GB981955A - Improvements in or relating to diagnostic compositions - Google Patents
Improvements in or relating to diagnostic compositionsInfo
- Publication number
- GB981955A GB981955A GB14043/62A GB1404362A GB981955A GB 981955 A GB981955 A GB 981955A GB 14043/62 A GB14043/62 A GB 14043/62A GB 1404362 A GB1404362 A GB 1404362A GB 981955 A GB981955 A GB 981955A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroperoxide
- dialdehyde
- added
- citrate buffer
- mixture
- 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
Links
- 239000000203 mixture Substances 0.000 title abstract 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 4
- 239000000463 material Substances 0.000 abstract 4
- 229920001282 polysaccharide Polymers 0.000 abstract 4
- 239000005017 polysaccharide Substances 0.000 abstract 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 3
- 240000007472 Leucaena leucocephala Species 0.000 abstract 3
- 235000010643 Leucaena leucocephala Nutrition 0.000 abstract 3
- 229920000715 Mucilage Polymers 0.000 abstract 3
- 239000000853 adhesive Substances 0.000 abstract 3
- 239000000839 emulsion Substances 0.000 abstract 3
- 229920000159 gelatin Polymers 0.000 abstract 3
- 239000008273 gelatin Substances 0.000 abstract 3
- 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 abstract 2
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 abstract 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 abstract 2
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical class N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 abstract 2
- 229920002085 Dialdehyde starch Polymers 0.000 abstract 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 abstract 2
- 239000004141 Sodium laurylsulphate Substances 0.000 abstract 2
- 235000010443 alginic acid Nutrition 0.000 abstract 2
- 229920000615 alginic acid Polymers 0.000 abstract 2
- 239000008280 blood Substances 0.000 abstract 2
- 210000004369 blood Anatomy 0.000 abstract 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 abstract 2
- 239000007979 citrate buffer Substances 0.000 abstract 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
- -1 dialdehyde polysaccharide Chemical class 0.000 abstract 2
- 239000006185 dispersion Substances 0.000 abstract 2
- 150000004676 glycans Chemical class 0.000 abstract 2
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 abstract 2
- 150000002432 hydroperoxides Chemical class 0.000 abstract 2
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 abstract 2
- CFJYNSNXFXLKNS-UHFFFAOYSA-N p-menthane Chemical compound CC(C)C1CCC(C)CC1 CFJYNSNXFXLKNS-UHFFFAOYSA-N 0.000 abstract 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 abstract 2
- 239000000243 solution Substances 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- OKIRBHVFJGXOIS-UHFFFAOYSA-N 1,2-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC=C1C(C)C OKIRBHVFJGXOIS-UHFFFAOYSA-N 0.000 abstract 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 abstract 1
- JRBJSXQPQWSCCF-UHFFFAOYSA-N 3,3'-Dimethoxybenzidine Chemical compound C1=C(N)C(OC)=CC(C=2C=C(OC)C(N)=CC=2)=C1 JRBJSXQPQWSCCF-UHFFFAOYSA-N 0.000 abstract 1
- 244000215068 Acacia senegal Species 0.000 abstract 1
- 102000009027 Albumins Human genes 0.000 abstract 1
- 108010088751 Albumins Proteins 0.000 abstract 1
- 229920002307 Dextran Polymers 0.000 abstract 1
- 239000001836 Dioctyl sodium sulphosuccinate Substances 0.000 abstract 1
- 108010010803 Gelatin Proteins 0.000 abstract 1
- 229920000084 Gum arabic Polymers 0.000 abstract 1
- 229920001202 Inulin Polymers 0.000 abstract 1
- 240000003183 Manihot esculenta Species 0.000 abstract 1
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 abstract 1
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- 239000004372 Polyvinyl alcohol Substances 0.000 abstract 1
