DD284050A5 - Verfahren zur kolorimetrischen bestimmung eines analyten mittels enzymatischer oxidation - Google Patents
Verfahren zur kolorimetrischen bestimmung eines analyten mittels enzymatischer oxidation Download PDFInfo
- Publication number
- DD284050A5 DD284050A5 DD89331554A DD33155489A DD284050A5 DD 284050 A5 DD284050 A5 DD 284050A5 DD 89331554 A DD89331554 A DD 89331554A DD 33155489 A DD33155489 A DD 33155489A DD 284050 A5 DD284050 A5 DD 284050A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- analyte
- electron acceptor
- color
- compounds
- oxidation
- Prior art date
Links
- 239000012491 analyte Substances 0.000 title claims abstract description 79
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 69
- 230000003647 oxidation Effects 0.000 title claims abstract description 63
- 238000000034 method Methods 0.000 title claims abstract description 51
- 230000002255 enzymatic effect Effects 0.000 title claims abstract description 33
- 230000008569 process Effects 0.000 title description 23
- 108090000854 Oxidoreductases Proteins 0.000 claims abstract description 39
- 102000004316 Oxidoreductases Human genes 0.000 claims abstract description 39
- 150000001875 compounds Chemical class 0.000 claims abstract description 37
- 239000000126 substance Substances 0.000 claims abstract description 36
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 30
- 230000002829 reductive effect Effects 0.000 claims abstract description 30
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 22
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 20
- 102000004190 Enzymes Human genes 0.000 claims description 37
- 108090000790 Enzymes Proteins 0.000 claims description 37
- 150000002832 nitroso derivatives Chemical class 0.000 claims description 25
- -1 aromatic N-oxide Chemical class 0.000 claims description 21
- 150000002923 oximes Chemical class 0.000 claims description 21
- 150000001204 N-oxides Chemical class 0.000 claims description 16
- 230000001419 dependent effect Effects 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 12
- 150000002443 hydroxylamines Chemical class 0.000 claims description 10
- NLRKCXQQSUWLCH-UHFFFAOYSA-N nitrosobenzene Chemical compound O=NC1=CC=CC=C1 NLRKCXQQSUWLCH-UHFFFAOYSA-N 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 101710088194 Dehydrogenase Proteins 0.000 claims description 3
- 108010020056 Hydrogenase Proteins 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 abstract description 8
- 239000000370 acceptor Substances 0.000 description 82
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 44
- 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 description 43
- 239000008103 glucose Substances 0.000 description 43
- 229940088598 enzyme Drugs 0.000 description 36
- 239000000523 sample Substances 0.000 description 31
- 238000012360 testing method Methods 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 25
- 230000009467 reduction Effects 0.000 description 22
- 239000000243 solution Substances 0.000 description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 125000000217 alkyl group Chemical group 0.000 description 16
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 16
- 239000001301 oxygen Substances 0.000 description 16
- 229910052760 oxygen Inorganic materials 0.000 description 16
- 229930027945 nicotinamide-adenine dinucleotide Natural products 0.000 description 14
- 230000001590 oxidative effect Effects 0.000 description 13
- 108010015776 Glucose oxidase Proteins 0.000 description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 230000008859 change Effects 0.000 description 12
- 239000003153 chemical reaction reagent Substances 0.000 description 12
- 229950006238 nadide Drugs 0.000 description 12
- BAWFJGJZGIEFAR-NNYOXOHSSA-N NAD zwitterion Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP([O-])(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 BAWFJGJZGIEFAR-NNYOXOHSSA-N 0.000 description 11
- 239000004366 Glucose oxidase Substances 0.000 description 10
- 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 description 10
- 229940116332 glucose oxidase Drugs 0.000 description 10
- 235000019420 glucose oxidase Nutrition 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- PLXBWHJQWKZRKG-UHFFFAOYSA-N Resazurin Chemical compound C1=CC(=O)C=C2OC3=CC(O)=CC=C3[N+]([O-])=C21 PLXBWHJQWKZRKG-UHFFFAOYSA-N 0.000 description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- 150000003839 salts Chemical group 0.000 description 9
