NZ713087B2 - Lutein composition suitable for infant food formulations - Google Patents

Lutein composition suitable for infant food formulations Download PDF

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Publication number
NZ713087B2
NZ713087B2 NZ713087A NZ71308714A NZ713087B2 NZ 713087 B2 NZ713087 B2 NZ 713087B2 NZ 713087 A NZ713087 A NZ 713087A NZ 71308714 A NZ71308714 A NZ 71308714A NZ 713087 B2 NZ713087 B2 NZ 713087B2
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NZ
New Zealand
Prior art keywords
composition
weight
composition according
lutein
total weight
Prior art date
Application number
NZ713087A
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NZ713087A (en
Inventor
Markus Beck
Andrea Hitzfeld
Christian Schaefer
Bernd Schlegel
Original Assignee
Dsm Ip Assets B V
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Publication date
Application filed by Dsm Ip Assets B V filed Critical Dsm Ip Assets B V
Priority claimed from PCT/EP2014/056126 external-priority patent/WO2014154788A1/en
Publication of NZ713087A publication Critical patent/NZ713087A/en
Publication of NZ713087B2 publication Critical patent/NZ713087B2/en

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Classifications

    • A—HUMAN NECESSITIES
    • 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
    • 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
    • A—HUMAN NECESSITIES
    • 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
    • A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/40—Complete food formulations for specific consumer groups or specific purposes, e.g. infant formula
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
    • A23P10/00—Shaping or working of foodstuffs characterised by the products
    • A23P10/40—Shaping or working of foodstuffs characterised by the products free-flowing powder or instant powder, i.e. powder which is reconstituted rapidly when liquid is added
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/045—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
    • A61K31/047—Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates having two or more hydroxy groups, e.g. sorbitol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
    • A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction

Abstract

The present invention is related to a powderous composition which comprises lutein and a hydrocolloid and which is used in infant food formulations or premixes for infant food formulations.

