US2799660A - Blood test composition and method - Google Patents
Blood test composition and method Download PDFInfo
- Publication number
- US2799660A US2799660A US423524A US42352454A US2799660A US 2799660 A US2799660 A US 2799660A US 423524 A US423524 A US 423524A US 42352454 A US42352454 A US 42352454A US 2799660 A US2799660 A US 2799660A
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- United States
- Prior art keywords
- tablet
- blood
- test
- water
- urine
- Prior art date
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- Expired - Lifetime
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- 239000000203 mixture Substances 0.000 title claims description 37
- 238000000034 method Methods 0.000 title description 8
- 238000009534 blood test Methods 0.000 title description 2
- 210000004369 blood Anatomy 0.000 claims description 30
- 239000008280 blood Substances 0.000 claims description 30
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- NUIURNJTPRWVAP-UHFFFAOYSA-N 3,3'-Dimethylbenzidine Chemical compound C1=C(N)C(C)=CC(C=2C=C(C)C(N)=CC=2)=C1 NUIURNJTPRWVAP-UHFFFAOYSA-N 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 10
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 claims description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 6
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims description 6
- 159000000021 acetate salts Chemical class 0.000 claims description 3
- 239000011973 solid acid Substances 0.000 claims description 3
- 239000002195 soluble material Substances 0.000 claims 1
- 239000003826 tablet Substances 0.000 description 68
- 238000012360 testing method Methods 0.000 description 37
- 210000002700 urine Anatomy 0.000 description 25
- 239000000463 material Substances 0.000 description 19
- VSGNNIFQASZAOI-UHFFFAOYSA-L calcium acetate Chemical compound [Ca+2].CC([O-])=O.CC([O-])=O VSGNNIFQASZAOI-UHFFFAOYSA-L 0.000 description 16
- 239000001639 calcium acetate Substances 0.000 description 16
- 235000011092 calcium acetate Nutrition 0.000 description 16
- 229960005147 calcium acetate Drugs 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 9
- 239000003153 chemical reaction reagent Substances 0.000 description 9
- UHCGLDSRFKGERO-UHFFFAOYSA-N strontium peroxide Chemical compound [Sr+2].[O-][O-] UHCGLDSRFKGERO-UHFFFAOYSA-N 0.000 description 9
- 229920002261 Corn starch Polymers 0.000 description 8
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 8
- 239000008120 corn starch Substances 0.000 description 8
- 229940099112 cornstarch Drugs 0.000 description 8
- 239000000049 pigment Substances 0.000 description 8
- 230000035945 sensitivity Effects 0.000 description 8
- 239000011975 tartaric acid Substances 0.000 description 8
- 235000002906 tartaric acid Nutrition 0.000 description 8
- 238000004040 coloring Methods 0.000 description 7
- 238000009472 formulation Methods 0.000 description 5
- 150000002978 peroxides Chemical class 0.000 description 5
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 229920002472 Starch Polymers 0.000 description 4
- 239000013049 sediment Substances 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000008107 starch Substances 0.000 description 4
- 235000019698 starch Nutrition 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 235000012222 talc Nutrition 0.000 description 4
- LUKPNZHXJRJBAN-UHFFFAOYSA-N 4-(4-amino-3-methylphenyl)-2-methylaniline;hydron;dichloride Chemical compound [Cl-].[Cl-].C1=C([NH3+])C(C)=CC(C=2C=C(C)C([NH3+])=CC=2)=C1 LUKPNZHXJRJBAN-UHFFFAOYSA-N 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- -1 alkali metal acetates Chemical class 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000002198 insoluble material Substances 0.000 description 2
- 239000001053 orange pigment Substances 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 239000001054 red pigment Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 239000001052 yellow pigment Substances 0.000 description 2
- AKVAGWOVWQDTAF-UHFFFAOYSA-N 1-bromo-4-(1-isocyanatoethyl)benzene Chemical compound O=C=NC(C)C1=CC=C(Br)C=C1 AKVAGWOVWQDTAF-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- SPAGIJMPHSUYSE-UHFFFAOYSA-N Magnesium peroxide Chemical compound [Mg+2].[O-][O-] SPAGIJMPHSUYSE-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 1
- 150000008041 alkali metal carbonates Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- ZJRXSAYFZMGQFP-UHFFFAOYSA-N barium peroxide Chemical compound [Ba+2].[O-][O-] ZJRXSAYFZMGQFP-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- HBHZKFOUIUMKHV-UHFFFAOYSA-N chembl1982121 Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O HBHZKFOUIUMKHV-UHFFFAOYSA-N 0.000 description 1
- ZLFVRXUOSPRRKQ-UHFFFAOYSA-N chembl2138372 Chemical compound [O-][N+](=O)C1=CC(C)=CC=C1N=NC1=C(O)C=CC2=CC=CC=C12 ZLFVRXUOSPRRKQ-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- WZHCOOQXZCIUNC-UHFFFAOYSA-N cyclandelate Chemical class C1C(C)(C)CC(C)CC1OC(=O)C(O)C1=CC=CC=C1 WZHCOOQXZCIUNC-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000007938 effervescent tablet Substances 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
- 229960004995 magnesium peroxide Drugs 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 235000011182 sodium carbonates Nutrition 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000007916 tablet composition Substances 0.000 description 1
- 210000001550 testis Anatomy 0.000 description 1
- WODGXFMUOLGZSY-UHFFFAOYSA-J tetrasodium phosphonatooxy phosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OOP([O-])([O-])=O WODGXFMUOLGZSY-UHFFFAOYSA-J 0.000 description 1