- 239000000758 substrate Substances 0.000 description 9
- WVMBPWMAQDVZCM-UHFFFAOYSA-N N-methylanthranilic acid Chemical compound CNC1=CC=CC=C1C(O)=O WVMBPWMAQDVZCM-UHFFFAOYSA-N 0.000 description 8
- 230000008878 coupling Effects 0.000 description 8
- 238000010168 coupling process Methods 0.000 description 8
- 238000005859 coupling reaction Methods 0.000 description 8
- NLRKCXQQSUWLCH-IDEBNGHGSA-N nitrosobenzene Chemical class O=N[13C]1=[13CH][13CH]=[13CH][13CH]=[13CH]1 NLRKCXQQSUWLCH-IDEBNGHGSA-N 0.000 description 8
- 238000005691 oxidative coupling reaction Methods 0.000 description 8
- 108020005199 Dehydrogenases Proteins 0.000 description 7
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 7
- 108010073450 Lactate 2-monooxygenase Proteins 0.000 description 7
- CMEWLCATCRTSGF-UHFFFAOYSA-N N,N-dimethyl-4-nitrosoaniline Chemical compound CN(C)C1=CC=C(N=O)C=C1 CMEWLCATCRTSGF-UHFFFAOYSA-N 0.000 description 7
- 108010042687 Pyruvate Oxidase Proteins 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 230000000875 corresponding effect Effects 0.000 description 7
- 238000001514 detection method Methods 0.000 description 7
- 108010054790 glycerol-3-phosphate oxidase Proteins 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 108010050375 Glucose 1-Dehydrogenase Proteins 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000000872 buffer Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- RWSXRVCMGQZWBV-WDSKDSINSA-N glutathione Chemical compound OC(=O)[C@@H](N)CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O RWSXRVCMGQZWBV-WDSKDSINSA-N 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 230000001603 reducing effect Effects 0.000 description 6
- 238000002835 absorbance Methods 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 125000003277 amino group Chemical group 0.000 description 5
- 239000008280 blood Substances 0.000 description 5
- 210000004369 blood Anatomy 0.000 description 5
- 235000012000 cholesterol Nutrition 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- RLFWWDJHLFCNIJ-UHFFFAOYSA-N 4-aminoantipyrine Chemical compound CN1C(C)=C(N)C(=O)N1C1=CC=CC=C1 RLFWWDJHLFCNIJ-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 229910018828 PO3H2 Inorganic materials 0.000 description 4
- 102000003992 Peroxidases Human genes 0.000 description 4
- 229910006069 SO3H Inorganic materials 0.000 description 4
- 150000005840 aryl radicals Chemical class 0.000 description 4
- 239000012131 assay buffer Substances 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- BOPGDPNILDQYTO-NNYOXOHSSA-N nicotinamide-adenine dinucleotide Chemical compound C1=CCC(C(=O)N)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]2[C@H]([C@@H](O)[C@@H](O2)N2C3=NC=NC(N)=C3N=C2)O)O1 BOPGDPNILDQYTO-NNYOXOHSSA-N 0.000 description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 description 4
- 108040007629 peroxidase activity proteins Proteins 0.000 description 4
- 210000002966 serum Anatomy 0.000 description 4
- AWUCVROLDVIAJX-GSVOUGTGSA-N sn-glycerol 3-phosphate Chemical compound OC[C@@H](O)COP(O)(O)=O AWUCVROLDVIAJX-GSVOUGTGSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 4
- RXGJTUSBYWCRBK-UHFFFAOYSA-M 5-methylphenazinium methyl sulfate Chemical compound COS([O-])(=O)=O.C1=CC=C2[N+](C)=C(C=CC=C3)C3=NC2=C1 RXGJTUSBYWCRBK-UHFFFAOYSA-M 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 108010024636 Glutathione Proteins 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical compound CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 3
- AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 description 3
- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 3
- TVWHNULVHGKJHS-UHFFFAOYSA-N Uric acid Natural products N1C(=O)NC(=O)C2NC(=O)NC21 TVWHNULVHGKJHS-UHFFFAOYSA-N 0.000 description 3
- 239000002250 absorbent Substances 0.000 description 3
- 230000002745 absorbent Effects 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000008033 biological extinction Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 229960003180 glutathione Drugs 0.000 description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 229910052750 molybdenum Inorganic materials 0.000 description 3
