFAOYSA-N 2,5-dihydroperoxy-2,5-dimethylhexane Chemical class OOC(C)(C)CCC(C)(C)OO JGBAASVQPMTVHO-UHFFFAOYSA-N 0.000 description 2
WXTMDXOMEHJXQO-UHFFFAOYSA-N 2,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC=C1O WXTMDXOMEHJXQO-UHFFFAOYSA-N 0.000 description 2
AKEUNCKRJATALU-UHFFFAOYSA-N 2,6-dihydroxybenzoic acid Chemical compound OC(=O)C1=C(O)C=CC=C1O AKEUNCKRJATALU-UHFFFAOYSA-N 0.000 description 2
UAIUNKRWKOVEES-UHFFFAOYSA-N 3,3',5,5'-tetramethylbenzidine Chemical compound CC1=C(N)C(C)=CC(C=2C=C(C)C(N)=C(C)C=2)=C1 UAIUNKRWKOVEES-UHFFFAOYSA-N 0.000 description 2
CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
229910021626 Tin(II) chloride Inorganic materials 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
230000002411 adverse Effects 0.000 description 2
230000001476 alcoholic effect Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000003153 chemical reaction reagent Substances 0.000 description 2
239000003638 chemical reducing agent Substances 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
230000001627 detrimental effect Effects 0.000 description 2
150000001989 diazonium salts Chemical class 0.000 description 2
150000002367 halogens Chemical group 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
239000000203 mixture Substances 0.000 description 2
CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 description 2
RDOWQLZANAYVLL-UHFFFAOYSA-N phenanthridine Chemical compound C1=CC=C2C3=CC=CC=C3C=NC2=C1 RDOWQLZANAYVLL-UHFFFAOYSA-N 0.000 description 2
DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 description 2
239000001509 sodium citrate Substances 0.000 description 2
NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 2
235000011150 stannous chloride Nutrition 0.000 description 2
239000001119 stannous chloride Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 2
RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
ZPKHRIKIPQGDKU-UHFFFAOYSA-N (4-chloroanilino)urea Chemical compound NC(=O)NNC1=CC=C(Cl)C=C1 ZPKHRIKIPQGDKU-UHFFFAOYSA-N 0.000 description 1
ZYKTTXOTZLXBES-UHFFFAOYSA-N (4-methylanilino)urea Chemical compound CC1=CC=C(NNC(N)=O)C=C1 ZYKTTXOTZLXBES-UHFFFAOYSA-N 0.000 description 1
OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 description 1
SBUBPFHJZHQNNT-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene hydrogen peroxide Chemical class OO.OO.CC(C)C1=CC=CC=C1C(C)C SBUBPFHJZHQNNT-UHFFFAOYSA-N 0.000 description 1
YWBMNCRJFZGXJY-UHFFFAOYSA-N 1-hydroperoxy-1,2,3,4-tetrahydronaphthalene Chemical class C1=CC=C2C(OO)CCCC2=C1 YWBMNCRJFZGXJY-UHFFFAOYSA-N 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
LIZVXGBYTGTTTI-UHFFFAOYSA-N 2-[(4-methylphenyl)sulfonylamino]-2-phenylacetic acid Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(C(O)=O)C1=CC=CC=C1 LIZVXGBYTGTTTI-UHFFFAOYSA-N 0.000 description 1
NUIURNJTPRWVAP-UHFFFAOYSA-N 3,3'-Dimethylbenzidine Chemical compound C1=C(N)C(C)=CC(C=2C=C(C)C(N)=CC=2)=C1 NUIURNJTPRWVAP-UHFFFAOYSA-N 0.000 description 1
MOMKYJPSVWEWPM-UHFFFAOYSA-N 4-(chloromethyl)-2-(4-methylphenyl)-1,3-thiazole Chemical compound C1=CC(C)=CC=C1C1=NC(CCl)=CS1 MOMKYJPSVWEWPM-UHFFFAOYSA-N 0.000 description 1
WXMQHPKQCPCDQO-UHFFFAOYSA-N 4-dimorpholin-4-ylphosphorylmorpholine Chemical compound C1COCCN1P(N1CCOCC1)(=O)N1CCOCC1 WXMQHPKQCPCDQO-UHFFFAOYSA-N 0.000 description 1
SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
239000001836 Dioctyl sodium sulphosuccinate Substances 0.000 description 1
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
RGHNJXZEOKUKBD-SQOUGZDYSA-N Gluconic acid Natural products OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 1
102000001554 Hemoglobins Human genes 0.000 description 1
108010054147 Hemoglobins Proteins 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
239000004141 Sodium laurylsulphate Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical compound NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
235000010323 ascorbic acid Nutrition 0.000 description 1
229960005070 ascorbic acid Drugs 0.000 description 1
239000011668 ascorbic acid Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
150000007514 bases Chemical class 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
230000000711 cancerogenic effect Effects 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
231100000357 carcinogen Toxicity 0.000 description 1
239000003183 carcinogenic agent Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
239000012954 diazonium Substances 0.000 description 1
238000006193 diazotization reaction Methods 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000835 fiber Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
235000004515 gallic acid Nutrition 0.000 description 1
229940074391 gallic acid Drugs 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
229960005219 gentisic acid Drugs 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
239000000174 gluconic acid Substances 0.000 description 1
235000012208 gluconic acid Nutrition 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
150000002429 hydrazines Chemical class 0.000 description 1
238000007654 immersion Methods 0.000 description 1
239000007788 liquid Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
239000003607 modifier Substances 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
229930004008 p-menthane Natural products 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
GKKCIDNWFBPDBW-UHFFFAOYSA-M potassium cyanate Chemical compound [K]OC#N GKKCIDNWFBPDBW-UHFFFAOYSA-M 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
230000001603 reducing effect Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
229940079862 sodium lauryl sarcosinate Drugs 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
235000019983 sodium metaphosphate Nutrition 0.000 description 1
ADWNFGORSPBALY-UHFFFAOYSA-M sodium;2-[dodecyl(methyl)amino]acetate Chemical compound [Na+].CCCCCCCCCCCCN(C)CC([O-])=O ADWNFGORSPBALY-UHFFFAOYSA-M 0.000 description 1
HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000010186 staining Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000008362 succinate buffer Substances 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
UJMBCXLDXJUMFB-GLCFPVLVSA-K tartrazine Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-GLCFPVLVSA-K 0.000 description 1
229960000943 tartrazine Drugs 0.000 description 1
235000012756 tartrazine Nutrition 0.000 description 1
239000004149 tartrazine Substances 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
- C12Q1/26—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
- C12Q1/28—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving peroxidase
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/14—Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
- Y10T436/142222—Hetero-O [e.g., ascorbic acid, etc.]
- Y10T436/143333—Saccharide [e.g., DNA, etc.]
- Y10T436/144444—Glucose

