Compositions and methods relating to salts of specialized pro-resolving mediators
The present invention relates to compounds of Formulas I-IV, which are salts of special lipid mediators of inflammation, compositions containing same, and methods of using same in the treatment of various diseases and disorders characterized by chronic or excessive inflammation, or both. Provided are pharmaceutical compositions adapted to deliver the compounds the lower gastrointestinal tract and methods of using same as monotherapy in the treatment of inflammatory diseases or disorders of the lower gastrointestinal tract, and in combination therapy with 5-aminosalicylate.
1. A pharmaceutical composition comprising a compound of Formula IV, or an enantiomer, polymorph, solvate, or hydrate thereof, adapted to deliver the compound to the lower gastrointestinal tract of a subject:
wherein
M is a divalent metal selected from magnesium (Mg 2+ ), calcium (Ca 2+ ), and zinc (Zn 2+ ),
A and B are each independently an SPM molecule selected from an E series resolvin,
A and B may be the same or different,
either A or B, but not both, may be absent,
R 1 and R 2 are each independently —(CH 2 ) 3 —Y 1 , and —(CH 2 ) 4 —Y 2 ,
where Y 1 and Y 2 are each selected from a positively charged primary amine, a positively charged secondary amine, a positively charged tertiary amine, and a positively charged guanidine,
X 1 and X 2 are each independently H or CO—Z and Z is a peptide comprising 1 to 5 amino acids.
2. The pharmaceutical composition of claim 1 , wherein the composition is an enema or suppository adapted to deliver the compound to the rectum.
3. The pharmaceutical composition of claim 1 , wherein the composition is an oral dosage form adapted to deliver the compound to the colon or ileum.
4. The pharmaceutical composition of claim 3 , wherein the oral dosage form comprises one or more of an enteric coating, an erodible and/or degradable matrix material, a gellable or swellable polymer, a poragen, and an osmotic pump mechanism.
5. The pharmaceutical composition of claim 4 , wherein M is selected from magnesium (Mg 2+ ) or calcium (Ca 2+ ).
6. The pharmaceutical composition of claim 5 , wherein R 1 and R 2 are independently selected from —(CH 2 ) 3 —Y 1 , and —(CH 2 ) 4 —Y 2 , and Y 1 and Y 2 are each selected from a positively charged primary amine, a positively charged secondary amine, a positively charged tertiary amine, and a positively charged guanidine.
7. The pharmaceutical composition of claim 6 , wherein X 1 and X 2 are each H.
8. The pharmaceutical composition of claim 7 , wherein R 1 and R 2 are each —(CH 2 ) 4 —Y 2 and Y 2 is —NH 3 + .
9. The pharmaceutical composition of claim 8 , wherein A and B are each independently an E series resolvin selected from the group consisting of resolvin E1 (RvE1), resolvin E2 (RvE2), resolvin E3 (RvE3), aspirin-triggered RvE1 (AT-RvE1), AT-RvE2, and AT-RvE3.
10. The pharmaceutical composition of claim 9 , wherein A and B are the same.
11. The pharmaceutical composition of claim 3 , wherein M is magnesium (Mg 2+ ), R 1 and R 2 are each —(CH 2 ) 4 —Y 2 and Y 2 is —NH 3 + , X 1 and X 2 are each H, and A and B are RvE1, which compound is referred to as bis RvE1 Mg-di-lysinate.
12. The pharmaceutical composition of claim 1 , wherein M is magnesium (Mg 2+ ), R 1 and R 2 are each —(CH 2 ) 4 —Y 2 and Y 2 is —NH 3 + , X 1 and X 2 are each H, and A and B are RvE1, which compound is referred to as bis RvE1 Mg-di-lysinate.
13. The pharmaceutical composition of claim 2 , wherein M is magnesium (Mg 2+ ), R 1 and R 2 are each —(CH 2 ) 4 —Y 2 and Y 2 is —NH 3 + , X 1 and X 2 are each H, and A and B are RvE1, which compound is referred to as bis RvE1 Mg-di-lysinate.
14. A method of treating an inflammatory disease or disorder of the lower gastrointestinal tract, the method comprising targeting the release of a compound of Formula IV, or an enantiomer, polymorph, solvate, or hydrate thereof, to the distal small intestine, colon, or rectum by administering to a subject in need of such treatment a pharmaceutical composition comprising a compound of Formula IV, or an enantiomer, polymorph, solvate, or hydrate thereof, adapted to deliver the compound to the lower gastrointestinal tract of a subject:
wherein
M is a divalent metal selected from magnesium (Mg 2+ ), calcium (Ca 2+ ), and zinc (Zn 2+ ),
A and B are each independently an SPM molecule selected from an E series resolvin,
A and B may be the same or different,
either A or B, but not both, may be absent,
R 1 and R 2 are each independently selected from —(CH 2 ) 3 —Y 1 , and —(CH 2 ) 4 —Y 2 ,
where Y 1 and Y 2 are each selected from a positively charged primary amine, a positively charged secondary amine, a positively charged tertiary amine, and a positively charged guanidine,
X 1 and X 2 are each independently H or CO—Z and Z is a peptide comprising 1 to 5 amino acids.
15. The method of claim 14 , wherein the disease or disorder is selected from inflammatory bowel disease, ulcerative colitis, and Crohn's disease.
16. The method of claim 15 , wherein M is magnesium (Mg 2+ ), R 1 and R 2 are each —(CH 2 ) 4 —Y 2 and Y 2 is —NH 3 + , X 1 and X 2 are each H, and A and B are RvE1, which compound is referred to as bis RvE1 Mg-di-lysinate.
17. The method of claim 14 , further comprising administering to the subject 5-aminosalicylate (5-ASA).
18. The method of claim 17 , wherein M is magnesium (Mg 2+ ), R 1 and R 2 are each —(CH 2 ) 4 —Y 2 and Y 2 is —NH 3 + , X 1 and X 2 are each H, and A and B are RvE 1 , which compound is referred to as bis RvE 1 Mg-di-lysinate.
19. The method of claim 14 , wherein M is magnesium (Mg 2+ ), R 1 and R 2 are each —(CH 2 ) 4 —Y 2 and Y 2 is —NH 3 + , X 1 and X 2 are each H, and A and B are RvE1, which compound is referred to as bis RvE1 Mg-di-lysinate.