http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100871988-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K47-34
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-30
filingDate 2007-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_84b581e82bc05d514bf5f08110b2e363
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a6e2b10416e1281935962511479a484f
publicationDate 2008-12-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100871988-B1
titleOfInvention Method for preparing biodegradable microsphere carrier in which water-soluble macromolecular drug is encapsulated without water-soluble solvent and biodegradable microsphere carrier
abstract The present invention provides a biodegradable microsphere carrier using a polyester-based polymer on a single organic solvent by dissolving a water-soluble macromolecular drug in an organic solvent using polyethylene glycol in an organic solvent or dispersing it in nano size without using an aqueous solution. The present invention relates to a biodegradable polymer microsphere carrier prepared by the method, and the biodegradable polymer microsphere carrier according to the present invention does not use an aqueous solution during the manufacturing process, so that an interface of an organic solvent / aqueous solution does not occur, so that it is water-soluble such as a protein. It has the advantage of not denaturing the properties of macromolecular drugs.
priorityDate 2007-06-25-04:00^^<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: 539.