Abstract: Extruded nutritional powders and methods of manufacturing the extruded nutritional powders , including extruded infant nutritional powders and extruded adult nutritional powders are provided. The processes utilize an extruder that is capable of internally mixing and emulsifying protein, and optionally , a carbohydrate with fat and water into an emulsion that can be dried into a powder having equivalent fat separation and dispersibility as compared to spray dried powders.
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application claims the benefit of U.S. Provisional Application
Nos. 61/717,799, filed October 24, 2012; 61/738,593, filed December 18, 2012; and
61/737,886, filed December 17, 2012; each of which is hereby incorporated by
reference herein in its entirety.
FIELD OF THE DISCLOSURE
[0002] The present disclosure relates to extruded nutritional powders having
emulsion and dispersibility characteristics upon reconstitution similar to conventional
spray dried nutritional powders. More particularly, the present disclosure relates to
extruded nutritional powders and methods of manufacturing extruded nutritional
powders, including infant nutritional powders and adult nutritional powders, by
emulsifying the powder ingredients completely within the extruder during the
manufacturing process.
BACKGROUND OF THE DISCLOSURE
[0003] Powdered nutritional products, including total nutrition products such
as powdered infant formulas, powdered follow on formulas, powdered pediatric
formulas, and powdered adult nutritional products, are widely commercially available
and their use has grown steadily over the years. These products typically contain at
least one of a fat, a carbohydrate, and a protein, along with various vitamins and
minerals, and potentially other nutritionally beneficial components. Prior to use, the
powdered formula or product is reconstituted in water or another suitable liquid at a
predetermined ratio to produce a ready-to-drink liquid. Such ready-to-drink liquids
are typically consumed within about 24 hours of reconstitution.
[0004] Conventional spray dried powdered nutritional products, including
both powdered infant formulas and powdered adult nutritional products, generally
contain from about 0.5% to about 35% by weight fat component to provide the
desired nutritional caloric density. In order for the finished powdered product to be
package stable (i.e., not subject to significant oxidation and rancidity over its shelf
life) and not have significant fat separation or creaming when reconstituted, during
manufacturing the fat component is generally sheared to globules having a size of
between about 0.1 and 20 microns, while simultaneously emulsifying the sheared fat
globules with hydrated protein and other additional emulsifiers.
[0005] This shearing and emulsifying has traditionally been accomplished
by preparing a high solids water slurry (i.e., 30% to 60% total solids) and pumping the
slurry through a high pressure homogenizer with a homogenization pressure between
2000 and 4500 psig. The slurry is then typically evaporated to about 45% to 60%
total solids and spray dried. This generally produces stable fat that is not subject to
substantial oxidation during storage and is easily reconstituted.
[0006] Extrusion methods are known as highly efficient methods that
significantly minimize the amount of water and energy needed and are capable of
producing pellets that can be dried and ground into powdered material. But extrusion
processes have generally not been used to date to produce powdered infant formulas
and powdered adult nutritional products because of the inability of the extrusion
process to produce a finished powder with a stable fat emulsion and with the
dispersibility capabilities of conventional spray dried nutritional powders. Extruded
nutritional powders have to date provided unwanted fat separation and creaming upon
reconstitution, which leads to a less commercially desirable product. Additionally,
extruded powders have also been unable to provide desirable dispersibility
characteristics such that unwanted clumping and sticking is not an issue.
[0007] As such, there is a need in the art for efficient methods for producing
extruded nutritional powders. It would be advantageous if the extruded nutritional
powder resisted fat separation upon reconstitution and had improved dispersibility
similar to spray dried nutritional powders.
SUMMARY OF THE DISCLOSURE
[0008] The present disclosure is directed to extruded nutritional powders and
processes for manufacturing extruded nutritional powders. The extruded powders
typically contain protein, fat, and carbohydrate, and may optionally include vitamins,
minerals, long chain polyunsaturated fatty acids, and the like. The high efficiency
extrusion manufacturing processes described herein utilize an extruder that is capable
of internally mixing and emulsifying protein, carbohydrate, or both, with fat and
water into an emulsion that can be suitably extruded, dried, and milled into a powder
having a desirable particle size distribution and water content. The extruded powders
as described herein, upon reconstitution with conventional amounts of an aqueous
solution, such as water, provide fat separation and dispersibility properties that are
similar to, or even improved, as compared to conventional spray dried nutritional
powders.
[0009] The present disclosure is further directed to a process for
manufacturing an extruded nutritional powder. The process comprises introducing
water into an extruder, introducing a dry blend comprising at least a portion of a
protein and, optionally, a carbohydrate into the extruder, introducing an oil blend
comprising a fat into the extruder, mixing the dry blend and oil blend to form an
emulsified mixture within the extruder, and extruding the emulsified mixture to form
an extrudate, drying the extrudate, and forming a powder from the dried extrudate. In
some aspects, the process includes introducing protein, vitamins, minerals and amino
acids, prior to mixing.
