US3266868A - Diagnostic composition and test indicator - Google Patents

Diagnostic composition and test indicator Download PDF

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Publication number
US3266868A
US3266868A US168553A US16855362A US3266868A US 3266868 A US3266868 A US 3266868A US 168553 A US168553 A US 168553A US 16855362 A US16855362 A US 16855362A US 3266868 A US3266868 A US 3266868A
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United States
Prior art keywords
glucose
iodide
molybdate
salt
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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
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US168553A
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English (en)
Inventor
Edward K Harvill
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Bayer Corp
Original Assignee
Miles Laboratories Inc
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Filing date
Publication date
Priority to NL288096D priority Critical patent/NL288096A/xx
Priority to BE627415D priority patent/BE627415A/xx
Application filed by Miles Laboratories Inc filed Critical Miles Laboratories Inc
Priority to US168553A priority patent/US3266868A/en
Priority to FR922431A priority patent/FR1344835A/fr
Priority to GB2915/63A priority patent/GB1018306A/en
Application granted granted Critical
Publication of US3266868A publication Critical patent/US3266868A/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
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S436/00Chemistry: analytical and immunological testing
    • Y10S436/904Oxidation - reduction indicators

Definitions

  • glucose indicator may also be used efficiently in routine urinalyses in hospitals and physicians oflices, in diabetes screening programs, in the differentiation of glucosuria from other meliturias, and the like.
  • a urine-sugar test to be of greatest value, must be conveniently rapid, simple enough for any patient to learn with ease, accurate enough to serve the clinician, and sensitive enough to reflect variations in the patients condition.
  • the reagent composition must be adequately stable.
  • the diagnostic composition according to the basic invention described in the copending application just referred to 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 the indicators by hydrogen peroxide formed in the oxidation of glucose.
  • Oxidized diamlnofluorene (blue color) The degree of blue color formation is immediately but accurately indicative of the glucose content of the fluid being tested.
  • an improved diagnostic composition for the detection of glucose which is not reduced in sensitivity by the presence of ketonic substances may be prepared by the incorporation of a metallic salt of a chelating agent into a formulation which contains a flavoprotein of glucose oxidase, an iodide salt, and a molybdate salt with a colorforming substance oxidizable by hydrogen peroxide in the presence of iodide and molybdate salts.
  • potassium iodide and sodium molybdate it is also possible, and therefore contemplated, to employ other equivalent iodide and molybdate salts.
  • other iodides such as sodium and ammonium iodides and other molybdates, such as potassium and ammonium molybdates may also be used.
  • As a colorforming substance 2,7-diamino-fluorene, o-tolidine, odianisidine, leucoindophenols, etc., may be used.
  • pH range may vary between 4 to 7.5, an especially preferred pH is 6.7.
  • test device itself may comprise the 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.
  • Bibulous strips such as filter paper cut into narrow strips
  • These strips are then dried in a drying tunnel or in a forced draft oven.
  • the test portion of these strips is of a red color. It will be understood 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 of this example are extraordinarily sensitive when compared to test strips commercially available but, as shown, their sensitivity is somewhat impaired by the presence of ketonic substances present in body fluids being tested.
  • Example II the formulation of the tests strips of Example I above was varied slightly by the incorporation into the formula of a heavy metallic salt of a chelating agent. This formulation is set out in detail in Example II as follows:
  • Example II The improved reagent strips of Example II were tested against the same urines as set out in Table I above with the following results:
  • molybdate salt used is the sodium salt and the iodide salt selected is the potassium salt. It is to be understood, of course, that other salts may be used.
  • operable molybdate salts include sodium and potassium.
  • Sodium and ammonium iodide may be used as the iodide salts.
  • the present invention relates to a diagnostic test for the detection of glucose in body fluids, especially in urine, which is not sensitive to interference by ketonic substances.
  • the improved composition of the instant invention consists of a bibulous material which has been impregnated with a composition comprising glucose oxidase, an iodide salt, a molybdate salt, an oxidizable substance which changes color in the presence of hydrogen peroxide and said salts and a metallic salt of a chelating agent.
  • the preferred embodiment of the present invention comprises a bibulous material which has been impregnated with a composition consisting of glucose oxidase, potassium iodide, sodium molyb-date, 2,7-diaminofluorene, and an iron salt of ethylene diamine tetraaeetic acid.
  • a diagnostic composition for detecting glucose which comprises glucose oxidase, an iodide salt selected from the group consisting of potassium iodide, sodium iodide, and ammonium iodide, a molybdate salt selected from the group. consisting of sodium molybdate, potassium molybdate, and ammonium molybdate, a color-forming substance oxidizable by hydrogen peroxide in the presence of said iodide and molybdate salts, and a metallic salt of a chelating agent selected from the group consisting of the copper, nickel, manganese and iron salts of ethylene diamine tetra-acetic acid.
  • a diagnostic composition for detecting glucose which com-prises glucose oxidase, an iodide salt selected from the group consisting of potassium iodide, sodium iodide, and ammonium iodide, a molybdate salt selected from the group consisting of sodium molybdate, potassium molybd'ate, and ammonium molybdate, a color-forming substance selected from the group consisting of 2,7-diaminofluorene, o-tolidine, and dianisidine and mixtures thereof, and a metallic salt of a chel-ating agent selected from the group consisting of the copper, iron, nickel and manganese salts of ethylene diamine tetraacetic acid.
  • an iodide salt selected from the group consisting of potassium iodide, sodium iodide, and ammonium iodide
  • a molybdate salt selected from the group consisting of sodium molybdate, potassium molybd'ate, and am
  • a diagnostic composition for detecting glucose which comprises glucose oxidase, potassium iodide, sodium molybdate, 2,7-diaminoiiuorene, o-tolidine and the ferric salt of ethylene diamine tetraacetic acid.
  • a test indicator for detecting glucose which comprises a bibulous 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, 2,7-diaminofluorene, o-tolidine, and the ferric salt of ethylene diamine tetraacetic acid.

