http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104758244-A

Outgoing Links

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
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filingDate 2015-04-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb14ca098017356fcf0e9e3e92ff64f2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5e82bf5736c7171419fd68552f650824
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publicationDate 2015-07-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104758244-A
titleOfInvention A nanogel, its preparation method, anti-tumor nanogel drug-loading system and its preparation method
abstract The application provides a nanogel and a preparation method thereof. In the presence of a phenylboronic acid initiator and a morpholine initiator, the L-glutamic acid oligoethylene glycol monomethyl ether ester-N-ring The internal acid anhydride is reacted in an organic solvent to obtain a reaction liquid; the reaction liquid is mixed with L-cystine-N-cyclic internal acid anhydride and L-phenylalanine-N-cyclic internal acid anhydride to react to obtain a nano-condensate glue; it includes phenylboronic acid group, morpholine group, glutamic acid oligoethylene glycol monomethyl ether ester chain link, phenylalanine chain link and cystine link; bonds to form a cross-linked network structure. The invention provides an anti-tumor nano gel drug-carrying system and a preparation method thereof. The surface of the drug-loaded particles has phenylboronic acid and morpholine groups to promote tumor targeting and endocytosis. In the present invention, a nanogel structure is formed through disulfide bond cross-linking, and after targeted enrichment and endocytosis at tumor sites, the drug-loaded particles can rapidly release drugs to achieve the effect of inhibiting tumors.
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priorityDate 2015-04-21-04:00^^<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: 34.