- MSLRPWGRFCKNIZ-UHFFFAOYSA-J tetrasodium;hydrogen peroxide;dicarbonate Chemical compound [Na+].[Na+].[Na+].[Na+].OO.OO.OO.[O-]C([O-])=O.[O-]C([O-])=O MSLRPWGRFCKNIZ-UHFFFAOYSA-J 0.000 description 1
- 150000004992 toluidines Chemical class 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/72—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood pigments, e.g. haemoglobin, bilirubin or other porphyrins; involving occult blood
- G01N33/721—Haemoglobin
- G01N33/725—Haemoglobin using peroxidative activity
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N31/00—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
- G01N31/22—Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/904—Oxidation - reduction indicators
Definitions
- This invention which relates to a diagnostic composition for detecting occult blood in animal fluids is a conatnt
- the present invention is directed to a tablet which is 7,
- the tablet of our invention is formed of a' mixture of a blood indicator such as, for example, o-a blood indicator
- tolidine, o-toluidine, benzidine, o-tolidine-dihydrochloride and similar compounds an oxidizing agent of the peroxide type such as sodium carbonate peroxide, sodium perbor silicate, strontium peroxide, sodium pyrophosphate peroxide, barium peroxide, magnesium peroxide, and urea peroxide; an acetate such as calcium acetate, sodium acetate, potassium acetate, lithium acetate and the like; a water insoluble pigment or dye; and a water-soluble solid acid which is stronger than acetic acid so that it can react with the aforementioned acetate salt to produce acetic acid.
- an oxidizing agent of the peroxide type such as sodium carbonate peroxide, sodium perbor silicate, strontium peroxide, sodium pyrophosphate peroxide, barium peroxide, magnesium peroxide, and urea peroxide
- an acetate such as calcium acetate, sodium acetate, potassium acetate
- Such acids are citric, fumaric, itaconic, maleic, rnalic, malonic, and mandelic acids.
- an effervescent couple comprising, for example, an acid in solid dry form and a carbonate or bicarbonate which is preferably any alkaline earth or alkali metal carbonate or bicarbonate such as sodium, potassium, and calcium carbonates and bicarbonates. Diluents and excipients' of the kind conventionally used in preparation of tablets are likewise used in conjunction with the aforementioned materials.
- the above composition is prepared in tablet form, each tablet containing conveniently 2 grains of material and being conveniently A; inch thick, and about A inch in diameter.
- the composition contain, in addition to the blood indicator and an oxidizing agent, an acetate, a water soluble organic acid such as tartaric acid which is capable of releasing acetic acid when contacted with an acetate, and an effervescent couple. Without the co-presence of these materials neither the degree of sensitivity nor the degree of reproducibility of test results will be adequate.
- Strontium peroxide From '5 to 15, preferably 9. Tartaric acid From 20 to 60, preferably 30. Calcium acetate From 20 to 75, preferably 60.
- Corn starch From 1 to 10, preferably 5.
- Effervescent couple From 5 to 20, preferably 10.
- o-Tolidine From 0.5-4, preferably 1.
- Stront um peroxide From 5-15 preferably 7.5.
- Succ mc acid From 20-75, preferably 40.
- Calcium acetate From 20-75, preferably 60.
- Corn starch From 1-10, preferably 5.
- Effervescent couple From 5-20, preferably 10.
- o-Tolidine From 1-6, preferably 4.
- Sodium perbor silicate From 8-20, preferably 10.
- Succrnic acid From 20-75, preferably 40.
- Calcium acetate From 20-75, preferably 60.
- Corn starch From 1-10, preferably 5.
- Effervescent couple From 5-20, preferably 10.
- o-Tolidine From 0.5-4, preferably 1.
- Strontium peroxide Itaconic acld Calcium acetate Corn starch Effervescent coup From 5-15, preferably 7.5. From 20-75, preferably 40. From 20-75, preferably 60. From 1-10, preferably 5.
- Benzidine hydrochloride From Strontium peroxide 'lartaric acid 1-5, preferably 1. 5-15, preferably 7.5. 20-60, preferably 30.
- Calcium acetate From 20-75, preferably 60.
- Efiervescent couple From 5-20, preferably 10.
- the present invention is particularly useful in the determination of occult blood in the presence of urine and, in sharp contrast with diagnostic compositions of the prior art, is sensitive to the extent of detecting of one part blod in 100,000 of uncentrifuged urine.
- tablet A is of the general type of prior art compositions such as are described, for example, in U. S. Patent 2,290,436, that tablet B is the composition of tablet A to which calcium acetate has been added and that tablet 'C is of the same composition as tablet A to which both calcium acetate and efliervescent couple have been added.
- Tablet D is the same composition as tablet C so modified as to include a water-insoluble pigment or dye.
- a water-insoluble pigment or dye To incorporate the pigment or dye in the tablet it is simply necessary that it is dry and finely divided and it is then mixed intimately with the remainder of the composition prior to compressing the material into tablets.
- the amount of pigment required would obviously vary depending on its hiding power and opacity, therefore the amount considered most satisfactory for any given pigment must be determined by trial. However, the necessary amount is generally not very much, being present
- the superior performance of tablet B over tablet A shows that the addition of calcium acetate increases considerably'the sensitivity of the test. Further it is obvious that tablet C is more uniform in reaction time than tablet B and in addition the sensitivity of the tablet within a given time period is very substantially improved.
