Biodegradable injectable nanoparticles
AssigneeMassachusetts Institute of Technology
InventorsRuxandra Gref, Yoshiharu Minamitake, Robert S. Langer
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AssigneeMassachusetts Institute of Technology
InventorsRuxandra Gref, Yoshiharu Minamitake, Robert S. Langer
Estimating the term…
Particles are provided that are not rapidly cleared from the blood stream by the macrophages of the reticuloendothelial system, and that can be modified to achieve variable release rates or to target specific cells or organs. The particles have a biodegradable solid core containing a biologically active material and poly(alkylene glycol) moieties on the surface. The terminal hydroxyl group of the poly(alkylene glycol) can be used to covalently attach onto the surface of the particles biologically active molecules, including antibodies targeted to specific cells or organs, or molecules affecting the charge, lipophilicity or hydrophilicity of the particle. The surface of the particle can also be modified by attaching biodegradable polymers of the same structure as those forming the core of the particles.
A nonoparticle or microparticle formed of a block copolymer consisting essentially of poly(alkylene glycol) and a biodegradable polymer selected from the group consisting of polyanhydride, polyhydroxybutyric acid, polyorthoesters, polysiloxanes, polycaprolactone, and copolymers prepared from the monomers of these polymers, wherein the biodegradable moieties of the copolymer are in the core of the resulting particle, and the poly(alkylene glycol) moieties are on the surface of the resulting particle in an amount effective to decrease uptake of the nanoparticle or microparticle by the reticuloendothelial system.
A nanoparticle or microparticle formed of a block copolymer consisting essentially of poly(alkylene glycol) and a biodegradable polymer selected from the group consisting of polyanhydrides, polyhydroxybutyric acid, polyorthoesters, polysiloxanes, polycaprolactone, poly(lactic-co-glycolic acid), poly(lactic acid), poly(glycolic acid) and copolymers prepared from the monomers of these polymers, wherein the biodegradable moieties of the copolymer are in the core of the resulting particle, and the poly(alkylene glycol) moieties are on the surface of the resulting nanoparticle or microparticle in an amount effective to decrease uptake of the nanoparticle or microparticle by the reticuloendothelial system, and wherein the copolymer is a diblock or multiblock copolymer comprising two or more poly(alkylene glycol) blocks.
A nanoparticle or microparticle formed of a block copolymer consisting essentially of poly(alkylene glycol) and a polymer selected from the group consisting of poly(lactic-co-glycolic acid), poly(lactic acid), and poly(glycolic acid), wherein the copolymer is blended with poly(lactic-co-glycolic acid) prior to forming the particle, and wherein the biodegradable moieties of the copolymer are in the core of the resulting particle, and the poly(alkylene glycol) moleties are on the surface of the resulting nanoparticle or microparticle in an amount effective to decrease uptake of the nanoparticle or microparticle. by the reticuloendothelial system.
A method for making a nanoparticle or microparticle with a core and a surface comprising:
A method for making a nanoparticle or microparticle with a core and a surface comprising:
A method for making a nanoparticle or microparticle with a core and a surface comprising:
A method for delivering a substance to a patient comprising administering to the patient a composition comprising nanoparticles or microparticles comprising a therapeutic or detectable amount of a substance to be delivered to a patient in need thereof and a block copolymer consisting essentially of poly(alkylene glycol) and a biodegradable polymer selected from the group consisting of polyanhydride, polyhydroxybutyric acid, polyorthoesters, polysiloxanes, polycaprolactone, and copolymers prepared from the monomers of these polymers, wherein the biodegradable moieties of the copolymer are in the core of the resulting particle, and the poly(alkylene glycol) moieties are on the surface or the resulting particle in an amount effective to decrease uptake of the nanoparticle or microparticle by the reticuloendothelial system.
Dependencies are inferred from the claim text.