Soft chewy confection comprising hmo
US-2024000098-A1 · Jan 4, 2024 · US
US9161563B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9161563-B2 |
| Application number | US-201113988967-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 21, 2011 |
| Priority date | Nov 23, 2010 |
| Publication date | Oct 20, 2015 |
| Grant date | Oct 20, 2015 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention discloses an oligosaccharide mixture comprising 5-70 wt % of at least one N-acetylated oligosaccharide, 5-90 wt % of at least one neutral oligosaccharide, 2-50 wt % of at least one sialylated oligosaccharide, and/or 5-70 wt % of at least one fucosylated oligosaccharide. The invention also discloses a food product, especially an infant formula, comprising said oligosaccharide mixture.
Opening claim text (preview).
The invention claimed is: 1. A food product comprising: hydrolyzed proteins; and an oligosaccharide mixture which comprises: 5-70 wt % of at least one N-acetylated oligosaccharide selected from the group consisting of N-acetyl-galactosaminyl-lactose and galactosyl-N-acetyl-galactosaminyl-lactose, 5-90 wt % of at least one galacto-oligosaccharide selected from the group consisting of Galβ1,6Gal, Galβ1,6Galβ1,4Glc, Galβ1,6Galβ1,6Glc, Galβ1,3Galβ1,3Glc, Galβ1,3Galβ1,4Glc, Galβ1,6Galβ1,6Galβ1,4Glc, Galβ1,6Galβ1,3Galβ1,4Glc, Galβ1,3Galβ1,6Galβ1,4Glc, Galβ1,3Galβ1,3Galβ1,4Glc, Galβ1,4Galβ1,4Glc and Galβ1,4Galβ1,4Galβ1,4Glc, 2-50 wt % of at least one sialylated oligosaccharide selected from the group consisting of 3′-sialyllactose and 6′-sialyllactose; and 2-70 wt % of at least one fucosylated oligosaccharide selected from the group consisting of 2′-fucosyllactose, 3-fucosyllactose, difucosyllactose, lacto-N-fucopentaoses, lacto-N-difucohexaose I, monofucosyllacto-N-hexaose, Difucosyllacto-N-hexaose I and Difucosyllacto-N-neohexaose II. 2. A food product according to claim 1 comprising a protein source, a fat source, and a carbohydrate source, wherein the protein source comprises the hydrolyzed proteins. 3. The food product according to claim 1 , which is selected from the group consisting of a starter infant formula, an infant formula, a baby food, an infant cereal composition, a follow-up formula and a growing-up milk. 4. The food product according to claim 1 , wherein the extent of hydrolysis of the hydrolysed proteins is between 50 and 100 of NPN/TN %. 5. The food product according to claim 1 , wherein a trinitrobenzenesulfonic acid reactive Nitrogen % that reacts with amino (lysine) N/TN of the hydrolysed proteins is from 8-15%. 6. A method for preventing and reducing the risk of food allergies and related food allergy effects on health of an individual, the method comprising: administering to the individual oligosaccharide mixture which comprises 5-70 wt % of at least one N-acetylated oligosaccharide selected from the group consisting of N-acetyl-galactosaminyl-lactose and galactosyl-N-acetyl-galactosaminyl-lactose, 5-90 wt % of at least one galacto-oligosaccharide selected from the group consisting of Galβ1,6Gal, Galβ1,6Galβ1,4Glc, Galβ1,6Galβ1,6Glc, Galβ1,3Galβ1,3Glc, Galβ1,3Galβ1,4Glc, Galβ1,6Galβ1,6Galβ1,4Glc, Galβ1,6Galβ1,3Galβ1,4Glc, Galβ1,3Galβ1,6Galβ1,4Glc, Galβ1,3Galβ1,3Galβ1,4Glc, Galβ1,4Galβ1,4Glc and Galβ1,4Galβ1,4Galβ1,4Glc, 2-50 wt % of at least one sialylated oligosaccharide selected from the group consisting of 3′-sialyllactose and 6′-sialyllactose; and 2-70 wt % of at least one fucosylated oligosaccharide selected from the group consisting of 2′-fucosyllactose, 3-fucosyllactose, difucosyllactose, lacto-N-fucopentaoses, lacto-N-difucohexaose I, monofucosyllacto-N-hexaose, Difucosyllacto-N-hexaose I and Difucosyllacto-N-neohexaose II. 7. The method according to claim 6 , wherein the effects are selected from the group consisting of (i) skin effects, atopic dermatitis, rash, or redness; (ii) effects on the immune system or inflammation status; or (iii) effects on the gastro-intestinal system. 