[0010] The present disclosure is further directed to a process for
manufacturing an extruded nutritional powder. The process comprises introducing
water into an extruder, introducing a dry blend comprising at least a portion of a
protein and, optionally, a carbohydrate into the extruder and hydrating the dry blend,
introducing an oil blend comprising a fat into the extruder, mixing the hydrated dry
blend and oil blend to form an emulsified mixture within the extruder, wherein water
comprises less than 22% by weight of total emulsified mixture, extruding the
emulsified mixture to form an extrudate, drying the extrudate, and grinding the dried
extrudate into a nutritional powder.
[001 1] The present disclosure is further directed to a process for
manufacturing an extruded nutritional powder. The process comprises introducing
water into an extruder, introducing a protein into the extruder, introducing an oil
blend comprising a fat into the extruder, introducing a carbohydrate into the extruder,
mixing and emulsifying the protein, water, oil blend, and carbohydrate within the
extruder to form an emulsified mixture, and extruding the emulsified mixture to form
an extrudate, drying the extrudate, and grinding the dried extrudate into a nutritional
powder. In some aspects, the process includes introducing a vitamin, mineral, amino
acid, and active component (e.g., polyphenols, CaHMB, flavors, color) prior to
mixing.
[0012] The present disclosure is further directed to an extruded powder
comprising fat, carbohydrate, and protein, wherein the extruded powder, upon
reconstitution with water, shows substantially no fat separation at 24 hours.
[0013] The present disclosure is further directed to an extruded powder
comprising fat, carbohydrate, and protein, wherein the extruded powder, upon
reconstitution with water, shows substantially no creaming defect at 24 hours.
[0014] The disclosure is further directed to methods for reducing the loss of
a heat labile vitamin in a powdered nutritional product using the disclosed extrusion
processes. The heat labile vitamins may include vitamin A, vitamin D , vitamin E,
vitamin K, pantothenic acid, vitamin C, thiamine, folic acid, riboflavin, vitamin B12,
biotin, and combinations thereof. The methods include the use of the disclosed
extrusion methods to produce full nutrition products while avoiding the need for
overfortification of the product.
[00 15] It has been unexpectedly found that extruded nutritional powders
having highly desirable properties and nutritional value can be prepared by forming
an emulsified mixture of ingredients interior of an extruder; that is, the ingredients are
introduced into an extruder at one or more times, areas, or both and then mixed and
emulsified completely within the extruder such that there is no external emulsification
required. The extruded nutritional powders, including infant formula powder,
pediatric and follow-on powder, and adult nutritional powder, produced utilizing the
extrusion methods described herein have good emulsion quality in that there is little to
no fat separation upon reconstitution. Additionally, the powders have equivalent
dispersibility as compared to conventional spray dried nutritional powders.
BRIEF DESCRIPTION OF THE DRAWINGS
[0016] FIG. 1 is a schematic diagram of the extrusion process according to
one embodiment of the present disclosure.
[0017] FIG. 2 is a schematic diagram of the extrusion process according to
one embodiment of the present disclosure.
[00 18] FIGS. 3A and 3B depict the fat separation of an extruded nutritional
powder and a spray dried nutritional powder as analyzed in Example 1.
[0019] FIGS. 4A and 4B depict the dispersibility of an extruded nutritional
powder and a spray dried nutritional powder as analyzed in Example 1.
DETAILED DESCRIPTION OF THE DISCLOSURE
[0020] The extruded nutritional powders and corresponding manufacturing
methods of preparing nutritional powders of the present disclosure are directed to
powders made by utilizing an extruder apparatus to mix and emulsify all components
internally; that is, the components are introduced into the extruder where they are
mixed and emulsified completely within the extruder. The resulting nutritional
powders of the present disclosure exhibit excellent emulsion and stability
characteristics, and disperse well when reconstituted with water.
[0021] These and other elements or limitations of the extruded nutritional
powders and methods of the present disclosure are described in detail hereinafter.
[0022] The term "nutritional powders" as used herein includes powdered
infant nutritional formulas, adult nutritional powders, and nutritional powders
generally.
[0023] The term "infant formula" as used herein includes both infant
formulas, toddler formulas, and follow-on formulas wherein infant formulas are
intended for infants up to 1 year of age and toddler and follow-on formulas are
intended for children from 1 year of age to about 10 years of age.
[0024] The terms "adult nutritional powder" and "adult nutritional product"
as used herein, are used interchangeably to refer to formulas for generally maintaining
or improving the health of an adult, and include those formulas designed for adults
who need to control their blood glucose.
[0025] The term "shelf life" as used herein refers to a product's
commercially viable life-span, after which the product is unfit or undesirable for sale,
consumption, or both.
[0026] References to process steps completed within the extruder (including,
e.g., "complete," "completely," "completed," "no external," etc.) as used herein, refer
to process steps that have been sufficiently completed within the extruder such that it
is unnecessary to continue those process steps external to the extruder to produce the
described nutritional products by the disclosed manufacturing process.
