http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2737025-T3

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filingDate 2013-08-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c61560e6beb873dbebd3895135c56221
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publicationDate 2020-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2737025-T3
titleOfInvention Methods and systems for screening compositions comprising sulfonated non-anticoagulant polysaccharides
abstract A method of evaluating or selecting a plurality of compositions comprising a NASP (non-anticoagulant sulfate polysaccharide) to identify a composition that is suitable for treating a subject having a blood clotting disorder, the method comprising: determining the characteristics of : the coagulation activity and chemical composition of each composition; the molecular structure of each NASP; wherein said determination of coagulation activity comprises evaluating the EC50 for the procoagulant activity of the composition by means of calibrated automated thrombography (CAT), the procoagulant window of the composition, and calculating the ratio of the procoagulant activity to the anticoagulant activity of the composition. ; wherein said determining the molecular structure comprises determining the molecular weight of the NASP, the percentage by weight of sulfur of the NASP and the content of fucosa and alginate of the NASP; and wherein said determination of the chemical composition comprises determining the elemental components of the composition, and wherein said determination of the elemental components of the composition comprises determining the impurity content of the composition; wherein said method further comprises comparing the determined characteristics of the plurality of compositions comprising a NASP; wherein said method further comprises determining that one or more of the plurality of compositions may be suitable for treating a subject having a blood clotting disorder when the composition comprises: an EC50 value for procoagulant activity of 0.3 µg / ml or less as determined by CAT; a procoagulant window of 0.1 to 100 µg / ml; a ratio of the procoagulant activity to the anticoagulant activity of the composition that is 10 or greater; a NASP molecular weight that is 160 kDa or less; a fucose content of the NASP that is 60% fucose or greater; NASP alginate content that is 10% alginate or less; a weight percentage of sulfur in the NASP that is 8% sulfur by weight or greater; and a weight percentage of impurities in the composition that is 0.1% impurities by weight or less.
priorityDate 2012-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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