Description

LUTEIN COMPOSITION SUITABLE FOR INFANT FOOD FORMULATIONS The present invention is related to a powderous composition which comprises lutein and which is used in infant food formulations or premixes for infant food formulations.
Lutein which has the following formula is obtained usually from plants or eggs.
It can also be synthesized chemically.
Due to the C-C double bonds lutein can have various stereochemical isomers (E/Z forms).
In the context of the present invention the different isomers do not have an essential effect. The term “lutein” always covers all stereochemical isomers.
It was found that lutein plays a vital role in eye health. The hypothesis for the natural concentration is that lutein helps keep the eyes safe from oxidative stress and the high- energy photons of blue light. Various research studies have shown that a direct relationship exists between lutein intake and pigmentation in the eye.
For that reason lutein is also an important ingredient in the diet for infants (Age 0 – 6).
Therefore, the goal of the present invention was to provide a composition which comprises lutein and which has excellent properties as such as well as allows to produce a (infant food) formulation comprising such a composition, which has also excellent properties.
It was found that a powderous composition comprising particles having (a) an inner phase, which comprises lutein, and (b) a matrix, which comprises at least one hydrocolloid, characterized in that (i) the inner phase has an average size D [3,2] of less than 30μm, and (ii) the particle has an average size D [3,2] of 10 – 150μm, and wherein the inner phase is always smaller than the particle, does show improved properties.
All the sizes of the inner phase D [3,2] as well as of the particles D [3,2] in the context of the present patent application were determined by using a Mastersizer 2000. The particle size of the inner phase was determined after redispersing the powderous composition in water, whereas the powderous particles of the composition were determined as such.
The composition according to the present invention is used in infant food formulations or in premixes (which are then used to produce infant food formulations).
The premix is usually in a dry form. The premix is usually produced by mixing the composition according to the present invention with other suitable ingredients, which are useful and/or essential in an infant formulation and/or premix (or which are useful and/or essential for the production of an infant formulation and/or premix).
The infant formulation in the context of the present invention is usually a dry formulation, which is then dissolved either in water or in milk.
Dry means that the water content is less than 5 weight-% (wt-%), based on the total weight of the composition, premix or formulation.
The advantages of the composition according to the present invention are: • the composition is storage stable • no colored (red) spots in the infant food formulation • no bleeding when the composition is blended to premix and/or an infant food formulation • no color formation, when the infant food formulation is dissolved in water (or milk).
Preferably the inner phase has an average size D [3,2] of 0.1μm to 30μm.
Preferably the inner phase has an average size D [3,2] of 0.2μm to 20μm.
Hydrocolloids are hydrophilic polymers, of vegetable, animal, microbial or synthetic origin, that generally contain many hydroxyl groups and may be polyelectrolytes.
A hydrocolloid is defined as a colloid system wherein the colloid particles are hydrophilic polymers dispersed in water. A hydrocolloid has colloid particles spread throughout water, and depending on the quantity of water available that can take place in different states, e.g., gel or sol (liquid). Hydrocolloids can be either irreversible (single-state) or reversible.
The hydrocolloids are preferably chosen from the group consisting of modified polysaccharides, maltodextrin, glucose syrup and gums.
The term “modified polysaccharide” as used in the present specification and claims refers to a polysaccharide which has been modified by known methods (chemically or physically, including enzymatic or thermal reactions) to be a good protective hydrocolloid for the stabilization of lipophilic surfaces in a fine dispersion in the aqueous medium.
Accordingly, the modified polysaccharide has been modified to have a chemical structure which provides it with a hydrophilic (affinity to water) portion and a lipophilic (affinity to dispersed phase) portion. This enables it to dissolve in the dispersed lipophilic phase and in the continuous water phase. Preferably the modified polysaccharide has a long hydrocarbon chain as part of its structure (preferably C ). -18 Modified polysaccharides are well known materials which are available commercially, or may be prepared by a skilled person using conventional methods. A preferred modified polysaccharide is modified starch. Modified starches are made from starches substituted by known chemical methods with hydrophobic moieties. For example starch may be treated with cyclic dicarboxylic acid anhydrides such as succinic anhydrides, substituted with a hydrocarbon chain (see Modified Starches: Properties and Uses, ed.
