IP Library Granted Patent US 7,387,900
Granted Patent B2
US 7,387,900 · App. 10/135,886 · Granted Jun 17, 2008

Colloidal metal compositions and methods

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Quick Facts
Patent No.
US 7,387,900
App. No.
10/135,886
Granted
Jun 17, 2008
Kind
B2
Abstract

The present invention comprises compositions and methods for delivery systems of agents, including therapeutic compounds, pharmaceutical agents, drugs, detection agents, nucleic acid sequences and biological factors. In general, these vector compositions comprise a colloidal metal, derivatized PEG (polyethylene glycol) and an agent. The invention also comprises methods and compositions for making such colloidal metal compositions and for treatment of cancer.

Claims (10)

1. A method for treating a solid tumor, comprising, administering to an organism having the solid tumor, a vector composition comprising a colloidal gold particle, at least one anti-cancer agent, and a polyethylene glycol derivative covalently bound to the colloidal gold particle.

2. The method of claim 1 , wherein the composition further comprises a targeting molecule.

3. The method of claim 1 , wherein the composition further comprises an integrating molecule.

4. The method of claim 1 , wherein the at least one anti-cancer agent is selected from the group consisting of tumor necrosis factor, endostatin, angiostatin, thalidomide, taxol, melphalan, paclitaxel, vinblastin, vincristine, doxorubicin, acyclovir, cisplatin, tacrine, 5-fluorouracil, mitaxantrone, VM-16, etoposide, VM-26, teniposide, and taxanes.

5. The method of claim 1 , wherein the polyethylene glycol derivative is a polyethylene glycol-thiol derivative.

6. The method of claim 1 , further comprising administering an anti-cancer agent after the administration of the vector composition.

7. The method of claim 1 , further comprising administering an anti-cancer agent prior to the administration of the vector composition.

8. The method of claim 1 , further comprising administering an anti-cancer agent concurrently with the administration of the vector composition.

9. The method of claim 1 , wherein the vector composition further comprises an immunostimulating molecule.

10. The method of claim 9 , wherein the immunostimulating molecule is selected from the group consisting of Interleukin-1, Interleukin-2, Interleukin-3, Interleukin-4, Interleukin-5, Interleukin-6, Interleukin-7, Interleukin-8, Interleukin-10, Interleukin-11, Interleukin-12, Interleukin-13, lipid A, phospholipase A2, endotoxins, staphylococcal enterotoxin B, Type I Interferon, Type II Interferon, Tumor Necrosis Factor alpha, Transforming Growth Factor beta, Lymphotoxin, Migration Inhibition Factor, Granulocyte-Macrophage Colony-Stimulating Factor, Monocyte-Macrophage Colony-Stimulating Factor, Granulocyte Colony-Stimulating Factor, Angiogenin, transforming growth factor alpha, fibroblast growth factor, cancer cell specific antigens, MART, MAGE, BAGE, B7 family of molecules and receptors, CD40ligand/receptor, basic fibroblast growth factor, and vascular endothelial growth factor.

Assignments (2)
RELEASE OF SECURITY INTEREST Recorded Sep 5, 2014
From: ITANI, HIDETAKA KENTARO
To: CYTIMMUNE SCIENCES, INC.
Reel/Frame 033692/0418 →
SECURITY AGREEMENT Recorded Sep 18, 2009
From: CYTIMMUNE SCIENCES, INC.
To: ITANI, HIDETAKA KENTARO
Reel/Frame 023254/0076 →