- the tablets B and C were both compared by testing them with the sediments obtained by centrifuging samples of urine containing very small quantities of blood.
- blood was diluted with normal urine to produce blood concentrations of 1 part in 50,000; 1 part in 100,- 000; 1 part in 300,000 and 1 part in 1,000,000 parts of urine.
- 15 cc. of one of the specimens was centrifuged in a conical tube at moderate speed. The *the mannerdescribed can be illustrated by the following supernatant liquid was drawn off and the sediment which remained tested by placing 1 drop of it on filter paper and then proceeding with the test as previously described.
- a Perthe added coloring material should be a water-insoluble Ohlde Whlhh h hberate hydrogeh. pehoxlde Water pigment or dye so that it will not leach away from the soluble .sohd.acld strohghr than achhc i ah acetate reagent material with which it is combined in the tablet Shh h whl rhact Wlth the last sand and to Produce when the whole mass is wetted as described in the test.
- the coloring materials should have the strontium peroxide, 20 to 60 parts tartaric acid, 20 to property of good opacity and hiding power so that they parts calcium acetate, 1 to 10 parts corn starch, 5 to 20 shall stand out well in contrast to blue and further they parts of a solid effervescent couple, and a minor amount shall cover up any tendency of the material of the test of a water-insoluble material contrasting in color with itself to turn blue. 75 the color formed in combination with blood by said The advantage of coloring the tableted composition in o-tolidine.
- composition-in tablet form comprisinglarmemberaofthe-group consisting-of o-tolidine, o--
- o-tolidine consisting of o-tolidine, o-toluidine, benzidine and o-tolidine dihydrochloride, a peroxide which will liberatelhy: drogen peroxide, an acetate selected from the group;-
- a method of determining occult blood in urine which comprises rwettingma portion of dry filter paper withaurine, placing-ontthe ..urine wetted portion of said paper, a tablet, composed of a mixture comprising by a water soluble acid stronger than acetic acid, and Ian 15 gh fIOm-abOI-It Parts of wmpound effervescent couple.
- a diagnostic composition in tablet form f0'l' 'dfi' tecting blood in the presence of urine comprising by weight from 0.5 to 4 parts o-tolidine, 5 to parts of 75 parts of calcium acetate, 1 to 10 parts cornstarch, and 5 to parts of a solid eflervescent couple, said tablet effecting a color change on urine wetted filter paper when placed on'suchlpaper andthe 'tablet'conta-cted with a small amount of water.
- A'diagnosti'c 'composition'in tablet form for detecting blood intliepresence of urine comprising 1 part of 'o-tolidine; 9parts of strontium peroxide, parts of tartaric acid, parts of calcium acetate, 5 parts of 'cornstarch, and 10'parts' of'a solid efiervescent couple, the 30 tablet efie'ctingea color change on urine-Wetted filter paper upon which said "tablet is placed, after a small amount of water is placed on said 'table't.
- composition of claim 2 wherein the said water- 5 insoluble material is'selected from the group consisting of red pigments, yellow pigments, and orange pigments.
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- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Analytical Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pathology (AREA)
- Urology & Nephrology (AREA)
- General Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Biomedical Technology (AREA)
- Physics & Mathematics (AREA)
- Medicinal Chemistry (AREA)
- Food Science & Technology (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Cell Biology (AREA)
- Biophysics (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Description
BLOOD TEST COMPGSITIQN AND METHOD Richard S. Nicholls and Dale E. Fonner, Elkhart, Ind., assignors to Miles Laboratories, Inc, Ellrhart, Ind, a corporation of Indiana No Drawing. Application April 15, 1954, Serial No. 423,524
Claims. (Cl. 252-408) This invention which relates to a diagnostic composition for detecting occult blood in animal fluids is a conatnt The present invention is directed to a tablet which is 7,
adapted for use in determining occult blood in such materials as urine and the like or in fluids containing urine which tablet is superior to the tableted compositions now available in several important respects, namely, in that with the present tablet the time of reaction is much more I uniform for any given concentration of blood, and fuf- I thermore, the sensitivity of the tablet within a given time is substantially and unexpectedly greater.
Generally, the tablet of our invention is formed of a' mixture of a blood indicator such as, for example, o-
tolidine, o-toluidine, benzidine, o-tolidine-dihydrochloride and similar compounds; an oxidizing agent of the peroxide type such as sodium carbonate peroxide, sodium perbor silicate, strontium peroxide, sodium pyrophosphate peroxide, barium peroxide, magnesium peroxide, and urea peroxide; an acetate such as calcium acetate, sodium acetate, potassium acetate, lithium acetate and the like; a water insoluble pigment or dye; and a water-soluble solid acid which is stronger than acetic acid so that it can react with the aforementioned acetate salt to produce acetic acid. Examples of such acids are citric, fumaric, itaconic, maleic, rnalic, malonic, and mandelic acids. Additionally, there must be present an effervescent couple comprising, for example, an acid in solid dry form and a carbonate or bicarbonate which is preferably any alkaline earth or alkali metal carbonate or bicarbonate such as sodium, potassium, and calcium carbonates and bicarbonates. Diluents and excipients' of the kind conventionally used in preparation of tablets are likewise used in conjunction with the aforementioned materials.
