US2019255083A1PendingUtilityA1

Use of purified 2'-fucosyllactose, 3-fucosyllactose and lactodifucotetraose as prebiotics

Assignee: Glycosyn LLCPriority: May 13, 2011Filed: May 3, 2019Published: Aug 22, 2019
Est. expiryMay 13, 2031(~4.8 yrs left)· nominal 20-yr term from priority
A61P 31/04A61P 43/00A61P 1/00A61P 1/14A23L 33/28A23L 33/40C07H 3/06A23L 33/10A61K 31/702A23V 2002/00A23L 2/52A23L 33/21Y02A50/473Y02A50/481Y02A50/30
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Claims

Abstract

The invention provides compositions and methods for utilizing synthetic human milk oligosaccharides as prebiotics.

Claims

exact text as granted — not AI-modified
What is claimed: 
     
         1 . A method for stimulating the growth of a probiotic bacteria in a gastrointestinal tract of a mammalian subject, comprising administering to said subject a composition comprising a purified 2′-FL, 3-FL, or LDFT. 
     
     
         2 . A prebiotic composition comprising a purified human milk oligosaccharide in an amount effective to stimulate the growth of bacteria, wherein said oligosaccharide comprises purified 2′-fucosyllactose (2′-FL), purified 3-fucosyllactose (3-FL), or purified lactodifucotetraose (LDFT). 
     
     
         3 . The prebiotic composition of  claim 2 , wherein said oligosaccharide comprises purified 2′-FL and purified 3-FL. 
     
     
         4 . The prebiotic composition of  claim 2 , wherein said oligosaccharide comprises purified 2′-FL, purified 3-FL, and purified LDFT. 
     
     
         5 . The prebiotic composition of  claim 2 , wherein said bacteria are commensal bacteria endogenous to the intestine of a mammalian subject. 
     
     
         6 . The prebiotic composition of  claim 2 , wherein said bacteria are exogenously administered to a mammalian subject. 
     
     
         7 . The prebiotic composition of  claim 2 , wherein said bacteria comprise bacteria of the genera  Bifidobacterium, Lactobacillus , or  Streptococcus.    
     
     
         8 . The prebiotic composition of  claim 2 , wherein said bacteria are selected from the group consisting of  Bifidobacterium bifidum, Bacteroides fragilis, Bacteroides thetaiotaomicron, Bifidobacterium infantis, Bifidobacterium longum, Lactobacillus acidophilus, Lactobacillus rhamnosus, Bacteroides vulgatus, Lactococcus lactis , and  Streptococcus thermophilus.    
     
     
         9 . The prebiotic composition of  claim 2 , wherein said composition comprises between 0.01 g 2′-FL and 1 g 2′-FL per gram of composition. 
     
     
         10 . The prebiotic composition of  claim 2 , wherein said 2′-FL comprises 90% to 99% by weight of said composition. 
     
     
         11 . The prebiotic composition of  claim 2 , wherein said composition is in the form of a tablet, a capsule, a powder, or an infant formula. 
     
     
         12 . The prebiotic composition of  claim 2 , wherein said composition is provided in dry milk, in mashed rice, in a banana, in a porridge, or in a gruel. 
     
     
         13 . The prebiotic composition of  claim 2 , wherein said composition further comprises probiotic bacteria. 
     
     
         14 . The prebiotic composition of  claim 2 , wherein said composition further comprises fructo-oligosaccharides (FOS) or galacto-oligosaccharides (GOS). 
     
     
         15 . A method of stimulating the growth of bacteria in the gastrointestinal tract of a subject comprising administering to the gastrointestinal tract a composition comprising an effective amount of a purified human milk oligosaccharide, wherein said oligosaccharide comprises purified 2′-fucosyllactose (2′-FL), purified 3-fucosyllactose (3-FL), or purified lactodifucotetraose (LDFT). 
     
     
         16 . The method of  claim 15 , wherein said 2′-FL, said 3-FL, or said LDFT is 95-99% pure. 
     
     
         17 . The method of  claim 15 , wherein the local pH in said gastrointestinal tract is decreased following administration of said composition. 
     
     
         18 . The method of  claim 15 , wherein the local lactate or lactic acid concentration in said gastrointestinal tract is increased following administration of said composition. 
     
     
         19 . The method of  claim 15 , wherein the growth of pathogenic bacteria in said gastrointestinal tract is inhibited following administration of said composition. 
     
     
         20 . The method of  claim 15 , wherein said probiotic bacteria is selected from the group consisting of  Bacteroides vulgates, Lactococcus lactis, Bifidobacterium bifidum, Bacteroides fragilis, Bacteroides thetaiotaomicron, Bifidobacterium infantis, Bifidobacterium longum, Lactobacillus acidophilus , and  Streptococcus thermophilus.    
     
     
         21 . The method of  claim 15 , wherein said composition comprises between 0.01 g 2′-FL and 1 g 2′-FL per gram of composition. 
     
     
         22 . The method of  claim 15 , wherein said composition further comprises probiotic bacteria selected from the group consisting of  Bifidobacterium bifidum, Bacteroides fragilis, Bacteroides thetaiotaomicron, Bifidobacterium infantis, Bifidobacterium longum, Lactobacillus acidophilus, Lactobacillus rhamnosus, Bacteroides vulgatus, Lactococcus lactis , and  Streptococcus thermophilus.    
     
     
         23 . The method of  claim 15 , wherein said composition further comprises fructo-oligosaccharides (FOS) or galacto-oligosaccharides (GOS). 
     
     
         24 . The method of  claim 19 , wherein said pathogenic bacteria 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.

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