IP Library Granted Patent US 9,289,511
Granted Patent B2
US 9,289,511 · App. 14/089,343 · Granted Mar 22, 2016

Bioconjugated nanoparticles

Inventor: Maurice P. Bianchi (Palos Verdes Estate, CA)
Assignee: The Boeing Company
A61K47/48376A61B18/18A61K33/06A61K33/22A61K33/24A61K33/30A61K33/44A61K41/0042A61K47/48092A61K47/48623A61K47/48723A61N5/0624B82Y5/00C07K16/2833A61N5/10A61N2005/1085Y10S977/774Y10S977/904Y10S977/911
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Quick Facts
Patent No.
US 9,289,511
App. No.
14/089,343
Granted
Mar 22, 2016
Kind
B2
Abstract

The present disclosure relates to compositions and methods for the treatment of a disease, e.g., cancer or pathogenic infection, using a bioconjugated nanoparticle comprising a biocompatible quantum dot conjugated to a targeting moiety. The targeting moiety allows for the nanopaticle to bind to a cancer cell or pathogenic organism. The quantum dot, upon excitation by soft x-rays, emits electromagnetic radiation at a frequency of ultraviolet light, thereby allowing for the disruption of the DNA found in the cancer cell or pathogenic organism.

Claims (26)

1. A method comprising the steps of:

administering an effective amount of electromagnetic radiation to a biocompatible quantum dot conjugated to a targeting moiety specific for a predictive marker of a target cell or a pathogenic organism;

wherein said electromagnetic radiation is soft x-rays from an external device having a wavelength in the range of 0.1 nm to 100 nm that interacts with the quantum dot thereby emitting light at an ultraviolet wavelength; and

inducing DNA damage or cellular membrane disruption to the target cell or the pathogenic organism from the emitted light at the ultraviolet wavelength.

2. The method of claim 1 , wherein said soft x-rays have a wavelength in the range of 1 nm to 15 nm.

3. The method of claim 1 , wherein said emitted ultraviolet light has a wavelength in the range of 100 nm to 260 nm.

4. The method of claim 1 , wherein said quantum dot comprises a and gap between 3 and 6.5 eV.

5. The method of claim 1 , wherein said quantum dot is selected from the group consisting of gallium nitride, gallium arsenide, zinc oxide, aluminum nitride, boron nitride and diamond.

6. The method of claim 1 , wherein said quantum dot is coated with a biocompatible material selected from the group consisting of a lipid, a carbohydrate, a polysaccharide, a protein, a polymer, a glycoprotein, and a glycolipid.

7. The method of claim 1 , further comprising a linker, wherein said linker attaches said targeting moiety to said quantum dot.

8. The method of claim 1 , wherein said targeting moiety is specific for a marker of said disease of the target cell.

9. The method of claim 1 , wherein said targeting moiety is selected from the group consisting of an antibody or fragments thereof, haptens, polypeptides, oligonucleotides, anti-sense RNA, Peptide Nucleic Acids, proteins, chimeric proteins, fusion proteins, and combinations thereof.

10. The method of claim 1 , further comprising, prior to the administrating the effective amount of radiation step, the steps of

culturing a disease sample in vitro;

determining the expression of a predictive marker of the disease;

providing the targeting moiety specific for said predictive marker;

attaching said targeting moiety to the quantum dot to form a bioconjugated nanoparticle; and then

administering said bioconjugated nanoparticle to a subject having or inflicted with the disease.

11. The method of claim 10 , wherein said disease is a cancer or a pathogenic infection.

12. The method of claim 10 , wherein said soft x-rays have a wavelength in the range of 1 nm to 15 nm.

13. The method of claim 10 , wherein said emitted ultraviolet light has a wavelength in the range of 100 nm to 260 nm.

14. A method comprising the steps of

introducing soft x-ray electromagnetic radiation of a wavelength between 0.1 nm and 100 nm from an external device to a biocompatible quantum dot conjugated to a targeting moiety of a target cell or a pathogenic organism; wherein the introducing of the soft x-ray electromagnetic radiation causes an emitting of light from the quantum dot at an ultraviolet wavelength in the range of 100 nm to 260 nm; and

inducing DNA damage within the target cell or the pathogenic organism and/or disrupting the cellular membrane associated with the target cell or the pathogenic organism.

15. The method of claim 14 , wherein said targeting moiety is linked to said quantum dot via a covalent bond.

16. The method of claim 14 , further comprising, prior to step (b), the step of administering to a subject in need thereof, an effective amount of the biocompatible quantum dot conjugated to the targeting moiety.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 25, 2013
From: BIANCHI, MAURICE P.
To: THE BOEING COMPANY
Reel/Frame 031672/0035 →
Continuity (2)
Division 11766285 · Jun 21, 2007
Related Publication 20140207126A1 · Jul 24, 2014