[0027] All percentages, parts and ratios as used herein, are by weight of the
total formulation, unless otherwise specified. All such weights as they pertain to
listed ingredients are based on the active level and, therefore, do not include solvents
or by-products that may be included in commercially available materials, unless
otherwise specified.
[0028] Numerical ranges as used herein are intended to include every
number and subset of numbers within that range, whether specifically disclosed or
not. Further, these numerical ranges should be construed as providing support for a
claim directed to any number or subset of numbers in that range. For example, a
disclosure of from 1 to 10 should be construed as supporting a range of from 2 to 8,
from 3 to 7, from 5 to 6, from 1 to 9, from 3.6 to 4.6, from 3.5 to 9.9, and so forth.
[0029] All references to singular characteristics or limitations of the present
disclosure shall include the corresponding plural characteristic or limitation, and vice
versa, unless otherwise specified or clearly implied to the contrary by the context in
which the reference is made.
[0030] All combinations of method or process steps as used herein can be
performed in any order, unless otherwise specified or clearly implied to the contrary
by the context in which the referenced combination is made.
[003 1] The various embodiments of the extruded nutritional powders
prepared using the processes of the present disclosure may also be substantially free
of any optional or selected essential ingredient or feature described herein, provided
that the remaining powder still contains all of the required ingredients or features as
described herein. In this context, and unless otherwise specified, the term
"substantially free" means that the selected powdered product contains less than a
functional amount of the optional ingredient, typically less than 0.1% by weight, and
also including zero percent by weight of such optional or selected essential ingredient.
[0032] The nutritional powders and corresponding manufacturing methods
of the present disclosure can comprise, consist of, or consist essentially of the
essential elements and limitations of the disclosure as described herein, as well as any
additional or optional ingredients, components, or limitations described herein or
otherwise useful in nutritional applications.
Product Form
[0033] The nutritional products produced utilizing the extrusion processes as
described herein are powdered nutritional products. The powdered nutritional
products are typically in the form of flowable or substantially flowable particulate
compositions. The compositions can easily be scooped and measured with a spoon or
similar other device, and can easily be reconstituted to a ready-to-feed state by the
intended user with a suitable aqueous liquid, typically water, to form a nutritional
composition for immediate oral or enteral use. In this context, "immediate" use
generally means within about 48 hours, most typically within about 24 hours, and
ideally immediately after preparation, preferably right after reconstitution. Where the
nutritional products are reconstituted in a ready-to-feed state, the reconstituted
products preferably contain a stable emulsion.
[0034] The extruded nutritional powders of the present disclosure generally
have a moisture content of from about 0.75% to about 5% by weight, including from
about 2% to about 5% by weight, including from about 2% to about 4% by weight,
including from about 2% to about 3% by weight, and including from about 2.5% to
about 3% by weight. Final moisture content is chosen based upon the water activity
of the dried powder that is designed to provide a microbiologically stable powder for
a low acid product (pH>4.6), less than 0.86 aw water activity, preferably less than 0.5
aw water activity. The water activity should be measured for each composition.
[0035] Having a low moisture content allows the water activity to remain
low, deterring the growth of microorganisms. This provides the extruded nutritional
powder with a longer shelf life. Particularly, the powders of the present disclosure
generally have a shelf life of at least 3 months, including at least 4 months, including
at least 5 months, including at least 12 months, including at least 18 months, including
at least 24 months, including at least 36 months, and including from about 6 to about
24 months.
[0036] The powders of the present disclosure may be formulated with
sufficient kinds and amounts of nutrients so as to provide a sole, primary, or
supplemental source of nutrition, or to provide a specialized nutritional formulation
for use in individuals afflicted with specific diseases or conditions.
[0037] One specific product form includes an infant formula powder
including a protein system that is substantially or even completely soy-based.
Another specific product form includes an infant formula powder that is substantially
or even completely lactose-free. Another specific product form includes an infant
formula powder that includes rice starch. Another specific product form includes an
infant formula powder that includes a protein system that is partially or even
completely based on milk-based proteins. Another specific product form includes an
infant formula powder that includes a protein system that is partially or even
completely based on hydrolyzed proteins.
Macronutrients
[0038] The extruded nutritional powders of the present disclosure comprise
at least one of a fat, a protein, and a carbohydrate, and in many embodiments
comprise fat, protein, and carbohydrate. Generally, any source of fat, protein, and
carbohydrate that is known or otherwise suitable for use in powdered nutritional
products may also be suitable for use in the extruded nutritional powders herein,
provided that such macronutrients are also compatible with the essential elements of
the nutritional compositions as defined herein.
[0039] Although total concentrations or amounts of the fat, protein, and
carbohydrates may vary depending upon the nutritional needs of the intended user,
such concentrations or amounts most typically fall within one of the following
embodied ranges, inclusive of any other essential fat, protein, and or carbohydrate
ingredients as described herein.
Carbohydrate
[0040] The extruded nutritional powders of the present disclosure may
comprise a carbohydrate source.