The above composition is prepared in tablet form, each tablet containing conveniently 2 grains of material and being conveniently A; inch thick, and about A inch in diameter. In determining the presence or absence of occult blood in a sample of urine a drop of the urine specimen is placed on a piece of dry filter paper, and when the drop has soaked into the paper a tablet prepared as above described is placed in the center of the drop and then two drops of water added to the tablet. With a positive test a ring of color appears on the filter paper surrounding the tablet, the color ranging fiom a very faint to a very deep blue, depending upon the concentration of blood in the sample. The higher the blood concentration, the deeper the color, and vice versa. The afore- 2,799,660 Patented July 16, 1957 said method of determining occult blood is found superior to the methods taught by the prior art, not only in the degree of sensitivity reached but also in the greater extent of reproducibility.
In connection with the composition and method of the present invention, it is absolutely essential that the composition contain, in addition to the blood indicator and an oxidizing agent, an acetate, a water soluble organic acid such as tartaric acid which is capable of releasing acetic acid when contacted with an acetate, and an effervescent couple. Without the co-presence of these materials neither the degree of sensitivity nor the degree of reproducibility of test results will be adequate.
While the formulation of our diagnositic composition may be varied in accordance with the procedures known to those skilled in the art, suitable formulations are as follows:
Strontium peroxide From '5 to 15, preferably 9. Tartaric acid From 20 to 60, preferably 30. Calcium acetate From 20 to 75, preferably 60.
Corn starch From 1 to 10, preferably 5. Effervescent couple From 5 to 20, preferably 10.
EXAMPLE II Components of reagent mixture:
o-Tolidine From 0.5-4, preferably 1. Stront um peroxide From 5-15 preferably 7.5. Succ mc acid From 20-75, preferably 40. Calcium acetate From 20-75, preferably 60. Corn starch From 1-10, preferably 5. Effervescent couple From 5-20, preferably 10.
EXAMPLE HI Components of reagent mixture:
o-Tolidine From 1-6, preferably 4. Sodium perbor silicate From 8-20, preferably 10. Succrnic acid From 20-75, preferably 40. Calcium acetate From 20-75, preferably 60. Corn starch From 1-10, preferably 5. Effervescent couple From 5-20, preferably 10.
EXAMPLE IV Components of reagent mixture:
o-Tolidine From 0.5-4, preferably 1.
Strontium peroxide Itaconic acld Calcium acetate Corn starch Effervescent coup From 5-15, preferably 7.5. From 20-75, preferably 40. From 20-75, preferably 60. From 1-10, preferably 5.
. From 5-20, preferably 10.
EXAMPLE V Components of reagent mixture:
Benzidine hydrochloride From Strontium peroxide 'lartaric acid 1-5, preferably 1. 5-15, preferably 7.5. 20-60, preferably 30.
Calcium acetate From 20-75, preferably 60.
Corn starch From 1-10, preferably 5.
Efiervescent couple From 5-20, preferably 10.
EXAMPLE VI Components of reagent mixture:
o-Tolidine-dihydrochloride- From 1-5, preferably 1.
The present invention is particularly useful in the determination of occult blood in the presence of urine and, in sharp contrast with diagnostic compositions of the prior art, is sensitive to the extent of detecting of one part blod in 100,000 of uncentrifuged urine.
The net effect of the effervescent couple and the acetate components of our formulation is to increase substantially the sensitivity, reproducibility and the speed of the test procedure. This is illustrated by tests performed with the following four (4) compositions, each being prepared as a 2 grain tablet:
4 only in trace amounts sufficient to establish a color tint in the tablet. Thus for the water insoluble coloring material D and C Red No. 35 it has been found that approximately one part in 1,000 parts of the remaining Tablet A 5 composition is adequate. Other suitable colors are D parts by Weight and C Yellow No. l1 and D and C Orange No. 17. HowoJIofidi 1 v r, almost any insoluble pigment or dye which con- Strontium peroxide 9 trasts strongly with blue would be satisfactory unless it Tartaric acid 30 sho ld In some other way interfere with the test as by Starch 5 10 reacting with another ingredient of the tablet. It is to Talcum 5 the general formulations of Examples I to VII above as 7 represented by tablets C and D that this application is Tablet B related, the peculiar merits of such formulations being Parts by welght made especially evident by comparison with the perf 1 formance of the other compositions of tablets A and B. strontium .Peroxlde 9 These tablets were tested as follows: 'f 30 Blood was diluted with normal urine to prepare sam- Calcmm acetate ples which contained blood in concentrations of 1:100,000, starch 5 l:20,000, and 1:40,000 parts of urine. To make the Talcum 5 test one drop of the specimen was placed on a filter aper T bl t C square laid out on a white tile. When the drop had Pa t by weight soaked into the paper a tablet was placed in the center o-Tolidine 1 of the wetted area and then two drops of Water added Strontium peroxide 9 so that they fell on the tablet and ran over onto the Tartari acid 30 paper. The examination of the test was made at the Calcium acetate 60 end of 2, 3, 4 and 5 minutes, the time being determined Starch 5 by a stop watch. Talcum 5 Each type table was tested a large number of times Efiervescent couple (tartaric acid and sodium biwith each of the 3 concentrations of blood. The results carbonate) 10 are recorded in Table I.
TABLE I Tablet A Tablet B Tablet 0 Concentration of blood added to urine Percent positive in Percent positive in Percent positive in No. No. No. Tests Tests Tests 2 3 4 a 2 3 4 5 2 3 4 5 min. min. min. min. min. min. min. min. min. min. min. min.
