WO2006019300A2 - Immune stimulatory infant nutrition - Google Patents
Immune stimulatory infant nutrition Download PDFInfo
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- WO2006019300A2 WO2006019300A2 PCT/NL2005/000609 NL2005000609W WO2006019300A2 WO 2006019300 A2 WO2006019300 A2 WO 2006019300A2 NL 2005000609 W NL2005000609 W NL 2005000609W WO 2006019300 A2 WO2006019300 A2 WO 2006019300A2
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- nutritional composition
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- DWRXFEITVBNRMK-JXOAFFINSA-N ribothymidine Chemical compound O=C1NC(=O)C(C)=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 DWRXFEITVBNRMK-JXOAFFINSA-N 0.000 description 1
- 125000005629 sialic acid group Chemical group 0.000 description 1
- 210000000813 small intestine Anatomy 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000001356 surgical procedure Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- 229940113082 thymine Drugs 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 125000005457 triglyceride group Chemical group 0.000 description 1
- DRTQHJPVMGBUCF-UHFFFAOYSA-N uracil arabinoside Natural products OC1C(O)C(CO)OC1N1C(=O)NC(=O)C=C1 DRTQHJPVMGBUCF-UHFFFAOYSA-N 0.000 description 1
- 229940045145 uridine Drugs 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- JCZSFCLRSONYLH-QYVSTXNMSA-N wyosin Chemical compound N=1C(C)=CN(C(C=2N=C3)=O)C=1N(C)C=2N3[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O JCZSFCLRSONYLH-QYVSTXNMSA-N 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
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- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/20—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
- A61K31/201—Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having one or two double bonds, e.g. oleic, linoleic acids
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- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/115—Fatty acids or derivatives thereof; Fats or oils
- A23L33/12—Fatty acids or derivatives thereof
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- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
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- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
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- A—HUMAN NECESSITIES
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- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
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- A—HUMAN NECESSITIES
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- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
Definitions
- the present invention relates to a nutritional composition for feeding infants, containing fat, protein, carbohydrate, a nucleotide component and to the use thereof.
- nucleotide components particularly nucleotides. It was found that by combining nucleotide components with negatively charged non-protein components the bioactive effects of the nucleotide component in nutritional formulations may be enhanced significantly.
- the present invention provides a nutritional composition containing a nucleotide component; and a non-proteinaceous negatively charged, glycan or glycoconjugate component with a molecular weight between 200 and 20.000 dalton (hereinafter referred to as NCC).
- NCC non-proteinaceous negatively charged, glycan or glycoconjugate component with a molecular weight between 200 and 20.000 dalton
- the improved activity is believed to be the result of an improved presentation and delivery of the negatively charged nucleotide component to the epithelial cells, due to interaction of the NCC and the nucleotide component e.g. via hydrogen and salt bridges.
- the biological active molecular anionic charge of nucleotides is condensed and the molecular distribution of charge is beneficially altered.
- the present nutritional composition can be even further improved by combining the nucleotide component and NCC with bivalent cations, preferably calcium and/or zinc.
- the cation will increase proximity of the nucleotide component and the NCC in a liquid environment (e.g. the intestinal tract) by formation of hydrogen/salt bridges, thereby further increasing the interactive effects between the NCC and the nucleotide components.
- the present invention provides a nutritional composition containing protein, fat and carbohydrate; and a nucleotide component selected from the group consisting of nucleic acid, nucleic acid derivatives, nucleotides, nucleoside polyphosphates, polynucleotides, nucleosides, ribose, desoxyribose, and dinucleosidpolyphosphates
- Nucleotide component contains a nucleotide component selected from the group consisting of nucleic acid, nucleic acid derivatives, nucleotides, nucleoside polyphosphates, polynucleotides, nucleosides, ribose, desoxyribose, and dinucleosidpolyphosphates (Np x N).
- Nucleic acids are typically heterocyclic pyrimidine bases cytosine, thymine, uridine and derivatives, like pseudouridine, dihyderouridine, ribothymidine, 4- thiouridine, 3-methylcytidine, N-acetylcytidine, lysidine as well as purine bases adenine and guanosine and derivatives, like 1-methyladenosine, N6- isopentenyladenosine, inosine, N7-methylguansine, N2-dimethylguanosine and wyosine.