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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)
Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

FI781015A 1977-04-09 1978-04-03 Stabiliserade snabbdiagnostiska medel innehaollande oxideringsindikatorer FI63637C (fi)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE2716060		1977-04-09
DE2716060A DE2716060C3 (de)	1977-04-09	1977-04-09	Stabilisierte Schnelldiagnostica mit Oxydationsindikatoren

Publications (3)

Publication Number	Publication Date
FI781015A7 FI781015A7 (fi)	1978-10-10
FI63637B FI63637B (fi)	1983-03-31
FI63637C true FI63637C (fi)	1983-07-11

Family

ID=6006093

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
FI781015A FI63637C (fi)	1977-04-09	1978-04-03	Stabiliserade snabbdiagnostiska medel innehaollande oxideringsindikatorer

Country Status (18)

Country	Link
US (1)	US4220713A (fr)
JP (1)	JPS53126996A (fr)
AR (1)	AR215172A1 (fr)
AT (1)	AT361132B (fr)
BE (1)	BE865701A (fr)
BR (1)	BR7802178A (fr)
CA (1)	CA1101318A (fr)
CH (1)	CH636964A5 (fr)
DD (1)	DD141361A5 (fr)
DE (1)	DE2716060C3 (fr)
FI (1)	FI63637C (fr)
FR (1)	FR2386823A1 (fr)
GB (1)	GB1571363A (fr)
HU (1)	HU177174B (fr)
IT (1)	IT1095396B (fr)
NL (1)	NL185177C (fr)
SE (1)	SE442680B (fr)
SU (1)	SU1457819A3 (fr)