Tablet D Parts by weight o-Tolidine 1 Strontium peroxide 9 Tartaric acid 30 Calcium acetate Starch 5 Talcum 5 Effervescent couple 10 Water-insoluble pigment or dye 0.1
It will be noticed that tablet A is of the general type of prior art compositions such as are described, for example, in U. S. Patent 2,290,436, that tablet B is the composition of tablet A to which calcium acetate has been added and that tablet 'C is of the same composition as tablet A to which both calcium acetate and efliervescent couple have been added.
Tablet D is the same composition as tablet C so modified as to include a water-insoluble pigment or dye. To incorporate the pigment or dye in the tablet it is simply necessary that it is dry and finely divided and it is then mixed intimately with the remainder of the composition prior to compressing the material into tablets. The amount of pigment required would obviously vary depending on its hiding power and opacity, therefore the amount considered most satisfactory for any given pigment must be determined by trial. However, the necessary amount is generally not very much, being present The superior performance of tablet B over tablet A shows that the addition of calcium acetate increases considerably'the sensitivity of the test. Further it is obvious that tablet C is more uniform in reaction time than tablet B and in addition the sensitivity of the tablet within a given time period is very substantially improved.
In the practice of our invention we have found that our test procedure which employs filter paper provides a much more sensitive test than other methods such as placing a drop of the sample directly on the tablet or dissolving the reagent mixture in water and adding it to the specimen. Under these latter conditions tablet A gives a negative test for blood at 1:0,000 and indeed only a very slowly formed positive with 1 part of blood in 1,000 parts of urine. The sensitivity of any of the compositions to blood dissolved in water is much higher than it is to blood in urine. Urine appears to contain a factor which inhibits the formation of color with o-tolidine, benzidine, etc., in the presence of blood and a peroxide. The use of the filter paper seems to a large extent to get around this difliculty and brings about a marked increase in sensitivity.
The tablets B and C were both compared by testing them with the sediments obtained by centrifuging samples of urine containing very small quantities of blood. In this case blood was diluted with normal urine to produce blood concentrations of 1 part in 50,000; 1 part in 100,- 000; 1 part in 300,000 and 1 part in 1,000,000 parts of urine. In making the test 15 cc. of one of the specimens was centrifuged in a conical tube at moderate speed. The *the mannerdescribed can be illustrated by the following supernatant liquid was drawn off and the sediment which remained tested by placing 1 drop of it on filter paper and then proceeding with the test as previously described.
record. j V
A number of urines wereobtained which were judged by microscopic examination of the sediment to contain The results of a series of tests are recorded in the follow- 5 no red blood cells, and could thereforebe expected to. ing table. give negative tests, that is there should be no blue color- TABLE II [Tests on sediment after centrifuging] Tablet B Tablet Concentration of blood added to Percent positive in Percent positive inunne No. No.
Tests 2 3 4 5 Tests 2 8 4 5 min. min. min. min. min. min. min. min.
It is again seen from the above results that with tablet ng on the P p Surrounding the tablet material- A C positive readings were obtained more consistently and Series f SW carried Out in Which a number of reliably than when tablet B was used. operators tested the two tablet compositions witheach Notwithstanding the very meritorious results obtained 0f the mines but in Such a manner that y did not by the use f t bl t C as d ib d b there i some run the tests with the two tablets concurrently and so were slight diificulty in deciding whether the test employing unable to compare their findings with one composition tablet C reads positive or negative when there is extremely against their findings With another on the Same urine little or no blood in the test sample. In these situations P Altogether 600 tests were carried out with each the subjective viewpoint of the person reading the result eempeslheh, the readings being taken at theme of 2 has considerable effect since he is not guided by any clearly mlhuteswith tablet C, the testshh these negative mines d fi d 1 h were considered to show at least. a faintly positive test When using such a tablet as represented by tablet C m 7 cases 125% of h tests run, he in h in the manner described above, the test is considered to 35 .Senes of teste Performed Wlth T eempeslheh e be positive when blue color appears on the paper surmg a red Plgment, tablet m the manner desenbed rounding the reacting tablet. However, it is a fact that above q 9 taste or 15% of the total e eonsldered as the effervescent tablet reacts, the material of the as jhowmg anythmg but a clear negahve test; tablet sloughs oif onto the paper in the area immediately lhe tablet of the Present mventlon thus Provides an around the tablet. In places where the amount on the 40 lmhmved mhans for detechng fields Such as paper is relatively little it is sometimes difficult to decide h by which Ihhhhs vhthal ehhhhahoh of false whether the paper should be considered as having turned poslhve readings 1S achleved 1h h dhhchhy detectable blue or whether the blue color which can be seen is areas of ehremely. 