- Nucleosides such as N-glycoside are pyrimidine or purine base glycoconjugates.
- Preferred nucleotides are phosphoesters of nucleosides, which are monomers or polymers in the form of oligo- or polynucleotides.
- hydrolysates of desoxyribonucleic acid and ribonucleic acid, t-ribonucleic acid and ribosomes derived from animal milk, animal and plant tissues, yeasts, bifido- and lactobacteria and synthetic molecules are suitable raw material sources.
- the present composition contains at least one, preferably at least two, even more preferably at least three nucleotides selected from the group consisting of cytidine monophosphate (CMP), guanosine monophosphate (GMP), adenosine monophosphate (AMP), uridine monophosphate (UMP), and inosine monophosphate (IMP).
- CMP cytidine monophosphate
- GMP guanosine monophosphate
- AMP adenosine monophosphate
- UMP uridine monophosphate
- IMP inosine monophosphate
- the present composition contains ribose as a nucleotide component, preferably D-ribose.
- D(-)Ribose is a pentose sugar that can be purchased as crystalline product. Ribose is a main constituent of nucleic acids.
- the present composition contains between 0.01 wt.% and 50 wt.% ribose based on dry weight of the product, more preferably between 0.05 and 10 wt.%, even more prefferably between 0.5 and 10 wt.%
- the present composition preferably comprises between 5 and 100 mg nucleosides and/or between 5 and 100 mg nucleotides per 100 gram dry weight of the composition, more preferably between 5 and 50 mg.
- the nucleotides and/or nucleosides further stimulate the immune system, acting synergistically with the NCC of the present composition.
- the present composition contains a negatively charged non-proteineous glycan and 5 glycoconjugate component (NCC) with a molecular weight between 200 and 20.000 dalton.
- NCC 5 glycoconjugate component
- the NCC is negatively charged in water with a pH of 7.
- the negative charge is preferably provided by a carboxylic, phosphate and/or sulphate group, most preferably by a carboxylic group.
- the NCC has a MW between 1000 and 10 10.000 Dalton.
- the weight ratio nucleotide component/NCC in the present nutritional composition is preferably between 100 and 0.1.
- the NCC is selected from the group consisting of glycosphingolipids, acid oligosaccharides, and sialysated oligosaccharides.
- the sialysated oligosaccharides is sialyllactose and/or disialo-lactoneotertaose (DS-LNT).
- 15 Glycosphingolipids are typically compounds with a monosaccharide attached directly to a ceramide.
- the NCC contains a ganglioside (a glycosphingolipid).
- Gangliosides are typically highly complex oligoglycosylceramides, which contain one or more sialic acid groups (iV-acyl, especially acetyl, derivatives of neuraminic acid, abbreviated 20 to "NANA") in addition to glucose, galactose and galactosamine.
- sialic acid groups iV-acyl, especially acetyl, derivatives of neuraminic acid, abbreviated 20 to "NANA”
- buttermilk, egg yolk lecithin are suitable raw material sources of gangliosides. ( Biochemistry, Donald Voet and Judith G. Voet, John Wiley and Sons, Inc NY second edition chapter 23).
- the present composition preferably contains egg yolk lecithin and/or buttermilk.
- the present composition contains a ganglioside selected from the group consisting GM3, GMl and GDI .
- the present composition contains sulfoglycosphingolipids as the NCC.
- Sulfoglycosphingolipids are sulfate esters of galactosylceramide and lactosylceramide (often referred as "sulfatides” or "lipid sulfates”), with a sulfate group linked to position 3 of the galactosyl moiety.
- the present composition preferably includes acidic oligosaccharides with a DP from 2 to 100, preferably from 2 to 60.
- acid or acidic oligosaccharide refers to oligosaccharides comprising at least one acidic group selected from the group consisting of N-acetylneuraminic acid, N-glycoloylneuraminic acid, free or esterified carboxylic acid, sulfuric acid group and phosphoric acid group.
