IP Library Granted Patent US 10,300,034
Granted Patent B2
US 10,300,034 · App. 12/033,431 · Granted May 28, 2019

Fatty acid formulations and methods of use thereof

Inventor: Claudia R. Morris (Oakland, CA)
Assignee: CHILDREN'S HOSPITAL OF OAKLAND RESEARCH INSTITUTE
A61K31/202A23L33/12A23L33/15A61K9/0053A61K9/48A61K31/122A61K31/201A61K31/205A61K31/355A61K31/375A61K31/385A61K31/593A61K31/661A61K33/30A61K38/43A61K45/06A23V2002/00
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 10,300,034
App. No.
12/033,431
Granted
May 28, 2019
Kind
B2
Abstract

The present invention provides dietary formulations comprising polyunsaturated fatty acids and vitamin E. The present invention further provides methods of treating various conditions, generally involving administering to an individual in need thereof an effective amount of a subject dietary formulation.

Claims (43)

1. A dietary formulation suitable for treating an autism spectrum disorder and/or apraxia, the formulation comprising:

a) eicosapentaenoic acid (EPA);

b) docosohexaenoic acid (DHA);

c) α-tocopherol;

d) γ-tocopherol;

e) vitamin K1;

f) vitamin K2; and

g) γ-linolenic acid (GLA),

wherein the ratio of EPA to DHA is in a range of from 1.5:1 to 5:1,

wherein the α-tocopherol is present in an amount of from 300 mg to 3000 mg per unit dose,

wherein the γ-tocopherol is present in an amount of from 200 mg to 1000 mg per unit dose,

wherein the EPA is present in an amount of from 500 mg to 3000 mg per unit dose,

wherein the DHA is present in an amount of from 100 mg to 400 mg per unit dose,

wherein the vitamin K1 is present in an amount of from 100 μg to 10 mg,

wherein the vitamin K2 is present in an amount of from 100 μg to 2 mg; and

wherein the GLA is present in an amount of from 50 mg to 75 mg.

2. The formulation of claim 1 , further comprising α-lipoic acid in an amount of from 50 mg to 600 mg per unit dose.

3. The formulation of claim 1 , further comprising carnitine in an amount of from 200 mg to 3000 mg per unit dose.

4. The formulation of claim 1 , further comprising an omega-9 fatty acid.

5. The formulation of claim 4 , wherein the omega-9 fatty acid is oleic acid.

6. The formulation of claim 1 , further comprising vitamin C in an amount of from 200 mg to 500 mg.

7. The formulation of claim 1 , further comprising phosphocholine.

8. The formulation of claim 1 , further comprising zinc.

9. The formulation of claim 1 , further comprising one or more additional components selected from coenzyme Q, selenium, vitamin A, vitamin B 1 , riboflavin, vitamin B 6 , vitamin B 12 , vitamin D, arginine, calcium, magnesium, vitamin B 7 , vitamin B 9 , vitamin B 5 , tetrahydrobiopterin, and vitamin B 3 .

10. The formulation of claim 1 , further comprising a pancreatic enzyme.

11. The formulation of claim 1 , further comprising a leukotriene inhibitor.

12. The formulation of claim 1 , wherein the formulation is in a dosage form selected from a tablet, a capsule, a powder, a gel, and a liquid.

13. The formulation of claim 1 , further comprising one or more food-grade components.

14. The formulation of claim 1 , further comprising an anti-oxidant.

15. The formulation of claim 1 , further comprising an anti-inflammatory agent.

16. The formulation of claim 1 , further comprising an amino acid.

17. The formulation of claim 16 , wherein the formulation further comprises arginine.

18. The formulation of claim 1 , further comprising an anti-fungal agent.

19. The formulation of claim 1 , further comprising one or more of β-tocopherol, δ-tocopherol, α-tocotrienol, β-tocotrienol, γ-tocotrienol, and δ-tocotrienol.

20. The formulation of claim 1 , wherein a unit dose of the formulation is effective to treat an autism spectrum disorder and/or apraxia.

21. A method of treating apraxia and/or autism spectrum disorder, the method comprising orally administering to an individual in need thereof an effective amount of the formulation of claim 1 .

22. The method of claim 21 , wherein the formulation is administered three times daily.

23. The method of claim 21 , wherein the formulation is administered twice daily.

24. The method of claim 21 , wherein the formulation is administered once daily.

25. The method of claim 21 , wherein said administration is effective to increase the percentile score of at least one of oral movement score, simple phonemic/syllabic score, complex phonemic/syllabic score, and spontaneous length and complexity score, by at least about 10 percentile points.

26. A method of treating an allergic disorder, the method comprising orally administering to an individual in need thereof an effective amount of the formulation of claim 1 .

27. The method of claim 26 , wherein the disorder is selected from celiac disease, sprue, gluten sensitivity, a malabsorption syndrome, asthma, food allergy, leaky gut syndrome, and/or eczema.

28. A method of treating an inflammatory condition, the method comprising orally administering to an individual in need thereof an effective amount of the formulation of claim 1 , wherein the inflammatory condition is rheumatic arthritis, diabetes, or cardiovascular disease.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 19, 2008
From: MORRIS, CLAUDIA R.
To: CHILDREN'S HOSPITAL & RESEARCH CENTER AT OAKLAND
Reel/Frame 020968/0435 →
Continuity (3)
Provisional Application 60891097 · Feb 22, 2007
Provisional Application 60981262 · Oct 19, 2007
Related Publication 20080213239A1 · Sep 4, 2008