US2022007704A1PendingUtilityA1

Nutritional compositions comprising hydrolyzed protein and a modified fat system and uses thereof

Assignee: ABBOTT LABPriority: Dec 28, 2015Filed: Sep 27, 2021Published: Jan 13, 2022
Est. expiryDec 28, 2035(~9.4 yrs left)· nominal 20-yr term from priority
A23V 2250/54246A23V 2250/30A23V 2200/322A23L 33/12A61K 31/685A23L 33/125A23L 33/115A61K 31/575A23L 33/19A61P 25/28A23V 2250/186A61K 38/018A23L 29/035A23V 2002/00A61K 2300/00A23V 2250/54252A23L 33/18A61K 45/06A23L 33/40A23V 2250/1842A23V 2250/192
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Claims

Abstract

Disclosed embodiments provide nutritional compositions and methods of enhancing maturation of an infant's brain. The methods include the step of administering to the infant a nutritional composition comprising a protein with a degree of hydrolysis of 10% to 75% in combination with at least one of a monoglyceride, a free fatty acid, a salt of a free fatty acid, a phospholipid, and cholesterol.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of inhibiting neuronal cell death in an individual in need thereof, the method comprising administering to the individual a nutritional composition comprising a protein with a degree of hydrolysis of 10% to 75% and at least one of a monoglyceride, a free fatty acid, a salt of a free fatty acid, a phospholipid, and cholesterol, and wherein after administration the individual's neuronal cell death is reduced. 
     
     
         2 . The method of  claim 1 , wherein the individual in need thereof is a preterm infant. 
     
     
         3 . The method of  claim 1 , wherein the nutritional composition comprises a mixture of a monoglyceride, a phospholipid, cholesterol, and at least one of a free fatty acid and a salt of a free fatty acid. 
     
     
         4 . The method of  claim 3 , wherein the monoglyceride comprises monoglycerol palmitate. 
     
     
         5 . The method of  claim 1 , wherein the nutritional composition is a human milk fortifier. 
     
     
         6 . The method of  claim 1 , wherein the nutritional composition is a powdered human milk fortifier. 
     
     
         7 . The method of  claim 1 , wherein the nutritional composition is an infant formula. 
     
     
         8 . The method of  claim 7 , wherein the nutritional composition is a preterm infant formula. 
     
     
         9 . The method of  claim 1 , wherein the nutritional composition further comprises a carbohydrate. 
     
     
         10 . A method of treating neuronal tissue inflammation in an individual in need thereof, the method comprising administering to the individual a nutritional composition comprising a protein with a degree of hydrolysis of 10% to 75% and at least one of a monoglyceride, a free fatty acid, a salt of a free fatty acid, a phospholipid and cholesterol, and wherein after administration the individual's neuronal tissue inflammation is reduced. 
     
     
         11 . The method of  claim 10 , wherein the nutritional composition comprises a mixture of a monoglyceride, a phospholipid, cholesterol, and at least one of a free fatty acid and a salt of a free fatty acid. 
     
     
         12 . The method of  claim 11 , wherein the monoglyceride comprises monoglycerol palmitate. 
     
     
         13 . The method of  claim 1 , wherein the nutritional composition is a human milk fortifier. 
     
     
         14 . The method of  claim 13 , wherein the nutritional composition is a powdered human milk fortifier. 
     
     
         15 . The method of  claim 1 , wherein the nutritional composition is an infant formula. 
     
     
         16 . The method of  claim 15 , wherein the nutritional composition is a preterm infant formula. 
     
     
         17 . A method for the prevention, delay of progression, or the treatment of a neurodegenerative disorder, comprising:
 administering to an individual in need thereof a nutritional composition comprising a therapeutically effective amount of a DPP-IV inhibiting protein.   
     
     
         18 . The method of  claim 17 , wherein the DPP-IV inhibiting protein has a degree of hydrolysis of 10% to 75%.

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