- the acidic oligosaccharide preferably comprises uronic acid units (i.e. uronic acid polymer), more preferably galacturonic acid units.
- the present composition preferably contains between 0.1 and 10 grams acid oligosaccharides per 100 gram dry weight of the present composition, more preferably between 1 and 6 grams per 100 gram dry weight.
- R is preferably selected from the group consisting of hydrogen, hydroxy or acid group, preferably hydroxy; and at least one selected from the group consisting of R2, R3, R4 and R5 represents N-acetylneuraminic acid, N-glycoloylneuraminic acid, free or esterified carboxylic acid, sulfuric acid group and phosphoric acid group, and the remaining of R2, R3, R4 and R5 representing hydroxy and/or hydrogen.
- one selected from the group consisting of R2, R3, R4 and R5 represents N-acetylneuraminic acid, N-glycoloylneuraminic acid, free or esterified carboxylic acid, sulfuric acid group or phosphoric acid group, and the remaining represent hydroxy and/or hydrogen.
- R2, R3, R4 and R5 represents free or esterified carboxylic acid and the remaining of R2, R3, R4 and R5 representing hydroxy and/or hydrogen; and n is an integer and refers to a number of hexose units (see also Degree of Polymerisation, below), which may be any hexose unit.
- n is an integer between 1-5000.
- the hexose unit(s) is a uronic acid unit.
- Rl, R2 and R3 represent hydroxy
- R4 represent hydrogen
- R5 represents carboxylic acid
- n is any number between 1 and 250, preferably between 1 and 10 and the hexose unit is galacturonic acid.
- the acid oligosaccharide has one, preferably two, terminal uronic acid units, which may be free or esterified.
- the terminal uronic acid unit is selected from the group consisting of galacturonic acid, glucuronic acid, guluronic acid, iduronic acid, mannuronic acid, riburonic acid and alturonic acid. These units may be free or esterified.
- the terminal hexose unit has a double bond, which is preferably situated between the C4 and C5 position of the terminal hexose unit.
- one of the terminal hexose units comprises the double bond.
- the terminal hexose e.g. uronic acid
- Fig. 2 Preferred terminal hexose acid group
- R is preferably selected from the group consisting of hydrogen, hydroxy or acid group, preferably hydroxy (see above); and at least one selected from the group consisting of R2, R3, R4 and R5 represents N-acetylneuraminic acid, N- glycoloylneuraminic acid, free or esterified carboxylic acid, sulfuric acid group and phosphoric acid group, and the remaining of R2, R3, R4 and R5 representing hydroxy and/or hydrogen.
- R2, R3, R4 and R5 represents N-acetylneuraminic acid, N-glycoloylneuraminic acid, free or esterified carboxylic acid, sulfuric acid group and phosphoric acid group, and the remaining of R2, R3, R4 and R5 represent hydroxy and/or hydrogen. Even more preferably one selected from the group consisting of R2, R3, R4 and R5 represents free or esterified carboxylic acid and the remaining of R2, R3, R4 and R5 represent hydroxy and/or hydrogen; and n is an integer and refers to a number of hexose units (see also Degree of Polymerisation, below), which may be any hexose unit.
- n is an integer between 1-100 representing the number of hexose units said hexose units preferably being uronic acid, even more preferably being galacturonic acid units.
- the carboxylic acid groups on these units may be free or (partly) esterified, and are preferably at least partly methylated.
- R2 and R3 represent hydroxy
- R4 represent hydrogen
- R5 represents free or esterified carboxylic acid.
- the acid oligosaccharides used in the invention are preferably prepared from pectin, pectate, alginate, chondroitine, hyaluronic acids, heparine, heparane, bacterial carbohydrates, sialoglycans, fucoidan, fucooligosaccharides or carrageenan, more preferably from pectin and/or alginate.
- pectin often biochemically depolymerized is used.
- pectin depolymerized with pectin lyase is used. Bivalent cation
- the present nutritional composition preferably contains a bivalent cation.
