IP Library Granted Patent US 10,596,131
Granted Patent B2
US 10,596,131 · App. 16/409,501 · Granted Mar 24, 2020

Non-racemic beta-hydroxybutyrate compounds and compositions enriched with the R-enantiomer and methods of use

Inventor: Gary Millet (Salt Lake City, UT)
Assignee: AXCESS GLOBAL SCIENCES, LLC
A61K31/19A61K9/0053A61K31/047
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Quick Facts
Patent No.
US 10,596,131
App. No.
16/409,501
Granted
Mar 24, 2020
Kind
B2
Abstract

Ketogenic compositions including a non-racemic mixture of beta-hydroxybutyrate (BHB) enriched with the R-enantiomer are formulated to increase ketone body level in a subject. The non-racemic mixture of BHB is enriched with the R-enantiomer to elevate ketone bodies and increase the rate at which ketosis is achieved yet contains an amount of the S-enantiomer sufficient to provide alternative benefits as discussed herein. In some aspects a composition for increasing ketone body level in a subject contains a dietetically or pharmaceutically acceptable carrier and a non-racemic mixture of R-beta-hydroxybutyrate and S-beta-hydroxybutyrate, wherein the non-racemic mixture of R-beta-hydroxybutyrate and S-beta-hydroxybutyrate contains from about 51% to 99.5% by enantiomeric equivalents of the R-beta-hydroxybutyrate and from about 49% to about 0.5% by enantiomeric equivalents of S-beta-hydroxybutyrate enantiomer.

Claims (31)

1. A composition for administering ketone bodies to a subject, comprising:

a non-racemic mixture of R-beta-hydroxybutyrate and S-beta-hydroxybutyrate containing more than 50% and up to 89% by enantiomeric equivalents of R-beta-hydroxybutyrate and less than 50% and at least 11% by enantiomeric equivalents of S-beta-hydroxybutyrate, with the proviso that the non-racemic mixture contains no more than 88% by enantiomeric equivalents of mono-ester of R-1,3-butanediol and R-beta-hydroxybutyrate,

wherein the composition is provided as or in a tablet, capsule, powder, food product, food additive, flavored beverage, vitamin fortified beverage, non-alcoholic beverage, flavored beverage additive, vitamin fortified beverage additive, non-alcoholic beverage additive, candy, sucker, pastille, food supplement, flavored mouth spray, or suppository.

2. The composition of claim 1 , wherein the non-racemic mixture contains from 51% to 89% by enantiomeric equivalents of the R-beta-hydroxybutyrate and 49% to 11% by enantiomeric equivalents of the S-beta-hydroxybutyrate.

3. The composition of claim 1 , wherein the non-racemic mixture contains from 52% to 89% by enantiomeric equivalents of the R-beta-hydroxybutyrate and 48% to 11% by enantiomeric equivalents of the S-beta-hydroxybutyrate.

4. The composition of claim 1 , wherein the non-racemic mixture contains from 53% to 89% by enantiomeric equivalents of the R-beta-hydroxybutyrate and 47% to 11% by enantiomeric equivalents of the S-beta-hydroxybutyrate.

5. The composition of claim 1 , wherein the non-racemic mixture contains from 57% to 87% by enantiomeric equivalents of the R-beta-hydroxybutyrate and 43% to 13% by enantiomeric equivalents of the S-beta-hydroxybutyrate.

6. The composition of claim 1 , wherein the non-racemic mixture comprises one or more salts of R-beta-hydroxybutyrate and/or one or more salts of S-beta-hydroxybutyrate.

7. The composition of claim 1 , wherein the non-racemic mixture comprises one or more esters of R-beta-hydroxybutyrate and/or one or more esters of S-beta-hydroxybutyrate.

8. The composition of claim 1 , wherein the non-racemic mixture comprises R-beta-hydroxybutyric acid and/or S-beta-hydroxybutyric acid.

9. The composition of claim 1 , further comprising at least one medium chain fatty acid having 6 to 12 carbons, or a mono-, di- or triglyceride of the at least one medium chain fatty acid.

10. The composition of claim 1 , further comprising at least one short chain fatty acid having fewer than 6 carbons, or a mono-, di- or triglyceride of the at least one medium chain fatty acid.

11. The composition of claim 1 , further comprising at least one long chain fatty acid having more than 12 carbons, or a mono-, di- or triglyceride of the at least one long chain fatty acid.

12. The composition of claim 1 , wherein the non-racemic mixture comprises at least one R-beta-hydroxybutyrate ester selected from the group consisting of mono-ester of ethanol, mono-ester of 1-propanol, mono- or di-ester of 1,3-propanediol, mono- or di-ester of S-1,3-butanediol, mono- or di-ester of R-1,3-butanediol, mono- or di-ester of S—R-1,3-butanediol, and mono-, di-, or tri-ester of glycerin.