8. The method according to claim 6 , wherein the composition provides enhancement of the oral tolerance to allergens. 9. The food product according to claim 1 , wherein the food product comprises at least one probiotic bacterial strain. 10. A method for reducing the severity and reducing the occurrence of food allergies and related food allergy effects on health, the method comprising: administering to an individual an oligosaccharide mixture comprising 5-70 wt % of at least one N-acetylated oligosaccharide selected from the group consisting of N-acetyl-galactosaminyl-lactose and galactosyl-N-acetyl-galactosaminyl-lactose, 5-90 wt % of at least one galacto-oligosaccharide selected from the group consisting of Galβ1,6Gal, Galβ1,6Galβ1,4Glc, Galβ1,6Galβ1,6Glc, Galβ1,3Galβ1,3Glc, Galβ1,3Galβ1,4Glc, Galβ1,6Galβ1,6Galβ1,4Glc, Galβ1,6Galβ1,3Galβ1,4Glc, Galβ1,3Galβ1,6Galβ1,4Glc, Galβ1,3Galβ1,3Galβ1,4Glc, Galβ1,4Galβ1,4Glc and Galβ1,4Galβ1,4Galβ1,4Glc, 2-50 wt % of at least one sialylated oligosaccharide selected from the group consisting of 3′-sialyllactose and 6′-sialyllactose, and/or 5-70 wt % of at least one fucosylated oligosaccharide selected from the group consisting of 2′-fucosyllactose, 3-fucosullactose, difucosyllactose, lacto-N-fucopentaoses, lacto-N-difucohexaose I, monofucosyllacto-N-hexaose, Difucosyllacto-N-hexaose I and Difucosyllacto-N-neohexaose II, as a synthetic nutritional composition. 11. A method for the enhancement of oral tolerance to allergens, the method comprising: administering to an individual a food product comprising 5-70 wt % of at least one N-acetylated oligosaccharide selected from the group consisting of N-acetyl-galactosaminyl-lactose and galactosyl-N-acetyl-galactosaminyl-lactose, 5-90 wt % of at least one galacto-oligosaccharide selected from the group consisting of Galβ1,6Gal, Galβ1,6Galβ1,4Glc, Galβ1,6Galβ1,6Glc, Galβ1,3Galβ1,3Glc, Galβ1,3Galβ1,4Glc, Galβ1,6Galβ1,6Galβ1,4Glc, Galβ1,6Galβ1,3Galβ1,4Glc, Galβ1,3Galβ1,6Galβ1,4Glc, Galβ1,3Galβ1,3Galβ1,4Glc, Galβ1,4Galβ1,4Glc and Galβ1,4Galβ1,4Galβ1,4Glc, 2-50 wt % of at least one sialylated oligosaccharide selected from the group consisting of 3′-sialyllactose and 6′-sialyllactose, and/or 5-70 wt % of at least one fucosylated oligosaccharide selected from the group comprising consisting of 2′-fucosyllactose, 3-fucosyllactose, difucosyllactose, lacto-N-fucopentaoses, lacto-N-difucohexaose I, monofucosyllacto-N-hexaose, Difucosyllacto-N-hexaose I and Difucosyllacto-N-neohexaose II, as a synthetic nutritional composition. 12. The method according to claims 10 , wherein the food product is a supplement. 13. The method according to claim 10 wherein the food product comprises fully hydrolyzed and/or partially hydrolyzed proteins. 14. The method according to claim 11 , wherein the food product is a supplement. 15. The method according to claim 11 wherein the food product comprises fully hydrolyzed and/or partially hydrolyzed proteins.
Drugs for immunological or allergic disorders · CPC title
Bacteria or derivatives thereof, e.g. probiotics · CPC title
Glucans · CPC title
Oligosaccharides, i.e. having three to five saccharide radicals attached to each other by glycosidic linkages · CPC title
having the esterifying carboxyl radicals attached to acyclic carbon atoms · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.