O.B.Wurzburg, CRC Press, Inc., Boca Raton, Florida (1991)). A particularly preferred modified starch of this invention has the following structure (I) wherein St is a starch, R is an alkylene group and R’ is a hydrophobic group.
Preferably the alkylene group is a lower alkylene group, such as dimethylene or trimethylene. R’ may be an alkyl or alkenyl group, preferably C to C . A preferred 18 compound of Formula I is starch sodium octenyl succinate. It is available commercially from, among other sources, Ingredion Inc., as Capsul® and Hicap®. Making this compound, and compounds of Formula I in general, is known in the art (see Modified Starches: Properties and Uses, ed. O.B.Wurzburg, CRC Press, Inc., Boca Raton, Florida (1991)).
Glucose syrup is a food syrup, made from the hydrolysis of starch.
A preferred gum in the context of the present invention is gum Arabic (= gum acacia).
The powderous composition according to the present invention comprises (a) 0.01 – 30 wt-%, based on the total weight of the composition, of lutein, and (b) 70 – 99.99 wt-%, based on the total weight of the composition, of at least one hydrocolloid, and (c) optionally up to 25 wt-%, based on the total weight of the composition, of at least one auxiliary agent.
It is clear that all the percentages always add up to 100.
A preferred powderous composition according to the present invention comprises (a) 0.1 – 15 wt-% based on the total weight of the composition, of lutein and (b) 70 – 90 wt-%, based on the total weight of the composition, of at least one hydrocolloid and (c) 15 – 25 wt-%, based on the total weight of the composition, of at least one auxiliary agent.
A preferred powderous composition according to the present invention comprises (a) 0.2 – 10 wt-% based on the total weight of the composition, of lutein and (b) 75 – 90 wt-%, based on the total weight of the composition, of at least one hydrocolloid and (c) 15 – 25 wt-%, based on the total weight of the composition, of at least one auxiliary agent.
These powderous compositions are dry but they could contain some water (less than 5 wt-%, based on the total weight of the composition, usually less than 3 wt-%).
The auxiliary agents can be any commonly known excipients, which are • useful for the composition and/or the premix and/or the infant food formulation and/or • useful for the production of the composition and/or of the premix and/or of the infant food formulation.
Such auxiliary agents are for example antioxidants (such as ascorbic acid or salts thereof, tocopherols (synthetic or natural); butylated hydroxytoluene (BHT); butylat-ed hydroxyanisole (BHA); propyl gallate; tert. butyl hydroxyquinoline and/or ascorbic acid esters of a fatty acid); ethoxyquin, plasticisers, stabilisers, humectants (such as glycerol, sorbitol, polyethylene glycol), dyes, fragrances, fillers and buffers.
Examples are i.e. sugar (saccharides), sodium ascorbate.
The hydrocolloids are preferably chosen from the group consisting of modified polysaccharides, maltodextrin, glucose syrup and gums, and especially OSA-starch, maltodextrin and glycose syrup.
The composition according to the present invention is produced by using methods known from the prior art.
Usually the composition according to the present invention is produced by: first preparing the water phase which comprises a) the hydrocolloid or a mixture of hydrocolloids, and b) optionally at least one auxiliary agent, such as sugar and/or sodium ascorbate, c) water by mixing the ingredients (in any sequence) into the water (usually under stirring) and at ambient temperature.
Afterwards this phase is heated up (to a temperature of between 40 and 90°C).
Then the lutein is added (still at elevated temperature) under vigorous dispersing, which is optionally followed by a homogenizing process.
Finally the suspension is dried by a method commonly used, such as spray drying.
The powderous compositions according to the present invention are used in infant food formulations and/or in premixes for infant food formulations.
By the term infant food formulations in the context of the present invention, dry formulations are meant (especially baby milk formulations), which are then dissolved in a suitable solvent (usually water or milk, preferably water) and the dissolved form (warm or cold) is then consumed by the infant.
The infant food formulation can be in any dry form, such powder, granules as well as tablets.
A preferred infant food formulation is a dry baby milk formulation (powder, granule as or tablets) wherein the powderous composition according the present invention is incorporated (lutein fortified baby milk formulation).
Therefore the powderous composition according to the present invention can added as such to all other ingredients to produce an infant food formulation; or the powderous composition according to the present invention can be mixed with other ingredients for an infant food formulation, which is called a premix. This premix is then used to produce an infant food formulation.
