USRE42524EExpiredUtility

Colloidal metal compositions and methods

Assignee: CYTIMMUNE SCIENCES INCPriority: Apr 30, 2001Filed: Oct 24, 2007Granted: Jul 5, 2011
Est. expiryApr 30, 2021(expired)· nominal 20-yr term from priority
A61P 37/04A61P 35/00C07K 16/241A61K 2039/55505C07K 14/525A61K 2039/55516A61K 39/39A61K 47/6923A61K 38/39A61P 35/04A61K 47/60A61K 2039/55522A61K 49/0013A61K 51/1244A61K 49/0065A61K 38/191A61K 49/0017A61K 49/0056
80
PatentIndex Score
2
Cited by
244
References
9
Claims

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

exact text as granted — not AI-modified
1. A composition comprising for treating a solid tumor consisting essentially of a pegylated colloidal gold particle and an anti-cancer therapeutic agent, wherein a polyethylene glycol derivative is covalently bound to the colloidal gold particle. 
     
     
       2. The composition of  claim 1 , further comprising an anticancer therapeutic agent. 
     
     
       3. The composition of claim  2  1, wherein the anti-cancer therapeutic agent comprises endostatin, angiostatin, thalidomide, taxol, melphalan, paclitaxel, taxanes, vinblastin, vincristine, doxorubicin, tumor necrosis factor, acyclovir, cisplatin or tacrine. 
     
     
       4. The composition of  claim 1 , further comprising a targeting molecule. 
     
     
       5. The composition of  claim 1 , further comprising wherein the anti-cancer therapeutic agent is bound to the colloidal gold particle by an integrating molecule. 
     
     
       6. The composition of  claim 1 , wherein the polyethylene glycol derivative is a polyethylene glycol-thiol derivative. 
     
     
       7. The composition of  claim 1 , further comprising an immunostimulating molecule. 
     
     
       8. The composition of  claim 7 , 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, RAGE, B7 family of molecules and receptors, CD40 ligand/receptor, basic fibroblast growth factor, and vascular endothelial growth factor. 
     
     
       9. The composition of claim 1, wherein the anti-cancer therapeutic agent is tumor necrosis factor alpha.

Join the waitlist — get patent alerts

Track USRE42524E — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.