Methods and compositions for treating conditions related to lack of blood supply, shock, and neuronal injuries
A pharmaceutical composition comprising a lipid component; an amphiphilic emulsifier; and a polar liquid carrier. The lipid component and the amphiphilic emulsifier form free-moving lipid-carrying micelles (LMs) in the polar liquid carrier. The pharmaceutical composition is free of hemoglobin and fluorocarbon and can be used for treating conditions related to lack of blood supply and to raise the blood pressure.
1. A pharmaceutical composition comprising:
a lipid component;
an amphiphilic emulsifier; and
a polar liquid carrier,
wherein the lipid component and the amphiphilic emulsifier form free-moving lipid-carrying micelles (LMs) or liposomes in the polar liquid carrier, wherein the pharmaceutical composition is free of hemoglobin and fluorocarbon, and wherein the pharmaceutical composition further comprises an effective amount of oxygen for enhancement of aerobic metabolism.
2. The pharmaceutical composition of claim 1 , wherein said LMs or liposomes have an average diameter of 300 nm or smaller.
3. The pharmaceutical composition of claim 1 , wherein said LMs or liposomes have an average diameter of 100 nm or smaller.
4. The pharmaceutical composition of claim 1 , wherein said LMs or liposomes have an average diameter of 30 nm or smaller.
5. The pharmaceutical composition of claim 1 , further comprising an amino acid at a final concentration of 0.2-50 mM.
6. The pharmaceutical composition of claim 1 , further comprising glycerol or mannitol in an amount of 2-5% (w/v).
7. The pharmaceutical composition of claim 1 , further comprising glycerol or mannitol in an amount of about 2.25% (w/v).
8. The pharmaceutical composition of claim 1 , further comprising albumin in an amount of 3-7% (w/v).
9. The pharmaceutical composition of claim 1 , further comprising albumin in an amount of about 5% (w/v).
10. The pharmaceutical composition of claim 1 , wherein said amphiphilic emulsifier is egg yolk phospholipids or α-phosphatidylcholine in an amount of 1%-5% (w/v).
11. The pharmaceutical composition of claim 10 , wherein said amphiphilic emulsifier is egg yolk phospholipids or α-phosphatidylcholine in an amount of about 2% (w/v).
12. The pharmaceutical composition of claim 1 , wherein said lipid component is selected from the group consisting of soybean oil, chia bean oil, pumpkin oil, flaxseed oil, fish oil and algae oil in an amount of 10%-70% (w/v) of said pharmaceutical composition.
13. The pharmaceutical composition of claim 12 , wherein said lipid component is selected from the group consisting of soybean oil, chia bean oil and algae oil in an amount of about 35% (w/v) of said pharmaceutical composition.
14. The pharmaceutical composition of claim 1 , wherein said composition is free of calcium, magnesium and potassium.
15. The pharmaceutical composition of claim 1 , wherein said composition is free of aluminium.
16. The pharmaceutical composition of claim 1 , wherein said LMs or liposomes have an average diameter of 2-300 nm.
17. The pharmaceutical composition of claim 1 , further comprising an amino acid at a final concentration of 0.1 fM-200 mM.
18. The pharmaceutical composition of claim 1 , further comprising an amino acid at a final concentration of 0.1 fM-10 mM.
19. The pharmaceutical composition of claim 1 , further comprising an amino acid at a final concentration of 0.01 mM-200 mM.
20. The pharmaceutical composition of claim 1 , further comprising an amino acid at a final concentration of 10 nM-10 μM.
21. The pharmaceutical composition of claim 1 , further comprising effective amounts of oxygen and nitric oxide for regulation of vascular function and cellular metabolism.
22. The pharmaceutical composition of claim 1 , further comprising erythrocyte ghosts that traps said lipid component.
23. The pharmaceutical composition of claim 1 , further comprising β-endorphin at a final concentration of 0.01-100 nM.
24. The pharmaceutical composition of claim 1 , further comprising 0.1 fM-10 mM histidine, cysteine, or an oligopeptide containing histidine or glycylglycine.
25. The pharmaceutical composition of claim 1 , further comprising 0.01-0.2 M histidine.
26. The pharmaceutical composition of claim 1 , wherein said lipid carrying micelles or liposomes have an average diameter of 90-120 nm.
27. The pharmaceutical composition of claim 1 , wherein said lipid carrying micelles or liposomes have an average diameter of 90-100 nm.
28. The pharmaceutical composition of claim 1 , wherein said lipid carrying micelles or liposomes have an average diameter of 100-110 nm.
29. The pharmaceutical composition of claim 1 , wherein said lipid carrying micelles or liposomes have an average diameter of 110-120 nm.
30. The pharmaceutical composition of claim 1 , further comprising one or more oncotic agents.
31. The pharmaceutical composition of claim 1 , further comprising one or more immunomodulatory agents.
32. The pharmaceutical composition of claim 1 , further comprising one or more anti-inflammatory agents.
33. The pharmaceutical composition of claim 1 , further comprising one or more coagulation enhancers.
34. The pharmaceutical composition of claim 1 , further comprising one or more additives selected from the group consisting of antioxidants, antibiotics, anti-fungal agents, vitamins, amino acids, vessel expanders, surfactants, antibodies and mediators of vascular potency.