http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-100794449-B1

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filingDate 2007-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fce2598a17f88fa3e9a22b697c3a5b0f
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publicationDate 2008-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-100794449-B1
titleOfInvention Cationic Phospholipid Nanoparticle Compositions for Nucleic Acid Delivery
abstract The present invention provides 1,2-dioleoyl-sn-glycero-3-ethylphosphocholine (1,2-dioleoyl-sn-glycero-3-ethylphosphocholine, EDOPC), 3b- [N- (N ', N '-Dimethylaminoethane) -carbamyl] cholesterol (3b- [N- (N' (N ', N'-dimethylaminoethane) -cabamyl] cholesterol, DC-cholesterol) and 1,2-dipitanoyl-sn-glycero-3 A cationic phospholipid liposome composition comprising phosphoethanolamine (1,2-diphytanoyl-sn-glycero-3-phosphoethanolamine, DPhPE), a liposome-nucleic acid complex forming a complex thereof, and a pharmaceutical composition comprising the same . The cationic phospholipid liposomes of the present invention have a nanoparticle diameter in the range of 30 to 450 nm, and are effective for reducing intracellular nucleic acid delivery ability and cytotoxicity as compared to conventional liposomes, and thus can be usefully used for gene therapy by introducing nucleic acids into cells. have.
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