Phosphorylated hexaacyl disaccharides (PHADs) for treating or preventing infections
The present disclosure relates to phosphorylated hexaacyl disaccharide (PHAD) compounds, compositions, and methods for treating or preventing infections.
1. A method for treating or preventing a bacterial infection or a fungal infection, comprising administering to a subject in need thereof a therapeutically effective amount of an active agent, wherein the active agent consists essentially of phosphorylated hexaacyl disaccharide (PHAD), 3-deacyl phosphorylated hexaacyl disaccharide (3D-PHAD), 3-D (6-acyl) phosphorylated hexaacyl disaccharide (3D(6-acyl) PHAD), or a pharmaceutically acceptable salt thereof, wherein the subject is recovering from surgery or the subject is recovering from trauma.
2. The method of claim 1 , wherein the active agent is phosphorylated hexaacyl disaccharide (PHAD).
3. The method of claim 1 , wherein the active agent is 3-deacyl phosphorylated hexaacyl disaccharide (3D-PHAD).
4. The method of claim 1 , wherein the active agent is 3-D (6-acyl) phosphorylated hexaacyl disaccharide (3D(6-acyl) PHAD).
5. The method of claim 1 , wherein the bacterial infection is a multi-drug resistant strain.
6. The method of claim 1 , wherein the bacterial infection is selected from Pseudomonas aeruginosa or Staphylococcus aureus.
7. The method of claim 1 , wherein the bacterial infection is a gram-negative bacteria.
8. The method of claim 1 , wherein the trauma is a burn.
9. The method of claim 1 , wherein the fungal infection is Candida albicans.
10. A method for treating or preventing a bacterial infection or a fungal infection, comprising administering to a subject in need thereof a therapeutically effective amount of a pharmaceutical composition comprising an active agent, wherein the active agent consists essentially of phosphorylated hexaacyl disaccharide (PHAD), 3-deacyl phosphorylated hexaacyl disaccharide (3D-PHAD), 3-D (6-acyl) phosphorylated hexaacyl disaccharide (3D(6-acyl) PHAD), or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier, wherein the subject is recovering from surgery or the subject is recovering from trauma.
11. The method of claim 10 , wherein the active agent is phosphorylated hexaacyl disaccharide (PHAD).
12. The method of claim 10 , wherein the active agent is 3-deacyl phosphorylated hexaacyl disaccharide (3D-PHAD).
13. The method of claim 10 , wherein the active agent is 3-D (6-acyl) phosphorylated hexaacyl disaccharide (3D(6-acyl) PHAD).
14. The method of claim 10 , wherein the bacterial infection is a multi-drug resistant strain.
15. The method of claim 10 , wherein the bacterial infection is selected from Pseudomonas aeruginosa or Staphylococcus aureus.
16. The method of claim 10 , wherein the bacterial infection is a gram-negative bacteria.