http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-102017011629-A2

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00
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filingDate 2017-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42ae9a716ed76ffaab7804e897e9071c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_82c5b3ce850df3755f2ba06e6982f4c8
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publicationDate 2018-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-102017011629-A2
titleOfInvention nanomicelles formed from methotrexate-conjugated poloxamer and incorporated from etoposide for the treatment of retinoblastoma and other malignant tumors
abstract nanomicelles formed from methotrexate - conjugated poloxamer and incorporated from etoposide for the treatment of retinoblastoma and other malignant tumors. The present invention relates to a pharmaceutical formulation composed of nanomicelles formed from methotrexate-conjugated poloxamer and incorporated by etoposide for the treatment of retinoblastoma and other malignant tumors. The aforementioned pharmaceutical formulation is composed of micellar nanometric systems formed by the methotrexate-conjugated poloxamer, which is positioned on the micellar surface, and incorporated with antitumor hydrophobic drugs, especially etoposide, present in the micellar hydrophobic nucleus. These nanomicels may be administered by the intraocular and / or parenteral routes. The formulation may be internalized by tumor cells expressing reduced folate and folate transporters due to the presence of methotrexate on the micellar surface. As a folic acid analogue, methotrexate acts as a recognition element for tumor cells. After cell uptake, methotrexate and etoposide are released to exert specific antitumor action. In addition, prolonged exposure of these drugs within the cell also ensures disruption of the cell cycle. poloxamer also exerts antiproliferative action. The proposed formulation further promotes antitumor effect specifically on tumor cells, which leads to the reduction of systemic side and / or toxic effects resulting from chemotherapy. In addition, it protects the incorporated etoposide from degradation processes due to ph variations and ensures its increased solubility in biological fluids, as well as that of other antineoplastic agents that have low aqueous solubility in the fluids.
priorityDate 2017-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID36462
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419506512
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID827177
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID180093
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID821250
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID189649

Total number of triples: 315.