US3016292A - Diagnostic composition - Google Patents

Diagnostic composition Download PDF

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Publication number
US3016292A
US3016292A US813336A US81333659A US3016292A US 3016292 A US3016292 A US 3016292A US 813336 A US813336 A US 813336A US 81333659 A US81333659 A US 81333659A US 3016292 A US3016292 A US 3016292A
Authority
US
United States
Prior art keywords
glucose
iodide
solution
molybdate
water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US813336A
Other languages
English (en)
Inventor
Bauer Robert
Ray L Mast
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer Corp
Original Assignee
Miles Laboratories Inc
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.)
Filing date
Publication date
Priority to NL251599D priority Critical patent/NL251599A/xx
Priority to BE590824D priority patent/BE590824A/xx
Priority to IT630626D priority patent/IT630626A/it
Priority to US813336A priority patent/US3016292A/en
Application filed by Miles Laboratories Inc filed Critical Miles Laboratories Inc
Priority to GB14249/60A priority patent/GB883744A/en
Priority to DEM45193A priority patent/DE1284124B/de
Priority to CH511860A priority patent/CH392109A/de
Priority to FR827161A priority patent/FR1256933A/fr
Application granted granted Critical
Publication of US3016292A publication Critical patent/US3016292A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/54Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving glucose or galactose
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/805Test papers
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/14Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
    • Y10T436/142222Hetero-O [e.g., ascorbic acid, etc.]
    • Y10T436/143333Saccharide [e.g., DNA, etc.]
    • Y10T436/144444Glucose

Definitions

  • This invention relates toa new and improved diagnostic 'guided in this regard by a regular check on urine glucose.
  • this glucose indicator may also be used efficiently inroutine urinalyses in hospitals and physicians offices, in diabetes detection screening programs, in the dilferentiation of glucosuria from other meliturias, and the like.
  • Glucose indicators in stick form present-ly' on the market depend for the detection of hydrogen peroxide on the action of enzymes,-s uch asperoxidases.
  • the glucose indicator of the present invention makes use of a non-enzymatic agent which permits a more accurately controllable and more definite composition. A very sensitive test for hydrogen peroxide and,faccordingly, glucose is'thus made possible.
  • a diagnostic composition according to the present'im vention comprises as essential constituents glucose oxidase, an iodide salt, such as potassium iodide, a molybdate salt, such as sodium molybdate, and a color-forming substance or indicator, such as 2,7-diaminofluorene.
  • an iodide salt such as potassium iodide
  • a molybdate salt such as sodium molybdate
  • a color-forming substance or indicator such as 2,7-diaminofluorene.
  • the glucose oxidase (glucose aerodehydrogenase), as is well known, catalyzes the aerobic oxidation of glucose to produce gluconic acid (gluconolactone) and hydrogen peroxide.
  • the iodide and molybdate salts are capable of inducing the oxidation of indicators by hydrogen peroxide formed in the oxidation of glucose.
  • the latter reaction may be represented by the following schematic equation: a
  • Oxidized diar'ninofiuorene blue color
  • potassium iodide and sodium molybdate it is also possible, and therefore contemplated, to employ other equivalent iodide and molybdatelsalts.
  • other iodides such as sodium and ammonium iodides and other molybdates, such as potassium 'and ammonium molybdates may also be used.
  • i2,7-diaminofluorene o-tolidine, o-dianisidine, leucoindophenols, etc. would be satisfactory indicators.
  • additives are incorporated in the reagent composition as suitable protective, thickening, wetting, suspending agents and the like as well as inert dyes to impart thereto a uniformrcolor background.
  • test device itself may comprise the reagent composition in the form of a'tablet, powder or other embodiment
  • reagent composition in the form of a'tablet, powder or other embodiment
  • Embodying the diagnostic composition in 'the form of test sticks insures ease and simplicity. of test procedure.
  • phosphate butter of pH 6.5 prepared by dissolving 43.55 gm. of dibasic potassium phosphate (K HPO and 39.0 gm. of monobasic sodium phosphate (NaH PO;.H O) in water and bringing. to a volume of 500 ml.) are added to solution No. 4 with constant stirring.
  • Bibulous strips such as filter paper cut into narrow strips
  • These strips are then dried in a. drying tunnel or in aforced draft oven.
  • the test portion of these strips is of a red color. It will be under stood that other porous or absorbing materials, 'such as small sticks of wood, etc. and other methods of applying the impregnating solution and of drying the impregnated sticks may likewise be employed.
  • Test strips are then prepared in accordance with the procedure recited in Example I.
  • gelatin-dye solution prepared by dis- (2) 1 gm. of KI, 3 gm. of glycine and 0.5 gm. of Na MoO .2H O are dissolved in 20 ml. of hot water. 10 ml. of 4% gelatin-dye solution is added to this solution.
  • the gelatin-dye solution is prepared as described in Example I. v
  • cation exchange cellulose has a two-fold purpose: it maintains the indicator in suspension so as to prevent it from precipitating, and it serves as a buffer for the reagent composition.
  • These functions in the embodiments of Examples I and II are performed, respectively, by polyvinyl alcohol and the buffer system.
  • this invention pertains to a diagnostic test for the detection of glucose in body fluids, especially in urine, consisting of a bibulous strip or stick that has been impregnated with a composition comprising glucose ox1- dase, potassium iodide, sodium molybdate and 2,7-diaminofluorene which is oxidizable by hydrogen peroxide formed in the glucose oxidase-catalyzed decomposition of glucose in the presence of said iodide and molybdate salts.
  • a diagnostic composition for detecting glucose which comprises glucoseoxidase, an iodide salt selected from the group consisting of potassium iodide, sodium iodide, and ammonium iodide, a molybdate salt for intensifying the action of the iodide and selected from the group consisting of sodium molybdate, potassium molybdate, and ammonium molybdate and a color-forming substance oxidizable by hydrogen peroxide in the presence of said iodide and molybdate salts.
  • an iodide salt selected from the group consisting of potassium iodide, sodium iodide, and ammonium iodide
  • a molybdate salt for intensifying the action of the iodide selected from the group consisting of sodium molybdate, potassium molybdate, and ammonium molybdate and a color-forming substance oxidizable by hydrogen peroxide in the presence of said iodide and molybdate
  • a diagnostic composition for detecting glucose which comprises glucose oxidase, an iodide salt selected from the group consisting of potassium iodide, sodium iodide,
  • a diagnostic composition for detecting glucose which comprises glucose oxidase, potassium iodide, sodium molybdate and 2,7-diaminofluorene.
  • a diagnostic composition for detecting glucose which comprises:
  • a test indicator for detecting glucose which comprises a bi-bulous material which contains therein the dried residue resulting from deposition on said material, followed by drying, of a liquid comprising glucose oxidase, potassium iodide, sodium molybdate and 2,7-diamino-' fiuorene.
  • a test indicator for detecting glucose which comprises a bibulous strip of paper which contains therein the diagnostic composition of claim 4.
  • ammonium molybdate and a color-forming substance se-

