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Publication numberUS3104209 A
Publication typeGrant
Publication dateSep 17, 1963
Filing dateFeb 2, 1960
Priority dateFeb 2, 1960
Publication numberUS 3104209 A, US 3104209A, US-A-3104209, US3104209 A, US3104209A
InventorsScott Don
Original AssigneeFermco Lab Inc
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Composition for determination of glucose
US 3104209 A
Abstract  available in
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Claims  available in
Description  (OCR text may contain errors)

taining material.

United States Patent Ofi ice Patented ,Sept. 17, 1963 COMPOSITION FOR DETERMINATION OF GLUCOSE v Don Scott, Chicago, Ill., assiguor to Fermco Laboratories,

This invention relates to a composition providing means for testing biological and chemical fluids for the presence of glucose. More particularly, it relates to a method of high sensitivity for testing body fluids for small quantities of glucose. Still more particularly, it relates to an enzyme system useful in the testing for glucose characterized by the absence of catalase activity.

A simple, rapid and reliable test for detecting the presence of glucose has been sought as an aid for rapid screening of samples as well as for assaying glucose concentration.

The most widely known and conventional method for determination of glucose is based upon the reduction of a metal ion by the glucose when the solution is rendered alkaline and subjected to heat. The Somogyi and Benedict tests are based upon the use of alkaline copper solutions.

Recently a composition has been used in the testing for glucose consisting of two enzymes, an indicator, a buffer and a stabilizer such as gelatin. known as glucose oxidase and peroxidase. The glucose oxidase enzyme in the presence of moisture and oxygen converts glucose to gluconic acid and at the same time produces hydrogen peroxide. The peroxidase enzyme The enzymes used are I acts to catalyze the oxidation of certain indicators such.

as oxidiza-ble dyes when present together with such dye and hydrogen peroxide. Such a system is limited to the use of indicators which are oxygen acceptors.

Peroxidase is a relatively diflicult and expensive enzyme to prepare. Elimination of peroxidase enzyme from test compositions so as to have a single enzyme system, offers a chance for a less expensive composition operating in a more reliable manner.

It has now been discovered that an eflective means for detecting glucose in various materials including body iodide salt and compound which undergoes a color reaction with iodine liberated by oxidation of iodide present in salts such as sodium iodide and potassium iodide or mixtures thereof.

Such a composition may be made into a suspension or solution and used to impregnate bibulous material such as paper, wood, fiber or the like having any desiredsize or shape. Compositions of this invention may be utilized by segregating a test quantity of aqueous solution of test material and adding a drop of the suspect glucose con- If the test solution develops color in accordance with the system used, glucose is present. A

of starch, starch-derivative such as cationic starch or lstarch degradation products such as erythrodextrine.

. tartrazine,

distinct color change will also be developed if glucose containing material is brought in contact with wet bibulous material impregnated with composition, or with dry impregnated bibulous material in the presence of an activating amount of moisture, as well as When a portion of composition is brought in contact with bibulous paper impregnated with test sample. In this situation color develops over the wetted'area on the paper.

In general, the compositions may comprise a system containing glucose oxidase, iodide salt and an indicator system, and optional constituents such as butters and contrasting background colors. Butlers serve a useful purpose through maintenance of an optimum pH for reaction, color change, and the like. Background colors make changes more apparent and thereby add to the sensitivity of the test.

Iodide salts useful in the test indicator compositions for detecting glucose are water soluble salts such as ammonium iodide, alkali metal iodides such as sodium iodide, potassium iodide, multivalent-metal iodides such as copper iodide, magnesium iodide, calcium iodide, ferrous iodide, cobaltous iodide, and nickel iodide.

The purpose of buffers in the compositions is to maintain reaction conditions generally in a specific range. When using an iodide salt such as sodium iodide, potassium iodide, .etc., the oxidation of iodide ion to iodine takes place at any pH. I-Iowever, a solution containing iodide salt is generally bulfered to maintain a pH between about 4.and about 7.5, which range is optimum for glucose oxidase activity. Suitable bulfers for use in these compositions are sodium phosphates, a mixture of citric acid and sodium citrate dihydrate, etc.

When contrast dyes are used in the compositions, the amount should not be such as to mask color changes. About 2-5 parts by weight of dye such as erythrosine, etc., usually produce sufficient contrast. Almost any contrasting color can be used which is different from the color exhibited by the indicator before and after the color change.

