Dendrimer based compositions and methods of using the same

• US 20070041934A1
• Filed: 08/14/2006
• Published: 02/22/2007
• Est. Priority Date: 08/12/2005
• Status: Abandoned Application

• Current Assignee: Board of Regents of the University of Michigan (University of Michigan)
• Original Assignee: Board of Regents of the University of Michigan (University of Michigan)
• Inventors: Baker, James, Shukla, Rameshwer, William, Bernell
• Application Number:
  US11/503,742
• Publication Number:
  US 20070041934A1
• Time in Patent Office: Days
• US Class Current: 424/78.300
• CPC Class Codes: A61K 31/787 containing heterocyclic rings having nitrogen as a ring hetero atom
• CPC Class Codes: C08G 73/0206 Polyalkylene(poly)amines
• CPC Class Codes: Y02A 50/30 Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Abstract

The present invention relates to novel therapeutic and diagnostic dendrimers. In particular, the present invention is directed to dendrimer based compositions and systems for use in disease diagnosis and therapy (e.g., cancer diagnosis and therapy). The compositions and systems comprise one or more components for targeting, imaging, sensing, and/or providing a therapeutic or diagnostic material and monitoring the response to therapy of a cell or tissue (e.g., a tumor).

Claims

1. A composition comprising a dendrimer, said dendrimer comprising a GCPII inhibitor.

2. The composition of claim 1, wherein said dendrimer is partially acetylated.

3. The composition of claim 1, wherein said dendrimer is a generation 5 (G5) polyamideamine (PAMAM) or polypropylamine (POPAM) dendrimer.

4. The composition of claim 1, wherein said dendrimer further comprises one or more functional groups, wherein said one or more functional groups are selected from the group consisting of a therapeutic agent, a targeting agent, an imaging agent, or a biological monitoring agent.

5. The composition of claim 1, wherein said GCPII inhibitor is 2-(Phosphonomethyl)-pentanedioic acid (2-PMPA).

6. The composition of claim 1, wherein said GCPII inhibitor and said one or more functional groups are conjugated to said dendrimer.

7. The composition of claim 4, wherein said therapeutic agent comprises a chemotherapeutic agent, an anti-oncogenic agent, an anti-angiogenic agent, a tumor suppressor agent, an anti-microbial agent, or an expression construct comprising a nucleic acid encoding a therapeutic protein.

8. The composition of claim 4, wherein said imaging agent comprises fluorescein isothiocyanate or 6-TAMARA.

9. The composition of claim 7, wherein said chemotherapeutic agent comprises methotrexate.

10. The composition of claim 9, wherein said methotrexate is conjugated to said dendrimer via an ester bond or an acid-labile linker.

11. The composition of claim 4, wherein said therapeutic agent is protected with a protecting group selected from photo-labile, radio-labile, and enzyme-labile protecting groups.

12. A method of targeting a therapeutic agent, an imaging agent or a biological monitoring agent to a cell expressing PSMA in a subject comprising providing a dendrimer comprising a GCPII inhibitor conjugated to said therapeutic agent, said imaging agent or said biological monitoring agent to said subject under conditions such that said dendrimer comprising a GCPII inhibitor interacts with said cell expressing PSMA.

13. The method of claim 12, wherein said cell expressing PSMA is a prostate specific cell.

14. The method of claim 13, wherein said prostate specific cell is a cancer cell.

15. The method of claim 14, wherein said cell expressing PSMA is a cell present within the neovasculature of a carcinoma.

16. The method of claim 12, wherein said therapeutic agent comprises a chemotherapeutic agent, an anti-oncogenic agent, an anti-angiogenic agent, a tumor suppressor agent, an anti-microbial agent, or an expression construct comprising a nucleic acid encoding a therapeutic protein.

17. The method of claim 14, wherein said method targets said cancer cell in a region of said subject outside of the prostate.

18. The method of claim 17, wherein detection of said cancer cell in a region of said subject outside of the prostate is indicative of metastasis.

19. The method of claim 12, wherein said targeting is used for staging of prostate cancer.