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US3649198A - Diagnostic method for the determination of uric acid in blood - Google Patents

Diagnostic method for the determination of uric acid in blood
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US3649198A
US3649198AUS38907AUS3649198DAUS3649198AUS 3649198 AUS3649198 AUS 3649198AUS 38907 AUS38907 AUS 38907AUS 3649198D AUS3649198D AUS 3649198DAUS 3649198 AUS3649198 AUS 3649198A
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uric acid
solution
added
blood
serum
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US38907A
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Robert L Rush
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Pfizer Inc
Warner Lambert Co LLC
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Pfizer Inc
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Assigned to WARNER-LAMBERT COMPANY, A CORP. OF DE.reassignmentWARNER-LAMBERT COMPANY, A CORP. OF DE.ASSIGNMENT OF ASSIGNORS INTEREST.Assignors: PFIZER INC.
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Abstract

A diagnostic method for the determination of uric acid in the blood of humans by detecting the color change of a copper neocuproine complex in the presence of N-ethylmaleimide.

Description

he States atei Rush 1 1 Mar. 14, 1972 [54] DIAGNOSTIC METHOD FQR THE [56] References Cited DETERMINATION 0F URIC ACID 1N UNITED STATES PATENTS 131.001)
3,349,006 10/1967 Albaum ..252/408 X [721 Invent Rush sprmgvaney 3,528,777 9/1970 Moran ..23/230 1; 73 Assigneez C Pfizer & C I New York, N Y 3,554,701 1/1971 (30111611, .1! ..252/408 X [22] Filed: May 19, 1970 Primary Examiner-Morris O. Wolk Assistant Examiner-R. E. Sew/in [21] App! 38907 Attorney-Connolly and Hutz [52] US. Cl 23/230 B, 252/408, 356/39, ABSTRACT 424/7 A dia gnost1c method for the determmauon of ur1c ac1d 1n the 51 11 1. c1 ..G0ln 33/16, 00111 31/22, GOln 21/24 blood of humans by detecting the change of a copper [58] Field of Search "23/230 253 TP; 25 neocuproine complex in the presence of N-ethylmaleimide.
2 Claims, No Drawings DIAGNOSTIC METHOD FOR THE DETERMINATION OF URIC ACID IN BLOOD BACKGROUND OF THE INVENTION This invention relates to a novel diagnostic test. More particularly, it relates to an improved diagnostic method for the determination of uric acid in the blood of humans, which is based on the detection of a color change of a copper neocuproine complex in the presence of N-ethylmaleimide.
The determination of uric acid is of particular importance in screening individuals for certain disease states. Uric acid is the metabolic end product of purines. The purines may be derived from nucleic acids, nucleotide cofactors, or from nucleic acids in food. In gout, the pool of uric acids is increased and urates are deposited in and around joints producing pain and swelling. Thus in gout, or in gouty arthritis, the blood uric acid level increases. High uric acid values are also found in nephritis, eclampsia, leukemia and other conditions affecting the excretory function of the kidneys.
Uric acid has been determined in several different ways. Two of the most common methods are by the reaction of uric acid with alkaline phosphotungstate and by the enzyme uricase. In the first method, uric acid is estimated by reducing alkaline phosphotungstate to tungsten blue and measuring the colored product in a colorimeter. The second method utilizes the property of uric acid of absorbing light at 290-293 M;/.. The products of the uricase reaction do not absorb at this wavelength. The decrease in absorbance is proportional to the amount of uric acid initially present.
Bittner, in US. Pat. No. 3,282,649, discloses a method for the determination of uric acid in deproteinized blood utilizing a preformed copper chelate of cuproine, neocuproine or bathocuproine at a pH of 5-6 and measuring the amount of copper reduced to the cuprous state by the uric acid present in the blood.
The new and novel features of the present invention over this prior art procedure will be obvious as the invention is further disclosed.
SUMMARY OF THE INVENTION This invention broadly comprises the steps of:
a. adding a solution of N-ethylmaleimide to a predetermined quantity of serum,
b. adding to said solution a predetermined volume of a neocuproine solution, followed by the addition of a predetermined quantity of a copper solution in the cupric state,
c. measuring the amount of copper reduced to the cuprous state by reference to the optical density of the solution and determining the amount of uric acid by comparing the optical density of a standard at a wavelength of from about 450 to 460 u.
Experimentally, it is preferred to use the following amounts of materials when carrying out the aforedescribed diagnostic test.
Serum 0.2 ml. Buffered N-ethylmaleimide solution (0.4 1: w/v). 1.0 ml. Buffered Neocuproine solution (0.04% w/v) 1.0 ml. Copper sulfate solution (0.02% w/v) 2.0 ml.
Of course, it is to be understood that any equivalent volume proportions may be used in lieu of these above; however, the above amounts are preferred since the total resulting volume is appropriate for the subsequent optical density measurements.
With regard to the wavelength at which the optical density measurements are carried out, it is preferred to use a wavelength of 445 My; however, a range of from about 450 to 460 Mp. is equally suitable.
This invention is an improvement over prior art methods in that it can be run directly on serum and eliminates the necessity of deproteinizing the blood to produce protein free serum. This results in a saving of valuable laboratory time and is a more convenient method. This important feature is attributable to the use of N-ethylmaleimide which increases the sensitivity of the copper-neocuproine reduction complex and makes the reaction more specific for uric acid which therefore allows ti to be run on serum.
DETAILED DESCRIPTION OF THE INVENTION The herein disclosed diagnostic method determines the amount of uric acid in human serum wherein said amount is measured by means of a change in optical density of a copperneocuproine complex in the presence of N-ethylmaleimide.
