IP Library › Granted Patent US 11,931,465
Granted Patent B2
US 11,931,465 · App. 16/083,416 · Granted Mar 19, 2024

Functionalized Prussian blue nanoparticles, combination Prussian blue nanoparticle-based nano-immunotherapy and applications thereof

Inventors: Rohan Fernandes (Washington, DC); Raymond W. Sze (Washington, DC); Conrad Russell Y. Cruz (Washington, DC); Anthony D. Sandler (Washington, DC); Catherine M. Bollard (Washington, DC); Elizabeth E. Sweeney (Washington, DC); Juliana Cano-Mejia (Washington, DC); Rachel Burga (Washington, DC); Matthieu F. Dumont (Washington, DC)
Assignee: Children's National Medical Center
A61K9/5146A61K9/127A61K9/5068A61K9/5169A61K33/26A61K35/17A61K38/193A61K38/195A61K38/20A61K38/21A61K39/39541A61K41/0052A61K45/06A61K47/6901A61K47/6935A61N5/0616A61N5/062A61N5/0624A61N5/0625A61P35/00A61N5/0601A61N2005/0659A61N2005/0663A61N5/067
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Quick Facts
Patent No.
US 11,931,465
App. No.
16/083,416
Granted
Mar 19, 2024
Kind
B2
Abstract

Combination treatment with Prussian blue nanoparticles and at least one immunotherapeutic treatment. Stable, functionalized Prussian blue nanoparticles, including those with enhanced stability under alkaline conditions, and methods of cancer, neoplasm, and tumor treatment using them, including photothermal treatment and combination immunotherapeutic treatments.

Claims (31)

1. A combined immunotherapeutic and photothermal method for treating a subject having a neoplasm, tumor, or cancer comprising:

treating the subject with an immunotherapy that comprises administering a checkpoint inhibitor which is an anti-CTLA-4 checkpoint inhibitor and/or an anti-PD-1/PD-L1 checkpoint inhibitor and wherein the checkpoint inhibitor is selected from the group consisting of ipilimumab, nivolumab, pembrolizumab and atezolizumab,

administering intratumorally Prussian blue nanoparticles comprising Prussian blue nanoparticles coated with first and second polymer coatings having opposite charges to each other; and

photothermally treating the subject; wherein the neoplasm, tumor or cancer is neuroblastoma; and wherein the first and second polymer coatings comprise polyallylamine hydrochloride and poly(acrylic acid).

2. The method of claim 1 , wherein the Prussian blue nanoparticles comprise a compound having the chemical formula:

A x B y M z [M′(CN 6 ] a ·n (H 2 O)

wherein:

A represents at least one of VO″, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, In, Ga, Sr, lr, Nb, Li, Na, K, Rb, Cs, Fr, TI, Mo, Ru, Rh, Pd, Ag, Cd, In, Lu, Ba, Hf, Ta, W, Os, Pt, Hg, La, Eu, Gd, Tb, Dy and Ho, in any oxidation state and any combination thereof;

B represents at least one of VO″, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, In, Ga, Sr, lr, Nb, Li, Na, K, Rb, Cs, Fr, TI, Mo, Ru, Rh, Pd, Ag, Cd, In, Lu, Ba, Hf, Ta, W, Os, Pt, Hg, La, Eu, Gd, Tb, Dy and Ho, in any oxidation state and any combination thereof;

M represents at least one of VO″, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, In, Ga, Sr, lr, Nb, Li, Na, K, Rh, Cs, Fr, TI, Mo, Ru, Rh, Pd, Ag, Cd, In, Lu, Ba, Hf, Ta, W, Os, Pt, Hg, La, Eu, Gd, Tb, Dy and Ho, in any oxidation state and any combination thereof;

M′ represents at least one of VO″, Ca, V, Cr, Mn, Fe, Co, Ni, Cu, In, Ga, Sr, lr, Nb, Li, Na, K, Rb, Cs, Fr, TI, Mo, Ru, Rh, Pd, Ag, Cd, In, Lu, Ba, Hf, Ta, W, Os, Pt, Hg, La, Eu, Gd, Tb, Dy and Ho, in any oxidation state and any combination thereof;

x is from 0.1 to about 1;

Y is from 0 to about 1;

z is from 0.1 to about 4;

a is from 0.1 to about 4; and

n is from 0.1 to about 24.

3. The method of claim 2 , wherein in the formula

A x B y M z [M′(CN 6 ] a ·n (H 2 O), A=B=K.

4. The method of claim 2 , wherein the Prussian blue nanoparticles comprise KFe(Fe(CN) 6 ).

5. The method of claim 2 , wherein in the formula

A x B y M z [M′(CN 6 ] a ·n (H 2 O), A=K and B=Gd.

6. The method of claim 2 , wherein in the formula A x B y M z [M′(CN 6 ] a ·n (H 2 O), A=K and B=Mn.

7. The method of claim 1 , wherein the immunotherapy further comprises administering T cells.

8. The method of claim 1 , wherein the immunotherapy further comprises administering T cells that recognize at least one cancer antigen.

9. The method of claim 1 , where in the first and second polymer coatings comprise polyallylamine hydrochloride (PAH) and poly(acrylic acid)(PAA) further coated with polyethylene glycol (PEG) in the following order from core to surface: Prussian blue nanoparticles, PAH, PAA and PEG.

10. The method of claim 1 , wherein the immunotherapy comprises administering the anti-CTLA-4 checkpoint inhibitor ipilimumab.

11. The method of claim 1 , wherein the immunotherapy comprises administering an anti-PD-1/PD-L1 checkpoint inhibitor comprising nivolumab, pembrolizumab or atezolizumab.

12. The method of claim 1 , wherein the T cells or the checkpoint inhibitors are conjugated to the Prussian blue nanoparticles.

13. The method of claim 1 , wherein the Prussian blue nanoparticles have an average size ranging from 1 nm to 10 microns.

14. The method of claim 1 , wherein the nanoparticles further comprise an antibody, aptamer, or other ligand that binds to a cancer cell antigen.

15. The method of claim 1 , wherein the photothermal treatment comprises radiating the Prussian blue nanoparticles with light having a wavelength of 600 nm to 1,200 nm.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2020
From: FERNANDES, ROHAN; SZE, RAYMOND W.; CRUZ, CONRAD RUSSELL Y.; SANDLER, ANTHONY D.; BOLLARD, CATHERINE M.; SWEENEY, ELIZABETH E.; CANO-MEJIA, JULIANA; BURGA, RACHEL; DUMONT, MATTHIEU F.
To: CHILDREN'S NATIONAL MEDICAL CENTER
Reel/Frame 051743/0157 →
Continuity (2)
Provisional Application 62305253 · Mar 8, 2016
Related Publication 20200163899A1 · May 28, 2020