Carrier-antibody compositions and methods of making and using the same
AssigneeMayo Foundation for Medical Education and Research
InventorsSvetomir N. MARKOVIC, Wendy K. NEVALA
Life of this patent
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Abstract
Described herein are compositions of antibodies and carrier proteins and methods of making and using the same, in particular, as a cancer therapeutic. Also described are lyophilized compositions of antibodies and carrier proteins and methods of making and using the same, in particular, as a cancer therapeutic.
Claims30
A lyophilized nanoparticle composition comprising nanoparticles having an outer surface, wherein each of the nanoparticles comprises:
- a) a carrier protein;
- b) between about 100 to about 1000 bevacizumab antibodies having a hydrophobic Fc portion and an antigen-binding portion;
- and
- c) optionally at least one therapeutic agent;
- said nanoparticles being lyophilized, and wherein upon reconstitution with an aqueous solution the antigen-binding portion of said antibodies are arranged on the outside surface of the nanoparticles and are capable of binding to VEGF in vivo and the Fc portion is associated with said carrier protein.
A lyophilized nanoparticle composition comprising nanoparticles having an outer surface, wherein each of the nanoparticles comprises:
- a) a carrier protein;
- b) between about 100 to about 1000 rituximab antibodies having a hydrophobic Fc portion and an antigen-binding portion;
- and
- c) optionally at least one therapeutic agent;
- said nanoparticles being lyophilized, and wherein upon reconstitution with an aqueous solution the antigen-binding portion of said antibodies are arranged on the outside surface of the nanoparticles and are capable of binding to CD20 in vivo and the Fc portion is associated with said carrier protein.
A lyophilized nanoparticle composition comprising nanoparticles having an outer surface, wherein each of the nanoparticles comprises:
- a) a carrier protein;
- b) between about 100 to about 1000 trastuzumab antibodies having a hydrophobic Fc portion and an antigen-binding portion;
- and
- c) optionally at least one therapeutic agent;
- said nanoparticles being lyophilized, and wherein upon reconstitution with an aqueous solution the antigen-binding portion of said antibodies are arranged on the outside surface of the nanoparticles and are capable of binding to HER2 in vivo and the Fc portion is associated with said carrier protein.
Dependencies are inferred from the claim text.