Composition of imaging nanoparticles
View Patent ↗The invention relates to a method of managing a tumor of an animal subject comprising imaging the tumor by delivering a dosage of imaging nanoparticles to the tumor site, the imaging nanoparticles consisting of positively charged chitosan, optionally a zero-charge substance or bioactive agent, and a negatively charged substrate having gadolinium (Gd) chelated to the negatively charged substrate.
1. A method of managing a tumor of an animal subject comprising imaging said tumor by delivering a dosage of imaging nanoparticles to the tumor site, the imaging nanoparticles consisting of positively charged chitosan, optionally a ligand or bioactive agent, and a negatively charged substrate having gadolinium (Gd) chelated to the negatively charged substrate.
2. The method of claim 1 , wherein said chitosan is N-trimethyl chitosan, EDTA-chitosan, low molecular weight chitosan, PEG-chitosan, mono-N-carboxymethyl chitosan, chitosan derivatives, or combinations thereof.
3. The method of claim 2 , wherein said ligand is attached to a free —NH 3 group of the N-trimethyl chitosan.
4. The method of claim 1 , wherein the ligand is galactosamine.
5. The method of claim 1 , wherein the ligand includes a substrate, inhibitor, activator, or neurotransmitter.
6. The method of claim 1 , wherein said negatively charged substrate is a PGA-complexone conjugate, γ-PGA, α-PGA, derivatives of PGA, salts of PGA, or combinations thereof.
7. The method of claim 6 , wherein the PGA-complexone conjugate is PGA-DTPA or PGA-EGTA.
8. The method of claim 1 , wherein said nanoparticles are delivered via an oral route or via a parenteral route.
9. The method of claim 1 , wherein the imaging is for brain tumor enhancement associated with degradation of a blood-brain barrier.
10. The method of claim 1 , wherein said nanoparticles are encapsulated in a capsule.
11. The method of claim 10 , wherein said capsule further comprises a pharmaceutically acceptable carrier, diluent, excipient, or absorption enhancer.
12. The method of claim 10 , wherein said capsule further comprises at least a solubilizer, bubbling agent, or emulsifier.
13. The method of claim 10 , wherein said capsule is treated with an enteric coating polymer.
14. The method of claim 1 , wherein said nanoparticles are freeze-dried, thereby said nanoparticles being in a powder form.
15. The method of claim 14 , wherein said freeze-dried nanoparticles are being re-constituted with sterile water prior to being delivered to the animal subject.
16. The method of claim 1 , wherein the nanoparticles are used in enhancing imaging contrast quality or property during an imaging procedure.
17. The method of claim 1 , wherein the bioactive agent is an anti-cancer drug.
18. The method of claim 1 , wherein the nanoparticles are treated with an enteric coating polymer.
19. The method of claim 1 , wherein the method further comprises a step of targeting said tumor by enclosing a tumor targeting moiety within the nanoparticles.
20. The method of claim 1 , wherein the bioactive agent is selected from the group consisting of nystatin, antifungal agent, itraconazole, fluconazole, mesalazine, prednisone, a TNF inhibitor, azathioprine (Imuran), methotrexate, or 6-mercaptopurine.