IP Library Granted Patent US 8,263,133
Granted Patent B2
US 8,263,133 · App. 12/708,520 · Granted Sep 11, 2012

Multivalent clustering targeting strategy for drug carriers

Assignee: The Regents of the University of California
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Quick Facts
Patent No.
US 8,263,133
App. No.
12/708,520
Granted
Sep 11, 2012
Kind
B2
Abstract

The present invention provides clustered ligand vehicles for the delivery of a nucleic acid therapeutic agent to a target expressing a receptor. The invention further provides methods for treating a disease state by targeting a nucleic acid therapeutic agent to a target expressing a receptor using clustered ligand vehicles.

Claims (16)

1. A clustered ligand vehicle for delivery of a therapeutic agent to a target expressing a receptor, said vehicle comprising:

one or more nanoparticles, each nanoparticle bearing a plurality of ligands, wherein said plurality of ligands comprises a combination of CAP peptides, wherein said CAP peptide are peptides that comprise the amino acid sequence Cys-Cys-Val-Val-Val-Thr (Seq ID NO:1): and CAP-RGD peptides, wherein said CAP-RGD peptides are peptides that comprise the amino acid sequence Cys-Cys-Val-Val-Val-Thr-Arg-Gly-Asp (SEQ ID NO:2); and

a carrier comprising said therapeutic agent, wherein each of the one or more nanoparticles is conjugated to the surface of the carrier.

2. The clustered ligand vehicle of claim 1 , wherein said CAP peptide and CAP-RGD peptides comprise a peptide selected from the group consisting of Cys-Cys-Val-Val-Val-Thr (Cap) (SEQ ID NO:1), Cys-Cys-Val-Val-Val-Thr-Arg-Gly-Asp (Cap-RGD) (SEQ ID NO:2), Cys-Cys-Val-Val-Val-Thr-Arg-Gly-Asp-Azidosalicylic Acid (Cap-RGD-ASA) (SEQ ID NO:3), and Cys-Cys-Val-Val-Val-Thr-Azidosalicylic Acid (Cap-ASA) (SEQ ID NO:4) peptides.

3. The clustered ligand vehicle according to any one of claims 1 and 2 , wherein the Cap peptides and Cap-RGD peptides are present in a ratio of from about 99:1 to about 85:15.

4. The clustered ligand of claim 3 , wherein the ratio of Cap peptides to Cap-RGD peptides is selected to promote clustering.

5. The clustered ligand vehicle of claim 1 , wherein said one or more nanoparticles are conjugated to the carrier by covalent bonding.

6. The clustered ligand vehicle of claim 1 , wherein the carrier comprises a cationic polymer.

7. The clustered ligand vehicle of claim 1 , wherein the carrier comprises poly(ethylene imine).

8. The clustered ligand vehicle of claim 1 , wherein the therapeutic agent comprises an agent selected from the group consisting of DNA, interfering RNA, small inhibitory RNA, and a ribozyme.

9. The clustered ligand vehicle of claim 8 , wherein the therapeutic agent comprises DNA.

10. The clustered ligand vehicle of claim 1 , wherein the therapeutic agent comprises DNA and the carrier comprises poly(ethylene imine).

11. The clustered ligand vehicle of claim 1 , wherein the clustered ligand vehicle is not larger than 200 nm in diameter.

12. The clustered ligand vehicle of claim 1 , wherein said one or more nanoparticles comprise a material selected from the group consisting of a metal, a semiconductor, and carbon.

13. The clustered ligand vehicle of claim 1 , wherein said one or more nanoparticles comprise gold.

14. The clustered ligand vehicle of claim 1 , wherein said one or more nanoparticles are conjugated to the carrier by a cross-linker.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 1, 2010
From: SEGURA, TATIANA; NG, QUINN
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 024624/0006 →
Continuity (2)
Provisional Application 61153581 · Feb 18, 2009
Related Publication 20100266695A1 · Oct 21, 2010