- 239000011733 molybdenum Substances 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- MMXZSJMASHPLLR-UHFFFAOYSA-N pyrroloquinoline quinone Chemical compound C12=C(C(O)=O)C=C(C(O)=O)N=C2C(=O)C(=O)C2=C1NC(C(=O)O)=C2 MMXZSJMASHPLLR-UHFFFAOYSA-N 0.000 description 3
- HSSLDCABUXLXKM-UHFFFAOYSA-N resorufin Chemical class C1=CC(=O)C=C2OC3=CC(O)=CC=C3N=C21 HSSLDCABUXLXKM-UHFFFAOYSA-N 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- AWDBHOZBRXWRKS-UHFFFAOYSA-N tetrapotassium;iron(6+);hexacyanide Chemical compound [K+].[K+].[K+].[K+].[Fe+6].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] AWDBHOZBRXWRKS-UHFFFAOYSA-N 0.000 description 3
- 229940116269 uric acid Drugs 0.000 description 3
- 210000002700 urine Anatomy 0.000 description 3
- YKFCISHFRZHKHY-NGQGLHOPSA-N (2s)-2-amino-3-(3,4-dihydroxyphenyl)-2-methylpropanoic acid;trihydrate Chemical compound O.O.O.OC(=O)[C@](N)(C)CC1=CC=C(O)C(O)=C1.OC(=O)[C@](N)(C)CC1=CC=C(O)C(O)=C1 YKFCISHFRZHKHY-NGQGLHOPSA-N 0.000 description 2
- JSTCPNFNKICNNO-UHFFFAOYSA-N 4-nitrosophenol Chemical compound OC1=CC=C(N=O)C=C1 JSTCPNFNKICNNO-UHFFFAOYSA-N 0.000 description 2
- 102000007698 Alcohol dehydrogenase Human genes 0.000 description 2
- 108010021809 Alcohol dehydrogenase Proteins 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
- 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 2
- 108010089254 Cholesterol oxidase Proteins 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- CKRZKMFTZCFYGB-UHFFFAOYSA-N N-phenylhydroxylamine Chemical class ONC1=CC=CC=C1 CKRZKMFTZCFYGB-UHFFFAOYSA-N 0.000 description 2
- XJLXINKUBYWONI-NNYOXOHSSA-O NADP(+) Chemical compound NC(=O)C1=CC=C[N+]([C@H]2[C@@H]([C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)OC[C@@H]3[C@H]([C@@H](OP(O)(O)=O)[C@@H](O3)N3C4=NC=NC(N)=C4N=C3)O)O2)O)=C1 XJLXINKUBYWONI-NNYOXOHSSA-O 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical class CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 239000012472 biological sample Substances 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 229940083181 centrally acting adntiadrenergic agent methyldopa Drugs 0.000 description 2
- 239000007979 citrate buffer Substances 0.000 description 2
- 239000005515 coenzyme Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 2
- OLNMJIHADFYHAK-UHFFFAOYSA-N n,n-diethyl-4-nitrosoaniline Chemical compound CCN(CC)C1=CC=C(N=O)C=C1 OLNMJIHADFYHAK-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 125000000018 nitroso group Chemical group N(=O)* 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- 238000005375 photometry Methods 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 230000027756 respiratory electron transport chain Effects 0.000 description 2
- 238000010517 secondary reaction Methods 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000661 sodium alginate Substances 0.000 description 2
- 235000010413 sodium alginate Nutrition 0.000 description 2
- 229940005550 sodium alginate Drugs 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 125000003831 tetrazolyl group Chemical group 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 1
- SJJCQDRGABAVBB-UHFFFAOYSA-N 1-hydroxy-2-naphthoic acid Chemical compound C1=CC=CC2=C(O)C(C(=O)O)=CC=C21 SJJCQDRGABAVBB-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- PHGRHSBQHVHQKZ-UHFFFAOYSA-N 2-(4-nitrosoanilino)ethane-1,1-diol Chemical compound OC(O)CNC1=CC=C(N=O)C=C1 PHGRHSBQHVHQKZ-UHFFFAOYSA-N 0.000 description 1
- RLEHYCNEHWSDLS-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)-4-nitrosoanilino]ethanol Chemical compound OCCN(CCO)C1=CC=C(N=O)C=C1 RLEHYCNEHWSDLS-UHFFFAOYSA-N 0.000 description 1
- 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 1
- PMYJGTWUVVVOFO-UHFFFAOYSA-N 4-phenyl-3-furoxancarbonitrile Chemical compound N#CC1=[N+]([O-])ON=C1C1=CC=CC=C1 PMYJGTWUVVVOFO-UHFFFAOYSA-N 0.000 description 1
- XTWYTFMLZFPYCI-KQYNXXCUSA-N 5'-adenylphosphoric acid Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O XTWYTFMLZFPYCI-KQYNXXCUSA-N 0.000 description 1
- KBZALDXXIMXRBJ-UHFFFAOYSA-N 5-methylphenazin-5-ium Chemical compound C1=CC=C2[N+](C)=C(C=CC=C3)C3=NC2=C1 KBZALDXXIMXRBJ-UHFFFAOYSA-N 0.000 description 1
- ZKHQWZAMYRWXGA-KQYNXXCUSA-J ATP(4-) Chemical compound C1=NC=2C(N)=NC=NC=2N1[C@@H]1O[C@H](COP([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O)[C@@H](O)[C@H]1O ZKHQWZAMYRWXGA-KQYNXXCUSA-J 0.000 description 1