The iodide component of an iodide salt, for example, potassium iodide, is converted to the free iodine state by hydrogen peroxide formed during the reaction of glucose and glucose oxidase. In the presence of starch, free iodine reactsto produce a characteristic color varying from: black to blue to red depending uponthe type Other compounds which undergo a color reaction when contacted with iodine are orthotolidine idihy-drochloride,

may be used.

When conducting a test with treated paper, for example,

.it is desirable'that there be a well defined area to provide contrast with unreacting portions of the paper. Such a well defined area can be produced by incorporating an agent such as higher molecular weight polyethylene glycols, methyl cellulose, hydroxy propyl methyl cellulose, sodium polypectate, pectin, peptone, gelatin, gelatinized starch, or mixture thereof in the impregnant for the paper or in solution applied to the paper in conducting the test which increases solution viscosity and/or acts as humectaut. Upon wetting papers treated to have these agents present, a well defined wetted area is obtained which promotes uniformity and intensity of color development over a desired test period of time. Of the agents disclosed, derivatives such as methyl cellulose, hydroxypropylmethylcellulose and the like are preferred because they produce a more uniform colored area than the peptones or gelatin.

Compositions are standardized so as to provide qualitative and/ or quantitative tests. Enzyme preparations containing glucose oxidase substantially free of catalase and amylase may be prepared in accordance with known procedures.

Components of the composition may be varied within wide limits. In general, impregnating solution should contain not less than 10 units/ml. of glucose oxidase activity unless extended reactions may be employed. Lesser concentrations are usually avoided because of a desire to maintain an appreciable color reaction within a 1 to 10 minute period. Glucose oxidase will generally have an activity between 200 and 1000 units per ml., a unit being determined by standard test as a quantity of enzyme giving predetermined rate of oxygen uptake at 30 C.

When desirable, the sample to be tested may be pretreated with an absorbent such as charcoal and the like to remove interfering substances prior to bringing it into contact with the compositions herein disclosed.

The invention will be more fully understood from the following examples which are given by way of illustration and without any intention of the invention being limited thereto.

EXAMPLE I A solution was prepared as follows:

5 ml. of solution containing 400 glucose oxidase units/ml.

essentially devoid of both catalase and amylase 5 ml. potassium iodide 10 ml. soluble starch solution (1.2% Lintner in pH 4.6

0.02 M acetate butter) Paper was impregnated therewith A second solution, prepared with substantially catalase free glucose oxidase enzyme 750 units/ml. containing amylase, turned blue virtually instantly and was discarded.

On testing solution A paper with varying glucose concentrations, the following results were obtained:

Table I Glucose Concentration I as llllll signs indicate extent of color change.

EXAMPLE II Two solutions were prepared as follows:

Each solution was used to impregnate Whatman #1 paper and the paper air-dried. Six strips measuring about 1 x 2 cm. were then cut from each paper and these were arranged on a white porcelain surface. Glucose solutions of Mercks anhydrous dextrose were prepared ranging in concentration from 0 to 2%. One drop of each concentration was then placed on separate pieces of each type of paper almost simultaneously. In the following table the degree of color development is given by the number of plus signs: a negative sign shows no color change.

Table II PAPER A Glucose Concentration Time in Minutes llllll APER B Illlll At the end of 10 minutes, Paper B with 2% glucose had developed only as much color as the paper, impregnated with solution A (the low catalase paper) containing 0.25% glucose developed in 1 /2 minutes.

EXAMPLE III A mixture was made up as follows:

3 ml. a solution contg. 750 units glucose oxidase and units catalase/m1.

10 m1. de-ionized water 5 ml. 10% KI solution 2 ml. o-tolidine solution (4% in 3A ethanol) Eaton-Dikeman papers #609 and 613 were impregnated with this solution and allowed to dry. Both developed dark blue coloring on addition of 3% glucose solution.

EXAMPLE IV A mixture was prepared as follows:

This was then split into 5 portions of 3 ml. each; gelatin was added as follows:

Table III M1. M1. 5% Final above gelatin Ml. H2O percent In gelatin (E ard D paper #613 was impregnated by dipping and airrie A 0.25% glucose solution was dropped on each. This drop remained intact on A'and B, spread on C, D, E.

Color development in test with 0.25% glucose solution is as follows:

values represent center color. Minus signs indicate no visible color change.