- 229920002125 Sokalan® Polymers 0.000 abstract 1
- 235000021307 Triticum Nutrition 0.000 abstract 1
- 244000098338 Triticum aestivum Species 0.000 abstract 1
- 240000008042 Zea mays Species 0.000 abstract 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 abstract 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract 1
- 235000010489 acacia gum Nutrition 0.000 abstract 1
- 239000000205 acacia gum Substances 0.000 abstract 1
- 150000001242 acetic acid derivatives Chemical class 0.000 abstract 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 abstract 1
- 239000000872 buffer Substances 0.000 abstract 1
- 230000003139 buffering effect Effects 0.000 abstract 1
- 235000010418 carrageenan Nutrition 0.000 abstract 1
- 229920001525 carrageenan Polymers 0.000 abstract 1
- 239000005018 casein Substances 0.000 abstract 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 abstract 1
- 235000021240 caseins Nutrition 0.000 abstract 1
- 239000001913 cellulose Substances 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 238000001514 detection method Methods 0.000 abstract 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 239000012467 final product Substances 0.000 abstract 1
- 235000019322 gelatine Nutrition 0.000 abstract 1
- 235000011852 gelatine desserts Nutrition 0.000 abstract 1
- 229960001867 guaiacol Drugs 0.000 abstract 1
- 229940029339 inulin Drugs 0.000 abstract 1
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 abstract 1
- 150000002672 m-cresols Chemical class 0.000 abstract 1
- 235000009973 maize Nutrition 0.000 abstract 1
- 150000002883 o-cresols Chemical class 0.000 abstract 1
- BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 abstract 1
- 150000002931 p-cresols Chemical class 0.000 abstract 1
- 229930004008 p-menthane Natural products 0.000 abstract 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 abstract 1
- 235000021317 phosphate Nutrition 0.000 abstract 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 abstract 1
- 125000005498 phthalate group Chemical class 0.000 abstract 1
- 229920002451 polyvinyl alcohol Polymers 0.000 abstract 1
- 229920001592 potato starch Polymers 0.000 abstract 1
- 235000018102 proteins Nutrition 0.000 abstract 1
- 102000004169 proteins and genes Human genes 0.000 abstract 1
- 108090000623 proteins and genes Proteins 0.000 abstract 1
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 abstract 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 abstract 1
- 150000003892 tartrate salts Chemical class 0.000 abstract 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Urology & Nephrology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Cell Biology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US107646A US3252762A (en) | 1961-05-04 | 1961-05-04 | Stabilized occult blood diagnostic |
Publications (1)
Publication Number | Publication Date |
---|---|
GB981955A true GB981955A (en) | 1965-02-03 |
Family
ID=22317688
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14043/62A Expired GB981955A (en) | 1961-05-04 | 1962-04-11 | Improvements in or relating to diagnostic compositions |
Country Status (7)
Country | Link |
---|---|
US (1) | US3252762A (enrdf_load_stackoverflow) |
BE (1) | BE617211A (enrdf_load_stackoverflow) |
CH (1) | CH427353A (enrdf_load_stackoverflow) |
DE (1) | DE1265453B (enrdf_load_stackoverflow) |
DK (1) | DK103213C (enrdf_load_stackoverflow) |
GB (1) | GB981955A (enrdf_load_stackoverflow) |
NL (1) | NL277911A (enrdf_load_stackoverflow) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1987001460A1 (en) * | 1985-08-30 | 1987-03-12 | Terje Silsand | Test device for determination of blood in faeces |
EP0123902A3 (en) * | 1983-03-31 | 1987-06-16 | Mallinckrodt Diagnostica Gmbh | Procedure for the determination of peroxidase activity by end dilution titration and means for its realization |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL126365C (enrdf_load_stackoverflow) * | 1963-06-24 | |||
