IP Library Granted Patent US 9,861,575
Granted Patent B2
US 9,861,575 · App. 13/668,558 · Granted Jan 9, 2018

Vitamin-containing nutrition infusion for administration through peripheral vein

Inventors: Kazuhiro Abiko (Shizuoka, JP); Toshiyuki Katsura (Shizuoka, JP)
Assignee: EA Pharma Co., Ltd.
A61K9/0019A23L33/15A61K31/197A61K31/375A61K31/4188A61K31/4415A61K31/455A61K31/51A61K31/525A61K31/7004A61K31/714A61K33/06A61K33/20A61K33/30
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,861,575
App. No.
13/668,558
Granted
Jan 9, 2018
Kind
B2
Abstract

A nutrition infusion is provided for administration through a peripheral vein that contains a vitamin B group and vitamin C stably and includes two solutions of a sugar solution and an amino acid solution. In the nutrition infusion for administration through a peripheral vein, the sugar solution contains vitamin B1, vitamin B12, and pantothenic acid and has a pH of 4.7 to 5.5, and the amino acid solution contains vitamin B2, folic acid, vitamin C, and biotin and has a pH of 7.0 to 7.5.

Claims (70)

1. A method of administering a nutrition infusion, comprising:

providing a kit comprising a first package containing a sugar solution comprising a reducing sugar, vitamin B1, vitamin B12, and pantothenic acid and having a pH of 4.7 to 5.5, and a second package separated from the first package and containing an amino acid solution comprising an amino acid, vitamin B2, folic acid, vitamin C, biotin, and sulfite in an amount of 25 mg/L to 100 mg/L, and having a pH of 7.0 to 7.5, wherein the sugar solution and the amino acid solution are prepared such that a nutrition infusion produced by mixing only the sugar solution and the amino acid solution contains 100 μg/L to 400 μg/L of the folic acid;

producing the nutrition infusion from the kit by mixing the sugar solution and the amino acid solution; and

administering the nutrition infusion through a peripheral vein of a subject.

2. The method according to claim 1 , wherein the reducing sugar in the sugar solution is glucose, and the sugar solution and the amino acid solution are prepared such that the nutrition infusion produced by mixing only the sugar solution and the amino acid solution has a glucose concentration of 4 w/v % to 10 w/v %.

3. The method according to claim 1 , wherein the sugar solution further comprises vitamin B6, and the amino acid solution further comprises a nicotinic acid derivative.

4. The method according to claim 1 , wherein the sugar solution further comprises acetic acid as a pH adjustor.

5. The method according to claim 1 , wherein the sugar solution and the amino acid solution are prepared such that the nutrition infusion produced by mixing only the sugar solution and the amino acid solution has a pH of 6.5 to 7.4.

6. The method according to claim 1 , wherein the sugar solution and the amino acid solution are prepared such that the nutrition infusion produced by mixing only the sugar solution and the amino acid solution further contains:

Vitamin B1 in an amount of 1 mg/L to 10 mg/L,

Vitamin B2 in an amount of 1 mg/L to 4 mg/L converted in terms of riboflavin,

Vitamin B6 in an amount of 1 mg/L to 5 mg/L,

Vitamin B12 in an amount of 1 μ/L to 10 μg/L,

Pantothenic acids in an amount of 4 mg/L to 16 mg/L,

Nicotinic acid derivative in an amount of 10 mg/L to 40 mg/L,

Biotin in an amount of 25 μg/L to 100 μg/L, and

Vitamin C in an amount of 50 mg/L to 200 mg/L.

7. The method according to claim 1 , wherein

the sugar solution further comprises sodium chloride in an amount of 0.5 g/L to 2 g/L, a calcium chloride hydrate in an amount of 0.2 g/L to 1 g/L, sodium lactate in an amount of 2 g/L to 15 g/L, a magnesium sulfate hydrate in an amount of 0.5 g/L to 2 g/L, and a zinc sulfate hydrate in an amount of 1 mg/L to 4 mg/L,

the amino acid solution comprises the amino acid in an amount of 50 g/L to 300 g/L in terms of a free amino acid, and

the volume ratio between the sugar solution and the amino acid solution is 2:1 to 3:1.

8. The method according to claim 1 , wherein the sugar solution and the amino acid solution are prepared such that the nutrition infusion produced by mixing only the sugar solution and the amino acid solution contains L-tryptophan in an amount of 0.04 g/L to 3.0 g/L, N-acetyl-L-cysteine in an amount of 0.01 g/L to 2.0 g/L, or both.

9. The method according to claim 1 , wherein the sugar solution has a pH of 4.9 to 5.5.

10. The method according to claim 1 , wherein the volume ratio of the sugar solution to the amino acid solution is 2:1 to 3:1.