10W cohcehtrahoh complete h some spilled over tablet material since there is a tendsehce h hh Wlth reshlhhg marked Improvement ency for the test material to take on a little gray or very test rehhhhlty pale blue color. Further than this, even when there is Havlhg thus described 9 lhvhhhoh 9 no question as to which is material and which is clear A hloohfdetechhg dlhghoshc composmoh m tablet paper there can be confusion from the shadows which form. hhhpnslhg a.c.ompohhd hh h the group the tablet throws on the paper because these often have h i of h ohohhdihe hehzldlhe h a light grayish cast and are irregular in outline since the tohdme dlhydrohhlonde a peroxlde which liberate tablet on efiervescing has lost its usual outline. hydrogehherohlde a Water Soluble .so'hd .ahld Stmhger We have found that these diiliculties can be eliminated than ahehc h acetate salt whlch react Wlth and the use of the test very greatly improved by the dethe Sald Sohd held to phohhce achhc h ah ehhervhh vice of coloring the material of the test tablet with a h and a Watehlhsolhhle hihterhh cohtrashhg coloring material which contrasts with the blue color of In Color h the color formed by sald color responslve a positive test in such a way that the contrasting color compouhh In Presehcehf i remains with the reagent material and does not diffuse A dlaghoshc composlhoh h tablet fohhhomphslhg out on its own into the paper and so hide the appearance ahlember h the group hh of h of a possible positive reaction. To achieve these objects h behzhhhe h .o'hhuhhhe dlhydrochlohhe a Perthe added coloring material should be a water-insoluble Ohlde Whlhh h hberate hydrogeh. pehoxlde Water pigment or dye so that it will not leach away from the soluble .sohd.acld strohghr than achhc i ah acetate reagent material with which it is combined in the tablet Shh h whl rhact Wlth the last sand and to Produce when the whole mass is wetted as described in the test. held ah ehervhsceht h and a water'soluble In addition, in order that the coloring material should perh h cohtrashhg m color Wlth the 00101 formed form its function of defining clearly where the reagent m combmatloh Wlth bleed by the Selected member of material is at the completion of the test, it is important Sald groupthat its color contrast strongly with the blue color which A diagnostic composition in a l t form for deforms on the paper when the test is positive and for this tecting blood in the presence of urine comprising by reason yellow, orange or red pigments are the most satisg from t0 4 P3115 O'tOIidhIle, 5 to 15 P511rts factory. Further, the coloring materials should have the strontium peroxide, 20 to 60 parts tartaric acid, 20 to property of good opacity and hiding power so that they parts calcium acetate, 1 to 10 parts corn starch, 5 to 20 shall stand out well in contrast to blue and further they parts of a solid effervescent couple, and a minor amount shall cover up any tendency of the material of the test of a water-insoluble material contrasting in color with itself to turn blue. 75 the color formed in combination with blood by said The advantage of coloring the tableted composition in o-tolidine.
8.--A diagnostic. composition-in tablet form comprisinglarmemberaofthe-group consisting-of o-tolidine, o--
toluidine. benzidine, o-tolidine ldihydrochloride, a, peroxidefor liberating hydrogen peroxide, alwater soluble 5 solidjacid stronger. than acetic acid and an effervescent couple, an acetic" sa'lt'which will react with the said solid acid to produce acetic acid, said tablet efiecting a color change on urine Wetted filter paper when placed thereon, and said tablet is contacted with asmall amount of form comprising a compound selected from thettgroupJfl W enwhen Said urine containslblood.
consisting of o-tolidine, o-toluidine, benzidine and o-tolidine dihydrochloride, a peroxide which will liberatelhy: drogen peroxide, an acetate selected from the group;-
consisting of calcium acetate and alkali metal acetates 9. A method of determining occult blood in urine which comprises rwettingma portion of dry filter paper withaurine, placing-ontthe ..urine wetted portion of said paper, a tablet, composed of a mixture comprising by a water soluble acid stronger than acetic acid, and Ian 15 gh fIOm-abOI-It Parts of wmpound effervescent couple.
6. A diagnostic composition in tablet form f0'l' 'dfi' tecting blood in the presence of urine comprising by weight from 0.5 to 4 parts o-tolidine, 5 to parts of 75 parts of calcium acetate, 1 to 10 parts cornstarch, and 5 to parts of a solid eflervescent couple, said tablet effecting a color change on urine wetted filter paper when placed on'suchlpaper andthe 'tablet'conta-cted with a small amount of water.
7. A'diagnosti'c 'composition'in tablet form for detecting blood intliepresence of urine comprising 1 part of 'o-tolidine; 9parts of strontium peroxide, parts of tartaric acid, parts of calcium acetate, 5 parts of 'cornstarch, and 10'parts' of'a solid efiervescent couple, the 30 tablet efie'ctingea color change on urine-Wetted filter paper upon which said "tablet is placed, after a small amount of water is placed on said 'table't.
lected from the-ugroup'consistingof o-tolidine, o-toluidine; benzidine' and o-tolidine dihydro-chloride; a peroxidezwhich liberates hydrogen peroxide, an acetate se-- lected from the group consisting of calcium acetate and strontium peroxide, 20 to 60 parts of tartaric acid, 20 to 20 alkali metal acetates, about 20 to Parts by Weight a water solublesolid acid stronger than acetic acid, and' about 5 to 20 parts of an eifervescentcouple and then adding'a small amount of water to said tablet.
10. The composition of claim 2 wherein the said water- 5 insoluble material is'selected from the group consisting of red pigments, yellow pigments, and orange pigments.
Kamlet July 21, 1942 Compton et al Oct. 23, 1945 UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 2,799,660 July 16, 1957 Richard S, Nicholle et 81.
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction and that the said Let oers Patent should read as corrected below.
Column 6, line 60, before "water" insert a line 63, after "acetic" strike out the comma; same line, for "water-soluble" read water-insoluble column 8 line 6, for "acetic" read acetate Signed and sealed this 8th day of October 1957.
