Parenteral nutrition composition containing iron
Bioavailable iron-containing parenteral nutrition compositions are provided that are physico-chemically stable. Iron is present in the form of soluble ferric pyrophosphate. Methods of preparation and use of the compositions are provide, as well as kits.
1. A composition suitable for parenteral nutrition comprising:
a therapeutically effective amount of soluble ferric pyrophosphate; lipid; amino acids; carbohydrate and a pharmaceutically acceptable carrier.
2. The composition according to claim 1 , wherein the composition is physic-chemically stable for at least about 24 hours following preparation, when the composition is maintained at about 25° C.
3. The composition according to claim 1 , herein the mean droplet size of the composition is less than about 500 nanometers for at least about 30 hours following preparation, when the composition is maintained at about 25° C.
4. The composition according to claim 1 , wherein the globule size distribution of the composition, expressed as the volume-weighted percent of fat greater than 5 μm in the composition, is less than about 0.05% at about 30 hours following preparation, when the composition is maintained at about 25° C.
5. The composition according to claim 1 , wherein elemental iron as soluble ferric pyrophosphate is present in the range of about 1 mg/L to about 150 mg/L.
6. The composition according to claim 5 , wherein elemental iron as soluble ferric pyrophosphate is present in the range of about 1 mg/L to about 50 mg/L.
7. The composition according to claim 1 , wherein the amino acids are present in the range from about 2.5% to about 7% (w/v).
8. The composition according to claim 1 , wherein the lipid is present in the range from about 2% to about 5% (w/v).
9. The composition according to claim 1 , wherein the carbohydrate is present in the range from about 5% to about 20% (w/v).
10. The composition according to claim 1 , wherein the carbohydrate comprises dextrose.
11. The composition according to claim 1 , further comprising one or more additional components selected from the group consisting of electrolytes, medicaments, vitamins and trace minerals not containing iron.
12. A method for preparing a composition suitable for parenteral nutrition, the method comprising aseptically combining soluble ferric pyrophosphate, lipids, amino acids, carbohydrate and a pharmaceutically acceptable carrier.
13. The method of claim 12 , comprising first forming a composition comprising amino acids, carbohydrate and a pharmaceutically acceptable carrier and mixing therewith soluble ferric pyrophosphate and lipid.
14. The method of claim 12 , comprising combining soluble ferric pyrophosphate with a composition comprising lipid, amino acids, carbohydrate and a pharmaceutically acceptable carrier.
15. The method according to claim 12 , wherein elemental iron, as the soluble ferric pyrophosphate, is present in the composition in the range from about 1 mg/L to about 150 mg/L.
16. The method according to claim 15 , wherein elemental iron, as the soluble ferric pyrophosphate, is present in the composition in the range from about 1 mg/L to about 50 mg/L.
17. The method according to claim 15 , wherein the composition is physico-chemically stable for at least about 4 hours following preparation, when the composition is maintained at about 25° C.
18. The method according to claim 12 , wherein the mean droplet size of the composition is less than about 500 nanometers for at least about 30 hours following preparation, when the composition is maintained at about 25° C.
19. The method according to claim 12 , wherein the globule size distribution of the composition, expressed as the volume-weighted percent of fat greater than 5 μm in the composition, is less than about 0.05% at about 30 hours following preparation, when the composition is maintained at about 25° C.
20. The method according to claim 12 , wherein said carbohydrate comprises dextrose.
21. A method for providing parenteral nutrition comprising bioavailable iron to an individual, the method comprising administering a composition according to claim 1 .
22. The method according to claim 21 , wherein elemental iron, as soluble ferric pyrophosphate, is present in the administered composition in the range from about 1 mg/l to about 150 mg/l.
23. The method according to claim 21 , wherein the composition is physic-chemically stable for at least about 24 hours following preparation, when the composition is maintained about 25° C.
24. The method according to claim 21 , wherein the mean droplet size of the composition is less than about 500 nanometers for at least about 30 hours following preparation, when the composition is maintained at about 25° C.
25. The method according to claim 21 , wherein the globule size distribution of the composition, expressed as the volume-weighted percent of fat greater than 5 μm in the composition, is less than about 0.05% at about 30 hours following preparation, when the composition is maintained at about 25° C.
26. A method for providing parenteral nutrition, comprising bioavailable iron to an individual, the method comprising intravenously administering a first composition comprising amino acids, lipid carbohydrates and a pharmaceutically acceptable carrier, and intravenously administering a second composition comprising lipid, at least one of the first and second compositions containing soluble ferric pyrophosphate.
27. A kit for providing parenteral nutrition comprising a first container containing a first composition comprising amino acids, lipid, carbohydrates and a pharmaceutically acceptable carrier, a second container containing a second composition comprising lipid, wherein at least one of the first and second compositions contains soluble ferric pyrophosphate.