[0041] When the extruded nutritional powder is an infant nutritional powder,
the carbohydrate component is present in an amount of from about 30% to about 85%,
including from about 45% to about 60%, including from about 50% to about 55% by
weight of the infant nutritional powder. The carbohydrate source may be any known
or otherwise suitable source that is safe and effective for oral administration and is
compatible with the essential and other ingredients in the powder.
[0042] When the extruded nutritional powder is an adult nutritional powder,
the carbohydrate component is present in an amount of from about 5% to about 60%,
including from about 7% to about 30%, including from about 10% to about 25%, by
weight of the adult nutritional powder. The carbohydrate source may be any known
or otherwise suitable source that is safe and effective for oral administration and is
compatible with the essential and other ingredients in the powder.
[0043] Suitable carbohydrates or carbohydrate sources for use in the
nutritional powders include glycerin, sucrose, dextrins in general and, specifically,
maltodextrin, tapioca maltodexrin, corn syrup, tapioca syrup, isomaltulose, lactose,
fructose, both unhydroyzed, partially hydrolyzed gums, gum Arabic, also known as
gum acacia, xanthan gum, gum tragacanth, and guar gum, gellan gum, carrageenans,
microcrystalline cellulose and carboxymethyl cellulose, glycerin, vegetable fibers,
glucose, maltose, cooked and uncooked waxy and non-waxy corn starch, cooked and
uncooked waxy and non-waxy tapioca starch, cooked and uncooked waxy and nonwaxy
rice starch, tagatose, galacto-oligosaccharides (GOS), fructo-oligosaccharides
(FOS) including short chain, moderate length chain, and long chain fructooligosaccharides,
alpha-lactose, beta-lactose, polydextrose, human milk
oligosaccharides, and combinations thereof.
[0044] Other suitable carbohydrates include any dietary fiber or fiber source,
non-limiting examples of which include insoluble dietary fiber sources such as oat
hull fiber, pea hull fiber, soy hull fiber, soy cotyledon fiber, sugar beet fiber, cellulose,
corn bran, and combinations thereof.
[0045] The carbohydrate for use in the extruded nutritional powder
formulation may therefore include soluble and/or insoluble fiber, or other complex
carbohydrate, preferably having a DE (dextrose equivalent) value of less than about
40, including less than 20, and also including from 1 to 10.
Fat
[0046] The extruded nutritional powders of the present disclosure may
comprise a fat or fat source.
[0047] When the extruded nutritional powder is an infant nutritional powder,
the fat component is present in an amount of from about 10% to about 35%, including
from about 25% to about 30%, and including from about 26% to about 28% by weight
of the infant nutritional powder. The fat may be any known or otherwise suitable
source that is safe and effective for oral administration and is compatible with the
essential and other ingredients in the powder.
[0048] When the extruded nutritional powder is an adult nutritional powder,
the fat component is present in an amount from about 0.5% to about 20%, including
from about 1% to about 10%, and also including from about 2% to about 5% by
weight of the adult nutritional powder. The fat may be any known or otherwise
suitable source that is safe and effective for oral administration and is compatible with
the essential and other ingredients in the powder.
[0049] Suitable fat or fat sources include coconut oil, soy oil, high oleic
safflower or sunflower oil, safflower oil, sunflower oil, corn oil, palm oil, palm kernel
oil, canola oil, triheptanoin, milk fat including butter, any animal fat or fraction
thereof, fish or crustacean oils containing docosahexaenoic acid (DHA),
eicosapentaenoic acid (EPA), or both, phospholipids from fish or crustacean
containing docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), or both,
concentrates of DHA, EPA, or both, from marine, vegetable, or fugal sources,
arachidonic acid (ARA) concentrate from fungal or other sources, a-linolenic acid
concentrate (ALA), flax seed oil, Borage oil or any other source of gamma linolenic
acid (GLA), phospholipids and fractions thereof, including soy lecithin and egg
lecithin, both partially hydrolyzed and unhydrolyzed, monoglycerides, diglycerides,
or both, from both vegetable and animal sources, and plant sterols and compounds
containing plant sterols, diacetyl tartaric acid of mono and diglycerides (DATEM) and
combinations thereof.
Protein
[0050] The extruded nutritional powders of the present disclosure may
comprise a protein or protein source, and desirably a non-gelling protein or protein
source.
[005 1] When the extruded nutritional powder is an infant nutritional
powder, the protein component is present in an amount of from about 5% to about
35%, including from about 8% to about 12%, and including from about 10% to about
12% by weight of the infant nutritional powder. The protein may be any known or
otherwise suitable source that is safe and effective for oral administration and is
compatible with the essential and other ingredients in the powder.
[0052] When the extruded nutritional product is an adult nutritional product,
the protein component is present in an amount of from about 10% to about 90%,
including from about 30% to about 80%, and also including from about 40% to about
75% by weight of the adult nutritional powder. The protein may be any known or
otherwise suitable source that is safe and effective for oral administration and is
compatible with the essential and other ingredients in the powder.
