NO128970B - - Google Patents
Download PDFInfo
- Publication number
- NO128970B NO128970B NO00504/70A NO50470A NO128970B NO 128970 B NO128970 B NO 128970B NO 00504/70 A NO00504/70 A NO 00504/70A NO 50470 A NO50470 A NO 50470A NO 128970 B NO128970 B NO 128970B
- Authority
- NO
- Norway
- Prior art keywords
- acid
- test device
- solution
- salt
- bilirubin
- Prior art date
Links
- 239000000243 solution Substances 0.000 claims description 52
- BPYKTIZUTYGOLE-IFADSCNNSA-N Bilirubin Chemical compound N1C(=O)C(C)=C(C=C)\C1=C\C1=C(C)C(CCC(O)=O)=C(CC2=C(C(C)=C(\C=C/3C(=C(C=C)C(=O)N\3)C)N2)CCC(O)=O)N1 BPYKTIZUTYGOLE-IFADSCNNSA-N 0.000 claims description 43
- 150000001989 diazonium salts Chemical class 0.000 claims description 23
- 239000012954 diazonium Substances 0.000 claims description 20
- 239000012876 carrier material Substances 0.000 claims description 18
- 239000003381 stabilizer Substances 0.000 claims description 15
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
- 150000004982 aromatic amines Chemical class 0.000 claims description 11
- WXHLLJAMBQLULT-UHFFFAOYSA-N 2-[[6-[4-(2-hydroxyethyl)piperazin-1-yl]-2-methylpyrimidin-4-yl]amino]-n-(2-methyl-6-sulfanylphenyl)-1,3-thiazole-5-carboxamide;hydrate Chemical compound O.C=1C(N2CCN(CCO)CC2)=NC(C)=NC=1NC(S1)=NC=C1C(=O)NC1=C(C)C=CC=C1S WXHLLJAMBQLULT-UHFFFAOYSA-N 0.000 claims description 9
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 claims description 9
- 239000002798 polar solvent Substances 0.000 claims description 9
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
- XTEGVFVZDVNBPF-UHFFFAOYSA-N naphthalene-1,5-disulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1S(O)(=O)=O XTEGVFVZDVNBPF-UHFFFAOYSA-N 0.000 claims description 7
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 claims description 6
- -1 aliphatic sulphonic acid salt Chemical class 0.000 claims description 6
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 6
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical group [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical group [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 4
- 239000002250 absorbent Substances 0.000 claims description 4
- 230000002745 absorbent Effects 0.000 claims description 4
- 235000019333 sodium laurylsulphate Nutrition 0.000 claims description 4
- 235000010288 sodium nitrite Nutrition 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- KQCMTOWTPBNWDB-UHFFFAOYSA-N 2,4-dichloroaniline Chemical group NC1=CC=C(Cl)C=C1Cl KQCMTOWTPBNWDB-UHFFFAOYSA-N 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims 1
- 229910021653 sulphate ion Inorganic materials 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 10
- 210000002700 urine Anatomy 0.000 description 9
- 239000003153 chemical reaction reagent Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000001514 detection method Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000001035 drying Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000012085 test solution Substances 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 210000001124 body fluid Anatomy 0.000 description 3
- 239000010839 body fluid Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- AVYGCQXNNJPXSS-UHFFFAOYSA-N 2,5-dichloroaniline Chemical compound NC1=CC(Cl)=CC=C1Cl AVYGCQXNNJPXSS-UHFFFAOYSA-N 0.000 description 2
- NIPDVSLAMPAWTP-UHFFFAOYSA-N 2-methoxy-5-nitroaniline Chemical compound COC1=CC=C([N+]([O-])=O)C=C1N NIPDVSLAMPAWTP-UHFFFAOYSA-N 0.000 description 2
- QSNSCYSYFYORTR-UHFFFAOYSA-N 4-chloroaniline Chemical compound NC1=CC=C(Cl)C=C1 QSNSCYSYFYORTR-UHFFFAOYSA-N 0.000 description 2
- TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 244000178870 Lavandula angustifolia Species 0.000 description 2
- 235000010663 Lavandula angustifolia Nutrition 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 150000008049 diazo compounds Chemical class 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 239000001102 lavandula vera Substances 0.000 description 2
- 235000018219 lavender Nutrition 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 2