- XTWYTFMLZFPYCI-UHFFFAOYSA-N Adenosine diphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(O)=O)C(O)C1O XTWYTFMLZFPYCI-UHFFFAOYSA-N 0.000 description 1
- ZKHQWZAMYRWXGA-UHFFFAOYSA-N Adenosine triphosphate Natural products C1=NC=2C(N)=NC=NC=2N1C1OC(COP(O)(=O)OP(O)(=O)OP(O)(O)=O)C(O)C1O ZKHQWZAMYRWXGA-UHFFFAOYSA-N 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 108091003079 Bovine Serum Albumin Proteins 0.000 description 1
- 229920003043 Cellulose fiber Polymers 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
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical class [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 108010003989 D-amino-acid oxidase Proteins 0.000 description 1
- 102000004674 D-amino-acid oxidase Human genes 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 102000057621 Glycerol kinases Human genes 0.000 description 1
- 108700016170 Glycerol kinases Proteins 0.000 description 1
- 102000008015 Hemeproteins Human genes 0.000 description 1
- 108010089792 Hemeproteins Proteins 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- 102000003855 L-lactate dehydrogenase Human genes 0.000 description 1
- 108700023483 L-lactate dehydrogenases Proteins 0.000 description 1
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 241000604136 Pediococcus sp. Species 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 241001620634 Roger Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 108010055297 Sterol Esterase Proteins 0.000 description 1
- 102000000019 Sterol Esterase Human genes 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- FVKALIMONZZWLL-UHFFFAOYSA-N [Pb].NC1=CCC(C2=NC3=CC=CC=C3N=C12)=O Chemical compound [Pb].NC1=CCC(C2=NC3=CC=CC=C3N=C12)=O FVKALIMONZZWLL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 238000013459 approach Methods 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
- 238000003556 assay Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000013060 biological fluid Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229940098773 bovine serum albumin Drugs 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- VDQQXEISLMTGAB-UHFFFAOYSA-N chloramine T Chemical class [Na+].CC1=CC=C(S(=O)(=O)[N-]Cl)C=C1 VDQQXEISLMTGAB-UHFFFAOYSA-N 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 239000007819 coupling partner Substances 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- ACKFDYCQCBEDNU-UHFFFAOYSA-J lead(2+);tetraacetate Chemical compound [Pb+2].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O ACKFDYCQCBEDNU-UHFFFAOYSA-J 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002730 mercury Chemical class 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- DZCCLNYLUGNUKQ-UHFFFAOYSA-N n-(4-nitrosophenyl)hydroxylamine Chemical compound ONC1=CC=C(N=O)C=C1 DZCCLNYLUGNUKQ-UHFFFAOYSA-N 0.000 description 1
- 229940101270 nicotinamide adenine dinucleotide (nad) Drugs 0.000 description 1
- 125000003544 oxime group Chemical group 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical class OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 1
- DHRLEVQXOMLTIM-UHFFFAOYSA-N phosphoric acid;trioxomolybdenum Chemical compound O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.OP(O)(O)=O DHRLEVQXOMLTIM-UHFFFAOYSA-N 0.000 description 1
- 210000002381 plasma Anatomy 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 238000009790 rate-determining step (RDS) Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- 229910001961 silver nitrate Inorganic materials 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- FTWCSAMTIKSPAT-UHFFFAOYSA-M sodium;nonyl sulfate Chemical compound [Na+].CCCCCCCCCOS([O-])(=O)=O FTWCSAMTIKSPAT-UHFFFAOYSA-M 0.000 description 1
- 239000008279 sol Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000000080 wetting agent 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
- C12Q1/32—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving dehydrogenase
-
- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R13/00—Details of coupling devices of the kinds covered by groups H01R12/70 or H01R24/00 - H01R33/00
- H01R13/73—Means for mounting coupling parts to apparatus or structures, e.g. to a wall
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K7/00—Constructional details common to different types of electric apparatus
- H05K7/02—Arrangements of circuit components or wiring on supporting structure