From this data it is apparent that there is a minimum concentration of material for iodide-containing compositions required to impart the limited hydrophobic properties to the test paper to maintain a well defined test area and to avoid diffusion of composition into migratory fringe areas of inconclusive color quality, shade and depth. For gelatin, concentrations between about 0.2 and about 0.7% are preferred for buifered compositions.

EXAMPLE V A mixture was prepared as follows:

7.5 ml. 2% soluble starch solution (Merck #74881) 0.25 gm. sodium salt of ethylene diam-inc tetraacetic acid 0.75 ml. 40% KI 2.0 ml. 5% gelatin 375 units-glucoseoxidase essentially free. of catalase and amylase Adjusted pH to 6.1

Citrate buffer was added to portions of the above composition as follows:

tion. Such builering action, however, should not be such as to slow down the reaction. Butler concentration in impregnating solution and for impregnated paper of between about 0.04 molar and about 0.004 molar is preferred.

Solutions were prepared as above except for the substitution of phosphate buffer for citrate buffer in equimolar amounts. A typical phosphate buffer consists of 13.4 grams of disodium hydrogen phosphate mixed with 58.5 grams of sodium dihydrogen phosphate (N3.H2PO4.H20)

This inorganic buffer shows substantially the same concentration effect as the butter containing salts of organic acids.

EXAMPLE VI A mixture was prepared as follows:

7.5 ml. 2% soluble starch (Merck #74881) 2.0 ml. 5% gelatin 0.36 gm. phosphate bufier prepared as in Example IV 1.25 ml.i% KI 375 units glucose oxidase essentially free of catalase and amylase Water to 15' ml.

7 The mixture was split into four portions of 3 ml. each. Concentrationof the sodium salt of ethylenediaminetetraacetic acid (indicated below by Na EDTA) was varied as follows:

Table VII Final percent M1. above M1. 2.5% MLHZO NazEDTAin mixture Na; ED TA impregnating solution Color development in tests with 0.25% glucose solution was as follows:

Table V I Table VIII M1. M1. Approx. Paper above buffer M1. final Time in Minutes mixture solution .HQO molarity citrate A B O D 2a is. as. 2 i [i] [if] [i] 3: 0 0 0 0 3 [++l [++1 lBufi lt'o c t dof25 solutionofeitrate mixture of33grams 5 citric aeir i rigniiiimiii e with fifi g rarns trisodium citrate duohydrate. ii ii H-i-H i Eaton-Dikeman #613 paper impregnated as before and air dried. Pieces of each were spotted with 0.25% glucose solution.

Color development in tests with 0.25% glucose solu- Consistent test results require the presence of some buffer to overcome the efiect of acid formed in the reac- The sodium salt of ethylenediaminetetraacetic acid acts as a sequestering agent. The presence of sequestering agents tend to stabilize impregnated paper. Paper impregnating with solutions containing in excess of about 0.5% of sodium salt of ethylenediaminetetraacetic acid are preferred.

It is apparent that the glucose oxidase concentration as well as other components of the composition can be varied to give a positive test at any predetermined glucose level with-in a specific test interval. In general, an impregnating solution should contain not less than about 10 units per ml. although greater amounts as evidenced by the examples can be used to produce a faster reaction. In the above examples, starch Wasused in amounts which would develop a strong depth of color in the period of 3 to 10 minutes. In general, soluble starch may beincorporated in the impregnating solutions in amounts of between 0.2 and 2% concentration.

EXAMPLE VII A stock solution was prepared as follows:

16.5 soluble starch solution (2% Lintner) 720 mg. phosphate buffer (solid mixture of disodium and mono sodium phosphate) 2.5 ml. 40% potassium iodide 250 mg. sodium salt of ethylenediaminetetraacetic acid Adjust pH to 6.0 and then add 750 units glucose oxidase essentially free of catalase and amylase 11 ml. water Paper impregnating solution was prepared as follows:

3 ml. stock solution 1.2 ml. of water 0.8 ml. of 2.5% solution of each of the materials listed below Four types of papers indicated E, F, G and H were prepared by impregnating Eaton-Dikeman #613 paper with solution containing hydroxypropylmethylcellulose (representative of methyl cellulose materials), sodium polypeotate, peptone and gelatin, respectively.

