IP Library Granted Patent US 11,135,316
Granted Patent B2
US 11,135,316 · App. 15/115,457 · Granted Oct 5, 2021

Imaging and treatment of pathophysiologic conditions by Cerenkov radiation

Inventors: Samuel Achilefu (St. Louis, MO); Nalinikanth Kotagiri (St. Louis, MO)
Assignee: Washington University
A61K49/0056A61K41/0038A61K41/0057A61K49/0013A61K49/0021A61K51/0474A61K51/0482
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,135,316
App. No.
15/115,457
Granted
Oct 5, 2021
Kind
B2
Abstract

The present disclosure discloses methods and compositions for administering Cerenkov radiation-induced therapy (CRIT). In an aspect, the invention encompasses a composition comprising at least two radiation-sensitive molecules. In another aspect, the invention encompasses a composition comprising a radiation-sensitive molecule and a targeting agent. In still another aspect, the invention encompasses a method for administering Cerenkov radiation-induced therapy (CRIT) to a target tissue in a subject. The method comprises administering to the subject an effective amount of a composition B comprising at least one radiation-sensitive molecule and administering to the subject an amount of a Cerenkov radiation (CR)-emitting radionuclide effective to activate the radiation-sensitive molecule, thereby administering CRIT to the target tissue in the subject.

Claims (19)

1. A composition, the composition comprising a biocompatible inorganic nanoparticle comprised of at least one of ZnO, Si, TiO 2 , CdSe, CdS, InP, PbS, or PbSe, wherein the nanoparticle is coated with a target agent, wherein the target agent is further bound to a photoinitiator.

2. The composition of claim 1 , wherein the nanoparticle is further coated with polyethylene glycol (PEG), dextran, pullulan, glycolipid, hyaluronic acid, orosomucoid, heparin, chitosan, pectin, a polysaccharide, or a combination thereof.

3. The composition of claim 1 , where in the target agent is a polypeptide, an antigen, a nucleic acid, a polysaccharide, a sugar, a fatty acid, a steroid, a purine, a pyrimidine, a ligand, an aptamer, a small molecule, albumin, or combinations thereof.

4. The composition of claim 3 , where in the target agent is transferrin.

5. The composition of claim 1 , where the photoinitiator comprises acetophenone, benzyl and benzoin compounds, benzophenone, cationic photoinitiators, thioxanthones, or a combination thereof.

6. The composition of claim 5 , where the photoinitiator is a biocompatible photoinitiator comprised of at least one of titanocene, titanocene dichloride, 2 hydroxy-1-[4-(hydroxyethoxy)phenyl]-2-methyl-1-propanone, 2 hydroxy-1-[4-(hydroxyethoxy)phenyl]-1-propanone, 1 hydroxycyclohexane acetophenone, 2,2-dymethoxy-2-phenyl acetophenone, THX (thioxanthone), Eosin Y, camphorquinone, camphorquinone derivatives, BAPO (bisacylphosphine oxide bis(2,4,6-trimethylbenzoyl) phenylphosphineoxide), and HAP (hydroxyalkylphenone).

7. The composition of claim 6 , where the biocompatible photoinitiator is titanocene.

8. The composition of claim 1 , comprising a biocompatible inorganic TiO 2 nanoparticle coated with transferrin, wherein the transferrin is further bound to titanocene.

9. The composition of claim 8 , wherein the composition is capable of being activated by Cerenkov radiation (CR)-emitting radionuclides.

10. The composition of claim 9 , wherein the CR-emitting radionuclides are selected from the group consisting of 18 F, 18 F-FDG, 64 Cu, 90 Y, 124 I, and 89 Zr.

11. The composition of claim 1 , wherein the composition is capable of being activated by Cerenkov radiation (CR)-emitting radionuclides.

12. The composition of claim 11 , wherein the CR-emitting radionuclides are selected from the group consisting of 18 F, 18 F-FDG, 64 Cu, 90 Y, 124 I, and 89 Zr.

13. A method for administering Cerenkov radiation (CR)-induced therapy (CRIT) to a target tissue in a subject, the method comprising:

a. administering to the subject a composition of claim 1 and

b. administering to the subject an amount of a CR-emitting radionuclide effective to activate the composition of claim 1 , thereby administering CRIT to the target tissue in the subject.

14. The method of claim 13 , wherein administering CRIT to a target tissue is used to treat a disease associated with the target tissue.

15. A method for treating a tumor in a subject, the method comprising:

a. administering to the subject a composition of claim 1 ; and

b. administering to the subject an amount of a Cerenkov radiation (CR)-emitting radionuclide effective to activate the composition of claim 1 , thereby treating the tumor.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2018
From: KOTAGIRI, NALINIKANTH
To: WASHINGTON UNIVERSITY
Reel/Frame 044593/0587 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2018
From: ACHILEFU, SAMUEL I.
To: WASHINGTON UNIVERSITY
Reel/Frame 044581/0372 →
CONFIRMATORY LICENSE Recorded Nov 22, 2016
From: WASHINGTON UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040662/0293 →
Continuity (3)
Provisional Application 61934073 · Jan 31, 2014
Provisional Application 62012086 · Jun 13, 2014
Related Publication 20170007724A1 · Jan 12, 2017