[0053] Suitable protein or protein sources include either intact, partially
hydrolyzed, or fully hydrolyzed, or a combination thereof, of lactase treated nonfat
dry milk, milk protein isolate, milk protein concentrate, whey protein concentrate,
glycomacropeptides, whey protein isolate, milk caseinates such as sodium caseinate,
calcium caseinate, or any combination of caseinate salts of any mineral, soy protein
concentrate, soy protein isolate, soy protein flour, pea protein isolate, pea protein
concentrate, any monocot or dicot protein isolate or protein concentrate, animal
collagen, gelatin, all amino acids, taurine, milk protein peptides, whey protein
peptides, bovine colostrum, human colostrum, other mammalian colostrum, genetic
communication proteins found in colostrum and in mammalian milk such as, but not
limited to, interleukin proteins, hydrolyzed animal collagen, hydrolyzed yeast, potato,
rice, hydrolyzed rice, mycoproteins, wheat, canola, hydrolyzed canola, and
combinations thereof.
Macronutrient Profile
[0054] The total amount or concentration of fat, carbohydrate, and protein in
the extruded nutritional powders of the present disclosure can vary considerably
depending upon the selected formulation and dietary or medical needs of the intended
user. Additional suitable examples of macronutrient concentrations are set forth
below. In this context, the total amount or concentration refers to all fat,
carbohydrate, and protein sources in the nutritional powder provided as a percentage
of total weight of the nutritional powder. For infant nutritional powders, such total
amounts or concentrations are most typically and preferably formulated within any of
the embodied ranges described in the following table (all numbers have "about" in
front of them).
[0055] In other embodiments, where the infant nutritional powders contain
heat labile vitamins, macronutrients amounts may be varied according to the
following table.
'All numerical values may be modified by the term
"about" From ready-to-feed liquid, reconstituted powder,
or diluted concentrate
[0056] For adult nutritional powders, such total amounts or concentrations
are most typically and preferably formulated within any of the embodied ranges of the
percentage of total weight as described in the following table (all numbers have
"about" in front of them).
Optional Ingredients
[0057] The extruded nutritional powders of the present disclosure may
further comprise other optional components that may modify the physical, chemical,
aesthetic or processing characteristics of the powders or serve as pharmaceutical or
additional nutritional components when used in the targeted population. Many such
optional ingredients are known or otherwise suitable for use in medical food or other
nutritional products or pharmaceutical dosage forms and may also be used in the
powder formulations herein, provided that such optional ingredients are safe and
effective for oral administration and are compatible with the essential and other
ingredients in the powders.
[0058] Non-limiting examples of such optional ingredients include
preservatives, anti-oxidants, emulsifying agents, buffers, pharmaceutical actives,
additional nutrients as described herein, vitamins, minerals, sweeteners including
artificial sweeteners (e.g., saccharine, aspartame, acesulfame K, Stevia extract, and
sucralose) colorants, flavorants in addition to those described herein, thickening
agents and stabilizers, emulsifying agents, lubricants, probiotics (such as acidophilus
bifidus bacteria, or both, both alive and inactive), prebiotics, beta-hydroxy betamethylbutyrate
(HMB), green tea polyphenols, Beta alanine, arginine, and glutamine.
[0059] Non-limiting examples of suitable minerals for use herein include
phosphorus, sodium, chloride, magnesium, manganese, iron, copper, zinc, iodine,
calcium, potassium, chromium, molybdenum, selenium, and combinations thereof.
[0060] Non-limiting examples of suitable vitamins for use herein include
carotenoids (e.g., beta-carotene, zeaxanthin, lutein, lycopene), biotin, choline, inositol,
folic acid, pantothenic acid, choline, vitamin A, thiamine (vitamin Bi), riboflavin
(vitamin B2), niacin (vitamin B3), pyridoxine (vitamin ) , cyanocobalamine (vitamin
B12), ascorbic acid (vitamin C), vitamin D, vitamin E, vitamin K, and various salts,
esters or other derivatives thereof, and combinations thereof. Any commercially
acceptable form of vitamins these may be utilized.
[006 1] In some embodiments, the vitamins used may include heat labile
vitamins. Exemplary heat labile vitamins include vitamins A, D, E, C, K, pantothenic
acid, thiamine, folic acid, riboflavin, vitamin B12, biotin, and combinations thereof,
In particular embodiments, the heat labile vitamin may be selected from pantothenic
acid, vitamin C, thiamine, folic acid, and a combination thereof.
[0062] Using the methods disclosed herein, at least about 80%, or at least
about 85%, or at least about 90%, or at least about 95% of the heat labile vitamins
may be retained in the nutritional compositions after processing via the extrusion
process.
