![]() Diagnostic agent for determining leukocytes in urine
专利摘要:
1. DIAGNOSTIC MEANS FOR DETERMINING LEUKOCYTES IN URINE, containing chromogen and buffer solution, characterized in that, in order to increase its specificity, as chromogen, it contains indoxyl or thiondoxyl ester of the general formula 0-A-B where R, jRj, Rj , R is hydrogen, halogen, alkyl with 1–3 carbon atoms, lower alkoxy, aryl, araloxyl, hydroxyl, carboxyl carboxyalkoxy, araloxycarbonylalkosyl, aralkyl, aralkoxycarbonyl,, nitro and lower acylamino, two adjacent mixtures of those mean a substituted halogen, a halo, a nitro and a lower acylaminogroup, two adjacent mixtures of those mean a substituted halogen, a halo, a nitro and a lower acylamino, two adjacent mixtures of the mean are substituted halogen, oannelirovanny residue; X is a sulfur atom or an imino group substituted by a residue of lower alkyl, arshta, and acyl; And the residue of glycocol, alanine, valine, leucine, glycerol, isoleucine, phenylalanine, tyrosine or 0-acetylthirazine, the residue of alanyl-alanine or osso residue of alanyl-alanyl-alanine; This is linked to the nitrogen atom of the amino acids of the A groups of the C — Cg-alkoxycarbonyl, C, —C — alkylsulfonyl 96 4 groups of formyl, acetyl or diphenylamino carbonyl of the O —CO — CH —CH —COOH group, or —C — O — C N / gO-SNZ 公开号:SU1184444A3 申请号:SU792853140 申请日:1979-12-19 公开日:1985-10-07 发明作者:Бергер Дитер;Браун Франц;Гютляйн Вегнер;Кур Манфред;Вернер ВОЛЬФГАНГ 申请人:Берингер Маннхайм Гмбх (Фирма); IPC主号:
专利说明:
-C-D the remainder "..about C - g upa -S-, -C-0 -C-S-. -C-, -S- or -C CH-C-; D is a valence trait or C, -Cj-alkylene; E is phenyl, 1-naphtsh1, 2-naphthyl, 2-furyl, 8-quinolyl, 2-thienyl, 3-pyridyl, cyclohexyl or H-piperidyl; , R, Rj and Rg may be the same or different and denote hydrogen, straight or branched C2-alkyl, C (-C3-alkoxy, nitro, halogen, di-C, -C3-alkylamino, acetylamino, hydroxyl, benzyloxy, HYDROXY-C-Szalkoxy-C | -Cz-alkoxy, methoxy-C-C-alkoxy-C (-Cz-alkoxy, hydroxy-C, -C J-.alkksh. halogen-C-C3-alkyl, cyano ,. carboxyl, C, -Cj-alkoxycarbonyl, benzyloxycarbonyl, carbamoyl, dis-C, -C, -alkylcarbamoyl, carboxyl-C, -C-alkyl, carboxyl-C, -C-alkoxy, carboxyl-C-C-alkylamino or phenyl , The following ratio of component.%: 0.2-9.0 Chromogen Buffer Solution Else 2. A diagnostic agent according to claim 1, characterized in that it further comprises a chemical in the amount of 8.9-28.4 wt.% 3. A diagnostic agent according to Claim 1, characterized in that it further comprises an oxidizing agent in an amount of 1.9-9.0 wt.%. 