IP Library Granted Patent US 8,916,606
Granted Patent B2
US 8,916,606 · App. 13/504,716 · Granted Dec 23, 2014

Therapeutic compositions and methods for targeted delivery of active agents

Inventors: James M. Tour (Bellaire, TX); Jacob Berlin (Monrovia, CA); Tam Pham (Renton, WA); Jeffrey N. Myers (Bellaire, TX); Daisuke Sano (Yokohama, JP)
Assignees: William Marsh Rice University; Board of Regents, The University of Texas System
C07K16/2854B82Y5/00A61K51/1268A61K47/48884A61K47/48961Y10S977/75Y10S977/746Y10S977/906Y10S977/842
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Quick Facts
Patent No.
US 8,916,606
App. No.
13/504,716
Granted
Dec 23, 2014
Kind
B2
Abstract

The present invention pertains to therapeutic compositions that comprise: (1) a nanovector, (2) an active agent; and (3) a targeting agent, wherein the active agent and the targeting agent are non-covalently associated with the nanovector. The present invention also pertains to methods of treating various conditions in a subject by utilizing the above-described therapeutic compositions. Methods of making the therapeutic compositions are also a subject matter the present invention.

Claims (41)

1. A therapeutic composition comprising:

a. a nanovector,

wherein said nanovector comprises an oxidized and ultra-short single-walled carbon nanotube (US-SWNT),

wherein said US-SWNT has open ends,

wherein said US-SWNT has lengths ranging from 20 nm to 80 nm,

wherein said nanovector is polyethylene-glycol-functionalized, and

wherein said nanovector is soluble in water;

b. an active agent non-covalently associated with said nanovector,

wherein said active agent comprises an anti-cancer drug; and

c. a targeting agent non-covalently associated with said nanovector,

wherein said targeting agent comprises an antibody.

2. The therapeutic composition of claim 1 , wherein said active agent is selected from the group consisting of small molecules, proteins, DNA, antisense oligonucleotides, miRNA, siRNA, and aptamers.

3. The therapeutic composition of claim 1 , wherein said active agent is Paclitaxel.

4. The therapeutic composition of claim 1 , wherein said targeting agent comprises a monoclonal antibody.

5. The therapeutic composition of claim 1 , wherein said targeting agent is an anti-epidermal growth factor receptor antibody.

6. A method of treating a condition in a subject, said method comprising administering a therapeutic composition to said subject, wherein said therapeutic composition comprises:

a. a nanovector,

wherein said nanovector comprises an oxidized and ultra-short single-walled carbon nanotube (US-SWNT),

wherein said US-SWNT has open ends,

wherein said US-SWNT has lengths ranging from 20 nm to 80 nm,

wherein said nanovector is polyethylene-glycol-functionalized, and

wherein said nanovector is soluble in water;

b. an active agent non-covalently associated with said nanovector,

wherein said active agent comprises an anti-cancer drug; and

c. a targeting agent non-covalently associated with said nanovector,

wherein said targeting agent comprises an antibody.

7. The method of claim 6 , wherein said active agent comprises Paclitaxel, and said targeting agent comprises Cetuximab.

8. The method of claim 6 , wherein said subject is a human being.

9. The method of claim 6 , wherein said administering said therapeutic agent comprises intravenous administration.

10. The method of claim 6 , further comprising administering radiation to said subject before, during or after said administering of said therapeutic composition.

11. A method of making a therapeutic composition, said method comprising:

a. non-covalently associating a nanovector with an active agent

wherein said active agent comprises an anti-cancer drug, and

wherein said nanovector comprises an oxidized and ultra-short single-walled carbon nanotube (US-SWNT),

wherein said US-SWNT has open ends,

wherein said US-SWNT has lengths ranging from 20 nm to 80 nm,

wherein said nanovector is polyethylene-glycol-functionalized, and

wherein said nanovector is soluble in water; and

b. non-covalently associating a targeting agent with said nanovector, wherein said targeting agent comprises an antibody.

12. The method of claim 11 , wherein said associating of said nanovector with said active agent occurs by sequestration.

13. The method of claim 11 , wherein said associating of said nanovector with said targeting agent occurs by sequestration.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 24, 2012
From: RICE UNIVERSITY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 028622/0226 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 3, 2012
From: TOUR, JAMES M.; PHAM, TAM; BERLIN, JACOB
To: WILLIAM MARSH RICE UNIVERSITY
Reel/Frame 028484/0389 →
Continuity (2)
Provisional Application 61255309 · Oct 27, 2009
Related Publication 20120302816A1 · Nov 29, 2012