- H05K7/12—Resilient or clamping means for holding component to structure
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01R—ELECTRICALLY-CONDUCTIVE CONNECTIONS; STRUCTURAL ASSOCIATIONS OF A PLURALITY OF MUTUALLY-INSULATED ELECTRICAL CONNECTING ELEMENTS; COUPLING DEVICES; CURRENT COLLECTORS
- H01R13/00—Details of coupling devices of the kinds covered by groups H01R12/70 or H01R24/00 - H01R33/00
- H01R13/46—Bases; Cases
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Immunology (AREA)
- Biochemistry (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Analytical Chemistry (AREA)
- Biophysics (AREA)
- Physics & Mathematics (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3826922A DE3826922A1 (de) | 1988-08-09 | 1988-08-09 | Verfahren zur kolorimetrischen bestimmung eines analyten mittels enzymatischer oxidation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD284050A5 true DD284050A5 (de) | 1990-10-31 |
Family
ID=6360464
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD89331554A DD284050A5 (de) | 1988-08-09 | 1989-08-07 | Verfahren zur kolorimetrischen bestimmung eines analyten mittels enzymatischer oxidation |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US5206147A (fr) |
| EP (1) | EP0354441B1 (fr) |
| JP (1) | JPH0687793B2 (fr) |
| KR (1) | KR920001449B1 (fr) |
| AT (1) | ATE122726T1 (fr) |
| AU (1) | AU614405B2 (fr) |
| CA (1) | CA1339058C (fr) |
| DD (1) | DD284050A5 (fr) |
| DE (2) | DE3826922A1 (fr) |
| ES (1) | ES2074457T3 (fr) |
| HK (1) | HK173796A (fr) |
| RU (1) | RU2015513C1 (fr) |
Families Citing this family (73)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3940010A1 (de) * | 1989-12-02 | 1991-06-06 | Boehringer Mannheim Gmbh | Verwendung eines schwer loeslichen salzes einer heteropolysaeure zur bestimmung eines analyts, entsprechendes bestimmungsverfahren sowie hierfuer geeignetes mittel |
| DE4003194A1 (de) * | 1990-02-03 | 1991-08-08 | Boehringer Mannheim Gmbh | Verfahren und sensorelektrodensystem zur elektrochemischen bestimmung eines analyts oder einer oxidoreduktase sowie verwendung hierfuer geeigneter verbindungen |
| ES2141172T3 (es) * | 1992-09-28 | 2000-03-16 | Roche Diagnostics Corp | Reactivo estable para sistemas indicadores de complejos de ion ferrico. |
| DE4311460A1 (de) * | 1993-04-08 | 1994-10-13 | Boehringer Mannheim Gmbh | Verfahren zur kolorimetrischen Bestimmung eines Analyten mittels Benzylalkoholdehydrogenase und einem chromogenen Redoxindikator |
| DE4311464A1 (de) * | 1993-04-08 | 1994-10-13 | Boehringer Mannheim Gmbh | Verfahren zur kolorimetrischen Bestimmung eines Analyten mit einer PQQ-abhängigen Dehydrogenase |
| US5620579A (en) * | 1995-05-05 | 1997-04-15 | Bayer Corporation | Apparatus for reduction of bias in amperometric sensors |
| US5989845A (en) | 1996-04-05 | 1999-11-23 | Mercury Diagnostics, Inc. | Diagnostic compositions and devices utilizing same |
| US5776719A (en) * | 1997-07-07 | 1998-07-07 | Mercury Diagnostics, Inc. | Diagnostic compositions and devices utilizing same |
| US6040151A (en) * | 1998-03-10 | 2000-03-21 | Mercury Diagnostics, Inc. | Diagnostic compositions and devices utilizing same |
| IL121279A (en) * | 1996-07-16 | 2001-05-20 | Roche Diagnostics Gmbh | An analytical system with means for testing samples with too small volumes |
| DE19628562A1 (de) | 1996-07-16 | 1998-01-22 | Boehringer Mannheim Gmbh | Analysesystem mit Mitteln zur Erkennung von Unterdosierungen |
| DE69809391T2 (de) | 1997-02-06 | 2003-07-10 | Therasense, Inc. | Kleinvolumiger sensor zur in-vitro bestimmung |
| US6391645B1 (en) | 1997-05-12 | 2002-05-21 | Bayer Corporation | Method and apparatus for correcting ambient temperature effect in biosensors |
| US6428974B1 (en) * | 1998-04-03 | 2002-08-06 | Kanto Kagaku Kabushiki Kaisha | Microplate for drug susceptibility testing containing a drug, a color reagent, and color suppressant |
| US6030802A (en) * | 1998-05-29 | 2000-02-29 | Roche Diagnostics Corporation | Liquid reagent set for L-lactate determination |
| US5902731A (en) * | 1998-09-28 | 1999-05-11 | Lifescan, Inc. | Diagnostics based on tetrazolium compounds |
| US6656697B1 (en) * | 1998-09-28 | 2003-12-02 | Lifescan, Inc. | Diagnostics based on tetrazolium compounds |
| JP3694424B2 (ja) | 1998-09-29 | 2005-09-14 | 松下電器産業株式会社 | グルコースセンサ |
| US6338790B1 (en) | 1998-10-08 | 2002-01-15 | Therasense, Inc. | Small volume in vitro analyte sensor with diffusible or non-leachable redox mediator |