4. The diagnostic agent according to claim 1, characterized in that it further comprises a herbal supplement in an amount of 78.5 May. % one This invention relates to clinical biochemistry, namely to a diagnostic tool for determining leukocytes in the urine. The purpose of the invention is to increase the specificity of an agent for determining leukocytes in the urine. P r and m er. The filtered paper is sequentially sewn with the following solutions and then dried at 60 ° C. Solution 1. Disodium tetraborate decahydrate, g1.91 Distilled water, ml 30 The solution is adjusted to pH 8.0 with 0.1 and hydrochloric acid and the total volume is adjusted to 100.0 ml with distilled water. Solution 2. (Benzyloxycarbonyl) -b-alanyloxy-indole, mg 33.8 Acetone, ml To. General; volume of 100.0. A colorless test paper is obtained which, when immersed in urine-containing urine, depending on the concentration of leukocytes, stains in color from light turquoise to blue. You can detect 5,000 leukocytes in 1 μl of urine in 2 minutes; 1000 white blood cells in 1 μl of urine for 6 minutes; 500 leukocytes in 1 μl of urine per 10 minutes; 200 white blood cells in 1 µl of urine in 15 min. The sensitivity of the test is 200 leukocytes. Per 1 μl. Evaluation can also be performed using remission photometry at 620 nm. Test paper with similar properties (sensitivity 200-2000 leukocytes per 1 μl) is obtained if, instead of (benzyloxycarbonyl 1) -b-alanyloxy-indole, the following substrates are used, it is also possible to give a color from light blue to blue paper and when immersed, urine containing leukocytes: (benzsuxycarbonyl) -l-al nyloxy-4-methyl-indole; (benzyloxycarbonyl) -l-al-nyloxy-5-methyl-indole; (benzyloxycarbonyl) -L-al-nyloxy-6-methyl-indole; (benzyloxycarbonyl) -l-al-nyloxy-7-methyl-indole; 3-tN- (benzyloxycarbonyl) -L-allyloxy-4,7-dimethyl-indole; (benzyloxycarbonyl) -L-al-nyloxy-4-chloro-indole; (benzyloxycarbonyl) -L-al-nyloxy-5-bromo-indole; (Benzyloxycarbonyl) -l-al-nyloxy-6-chloro-indole. Coloring from colorless to purple: “(toluene-4-sulfonyl) -b-alanyloxy-4-chloro-5-bromo-indole; (toluene-4-sulfonyl) -b-alanyloxy | -4, 5,7-trichloro-indole; (toluene-4-sulfonyl) -, - alanyloxy-4-chloro-5-bromo-7-me indole; (tolu-4-sulfonyl) -l-alanyloxy-5-hydroxyindole; (benzyloxycarbonyl) -l-allyloxy-5-methoxy-indole; (toluene-4-sulfonyl) -L-alanyloxy 3-5-benzyloxy-indole; (toluene-4-sulfonyl) -L-alanyloxy1-4 carboxyindole; - city (toluene-4-sulfonyl) -L-alanyloxy-4-benzyl-carbox indole; (toluene-4-sulfonyl) -L-alanyloxy-5-carboxy-methoxyj-indole; 3-H- (toluene-4-sulfonyl) -b-alanypoxy-3-benzyloxycarbonyl-meth: 5th and VD ° - (toluene-4-sulfonyl) -L-alanyloxyT-b-nitro-indole; (toluene-4-sulfonyl) -L-alanyloxy-6-acetylamino-indole (toluene-4-sulfonyl) -L-alanyloxy 3-benzene (§ / -indole, Coloring from colorless to friable: 1-methyl-3-LN- (Benzyloxycarbo-L-alanyloxy-1-indole; 1-benzyl-3-N- (tolu-4-ssub NIL) -L-alanyloxy-indole; 1-phenyl-3-N- (toluene-4-sulphyl) -L -alanyloxy-indol. 