Soft chewy confection comprising hmo
US-2024000098-A1 · Jan 4, 2024 · US
US9567361B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9567361-B2 |
| Application number | US-201213469499-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 11, 2012 |
| Priority date | May 13, 2011 |
| Publication date | Feb 14, 2017 |
| Grant date | Feb 14, 2017 |
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The invention provides compositions and methods for utilizing synthetic human milk oligosaccharides as prebiotics.
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What is claimed: 1. A method for stimulating the growth of an exogenously administered probiotic bacterium in a gastrointestinal tract of a mammalian subject, comprising: administering to said subject a composition comprising an oligosaccharide, wherein said oligosaccharide consists of (a) purified 2′-fucosyllactose (2′-FL), (b) purified 3-fucosyllactose (3-FL), (c) purified lactodifucotetraose (LDFT), or (d) a combination thereof, wherein the composition further comprises a probiotic bacterium selected from the group consisting of Bifidobacterium bifidum, Bacteroides fragilis, Bacteroides thetaiotaomicron, Lactobacillus acidophilus, Lactobacillus rhamnosus, Bacteroides vulgatus, Lactococcus lactis , and Streptococcus thermophilus , wherein said 2′-FL, said 3-FL, or said LDFT is at least 95%, 98%, or 99% pure, and wherein said oligosaccharide selectively stimulates the growth of said probiotic bacterium. 2. The method of claim 1 , wherein the local pH in said gastrointestinal tract is decreased following administration of said composition. 3. The method of claim 1 , wherein the local lactate or lactic acid concentration in said gastrointestinal tract is increased following administration of said composition. 4. The method of claim 1 , wherein the growth of a pathogenic bacterium in said gastrointestinal tract is inhibited following administration of said composition. 5. The method of claim 1 , wherein said composition comprises between 0.01 g 2′ FL and 1 g 2′-FL per gram of composition. 6. The method of claim 4 , wherein said pathogenic bacterium is selected from the group consisting of Clostridium histolyticum, Clostridium difficile, Clostridium perfringens, Enterobacter aerogenes, Listeria monocytogenes, Staphylococcus aureus, Salmonella enterica, Yersinia enterocolitica , enterotoxigenic E. coli , and enteropathogenic E. coli. 7. The method of claim 1 , wherein said subject is an infant. 8. The method of claim 1 , wherein said composition is in the form of an infant formula. 9. The method of claim 1 , wherein said composition is provided in dry milk, in mashed rice, in a banana, in a porridge, or in a gruel. 10. A method for stimulating the growth of an exogenously administered probiotic bacterium in a gastrointestinal tract of a mammalian subject, comprising: administering to said subject a composition comprising (a) purified 2′-fucosyllactose (2′-FL), (b) purified 3-fucosyllactose (3-FL), (c) purified lactodifucotetraose (LDFT), or (d) a combination thereof, wherein said 2′-FL, said 3-FL, or said LDFT is at least 95%, 98%, or 99% pure, wherein said oligosaccharide selectively stimulates the growth of said probiotic bacterium and wherein the exogenously administered probiotic bacterium comprises a probiotic bacterium selected from the group consisting of Bifidobacterium bifidum, Bacteroides fragilis, Bacteroides thetaiotaomicron, Lactobacillus acidophilus, Lactobacillus rhamnosus, Bacteroides vulgatus, Lactococcus lactis , and Streptococcus thermophilus. 11. A method for stimulating the growth of an exogenously administered probiotic bacterium in a gastrointestinal tract of a mammalian subject, comprising: administering to said subject a composition comprising 2′-fucosyllactose (2′-FL), a probiotic bacterium selected from the group consisting of Bifidobacterium bifidum, Bacteroides fragilis, Bacteroides thetaiotaomicron, Lactobacillus acidophilus, Lactobacillus rhamnosus, Bacteroides vulgatus, Lactococcus lactis , and Streptococcus thermophilus , and a pharmaceutically-acceptable excipient or inactive ingredient, wherein said 2′-FL is at least 95%, 98%, or 99% pure, and wherein said 2′-FL selectively stimulates the growth of said probiotic bacterium. 12. The method of claim 1 , wherein said probiotic bacterium is selected from the group consisting of Bifidobacterium bifidum BB-12, Lactobacillus acidophilus RC-14 , Lactobacillus acidophilus NCFM, Lactobacillus acidophilus CL 1285, Lactobacillus rhamnosus GG, and Lactobacillus rhamnosus GR-1. 13. The method of claim 10 , wherein said probiotic bacterium is selected from the group consisting of Bifidobacterium bifidum BB-12, Lactobacillus acidophilus RC-14 , Lactobacillus acidophilus NCFM, Lactobacillus acidophilus CL 1285, Lactobacillus rhamnosus GG, and Lactobacillus rhamnosus GR-1. 14. The method of claim 1 , wherein said probiotic bacterium further comprises Bifidobacterium infantis or Bifidobacterium longum. 15. The method of claim 1 , wherein said composition comprises yogurt or a probiotic beverage. 16. The method of claim 1 , wherein said probiotic bacterium is Bacteroides fragilis, Bacteroides thetaiotaomicron , or Bacteroides vulgatus. 17. The method of claim 1 , wherein said composition comprises a weaning food. 18. The method of claim 1 , wherein said mammalian subject is not an infant. 19. The method of claim 18 , wherein said mammalian subject is a child. 20. The method of claim 18 , wherein said mammalian subject is an adult. 21. The method of claim 6 , wherein said pathogenic bacterium is selected from the group consisting of Enterobacter aerogenes, Listeria monocytogenes, Staphylococcus aureus, Salmonella enterica , and Yersinia enterocolitica.
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