Manufacture of Nutritional Powders Using Extrusion Process
[0063] The processes of the present disclosure incorporate the use of an
extruder apparatus to provide extruded nutritional powders having similar physical
properties to that of spray dried nutritional powders. In some embodiments of the
manufacturing processes described herein, the extruder apparatus may utilize
ultrasonic energy at one or more zones or elements of the process. In one desirable
embodiment, ultrasonic energy may be applied to the extruder apparatus at the time of
the formation of the emulsion in the interior of the extruder as described in detail
herein. Ultrasonic energy may be particularly beneficial at those stages of the process
where there is relatively low solids content and low viscosity.
[0064] Particularly, the extruded nutritional powders have similar
dispersibility as compared to spray dried nutritional powders. The extruded
nutritional powder completely dissolves when placed in room temperature water after
a period of less than three minutes. The extruded nutritional powder completely
dissolves when placed in water having a temperature of about 105°F (40.6°C) after a
period of about 30 seconds. Powder dispersibility describes the degree of firmness
and solubility of particles of gel, sediment, and creaming with a product.
Dispersibility is evaluated using a visual evaluation with a scale of 1-6 that rates
undissolved powder residue after reconstitution remaining on a 5 inch diameter 80
mesh screen. A score of 1 is a powder that dissolves completely with almost no
residue and a score of 6 is a powder that does not dissolve well with significant
residue. The method specifies the amount of powder to be added to 180 mL of 105
degree F water, which is then placed in an eight ounce bottle with a lid and shaken
moderately for 30 seconds. The contents of the bottle are then emptied into a 5 inch
diameter 80 mesh screen. Several handfuls of tap water are then used to wash away
foam through the screen to expose remaining undissolved particles or gel particles. A
score of 1-4 is an acceptable powder dispersibility score. A score of 4 has
approximately 25% of the 80 mesh screen with undissolved particles. A score of 5 or
greater has approximately 40% or more of the screen with undissolved particles. A
score of 5 or 6 is an unacceptable powder dispersibility score.
[0065] Additionally, the extruded nutritional powders have good emulsion
stability in that there is little to no fat (oil) separation upon reconstitution.
Surprisingly, the extruded nutritional powders have no fat separation after a period of
at least 15 minutes, including at least 20 minutes, including at least 25 minutes, and
including at least 30 minutes when placed in room temperature water. Further, the
extruded nutritional powders have no fat separation after a period of at least 1 hour,
including at least 3 hours, including at least 8 hours, including at least 10 hours,
including at least 15 hours, including at least 20 hours, and including at least 24 hours
when refrigerated at 1 degree C to 4.5 degree C. Furthermore, in some embodiments,
the extruded nutritional powders also maintain emulsion stability following
reconstitution to a ready-to-feed form.
[0066] The extruder apparatus may be used to produce extruded powder in
batch format, or in a continuous process. For preparing the mixture to be emulsified,
the various components to be mixed and emulsified are typically added successively
to the extruder. Any suitable extruder known for use in the nutritional art may be
used with the processes of the present disclosure. The extruder may be a single
screw, multi screw, ring screw, planetary gear extruder, and the like. In one
particularly suitable embodiment, the extruded is a co-rotating, twin screw extruder
that may be used to continuously process nutritional powders.
[0067] One embodiment of preparing the mixture to be extruded to form an
extrudate includes initially introducing a dry blend into an extruder. The dry blend
may include at least one or more of a protein (or portion of a protein component; that
is, from 1% to 100% by weight of the protein component, desirably 22% to about
30% by weight) and optionally a carbohydrate as discussed herein, wherein the
optional carbohydrate may optionally be lactose-free. In some embodiments,
vitamins and minerals are optionally introduced with the dry blend. In other
embodiments, the dry blend may include a protein and lactose preblend. The protein,
or portion of the protein, may, in some embodiments, be dryblended with ingredients,
such as citrates, that one skilled in the art based on the disclosure herein would know
to aid in the hydration of proteins by complexing divalent minerals that interfere with
solubility of the protein. In addition or in place of, a small amount of the total oil
(such as 0.1% to about 3% by weight of the total oil, including about 1.4% by weight
of the total oil) adequate to coat the outside of the powder particles, may also be
introduced prior to water to aid in the protein hydration by slowing hydration of the
outside of the particle and thereby allowing complete hydration of the total protein
particle.
[0068] Water may then be introduced into the extruder to hydrate the dry
blend. Water soluble vitamins and minerals may optionally be added at this hydration
stage. Following hydration, emulsification is initiated by introducing an oil blend
including fat and fat soluble vitamins along with fat soluble ingredients such as
carotenoids into the extruder. Finally, dispersive mixing of any additional
carbohydrates (also referred to as carbohydrate blend), water soluble vitamins and
minerals, or additional optional liquid or dry components for use in the resulting
extruded nutritional powders may be introduced simultaneously or successively into
the extruder. The hydration, emulsification, and dispersive mixing steps of extrusion
are entirely within the extruder. That is, there is no external emulsification of the
components outside the extruder.
[0069] In alternative embodiments, water is added to the extruder prior to
adding the dry blend to help ensure hydration of the powdered ingredients when
added. Improved hydration allows the powdered ingredients to mix better so that they
do not stick as readily to the inside of the extruder.