This new method is an advance over prior art methods in that the new method is run directly on serum whereas prior art procedures are run on protein-free filtrates. The new method utilizes N-ethyl maleimide which a. increases the sensitivity of the copper-neocuproine reduction complex,
b. enhances the linearity of the reaction, and
c. increases the accuracy of recovery experiments when two serums of divergent values are mixed.
In the new method, the serum is treated successively with the N-ethyl maleimide, neocuproine and finally with a separate cupric solution.
Experimentally the diagnostic procedures may be carried out in the following manner: A sample of blood serum, from about 0.1 ml. to about 0.8 ml., with the preferred amount being 0.2 ml., is mixed with about 0.5 to about 4.0 ml., the preferred amount being 1.0 ml. of a buffered N-ethylmaleimide solution having a concentration of about 0.4 percent w/v. The pH of said buffered solution is from about 7.0 to 8.0, the preferred pH being 7.5.
To this is then added from about 0.5 ml. to about 4.0 ml., the preferred amount being 1.0 ml. of a buffered neocuproine solution having a concentration of about 0.04 percent w/v. Said mixture is then allowed to incubate at ambient tempera ture for about 15 to about 30 minutes. The preferred time, however, is 20 minutes. Copper sulfate solution having a concentration of about 0.02 percent w/v is then added. The usual amount is from about 0.5 ml. to about 4.0 ml., with the preferred amount being 2.0 ml. The mixture is then allowed to incubate for an additional time period of from about 10 to about 20 minutes, the preferred time being 15 minutes. The optical density is determined at a wave length of from about 450 to 460 My; however 455 Mn is the preferred wave length. The quantity of uric acid present is then determined from a standard curve, determined by measurements made on samples made up to known uric acid concentrations.
PREPARATION OF REAGENTS A. Buffered N-Ethylmaleimide Solution To a 2-liter volumetric flask is added 8.0 g. of N-ethylmaleimide, 1.03 g. of sodium dihydrogen phosphate, and 3.19 g. of disodium hydrogen phosphate. Distilled water (800 ml.) is added and the mixture stirred until the solids are in solution. This solution is adjusted to a pH of 7.5 using 1 N NaOH. Sufficient distilled water is then added with mixing to give a 2-liter solution.
B. Buffered Neocuproine Solution Neocuproine hemihydrate (0.720 g.) is added to 200 ml. of distilled water. Some solid remains undissolved. Sufficient 5 N HCl is added to adjust the pH to 2.0. At this point all of the solids are in solution. Sufficient 5 N NaOH is then added in order to adjust to a final pH of5.0.
Glycine (15 g.) is added to 200 ml. of distilled water and mixed until dissolved. Sufficient 5 N NaOH is then added to adjust the pH to 9.0.
To a 2-liter volumetric flask containing 600 ml. of distilled water is added the neocuproine solution and glycine solution described above. The pH of the combined solution is then adjusted to 9.0 using 5 N NaOH. SuiTicient distilled water is then added to give a 2-liter solution.
C. Copper Sulfate Solution To 60 ml. of distilled water in a 2-liter volumetric flask is added 152 ml. of 2-amino-2-methyl propanol. The pH of the solution is then adjusted to 9.0 with 5 N HCl or 5 N NaOH.
Anhydrous copper sulfate 0.39 g. is dissolved in m]. of distilled water.
The copper sulfate solution is then added to the solution of Z-amino-Z-methyl propanol. The pH is then adjusted to pH 9.0 with 5 N NaOH. Sufficient distilled water is added to give a 2- liter solution.
D. Uric Acid Stock Solution To 150 ml. of distilled water in a l-liter volumetric flask is added and dissolved 0.6 g. of lithium carbonate and 1.0 g. of uric acid. The pH is adjusted to 12.0 with l N NaOH in order to dissolve the uric acid. Formalin 40 percent (20 ml.) and 330 ml. of distilled water is then added. The pH is readjusted to pH 2.9 with l N H 80 Sufficient distilled water is added to give a l-liter solution.
EXAMPLE I l. Reagent A, 1.0 ml. is pipetted into each of two 95 l5 mm. test tubes labeled sample and reagent blank."
2. The serum to be tested, 0.2 ml. is added to the sample" tube and 0.2 ml. of distilled water to the reagent blank" blank tube.
3. Reagent B. 1.0 ml. is added to each tube.
4. The tubes are then allowed to remain for 20 minutes at room temperature.
5. Reagent C, 2.0 ml. is then added to each tube, followed by an additional minutes waiting period.
6. Spectrophometric readings are then made at 455 My. by adjusting the zero point of the spectrophotometer with the reagent blank" and determining the absorptivity of the sam ple."
Serum blanks are determined by adding 4.0 ml. of distilled water to each three x15 mm. test tubes. To each tube is added 0.2 ml. of serum. Spectrophometric determinations are then made by using distilled water to adjust the zero point and determining the absorptivity of each serum blank. The results are then averaged and the following optical density (OD") calculation made:
sumple sumplP blank mrIc acid The uric acid concentration is then read from a standard curve which is obtained by treating a series of dilutions of Reagent D in the same manner and plotting the resulting optical densities vs. uric acid concentration.
EXAMPLE I] The procedure of Example I is repeated wherein the following amounts of serum sample and reagents are used:
I. Sample 0.4 ml. Reagent A 2 ml. Reagent B 2 ml. Reagent C 4 ml.
ll. Sample 0.8 ml.
Reagent A 4 ml. Reagent B 4 ml. Reagent C 8 ml.
Equivalent results are obtained. What is claimed is: l. A method for determining uric acid concentration in human blood serum which comprises:
a. adding aqueous N-ethylmaleimide solution to a measured quantity of said serum, b. adding to the thus-treated serum aqueous neocuproine solution, followed by an aqueous solution of cupric salt, c. and comparing the optical density of the resulting solution with that of the standard. 2. The method of claim 1 wherein said optical density is determined at a wavelength of from about 450 to 460 my

