Magnetic tracer compositions
AssigneeFerronova Pty Ltd
InventorsStewart Gavin BARTLETT, Melanie Ruth Maria NELSON, Benjamin THIERRY, Aidan COUSINS, Thi Hanh Nguyen PHAM, Brian Stanley HAWKETT
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Abstract
Disclosed herein are pharmacologically acceptable magnetic nanoparticles suitable for administration to a subject.
Claims20
A pharmacologically acceptable magnetic nanoparticle suitable for administration to a subject, the magnetic nanoparticle having a polymer composition coating, the polymer composition comprising:
- (i) a polymeric steric stabilizer that promotes dispersion of the magnetic nanoparticles in a liquid, the polymeric steric stabilizer comprising (i) an anchoring polymer segment having one or more binding groups that bind the polymeric steric stabilizer to the magnetic nanoparticle, and (ii) a steric stabilizing polymer segment comprising a polyacrylamide-co-polyalkylene oxide block copolymer, wherein the anchoring polymer segment is different from the steric stabilizing polymer segment;
- and
- (ii) a polymeric targeting moiety, comprising (i) an anchoring polymer segment having one or more binding groups that bind the polymeric targeting moiety to the magnetic nanoparticle, (ii) a linking polymer segment consisting of polyacrylamide, wherein the anchoring polymer segment is different from the linking polymer segment, and (iii) one or more targeting groups, each targeting group independently being a monosaccharide group for selectively targeting monosaccharide receptors, or an antibody, an antibody fragment, or an inhibitor for selectively targeting Prostate Specific Membrane Antigen (PSMA).
The pharmacologically acceptable magnetic nanoparticle of claim 8, wherein the linker has (i) more polymerized monomer residue units than the steric stabilising polymer segment and (ii) about 10 to about 100 polymerized monomer residue units.
The pharmacologically acceptable magnetic nanoparticle of claim 8, wherein the linker consists of polyacrylamide.
Dependencies are inferred from the claim text.