IP Library Granted Patent US 10,596,122
Granted Patent B2
US 10,596,122 · App. 15/033,750 · Granted Mar 24, 2020

Amorphous magnesium-substituted calcium phosphate compositions and their uses

Inventors: Jonathan Joseph Powell (Cambridge, GB); Nuno Jorge Rodriguez Faria (Bedfordshire, GB); Laetitia Pele (Cambridge, GB); Rachel Hewitt (Cambridge, GB); Emma Thomas-McKay (Oxfordshire, GB)
Assignee: Medical Research Council
A61K9/501A61K9/1611A61K9/5115A61K47/02A61K49/0002C01B25/32A61K39/00
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Quick Facts
Patent No.
US 10,596,122
App. No.
15/033,750
Granted
Mar 24, 2020
Kind
B2
Abstract

Amorphous magnesium-substituted calcium, phosphate compositions and their medical uses are described, in particular for use in delivering cargo materials, such as cargo molecules or cargo nanoparticles contained in pores of the amorphous magnesium-substituted calcium phosphate to cells of the immune system, for example as therapeutic approaches for the treatment of inflammatory bowel diseases, and in particular Crohn's disease, autoimmune diseases, allergy and for therapeutic vaccination.

Claims (12)

1. A method of treating a condition by delivering a biologically active cargo material to the gastrointestinal tract, the method comprising administering to a subject in need of treatment a composition comprising amorphous magnesium-substituted calcium phosphate (AMCP) which entraps the biologically active cargo material that is capable of promoting PD-L1 expression, thereby enabling the cargo material to be delivered to a site of interest in the gastrointestinal tract, wherein said condition is selected from Crohn's disease, or inflammatory bowel disease, wherein the cargo materials are selected from the group consisting of muramyl dipeptide (MDP), lipopolysaccharides (LPS), polyinosinic:polycytidylic acid (Poly I:C) and retinoic acid (RA).

2. The method of treatment of claim 1 , wherein the magnesium-substituted calcium phosphate is amorphous as determined by X-ray diffraction.

3. The method of treatment of claim 1 , wherein the X-ray diffraction pattern of the amorphous magnesium-substituted calcium phosphate lacks one or more peaks associated with the X-ray diffraction pattern of crystalline hydroxyapatite.

4. The method of treatment of claim 1 , wherein the amorphous magnesium-substituted calcium phosphate is capable of dispersing to form nanoparticles that are capable of uptake by cells in the gastrointestinal tract.

5. The method of treatment of claim 4 , wherein the nanoparticles are capable of uptake by gut mucosal immune cells.

6. The method of treatment of claim 1 , wherein the composition delivers the biologically active cargo material to Peyer's patches or to Mesenteric Lymph Nodes (MLN).

7. The method of treatment of claim 1 , wherein the amorphous magnesium-substituted calcium phosphate comprises aggregated nanoparticles that are capable of dispersing to deliver the biologically active cargo molecule to the site of interest.

8. The method of treatment of claim 7 , wherein the nanoparticles are metal-based nanoparticles or metal oxo-hydroxide based nanoparticles.

9. The method of treatment of claim 1 , wherein the amorphous magnesium-substituted calcium phosphate is a silent delivery platform that does not cause an adjuvant response to the amorphous magnesium-substituted calcium phosphate at the site of interest that differs substantially to the response to the biologically active cargo material alone.

10. The method of treatment of claim 1 , wherein the ratio of Mg:Ca in the amorphous magnesium-substituted calcium phosphate is selected from at least 1:25, at least 1:20, at least 1:10, at least 1:5, at least 1:4 and 1:3.

11. A method of treating a condition by delivering a biologically active cargo material to the gastrointestinal tract, the method comprising administering to a subject in need of treatment a composition comprising amorphous magnesium-substituted calcium phosphate (AMCP) which entraps the biologically active cargo material that is capable of promoting PD-L1 expression, thereby enabling the cargo material to be delivered to a site of interest in the gastrointestinal tract, wherein said condition is selected from Crohn's disease, or inflammatory bowel disease, wherein said cargo material is polyinosinic:polycytidylic acid (Poly I:C).

12. The method of claim 1 , wherein said cargo material further comprises protein antigens, bioactive cytokines, peptidoglycans, low molecular weight organic molecules, a nutrient, a nanoparticle, a therapeutic molecule, DNA or RNA and nanoparticles.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 11, 2020
From: POWELL, JONATHAN JOSEPH; FARIA, NUNO JORGE RODRIGUES; HEWITT, RACHEL; THOMAS-MCKAY, EMMA; PELE, LAETITIA
To: MEDICAL RESEARCH COUNCIL
Reel/Frame 051779/0828 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2018
From: MEDICAL RESEARCH COUNCIL
To: UNITED KINGDOM RESEARCH AND INNOVATION
Reel/Frame 046469/0108 →
Priority Claims (1)
GB 1319548.2 · Nov 5, 2013 · national
Continuity (1)
Related Publication 20160235683A1 · Aug 18, 2016