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US4329317A (en)	1981-01-29	1982-05-11	Smithkline Instruments, Inc.	Method of stabilizing a specimen slide for occult blood testing
US4382064A (en)	1981-01-29	1983-05-03	Smithkline Instruments, Inc.	Specimen slide for occult blood testing
DE3134585A1 (de) *	1981-09-01	1983-03-10	Terumo Corp., Tokyo	Testeinheit zum nachweis von okkultem blut
US4956300A (en) *	1982-01-05	1990-09-11	Helena Laboratories Corporation	Aid for determining the presence of occult blood, method of making the aid, and method of using the aid
PH23572A (en) *	1982-05-28	1989-09-11	Smithkline Diagnostics Inc	Specimen test slide for occult blood testing
US5702913A (en) *	1983-12-21	1997-12-30	Helena Laboratories Corporation	Chromgen-reagent test system
US5273888A (en) *	1984-01-16	1993-12-28	Helena Laboratories Corporation	Chemical test kit and method for determining the presence of blood in a specimen and for verifying the effectiveness of the chemicals
JPH0653074B2 (ja) *	1984-02-24	1994-07-20	大日本印刷株式会社	体液検査体
DE3425118A1 (de) *	1984-07-07	1986-01-16	Boehringer Mannheim Gmbh, 6800 Mannheim	Neue redox-indikatoren
US4615982A (en) *	1984-12-11	1986-10-07	Lawrence Paul J	Fecal occult blood test
US4818702A (en) *	1986-06-02	1989-04-04	Litmus Concepts, Inc.	Fecal occult blood test reagent
DE3625852A1 (de) *	1986-07-31	1988-02-04	Miles Lab	Verbesserte testmittel und verfahren zu deren herstellung
US5081040A (en) *	1987-06-29	1992-01-14	Helena Laboratories Corporation	Composition and kit for testing for occult blood in human and animal excretions, fluids, or tissue matrixes
JP2645429B2 (ja) *	1987-09-16	1997-08-25	スミスクライン・ダイアグノスティクス・インコーポレイテッド	改良された糞便潜血用テスト
US5310680A (en) *	1987-09-16	1994-05-10	Smithkline Diagnostics, Inc.	Test for fecal occult blood
US4895798A (en) *	1987-11-13	1990-01-23	Miles, Inc.	Test devices for determination of occult blood
JPH01177824A (ja) *	1988-01-08	1989-07-14	Toshiba Corp	ネットワーク継電装置
US5116729A (en) *	1989-03-10	1992-05-26	Miles Inc.	Stabilization of oxidase enzyme-based test strips
US5185247A (en) *	1989-03-10	1993-02-09	Miles Inc.	Stabilization of oxidase enzyme-based test strips
US5217874A (en) *	1989-04-04	1993-06-08	Helena Laboratories Corporation	Fecal occult blood test product with positive and negative controls
US5196167A (en) *	1989-04-04	1993-03-23	Helena Laboratories Corporation	Fecal occult blood test product with positive and negative controls
JP2836865B2 (ja) *	1989-10-23	1998-12-14	東亜医用電子株式会社	血液中の白血球およびヘモグロビンの測定用試薬
DE3942356A1 (de) *	1989-12-21	1991-06-27	Boehringer Mannheim Gmbh	Verwendung von 1-arylsemicarbaziden zur stabilisierung von enzymsubstraten, entsprechende verfahren und diagnostisches mittel enthaltend einen solchen stabilisator
US5212066A (en) *	1991-11-14	1993-05-18	Miles Inc.	Use of inhibitors of color generation in chromogenic assays
US5334502A (en) *	1991-11-27	1994-08-02	Osborn Laboratories, Inc.	Method of collecting, identifying, and quantifying saliva
US5447868A (en) *	1993-09-14	1995-09-05	Propper Manufacturing Co. Inc.	Method, reagent and kit for the detection of fecal occult blood
US5885789A (en) *	1997-03-20	1999-03-23	Stc Technologies Incorporated	Solution-based assay for peroxidatively-active substances in bodily fluids
ES2183999T3 (es) *	1996-03-22	2003-04-01	Roche Diagnostics Gmbh	Estabilizacion de bilirrubina en sueros de control y en calibradores.
DE19849008A1 (de) *	1998-10-23	2000-04-27	Roche Diagnostics Gmbh	Spreitschichten, Netzmittel zu ihrer Herstellung und deren Verwendung in Teststreifen
DE19912365A1 (de)	1999-03-19	2000-09-21	Roche Diagnostics Gmbh	Mehrschichtiges analytisches Hilfsmittel
EP2193779A1 (fr) *	2008-12-05	2010-06-09	Cognis IP Management GmbH	Blanchisseur de la peau
CN102128919B (zh) *	2010-11-18	2013-12-04	艾康生物技术(杭州)有限公司	一种组合物及其应用
RU2477469C1 (ru) *	2012-03-16	2013-03-10	Федеральное государственное бюджетное учреждение науки Институт химической физики им. Н.Н. Семенова Российской академии наук (ИХФ РАН)	Способ контроля качества меда
RU2477470C1 (ru) *	2012-03-16	2013-03-10	Федеральное государственное бюджетное учреждение науки Институт химической физики им. Н.Н. Семенова Российской академии наук (ИХФ РАН)	Способ количественного определения пероксида водорода в натуральных медах и других продуктах пчеловодства
CN109856409B (zh) *	2019-01-03	2023-03-31	桂林优利特医疗电子有限公司	干式血红蛋白检测系统用血红蛋白质控液的应用