[0070] The processes of the present disclosure reduce the moisture levels of
the components within the extruder from upwards of 37.5% by total weight of the
components (e.g., dry blend, water, oil blend, etc.) to less than about 14% by total
weight of the components. Typically, water comprises less than about 22% by weight
of the total dry blend, water, oil blend and the like, including less than about 14% by
weight of total dry blend, water, oil blend, and the like, including less than about
13.5% by weight, including less than about 13% by weight, including less than about
12% by weight, including less than about 11% by weight, including less than about
10% by weight, including less than about 9% by weight, including less than about 8%
by weight, also including from about 6% by weight to about 14% by weight,
including from about 7.5% by weight to about 13.2% by weight, and including from
about 8% by weight to about 10% by weight of the total dry blend, water, oil blend,
and the like.
[0071] Typically, the temperature of the mixing and emulsifying may be
adjusted throughout the extruder dependent on the components to be added and the
function of the work to be carried out. Typically, the temperatures of the mixing and
emulsification process range from about 25°C to about 100°C, including from about
55°C to about 78°C, including from about 60°C to about 70°C. In those embodiments
where heat labile vitamins are used, the mixing and emulsification temperature may
be slightly modified. In those embodiments, mixing and emulsification may be
carried out at a temperature of from about 70°C to about 100°C, or from about 80°C
to about 95°C, or at a temperature of about 90°C.
[0072] Additionally, the pressure may be adjusted accordingly from above
atmospheric pressure (mixing and emulsification) up to between about 200 kPa and
about 10 MPa (dispersive mixing, plasticizing, and extruding). Further, the
components are mixed and emulsified within the extruder for a time period of about
30 seconds to about 300 seconds and including from about 55 seconds to about 180
seconds, including from about 75 seconds to about 120 seconds, and including from
about 90 seconds to about 110 seconds. In those embodiments where heat labile
vitamins are used, mixing and emulsification may occur for a period of about two
minutes to about ten minutes, or from about three minutes to about eight minutes or
about four minutes to about seven minutes, or about five minutes to about six minutes.
In a particular embodiment, mixing and emulsification is carried out for about four
minutes.
[0073] Referring now to FIG. 1, one suitable mixing and emulsifying
process of the present disclosure includes an extruder having twelve different
elements with multiple feed zones. One or more proteins are introduced into zone 1,
water is introduced into zone 2 (start of hydration), the oil blend including oil soluble
vitamins and oil soluble ingredients is introduced into zone 5 (start of emulsification),
and finally the carbohydrates (e.g., lactose blend and galactooligosaccharides (GOS)
and/or fructooligosaccharides (FOS)) are introduced into zone 8 (start of dispersive
mixing). Optionally, water-soluble vitamins and minerals can be introduced in one or
both of zones 2 and 8, optional liquid components may be introduced into zone 8, and
optional dry powdered components may be introduced into zone 11. Temperatures in
the zones of the extruder of this embodiment include: a temperature of about 80°C in
zones 1-7 and a temperature of about 60°C in zones 8-12 with a total residence time in
the extruder of from about 55 seconds to about 180 seconds.
[0074] The feed rates for the different components, as well as the flow rate
for the final extruded mixture and sizes of the entry points to the different feed zones,
are dependent on the size of the extruder.
[0075] Now referring to FIG. 2, another suitable embodiment of the mixing
and emulsifying process of the present disclosure includes introducing a dry blend
including at least a portion of a protein and optionally a portion of the carbohydrate
into zone 1, water is introduced into zone 2 (start of hydration), and the oil blend
including the oil soluble vitamins and oil soluble ingredients is introduced into zone 5
(start of emulsification). Optionally, water-soluble vitamins and minerals can be
introduced in one or both of zones 1 and 2, optional liquid components may be
introduced into zone 8 (start of dispersive mixing), and optional dry powdered
components may be introduced into zone 11.
[0076] Once the components are mixed and emulsified as described herein,
the emulsified mixture is extruded from the extruder and dried. In some optional
embodiments, the extrudate may be cut into desired sizes upon exiting the extruder.
The emulsified mixture may be extruded as a cake, or may optionally be extruded
through a die, which may potentially reduce the amount of shear that the finished
product is exposed to. The shear applied at any time during the manufacturing
process, and suitable during the emulsification process, may be continuous shear or
non-continuous shear.
[0077] Numerous conventional drying means are suitable for drying the
extrudate to the desired water content of the final product. For example, the extrudate
may be dried using a vacuum belt dryer, a continuous microwave dryer, or a vacuum
drum dryer. Other drying processes, including infrared drying or spray drying may
also be used in some embodiments to produce a suitably dry extruded nutritional
powder. Typically, the extrudate is dried at a temperature of from about 80°C to
about 160°C, including from about 90°C to about 150°C, and including from about
105°C to about 130°C. Drying including microwave drying, radiant drying, and
conduction drying may suitably be used.