Therefore a further embodiment of the present invention is a process of production of a dry premix and/or a dry infant food formulation comprising at least one powderous composition as described above.
The amount of the powderous composition according to the present invention in such a premix and/or infant food formulation can vary.
The concentration of lutein is usually not more than 0.25 ppm in the liquid infant food formulation (dry infant food formulation dissolved in milk or preferably in water).
Therefore a further embodiment of the present invention is a dry premix and/or a dry infant food formulation comprising at least one powderous composition as described above.
The following examples serve to illustrate the invention. The percentages are expressed in weight percentages and the temperatures are degrees Celsius, if not otherwise defined.
Examples Example 1 408.5 g Maltodextrin and 432.2. g HiCap IMF and 210.7g Glucidex 28 E were added to 600 g distilled water. The mixture was stirred and after a few minutes the mixture was heated to about 60°C. After 20 minutes 10.8 g sodiu m ascorbate was added under stirring. 10 minutes later 9.6 g lutein was added and the mixture was vigorously dispersed.
Afterwards the suspension was spray dried.
The following table shows the amounts of the various ingredients after spray drying: Ingredients Amount [wt-%] Lutein 1.2 HiCap IMF 40.2 Maltodextrin 38.0 Glucidex 28 E 19.6 Na-Ascorbate 1.0 The average size of the inner phase D[3,2] was 3.19 μm and the average particles size was 45.92 μm.
Example 2 The same process as in Example 1 was repeated but instead of Glucidex 28 E sugar was used.
The following table shows the amounts of the various ingredients after spray drying: Ingredients Amount [wt-%] Lutein 1.2 HiCap IMF 40.2 Maltodextrin 38.0 Sugar 19.6 Na-Ascorbate 1.0 The average size of the inner phase D[3,2] was 3.02 μm and the average particles size was 81.82 μm.
Both compositions did not bleed when added to a premix or a infant food formulation.
Furthermore, no color formation was observed when the infant food formulation (baby milk powder) comprising one of these compositions were dissolved in water.
Example 3: Baby milk powder comprising composition of Example 1 The composition of Example 1 was used adding to a baby milk powder formulation. 0.83 g of the powderous composition of Example 1 were incorporating (by mixing).
The following table shows the list of ingredients of the lutein fortified baby milk powder: Ingredients unit Content per 100g Content per 100ml serving powder Protein g 9.20 1.4 Carbohydrates g 53.2 8.1 Fat g 23 3.5 Sodium g 0.13 0.02 Potassium mg 493 75 Calcium mg 348 53 Phosphorus mg 197 30 Chloride mg 276 42 Magnesium mg 32.2 4.9 Iron mg 4.60 0.7 Zinc μg 3.3 0.5 Copper μg 263 40 Iodine μg 65 9.9 Manganese μg 46 7 Selenium μg 9.85 1.5 Fluorid μg 38.8 5.9 Vitamin C mg 67.7 10.3 Vitamin A μg 460 70 Vitamin D μg 7.88 1.2 Vitamin E μg 4.6 0.7 Vitamin B1 μg 394 60 Vitamin B2 μg 834 127 Vitamin B6 μg 263 40 Vitamin B12 μg 1 0.15 Folic acid μg 67.7 10.3 Pantotenic acid μg 3258 496 Vitamin K μg 32.2 4.9 Biotin μg 10.51 1.6 Niacin μg 2621 399 Choline mg 99.2 15.1 Inositol mg 32.2 4.9 Lutein μg 1000 152 This lutein fortified baby milk powder showed excellent storage stability. No bleeding was observed during and after the addition of the composition of Example 1. No colored (red) spots have been seen in the fortified baby milk powder. Furthermore the baby milk powder shows excellent dissolving properties in water (dissolves fast) and no color change of the dissolved baby milk formulation.
Example 4: Baby milk powder comprising composition of Example 1 For this baby milk formulation a lower concentration of the composition of Example 1 was added (all the other ingredients are the same in the same concentration) Ingredients unit Content per 100g Content per 100ml serving powder Protein g 9.20 1.4 Carbohydrates g 53.2 8.1 Fat g 23 3.5 Sodium g 0.13 0.02 Potassium mg 493 75 Calcium mg 348 53 Phosphorus mg 197 30 Chloride mg 276 42 Magnesium mg 32.2 4.9 Iron mg 4.60 0.7 Zinc μg 3.3 0.5 Copper μg 263 40 Iodine μg 65 9.9 Manganese μg 46 7 Selenium μg 9.85 1.5 Fluorid μg 38.8 5.9 Vitamin C mg 67.7 10.3 Vitamin A μg 460 70 Vitamin D μg 7.88 1.2 Vitamin E μg 4.6 0.7 Vitamin B1 μg 394 60 Vitamin B2 μg 834 127 Vitamin B6 μg 263 40 Vitamin B12 μg 1 0.15 Folic acid μg 67.7 10.3 Pantotenic acid μg 3258 496 Vitamin K μg 32.2 4.9 Biotin μg 10.51 1.6 Niacin μg 2621 399 Choline mg 99.2 15.1 Inositol mg 32.2 4.9 Lutein μg 164 25 Also this lutein fortified baby milk powder showed excellent storage stability. No bleeding was observed during and after the addition of the composition of Example 1. No colored (red) spots have been seen in the fortified baby milk powder. Furthermore the baby milk powder shows excellent dissolving properties in water (dissolves fast) and no color change of the dissolved baby milk formulation.