(SEAL) Attest:
KARL H. AXLI NE ROBERT C. WATSON Attesting Oi'ficr Comnissioner of Patents
Claims (1)
- 2. A DIAGNOSTIC COMPOSITION IN TABLET FORM COMPRISING A MEMBER OF THE GROUP CONSISTING OF O-TOLIDINE, O-TOLUIOXIDE WHICH WILL LIBERATE HYDROGEN PEROXIDE, WATER DINE, BENZIDINE AND O-TOLUIDINE DIHYDROCHLORIDE, A PERSOLUBLE SOLID ACID STRONGER THAN ACETIC ACID AN ACETATE SALT WHICH WILL REACT WITH THE LAST SAID ACID TO PRODUCE ACETIC, ACID, AN EFFERVESCENT COUPLE, AND A WATER-SOLUBLE MATERIAL CONTRASTING IN COLOR WITH THE COLOR FORMED IN COMBINATION WITH BLOOD BY THE SELECTED MEMBER OF SAID GROUP.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB11558/52A GB708996A (en) | 1954-04-15 | 1952-05-07 | Improvements in or relating to diagnostic compositions |
| US423524A US2799660A (en) | 1954-04-15 | 1954-04-15 | Blood test composition and method |
| GB37258/54A GB772374A (en) | 1954-04-15 | 1954-12-23 | Blood test |
| FR1119775D FR1119775A (en) | 1954-04-15 | 1955-01-11 | Diagnostic composition |
| CH339401D CH339401A (en) | 1954-04-15 | 1955-01-14 | Reagent for the detection of blood for diagnostic purposes |
| DEM26333A DE1004398B (en) | 1954-04-15 | 1955-03-05 | Diagnostic preparation in tablet form for the detection of blood |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US423524A US2799660A (en) | 1954-04-15 | 1954-04-15 | Blood test composition and method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2799660A true US2799660A (en) | 1957-07-16 |
Family
ID=23679205
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US423524A Expired - Lifetime US2799660A (en) | 1954-04-15 | 1954-04-15 | Blood test composition and method |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US2799660A (en) |
| CH (1) | CH339401A (en) |
| DE (1) | DE1004398B (en) |
| FR (1) | FR1119775A (en) |
| GB (2) | GB708996A (en) |
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2905594A (en) * | 1956-04-25 | 1959-09-22 | Herman J Morris | Means for detecting enzyme activity |
| US2970945A (en) * | 1958-10-03 | 1961-02-07 | Miles Lab | Diagnostic composition |
| US3068855A (en) * | 1957-04-29 | 1962-12-18 | Jr Norman B Furlong | Disposable blood-gas analyzer |
| US3252762A (en) * | 1961-05-04 | 1966-05-24 | Miles Lab | Stabilized occult blood diagnostic |
| US3335793A (en) * | 1964-11-30 | 1967-08-15 | Cities Service Oil Co | Method and composition for improving and maintaining the capacity of water injection wells |
| US3411887A (en) * | 1964-06-15 | 1968-11-19 | Miles Lab | Diagnostic composition |
| USRE28575E (en) * | 1971-03-01 | 1975-10-21 | Indicator for detecting hydrogen peroxide and peroxidative compounds containing alpha naphthoflavone | |
| US4148611A (en) * | 1978-06-28 | 1979-04-10 | Miles Laboratories, Inc. | Test composition, device and method for the detection of peroxidatively active substances |
| US4175923A (en) * | 1978-06-26 | 1979-11-27 | Friend William G | Method and apparatus for occult blood testing in the home |
| US4394452A (en) * | 1977-05-31 | 1983-07-19 | Rohm Gmbh | Synthetic stool |
| EP0177244A3 (en) * | 1984-09-26 | 1986-12-17 | Warner-Lambert Company | A method for the detection of peroxidase activity |
| US4676950A (en) * | 1984-02-03 | 1987-06-30 | Foster Research Corporation | Indicator and test device for detecting occult blood |
| EP0227602A3 (en) * | 1985-12-20 | 1988-04-06 | Warner-Lambert Company | Free flowing granular indicator material for peroxidase-like activity |
| US4956300A (en) * | 1982-01-05 | 1990-09-11 | Helena Laboratories Corporation | Aid for determining the presence of occult blood, method of making the aid, and method of using the aid |
| US5081040A (en) * | 1987-06-29 | 1992-01-14 | Helena Laboratories Corporation | Composition and kit for testing for occult blood in human and animal excretions, fluids, or tissue matrixes |
| US5196167A (en) * | 1989-04-04 | 1993-03-23 | Helena Laboratories Corporation | Fecal occult blood test product with positive and negative controls |
| US5217874A (en) * | 1989-04-04 | 1993-06-08 | Helena Laboratories Corporation | Fecal occult blood test product with positive and negative controls |
| US5273888A (en) * | 1984-01-16 | 1993-12-28 | Helena Laboratories Corporation | Chemical test kit and method for determining the presence of blood in a specimen and for verifying the effectiveness of the chemicals |
| US5702913A (en) * | 1983-12-21 | 1997-12-30 | Helena Laboratories Corporation | Chromgen-reagent test system |
| US6046019A (en) * | 1991-07-09 | 2000-04-04 | Goumeniouk; Alexander P. | Diagnostic kits and methods for making granulocyte cell counts |
| US6225123B1 (en) * | 1997-04-30 | 2001-05-01 | Becton Dickinson And Company | Additive preparation and method of use thereof |
| US6534016B1 (en) | 1997-04-30 | 2003-03-18 | Richmond Cohen | Additive preparation and method of use thereof |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3164534A (en) * | 1954-04-13 | 1965-01-05 | Miles Lab | Diagnostic composition |