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US38907A1970-05-191970-05-19Diagnostic method for the determination of uric acid in bloodExpired - LifetimeUS3649198A (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US4072627A (en)*1976-08-021978-02-07Pierce Chemical CompanyUric acid determination
US4095948A (en)*1973-10-191978-06-20Hoffmann-La Roche Inc.Determination of uric acid
US4234313A (en)*1974-11-111980-11-18Burroughs Wellcome Co.Device and method for quantitative uric acid testing
US4348208A (en)*1981-10-261982-09-07American Monitor CorporationUric acid assay and reagent system therefor
US6699720B1 (en)2000-05-262004-03-02Development Center For BiotechnologyInterference-eliminating membranes, test strips, kits and methods for use in uric acid assay
US6753159B1 (en)1998-08-062004-06-22Jin Po LeeUric acid assay device with stabilized uricase reagent composition
CN113017995A (en)*2021-03-032021-06-25杭州可靠护理用品股份有限公司Adult diaper with uric acid prompting function

Citations (3)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3349006A (en)*1963-06-171967-10-24Miles LabProcess and composition for the enzymatic determination of uric acid
US3528777A (en)*1968-09-271970-09-15Hycel IncProcess and compositions for determination of uric acid in blood serum
US3554701A (en)*1969-01-231971-01-12Bio Dynamics IncUric acid test procedure

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3349006A (en)*1963-06-171967-10-24Miles LabProcess and composition for the enzymatic determination of uric acid
US3528777A (en)*1968-09-271970-09-15Hycel IncProcess and compositions for determination of uric acid in blood serum
US3554701A (en)*1969-01-231971-01-12Bio Dynamics IncUric acid test procedure

Cited By (8)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US4095948A (en)*1973-10-191978-06-20Hoffmann-La Roche Inc.Determination of uric acid
US4234313A (en)*1974-11-111980-11-18Burroughs Wellcome Co.Device and method for quantitative uric acid testing
US4072627A (en)*1976-08-021978-02-07Pierce Chemical CompanyUric acid determination
US4348208A (en)*1981-10-261982-09-07American Monitor CorporationUric acid assay and reagent system therefor
WO1983001513A1 (en)*1981-10-261983-04-28American Monitor CorpUric acid assay and reagent system therefor
US6753159B1 (en)1998-08-062004-06-22Jin Po LeeUric acid assay device with stabilized uricase reagent composition
US6699720B1 (en)2000-05-262004-03-02Development Center For BiotechnologyInterference-eliminating membranes, test strips, kits and methods for use in uric acid assay
CN113017995A (en)*2021-03-032021-06-25杭州可靠护理用品股份有限公司Adult diaper with uric acid prompting function

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AR194193A1 (en)1973-06-29
SE372103B (en)1974-12-09
GB1294518A (en)1972-11-01
DE2123032A1 (en)1971-12-02

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Owner name:WARNER-LAMBERT COMPANY, 201 TABOR RD., MORRIS PLAI

Free format text:ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:PFIZER INC.;REEL/FRAME:003853/0905

Effective date:19810409


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