US2018055864A1PendingUtilityA1
Nutritional formulations including human milk oligosaccharides and antioxidants and uses thereof
Est. expiryDec 31, 2030(~4.4 yrs left)· nominal 20-yr term from priority
A61P 39/06A61P 37/00A61P 29/00A61P 31/12A61P 31/00A61P 11/00A61P 1/00A23V 2200/324A23V 2250/1882A61K 45/06A61K 2300/00A23V 2002/00A23V 2250/28A23L 33/40A23L 33/12A61K 31/202A61K 31/702A61K 31/7016A23V 2200/3202
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Claims
Abstract
Disclosed are nutritional compositions including human milk oligosaccharides in combination with long chain polyunsaturated fatty acids and/or carotenoids that can be administered to preterm infants, term infants, toddlers, and children for reducing inflammation and the incidence of inflammatory diseases.
Claims
exact text as granted — not AI-modified1 . A synthetic pediatric formula comprising a human milk oligosaccharide and from about 0.025 mM to about 1 mM of a long chain polyunsaturated fatty acid.
2 . The synthetic pediatric formula of claim 1 , wherein the human milk oligosaccharide is selected from the group consisting of 6′-sialyllactose, 3′-sialyllactose, 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, lacto-N-fucopentaose, and combinations thereof.
3 . The synthetic pediatric formula of claim 1 , wherein the human milk oligosaccharide is present in an amount of from about 0.001 mg/mL to about 20 mg/mL and is selected from the group consisting of 6′-sialyllactose, 3′-sialyllactose, 2′-fucosyllactose, lacto-N-neotetraose, and combinations thereof.
4 . The synthetic pediatric formula of claim 1 , wherein the long chain polyunsaturated fatty acid is selected from the group consisting of linoleic acid, linolenic acid, arachidonic acid, docosahexaenoic acid, eicosapentaenoic acid, docosapentaenoic acid, and combinations thereof.
5 . The synthetic pediatric formula of claim 1 , wherein the long chain polyunsaturated fatty acid is arachidonic acid, docosahexaenoic acid, or a combination of both.
6 . The synthetic pediatric formula of claim 1 , wherein the human milk oligosaccharide is 6′-sialyllactose.
7 . The synthetic pediatric formula of claim 6 , wherein the 6′-sialyllactose is present in a concentration of from about 0.001 mg/mL to about 20 mg/mL.
8 . The synthetic pediatric formula of claim 1 , wherein the human milk oligosaccharide is 2′-fucosyllactose.
9 . The synthetic pediatric formula of claim 8 , wherein the 2′-fucosyllactose is present in a concentration of from about 0.001 mg/mL to about 1 mg/mL.
10 . The synthetic pediatric formula of claim 1 , further comprising from about 0.001 μg/mL to about 10 μg/mL of a carotenoid.
11 . The synthetic pediatric formula of claim 10 , wherein the carotenoid is present in a concentration of from about 0.001 μg/mL to about 5 μg/mL.
12 . The synthetic pediatric formula of claim 10 , wherein the carotenoid is selected from the group consisting of lutein, lycopene, beta-carotene, and combinations thereof.
13 . The synthetic pediatric formula of claim 1 further comprising from about 10 mg/L to about 200 mg/L of a nucleotide.
14 . The synthetic formula of claim 13 , wherein the nucleotide is present in an amount of from about 42 mg/L to about 102 mg/L.
15 . A synthetic formula selected from a synthetic pediatric formula and a synthetic child formula, the synthetic formula comprising a human milk oligosaccharide selected from the group consisting of 6′-sialyllactose, 3′-sialyllactose, 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, lacto-N-fucopentaose, and combinations thereof, from about 0.025 mM to about 1 mM of a long chain polyunsaturated fatty acid, and from about 0.001 μg/mL to about 10 μg/mL of a carotenoid.
16 . The synthetic formula of claim 15 , wherein the human milk oligosaccharide is selected from the group consisting of 6′-sialyllactose, 3′-sialyllactose, 2′-fucosyllactose, lacto-N-neotetraose, and combinations thereof.
17 . The synthetic formula of claim 15 , wherein the long chain polyunsaturated fatty acid is selected from the group consisting of linoleic acid, linolenic acid, arachidonic acid, docosahexaenoic acid, eicosapentaenoic acid, docosapentaenoic acid, and combinations thereof.
18 . The synthetic formula of claim 15 , wherein the long chain polyunsaturated fatty acid is arachidonic acid, docosahexaenoic acid, or a combination of both.
19 . The synthetic formula of claim 15 , wherein the carotenoid is present in a concentration of from about 0.001 μg/mL to about 5 μg/mL.
20 . The synthetic formula of claim 15 , wherein the carotenoid is selected from the group consisting of lutein, lycopene, beta-carotene, and combinations thereof.
21 . The synthetic formula of claim 15 , wherein the human milk oligosaccharide is present in an amount of about 0.1 mg/mL to about 2 mg/mL.
22 . A method of reducing inflammation in an infant, toddler, or child in need thereof, the method comprising administering to the infant, child or toddler a synthetic formula selected from a synthetic pediatric formula and a synthetic child formula, the synthetic formula comprising a human milk oligosaccharide, from about 0.025 mM to about 1 mM of a long chain polyunsaturated fatty acid, and from about 0.001 μg/mL to about 10 μg/mL of a carotenoid.
23 . The method of claim 22 , wherein the human milk oligosaccharide is selected from the group consisting of 6′-sialyllactose, 3′-sialyllactose, 2′-fucosyllactose, 3-fucosyllactose, lacto-N-tetraose, lacto-N-neotetraose, lacto-N-fucopentaose, and combinations thereof.
24 . The method of claim 22 , wherein the human milk oligosaccharide is selected from the group consisting of 6′-sialyllactose, 3′-sialyllactose, 2′-fucosyllactose, lacto-N-neotetraose, and combinations thereof.
25 . The method of claim 22 , wherein the long chain polyunsaturated fatty acid is selected from the group consisting of linoleic acid, linolenic acid, arachidonic acid, docosahexaenoic acid, eicosapentaenoic acid, docosapentaenoic acid, and combinations thereof.
26 . The method of claim 25 , wherein the long chain polyunsaturated fatty acid is arachidonic acid, docosahexaenoic acid, or a combination of both.
27 . The method of claim 22 , wherein the carotenoid is present in a concentration of from about 0.001 μg/mL to about 5 μg/m L.
28 . The method of claim 28 , wherein the carotenoid is selected from the group consisting of lutein, lycopene, beta-carotene, and combinations thereof.
29 . The method of claim 22 , wherein the synthetic formula further comprises from about 10 mg/L to about 200 mg/L of a nucleotide.
30 . The method of claim 29 , wherein the nucleotide is present in an amount of from about 42 mg/L to about 102 mg/L.Join the waitlist — get patent alerts
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