DE2235127C2 (de) * | 1972-07-18 | 1974-08-08 | Boehringer Mannheim Gmbh, 6800 Mannheim | Diagnostisches Mittel zum Nachweis von Blut und anderen peroxidatisch wirksamen Substanzen in Körperflüssigkeiten |
GB1456234A (en) * | 1973-05-24 | 1976-11-24 | Kodak Ltd | Formaldehyde testing material |
US3975162A (en) * | 1974-03-13 | 1976-08-17 | Marine Colloids, Inc. | Applying reagent to medium and device therefor |
CS175782B1 (enrdf_load_stackoverflow) * | 1974-10-16 | 1977-05-31 | ||
JPS5263794A (en) * | 1975-11-21 | 1977-05-26 | Shionogi Seiyaku Kk | Test piece for latent blood |
US4071321A (en) * | 1977-03-14 | 1978-01-31 | Miles Laboratories, Inc. | Test composition and device for determining peroxidatively active substances |
US4071317A (en) * | 1977-03-14 | 1978-01-31 | Miles Laboratories, Inc. | Test composition and device for determining peroxidatively active substances and process for preparing same |
US4071318A (en) * | 1977-03-14 | 1978-01-31 | Miles Laboratories, Inc. | Test composition and device for determining peroxidatively active substances |
US4175923A (en) * | 1978-06-26 | 1979-11-27 | Friend William G | Method and apparatus for occult blood testing in the home |
US4526869A (en) * | 1980-09-24 | 1985-07-02 | Regents Of The University Of Minnesota | Method for quantitatively determining the concentration of hemoglobin in a biological sample |
US4329317A (en) * | 1981-01-29 | 1982-05-11 | Smithkline Instruments, Inc. | Method of stabilizing a specimen slide for occult blood testing |
US4382064A (en) * | 1981-01-29 | 1983-05-03 | Smithkline Instruments, Inc. | Specimen slide for occult blood testing |
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 |
US4447542A (en) * | 1983-04-04 | 1984-05-08 | Miles Laboratories, Inc. | Analytical test composition, device and method for the determination of peroxidatively active substances |
US4556640A (en) * | 1983-06-29 | 1985-12-03 | Miles Laboratories, Inc. | Stabilized test composition, device and method for the determination of peroxidatively active substances |
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 |
US4615982A (en) * | 1984-12-11 | 1986-10-07 | Lawrence Paul J | Fecal occult blood test |
US4818702A (en) * | 1986-06-02 | 1989-04-04 | Litmus Concepts, Inc. | Fecal occult blood test reagent |
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 |
US4895798A (en) * | 1987-11-13 | 1990-01-23 | Miles, Inc. | Test devices for determination of occult blood |
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 |
DE3925938C1 (enrdf_load_stackoverflow) * | 1989-08-03 | 1990-04-12 | Geb. Sehl Claudia 1000 Berlin De Keck | |
US7604807B2 (en) * | 2000-12-01 | 2009-10-20 | Auburn University | Use of pullulan to isolate and preserve biological material |
AU2002241550A1 (en) * | 2000-12-01 | 2002-06-11 | Auburn University | Use of acacia gum (arabic gum) to isolate and preserve biological material |
US6850633B2 (en) * | 2001-02-23 | 2005-02-01 | Beckman Coulter, Inc. | Devices and methods for reading and interpreting guaiac-based occult blood tests |
GB201107466D0 (en) | 2011-05-05 | 2011-06-15 | Loktionov Alexandre | Device and method for non-invasive collection of colorectal mucocellular layer and disease detection |
KR20240161711A (ko) | 2018-03-27 | 2024-11-12 | 이그잭트 사이언시즈 코포레이션 | 헤모글로빈 안정화 방법 및 동일한 수행을 위한 시약 |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2290436A (en) * | 1940-09-26 | 1942-07-21 | Miles Lab | Diagnostic composition and method |
US2754289A (en) * | 1952-02-29 | 1956-07-10 | Shell Dev | Process for polymerizing unsaturated compounds by conducting droplets through an aqueous medium with control of pressure fluctuations |
BE530008A (enrdf_load_stackoverflow) * | 1953-06-30 | |||