44 Coloring from colorless to blue-green: 1-acetyl-Z-N- (, toluene-4-sulfonyl) -b-alanyloxy1-indole. Coloring from colorless to red: 1-benzoyl-3-H - (toluene-4-sulfonyl) -b-alanyloxy | -indole. Coloring from colorless to violet: (benzyloxycarbonyl a) -glycyloxyP-indole; (toluene-4-sulfonyl) -glycyloxy-indole; 3- (N- (toluene-2-sulfonyl) -b-alanyloxy-indole:, (toluene-3-sulfonyl) -L-alanyloxy - indole; (toluene-4-sulfonyl) -b-alanyloxy-indole; 3-N- (toluene-4-sulfonyl) -0-alanyloxyT-indole; 3-K- (benzyloxycarbonl) -0, L-alanyloxy-indole; (Benzyloxycarbonyl) -L-valyloxy-indole; (toluene-4-sulfonyl) -L-valyloxy-indole; (benzyloxycarbonyl) -L-leucyloxy-indole; (benzyloxycarbonyl) -L-isolecyloxy-indole; 3- N- (benzyloxycarbonyl) -L-phenylalanyloxy3-indole; (toluene-4-sulfonyl) -L-fesh lalanyloxy-indole; . (acetyl-L-tyrosyloxide) -indole; 3- (N-benzoyl-L-tyrosyloxide) -indole; (benzyloxycarbonyl) -L-tyrosyloxy-indole; (toluene-4-sulfonyl) -L-tyrosyloxy-indole; (toluene-4-sulfonyl) -0-acetyl-L-tyrosyl-indole; (benz shoxicarbonium) -L-alanyl-L-alaniloxio-alder; (toluene-4-sulfonyl) -D-alanyl-L-alaminoxy-indol; (benzyloxycarbonyl) -L-alanyl-L-alanyl-alanyl-L-oxy-indole; 3-s-Stoluuol-4-sulfonyl) -p-alanch I-D-alanyl-L-alenchl-oxy -indole; 3- (N-formyl-L-alaminoxy) -indole; 3- (N-acetyl-L-alaminoxy) -indole; 3- (N-cycenyl-L-alaminoxy) -indole; 3- (N-benzoyl-B, L-alanyloxy) -indole; 3- (L-phthaloyl-b-alanyloxy) -indole (ethoxycarbonyl) -b-alanyloxy-indole; 3-Gk- (tert-butyloxycarbonyl) -L1-alanyloxyJ-indole; (3, 6-dioxane-n-heptyloxycarbonyl) -b-alanyloxy-indole; (cyclohexyloxycarbonyl) -b-alanyloxy-indole; 3- N- (phenyloxycarbonyl) -L-alanyoxy-indole; (4-methyl-benzyloxycarbonyl) -L-alenyloxy-J-indole; 3-fN- (4-methoxy-benzyloxycarbo NRL J-L-alanyloxy j-indole; 3-Gy- (4-nitro-benzyloxycarboL .-. NIL) -L-ala-nioxy-J-indole; 3-TN-FN- (piperidine) -oxycarbonyl-l-alanyloxy-indole; 3-Hfuryl- (2) -methoxycarbonyl-1-alanyloxy-indole; Z-Gy-Gtienil- (2) -methoxycarbonyl-gananyloxy-INDol; Z-Gy- (benzylthiocarbonyl) -b-alanyloxy-indole; 3-Hm- (methanesulfonyl) -b-alanyloxy1-indole; 3-y- (benzylsulfonyl) -j-alanshloxn-indole; 3-to- (benzenesulfonyl) -b-alanyl-T-indole; (4-bromo-benzolylfcnshI) -L-linearoksy-indol; (4-nitro-benzenesulfonyl) -L-alanyloxy-indole; . J (4-dimethylamino-benzenesulfonyl) -b-alanyloxy-indole; (4-acetylamino-benzenesulfonyl) -b-alanyloxy} -indole; 3-N- (4-n-butyl-benzenesulfonyl-b-alanyloxy-indole; (4-tert-butyl-benzenesulfonyl) -b-alanyloxy-indole; (4-n-octyl-benzenesulfonyl) -b-alanyloxy-indole; (4-hydroxy-benzene sulfonyl) -b-alanyloxy-indole; (4-methoxy-benzenesulfonyl) -b-alanyloxy-indole; (4-benzyloxy-benzenesulfonyl) -b-alanyloxyJ-indole; 3-Gy- 4- (2 -oxy-ethoxy) -benzenesulfonyl-L-alanyloxy (-indole; 3-Hn-4 - (3 -oxy-5-hydroxy-n-pentyloxy) -benzenesulfonyl-L-alanyloxy J-indole; 4 - (3, d-ixi-n-reptschioxy) -benzenesulfonyl-1-b-alanyloxyT-indole, H-W-4 - (2 -oxy-ethyl) -benzenesulfonyl-L-alanyloxyJ-indole; - (2 - | 4-nitro-benzyl-T-ethyl) -benzolylphosphine-L-alanyloxy J -indol; -ft- (2-chloro-ethyl) -benzenesulfonyl -b-alanyloxy-indole; (4-adhethyl-benzenesulfonyl) -L-alanyloxy-indole; (4-cyano-benzenesulfonyl) -b-alanyloxy-indole; (4-carboxy-benzenesulfonium-L-alanyloxy-indole; (4-methoxycarbonyl-benzenesulfonyl) -b-alansh10xy1-indole; (4-benzyloxycarbonyl-benzenesulfonyl) -b-alanyl-oxy1-indole; (4 -carbamoyl-benzenesulfonyl) -L-alanyloxyJ-indole; 3- | m- (4 - (dimesh1carbamoyl) -bunzolsulfonishP-L-alanyloxyT -indole; (4 -carboxymethyl-benzenesulfonyl) -L-alanyloxyT-indole; 3- N- (4-carboxymethoxy-benzenesulfonyl) -b-alanyloxy-indole; (4-carboxyethylamino-benzenesulfonyl) -b-alanyloxy-indole; - (Benztoxycarbonyl-methyl amino) -benzene sulfonyl-L-alanyloxy-indole; 3- N- (4-fluoro-benzenesulfonyl) -b-alanyloxy-indole; (4-fluorosulfonyl-benzenesulfonyl) -L-alanyloxy-indole; 3-rN- (4 -sulfamoyl-benzenesulL. fonil) -L-alaminoxy-J-indole; 3-M-metsh-1- K- (toluene-4-sulfonyl) -b-alanx 1 Oxy 3 -indole; 3-N-acetyl-L- (toluene-4-sulfonyl) -L-alanyloxy-indole; (2, 4, b-trimethyl-benzenesulfonyl) - -alanyloxy-indole; (biphenyl-4-sulfonyl) -b-alanyloxy-indole; (naphthalene-2 -sulfonyl) -L-alanyloxy-indole; (4-acetylamino-naphthalene-L-sulfonyl) -L-alanyloxy-indole; (5-dimethylamino-naphthalene-1 -sulfonyl) -b-alanch1oxy-indole (xinolin-8-sulfonyl) -L-alanyloxy-indole; (pyridin-3-sulfonyl) -L-alanyloxy-indole; (2-nitro-benzenesulfonyl) -b-alanyloxy indole. Yellow to green staining: with (l -methyl-2-benzoyl-vinyl) -L-apanyloxyZ-indole; . (5, 5-dimethyl-3-oxo-cyclohexen-1 -yl) -alanyloxy-indole; (diphenylcarbamoyl) -l-alanyl-10 oxy 3 -indole; (4-nitrobenzyl) phosphoryl-L-alanyloxy-indole; 3- {N-flH- (4-bromobenzyl) -phosphoryl-L-alanyloxy} -indole; 3-p1- (toluene-4-sulfonyl) -b-alanyloxy-5-benz-1-indole; (toluene-4-sulfonyl) -b-alanyloxy-5-phenyl-indole; (toluene-4-sulfonyl) -b-alanyloxy-5-methoxy-indole.