| DE19945828B4 (de) | 1999-09-24 | 2011-06-01 | Roche Diagnostics Gmbh | Analysenelement und Verfahren zur Bestimmung eines Analyten in Flüssigkeit |
| US7005048B1 (en) | 1999-10-05 | 2006-02-28 | Matsushita Electric Industrial Co., Ltd. | Glucose sensor |
| DE10001529A1 (de) * | 2000-01-15 | 2001-07-19 | Roche Diagnostics Gmbh | Stabilisierte Coenzym-Lösungen und deren Verwendung zur Bestimmung von Dehydrogenasen bzw. deren Substrate |
| US6420128B1 (en) * | 2000-09-12 | 2002-07-16 | Lifescan, Inc. | Test strips for detecting the presence of a reduced cofactor in a sample and method for using the same |
| EP1416851B1 (fr) * | 2001-06-08 | 2006-08-09 | Roche Diagnostics GmbH | Dispositif de prelevement de liquide corporel et cassette a support d'essai destinee a etre utilisee avec ledit dispositif |
| US7163616B2 (en) * | 2001-09-14 | 2007-01-16 | Bayer Corporation | Reagents and methods for detecting analytes, and devices comprising reagents for detecting analytes |
| US6982152B2 (en) * | 2002-04-17 | 2006-01-03 | Promega Corporation | Cytotoxicity assay |
| US6759190B2 (en) * | 2002-06-15 | 2004-07-06 | Acon Laboratories, Inc. | Test strip for detection of analyte and methods of use |
| DE10248555B4 (de) * | 2002-10-18 | 2004-12-02 | Roche Diagnostics Gmbh | Verfahren und Analysesystem zur Ermittlung der Konzentration eines Analyten in einer Probe, die aus dem Analyten und der Probenmatrix besteht und Testelement dafür |
| US7572237B2 (en) | 2002-11-06 | 2009-08-11 | Abbott Diabetes Care Inc. | Automatic biological analyte testing meter with integrated lancing device and methods of use |
| DE10304448A1 (de) | 2003-02-04 | 2004-08-12 | Roche Diagnostics Gmbh | Fluorimetrische Bestimmung von Analyten durch Amin-N-Oxide als Redoxindikatoren |
| DE10346863A1 (de) * | 2003-10-09 | 2005-05-04 | Roche Diagnostics Gmbh | On-Board-Kontrolle für Analyseelemente |
| JP4839219B2 (ja) | 2003-10-24 | 2011-12-21 | バイエル・ヘルスケア・エルエルシー | 酵素的電気化学的バイオセンサ |
| CN1914331A (zh) * | 2004-02-06 | 2007-02-14 | 拜尔健康护理有限责任公司 | 作为生物传感器的内部参照的可氧化种类和使用方法 |
| BRPI0509296A (pt) | 2004-03-31 | 2007-09-18 | Bayer Healthcare Llc | método e aparelho para implementar funções corretivas baseadas em limiares para biossensores |
| US20060024835A1 (en) * | 2004-07-30 | 2006-02-02 | Matzinger David P | Analytical test strip with control zone |
| DE602006015295D1 (de) * | 2005-04-04 | 2010-08-19 | Facet Technologies Llc | Lanzettenvorrichtung mit schmalem profil |
| WO2007013915A1 (fr) | 2005-07-20 | 2007-02-01 | Bayer Healthcare Llc | Amperometrie a declenchement periodique |
| WO2007040913A1 (fr) | 2005-09-30 | 2007-04-12 | Bayer Healthcare Llc | Voltamperometrie commandee |
| US7955484B2 (en) * | 2005-12-14 | 2011-06-07 | Nova Biomedical Corporation | Glucose biosensor and method |
| DE102006043718B4 (de) | 2006-09-18 | 2014-12-31 | Alexander Adlassnig | Bestimmung von Wasserstoffperoxidkonzentrationen |
| EP3543348B1 (fr) | 2006-09-22 | 2020-11-18 | Ascensia Diabetes Care Holdings AG | Système de biocapteur présentant une stabilité améliorée et une fonction de mesure d'hématocrite |
| EP3753481B1 (fr) | 2006-10-24 | 2024-07-17 | Ascensia Diabetes Care Holdings AG | Dispositif pour amperométrie de decroissance transitoire |
| EP1964927A1 (fr) * | 2007-02-27 | 2008-09-03 | F. Hoffmann-La Roche AG | Quinone en tant que médiateurs pour tests photométriques |
| CA2716603A1 (fr) * | 2007-03-05 | 2009-09-12 | Advanced Liquid Logic, Inc. | Dosages sur gouttelettes du peroxyde d'hydrogene |
| WO2009076302A1 (fr) | 2007-12-10 | 2009-06-18 | Bayer Healthcare Llc | Marqueurs de contrôle pour la détection automatique d'une solution de contrôle et procédés d'utilisation |
| JP5856371B2 (ja) | 2007-12-10 | 2016-02-09 | バイエル・ヘルスケア・エルエルシーＢａｙｅｒ ＨｅａｌｔｈＣａｒｅＬＬＣ | 分析対象物を検出するための試薬及び方法 |
| EP3187866B1 (fr) | 2007-12-10 | 2019-04-17 | Ascensia Diabetes Care Holdings AG | Capteur d'analyse électrochimique |
| WO2009076268A1 (fr) * | 2007-12-10 | 2009-06-18 | Bayer Healthcare Llc | Procédé de fabrication de médiateur de 3-phénylimino-3h-phénothiazine ou de 3-phénylimino-3h-phénoxazine |
| US20090219509A1 (en) * | 2008-02-29 | 2009-09-03 | Hiroshi Nomura | Optical sensor with enhanced reflectance |
| US8008068B2 (en) * | 2008-02-29 | 2011-08-30 | Light Pointe Medical, Inc. | Nonhemolytic optical sensor with enhanced reflectance |