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  • 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)
  • Investigating Or Analysing Biological Materials (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
US168553A 1962-01-24 1962-01-24 Diagnostic composition and test indicator Expired - Lifetime US3266868A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
NL288096D NL288096A (ja) 1962-01-24
BE627415D BE627415A (ja) 1962-01-24
US168553A US3266868A (en) 1962-01-24 1962-01-24 Diagnostic composition and test indicator
FR922431A FR1344835A (fr) 1962-01-24 1963-01-23 Composition perfectionnée pour doser et déceler le glucose dans les fluides biologiques
GB2915/63A GB1018306A (en) 1962-01-24 1963-01-23 Improved diagnostic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US168553A US3266868A (en) 1962-01-24 1962-01-24 Diagnostic composition and test indicator

Publications (1)

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US3266868A true US3266868A (en) 1966-08-16

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US168553A Expired - Lifetime US3266868A (en) 1962-01-24 1962-01-24 Diagnostic composition and test indicator

Country Status (4)

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US (1) US3266868A (ja)
BE (1) BE627415A (ja)
GB (1) GB1018306A (ja)
NL (1) NL288096A (ja)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3367842A (en) * 1965-02-17 1968-02-06 Miles Lab Test composition and device for the detection of galactose in fluids
US3411887A (en) * 1964-06-15 1968-11-19 Miles Lab Diagnostic composition
DE2500689A1 (de) * 1974-01-09 1975-07-10 Shionogi & Co Diagnosemittel und diese enthaltende diagnosevorrichtung
US4132527A (en) * 1974-01-09 1979-01-02 Shionogi & Co., Ltd. Diagnostic compositions, diagnosing instruments, and methods of manufacturing same
US4143080A (en) * 1976-11-25 1979-03-06 The Goodyear Tire & Rubber Company Method and reagent for the assay of hydroperoxide
US4288541A (en) * 1979-10-15 1981-09-08 Miles Laboratories, Inc. Ascorbate resistant composition, test device and method for detecting a component in a liquid test sample
US4303409A (en) * 1979-04-24 1981-12-01 Shionogi & Co., Ltd. Method, composition and test strip for colorimetric analysis of ascorbic acid
US4469110A (en) * 1981-06-25 1984-09-04 Slama Gerard J Device for causing a pinprick to obtain and to test a drop of blood
US4587220A (en) * 1983-03-28 1986-05-06 Miles Laboratories, Inc. Ascorbate interference-resistant composition, device and method for the determination of peroxidatively active substances
US4658833A (en) * 1983-03-08 1987-04-21 Stuart James F B Monitoring of drug levels
US6583722B2 (en) 2000-12-12 2003-06-24 Kimberly-Clark Worldwide, Inc. Wetness signaling device
US6603403B2 (en) 2000-12-12 2003-08-05 Kimberly-Clark Worldwide, Inc. Remote, wetness signaling system
US9121831B2 (en) 2011-08-24 2015-09-01 Multisorb Technologies, Inc. Copper, starch and iodide moisture indicator