权利要求:
Claims (4) [1] 1. DIAGNOSTIC MEANS FOR DETERMINING LEUKOCYTES IN URINE, containing a chromogen and a buffer solution, characterized in that, in order to increase its specificity, it contains an indoxyl or thionoxyl ether of the general formula where R,, Rj, R 3 , ® · 4 as a chromogen hydrogen, halogen, alkyl with 1-3 carbon atoms, lower alkoxyl, aryl, araloxyl, hydroxyl, carboxyl, carboxyalkoxyl, araloxycarbonylalkosyl, aralkyl, aralkoxycarbonyl, nitro lower acylamino group, two adjacent substituents mean substituted benzene halogen nny residue; X is a sulfur atom or an imino group substituted by a residue of lower alkyl, aryl and acyl; A is the residue of glycocol, alanine, valine, leucine, glycerol, isolecin, phenylalanine, tyrosine or 0-acetyl tyrazine, the residue of alanyl-alanine or a residue of alanyl-alanyl-alanine; B - a group of C 4 -C 6 alkoxycarbonyl, C, —C ^ alkylsulfonyl formyl, acetyl or diphenylaminocarbonyl group bonded to the nitrogen atom of the amino acids specified in A ABOUT V Ί -so-sn 2 -sn 2 -soon, or —С _ 0 _ С 2 Нц. About SPZ "> or balance C-d 0 with w -S-, -C-O, -CS-, 'Sn 3 ' o '-S- or —C = CH-C-; group h-s-, valency line or C ( -C 3 alkylene; E is phenyl, 1-naphthyl, 2-naphthyl, 2-furyl, 8-quinolyl, 2-thienyl, 3-pyridyl, cyclohexyl or N-piperidyl; R 5 , R & R and Rg may be the same or different and denote hydrogen, straight or branched C 1 -Cg alkyl, C (-Cz ~ alkoxy, nitro, halo'gen, di-C, -Cj-alkylamino, acetylamino, hydroxyl, benzyloxy, hydroxy -Cf-Cj alkoxy — C (—C e -alkoxy, methoxy-C, -C 3 -alkoxy-C ( -C 3 -alk- * -oxy, hydroxy-C, -C -Alkyl, halogen-C ^ -C 3 -alkyl, cyano ,, carboxyl, C G -C 3 ~ alkoxycarbonyl ~ benzyl, benzyloxycarbonyl, carbamoyl, dis-C, -C, -alkylcarbamoyl, carboxyl-C, -C 3 ~ -alkyl, carboxyl-C, -C 3- alkoxy, carboxyl-C, -C 3 -alkylamino or phenyl, in the following ratio, wt.%: Chromogen 0.2-9.0 Buffer solution Else [2] 2. The diagnostic tool according to π.1, characterized in that it additionally contains a wetting agent in the amount of 8.9-28.4 wt.%. [3] 3. The diagnostic tool according to claim 1, characterized in that it further comprises an oxidizing agent in an amount of 1.9-9.0 wt.%. [4] '4. The diagnostic tool according to claim 1, characterized in that it further comprises a galenic additive in an amount of 78.5 may. Z.