| US8008037B2 (en) | 2008-03-27 | 2011-08-30 | Roche Diagnostics Operations, Inc. | Matrix composition with alkylphenazine quaternary salt and a nitrosoaniline |
| WO2011012754A2 (fr) | 2009-07-30 | 2011-02-03 | Fundacion Cidetec | Détecteur électrochimique pour la détection d'analytes dans des milieux liquides |
| EP2287295A1 (fr) | 2009-08-03 | 2011-02-23 | Roche Diagnostics GmbH | Muté fructosyl oxydase d'acide aminé |
| EP2281900A1 (fr) | 2009-08-03 | 2011-02-09 | Roche Diagnostics GmbH | Fructosyl-oxydase peptidique et capteur pour la détermination des protéines glycées |
| JP6055236B2 (ja) * | 2011-08-17 | 2016-12-27 | 株式会社三和化学研究所 | 測定方法 |
| EP2562251B1 (fr) | 2011-08-25 | 2016-08-17 | Roche Diagnostics GmbH | Oxydase de cholestérol |
| WO2013026575A2 (fr) | 2011-08-25 | 2013-02-28 | Roche Diagnostics Gmbh | Glucose oxydase |
| KR101609083B1 (ko) * | 2011-09-28 | 2016-04-04 | 에프. 호프만-라 로슈 아게 | 아조 매개체 |
| US9572922B2 (en) | 2012-12-21 | 2017-02-21 | Larry Leonard | Inventive diabetic systems, tools, kits, and supplies for better diabetic living and mobility |
| KR101728597B1 (ko) | 2012-04-19 | 2017-04-19 | 에프. 호프만-라 로슈 아게 | 혈액 내 분석물 농도를 결정하는 방법 및 디바이스 |
| CN104870982B (zh) | 2012-12-20 | 2019-02-15 | 霍夫曼-拉罗奇有限公司 | 用于评估医学测量曲线的方法 |
| KR101750638B1 (ko) | 2012-12-20 | 2017-06-23 | 에프. 호프만-라 로슈 아게 | 체액의 샘플을 분석하는 방법 |
| JP6427110B2 (ja) | 2013-01-28 | 2018-11-21 | エフ ホフマン−ラ ロッシュ アクチェン ゲゼルシャフト | アスペルギルスニガー由来の新規グルコース酸化酵素 |
| EP2781919A1 (fr) | 2013-03-19 | 2014-09-24 | Roche Diagniostics GmbH | Procédé/dispositif permettant de générer une valeur corrigée de concentration d'un analyte dans un échantillon d'un fluide corporel |
| EP2796547B1 (fr) | 2013-04-24 | 2016-09-14 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Nouveaux variants d'oxydase de glucose |
| EP3406732B1 (fr) * | 2016-01-22 | 2020-11-04 | National Agriculture and Food Research Organization | Procédé de mesure d'activité d'oxydoréductase |
| CA3035874C (fr) | 2016-10-05 | 2025-09-09 | F. Hoffmann-La Roche Ag | Reactifs de detection et agencements d'electrodes pour elements de test de diagnostic multi-analytes, ainsi que leurs procedes d'utilisation |
| EP3339431A1 (fr) | 2016-12-22 | 2018-06-27 | Roche Diabetes Care GmbH | Variantes de glucose déshydrogénase à propriétés améliorées |
| DE102017208461A1 (de) | 2017-05-18 | 2018-11-22 | Diabetes.Online Ag | Multianalytmessung |
| EP3759231B1 (fr) | 2018-02-28 | 2023-10-18 | F. Hoffmann-La Roche AG | Revêtement de biocompatibilité pour la mesure continue d'analytes |
| JPWO2020122231A1 (ja) | 2018-12-13 | 2021-10-21 | キッコーマン株式会社 | エタノールアミンリン酸の定量方法、定量用のオキシドレダクターゼ、定量用組成物、定量用キット及び定量用センサー |
| KR102178443B1 (ko) * | 2018-12-17 | 2020-11-13 | 주식회사 포스코 | 글로우 방전 광학 방출 분광법의 다변량 분석을 이용한 철강 표면 산화철의 정량 분석 방법 |
| US12116610B2 (en) | 2021-01-26 | 2024-10-15 | The University Of North Carolina At Chapel Hill | Glycerol 3-phosphate oxidase mutants, compositions, devices, kits and uses thereof |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4105800A (en) * | 1976-07-26 | 1978-08-08 | Board Of Regents For Education Of The State Of Rhode Island | Immobilized enzyme method to assess fish quality |
| US4645760A (en) * | 1982-07-30 | 1987-02-24 | Health Research Inc. | Activated aminoglycosides and aminoglycoside-aminocyclitols pharmaceutical compositions and method of use |
| DE3311027A1 (de) * | 1983-03-25 | 1984-09-27 | Boehringer Mannheim Gmbh, 6800 Mannheim | Nad(p)-unabhaengige glycerindehydrogenase, verfahren zu deren herstellung sowie deren verwendung zur bestimmung von glycerin und triglyceriden |
| AU1469983A (en) * | 1983-05-19 | 1984-11-22 | Imperial Chemical Industries Plc | Glucose determination using glucose d.h. and reducible cpd to change e.m. radiation |
| US4629689A (en) * | 1984-08-29 | 1986-12-16 | Allied Corporation | Binding assay with amplified read-out and gas-phase detection |
| JPS62239999A (ja) * | 1986-04-11 | 1987-10-20 | Arinobu Fujimura | Ｎａｄ（ｐ）ｈの半定量法 |
| DE3820404A1 (de) * | 1987-06-15 | 1988-12-29 | Toyo Boseki | Pyruvat-dehydrogenase und ihre verwendung in einem analytischen verfahren |
| DE3720506A1 (de) * | 1987-06-20 | 1988-12-29 | Draegerwerk Ag | Verfahren zum nachweis gasfoermiger stoffe mittels einer enzymatischen redox-reaktion |
| US5000815A (en) * | 1988-12-19 | 1991-03-19 | Ncr Corporation | Apparatus for applying a correction sticker to a document |
