US2014093554A1PendingUtilityA1
Nutritional compositions with large lipid globule size
Est. expiryDec 11, 2028(~2.4 yrs left)· nominal 20-yr term from priority
Inventors:Eline Marleen Van Der BeekGelske SpeelmansAntonie Van BaalenAnnemarie OostingGünther Boehm
A61P 3/06A61P 19/00A61P 19/10A61P 19/08A23L 33/00A23L 33/12A23L 33/115A61K 35/66A61K 35/60A61K 9/1276A61K 35/20A61K 31/688A61K 31/20A61K 36/06A23V 2002/00A61K 9/14A23L 33/40A61K 36/02A61K 31/202A61K 31/575A23C 9/1528A23L 1/296A23L 1/3008
49
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Claims
Abstract
The present invention relates to a nutritional composition for infants and/or toddlers comprising a lipid component which has a large lipid globule size. The composition can be used to increase bone mineral content and/or bone mass density.
Claims
exact text as granted — not AI-modified1 - 19 . (canceled)
20 . A method of increasing bone mass density and/or increasing bone mineral content, comprising administering to a human subject at risk of developing osteoporosis or in need of enhancement of bone formation and/or bone mass maximization, a composition comprising 10 to 50 wt. % vegetable lipids, based on dry weight of the composition, wherein the vegetable lipids are comprised in lipid globules having:
i) a volume-weighted mode diameter above 1.0 μm, and/or ii) a diameter of 2 to 12 μm in an amount of at least 45 volume % based on total lipid, wherein the increasing bone mass density and/or increasing bone mineral content occurs later in life.
21 . The method according to claim 20 , wherein the lipid globules have:
i) a volume-weighted mode diameter of 1.0-10 μm, and/or ii) a diameter of 2 to 12 μm in an amount of at least 55 volume % based on total lipid.
22 . The method according to claim 20 , wherein the administration is to a human subject between 0 and 36 months of age.
23 . The method according to claim 20 , wherein the increasing bone mass density and/or increasing bone mineral content occurs in a human subject of 36 months of age or older.
24 . The method according to claim 23 , wherein the increasing bone mass density and/or increasing bone mineral content occurs in a human subject above 5 years of age.
25 . The method according to claim 24 , wherein the composition comprises 0.5-10 wt. % phospholipids, based on total lipid.
26 . The method according to claim 25 , wherein the phospholipids are derived from milk lipids.
27 . The method according to claim 20 , wherein the composition comprises glycosphingolipids, cholesterol, or both.
28 . The method according to claim 27 , wherein the composition comprises 0.6 to 12 wt. % polar lipids based on total lipid, wherein the polar lipids are the sum of phospholipids, glycosphingolipids and cholesterol.
29 . The method according to claim 27 , wherein the composition comprises glycosphingolipids.
30 . The method according to claim 20 , wherein the composition comprises gangliosides.
31 . The method according to claim 20 , wherein the composition comprises sphingomyelin.
32 . The method according to claim 21 , wherein the lipid globules have a volume-weighted mode diameter of 4.0 μm or above.
33 . The method according to claim 32 , wherein at least 75 volume % of the lipid globules have a diameter between 4 to 10 μm, based on total lipid.
34 . The method according to claim 21 , wherein the lipid globules have a diameter of 2 to 12 μm in an amount of at least 75 volume % based on total lipid.
35 . The method according to claim 34 , wherein at least 75 volume % of the lipid globules have a diameter between 4 to 10 μm, based on total lipid.
36 . The method according to claim 20 , wherein the composition has a fatty acid profile with a linoleic acid to alpha-linolenic acid weight ratio between 4 and 7.
37 . The method according to claim 20 , wherein the lipids comprise at least 16 wt. % palmitic acid based on total fatty acids.
38 . The method according to claim 37 , wherein over 75 wt. % of the palmitic acid is in the sn-1 or sn-3 position.
39 . The method according to claim 20 , wherein the composition further comprises at least one lipid selected from the group consisting of fish oil, marine oil, algal oil, fungal oil and microbial oil.
40 . The method according to claim 20 , wherein the composition further comprises non-digestible oligosaccharides.
41 . The method according to claim 20 , wherein the composition is a powder suitable for making a liquid composition after reconstitution with an aqueous solution.
42 . The method according to claim 41 , wherein the aqueous solution is water.
43 . A method of treating osteoporosis and/or ostopenia, comprising administering to a human subject at risk of developing osteoporosis and/or ostopenia a composition comprising 10 to 50 wt. % vegetable lipids, based on dry weight of the composition, wherein the vegetable lipids are comprised in lipid globules having:
i) a volume-weighted mode diameter above 1.0 μm, and/or ii) a diameter of 2 to 12 μm in an amount of at least 45 volume % based on total lipid.
44 . The method according to claim 43 , wherein the lipid globules have:
i) a volume-weighted mode diameter of 1.0-10 μam, and/or ii) a diameter of 2 to 12 μm in an amount of at least 55 volume % based on total lipid.
45 . A method of treating obesity, comprising administering to a human subject at risk of developing obesity a composition comprising 10 to 50 wt. % vegetable lipids, based on dry weight of the composition, wherein the vegetable lipids are comprised in lipid globules having:
i) a volume-weighted mode diameter above 1.0 μm, and/or ii) a diameter of 2 to 12 μm in an amount of at least 45 volume % based on total lipid.
46 . A nutritional composition comprising 10 to 50 wt. % vegetable lipids based on dry weight of the composition and 0.6 to 12 wt. % polar lipids based on total lipid weight, wherein the polar lipids are phospholipids, glycosphingolipids and cholesterol, and wherein the vegetable lipids are comprised in lipid globules having:
i) a volume-weighted mode diameter above 1.0 μm, and/or ii) a diameter of 2 to 12 μm in an amount of at least 45 volume % based on total lipid.Join the waitlist — get patent alerts
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