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Emergency Medicine (AREA)
  • Immunology (AREA)
  • Microbiology (AREA)
  • Molecular Biology (AREA)
  • Biophysics (AREA)
  • Physics & Mathematics (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
US813336A 1959-05-15 1959-05-15 Diagnostic composition Expired - Lifetime US3016292A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
NL251599D NL251599A (US06262066-20010717-C00315.png) 1959-05-15
BE590824D BE590824A (US06262066-20010717-C00315.png) 1959-05-15
IT630626D IT630626A (US06262066-20010717-C00315.png) 1959-05-15
US813336A US3016292A (en) 1959-05-15 1959-05-15 Diagnostic composition
GB14249/60A GB883744A (en) 1959-05-15 1960-04-22 Diagnostic composition
DEM45193A DE1284124B (de) 1959-05-15 1960-05-04 Diagnostisches Mittel und Testindikator zum Nachweis von Glucose in Koerperfluessigkeiten
CH511860A CH392109A (de) 1959-05-15 1960-05-05 Diagnostische Zusammensetzung
FR827161A FR1256933A (fr) 1959-05-15 1960-05-13 Composition de détection du glucose dans l'urine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US813336A US3016292A (en) 1959-05-15 1959-05-15 Diagnostic composition

Publications (1)

Publication Number Publication Date
US3016292A true US3016292A (en) 1962-01-09

Family

ID=25212086

Family Applications (1)

Application Number Title Priority Date Filing Date
US813336A Expired - Lifetime US3016292A (en) 1959-05-15 1959-05-15 Diagnostic composition

Country Status (7)

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US (1) US3016292A (US06262066-20010717-C00315.png)
BE (1) BE590824A (US06262066-20010717-C00315.png)
CH (1) CH392109A (US06262066-20010717-C00315.png)
DE (1) DE1284124B (US06262066-20010717-C00315.png)
GB (1) GB883744A (US06262066-20010717-C00315.png)
IT (1) IT630626A (US06262066-20010717-C00315.png)
NL (1) NL251599A (US06262066-20010717-C00315.png)

