Multifunction nanoconjugates for imaging applications and targeted treatment
The present invention relates to nanoconjugates. In particular, the present invention provides nanoconjugates for diagnostic (e.g., imaging), research, and clinical (e.g., targeted treatment) applications.
1. A multifunctional nanoconjugate comprising:
a) a nanoparticle comprising a magnetic or superparamagnetic iron oxide core covered by a TiO 2 nanoparticle shell;
b) at least one biological molecule conjugated to said nanoparticle core; and
c) an imaging contrast agent conjugated to the surface of said nanoparticle, wherein said imaging contrast agent comprises PGA-1,6-hexanediamine-(Gd-DOTA)-dopamine.
2. The nanoconjugate of claim 1 , wherein said nanoparticles are between 100 nm and 0.1 nm in diameter.
3. The nanoconjugate of claim 2 , wherein said nanoparticles are approximately 5 nm in diameter.
4. The nanoconjugate of claim 1 , wherein said biological molecule is selected from the group consisting of a nucleic acid, a peptide-nucleic acid (PNA), a peptide, a polypeptide and an antibody.
5. The nanoconjugate of claim 4 , wherein said biological molecule specifically intertacts with an in vivo target.
6. The nanoconjugate of claim 4 , wherein said in vivo target is a cancer marker.
7. The nanoconjugate of claim 1 , wherein said nanconjugate further comprises a therapeutic agent.
8. The nanoconjugate of claim 7 , wherein said therapeutic agent is selected from the group consisting of a chemotherapeutic agent and a photosensitizer agent for photodynamic therapy.
9. The nanoconjugate of claim 1 , wherein said PGA-1,6-hexanediamine-(Gd-DOTA)-dopamine comprises 28 molecules of gadolinium.
10. A method of targeting an in vivo target, comprising:
contacting an organism with the nanoconjugate of claim 1 under conditions such that said nanoconjugate interacts with said in vivo target.
11. The method of claim 10 , wherein said nanoparticles are between 100 nm and 0.1 nm in diameter.
12. The method of claim 11 , wherein said nanoparticles are approximately 5 nm in diameter.
13. The method of claim 10 , further comprising the step of visualizing said nanoconjugate in said organism.
14. The method of claim 13 , wherein visualizing said imaging agent utilizes an imaging technique selected from the group consisting of X-ray imaging, computer tomography (CT) imaging, and magnetic reasonance imaging (MRI).
15. The method of claim 10 , wherein said biological molecule is selected from the group consisting of a nucleic acid, a PNA, a peptide, a polypeptide and an antibody.
16. The method of claim 10 , wherein said in vivo target is a cancer marker.
17. The method of claim 10 , further comprising the step of destroying said in vivo target.
18. The method of claim 17 , wherein the step of destroying said in vivo target comprises a technique selected from the group consisting of neutron capture therapy by said nanoconjugate or generation of reactive oxygen species by said nanoconjuqate.
19. The method of claim 17 , said nanoconjugate further comprising a therapeutic agent and wherein the step of destroying said in vivo target comprises contacting said in vivo target with said therapeutic agent.
20. The method of claim 19 , wherein said therapeutic agent is selected from the group consisting of a chemotherapeutic agent and a photosensitizer agent for photodynamic therapy.