发明名称 Nanoparticle-based tumor-targeted drug delivery
摘要 The present invention provides an aqueous tumor-targeting liposome nanoparticle composition comprising an aqueous dispersion of liposome nanoparticles. The nanoparticles preferably encapsulate an anti-cancer chemotherapeutic agent, which can be added to a pre-formed liposome composition or can be incorporated in the liposomes during the formation of the liposomes. The liposome nanoparticles comprise a legumain-targeting lipid admixed with one or more other micelle or vesicle-forming lipid materials in the form of nanoparticulate liposomes dispersed in an aqueous carrier. A preferred tumor-targeting liposome nanoparticle composition comprises (a) a legumain-targeting lipid component, (b) a zwitterionic lipid component; (c) an amino-substituted lipid component; (d) a neutral lipid component; and (e) polyethylene glycol-conjugated lipid component. The legumain-targeting lipid component comprising a hydrophobic lipid portion covalently attached to a legumain-binding moiety.
申请公布号 US9616137(B2) 申请公布日期 2017.04.11
申请号 US201113224399 申请日期 2011.09.02
申请人 The Scripps Research Institute 发明人 Reisfeld Ralph A.;Xiang Rong;Luo Yunping;Liao Debbie;Liu Ze;Chen Tingmei;Chen Si;Lu Dan
分类号 A61K47/48;B82Y5/00;A61K9/127 主分类号 A61K47/48
代理机构 Olson & Cepuritis, Ltd. 代理人 Olson & Cepuritis, Ltd.
主权项 1. A nanoparticle composition comprising lipid nanoparticles in which the nanoparticles include a lipid comprising a lipid component covalently bound to a legumain-binding moiety; wherein the lipid comprises a compound of Formula (II): wherein the lipid is admixed with one or more micelle or vesicle-forming lipid materials in the nanoparticles; and the legumain-binding moiety comprises an aza-Asn legumain inhibitor.
地址 La Jolla CA US