- RUDCBGCNXOSCTI-UHFFFAOYSA-N n-methoxy-4-[4-(methoxyamino)phenyl]aniline Chemical compound C1=CC(NOC)=CC=C1C1=CC=C(NOC)C=C1 RUDCBGCNXOSCTI-UHFFFAOYSA-N 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000001575 pathological effect Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 210000002966 serum Anatomy 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 206010023126 Jaundice Diseases 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 1
- AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000002390 adhesive tape Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- RAFRTSDUWORDLA-UHFFFAOYSA-N phenyl 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=CC=C1 RAFRTSDUWORDLA-UHFFFAOYSA-N 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 235000010289 potassium nitrite Nutrition 0.000 description 1
- 239000004304 potassium nitrite Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 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
- G01N33/728—Bilirubin; including biliverdin
-
- 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
- Y10S436/903—Diazo reactions
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T436/00—Chemistry: analytical and immunological testing
- Y10T436/14—Heterocyclic carbon compound [i.e., O, S, N, Se, Te, as only ring hetero atom]
- Y10T436/145555—Hetero-N
- Y10T436/146666—Bile pigment
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)
- Biochemistry (AREA)
- Cell Biology (AREA)
- Food Science & Technology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Analytical Chemistry (AREA)
- Microbiology (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)
- Investigating Materials By The Use Of Optical Means Adapted For Particular Applications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79992869A | 1969-02-17 | 1969-02-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO128970B true NO128970B (fr) | 1974-02-04 |
Family
ID=25177106
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO00504/70A NO128970B (fr) | 1969-02-17 | 1970-02-13 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US3585001A (fr) |
| JP (1) | JPS4929475B1 (fr) |
| BE (1) | BE746099A (fr) |
| BR (1) | BR7016743D0 (fr) |
| CH (1) | CH533837A (fr) |
| DE (1) | DE2007013B2 (fr) |
| DK (1) | DK134872B (fr) |
| ES (1) | ES374872A1 (fr) |
| FR (1) | FR2035492A5 (fr) |
| GB (1) | GB1298762A (fr) |
| NL (1) | NL7001638A (fr) |
| NO (1) | NO128970B (fr) |
| SE (1) | SE374821B (fr) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2130559C3 (de) * | 1971-06-19 | 1973-11-22 | Boehringer Mannheim Gmbh, 6800 Mannheim | Diagnostisches Mittel zum Nach weis von Urobihnogen |
| DE2229611C3 (de) * | 1972-06-19 | 1980-07-17 | Boehringer Mannheim Gmbh, 6800 Mannheim | Diagnostischer Nachweis von Urobilinogen-Körpern |
| DE2240471C3 (de) * | 1972-08-17 | 1975-04-03 | Boehringer Mannheim Gmbh, 6800 Mannheim | Testpapier zum Nachweis von Bilirubin in Körperflüssigkeiten |
| DE2240357C2 (de) * | 1972-08-17 | 1974-09-12 | Boehringer Mannheim Gmbh, 6800 Mannheim | Testpapier zum Nachweis von Bilirubin in Körperflüssigkeiten |
| US3825411A (en) * | 1972-08-30 | 1974-07-23 | Medico Electronic Inc | Reagent and method for bilirubin determination |
| US3923459A (en) * | 1972-12-14 | 1975-12-02 | Union Carbide Corp | Process for the determination of bilirubin in fluids |
| US4038031A (en) * | 1975-10-02 | 1977-07-26 | Miles Laboratories, Inc. | Test composition, device and method for detecting bilirubin |
| US4288344A (en) * | 1976-11-22 | 1981-09-08 | Andre Reiss | Stable diazonium salt generator for improved marijuana analysis |
| US4190419A (en) * | 1978-09-22 | 1980-02-26 | Miles Laboratories, Inc. | Device for detecting serum bilirubin |
| DE2855363B1 (de) * | 1978-12-21 | 1980-05-29 | Boehringer Mannheim Gmbh | Kontrollreagens fuer Teststreifen zum Nachweis von Urobilinogen im Harn |
| DE3017721A1 (de) * | 1980-05-09 | 1981-11-26 | Boehringer Mannheim Gmbh, 6800 Mannheim | Mittel zum nachweis esterolytischer und/oder proteolytischer enzyme und dafuer geeignete substrate |