| 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 |
| IT568716A (en) * | 1956-02-03 | |||
| IT569423A (en) * | 1956-04-12 | |||
| JP3003152B2 (en) * | 1990-03-20 | 2000-01-24 | 吉富製薬株式会社 | Method for measuring free hemoglobin and reagent kit for measuring free hemoglobin used therefor |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2290436A (en) * | 1940-09-26 | 1942-07-21 | Miles Lab | Diagnostic composition and method |
| US2387244A (en) * | 1942-06-19 | 1945-10-23 | Miles Lab | Tablet and method of dissolving same |
-
1952
- 1952-05-07 GB GB11558/52A patent/GB708996A/en not_active Expired
-
1954
- 1954-04-15 US US423524A patent/US2799660A/en not_active Expired - Lifetime
- 1954-12-23 GB GB37258/54A patent/GB772374A/en not_active Expired
-
1955
- 1955-01-11 FR FR1119775D patent/FR1119775A/en not_active Expired
- 1955-01-14 CH CH339401D patent/CH339401A/en unknown
- 1955-03-05 DE DEM26333A patent/DE1004398B/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2290436A (en) * | 1940-09-26 | 1942-07-21 | Miles Lab | Diagnostic composition and method |
| US2387244A (en) * | 1942-06-19 | 1945-10-23 | Miles Lab | Tablet and method of dissolving same |
Cited By (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2905594A (en) * | 1956-04-25 | 1959-09-22 | Herman J Morris | Means for detecting enzyme activity |
| US3068855A (en) * | 1957-04-29 | 1962-12-18 | Jr Norman B Furlong | Disposable blood-gas analyzer |
| US2970945A (en) * | 1958-10-03 | 1961-02-07 | Miles Lab | Diagnostic composition |
| DE1265453B (en) * | 1961-05-04 | 1968-04-04 | Miles Lab | Diagnostic agent intended for the detection of blood |
| US3252762A (en) * | 1961-05-04 | 1966-05-24 | Miles Lab | Stabilized occult blood diagnostic |
| US3411887A (en) * | 1964-06-15 | 1968-11-19 | Miles Lab | Diagnostic composition |
| US3335793A (en) * | 1964-11-30 | 1967-08-15 | Cities Service Oil Co | Method and composition for improving and maintaining the capacity of water injection wells |
| USRE28575E (en) * | 1971-03-01 | 1975-10-21 | Indicator for detecting hydrogen peroxide and peroxidative compounds containing alpha naphthoflavone | |
| US4394452A (en) * | 1977-05-31 | 1983-07-19 | Rohm Gmbh | Synthetic stool |
| US4175923A (en) * | 1978-06-26 | 1979-11-27 | Friend William G | Method and apparatus for occult blood testing in the home |
| US4148611A (en) * | 1978-06-28 | 1979-04-10 | Miles Laboratories, Inc. | Test composition, device and method for the detection of peroxidatively active substances |
| US4956300A (en) * | 1982-01-05 | 1990-09-11 | Helena Laboratories Corporation | Aid for determining the presence of occult blood, method of making the aid, and method of using the aid |
| US5702913A (en) * | 1983-12-21 | 1997-12-30 | Helena Laboratories Corporation | Chromgen-reagent test system |
| US5273888A (en) * | 1984-01-16 | 1993-12-28 | Helena Laboratories Corporation | Chemical test kit and method for determining the presence of blood in a specimen and for verifying the effectiveness of the chemicals |
| US4676950A (en) * | 1984-02-03 | 1987-06-30 | Foster Research Corporation | Indicator and test device for detecting occult blood |
| EP0177244A3 (en) * | 1984-09-26 | 1986-12-17 | Warner-Lambert Company | A method for the detection of peroxidase activity |
| EP0227602A3 (en) * | 1985-12-20 | 1988-04-06 | Warner-Lambert Company | Free flowing granular indicator material for peroxidase-like activity |
| US5081040A (en) * | 1987-06-29 | 1992-01-14 | Helena Laboratories Corporation | Composition and kit for testing for occult blood in human and animal excretions, fluids, or tissue matrixes |
| US5196167A (en) * | 1989-04-04 | 1993-03-23 | Helena Laboratories Corporation | Fecal occult blood test product with positive and negative controls |
| US5217874A (en) * | 1989-04-04 | 1993-06-08 | Helena Laboratories Corporation | Fecal occult blood test product with positive and negative controls |
| US6046019A (en) * | 1991-07-09 | 2000-04-04 | Goumeniouk; Alexander P. | Diagnostic kits and methods for making granulocyte cell counts |
| US6225123B1 (en) * | 1997-04-30 | 2001-05-01 | Becton Dickinson And Company | Additive preparation and method of use thereof |
| US6534016B1 (en) | 1997-04-30 | 2003-03-18 | Richmond Cohen | Additive preparation and method of use thereof |
| EP0875756B1 (en) * | 1997-04-30 | 2004-02-18 | Becton, Dickinson and Company | Additive preparation and method of use thereof |
| KR100473726B1 (en) * | 1997-04-30 | 2005-07-18 | 벡톤 디킨슨 앤드 컴퍼니 | Additives and how to use them |
Also Published As
| Publication number | Publication date |
|---|---|
| CH339401A (en) | 1959-06-30 |
| GB772374A (en) | 1957-04-10 |
| DE1004398B (en) | 1957-03-14 |
| FR1119775A (en) | 1956-06-25 |
| GB708996A (en) | 1954-05-12 |
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