- the bivalent cation enhances proximity of the nucleotide component and the NCC, further modifying the charge density and improving biological activity.
- the present composition contains at least one bivalent cation selected from the group consisting of magnesium, calcium, iron, chromium, manganese, molybdenum, copper and zinc.
- the present composition contains at least calcium and/or zinc.
- Zinc is advantageously included in the present composition.
- Zinc enhances the biological activity of the nucleotides when combined with the present NCC, and also s an essential micronutrient for growth and development of the immune function, particularly for infants.
- Zinc deficiency impairs overall immune function and resistance to infection.
- the present composition advantageously comprises zinc, preferably in an amount of 2 to 100 mg zinc per 100 gram dry weight of the present composition, even more preferably between 3 and 25 mg zinc per 100 g dry weight of the present composition.
- the weight of zinc is calculated as elementary zinc.
- the present composition contains calcium for improved charge interaction. Calcium is also essential in an infants diet, and hence advantageously included in the present composition. Preferably the present composition contains between 150 and 1000 mg calcium by weight total dry weight of the composition.
- the present composition can be advantageously used as an infant formula,.
- the infant formula preferably administered to the infant in liquid form.
- the term infant includes weaning infants, and toddlers.
- the present invention relates to an nutritional composition which provides the macronutrients of the infant diet.
- the present composition preferably contains 30 to 60 en% lipid; 5 to 15 en% protein; and 25 to 65 en% carbohydrate.
- the present composition contains 43 to 53 en% lipid; 7 to 11 en% protein; and 43 to 53 en% carbohydrate (en% is short for energy percentage and represents the relative amount each constituent contributes to the total caloric value of the preparation).
- the term "protein” or protein component in this context is the cumulative of protein, polypeptides, peptides and amino acids.
- the carbohydrate in the present composition is preferably provided largely by lactose, i.e. preferably at least 75 wt.% of total digestible carbohydrate is provided by lactose, preferably at least 90 wt.%.
- the present composition preferably contains at least 10 wt.% linoleic acid (LA) based on total fatty acids, preferably between 11 and 20 wt.%, more preferably between 12 and 15 wt.%.
- the present composition preferably contains at least 1 wt.% alpha linolenic acid (ALA) based on total fatty acids, preferably between 1.5 and 4 wt.% ALA, even more preferably between 2 and 2.5 wt.%.
- the weight ratio LA/ALA is preferably between 2 and 10, preferably between 5 and 7.5.
- the present composition preferably includes between 0.05 and 5 wt% gamma-linolenic acid (GLA) based on total fatty acids, preferably between 0.1 and 1 wt.%.
- GLA gamma-linolenic acid
- STA steraidonic acid
- the present composition preferably comprises at least one long chain- polyunsaturated fatty acid with 20 or 22 carbon atoms (LCPUFA) in an amount exceeding 0.1 wt.% based on total fatty acids, selected from the group consisting of docosahexaenoic acid (DHA), arachidonic acid (AA) and eicosapentaenoic acid (EPA).
- DHA docosahexaenoic acid
- AA arachidonic acid
- EPA eicosapentaenoic acid
- the composition contains DHA in an amount exceeding 0.1 wt.% based on total fatty acids; and AA in an amount exceeding 0.1 wt.% based on total fatty acids.
- At least one LCPUFA of this group is included in an amount between
- the composition contains AA and DHA, even more preferably AA, DHA and EPA.
- the AA content preferably does not exceed 5 wt.%, more preferably does not exceed 1 wt.%, most preferably between 0.1 and 0.6 wt.% of the total fatty acids.
- EPA and/or DHA are advantageously added to balance the action of AA, e.g. reduce the potential pro -inflammatory action of AA metabolites. Excess metabolites from AA may cause inflammation.
- the present composition preferably comprises AA, EPA and/or DHA, wherein the weight ratio AA/DHA preferably is above 0.25, preferably above 0.5, even more preferably above 1.
- the ratio AA/DHA is preferably below 25, preferably below 10.
- the weight ratio AA/EPA is preferably between 1 and 100, more preferably between 5 and 20.
