IP Library Granted Patent US 9,107,944
Granted Patent B2
US 9,107,944 · App. 13/755,105 · Granted Aug 18, 2015

Immunologically modified carbon nanotubes for cancer treatment

Inventor: Wei R. Chen (Edmond, OK)
Assignee: The University of Central Oklahoma
A61K41/0057A61K39/0011A61K41/0052A61N5/062B82Y5/00C12N5/0068A61K2039/55583A61K2039/6087C12N2533/30Y10S977/746Y10S977/918
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Quick Facts
Patent No.
US 9,107,944
App. No.
13/755,105
Granted
Aug 18, 2015
Kind
B2
Abstract

A method for constructing a compound of immunologically modified nanotubes and method for using the compound to deliver immunoadjuvants to tumor cells and to produce targeted, synergistic photophysical and immunological reactions for cancer treatment. To prepare the immunologically modified nanotubes, carbon nanotubes are dissolved in a solution of glycated chitosan, an immunostimulant, hence using glycated chitosan as a surfactant for rendering the aqueous solution of nanotubes stable. The compound can be used for treatment of cancer. The method includes steps of intratumorally administering immunologically modified nanotubes and administering laser irradiation of the target tumor. The nanotube serves as a carrier to deliver immunoadjuvants to the tumor cells and serves as a light-absorbing agent in a cell body of a tumor in a host. Upon laser irradiation of target tumor cells, immunologically modified nanotubes inside the tumor cells can produce spatially and temporally synchronized photothermal and immunological reactions for cancer treatment.

Claims (17)

1. A method of delivering an immunostimulant to a cell body and of producing targeted, synergistic photophysical and immunological reactions comprising:

coating a nanostructure with glycated chitosan;

penetrating a cell membrane of a cell body with said nanostructure;

irradiating said nanostructure after said step of penetrating; wherein

said nanostructure is a singled-walled carbon nanotube; and wherein

said step of irradiating comprises exposing said cell body with near-infrared light for facilitating synergistic, simultaneous photothermal and immunological reactions.

2. The method according to claim 1 wherein:

said near-infrared light is produced by a 980-nm laser.

3. The method according to claim 2 wherein:

said laser has a laser power density of 0.75 to 2 W/cm; and

said step of irradiating comprises administering said laser with an irradiating duration of 10 to 30 minutes.

4. The method according to claim 1 wherein:

said step of irradiating comprises exposing said cell body with radiofrequency radiation for facilitating synergistic, simultaneous photothermal and immunological reactions.

5. The method according to claim 1 further comprising the step of:

dissolving and stabilizing said nanostructure with an immunostimulant.

6. The method according to claim 1 wherein:

said nanostructure has an absorption peak in the range of 800 to 1200 nm.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jun 21, 2016
From: UNIVERSITY OF CENTRAL OKLAHOMA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039093/0924 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 21, 2013
From: CHEN, WEI R.
To: THE UNIVERSITY OF CENTRAL OKLAHOMA
Reel/Frame 029848/0568 →
Continuity (2)
Division 13037171 · Feb 28, 2011
Related Publication 20130172848A1 · Jul 4, 2013