Functionalized nanoparticles and methods of use thereof
Certain embodiments of the present invention provide functionalized nanoparticles and methods of use thereof. Certain embodiments provide nanoparticles functionalized with streptokinase. Certain embodiments of the present invention provide methods for treating a pathological fibrin associated disorder (e.g., cancer) in an animal.
1. A nanoparticle comprising a polymer and one or more units of formula (I):
A-B-C-D (I)
wherein A is poly-lactic acid or poly-(lactic-co-glycolic acid); B is poly-(ethylene glycol); C is a linking group and D is one or more moieties independently selected from tissue plasminogen activator (tPA) and recombinant tissue plasminogen activator (r-tPA), wherein the r-tPA is alteplase or reteplase.
2. The nanoparticle of claim 1 , wherein A is embedded or partially embedded in the polymer.
3. The nanoparticle of claim 1 , wherein A is poly-lactic acid.
4. The nanoparticle of claim 1 , wherein A is poly-(lactic-co-glycolic acid).
5. The nanoparticle of claim 1 , wherein the linking group is a direct bond or —OC(═O)(CH 2 ) n C(═O)O—, wherein n is 1-10.
6. The nanoparticle of claim 1 , wherein the linking group is derivable from carboxy and is —C(═O)—.
7. The nanoparticle of claim 1 , wherein the linking group is derivable from maleimide and is:
8. The nanoparticle of claim 1 , wherein D is tPA.
9. The nanoparticle of claim 1 , wherein D is reteplase.
10. The nanoparticle of claim 1 , wherein D is alteplase.
11. The nanoparticle of claim 1 , wherein the polymer is selected from poly-(lactic-co-glycolic acid), polyanhydride, poly sulfonamide, alginate, chitosan, polyethyleneimine, polyethylene glycol, poly-L-lysisne, polyglutamic acid, cellulosic derivatives, and acrylic acid based polymers.
12. The nanoparticle of claim 1 , wherein the polymer is poly (lactic-co-glycolic acid).
13. The nanoparticle of claim 1 , further comprising one or more therapeutic agents.
14. The nanoparticle of claim 13 , wherein the one or more therapeutic agents is an anti-cancer agent.
15. The nanoparticle of claim 14 , wherein the anti-cancer agent is selected from All-trans retinoic acid, Azacitidine, Azathioprine, Bleomycin, Bortezomib, Carboplatin, Capecitabine, Cisplatin, Chlorambucil, Cyclophosphamide, Cytarabine, Daunorubicin, Docetaxel, Doxifluridine, Doxorubicin, Epirubicin, Epothilone, Etoposide, Fluorouracil, Gemcitabine, Hydroxyurea, Idarubicin, Imatinib, Mechlorethamine, Mercaptopurine, Methotrexate, Mitoxantrone, Oxaliplatin, Paclitaxel, silicate prodrug of Paclitaxel, Pemetrexed, Teniposide, Tioguanine, Valrubicin, Vinblastine, Vincristine, Vindesine, Vinorelbine, a tyrosine kinase inhibitor, an antibody, trastuzumab, bevacizumab and pharmaceutically acceptable salts thereof, or combinations thereof.
16. The nanoparticle of claim 1 , further comprising one or more imaging agents independently selected from coumarin-6, SDB5491, rhodamine derivatives, cy5.5, radiolabels for PET imaging and diagnostic agents suitable for MM imaging.
17. A pharmaceutical composition comprising a nanoparticle as described in claim 1 and a pharmaceutically acceptable carrier.
18. A compound of formula (I):
A-B-C-D (I)
wherein A is poly-lactic acid or poly-(lactic-co-glycolic acid); B is poly-(ethylene glycol); C is a linking group and D is one or more moieties independently selected tissue plasminogen activator (tPA) and recombinant tissue plasminogen activator (r-tPA), wherein the r-tPA is alteplase or reteplase.
19. The compound of claim 18 , wherein the linking group is a direct bond or —OC(═O)(CH 2 ) n C(═O)O—, wherein n is 1-10.
20. The compound of claim 18 , wherein D is tPA.
21. The compound of claim 18 , wherein D is reteplase.
22. The compound of claim 18 , wherein D is alteplase.
23. A method for treating myocardial infarction in an animal, comprising administering to the animal a nanoparticle as described in claim 1 .
24. A method for treating cancer in an animal, comprising administering to the animal a nanoparticle as described in claim 14 .