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公开号 | 公开日 EP0012957B1|1981-09-16| AU5383879A|1980-06-26| EP0012957A1|1980-07-09| CS245763B2|1986-10-16| PT70608A|1980-01-01| FI77229C|1989-02-10| DE2960857D1|1981-12-03| BR7908306A|1980-09-09| PL127198B1|1983-10-31| AU515190B2|1981-03-19| ES486932A1|1980-05-16| PL220526A1|1980-12-01| AR223505A1|1981-08-31| DE2854987A1|1980-06-26| YU311579A|1984-04-30| CA1130801A|1982-08-31| JPS5585561A|1980-06-27| JPS593475B2|1984-01-24| SU1156595A3|1985-05-15| HU180431B|1983-03-28| FI793986A|1980-06-21| DD147845A5|1981-04-22| FI77229B|1988-10-31| US4278763A|1981-07-14| DK155318B|1989-03-28| ZA796880B|1980-12-31| DK535679A|1980-06-21| AT230T|1981-10-15| DK155318C|1989-08-28|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 US3087794A|1960-05-23|1963-04-30|Miles Lab|Chemical test for differentiating leucocytes from erythrocytes| BE615395A|1962-03-21| GB1128371A|1965-10-04|1968-09-25|Miles Lab|Diagnostic composition| DE2118455B1|1971-04-16|1972-09-21|Boehringer Mannheim Gmbh|Test strips| US4061625A|1975-07-11|1977-12-06|Ab Kabi|Novel chromogenic thrombin substrates| JPS5263794A|1975-11-21|1977-05-26|Shionogi Seiyaku Kk|Test piece for latent blood| JPS6134439B2|1977-04-22|1986-08-07|Takeda Chemical Industries Ltd| JPS6111219B2|1977-05-30|1986-04-01|Wako Pure Chem Ind Ltd| US4216142A|1978-12-18|1980-08-05|Abbott Laboratories|Chromogenic substrates for the proteolytic enzymes|DE3005845A1|1980-02-16|1981-09-03|Boehringer Mannheim Gmbh, 6800 Mannheim|AMINO ACID AND PEPTIDESTERS OF LEUKO-INDOANILINES, METHOD FOR THE PRODUCTION THEREOF AND MEANS CONTAINING THESE COMPOUNDS FOR DETECTING PROTEOLYTIC ENZYMS| DE3017721A1|1980-05-09|1981-11-26|Boehringer Mannheim Gmbh, 6800 Mannheim|AGENT FOR DETECTING ESTEROLYTIC AND / OR PROTEOLYTIC ENZYME AND SUBSTRATES SUITABLE FOR THIS| DE3164437D1|1980-08-25|1984-08-02|Kabivitrum Ab|Peptide substrates for determination of protease activity| US4499185A|1982-05-17|1985-02-12|Miles Laboratories, Inc.|Test for esterase activity in a liquid sample| US4676950A|1984-02-03|1987-06-30|Foster Research Corporation|Indicator and test device for detecting occult blood| DE3413077A1|1984-04-06|1985-10-17|Miles Laboratories, Inc., Elkhart, Ind.|CHROMOGENEIC AMINO ACID AND PEPTIDESTERS, METHOD FOR THE PRODUCTION THEREOF, USE OF THESE COMPOUNDS IN ANALYZING METHODS AND MEANS FOR DETECTING ESTEROLYTIC AND / OR PROTEOLYTIC ENZYMES| US4637979A|1984-04-06|1987-01-20|Miles Laboratories, Inc.|Composition and test device for determining the presence of leukocytes containing a zwitterion coupling agent| US4716236A|1984-04-06|1987-12-29|Miles Laboratories, Inc.|Method for synthesizing esters| US4657855A|1984-04-06|1987-04-14|Miles Laboratories, Inc.|Composition and test device for determining the presence of leukocytes, esterase and protease in a test sample| DE3413078A1|1984-04-06|1985-10-24|Miles Laboratories, Inc., Elkhart, Ind.|CHROMOGENEIC AMINO ACID AND PEPTIDESTERS, METHOD FOR THE PRODUCTION THEREOF, USE OF THESE COMPOUNDS IN ANALYZING METHODS AND MEANS FOR DETECTING ESTEROLYTIC AND / OR PROTEOLYTIC ENZYMES| IL73998A|1984-04-06|1988-08-31|Miles Lab|Preparation of 3--pyrrole compounds| DE3412939A1|1984-04-06|1985-10-17|Behringwerke Ag, 3550 Marburg|SUBSTRATES FOR HYDROLASES, METHOD FOR THEIR PRODUCTION AND THEIR USE| US4645842A|1984-04-06|1987-02-24|Miles Laboratories, Inc.