http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102614135-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_69c4789fc0d026b6389737378673435f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-19
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-00
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-42
filingDate 2012-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f708a5a3e7a6afc93e1535923937bfa3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3781e7acc8cf62070a72747fdbd44f9d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_087319599fe11590ed92684740e0cc0b
publicationDate 2013-08-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102614135-B
titleOfInvention Cytidine disodium triphosphate suspension powder injection and preparation method thereof
abstract The invention relates to novel preparation formulation of cytidine disodium triphosphate, in particular to cytidine disodium triphosphate suspension powder injection and a preparation method thereof. The powder-injection comprises the following components as per parts by weight: 1 part of cytidine disodium triphosphate, 0.1 to 10 parts of surface active agent and 2 to 15 parts of cryoprotectant. The powder injection improves the stability of cytidine disodium triphosphate, can be slowly administrated in body for a long time, and greatly improves the bioavailability. Protein of the surface active agent (stabilizing agent) is degraded in body, has no toxicity and immunogenicity, can effectively increase the pharmacological treatment index, and reduces the drug toxicity and the drug side-effect.
priorityDate 2012-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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