http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2018151602-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_18e7652388f26aef216235b6cb71e0bc |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-974 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N2333-968 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G01N33-86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-56 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-86 |
| filingDate | 2018-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d344f2671aa5e68aa78b25552d8092a |
| publicationDate | 2018-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | WO-2018151602-A1 |
| titleOfInvention | Self-calibrated assay for determining proteolytic enzyme generation, dedicated means and uses thereof |
| abstract | A method is described to measure the course of enzyme activity when a proteolytic enzyme is generated in a sample of blood or plasma. The activity, like in previous art, is monitored through its action on a substrate that upon action of the enzyme releases a fluorescent product. Contrary to previous art a small fluorescent moiety is made to be present at zero time, either because the substrate itself has native fluorescence or because a small amount of fluorescent product (0.1 - 10 mole % of the concentration of substrate) is added before the reaction starts, giving rise to a small initial signal (F o ). Also, the maximal signal (F max ), occurring when all substrate has been converted into product is determined. The experimental fluorescent signal (F exp .t) is converted into the normalized ratio of the signal (R t ) according to the formula R t =(F exp.t -F o )/(F max -F o ). It is demonstrated that the course of enzyme activity (Et) can be obtained from: E t =dR t /dt.(S o +K m /(1 -R t ))/k cat . The use of this method has the following advantages: • Strong reduction of experimental noise • No external calibration is required, i.e. no second sample with known enzymatic activity has to be used. • No correction for substrate consumption is required. • Thrombin or plasmin generation curves obtained with macromolecular substrates can be calibrated despite the fact that such substrates are insensitive to the action of α2macroglobulin- thrombin complexes. |
| priorityDate | 2017-02-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 145.