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2290436A (en) *	1940-09-26	1942-07-21	Miles Lab	Diagnostic composition and method
NL126252C (fr) *	1961-07-28	1900-01-01	United States Rubber Co
NL6708558A (fr) *	1967-06-20	1968-12-23
US3947377A (en) *	1972-02-08	1976-03-30	Boehringer Mannheim Gmbh	Stabilized indicator compositions containing 9-γ-aminopropyl)-3-aminocarbazole
DE2235152C2 (de) *	1972-07-18	1975-07-10	Boehringer Mannheim Gmbh, 6800 Mannheim	Diagnostisches Mittel zum Nachweis von Blut und anderen peroxidatisch wirksamen Substanzen in Körperflüssigkeiten
DK153334C (da) *	1974-01-09	1988-11-14	Shionogi & Co	Diagnostiske praeparater
US4017420A (en) *	1975-12-22	1977-04-12	Smithkline Corporation	Stable oxidase reagent solutions
US4089747A (en) *	1976-08-09	1978-05-16	Eastman Kodak Company	Compositions for the detection of hydrogen peroxide

1977
- 1977-04-09 DE DE2716060A patent/DE2716060C3/de not_active Expired
1978
- 1978-03-30 CA CA300,069A patent/CA1101318A/fr not_active Expired
- 1978-03-31 US US05/892,362 patent/US4220713A/en not_active Expired - Lifetime
- 1978-04-03 FI FI781015A patent/FI63637C/fi not_active IP Right Cessation
- 1978-04-04 AR AR271682A patent/AR215172A1/es active
- 1978-04-05 CH CH367278A patent/CH636964A5/de not_active IP Right Cessation
- 1978-04-05 BE BE186573A patent/BE865701A/fr not_active IP Right Cessation
- 1978-04-05 GB GB13292/78A patent/GB1571363A/en not_active Expired
- 1978-04-06 IT IT22064/78A patent/IT1095396B/it active
- 1978-04-06 DD DD78204630A patent/DD141361A5/de unknown
- 1978-04-06 SE SE7803889A patent/SE442680B/sv not_active IP Right Cessation
- 1978-04-07 FR FR7810369A patent/FR2386823A1/fr active Granted
- 1978-04-07 SU SU782599514A patent/SU1457819A3/ru active
- 1978-04-07 NL NLAANVRAGE7803722,A patent/NL185177C/xx active Search and Examination
- 1978-04-07 HU HU78BO1709A patent/HU177174B/hu unknown
- 1978-04-07 BR BR7802178A patent/BR7802178A/pt unknown
- 1978-04-07 AT AT248578A patent/AT361132B/de not_active IP Right Cessation
- 1978-04-10 JP JP4205278A patent/JPS53126996A/ja active Granted