-
1988
- 1988-08-09 DE DE3826922A patent/DE3826922A1/de not_active Withdrawn
-
1989
- 1989-08-01 DE DE58909232T patent/DE58909232D1/de not_active Expired - Lifetime
- 1989-08-01 AT AT89114143T patent/ATE122726T1/de not_active IP Right Cessation
- 1989-08-01 EP EP89114143A patent/EP0354441B1/fr not_active Expired - Lifetime
- 1989-08-01 ES ES89114143T patent/ES2074457T3/es not_active Expired - Lifetime
- 1989-08-02 AU AU39222/89A patent/AU614405B2/en not_active Expired
- 1989-08-06 RU SU894614868A patent/RU2015513C1/ru active
- 1989-08-07 DD DD89331554A patent/DD284050A5/de unknown
- 1989-08-08 CA CA000607703A patent/CA1339058C/fr not_active Expired - Lifetime
- 1989-08-09 JP JP1204927A patent/JPH0687793B2/ja not_active Expired - Lifetime
- 1989-08-09 US US07/390,946 patent/US5206147A/en not_active Expired - Lifetime
- 1989-08-09 KR KR1019890011395A patent/KR920001449B1/ko not_active Expired
-
1993
- 1993-01-14 US US08/004,587 patent/US5334508A/en not_active Expired - Lifetime
-
1996
- 1996-09-12 HK HK173796A patent/HK173796A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP0354441A3 (fr) | 1992-04-08 |
| AU3922289A (en) | 1990-02-15 |
| RU2015513C1 (ru) | 1994-06-30 |
| ATE122726T1 (de) | 1995-06-15 |
| DE3826922A1 (de) | 1990-02-22 |
| ES2074457T3 (es) | 1995-09-16 |
| US5206147A (en) | 1993-04-27 |
| EP0354441B1 (fr) | 1995-05-17 |
| US5334508A (en) | 1994-08-02 |
| DE58909232D1 (de) | 1995-06-22 |
| EP0354441A2 (fr) | 1990-02-14 |
| KR900003378A (ko) | 1990-03-26 |
| JPH0687793B2 (ja) | 1994-11-09 |
| AU614405B2 (en) | 1991-08-29 |
| KR920001449B1 (ko) | 1992-02-14 |
| HK173796A (en) | 1996-09-20 |
| JPH02174695A (ja) | 1990-07-06 |
| CA1339058C (fr) | 1997-07-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0354441B1 (fr) | Procédé de détermination colorimétrique d'analyse utilisant l'oxidation enzymatique | |
| EP0037056B1 (fr) | Procédé et agents diagnostiques pour la détection des réactions d'oxido-réduction | |
| DE3003490C2 (fr) | ||
| DE3788239T2 (de) | Kontrollierte Farbton-Vorrichtung. | |
| DE3247894A1 (de) | Testsystem und verfahren zur bestimmung von nad(p)h | |
| DE3940010A1 (de) | Verwendung eines schwer loeslichen salzes einer heteropolysaeure zur bestimmung eines analyts, entsprechendes bestimmungsverfahren sowie hierfuer geeignetes mittel | |
| EP0748866B1 (fr) | Méthode et moyens pour la détermination colorimétrique et électrochimique simultanées d'un analyte | |
| DE3788828T2 (de) | Stabilisierte flüssige Enzymzusammensetzung zur Bestimmung von Glucose. | |
| DE69228554T2 (de) | Reagenzien und untersuchungsverfahren einschliesslich eines phenazin enthaltenden indikators | |
| DE69129308T2 (de) | Hochempfindliche bestimmung von d-3-hydroxybutiersäure oder acetessigsäure und zusammensetzung dafür | |
| DE3125667C2 (de) | Verfahren und Mittel zum Nachweis von Wasserstoffperoxid | |
| DE3852889T2 (de) | Test von salicylaten oder reduzierten pyridin-nukleotiden. | |
| DE2224132B1 (de) | Verfahren und reagenz zur bestimmung von cholesterin | |
| DE3403250C2 (de) | Neue hochempfindliche enzymatische Testmethode | |
| DE3882770T2 (de) | Verfahren und Reagens zur Bestimmung von Dehydrogenase oder ihrem Substrat. | |
| DE2459087A1 (de) | Verfahren und reagenz zur bestimmung von serumtriglyceriden | |
| CH646792A5 (de) | Testvorrichtung fuer die bestimmung von harnsaeure. | |
| DE3851316T2 (de) | Verfahren zur Messung der Menge der Polyamine in einer biologischen Probe. | |
| DE3703081A1 (de) | Verfahren und mittel zum nachweis von thiolen | |
| DE2910737A1 (de) | Verfahren zur ausschaltung stoerender begleitreaktionen bei enzymatischen analysenverfahren | |
| EP1120468B1 (fr) | Solutions stabilisés de co-enzymes et leur utilisation pour la détermination des déshydrogénases ou leurs substrates | |
| DE3485906T2 (de) | Verfahren zur zersetzung von askorbinsaeure. | |
| DE3117952C2 (fr) | ||
| DE69215797T2 (de) | Verfahren zur Messung von NADH und NADPH | |
| DE3820404C2 (fr) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RPI | Change in the person, name or address of the patentee (searches according to art. 11 and 12 extension act) | ||
| ASS | Change of applicant or owner |
Owner name: ROCHE DIAGNOSTICS GMBH, MANNHEIM Effective date: 19990128 |
|
| IF04 | In force in the year 2004 |
Expiry date: 20090808 |