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3066081A (en) * 1961-05-05 1962-11-27 Edward S Rorem Means for detecting galactose
US3183173A (en) * 1963-06-10 1965-05-11 Miles Lab Test composition for detecting hydrogen peroxide
US3266868A (en) * 1962-01-24 1966-08-16 Miles Lab Diagnostic composition and test indicator
US3329486A (en) * 1965-09-10 1967-07-04 Miles Lab Composition and device for testing for chloride, bromide, iodide, cyanide, and thiocyanate
US3350278A (en) * 1962-12-03 1967-10-31 Miles Lab Enzymatic glucose test composition and device
US3371019A (en) * 1965-01-08 1968-02-27 Searle & Co Diagnostic indicator
US3453180A (en) * 1965-08-02 1969-07-01 Miles Lab Test article
US3528780A (en) * 1968-04-05 1970-09-15 Us Air Force Visual ammonia detector
US4143080A (en) * 1976-11-25 1979-03-06 The Goodyear Tire & Rubber Company Method and reagent for the assay of hydroperoxide
US4331759A (en) * 1979-09-10 1982-05-25 E.N.I. Ente Nazionale Idrocarburi Composition suitable for testing biological tissues and/or liquids, and the method of use
WO1982002251A1 (en) * 1980-12-19 1982-07-08 Mining & Mfg Minnesota Method and article for determining free acid concentration in liquid
US4654309A (en) * 1980-12-19 1987-03-31 Minnesota Mining And Manufacturing Co. Test method and article for estimating the concentration of free acid in liquid
EP0266216A2 (en) * 1986-10-31 1988-05-04 Fuji Photo Film Co., Ltd. Control or calibration solutions for fluid analysis
US5382523A (en) * 1989-12-02 1995-01-17 Boehringer Mannheim Gmbh Use of sparingly soluble salt of a heteropoly acid for the determination of an analyte, a corresponding method of determination as well as a suitable agent thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2848308A (en) * 1955-12-05 1958-08-19 Miles Lab Composition of matter
US2881213A (en) * 1957-12-17 1959-04-07 Standard Oil Co Process for the conversion of acrolein and methacrolein to the corresponding unsaturated acids

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB784548A (en) * 1955-07-07 1957-10-09 Lilly Co Eli Improvements in or relating to glucose indicator

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2848308A (en) * 1955-12-05 1958-08-19 Miles Lab Composition of matter
US2881213A (en) * 1957-12-17 1959-04-07 Standard Oil Co Process for the conversion of acrolein and methacrolein to the corresponding unsaturated acids

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3066081A (en) * 1961-05-05 1962-11-27 Edward S Rorem Means for detecting galactose
US3266868A (en) * 1962-01-24 1966-08-16 Miles Lab Diagnostic composition and test indicator
US3350278A (en) * 1962-12-03 1967-10-31 Miles Lab Enzymatic glucose test composition and device
US3183173A (en) * 1963-06-10 1965-05-11 Miles Lab Test composition for detecting hydrogen peroxide
US3371019A (en) * 1965-01-08 1968-02-27 Searle & Co Diagnostic indicator
US3453180A (en) * 1965-08-02 1969-07-01 Miles Lab Test article
US3329486A (en) * 1965-09-10 1967-07-04 Miles Lab Composition and device for testing for chloride, bromide, iodide, cyanide, and thiocyanate
US3528780A (en) * 1968-04-05 1970-09-15 Us Air Force Visual ammonia detector
US4143080A (en) * 1976-11-25 1979-03-06 The Goodyear Tire & Rubber Company Method and reagent for the assay of hydroperoxide
US4331759A (en) * 1979-09-10 1982-05-25 E.N.I. Ente Nazionale Idrocarburi Composition suitable for testing biological tissues and/or liquids, and the method of use
US4376820A (en) * 1979-09-10 1983-03-15 E.N.I. Ente Nazionale Idrocarburi Composition suitable for testing biological tissues and/or liquids, and the method of use
WO1982002251A1 (en) * 1980-12-19 1982-07-08 Mining & Mfg Minnesota Method and article for determining free acid concentration in liquid
US4654309A (en) * 1980-12-19 1987-03-31 Minnesota Mining And Manufacturing Co. Test method and article for estimating the concentration of free acid in liquid
EP0266216A2 (en) * 1986-10-31 1988-05-04 Fuji Photo Film Co., Ltd. Control or calibration solutions for fluid analysis
EP0266216B1 (en) * 1986-10-31 1993-12-15 Fuji Photo Film Co., Ltd. Control or calibration solutions for fluid analysis
US5382523A (en) * 1989-12-02 1995-01-17 Boehringer Mannheim Gmbh Use of sparingly soluble salt of a heteropoly acid for the determination of an analyte, a corresponding method of determination as well as a suitable agent thereof
US5521060A (en) * 1989-12-02 1996-05-28 Boehringer Mannheim Gmbh Use of a sparingly soluable salt of a heteropoly acid for the determination of an analyte, a corresponding method of determination as a suitable agent therefor

Also Published As

Publication number Publication date
GB883744A (en) 1961-12-06
IT630626A (US06262066-20010717-C00315.png)
CH392109A (de) 1965-05-15
NL251599A (US06262066-20010717-C00315.png)
BE590824A (US06262066-20010717-C00315.png)
DE1284124B (de) 1968-11-28

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