GB708996A (en) * | 1954-04-15 | 1954-05-12 | Miles Lab | Improvements in or relating to diagnostic compositions |
NL226920A (enrdf_load_stackoverflow) * | 1957-04-23 | |||
US2986453A (en) * | 1957-11-13 | 1961-05-30 | Miles Lab | Diagnostic compositions |
US2886445A (en) * | 1958-12-08 | 1959-05-12 | Gen Foods Corp | Process for making chewing gum and product |
US3043782A (en) * | 1958-12-22 | 1962-07-10 | Upjohn Co | Process for preparing a more impermeable coating by liquid-liquid phase separation |
NL102893C (enrdf_load_stackoverflow) * | 1959-03-27 | |||
US3057723A (en) * | 1959-06-24 | 1962-10-09 | Eastman Kodak Co | Hardening of gelatin with oxystarch |
US3092463A (en) * | 1959-11-02 | 1963-06-04 | Miles Lab | Stable blood detecting composition |
-
0
- NL NL277911D patent/NL277911A/xx unknown
-
1961
- 1961-05-04 US US107646A patent/US3252762A/en not_active Expired - Lifetime
-
1962
- 1962-04-11 GB GB14043/62A patent/GB981955A/en not_active Expired
- 1962-05-02 CH CH524662A patent/CH427353A/de unknown
- 1962-05-03 DE DEM52734A patent/DE1265453B/de not_active Withdrawn
- 1962-05-03 BE BE617211A patent/BE617211A/fr unknown
- 1962-05-03 DK DK200362AA patent/DK103213C/da active
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0123902A3 (en) * | 1983-03-31 | 1987-06-16 | Mallinckrodt Diagnostica Gmbh | Procedure for the determination of peroxidase activity by end dilution titration and means for its realization |
WO1987001460A1 (en) * | 1985-08-30 | 1987-03-12 | Terje Silsand | Test device for determination of blood in faeces |
Also Published As
Publication number | Publication date |
---|---|
CH427353A (de) | 1966-12-31 |
NL277911A (enrdf_load_stackoverflow) | |
BE617211A (fr) | 1962-08-31 |
DK103213C (da) | 1965-11-29 |
US3252762A (en) | 1966-05-24 |
DE1265453B (de) | 1968-04-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB981955A (en) | Improvements in or relating to diagnostic compositions | |
US3290117A (en) | Occult blood diagnostic composition with color enhancing agent | |
US4063894A (en) | Test strip for the detection of occult blood in excreta | |
US3290228A (en) | Test composition and device for detecting glucose | |
GB893318A (en) | Stable blood detecting composition | |
Kuninaka et al. | Nature of enhanced mitochondrial oxidative metabolism by a calf blood extract | |
Kveder et al. | 5-Hydroxytryptophol: a metabolite of 5-hydroxytryptamine in rats | |
Brown | The estimation of vitamin E. 1. Separation of tocopherol mixtures occurring in natural products by paper chromatography | |
GB960167A (en) | Improvements in or relating to diagnostic compositions | |
GB911181A (en) | Diagnostic composition for glucose | |
US3964870A (en) | Diagnostic composition for the determination of glucose | |
GB1171788A (en) | Diagnostic Device for Various Sugars. | |
US3066081A (en) | Means for detecting galactose | |
GB1182898A (en) | Process and Diagnostic Agent for the Determination of Hydroperoxides and of Peroxidate-Active Substances | |
GB883744A (en) | Diagnostic composition | |
US3104209A (en) | Composition for determination of glucose | |
GB1035911A (en) | Improvements in or relating to diagnostic compositions | |
GB1062361A (en) | Means for detecting the fertile period | |
GB1529148A (en) | Method of hardening gelatin and gelatin-containing compositions | |
USRE28575E (en) | Indicator for detecting hydrogen peroxide and peroxidative compounds containing alpha naphthoflavone | |
Chan et al. | Differential effects of dietary vitamin E and antioxidants on eicosanoid synthesis in young rabbits | |
EP0374946A2 (de) | Verfahren zum Nachweis von kohlenhydrathaltigen Verbindungen | |
GB889676A (en) | Water insoluble films | |
KR830004414A (ko) | 마이코페놀산 유도체의 제조방법 | |
GB638908A (en) | Diazo type papers containing an alginate sizing |