Claims (13)

Claims 1.
1. Powderous composition comprising particles having (a) an inner phase, which comprises 0.01 – 30 weight-%, based on the total 5 weight of the composition, of lutein, (b) a matrix, which comprises 70 – 99.99 weight-%, based on the total weight of the composition, of at least one hydrocolloid, and (c) optionally up to 25 weight-%, based on the total weight of the composition, of at least one auxiliary agent, 10 characterized in that (i) the inner phase has an average size D [3,2] of 0.1μm to 30μm, and (ii) the particle has an average size D [3,2] of 10 μm – 150 μm, and wherein the inner phase is always smaller than the particle. 15
2. Composition according to claim 1, wherein the inner phase has an average size D [3,2] of 0.2 μm to 20 μm.
3. Composition according to any one of the preceding claims, wherein the hydrocolloid is chosen from the group consisting of polysaccharides, modified polysaccharides, 20 maltodextrin, glucose syrup and gums.
4. Composition according to any one of the preceding claims, wherein the modified polysaccharide is a modified starch of structure (I) wherein St is a starch, R is an alkylene group and R’ is a hydrophobic group.
5. Composition according to any one of the preceding claims, wherein the gum is gum Arabic.
6. Composition according to any one of the preceding claims 1 – 5, comprising (a) 0.1 – 15 weight-% based on the total weight of the composition, of lutein and (b) 70 – 90 weight-%, based on the total weight of the composition, of at least one hydrocolloid and (c) 15 – 25 weight-%, based on the total weight of the composition, of at least one 5 auxiliary agent.
7. Composition according to any one of the preceding claims 1 – 5, comprising (a) 0.2 – 10 weight-% based on the total weight of the composition, of lutein and (b) 75 – 90 weight-%, based on the total weight of the composition, of at least one 10 hydrocolloid and (c) 15 – 24.8 weight-%, based on the total weight of the composition, of at least one auxiliary agent.
8. Composition according to claim 6 or claim 7, wherein the auxiliary agent is chosen 15 from the group consisting of antioxidants; ethoxyquin, plasticisers, stabilisers, humectants, dyes, fragrances, fillers and buffers.
9. Composition according to claim 8, wherein when the auxiliary agent is an antioxidant, said antioxidant is chosen from the group consisting of ascorbic acid or salts 20 thereof, natural and synthetic tocopherols, butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), propyl gallate, tert-butyl hydroxyquinoline and ascorbic acid esters of a fatty acid.
10. Composition according to claim 8, wherein when the auxiliary agent is a humectant, 25 said humectant is chosen from the group consisting of glycerol, sorbitol and polyethylene glycol.
11. Process of production of a dry premix and/or a dry infant food formulation comprising a step of mixing at least one powderous composition according to any one of 30 claims 1 – 10 with other suitable ingredients.
12. A dry premix and/or a dry infant food formulation comprising at least one powderous composition according to any one of claims 1 – 10.
13. Process for production of a composition according to any one of claims 1 – 10, comprising the steps: preparing a water phase at ambient temperature which comprises: a) the at least one hydrocolloid, 5 b) water, and c) optionally the at least one auxiliary agent; heating the water phase to a temperature of between 40 and 90 ºC; adding lutein to the heated water phase with dispersing to form a suspension; optionally followed by a homogenizing process; and 10 drying the suspension.
NZ713087A 2013-03-28 2014-03-27 Lutein composition suitable for infant food formulations NZ713087B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP13161534 2013-03-28
EP13161534.6 2013-03-28
PCT/EP2014/056126 WO2014154788A1 (en) 2013-03-28 2014-03-27 Lutein composition suitable for infant food formulations

Publications (2)

Publication Number Publication Date
NZ713087A NZ713087A (en) 2020-09-25
NZ713087B2 true NZ713087B2 (en) 2021-01-06

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