发明名称 Composition and method for sulfated non-anticoagulant low molecular weight heparins in cancer and tumor metastasis
摘要 A nanoformulation that includes nanoparticles. Each nanoparticle includes a shell in which a glycosaminoglycan (GAG is encapsulated. The GAG is ionically or covalently bonded to the shell. The GAG is selected from the group consisting of sulfated non-anticoagulant heparin (SNACH), super-sulfated non-anticoagulant heparin (S-SNACH), and a combination thereof. The shell includes Poly (lactic-co-glycolic acid) (PLGA), Polyethylene Glycol (PEG)-PLGA, maleimide-PEG-PLGA, chitosan, chitosan-PLGA, methoxy-polyethyleneglycol-poly (lactide-co-glycolide) (MPEG-PLGA)-(maleimide-PEG-PLGA), PLGA-Polycaprolate, or calcium alginate. A method of using the nanoformulation to treat a cancer in a subject includes administering to the patient a therapeutically effective amount of the nanoformulation for treating the cancer.
申请公布号 US9572831(B2) 申请公布日期 2017.02.21
申请号 US201414526660 申请日期 2014.10.29
申请人 Mousa Shaker A. 发明人 Mousa Shaker A.
分类号 A61K31/704;A61K31/727;A61K47/48;A61K31/7068;A61K33/24 主分类号 A61K31/704
代理机构 Schmeiser, Olsen & Watts, LLP 代理人 Schmeiser, Olsen & Watts, LLP
主权项 1. A nanoformulation, comprising: nanoparticles, each nanoparticle comprising a shell within which a glycosaminoglycan (GAG) is encapsulated, said GAG being ionically or covalently bonded to the shell, wherein the GAG is selected from the group consisting of sulfated non-anticoagulant heparin (SNACH), super-sulfated non-anticoagulant heparin (S-SNACH), and a combination thereof, and wherein the shell comprises Poly(lactic-co-glycolic acid) (PLGA), Polyethylene Glycol (PEG)-PLGA, maleimide-PEG-PLGA,chitosan, chitosan-PLGA, a blend of methoxy-polyethyleneglycol-poly(lactide-co-glycolide)(MPEG-PLGA) and maleimide-PEG-PLGA, or calcium alginate, wherein the nanoparticles are conjugated to Poly L-arginine via an amide link between the GAG and the Poly L-arginine, wherein the shell encapsulates a chemotherapeutic agent for treating cancer, and wherein a targeted moiety is conjugated to the shell of the nanoparticle to effectuate a targeted delivery of the nanoparticle to a specified target for increasing the efficacy of the chemotherapeutic agent.
地址 Wynantskill NY US