13. A composition for administering ketone bodies to a subject, comprising:

a dietetically or pharmaceutically acceptable carrier selected from the group consisting of tablet, capsule, powder, food product, food additive, flavored beverage, vitamin fortified beverage, non-alcoholic beverage, flavored beverage additive, vitamin fortified beverage additive, non-alcoholic beverage additive, candy, sucker, pastille, food supplement, flavored mouth spray, and suppository; and

a non-racemic mixture of R-beta-hydroxybutyrate and S-beta-hydroxybutyrate containing more than 50% and up to 89% by enantiomeric equivalents of R-beta-hydroxybutyrate and less than 50% and at least 11% by enantiomeric equivalents of S-beta-hydroxybutyrate, with the proviso that the non-racemic mixture contains no more than 88% by enantiomeric equivalents of mono-ester of R-1,3-butanediol and R-beta-hydroxybutyrate.

14. A kit for administering ketone bodies to a subject, comprising: the composition of claim 1 ; a container in which the composition is placed, wherein the container is selected from the group consisting of carton, box, can, jar, bag, pouch, bottle, jug, and keg; and a measuring device configured to hold therein a unit dose, or fraction thereof, of the composition, wherein a unit dose of the composition contains about 0.5 g to about 25 g of the non-racemic mixture of R-beta-hydroxybutyrate and S-beta-hydroxybutyrate, wherein the measuring device is selected from the group consisting of cup, scoop, syringe, dropper, spoon, and colonic irrigation device.

15. The kit of claim 14 , the composition further comprising at least one medium chain fatty acid having 6 to 12 carbons, or a mono-, di- or triglyceride of the at least one medium chain fatty acid.

16. A composition for increasing ketone body level in a subject, comprising:

a non-racemic mixture of R-beta-hydroxybutyrate and S-beta-hydroxybutyrate,

wherein the non-racemic mixture contains from 51% to 89% by enantiomeric equivalents of the R-beta-hydroxybutyrate and 49% to 11% by enantiomeric equivalents of the S-beta-hydroxybutyrate,

wherein the non-racemic mixture comprises one or more salts of R-beta-hydroxybutyrate.

17. A composition for increasing ketone body level in a subject, comprising:

a non-racemic mixture of R-beta-hydroxybutyrate and S-beta-hydroxybutyrate containing more than 50% and up to 89% by enantiomeric equivalents of the R-beta-hydroxybutyrate and less than 50% and at least 11% by enantiomeric equivalents of the S-beta-hydroxybutyrate,

wherein the non-racemic mixture comprises one or more salts or esters of R-beta-hydroxybutyrate with the proviso that the non-racemic mixture contains less than 85% by enantiomeric equivalents of mono-ester of R-1,3-butanediol and R-beta-hydroxybutyrate.

18. A composition for increasing ketone body level in a subject, comprising:

a non-racemic mixture of R-beta-hydroxybutyrate and S-beta-hydroxybutyrate containing more than 50% and up to 89% by enantiomeric equivalents of R-beta-hydroxybutyrate and less than 50% and at least 11% by enantiomeric equivalents of S-beta-hydroxybutyrate, and

at least one short-, medium-, or long-chain fatty acid, or a mono-, di- or triglyceride of the at least one short-, medium-, or long-chain fatty acid.

19. The kit of claim 14 , wherein the non-racemic mixture comprises 51% to 99.5% by enantiomeric equivalents of the R-beta-hydroxybutyrate and 49% to 0.5% by enantiomeric equivalents of the S-beta-hydroxybutyrate.

20. The kit of claim 14 , wherein the non-racemic mixture contains from 52% to 99% by enantiomeric equivalents of the R-beta-hydroxybutyrate and 48% to 1% by enantiomeric equivalents of the S-beta-hydroxybutyrate.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2019
From: MILLET, GARY
To: AXCESS GLOBAL SCIENCES, LLC
Reel/Frame 049153/0633 →
Continuity (5)
Continuation In Part 16272165 · Feb 11, 2019
Continuation In Part 16224408 · Dec 18, 2018
Division 15936820 · Mar 27, 2018
Provisional Application 62590063 · Nov 22, 2017
Related Publication 20190262293A1 · Aug 29, 2019
Cited By (13)
US 12,186,297 US 12,251,362 US 12,329,734 US 12,350,243 US 12,433,912 US 12,472,200 US 12,496,283 US 12,521,378 US 12,533,331 US 12,533,346 US 12,551,455 US 12,599,579 US 12,622,889