- the weight ratio EPA/DHA is preferably 1 or lower, more preferably below 0.5.
- the content of LCPUFA does not exceed 3 wt.% of the total fatty acids as it is desirable to mimic human milk as closely as possible.
- the present composition preferably contains less than 1 gram omega-3 LCPUFA per 100 gram fatty acids, more preferably between 0.1 and 0.75 gram per 100 gram fatty acids.
- the omega-6 LCPUFA content preferably does not exceed 2 gram per 100 gram fatty acids and is preferably between 0.1 and 0.75 gram per 100 gram fatty acids.
- the LCPUFAs and the other fatty acids may be provided as free fatty acids, in triglyceride form, in phospholipid form, or as a mixture of one of more of the above.
- the present composition advantageously comprises at least one of AA and DHA in phospholipid form, as these reduce the incidence of inflammatory disorders of the intestine.
- the present composition preferably comprises between 0.1 and 5 mg AA from phospholipid per gram total fat and between 0.1 and 5 mg DHA from phospholipid per gram total fat.
- the AA and/or DHA are at least partly present in the form of phosphatidylcholine (PC) and/or phosphatidylethanolamine (PE), e.g. AA and/or DHA containing PE and/or PC.
- the present composition preferably comprises indigestible oligosaccharides with a degree of polymerisation (DP) of between 2 and 100.
- the oligosaccharides are believed to be important for providing a suitable intestinal environment for improved presentation and charge density of the combination of nucleotide 5 component and NCC.
- the indigestible oligosaccharides reduce the pH of the intestinal environment, improving biological activity of the nucleotides.
- the present composition contains 0.1 to 12 grams indigestible oligosaccharides per 100 gram dry weight of the composition, preferably between 3 and 8 grams, more preferably between 5 and 7.5 grams.
- indigestible oligosaccharides provide the desired effects without causing intestinal discomfort.
- Suitable indigestible oligosaccharides are not or only partially digested in the intestine by the action of acids or digestive enzymes present in the human upper digestive tract (small intestine and stomach), but are
- the oligosaccharides are preferably water-soluble (exceeding a solubility of 1 gram oligosaccharide per liter water).
- the average DP of the present oligosaccharide is preferably below 40, even more preferably below 20.
- the present composition comprises between 2 and 12 grams oligosaccharides with a DP of 2 to 60, more preferably with a DP of 2 to
- At least one of the oligosaccharides of the present composition is selected from the group consisting of inulin, fructooligosaccharides, indigestible dextrins, galactooligosaccharides (including 25 transgalactooligosaccharides), xylooligosaccharides, arabinooligosaccharides, glucooligosaccharides, mannooligo-saccharides, lacto-N-neotetraose, fucooligosaccharides (containing at least one fucose saccharide unit), acidic oligosaccharides (e.g. uronic acid oligosaccharides such as pectin oligosaccharides) and mixtures thereof.
- inulin fructooligosaccharides, indigestible dextrins
- galactooligosaccharides including 25 transgalactooligosaccharides
- xylooligosaccharides arab
- the present composition comprises at least one selected from the group consisting of inulins and fructooligosaccharides and at least one selected from the group consisting of galactooligosaccharides (including transgalactooligosaccharides) and pectin hydrolysate.
- the present composition comprises 2 to 12 grams oligosaccharides with a DP of 2 to 10 and ⁇ -linked galactose and glucose saccharides, more preferably transgalactooligosaccharides (i.e. [gal] n -glu, wherein n is 2 to 10).
- the present composition comprises transgalactooligosaccharides (i.e.
- oligosaccharide is preferably derived from animal milk, a mixture of oligosaccharides derived from animal milk or a fucosylated oligosaccharide (oligosaccharide containing at least one fucose saccharide unit).
- At least 10 wt.% of the oligosaccharides in the present composition has a DP of 2 to 5 (i.e. 2, 3, 4 and/or 5) and at least 5 wt.% has a DP of 10 to 100.
