US2022378078A1PendingUtilityA1
Compositions and their use
Est. expiryDec 14, 2035(~9.4 yrs left)· nominal 20-yr term from priority
A23L 33/12A61P 25/28A61K 31/70A61K 33/26A23L 33/40A23L 33/16A23V 2250/1588A23V 2250/1564A61K 33/06A61K 31/661A23V 2250/1618A23V 2250/161A23V 2250/5424A61K 31/14A61K 45/06A61K 33/42A61K 31/519A23L 33/15A61K 33/30A61P 25/00A61K 9/0095A23V 2200/322A61K 31/714A23V 2250/1886A24B 15/38A23V 2250/1852A23V 2250/1578A23V 2002/00A61K 31/202A23L 33/115A23V 2250/706A23V 2250/185A23V 2250/7056A23V 2250/1846A61K 33/00A23L 33/30A23V 2250/1592A23V 2250/1862A23V 2250/1642A23L 33/10
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Claims
Abstract
A synthetic nutritional composition comprising a vitamin for use to promote, support or optimise de novo myelination, in particular the de novo myelination trajectory, and/or brain structure, and/or brain connectivity, and/or intellectual potential and/or cognitive potential and/or learning potential and/or cognitive functioning in a subject, in particular a formula fed subject.
Claims
exact text as granted — not AI-modified1 . A method for promoting, supporting or optimizing de novo myelination, in particular the de novo myelination trajectory, and/or brain structure, and/or brain connectivity, and/or intellectual potential, and/or cognitive potential, and/or learning potential and/or cognitive functioning in a formula fed subject comprising administering to the subject a synthetic nutritional composition comprising a vitamin, wherein brain structure refers to the amount and/or spatial distribution of myelinated matter throughout the brain, and/or in specific brain regions, and wherein said cognitive function is optimized if the subject's scores in a standardized neurodevelopmental test are less than one standard deviation different from that of an exclusively breastfed subject of a well-nourished mother.
2 . A method according to claim 1 wherein the subject is a human infant or child.
3 . A method according to claim 1 wherein the vitamin is vitamin B12 and/or folic acid.
4 . A method according to claim 3 wherein, the composition comprises folic in an amount greater than 50 mcg/100 g dry weight of the composition and/or vitamin B12 in an amount greater than 0.01 mcg/100 g dry weight of the composition.
5 . A method according to claim 1 wherein the composition further comprises an ingredient selected from the group consisting of a mineral, choline, a phospholipid, and a fatty acid derivative.
6 . A method according to claim 5 wherein the mineral is selected from the group consisting of iron, zinc, calcium, phosphorus, copper and combinations thereof; wherein the fatty acid derivative comprises docosahexaenoic acid and/or arachidonic acid and/or stearic acid and/or nervonic acid, and wherein the phospholipid is a compound of formula (I) or a mixture of compounds of formula (I)
wherein,
R 1 is O;
X is NH or O;
R 2 is a C2-C44 saturated or unsaturated, linear or branched acyl group;
R 3 is a substituent of formula (II) or formula (III):
Wherein, R 5 is a C2-C44 saturated or unsaturated, linear or branched acyl group and
R 6 is a C2-C44 saturated alkyl or alkenyl group; and
R 4 is selected from; a C5 or C6 substituted or unsubstituted cyclic alkyl or alkenyl group, or,
—(CH2)n-R 7 , wherein n is an integer ranging from 1 to 4, in particular 1 to 2 and R 7 is —N(CH3)3+, NH3+, or a substituent of formula (IV) and,
7 . A method according to claim 6 wherein the phospholipid is selected from the group consisting of sphingomyelin, phosphatidylcholine, phosphatidylinositole, phosphatidylserine, and mixture of the foregoing.
8 . A method according to claim 6 wherein, if iron is present in the composition it is comprised in an amount greater than 5 mg/100 g dry weight of the composition, wherein if sphingomyelin is in the composition it is in an amount greater than 300 mg/kg dry weight of the composition wherein if a fatty acid derivative comprising DHA is in the composition it is in an amount of 60 to 350 mg/100 g dry weight of the composition, and wherein if a fatty acid derivative comprising arachidonic acid is in the composition it is in an amount of 60 to 350 mg/100 g dry weight of the composition.
9 . A method according to claim 1 wherein the composition is a composition selected from the group consisting of; an infant formula, a growing up milk, a composition for infants that is intended to be added or diluted with human breast milk, and a food stuff intended for consumption by an infant and/or child either alone or in combination with human breast milk.
10 - 12 . (canceled)
13 . A method to promote, support or optimise de novo myelination, in particular the de novo myelination trajectory, and/or brain structure, and/or brain connectivity, and/or intellectual potential, and/or cognitive potential, and/or learning potential and/or cognitive functioning in a subject, the method comprising feeding to the subject a vitamin and an ingredient selected from the group consisting of a mineral, choline, a phospholipid, and a fatty acid derivative, wherein brain structure refers to the amount and/or spatial distribution of myelinated matter throughout the brain, and/or in specific brain regions, and wherein said cognitive function is optimised if said subject's scores in a standardized neurodevelopmental test are less than one standard deviation different from that of an exclusively breastfed subject of a well-nourished mother.
14 - 18 . (canceled)Join the waitlist — get patent alerts
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