Formulation and delivery method to enhance antioxidant potency of Vitamin E
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A01N-043/16
A01N-043/02
A61K-009/48
A61K-009/66
A61K-009/52
출원번호
US-0720907
(2003-11-24)
발명자
/ 주소
Rich,Mel
Udell,Ronald G.
Hari,Siva P.
출원인 / 주소
Rich,Mel
Udell,Ronald G.
Hari,Siva P.
대리인 / 주소
Dorsey &
인용정보
피인용 횟수 :
4인용 특허 :
20
초록▼
A formulation to deliver a full-spectrum of Vitamin E isomers for improved antioxidant capacity, bioavailability, dissolution and efficacy. The formulation includes dl-α-tocopheryl acetate or dl-α-tocopheryl succinate (synthetic Vitamin E), natural Vitamin E and mixed tocopherols, such as
A formulation to deliver a full-spectrum of Vitamin E isomers for improved antioxidant capacity, bioavailability, dissolution and efficacy. The formulation includes dl-α-tocopheryl acetate or dl-α-tocopheryl succinate (synthetic Vitamin E), natural Vitamin E and mixed tocopherols, such as α-, β-, γ-and δ-tocopherol, as well as four isomers (α, β, γ and δ) of tocotrienols. This formulation is designed to deliver at least 17-times the antioxidant capacity of synthetic Vitamin E (dl-α-tocopheryl acetate), and at least twice the antioxidant capacity of natural Vitamin E (d-α-tocopherol) as measured by oxygen radical absorbance capacity (ORAC) assay. The potent antioxidant capacity of this formula affords protection against oxidative damage of cell membranes, heart disease, cancer and eye and skin disease.
대표청구항▼
What is claimed is: 1. A method of treating cell oxidative damage in humans, comprising administering a formulation comprising: Vitamin E as d-α-tocopherol; Vitamin E as dl-α-tocopheryl; Vitamin E mixed tocopherols; and tocotrienols in the forms comprising inseparable tocopherols. 2.
What is claimed is: 1. A method of treating cell oxidative damage in humans, comprising administering a formulation comprising: Vitamin E as d-α-tocopherol; Vitamin E as dl-α-tocopheryl; Vitamin E mixed tocopherols; and tocotrienols in the forms comprising inseparable tocopherols. 2. The method of claim 1 wherein said tocotrienols are in the forms α, γ, β, and δ, and said inseparable tocopherols are in the forms of α, γ, β, and δ, said tocotrienols and said tocopherols being from rice, whereby said formulation is beneficial for antioxidant protection of cells in the human body containing a lipid layer membrane. 3. The method of claim 1 wherein said tocotrienols are in the forms α, γ, β, and δ, and said inseparable tocopherols are in the forms of α, γ, β, and δ, said tocotrienols and said tocopherols being from palm, whereby said formulation is beneficial for antioxidant protection of cells in the human body containing a lipid layer membrane. 4. The method of claim 1 wherein said Vitamin E mixed tocopherols are in the forms α, γ, β, and δ and are a blend of synthetic and natural sources of Vitamin E. 5. The method of claim 1 wherein said Vitamin E dl-α-tocopheryl is present at about 90 weight % of said active ingredients. 6. The method of claim 1 wherein said Vitamin E mixed tocopherols are present at about 5 weight % of said active ingredients. 7. The method of claim 1 wherein said tocotrienols from natural sources are present at about 5 weight % of said active ingredients. 8. A method of treating cell oxidative damage in humans, comprising administering a formulation comprising: Vitamin E selected from at least one of the ester group consisting of: dl-α-tocopheryl acetate; and dl-α-tocopheryl succinate; Vitamin E as d-α-tocopherol; Vitamin E mixed tocopherols in the forms α, β, γ, and δ; tocotrienols in the forms α, β, γ, and δ. 9. The method of claim 8 wherein said Vitamin E as dl-α-tocopheryl ester, said Vitamin E as d-α-tocopherol, and said Vitamin E mixed tocopherols in the forms α, β, γ, and δ is a blend of synthetic and natural sources of Vitamin E, and said tocotrienols are from a natural source. 