Citations (10)

* 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
US2981606A (en) * 1955-06-20 1961-04-25 Lilly Co Eli Glucose indicator and method
US2982700A (en) * 1961-05-02 Diagnostic composition
US2990253A (en) * 1959-05-21 1961-06-27 Miles Lab Diagnostic composition
US2990338A (en) * 1959-11-24 1961-06-27 Gibson Jacob John Composition for determination of glucose in body fluids
US3016292A (en) * 1959-05-15 1962-01-09 Miles Lab Diagnostic composition
US3042496A (en) * 1959-03-27 1962-07-03 Miles Lab Diagnostic composition
US3104209A (en) * 1960-02-02 1963-09-17 Fermco Lab Inc Composition for determination of glucose
US3123443A (en) * 1960-04-18 1964-03-03 Composition for diagnosing glucose
US3143476A (en) * 1954-09-15 1964-08-04 Curtis Helene Ind Inc Cold wave neutralizing composition and process

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2982700A (en) * 1961-05-02 Diagnostic composition
US3143476A (en) * 1954-09-15 1964-08-04 Curtis Helene Ind Inc Cold wave neutralizing composition and process
US2981606A (en) * 1955-06-20 1961-04-25 Lilly Co Eli Glucose indicator and method
US2848308A (en) * 1955-12-05 1958-08-19 Miles Lab Composition of matter
US3042496A (en) * 1959-03-27 1962-07-03 Miles Lab Diagnostic composition
US3016292A (en) * 1959-05-15 1962-01-09 Miles Lab Diagnostic composition
US2990253A (en) * 1959-05-21 1961-06-27 Miles Lab Diagnostic composition
US2990338A (en) * 1959-11-24 1961-06-27 Gibson Jacob John Composition for determination of glucose in body fluids
US3104209A (en) * 1960-02-02 1963-09-17 Fermco Lab Inc Composition for determination of glucose
US3123443A (en) * 1960-04-18 1964-03-03 Composition for diagnosing glucose

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3411887A (en) * 1964-06-15 1968-11-19 Miles Lab Diagnostic composition
US3367842A (en) * 1965-02-17 1968-02-06 Miles Lab Test composition and device for the detection of galactose in fluids
DE2500689A1 (de) * 1974-01-09 1975-07-10 Shionogi & Co Diagnosemittel und diese enthaltende diagnosevorrichtung
US4132527A (en) * 1974-01-09 1979-01-02 Shionogi & Co., Ltd. Diagnostic compositions, diagnosing instruments, and methods of manufacturing same
US4143080A (en) * 1976-11-25 1979-03-06 The Goodyear Tire & Rubber Company Method and reagent for the assay of hydroperoxide
US4303409A (en) * 1979-04-24 1981-12-01 Shionogi & Co., Ltd. Method, composition and test strip for colorimetric analysis of ascorbic acid
US4288541A (en) * 1979-10-15 1981-09-08 Miles Laboratories, Inc. Ascorbate resistant composition, test device and method for detecting a component in a liquid test sample
US4469110A (en) * 1981-06-25 1984-09-04 Slama Gerard J Device for causing a pinprick to obtain and to test a drop of blood
US4658833A (en) * 1983-03-08 1987-04-21 Stuart James F B Monitoring of drug levels
US4587220A (en) * 1983-03-28 1986-05-06 Miles Laboratories, Inc. Ascorbate interference-resistant composition, device and method for the determination of peroxidatively active substances
US6583722B2 (en) 2000-12-12 2003-06-24 Kimberly-Clark Worldwide, Inc. Wetness signaling device
US6603403B2 (en) 2000-12-12 2003-08-05 Kimberly-Clark Worldwide, Inc. Remote, wetness signaling system
US9121831B2 (en) 2011-08-24 2015-09-01 Multisorb Technologies, Inc. Copper, starch and iodide moisture indicator

Also Published As

Publication number Publication date
GB1018306A (en) 1966-01-26
NL288096A (ja)
BE627415A (ja)

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