|Pyrrole compounds for detecting the presence of hydrolytic analytes| DE3446714A1|1984-12-21|1986-06-26|Boehringer Mannheim Gmbh|METHOD FOR DETECTING THE PRESENCE OF AN ALLERGY AND FOR SPECIFIC DETECTING THE ALLERGY RESPONSIBLE FOR THE ALLERGY| US5179112A|1985-04-17|1993-01-12|Ici Americas Inc.|Heterocyclic amide derivatives and pharmaceutical use| GB8607294D0|1985-04-17|1986-04-30|Ici America Inc|Heterocyclic amide derivatives| GB8623429D0|1985-10-17|1986-11-05|Ici America Inc|Carboximide derivatives| NO864131L|1985-10-17|1987-04-21|Ici America Inc|PROCEDURE FOR THE PREPARATION OF THERAPEUTIC ACTIVE INDOL AND INDAZOL-KETOSULPHONE DERIVATIVES.| GB8609175D0|1986-04-15|1986-05-21|Ici America Inc|Heterocyclic carboxamides| JP3043063B2|1989-04-27|2000-05-22|バイオコントロールシステムズインコーポレイテッド|Precipitation test for microorganisms| US5589328A|1994-08-04|1996-12-31|Mahant; Vijay K.|Chemiluminescence assays based on indoxyl substrates, thioindoxyl substrates and other substrates| US5464739A|1994-08-22|1995-11-07|Bayer Corporation|Composition method for determining the presence of leukocyte cells, esterase or protease in a test sample| CA2161574A1|1994-11-15|1996-05-16|James Noffsinger|Methodology for colorimetrically determining the concentration of white blood cells in a biological fluid| FR2751663B1|1996-07-29|1998-10-02|Bio Merieux|METHOD FOR EVIDENCE OF AN ENZYMATIC ACTIVITY OF MICROORGANISMS| DE19651886A1|1996-12-13|1998-06-18|Merck Patent Gmbh|Means and methods for the determination of hydrolytic enzymes| GB2326712B|1997-06-25|2001-09-26|Fujirebio Kk|Colour devoloping method,enzyme immunoassay using the colour developing method,and immunochromatography incorporating the enzyme immunoassay| DE19735614A1|1997-08-16|1999-02-18|Lothar Dr Seik|Detection of protease activity for insulin-like growth factor binding proteins| DE19829707C2|1998-07-03|2002-07-18|Macherey Nagel Gmbh & Co Hg|Diagnostic agent for the detection of leukocytes, elastases, esterases and proteases| US6528652B1|1999-01-21|2003-03-04|Chronimed|Composition and device for detecting leukocytes in urine| US6348324B1|1999-01-21|2002-02-19|Hypoguard America Limited|Composition and device for detecting leukocytes in urine| US6709868B2|2002-05-20|2004-03-23|Portascience Inc.|Method and apparatus for measuring white blood cell count| JP5009808B2|2004-12-13|2012-08-22|バイエル・ヘルスケア・エルエルシー|A method for distinguishing blood from a control solution containing a common analyte| GB2426334A|2005-05-20|2006-11-22|Orion Diagnostica Oy|Application of a reagent to a matrix material| US7504235B2|2005-08-31|2009-03-17|Kimberly-Clark Worldwide, Inc.|Enzyme detection technique| US7727206B2|2005-12-27|2010-06-01|Gorres Geoffrey H|Device for monitoring a patient for a urinary tract infection| US9103796B2|2007-12-14|2015-08-11|Kimberly-Clark Worldwide, Inc.|Multi-layered devices for analyte detection| US11104933B1|2016-03-22|2021-08-31|Cleu Diagnostics, Llc|Compositions and methods for determining the presence of active leukocyte cells using an electrochemical assay|
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申请号 | 申请日 | 专利标题 DE2854987A|DE2854987A1|1978-12-20|1978-12-20|DIAGNOSTIC AGENTS FOR DETECTING PROTEOLYTIC ENZYMS AND CHROMOGENS SUITABLE FOR THIS| 相关专利
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