http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-108728496-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K48-0041
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G83-004
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G69-48
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G83-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K48-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G69-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-87
filingDate 2018-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2021-09-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-108728496-B
titleOfInvention Polycation gene vector, preparation method and application thereof
abstract The invention provides a polycation gene vector, a preparation method and application thereof, wherein the polycation gene vector comprises a grafting framework and arginine protected by tosyl grafted with the grafting framework; the raw material of the grafting framework is selected from dendritic polyamide-amine, hyperbranched polylysine with molecular weight of 2000-100000 g/mol or linear epsilon-polylysine with molecular weight of 2000-50000 g/mol; the dendritic polyamidoamine is selected from one or more of model PAMAM-G3, model PAMAM-G4 and model PAMAM-G5. The polycation gene vector provided by the invention grafts the arginine protected by the tosyl on a specific grafting framework, and can obviously improve the transfection efficiency of the compound nanoparticles prepared by the polycation vector. In addition, the charge density of the nano-composite particles can be effectively reduced, and the cytotoxicity of the nano-composite particles is further reduced.
priorityDate 2018-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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