US2019008783A1PendingUtilityA1
Ubiquinol and alpha lipoic acid compositions
Est. expiryMar 15, 2027(~0.6 yrs left)· nominal 20-yr term from priority
Inventors:Michael Fantuzzi
A61K 9/4825A61K 31/122A61K 9/4858A61K 47/12A61K 31/09A61K 47/22
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Claims
Abstract
The present invention is directed to compositions and methods of delivery of CoQ that is reduced in the presence of lipoic acid and, optionally a fatty acid and/or optionally in a monoterpene. The compositions that include the reduced CoQ can be formulated in soft gel capsules.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A soft gelatin capsule, comprising an encapsulated solution comprising:
a ubiquinol; a sufficient quantity of lipoic acid to maintain the ubiquinol in its reduced form; and one or more fatty acids, such that the ubiquinol comprises about 95% by weight of a total amount of ubiquinol and coenzyme Q in the solution.
2 . The soft gelatin capsule of claim 1 , wherein the ubiquinol content is about 98% by weight of the total weight of ubiquinol and coenzyme Q in the solution.
3 . The soft gelatin capsule of claim 2 , wherein the ubiquinol content is about 99% by weight of the total weight of ubiquinol and coenzyme Q in the solution.
4 . The soft gelatin capsule of claim 1 , wherein the molar ratio of lipoic acid to ubiquinol is from about 0.1:1 to about 2.5:1.
5 . The soft gelatin capsule of claim 1 , wherein the fatty acid is butanoic acid, hexanoic acid, octanoic acid, decanoic acid, dodecanoic acid, tetradecanoic acid, hexadecanoic acid, 9-hexadecenoic acid, octadecanoic acid, 9-octadecenoic acid, 12-hydroxy-9-octadecenoic acid, 11-octadecenoic acid, 9,12-octadecadienoic acid, 9,12,15-octadecatrienoic acid, 6,9,12-octadecatrienoic acid, eicosanoic acid, 9-eicosenoic acid, 5,8,11,14-eicosatetraenoic acid, 5,8,11,14,17-eicosapentaenoic acid, docosanoic acid, 13-docosenoic acid, 4,7,10,13,16,19-docosahexaenoic, tetracosanoic acid or mixtures thereof.
6 . The soft gelatin capsule of claim 5 , wherein the fatty acid is a combination of decanoic acid and octanoic acid.
7 . The soft gelatin capsule of claim 6 , wherein the ratio of decanoic acid to octanoic acid is 3:7.
8 . The soft gelatin capsule of claim 1 , further comprising a monoterpene.
9 . The soft gelatin capsule of claim 8 , wherein the monoterpene is limonene or a derivative thereof.
10 . The soft gelatin capsule of claim 9 , wherein the limonene derivative is perillyl alcohol, perillic acid, cis-dihydroperillic acid, trans-dihydroperillic acid, methyl esters of perillic acid, methyl esters of dihydroperillic acid, limonene-2-diol, uroterpenol, or a combination thereof.
11 . The soft gelatin capsule of claim 1 , wherein the encapsulated ubiquinol solution is stable to oxidation for at least about 30 days, such that about 95% ubiquinol remains from the original total amount of ubiquinol and coenzyme Q in the solution.
12 . The soft gelatin capsule of claim 1 , wherein the encapsulated ubiquinol solution is stable to oxidation for at least about 120 days, such that about 95% ubiquinol remains from the original total amount of ubiquinol and coenzyme Q in the solution.
13 . The soft gelatin capsule of claim 1 , wherein the encapsulated ubiquinol solution is stable to oxidation for at least about 365 days, such that about 95% ubiquinol remains from the original total amount of ubiquinol and coenzyme Q in the solution.
14 . A method for the delivery of an effective amount of ubiquinol to an individual in need thereof, comprising the steps of
providing a soft gelatin capsule as claimed in claim 1 , such that an effective amount of ubiquinol is provided to an individual.
15 . A method to prevent oxidation of a ubiquinol to a ubiquinone or a semi-ubiquinone, comprising the step of:
contacting a sufficient amount of alpha lipoic acid with ubiquinol, such that oxidation of the ubiquinol to a ubiquinone or a semi-ubiquinone does not occur.
16 . A soft gelatin capsule, comprising an encapsulated solution comprising:
a ubiquinol; a sufficient quantity of lipoic acid to maintain the ubiquinol in its reduced form; and a monoterpene, such that the ubiquinol comprises about 95% by weight of a total amount of ubiquinol and coenzyme Q in the solution.
17 . The soft gelatin capsule of claim 16 , wherein the ubiquinol content is about 98% by weight of the total weight of ubiquinol and coenzyme Q in the solution.
18 . The soft gelatin capsule of claim 16 , wherein the ratio of lipoic acid to ubiquinol is from about 0.1:1 to about 2.5:1.
19 . The soft gelatin capsule of claim 16 , wherein the monoterpene is limonene or a derivative thereof.
20 . The soft gelatin capsule of claim 19 , wherein the limonene derivative is perillyl alcohol, perillic acid, cis-dihydroperillic acid, trans-dihydroperillic acid, methyl esters of perillic acid, methyl esters of dihydroperillic acid, limonene-2-diol, uroterpenol, or a combination thereof.
21 . The soft gelatin capsule of claim 16 , wherein the encapsulated ubiquinol solution is stable to oxidation for at least about 365 days, such that about 95% ubiquinol remains from the original total amount of ubiquinol and coenzyme Q in the solution.
22 . A method for the delivery of an effective amount of ubiquinol to an individual in need thereof, comprising the steps of
providing a soft gelatin capsule as claimed in claim 16 , such that an effective amount of ubiquinol is provided to an individual.Join the waitlist — get patent alerts
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