IP Library Granted Patent US 10,918,126
Granted Patent B2
US 10,918,126 · App. 16/016,023 · Granted Feb 16, 2021

Isotopically modified compounds and their use as food supplements

Inventor: Mikhail Sergeevich Shchepinov (Kingston Upon Thames, GB)
Assignee: Retrotope, Inc.
A23L33/12A23D9/00A23D9/007A23K10/12A23K50/80A23L33/10A23L33/105A23L33/13A23L33/135A23L33/175A23L33/18A23L33/20A61K9/0019A61K31/201C07C57/03C07C229/26C07C255/30C07C279/14C07H19/16A23V2002/00C07B2200/05
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Quick Facts
Patent No.
US 10,918,126
App. No.
16/016,023
Granted
Feb 16, 2021
Kind
B2
Abstract

A nutrient composition comprises an essential nutrient in which at least one exchangeable H atom is 2 H and/or at least one C atom is 13 C. The nutrient is thus protected from, inter alia, active oxygen species.

Claims (22)

1. A medicament composition, comprising an effective amount of an isotopically modified compound, wherein the isotopically modified compound reduces oxidative damage of a bodily constituent in a patient after the isotopically modified compound is administered and incorporated into the bodily constituent, wherein the isotopically modified compound is a nucleic acid, lipid, or amino acid, and wherein the lipid is a fatty acid or fatty acid ester isotopically modified at least at one or more bis-allylic positions.

2. The medicament composition of claim 1 , wherein the isotopically modified compound is a lipid.

3. The medicament composition of claim 2 , wherein the lipid is a deuterated fatty acid.

4. The medicament composition of claim 3 , wherein the deuterated fatty acid is a deuterated ω-3 fatty acid or a deuterated ω-6 fatty acid.

5. The medicament composition of claim 3 , wherein the deuterated fatty acid is deuterated at least at one or more bis-allylic positions.

6. The medicament composition of claim 3 , wherein the deuterated fatty acid is 11-D-linoleic acid or 11,11-D2-linoleic acid.

7. The medicament composition of claim 2 , wherein the lipid is a deuterated fatty acid ester.

8. The medicament composition of claim 7 , wherein the lipid is a 11-D-linoleic acid ester or 11,11-D2-linoleic acid ester.

9. The medicament composition of claim 2 , wherein the bodily constituent of the patient is a fat.

10. The medicament composition of claim 1 , wherein the isotopically modified compound is a nucleic acid or an amino acid.

11. The medicament composition of claim 10 , wherein the amino acid is selected from the group consisting of Phe, Val, Trp, Thr, Ile, Met, His, Leu, Lys and Arg.

12. The medicament composition of claim 10 , wherein the amino acid is selected from the group consisting of Lys-D 2 , Arg-D 2 , Trp-D, Thr-D, Phe-D 4 , His-D, Lys-D 3 13 C 2 , Arg-D 3 13 C 2 , Trp-D 4 13 C 4 , Val-D 3 13 C 3 , Thr-D 2 13 C 2 ; (S)-2,6-diaminohexanoic acid-6,6-D 2 , (S)-2-amino-5-guanidino pentanoic acid-5- 13 C,5,5-D 2 , and (S)-2-amino-5-guanidino pentanoic acid-5,5-D 2 .

13. The medicament composition of claim 1 , wherein the medicament composition is in a form of a tablet or pill.

14. The medicament composition of claim 1 , wherein the medicament composition is in a form suitable for intravenous delivery.

15. The medicament composition of claim 1 , wherein the medicament composition is in a liquid form.

16. A method for reducing oxidative damages in vivo in a human, comprising repeatedly administering to the human a medicament composition, comprising an effective amount of an isotopically modified compound, wherein the isotopically modified compound reduces oxidative damage of a bodily constitutent in the human after the isotopically modified compound is administered and incorporated into the bodily constitutent, wherein the isotopically modified compound is a nucleic acid, lipid, or amino acid, and wherein the lipid is a fatty acid or fatty acid ester isotopically modified at least at ione or more bis-allylic positions.

17. The method of claim 16 , wherein the isotopically modified compound is a lipid.

18. The method of claim 17 , wherein the lipid is a deuterated fatty acid.

19. The method of claim 18 , wherein the deuterated fatty acid is deuterated at least at one or more bis-allylic positions.

20. The method of claim 18 , wherein the deuterated fatty acid is 11-D-linoleic acid or 11,11-D2-linoleic acid.

21. The method of claim 17 , wherein the lipid is a deuterated fatty acid ester.

22. The method of claim 21 , wherein the lipid is a 11-D-linoleic acid ester or 11,11-D2-linoleic acid ester.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Sep 9, 2022
From: RTMFP ENTERPRISES INC.
To: RETROTOPE, INC.
Reel/Frame 061403/0670 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2022
From: RETROTOPE, INC.
To: RTMFP ENTERPRISES INC.
Reel/Frame 061403/0835 →
CHANGE OF NAME Recorded Sep 9, 2022
From: RTMFP ENTERPRISES INC.
To: BIOJIVA LLC
Reel/Frame 061405/0819 →
SECURITY INTEREST Recorded Mar 30, 2022
From: RETROTOPE, INC.
To: RTMFP ENTERPRISES, INC.
Reel/Frame 059442/0414 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2018
From: SHCHEPINOV, MIKHAIL SERGEEVICH
To: RETROTOPE, INC.
Reel/Frame 046195/0427 →
Priority Claims (1)
GB 0604647 · Mar 8, 2006 · national
Continuity (5)
Continuation 15446922 · Mar 1, 2017
Division 15078853 · Mar 23, 2016
Division 14551450 · Nov 24, 2014
Division 12281957
Related Publication 20180303145A1 · Oct 25, 2018
Cited By (1)
US 12,398,176