- at least 50 wt.%, more preferably at least 75 wt.% of the oligosaccharides have a DP of 2 to 10 (i.e. 2, 3, 4, 5, 6, 7, 8, 9 and/or 10), because these are believed to work throughout the ileum and proximal and middle parts of the colon and because the weight percentage of oligosaccharides that needs to be incorporated in the composition to achieve the desired effect is reduced.
- the weight ratios i.e. 2, 3, 4 and/or 5
- oligosaccharides with DP 2 to 5 are both above 1.
- oligosaccharides with DP 6 to 9 are both above 1.
- oligosaccharides with DP 10 to 100 are both above 1.
- Preferably both weight ratios are above 2, even more preferably above 5.
- the present composition preferably comprises 0.5 to 10 gram galactooligosaccharide with DP between 2 and 10 per 100 gram dry weight of the composition, more preferably between 1 and 5 gram.
- the preferred galactooligosaccharides is transgalactooligosaccharide, as this best mimics human milk oligosaccharides.
- the present invention preferably comprises 0.5 to 10 gram fructopolysaccharide with DP between 10 and 60 per 100 gram dry weight of the composition, more preferably between 1 and 5 gram.
- the term "fructopolysaccliaride” refers to a polysaccharide carbohydrate comprising a chain of at least 10 ⁇ -linked fructose units.
- the present nutritional composition is preferably in powder or liquid form or in tablet form, wherein said tablet has a weight between 5 and 25 grams.
- the present composition is provided in powered form as this increases shelf life.
- the present composition is preferably administered orally in liquid form. Prior to the administration of the present composition, it is preferably admixed with a liquid, preferably water.
- Stool irregularities e.g. hard stools, insufficient stool volume, diarrhea
- Stool irregularities is a major problem in many babies and ill subjects that receive liquid foods. It was found that stool problems may be reduced by administering the present composition in liquid form, having an osmolality between 50. and 500 m ⁇ sm/kg, more preferably between 100 and 400 m ⁇ sm/kg, most preferably between 220 and 300 m ⁇ sm/kg.
- the liquid food does not have an excessive caloric density as this causes significant intestinal stress.
- the formula needs to provide sufficient calories to feed the infant.
- the liquid food preferably has a caloric density between 0.5 and 0.9 kcal/ml, preferably between 0.6 and 0.8 kcal/ml.
- the present composition is advantageously administered to infants with the age between 0 and 2 years.
- the present composition can also be advantageously used in a method for providing the nutritional requirements of a premature infant (an infant born before 37 weeks gestation).
- the present invention provides a method for feeding infants with an age between 0 and 30 day.
- the present composition can be advantageously used to treat or prevent diseases wherein a comprised immune system and/or intestinal barrier immaturity is underlying the development of the course of the disease.
- the present composition can thus be advantageously used to treat or prevent diarrhea or allergy, particularly in infants with an age between 0 and 2.
- the present composition is particularly suitable for the treatment and/or prevention of allergic rhinitis, allergic conjunctivitis, allergic dermatitis, atopic dermatitis and/or food allergy.
- the present method provides for a method for the treatment and/or prevention of infections, said method comprising administering the present composition.
- Example 1 Infant nutrition
- a liquid infant nutrition prepared by admixing 13.9 g powder with water to yield 100 ml final product, said liquid product comprising per 100 ml:
- Fibre 0.8 g (containing 0.05 g fructopolysaccharide (Raftiline HPTM, Orafti,
- Uridine-5-monophosphate 0.82 mg Adenosine-5-monophosphate; 0.20 mg Guanosine-5-monophosphate; 0.34 mg Inosine-5monophosphate.
- NCC 0.55 mg Uridine-5-monophosphate; 0.82 mg Adenosine-5-monophosphate; 0.20 mg Guanosine-5-monophosphate; 0.34 mg Inosine-5monophosphate.
- composition further contains choline (6 mg/100 ml) and taurine (6.3 mg/100 ml); minerals and trace elements and vitamins in amounts in compliance with the international guidelines for infant milk formula.
