http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102212197-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_be2c55a9de09e08e3404c0a5a1ae4dc7
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K47-34
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filingDate 2011-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d182ef94fad363cedb96cf2d1cb709c6
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publicationDate 2011-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102212197-A
titleOfInvention Hyperbranched star polylactic acid-polydimethylaminoethyl methacrylate amphiphilic block copolymer and preparation method thereof
abstract The invention relates to a hyperbranched star polylactic acid-polydimethylaminoethyl methacrylate amphiphilic block copolymer and a preparation method thereof. The preparation method comprises the following steps of: synthesizing a hyperbranched star amphiphilic polymer of which the surface contains a cationic group and a core has a hydrophobic structure by an arm-first method, and synthesizing polydimethylaminoethyl methacrylate containing a terminal alkynyl functional group through atom transfer radical polymerization by taking an esterification reaction product 2-butynol ester bromoisobutyrate of butynol and 2-bromoisobutyryl bromide as an initiator, and cuprous bromide and 1,4,7,10,10-hexamethyltriethylenetetramine as a catalyst system; synthesizing polylactic acid containing a nitrine functional group by a lactide ring-opening polymerization method by taking pentaerythritol tribromide azide as the initiator and stannous octoate as a catalyst, and performing an esterification reaction of an obtained product and trimesoyl chloride to synthesize star polylactic acid azide, namely a star polymer core; and coupling a polydimethylaminoethyl methacrylate arm with the polylactic acid containing the nitrine functional group to obtain the A3 (B3) 3 type star polylactic acid-polydimethylaminoethyl methacrylate amphiphilic block copolymer. The hyperbranched star polymer prepared by the method has high biocompatibility and stability, and has good application prospect in the aspect of antitumor medicine carriers.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104629059-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104629059-B
priorityDate 2011-05-10-04:00^^<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: 24.