http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2016038607-A1

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filingDate 2014-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_97ca431a8b95a2e5a4a27a09c70254c9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_13326600cea66999a95e043e68cc4855
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publicationDate 2016-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2016038607-A1
titleOfInvention Nanoparticle drug delivery systems
abstract The invention provides pharmaceutical compositions and method of using the compositions, wherein the compositions comprise liposomes or micelles that contain one or more targeting peptides and/or anticancer drugs. In various embodiments, the components of the liposomes can include a) a phospholipid and optionally a lipid that is not a phospholipid; b) a pegylated lipid; c) a peptide-ethylene glycol (EG)-lipid conjugate wherein the peptide is a targeting ligand, and d) one or more drug-conjugated lipid, encapsulated drugs, or a combination thereof. The peptide-EG-lipid conjugate can be, for example, a compound of Formula (I) or Formula (II). The ethylene glycol (EG) segments of the peptide-EG-lipid conjugate can be, for example, EG6 to about EG36; and the EG segment can be conjugated to one or more lysine moieties.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2016375072-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2021361575-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2014341973-A1
priorityDate 2013-02-04-04:00^^<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: 470.