US2012252750A1PendingUtilityA1
Formulations for reducing neuronal degeneration
Est. expiryJul 25, 2023(expired)· nominal 20-yr term from priority
A61P 25/16A23L 33/15A23V 2002/00A61K 31/355A61K 31/00A61P 25/28A61K 31/525A61K 31/22
39
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Abstract
Nutriceutical and pharmaceutical formulations for treating neurodegenerative disorders such as Alzheimer's disease are provided. Nutriceutical formulations include two or more of folate, vitamin E, and acetyl-L-carnitine (ALCAR). Pharmaceutical formulations include two or more of 3-deaza-adenosine (DZA), N-acetyl-L-cysteine (NAC), and S-adenosylmethionine (SAM).
Claims
exact text as granted — not AI-modified1 . A method for treating a neurodegenerative disorder in a mammal, the method comprising administering to the mammal an amount of a formulation effective to reduce a level of reactive oxygen species (ROS) in an in vitro neural cell culture, wherein the formulation comprises, folate, vitamin E, acetyl-L-carnitine (ALCAR), and at least two of 3-deaza-adenosine (DZA), N-acetyl-L-cysteine (NAC), and S-adenosylmethionine (SAM), in combination or in individual dosage forms.
2 . The method of claim 1 , wherein the formulation comprises folate, vitamin E, ALCAR, NAC, and SAM.
3 . The method of claim 1 , wherein the mammal suffers from a neurodegenerative disorder selected from the group consisting of Alzheimer's disease, Parkinson's disease, or amyotrophic lateral sclerosis (ALS).
4 . The method of claim 1 , wherein the mammal is a human.
5 . The method of claim 1 , wherein a level of reactive oxygen species (ROS) in the mammal is reduced compared to a reference.
6 . A composition comprising, folate, vitamin E, acetyl-L-carnitine (ALCAR), and at least two of 3-deaza-adenosine (DZA), N-acetyl-L-cysteine (NAC), and S-adenosylmethionine (SAM), in combination or in individual dosage forms, wherein a unit dose of the composition reduces a level of reactive oxygen species (ROS) in an in vitro neural cell culture.
7 . The composition of claim 6 , wherein the composition comprises folate, vitamin E, ALCAR, NAC, and SAM.
8 - 25 . (canceled)
26 . The composition of claim 6 , wherein the unit dose comprises about 200-2000 μg folate.
27 . The composition of claim 6 , wherein the unit dose comprises about 50-3000 I.U. vitamin E.
28 . The composition of claim 6 , wherein the unit dose comprises about 200-4000 mg ALCAR.
29 . The composition of claim 6 , wherein the unit dose comprises about 200-2000 mg NAC.
30 . The composition of claim 6 , wherein the unit dose comprises about 400-2000 mg SAM.
31 . The composition of claim 6 , wherein the unit dose comprises about 20-500 mg DZA.
32 . The composition of claim 7 , wherein the unit dose comprises about 200-2000 μg folate, about 50-3000 I.U. vitamin E, about 200-4000 mg ALCAR, about 200-2000 mg NAC, and about 400-2000 mg SAM.
33 . The composition of claim 7 , wherein the unit dose comprises about 400-1500 μg folate, about 50 I.U. vitamin E, about 500-3000 mg ALCAR, about 500-1500 mg NAC, and about 400-1500 mg SAM.
34 . The composition of claim 7 , wherein the unit dose of the composition comprises about 200-2000 μg folate, about 200-4000 mg ALCAR, about 400-2000 mg SAM, and about 200-2000 mg NAC.
35 . The composition of claim 7 , wherein the unit dose of the composition comprises about 400-1500 μg folate, about 500-3000 mg ALCAR, about 400-1500 mg SAM, and about 500-1500 mg NAC.
36 . A composition comprising folate, vitamin E, acetyl-L-carnitine (ALCAR), and at least two of 3-deaza-adenosine (DZA), N-acetyl-L-cysteine (NAC), and S-adenosylmethionine (SAM), in combination or in individual dosage forms, wherein a unit dose of the composition improves memory in a subject.
37 . A method of improving memory in a subject, comprising administering a composition of any one of claim 6 , 7 , or 26 - 35 to the subject, such that memory is improved.Cited by (0)
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