Method of inhibiting restenosis using bisphosphonates
OwnerGershon Golomb, Haim Danenberginventors
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OwnerGershon Golomb, Haim Danenberginventors
Estimating the term…
A method of inhibiting the activity or production of cytokines or growth factors associated with vascular restenosis, by administering to an individual an effective amount of an active ingredient comprising a bisphosphonate particle or a bisphosphonate particulate. The bisphosphonate may be encapsulated, embedded or adsorbed within the particle, dispersed uniformly in the polymer matrix, adsorbed on the particle surface, or in combination of any of these forms. The particles include liposomes or inert polymeric particles, such as microcapsules, nanocapsules, nanoparticles, nanospheres, or microparticles. The particulates include any suspended or dispersed form of the bisphosphonate which is not encapsulated, entrapped, or adsorbed within a polymeric particle. The particulates include suspended or dispersed colloids, aggregates, flocculates, insoluble salts and insoluble complexes of the active ingredient. The cytokines and growth factors include, but are not limited to interleukin 1-β, matrix metalloproteinase-2, and platelet-derived growth factor β (PDGFβ).
A pharmaceutical composition comprising bisphosphonate that has been formulated into an insoluble particulate having a size of 0.01-1.0 microns, together with a pharmaceutically acceptable carrier.
A pharmaceutical composition comprising an active ingredient encapsulated in, embedded in, absorbed onto, or linked to an insoluble particle wherein the particle is non-liposomal and is selected from the group consisting of a bisphosphonate microparticle, a bisphosphonate nanoparticle, a bisphosphonate nanosphere, a bisphosphonate microcapsule, a bisphosphonate nanocapsule, and a bisphosphonate polymeric particle together with a pharmaceutically acceptable carrier, the particle having a size of 0.01-1.0 microns in diameter.
A pharmaceutical composition comprising an active ingredient encapsulated in, embedded in, absorbed onto, or linked to an insoluble particle wherein the particle is a liposome having a size of 0.01-1.0 microns in diameter.
Dependencies are inferred from the claim text.