| JPS60233559A (ja) * | 1984-05-02 | 1985-11-20 | Terumo Corp | 試験片 |
| US6377230B1 (en) * | 1995-10-05 | 2002-04-23 | Semiconductor Energy Laboratory Co., Ltd. | Three dimensional display unit and display method |
| ES2143434B1 (es) * | 1998-09-16 | 2000-12-16 | Cerrato Paula Jimenez | Pañal con indicadores sensibles al estado de la orina que lo impregna visualiazables desde el exterior. |
| SG120277A1 (en) * | 2004-08-27 | 2006-03-28 | Zellweger Analytics Ag | Extended life mineral acid detection tape |
-
1969
- 1969-02-17 US US799928A patent/US3585001A/en not_active Expired - Lifetime
- 1969-12-23 ES ES374872A patent/ES374872A1/es not_active Expired
-
1970
- 1970-02-03 GB GB5174/70D patent/GB1298762A/en not_active Expired
- 1970-02-04 CH CH161070A patent/CH533837A/de not_active IP Right Cessation
- 1970-02-05 NL NL7001638A patent/NL7001638A/xx unknown
- 1970-02-13 BR BR216743/70A patent/BR7016743D0/pt unknown
- 1970-02-13 NO NO00504/70A patent/NO128970B/no unknown
- 1970-02-16 DK DK74170AA patent/DK134872B/da unknown
- 1970-02-16 FR FR7005475A patent/FR2035492A5/fr not_active Expired
- 1970-02-16 DE DE2007013A patent/DE2007013B2/de active Pending
- 1970-02-16 JP JP45012668A patent/JPS4929475B1/ja active Pending
- 1970-02-16 SE SE7001954A patent/SE374821B/xx unknown
- 1970-02-17 BE BE746099D patent/BE746099A/fr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US3585001A (en) | 1971-06-15 |
| BR7016743D0 (pt) | 1973-01-09 |
| DK134872B (da) | 1977-01-31 |
| JPS4929475B1 (fr) | 1974-08-05 |
| SE374821B (fr) | 1975-03-17 |
| DE2007013A1 (de) | 1970-09-03 |
| DK134872C (fr) | 1977-06-20 |
| FR2035492A5 (fr) | 1970-12-18 |
| ES374872A1 (es) | 1972-02-16 |
| GB1298762A (en) | 1972-12-06 |
| NL7001638A (fr) | 1970-08-19 |
| CH533837A (de) | 1973-02-15 |
| DE2007013B2 (de) | 1974-12-19 |
| BE746099A (fr) | 1970-07-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO128970B (fr) | ||
| NO128837B (fr) | ||
| DE1598153C3 (de) | Diagnostisches Mittel zum Nach weis der Inhaltsstoffe von Korperflus sigkeiten | |
| US5055195A (en) | Erythrocyte-retention substrates | |
| AU714671B2 (en) | Chemical timer for a visual test strip | |
| EP0154839B1 (fr) | Dispositif d'essai et méthode pour la détection d'un constituent d'un échantillon liquide | |
| NO130520B (fr) | ||
| EP0735369B1 (fr) | Système chimique de mesure du temps pour la lecture directe de bandes de test | |
| Fairbridge et al. | The direct colorimetric estimation of reducing sugars and other reducing substances with tetrazolium salts | |
| FI79615B (fi) | Testband foer upptagning av blodsockerdagsprofiler samt foerfarandet foer dess framstaellning. | |
| DE1005759B (de) | Zur Bestimmung von Blutgruppen verwendbare Karte | |
| CA1132891A (fr) | Dispositif et methode de determination semiquantitative de glucose dans des fluides aqueux | |
| Leibman et al. | Interrelations of plasma potassium concentration, plasma sodium concentration, arterial pH and total exchangeable potassium | |
| US4440724A (en) | Composition for detecting ketone bodies and method of preparation | |
| CN102520182A (zh) | 一种可视血糖试纸及其制备方法 | |
| EP3614141A1 (fr) | Indicateur d'urine stable à détection lente | |
| Maizels et al. | Mercaptomerin and water exchange in cortex slices of rat kidney | |
| US5215925A (en) | Method and composition for magnesium ion detection using hydroxy-substituted cyanoformazans | |
| JP3855008B2 (ja) | 酸含有状態下あるいは酸性条件下で使用する濾紙およびそれを用いて形成される試験片 | |
| DE2264438C3 (de) | Teststreifen zum Nachweis von Wasserstoffperoxid oder Wasserstoffperoxid erzeugenden Systemen | |
| Chrastil | Colorimetric determination of aniline in the presence of 4-aminophenol and other oxidation products | |
| JP3723828B2 (ja) | 液体中のアスコルビン酸濃度の測定方法、及び液体中のアスコルビン酸濃度測定用試験片 | |
| Hunter | Enzyme Systems in Stylonychia pusulata. I. Cytochemical Studies on the Oxidation of the Dicarboxylic Acid Substrates | |
| CN113030077A (zh) | 一种n-乙酰氨基葡萄糖苷酶检测试纸及其制备方法 | |
| Randles Jr et al. | The buffering capacities of allantoic and amniotic fluids of the chick |