US2019075808A1PendingUtilityA1

Human milk compositions and methods of making and using same

79
Assignee: PROLACTA BIOSCIENCE INCPriority: Aug 30, 2006Filed: Nov 14, 2018Published: Mar 14, 2019
Est. expiryAug 30, 2026(~0.1 yrs left)· nominal 20-yr term from priority
A23L 33/15A23L 2/52A23L 33/16A23L 33/10A23L 2/66A23L 33/40A23L 33/19A23C 9/206
79
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Claims

Abstract

The disclosure features human milk fortifier compositions, standardized human milk, and methods of making and using same. In one embodiment, a pasteurized human milk composition includes a human protein constituent of about 35-85 mg/mL; a human fat constituent of about 60-110 mg/mL; and a human carbohydrate constituent of about 60-140 mg/mL.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A human milk fortifier composition comprising 35-95 mg/mL protein, calcium, and phosphorus, wherein the calcium is present in the composition at a concentration of about 4.0 to about 5.55 mg/mL, and wherein the composition comprises a calcium to phosphorus ratio of no more than 2:1. 
     
     
         2 . The human milk fortifier composition of  claim 1 , wherein the calcium to phosphorus ratio is about 1.8:1 to 2:1. 
     
     
         3 . The human milk fortifier composition of  claim 1 , wherein the phosphorus is present in the composition at a concentration of about 2.0 to about 3.05 mg/mL. 
     
     
         4 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier does not comprise xenogeneic components. 
     
     
         5 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier comprises about 35-85 mg/mL protein. 
     
     
         6 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier comprises about 55-65 mg/mL protein. 
     
     
         7 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier comprises about 60-110 mg/mL fat. 
     
     
         8 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier comprises about 85-95 mg/mL fat. 
     
     
         9 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier comprises about 60-140 mg/mL carbohydrates. 
     
     
         10 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier comprises about 70-120 mg/mL carbohydrates. 
     
     
         11 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier comprises about 55-65 mg/mL protein, about 85-95 mg/mL fat, and about 70-120 mg/mL carbohydrates. 
     
     
         12 . The human milk fortifier composition of  claim 1 , further comprising one or more added minerals selected from the group consisting of chloride, copper, iron, magnesium, manganese, potassium, sodium, and zinc. 
     
     
         13 . The human milk fortifier composition of  claim 1 , wherein the human milk fortifier is prepared from donor milk obtained from a qualified human breast milk donor. 
     
     
         14 . The human milk fortifier composition of  claim 13 , wherein the donor is qualified by screening a biological sample from the donor for the presence of pathogens and drugs of abuse. 
     
     
         15 . The human milk fortifier composition of  claim 14 , wherein the pathogens are selected from HIV 1, HIV2, HTLV I, HTLV II, HBV, HCV, syphilis, and  B. cereus.    
     
     
         16 . The human milk fortifier composition of  claim 14 , wherein the drugs of abuse are selected from the group consisting of cocaine, opiates, methamphetamines, benzodiazepine, amphetamines, and THC. 
     
     
         17 . The human milk fortifier composition of  claim 13 , wherein the donor is re-qualified periodically. 
     
     
         18 . The human milk fortifier composition of  claim 13 , wherein a biological sample from the qualified human breast milk donor is tested for one or more genetic markers. 
     
     
         19 . The human milk fortifier composition of  claim 18 , wherein the donor milk is tested for one or more genetic markers, and wherein the genetic markers of the donor milk are compared to the genetic markers of the biological sample from the qualified human breast milk donor, to determine if the donor milk is obtained from the qualified human breast milk donor. 
     
     
         20 . The human milk fortifier composition of  claim 13 , wherein the donor milk is screened for the presence of pathogens and drugs of abuse prior to preparing the human milk fortifier. 
     
     
         21 . The human milk fortifier composition of  claim 20 , wherein the pathogens are selected from the group consisting of HIV 1, HIV2, HTLV I, HTLV II, HBV, HCV, syphilis, and  B. cereus.    
     
     
         22 . The human milk fortifier composition of  claim 1 , prepared by pooling milk from a human donor to generate the fortifier composition, wherein the donor milk is pooled to at least about 75 to 2,000 liters per lot. 
     
     
         23 . The human milk fortifier composition of  claim 1 , prepared by pooling milk from a human donor and concentrating the nutrients in the pooled milk to obtain the human milk fortifier composition. 
     
     
         24 . The human milk fortifier composition of  claim 23 , wherein the concentrating step comprises filtration. 
     
     
         25 . The human milk fortifier composition of  claim 24 , wherein the filtering comprises ultrafiltration. 
     
     
         26 . The human milk fortifier composition of  claim 1 , prepared by pooling milk from a human donor and processing the donor milk to reduce the bioburden. 
     
     
         27 . The human milk fortifier composition of  claim 26 , wherein the bioburden of the pooled human milk is reduced by heat treatment. 
     
     
         28 . The human milk fortifier composition of  claim 26 , wherein the bioburden of the pooled human milk is reduce by filtration. 
     
     
         29 . The human milk fortifier composition of  claim 1 , prepared by a method comprising pooling milk from a qualified human donor, screening the pooled milk for the presence of pathogens, and filtering the pooled milk. 
     
     
         30 . The human milk fortifier composition of  claim 29 , wherein the filtering comprises ultrafiltration. 
     
     
         31 . The human milk fortifier composition of  claim 29 , wherein the method further comprises pasteurization. 
     
     
         32 . The human milk fortifier composition of  claim 29 , wherein the method further comprises separating the pooled milk into a skim portion and a cream portion. 
     
     
         33 . The human milk fortifier composition of  claim 32 , wherein the method further comprises filtering the skim portion through one or more skim filters to obtain a permeate portion and a protein rich skim portion; and mixing a fraction of the cream portion with the protein rich skim portion. 
     
     
         34 . The human milk fortifier composition of  claim 33 , wherein the method further comprises washing the one or more skim filters with permeate to obtain a protein wash, and adding the protein wash to the protein rich skim portion. 
     
     
         35 . A human milk composition prepared by a method comprising mixing the human milk fortifier composition of  claim 1  with a volume of human milk, at a milk:fortifier ratio of about 80:20. 
     
     
         36 . A method for providing fortified human milk to a preterm or low birth weight infant, comprising administering a human milk composition of  claim 35  to the premature or low birth weight infant. 
     
     
         37 . The method of  claim 36 , wherein the infant was born at less than 37 weeks gestational age. 
     
     
         38 . The method of  claim 36 , wherein the infant weighs less than 2500 grams at birth. 
     
     
         39 . The method of  claim 36 , wherein the infant weighs less than 1500 grams at birth. 
     
     
         40 . The method of  claim 36 , wherein the human milk composition is administered to the infant as a bolus feeding or through a syringe infusion pump for continuous feeding. 
     
     
         41 . A method for promoting growth of a preterm or low birth weight infant, comprising administering the human milk composition of  claim 35  to the premature or low birth weight infant. 
     
     
         42 . A method for promoting the immunological development of a preterm or low birth weight infant, comprising administering the human milk composition of  claim 35  to the premature or low birth weight infant. 
     
     
         43 . A method for treating or preventing necrotizing enterocolitis (NEC) in a preterm or low birth weight infant, comprising administering the human milk composition of  claim 35  to the premature or low birth weight infant.

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