초록

A method of detecting creatinine in body fluids using an indicator which produces a fluorescent response when oxidized in the presence of a copperII/creatinine complex. A preferred indicator is 4-(1-methylhydrazino)-7-nitro benzooxadiazole (MNBDH).

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1. A method for the detection of creatinine in fluids comprising contacting a sample of said fluid with a reagent system comprising cupric ions, a hydroperoxide and an indicator which produces a fluorescent response when oxidized in the presence of a pseudoperoxidase, wherein said indicator is a 4-(

1. A method for the detection of creatinine in fluids comprising contacting a sample of said fluid with a reagent system comprising cupric ions, a hydroperoxide and an indicator which produces a fluorescent response when oxidized in the presence of a pseudoperoxidase, wherein said indicator is a 4-(1-alkylhydrazino)-7-substituted benzooxadiazole having the formula: where:R1 is C1-C7 R2 is NO2, R3NHSO2, (R3)2NSO2 R3 is hydrogen, alkyl, substituted alkyl, phenyl, substituted phenyl. 2. A method of claim 1, wherein said indicator is 4-(1-methylhydrazino)-7-nitro-benzooxadiazole (MNBDH).3. A method of claim 1 wherein said reagent system further comprises citric acid.4. A method of claim 1 wherein said cupric ions are supplied by a member of the group consisting of copper sulfate, copper chloride, copper phosphate, and copper hydroxide.5. A method of claim 1 wherein said hydroperoxide is diisopropylbenzene dihydroperoxide or cumene hydroperoxide.6. A method of claim 1 wherein said reagent system is placed on a test strip.7. A method of claim 1 wherein said alkyl or said phenyl of R3 are substituted to provide predetermined solubility and/or optical properties.8. A method of claim 7 wherein said phenyl is substituted with at least one group selected from the group consisting of methoxy, nitro, chloride, bromide, or iodide to provide predetermined fluorescent properties.9. A method of claim 7 wherein said phenyl is substituted with at least one substituent selected from the group consisting of sulfo, carboxy, dimethylamino, trialkylammonio, and ethylene glycol to increase water solubility.10. A method of claim 7 wherein said alkyl is methyl, ethyl, or a longer alkyl chain to increase lipophilicity.11. A method of claim 7 wherein said alkyl is selected from the group consisting of 2-sulfoethyl, carboxymethyl, and dimethylaminopropyl to increase water solubility.12. A method of claim 7 wherein said alkyl is an n-(ethylene glycol)ethyl to increase both lipophilicity and water solubility.13. A method of claim 7 wherein said alkyl is substituted with at least one member of the group consisting of hydroxyl, amino, and trialkylammonio.14. In a method for the detection of creatinine in blood or other bodily fluids wherein a sample of said fluids is contacted with a reagent system comprising cupric ions, a hydroperoxide and an indicator, the improvement comprising the use of an indicator which produces a fluorescent response when oxidized in the presence of a pseudoperoxidase, wherein said indicator is a 4-(1-alkylhydrazino-7-substituted benzooxadiazole having the formula: where:R1 is C1-C7 R2 is NO2, R3NHSO2, (R3)2NSO2 R3 is hydrogen, alkyl, substituted alkyl, phenyl, substituted phenyl. 15. The method of claim 14 wherein said indicator is 4-(N-methylhydrazino)-7-nitrobenzooxadiazole (MNBDH).16. The method of claim 14 wherein said reagent system further comprises citric acid.17. The method of claim 14 wherein said cupric ions are supplied by a member of the group consisting of copper sulfate, copper chloride, copper phosphate, and copper hydroxide.18. The method of claim 14 wherein said hydroperoxide is diisopropylbenzene dihydroperoxide or cumene hydroperoxide.19. The method of claim 14 wherein said reagent system is placed on a test strip.20. A method of claim 14 wherein said alkyl or said phenyl of R3 are substituted to provide predetermined solubility and/or optical properties.21. A method of claim 20 wherein said phenyl is substituted with at least one group selected from the group consisting of methoxy, nitro, chloride, bromide, or iodide to provide predetermined fluorescent properties.22. A method of claim 20 wherein said phenyl is substituted with at least one substituent selected from the group consisting of sulfo, carboxy, dimethylamino, trialkylammonio, and ethylene glycol to increase water solubility.23. A method of claim 20 wherein said alkyl is methyl, ethyl, or a longer alkyl chain to increase lipophilicity.24. A method of claim 20 wherein said alkyl is selected from the group consisting of 2-sulfoethyl, carboxymethyl, and dimethylaminopropyl to increase water solubility.25. A method of claim 20 wherein said alkyl is an n-(ethylene glycol) ethyl to increase both lipophilicity and water solubility.26. A method of claim 20 wherein said alkyl is substituted with at least one member of the group consisting of hydroxyl, amino, and trialkylammonio.27. An assay for creatinine in fluids in which assay a fluid sample is contacted with a reagent system comprising cupric ions, a hydroperoxide, and an indicator which produces a fluorescent response when oxidized in the presence of a pseudoperoxide, wherein said indicator is a 4-(1-alkylhydrazino)-7-substituted benzooxadiazole having the formula: where:R1 is C1-C7 R2 is NO2, R3NHSO2, (R3)2NSO2 R3 is hydrogen, alkyl, substituted alkyl, phenyl, substituted phenyl. 28. An assay of claim 27 wherein said indicator is 4-(N-methylhydrazino)-7-nitrobenzooxadiazole (MNBDH).29. An assay of claim 27 further comprising citric acid.30. An assay of claim 27 wherein said cupric ions are supplied by a member of the group consisting of copper sulfate, copper chloride, copper phosphate, and copper hydroxide.31. An assay of claim 27 wherein said hydroperoxide is diisopropylbenzene dihydroperoxide or cumene hydroperoxide.32. An assay of claim 27 wherein said reagent system further comprises a substrate.33. An assay of claim 32 wherein said substrate is a test strip.