Also Published As

Publication number	Publication date
IT1095396B (it)	1985-08-10
JPS53126996A (en)	1978-11-06
US4220713A (en)	1980-09-02
SE7803889L (sv)	1978-10-10
DE2716060B2 (de)	1979-10-04
JPS5643238B2 (fr)	1981-10-09
FI63637B (fi)	1983-03-31
CA1101318A (fr)	1981-05-19
BR7802178A (pt)	1978-12-19
DE2716060C3 (de)	1980-06-12
AT361132B (de)	1981-02-25
AR215172A1 (es)	1979-09-14
GB1571363A (en)	1980-07-16
DE2716060A1 (de)	1978-10-12
DD141361A5 (de)	1980-04-23
FR2386823A1 (fr)	1978-11-03
SU1457819A3 (ru)	1989-02-07
SE442680B (sv)	1986-01-20
FR2386823B1 (fr)	1983-03-11
BE865701A (fr)	1978-10-05
CH636964A5 (de)	1983-06-30
ATA248578A (de)	1980-07-15
IT7822064A0 (it)	1978-04-06
HU177174B (en)	1981-08-28
NL185177C (nl)	1990-02-01
NL7803722A (nl)	1978-10-11
FI781015A7 (fi)	1978-10-10

Legal Events

Date	Code	Title	Description
1978-04-03	MA	Patent expired
2004-08-31	MA	Patent expired	Owner name: BOEHRINGER MANNHEIM GMBH

Publication	Publication Date	Title
FI63637C (fi)	1983-07-11	Stabiliserade snabbdiagnostiska medel innehaollande oxideringsindikatorer
CA1060906A (fr)	1979-08-21	3,3',5,5'-tetraalkylbenzidines; emploi comme indicateurs dans les diagnostiques
KR920001449B1 (ko)	1992-02-14	효소적산화에 의한 검체의 비색적 측정방법 및 시약
FI80072B (fi)	1989-12-29	Askorbatresistant, pao brett omraode verkande glukostestkomposition, testapparat och -metod.
US4071317A (en)	1978-01-31	Test composition and device for determining peroxidatively active substances and process for preparing same
DK167826B1 (da)	1993-12-20	Stabil reagenssammensaetning til bestemmelse af et peroxidativt aktivt stof i en proeve, reagensmateriale indeholdende sammensaetningen samt fremgangsmaade til fremstilling af et stabilt, ascorbat-resistent reagensmateriale
RU2244706C2 (ru)	2005-01-20	Аналоги 8-(анилино)-1-нафталинсульфоната и их применение в тестах обнаружения аналита
JP2922003B2 (ja)	1999-07-19	過酸化活性物質の検定のための組成物、用具及び方法の改良
US4556640A (en)	1985-12-03	Stabilized test composition, device and method for the determination of peroxidatively active substances
US3668076A (en)	1972-06-06	Diagnostic agent
US4071318A (en)	1978-01-31	Test composition and device for determining peroxidatively active substances
JPS6326869B2 (fr)	1988-05-31
JPS583679B2 (ja)	1983-01-22	タイエキチユウノカサンカセイサヨウブツシツオケンシユツスルタメノシケンヘン
JPS5813398A (ja)	1983-01-25	過酸化水素もしくは過酸化水素を形成する基質またはペルオキシダ−ゼもしくはペルオキシダ−ゼのように作用する物質を検出するための剤および方法
JP2000210100A5 (fr)	2006-11-09
EP0038205B1 (fr)	1985-08-28	Méthode et réactif d'essai pour la détermination de peroxyde
JPS62298573A (ja)	1987-12-25	酸化還元反応指示薬としてのトリアリ−ル−及びトリヘタリルメタン誘導体及びそれらの使用
JPH0225152B2 (fr)	1990-05-31
US3627697A (en)	1971-12-14	Hydroperoxide diagnostic agents containing a chromogen indicator
EP0504663A1 (fr)	1992-09-23	Système indicateur pour l'activité peroxidatique pour le milieu basique
JP2009072136A (ja)	2009-04-09	還元系色素を用いた安定な測定方法、およびその試薬
Baird et al.	1986	Effects of nine synthetic putative metabolites of primaquine on activity of the hexose monophosphate shunt in intact human red blood cells in vitro
US4481295A (en)	1984-11-06	Substituted or condensed pyridines in a process for the detection of substances having a peroxidatic effect and a diagnostic agent containing such pyridines
US4801538A (en)	1989-01-31	Process for determining superoxide dismutase activity
JP4200467B1 (ja)	2008-12-24	総分岐鎖アミノ酸測定用液状試薬