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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-704
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-704
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-60
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-61
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
filingDate 2016-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-01-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105943496-B
titleOfInvention The adriamycin bonded pro-drug of galactose chitosan-polyethylene glycol polymer and its preparation and use of pH response
abstract PH response adriamycin bonded pro-drug of galactose chitosan-polyethylene glycol polymer that the present invention relates to a kind of with neighboring group effect and preparation method thereof and purposes in medicine.It is characterized in that: (1) monomethyl ether polyethylene glycol first pass around carboxylated, then forms amido bond with amino in galactose chitosan, chitosan-polyethylene glycol medicine carrier is prepared;(2) amino in histidine and glutaraldehyde react to obtain the histidine with aldehyde radical;(3) amino on adriamycin is protected, then carries out the esterification of hydroxyl in histidine carboxyl and adriamycin, be then deprotected;(4) the histidine adriamycin ester containing aldehyde radical and chitosan-polyethylene glycol carry out schiff base reaction, and are restored with sodium cyanoborohydride;(5) carrier micelle is prepared by dialysis;(6) carrier micelle prepared by has good pH responsiveness and hepatic targeting, can further develop to treat the novel targeted preparation of liver cancer.
priorityDate 2016-04-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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