Color development in test with 0.25% glucose solution is as follows:

Table IX Time in Minutes E F G H 1 [fl l-] [fl 2 +l [t] [++1 3 [ti-1 H-i-H [+-i-+l 5 l++++1 l++++l l++++l I claim:

1. A composition for detecting the presence of glucose which comprises glucose oxidase enzyme substantially free of proteinaceous material functioning to produce peroxidase and catalase activity, iodide salt, a compound which undergoes a color reaction when contacted with iodine produced from the iodide of the salt, and a sequestering agent.

2. A composition for detecting the presence of glucose which comprises glucose oxidase substantially free of proteinaceous material functioning to produce peroxidase and catalase activity, iodide salt,.a compound which undergoes a color reaction when contacted with iodine produced by oxidation of the iodide and the sodium salt of ethylenediarninetetraacetic acid.

3. A composition for detecting the presence of glucose which comprises glucose oxidase enzyme substantially free of proteinaceous material functioning to produce peroxidase and catalase activity, iodide salt, a compound which undergoes a color reaction when contacted with iodine produced from the iodide of the salt, a compound selected from the group consisting of higher molecular weight polyethylene glycols, methyl cellulose, hydroxy propyl methyl cellulose, sodium polypectate, pectin, peptone, gelatin, gelatinized starch, and mixtures thereof in quantities adapted to impart limited hydrophobic properties to bibulous material, and a sequestering agent.

4. A composition for detecting the presence of glucose which comprises glucose oxidase substantially free of proteinaceous material functioning to produce peroxidase and catalase activity, alkali metal iodide, a butter for maintaining a pH in the range between about 4 and about 7.5, ortho tolidine dihydrochloride and a sequestering agent.

References Cited in the file of this patent UNITED STATES PATENTS 2,848,308 Free Aug. 19, 1958 FOREIGN PATENTS 203,451 Australia Sept. 27, 1956 OTHER REFERENCES Annalen der Chemie, vol. 541, pages 141-142, 1939.

Specific Colorimetric Enzymatic Analytical Reagents for Glucose, lby Keston, Abstract of Papers, 129th Meeting, A.C.S., Dallas, Texas, April 1956, p. 31.C.

Methocel, publication by Dow Chemical Co., 1957.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2848308 *Dec 5, 1955Aug 19, 1958Miles LabComposition of matter
AU203451B * Title not available
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3266868 *Jan 24, 1962Aug 16, 1966Miles LabDiagnostic composition and test indicator
US3411887 *Jun 15, 1964Nov 19, 1968Miles LabDiagnostic composition
US3920580 *Jul 12, 1973Nov 18, 1975Miles LabLiquid control solution
US3964870 *Mar 4, 1975Jun 22, 1976Boehringer Mannheim G.M.B.H.Diagnostic composition for the determination of glucose
US4092115 *May 20, 1977May 30, 1978Miles Laboratories, Inc.Method, device and test reagent for detecting free available chlorine in aqueous fluids
US4098574 *Aug 1, 1977Jul 4, 1978Eastman Kodak CompanyGlucose detection system free from fluoride-ion interference
US4303409 *Apr 15, 1980Dec 1, 1981Shionogi & Co., Ltd.Method, composition and test strip for colorimetric analysis of ascorbic acid
US4390621 *Mar 1, 1982Jun 28, 1983Miles Laboratories, Inc.Method and device for detecting glucose concentration
US4539180 *Mar 31, 1983Sep 3, 1985Regents Of The University Of MinnesotaApparatus for quantitatively determining the level of hemoglobin in a biological sample
US4587220 *Feb 2, 1984May 6, 1986Miles Laboratories, Inc.Ascorbate interference-resistant composition, device and method for the determination of peroxidatively active substances
US4851353 *Feb 4, 1987Jul 25, 1989Kyowa Hakko Kogyo Co., Ltd.Method and test composition for determination of lipid peroxide
US7138268Jun 29, 2001Nov 21, 2006Agilent Technologies, Inc.Dry biochemical assay plate and method for making the same
US20010046682 *Jun 29, 2001Nov 29, 2001Kay LichtenwalterDry biochemical assay plate and method for making the same
Classifications
U.S. Classification435/14, 435/805, 436/95, 422/420, 422/428
International ClassificationC12Q1/54
Cooperative ClassificationC12Q1/54, Y10S435/805
European ClassificationC12Q1/54