10. The method of claim 8 wherein said Vitamin E as dl-α-tocopheryl ester is present at from 5 mg to 400 mg. 11. The method of claim 8 wherein said Vitamin E as d-α-tocopherol is present at from 5 mg to 400 mg. 12. The method of claim 8 wherein said Vitamin E as mixed tocopherols is present at from 5 mg to 200 mg. 13. The method of claim 8 wherein said Vitamin E as mixed tocotrienols in the forms α, β, γ, and δ is present at from 5 mg to 50 mg with variable composition of isomers: α tocotrienol at 1 to 30%; β tocotrienol at 0.1 to 30%; γ tocotrienol at 1 to 30%; and δ tocotrienol at 0.1 to 30%. 14. The method of claim 13 wherein the formulation further comprises: inseparable variable content of carotenoids comprising: alpha carotene; beta carotene; gamma carotene; lycopene; and phytosterols and squalene. 15. The method of claim 8 wherein the formulation further comprises: a marker selected from at least one of the group consisting of: coenzyme Q10; rosemary oil; green tea; a lipoic acid; lycopene; grape seed extract; pine bark extract; vitamin C; natural beta carotene; synthetic beta carotene; γ-oryzanol; selenium; and lutein. 16. A method of treating cell oxidative damage in humans, comprising administering a formulation comprising: Vitamin E selected from at least one of the ester group consisting of: dl-α-tocopheryl acetate; and dl-α-tocopheryl succinate; Vitamin E as d-α-tocopherol; Vitamin E mixed tocopherols in the forms α, β, γ, and δ; and tocotrienols in the forms α, β, γ, and δ. 17. The method of claim 16 wherein said Vitamin E as dl-α-tocopheryl ester, said Vitamin E as d-α-tocopherol, and said Vitamin E mixed tocopherols in the forms α, β, γ, and δ is a blend of synthetic and natural sources of Vitamin E, and said tocotrienols are from a natural source. 18. The method of claim 16 wherein said Vitamin E as dl-α-tocopheryl ester is present at from 5 mg to 2000 mg. 19. The method of claim 16 wherein said Vitamin E as d-α-tocopherol is present at from 5 mg to 2000 mg. 20. The method of claim 16 wherein said Vitamin E as mixed tocopherols is present at from 5 mg to 2000 mg. 21. The method of claim 16 wherein said Vitamin E as mixed tocotrienols in the forms α, β, γ, and δ is present at from 5 mg to 500 mg with variable composition of isomers: α tocotrienol at 1 to 30%; β tocotrienol 0.1 to 30%; γ tocotrienol at 1 to 30%; and δ tocotrienol at 0.1 to 30%. 22. The method of claim 16 wherein said Vitamin E as dl-α-tocopheryl ester, said Vitamin E as d-α-tocopherol, and said Vitamin E mixed tocopherols in the forms α, β, γ, and δ is a blend of synthetic and natural sources of Vitamin E, and said tocotrienols are from a natural source. 23. The method of claim 16 wherein said formulation is formed in a soft gel capsule further comprising: gelatin; glycerin; and water for said soft gelatin formulation. 24. The method of claim 16 wherein the formulation further comprises: a marker selected from at least one of the group consisting of: coenzyme Q10; rosemary oil; green tea; α lipoic acid; lycopene; grape seed extract; pine bark extract; vitamin C; natural beta carotene; synthetic beta carotene; γ-oryzanol; selenium; and lutein. 25. A method of protecting against cell oxidative damage in humans, comprising administering a formulation comprising: Vitamin E as d-α-tocopherol; Vitamin E as dl-α-tocopheryl; Vitamin E mixed tocopherols; and tocotrienols in the forms comprising inseparable tocopherols. 26. The method of claim 25 wherein said tocotrienols are in the forms α, γ, β, and δ, and said inseparable tocopherols are in the forms of α, γ, β, and δ, said tocotrienols and said tocopherols being from rice, whereby said formulation is beneficial for antioxidant protection of cells in the human body containing a lipid layer membrane. 27. The method of claim 25 wherein said tocotrienols are in the forms α, γ, β, and δ, and said inseparable tocopherols are in the forms of α, γ, β, and δ, said tocotrienols and said tocopherols being from palm, whereby said formulation is beneficial for antioxidant protection of cells in the human body containing a lipid layer membrane. 28. The method of claim 25 wherein said Vitamin E mixed tocopherols are in the forms α, γ, β, and δ and are a blend of synthetic and natural sources of Vitamin E. 29. The method of claim 25 wherein said Vitamin E dl-α-tocopheryl is present at about 90 weight % of said active ingredients. 