http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S54122711-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K38-17
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K35-14
filingDate 1978-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a03b3347ea2a52318d01afe03b799fb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2c4ea4a33b874d713cb0d0579d5fd1d
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publicationDate 1979-09-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S54122711-A
titleOfInvention Preparation of blood extract solution
abstract PURPOSE: To prepare a blood extract solution having excellent aging stability and excellent pharmacological activity, and free from precipitation and pH variation, by the successive treatments comprising removal of fibrin from the blood of a low- potassium animal, hemolyzation, removal of protein, concentration, pH adjustment, removal of precipitate, and degassing. n CONSTITUTION: Animal blood containing ≤80 mg/1 of potassium, usually cattle blood, is stirred, and after separating and removing the formed fibrin from the blood, hemolyzed by the freezing and thawing. Protein is removed from the hemolyzed blood by dialysis using distilled water as ecternal liquid. The product is concentrated at 30W60°C under reduced pressure to a solid concentration of about 30W60 mg/ml. The objective blood extract solution is obrained by adjusting the pH of the solution between 9.5 and 11.5, removing the precipitate, and finally removing the dissolved gas at pH≤5. n COPYRIGHT: (C)1979,JPO&Japio
priorityDate 1978-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 20.