US2010222428A1PendingUtilityA1
Fatty Acid Nutritional Supplement
Est. expiryFeb 5, 2019(expired)· nominal 20-yr term from priority
Inventors:Charles R. Roe
A23L 33/12A61K 31/20
65
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Abstract
A seven-carbon fatty acid or derivative thereof has been identified as an excellent energy source for humans or human infants. A nutritional supplement suitable for humans or human infants comprising a seven carbon fatty acid chain compound or derivative thereof can be used to increase energy production derived from fatty acid metabolism. For example, administering a seven carbon fatty acid chain compound or derivative thereof can be used to accelerate the growth rate of a prematurely born human infant.
Claims
exact text as granted — not AI-modified1 . A method of accelerating the growth rate of a prematurely-born human infant by administering to said infant a seven carbon fatty acid compound or derivative thereof, wherein said compound or derivative thereof is able to readily enter the mitochondrion without special transport enzymes.
2 . The method of claim 1 , wherein said seven carbon fatty acid compound comprises n-heptoanoic acid.
3 . The method of claim 1 , wherein said seven carbon fatty acid compound comprises a triglyceride comprising n-heptanoic acid.
4 . The method of claim 3 , wherein said triglyceride comprises triheptanoin.
5 . The method of claim 1 wherein said derivative is a five carbon fatty acid chain.
6 . The method of claim 1 , wherein said derivative is selected from the group consisting of 4-methylhexanoate, 4-methylhexenoate, 3-hydroxy-4-methylhexanoate, 5methylhexanoate, 5-methylhexenoate and 3-hydroxy-5-methylhexanoate.
7 . The method of claim 1 , wherein said compound or derivative thereof is capable of being broken down by normal J3-oxidation in humans to methylbutyric acid.
8 . The method of claim 1 , wherein said compound or derivative thereof is capable of being broken down by normal J3-oxidation in humans to isovaleric acid.
9 . The method claim 1 , wherein said compound or derivative is capable of being broken down by normal J3-oxidation in humans to n-valeryl-CoA.
10 . The method of claim 1 , wherein said compound or derivative is capable of being broken down by normal J3-oxidation in humans to propionyl-CoA in one or more oxidative procedures.
11 . The method of claim 1 , wherein said compound or derivative thereof is provided to said human infant in an amount comprising at least about 25% of the dietary caloric requirement for said infant.
12 . The method of claim 1 , wherein said compound or derivative is provided orally.
13 . The method of claim 1 , wherein said compound or derivative is provided parenterally.
14 . The method of claim 1 , wherein said compound or derivative is provided intraperitoneally.Cited by (0)
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