30. The method of claim 25 wherein said Vitamin E mixed tocopherols are present at about 5 weight % of said active ingredients. 31. The method of claim 25 wherein said tocotrienols from natural sources are present at about 5 weight % of said active ingredients. 32. A method of protecting against cell oxidative damage in humans, comprising administering a formulation comprising: Vitamin E selected from at least one of the ester group consisting of: dl-α-tocopheryl acetate; and dl-α-tocopheryl succinate; Vitamin E as d-α-tocopherol; Vitamin E mixed tocopherols in the forms α, β, γ, and δ; tocotrienols in the forms α, β, γ, and δ. 33. The method of claim 32 wherein said Vitamin E as dl-α-tocopheryl ester, said Vitamin E as d-α-tocopherol, and said Vitamin E mixed tocopherols in the forms α, β, γ, and δ is a blend of synthetic and natural sources of Vitamin E, and said tocotrienols are from a natural source. 34. The method of claim 32 wherein said Vitamin E as dl-α-tocopheryl ester is present at from 5 mg to 400 mg. 35. The method of claim 32 wherein said Vitamin E as d-α-tocopherol is present at from 5 mg to 400 mg. 36. The method of claim 32 wherein said Vitamin E as mixed tocopherols is present at from 5 mg to 200 mg. 37. The method of claim 32 wherein said Vitamin E as mixed tocotrienols in the forms α, β, γ, and δ is present at from 5 mg to 50 mg with variable composition of isomers: α tocotrienol at 1 to 30%; β tocotrienol at 0.1 to 30%; γ tocotrienol at 1 to 30%; and δ tocotrienol at 0.1 to 30%. 38. The method of claim 37 wherein the formulation further comprises: inseparable variable content of carotenoids comprising: alpha carotene; beta carotene; gamma carotene; lycopene; and phytosterols and squalene. 39. The method of claim 32 wherein the formulation further comprises: a marker selected from at least one of the group consisting of: coenzyme Q10; rosemary oil; green tea; α lipoic acid; lycopene; grape seed extract; pine bark extract; vitamin C; natural beta carotene; synthetic beta carotene; γ-oryzanol; selenium; and lutein. 40. A method of protecting against cell oxidative damage in humans, comprising administering a formulation comprising: Vitamin E selected from at least one of the ester group consisting of: dl-α-tocopheryl acetate; and dl-α-tocopheryl succinate; Vitamin E as d-α-tocopherol; Vitamin E mixed tocopherols in the forms α, β, γ, and δ; and tocotrienols in the forms α, β, γ, and δ. 41. The method of claim 40 wherein said Vitamin E as dl-α-tocopheryl ester, said Vitamin E as d-α-tocopherol, and said Vitamin E mixed tocopherols in the forms α, β, γ, and δ is a blend of synthetic and natural sources of Vitamin E, and said tocotrienols are from a natural source. 42. The method of claim 40 wherein said Vitamin E as dl-α-tocopheryl ester is present at from 5 mg to 2000 mg. 43. The method of claim 40 wherein said Vitamin E as d-α-tocopherol is present at from 5 mg to 2000 mg. 44. The method of claim 40 wherein said Vitamin E as mixed tocopherols is present at from 5 mg to 2000 mg. 45. The method of claim 40 wherein said Vitamin E as mixed tocotrienols in the forms α, β, γ, and δ is present at from 5 mg to 500 mg with variable composition of isomers: α tocotrienol at 1 to 30%; β tocotrienol at 0.1 to 30%; γ tocotrienol at 1 to 30%; and δ tocotrienol at 0.1 to 30%. 46. The method of claim 40 wherein said Vitamin E as dl-α-tocopheryl ester, said Vitamin E as d-α-tocopherol, and said Vitamin E mixed tocopherols in the forms α, β, γ, and δ is a blend of synthetic and natural sources of Vitamin E, and said tocotrienols are from a natural source. 47. The method of claim 40 wherein said formulation is formed in a soft gel capsule further comprising: gelatin; glycerin; and water for said soft gelatin formulation. 48. The method of claim 40 wherein the formulation further comprises: a marker selected from at least one of the group consisting of: coenzyme Q10; rosemary oil; green tea; α lipoic acid; lycopene; grape seed extract; pine bark extract; vitamin C; natural beta carotene; synthetic beta carotene; γ-oryzanol; selenium; and lutein.
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