- Example 2 Composition according to example 1, wherein the nucleotide component is replaced by dinucleosidporyphosphates (NpxN) Gp4G
- composition according to example 1, wherein the nucleotide component is an DNA/RNA oligomers extract
- composition according to example 1 comprising 1 wt.% D-ribose based on total dry weight of the composition.
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Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BRPI0514498-1A BRPI0514498A (en) | 2004-08-20 | 2005-08-22 | nutritional composition and use of nutritional composition |
NZ553299A NZ553299A (en) | 2004-08-20 | 2005-08-22 | Immune stimulatory infant formula with nucleotides and a negatively charged glycan or glycoconjugate |
CA002577698A CA2577698A1 (en) | 2004-08-20 | 2005-08-22 | Infant formula |
AU2005273099A AU2005273099B2 (en) | 2004-08-20 | 2005-08-22 | Immune stimulatory infant nutrition |
US11/573,939 US20080125346A1 (en) | 2004-08-20 | 2005-08-22 | Infant Formula |
JP2007527084A JP2008510697A (en) | 2004-08-20 | 2005-08-22 | Infant formula |
EP05775170A EP1781306A2 (en) | 2004-08-20 | 2005-08-22 | Immune stimulatory infant nutrition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04019856A EP1634599A1 (en) | 2004-08-20 | 2004-08-20 | Iimmune stimulatory infant nutrition |
EP04019856.6 | 2004-08-20 |
Publications (2)
Publication Number | Publication Date |
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WO2006019300A2 true WO2006019300A2 (en) | 2006-02-23 |
WO2006019300A3 WO2006019300A3 (en) | 2006-06-01 |
Family
ID=34926246
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
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PCT/EP2005/008999 WO2006018314A2 (en) | 2004-08-20 | 2005-08-19 | Immune stimulatory infant nutrition |
PCT/NL2005/000609 WO2006019300A2 (en) | 2004-08-20 | 2005-08-22 | Immune stimulatory infant nutrition |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2005/008999 WO2006018314A2 (en) | 2004-08-20 | 2005-08-19 | Immune stimulatory infant nutrition |
Country Status (15)
Country | Link |
---|---|
US (3) | US8114441B2 (en) |
EP (3) | EP1634599A1 (en) |
JP (2) | JP4965444B2 (en) |
CN (3) | CN101766228B (en) |
AT (1) | ATE427112T1 (en) |
AU (2) | AU2005274266B2 (en) |
BR (2) | BRPI0514526A (en) |
CA (2) | CA2576042C (en) |
DE (1) | DE602005013679D1 (en) |
ES (1) | ES2322380T3 (en) |
NZ (2) | NZ553248A (en) |
PL (1) | PL1781307T3 (en) |
RU (2) | RU2426549C2 (en) |
UA (1) | UA88918C2 (en) |
WO (2) | WO2006018314A2 (en) |
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- 2004-08-20 EP EP04019856A patent/EP1634599A1/en not_active Withdrawn
-
2005
- 2005-08-19 CN CN200910225789XA patent/CN101766228B/en not_active Expired - Fee Related
- 2005-08-19 AU AU2005274266A patent/AU2005274266B2/en not_active Ceased
- 2005-08-19 CA CA2576042A patent/CA2576042C/en not_active Expired - Fee Related
- 2005-08-19 AT AT05777309T patent/ATE427112T1/en not_active IP Right Cessation
- 2005-08-19 BR BRPI0514526-0A patent/BRPI0514526A/en not_active Application Discontinuation
- 2005-08-19 NZ NZ553248A patent/NZ553248A/en not_active IP Right Cessation
- 2005-08-19 ES ES05777309T patent/ES2322380T3/en active Active
- 2005-08-19 CN CNA2005800281714A patent/CN101048167A/en active Pending
- 2005-08-19 PL PL05777309T patent/PL1781307T3/en unknown
- 2005-08-19 DE DE602005013679T patent/DE602005013679D1/en active Active
- 2005-08-19 US US11/660,594 patent/US8114441B2/en not_active Expired - Fee Related
- 2005-08-19 EP EP05777309A patent/EP1781307B1/en not_active Revoked
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