11. The method according to claim 1 , wherein the amino acid solution has a pH of 7.0 to 7.2.

12. The method according to claim 1 , wherein the amino acid solution has a pH of 7.1 to 7.5.

13. The method according to claim 1 , wherein the amino acid solution has a pH of 7.1 to 7.2.

14. The method according to claim 1 , wherein the sugar solution and the amino acid solution are prepared such that the nutrition infusion produced by mixing only the sugar solution and the amino acid solution further contains:

L-Isoleucine in an amount of 0.2 g/L to 14.0 g/L,

L-Leucine in an amount of 0.4 g/L to 20.0 g/L,

L-Lysine in an amount of 0.2 g/L to 14.0 g/L,

L-Methionine in an amount of 0.1 g/L to 8.0 g/L,

L-Phenyl alanine in an amount of 0.2 g/L to 12.0 g/L,

L-Threonine in an amount of 0.1 g/L to 8.0 g/L,

L-Tryptophan in an amount of 0.04 g/L to 3.0 g/L,

L-Valine in an amount of 0.1 g/L to 16.0 g/L,

L-Alanine in an amount of 0.2 g/L to 14.0 g/L,

L-Arginine in an amount of 0.2 g/L to 14.0 g/L,

L-Aspartic acid in an amount of 0.01 g/L to 4.0 g/L,

L-Glutamic acid in an amount of 0.01 g/L to 6.0 g/L,

L-Histidine in an amount of 0.1 g/L to 8.0 g/L,

L-Proline in an amount of 0.1 g/L to 10.0 g/L,

L-Serine in an amount of 0.1 g/L to 6.0 g/L,

L-Tyrosine in an amount of 0.01 g/L to 2.0 g/L,

Glycine in an amount of 0.1 g/L to 12.0 g/L, and

L-Cysteine in an amount of 0.01 g/L to 2.0 g/L.

15. The method according to claim 1 , wherein the first package and the second package are formed in a container made of at least one material selected from the group consisting of polyethylene, polypropylene, and cyclic polyolefin.

16. The method according to claim 1 , wherein the amino acid solution further comprises citric acid as a pH adjustor.

17. The method according to claim 1 , wherein the amino acid solution further comprises citric acid such that the nutrition infusion produced by mixing only the sugar solution and the amino acid solution further contains 5 mEq/L to 15 mEq/L of the citric acid.

18. A method of administering a nutrition infusion, comprising:

administering, through a peripheral vein of a subject, a nutrition infusion prepared by mixing a sugar solution comprising a reducing sugar, vitamin B1, vitamin B12, and a pantothenic acid and having a pH of 4.7 to 5.5, and an amino acid solution comprising an amino acid, vitamin B2, folic acid, vitamin C, biotin, and sulfite in an amount of 25 mg/L to 100 mg/L, and having a pH of 7.0 to 7.5,

wherein the nutrition infusion comprises 100 μg/L to 400 μg/L of the folic acid, and the nutrition infusion has a pH of 6.5 to 7.4.

19. The method according to claim 18 , wherein the reducing sugar in the sugar solution is glucose, and the nutrition infusion has a glucose concentration of 4 w/v % to 10 w/v %.

20. The method according to claim 18 , wherein the sugar solution further comprises vitamin B6, and the amino acid solution further comprises a nicotinic acid derivative.

21. The method according to claim 18 , wherein the sugar solution further comprises acetic acid as a pH adjustor.

22. The method according to claim 18 , wherein the nutrition infusion has a pH of 6.8 to 7.4.

23. The method according to claim 18 , wherein the nutrition infusion contains:

Vitamin B1 in an amount of 1 mg/L to 10 mg/L,

Vitamin B2 in an amount of 1 mg/L to 4 mg/L converted in terms of riboflavin,

Vitamin B6 in an amount of 1 mg/L to 5 mg/L,

Vitamin B12 in an amount of 1 μg/L to 10 μg/L,

Pantothenic acids in an amount of 4 mg/L to 16 mg/L,

Nicotinic acid derivative in an amount of 10 mg/L to 40 mg/L,

Biotin in an amount of 25 μg/L to 100 μg/L, and

Vitamin C in an amount of 50 mg/L to 200 mg/L.

24. The method according to claim 18 , wherein the sugar solution further comprises sodium chloride in an amount of 0.5 g/L to 2 g/L, a calcium chloride hydrate in an amount of 0.2 g/L to 1 g/L, sodium lactate in an amount of 2 g/L to 15 g/L, a magnesium sulfate hydrate in an amount of 0.5 g/L to 2 g/L, and a zinc sulfate hydrate in an amount of 1 mg/L to 4 mg/L,

the amino acid solution comprises the amino acid in an amount of 50 g/L to 300 g/L in terms of a free amino acid, and

the volume ratio between the sugar solution and the amino acid solution is 2:1 to 3:1.

25. The method according to claim 18 , wherein the amino acid solution further comprises citric acid as a pH adjustor.

26. The method according to claim 18 , wherein the amino acid solution further comprises citric acid such that the nutrition infusion produced by mixing only the sugar solution and the amino acid solution further contains 5 mEq/L to 15 mEq/L of the citric acid.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2018
From: EA PHARMA CO., LTD.
To: AY PHARMACEUTICALS CO., LTD.
Reel/Frame 046886/0253 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2016
From: AJINOMOTO CO., INC.
To: EA PHARMA CO., LTD.
Reel/Frame 039094/0087 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 12, 2013
From: ABIKO, KAZUHIRO; KATSURA, TOSHIYUKI
To: AJINOMOTO CO., INC.
Reel/Frame 029797/0512 →
Priority Claims (1)
JP 2010-107429 · May 7, 2010 · national
Continuity (2)
Continuation PCTJP2011060899 · May 2, 2011
Related Publication 20130078228A1 · Mar 28, 2013