http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2093831-C1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3f0579cce196bf72d7d54444b3f5391d |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-52 |
| filingDate | 1994-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1997-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1bba542ae6c4cbba626ada7d43d32a34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bcc73745d6be326689a640740a1ffa95 |
| publicationDate | 1997-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2093831-C1 |
| titleOfInvention | Method of determination of creatinine concentration in biological fluids |
| abstract | FIELD: medicinal and clinical biochemistry, analytical biochemistry. SUBSTANCE: examined blood or urea sample in incubated with picric acid for 20 min firstly in alkaline medium and then optical density of reaction mixture is measured. Then mixture is acidified with buffer solution glycine- HCl to pH = 3.5-5.0, incubated for 15 min and optical density of reaction mixture is measured again. For mixture acidification 3.2 M glycine-HCl buffer, pH = 2.2 is used mainly. Creatinine concentration is calculated by difference of optical densities of reaction mixture in alkaline and acid medium. EFFECT: improved method of analysis. 2 cl, 1 dwg |
| priorityDate | 1994-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 26.