[0078] An exemplary vacuum belt dryer is the Merk Vacuum belt dryer
which includes an infrared component and a direct contact heater. Where used, the
amount of drying time will depend on the amount of water added to the extruder. For
example, about 1.0 to about 1.6 kg/hr of water may require about 5 to about 45
minutes of drying time, such as about 25 minutes. The vacuum pressure may be
about 20 to about 50 mbar, such as about 30 mbar. The vacuum drying temperature
may be about 100°C to about 170°C.
[0079] Alternatively, the extrudate may be dried by subjecting it to radiation
via a continuous microwave dryer. The extruded material may be transported through
the microwave dryer via a conveyor passing through the microwave dryer. The
conveyor may deposit the extruded material across the conveyor at a uniform density
and a uniform thickness for uniform product characteristics. The desired depth of the
product may vary depending on the penetration depth of the microwave emitter.
[0080] The microwave dryer may use air flow in the interior of the
microwave dryer to further aid in drying the wet extrudate. The air flow may be
heated, dried, or both, prior to entering the microwave dryer, or the air may be
ambient air as it exists near the process site. For instance, the wet extrudate may be
dried in the microwave dryer for a period of about 5 to about 20 minutes. The
microwave dryer may have a vacuum pressure of about 20 mbar to about 30 mbar and
a power of about 0.3 to about 1.0 KW.
[008 1] Alternatively, the extrudate may be dried using a vacuum drum dryer.
The drum dryer may include a pair of drums positioned substantially parallel with
each other. Although the present example includes two drums, any other suitable
number of drums may be used. The drums may be spaced apart to form gap distance
about 0.1mm to about 2 mm between the drums. The drums may rotate in opposing
directions. The drums may be made of carbon or stainless steel and coated in a hard
chrome-plated metal. The drums may be positioned within a housing.
[0082] The wet extrudate may be distributed between the drums such that
the extrudate is adhered to the drums as the extrudate passes through the gap between
the drums. The extrudate may be applied such that the extrudate is distributed
substantially evenly onto the drums. The wet extrudate may be fed from above the
drums such that the extrudate is fed through the drums by gravity. Alternatively, a
belt system or other suitable system may be used to feed the extrudate through the
drums.
[0083] The drums may be heated, such as with steam or thermal oil, to dry
the wet extrudate applied to the drums. As the extrudate is applied to and rotates on
the heated drums, the moisture content of the extrudate evaporates. A scrapper may
be positioned adjacent to each drum such that the scrappers remove the extrudate
adhered to the drum as the drum rotates against the scrapper. The scrappers may be
positioned about 270 degrees around the circumference of the drum from the entry
point of the extrudate such that the extrudate is applied to the drums for about a ¾
turn. For instance, the drums may rotate between about 0.5 to about 3 rpm, such as
about 2 rpm. The wet extrudate may be dried in the drum dryer for a period of about
15 to about 90 seconds at a temperature of about 90°C to about 140°C. The rotary
drum dryer may have a vacuum pressure of about 50 mbar.
[0084] In one particularly suitable embodiment, the dried extrudate includes
water in an amount of no more than about 5% by weight. The extrudate may be dried
to a water content of from about 0.5% by weight to about 5% by weight, including
from about 0.75% by weight to about 5% by weight, including from about 2% by
weight to about 4% by weight, including about 2% by weight to about 3% by weight,
and including about 2.5% by weight to about 3% by weight.
[0085] In some embodiments, after the emulsified mixture is sufficiently
dried to the desired water level, one or more optional encapsulated ingredients may
further be added to the dried emulsified mixture via dryblending or drymixing.
Dryblending or drymixing procedures are known in the art and include the addition of
one or more dry or substantially dry ingredients to a dried base powder, such as a
dried extruded base nutritional powder. These optional ingredients include proteins,
carbohydrates, vitamins, minerals, long chain polyunsaturated acids such as DHA,
ARA, and/or EPA, flavors, nucleotides, nucleosides and other optional ingredients as
discussed herein. In one specific embodiment, the dryblended ingredients are
substantially or completely lactose-free.
[0086] Finally, the dried emulsified mixture may be ground into an extruded
nutritional powder having a desired particle size. Dryblending or drymixing may also
be applied to the ground nutritional powder, i.e., dryblending may occur subsequent to
grinding the dried extrudate to the nutritional powder or forming the nutritional
powder from the dried extrudate. Typically, the mixture is ground using high impact
milling, although other conventional grinding methodologies may suitably be used in
accordance with the present disclosure. The granules of the extruded nutritional
powder may have a bulk density of from about 400 g/1 to about 700 g/1 with a particle
size range of 100-300 microns, preferably 100-250 microns, most preferably 100-225
microns. The extruded nutritional powders may be an extruded infant nutritional
powder, an extruded pediatric nutritional powder, an extruded follow on formula
nutritional powder, or may be an extruded adult nutritional powder.
[0087] As noted above, the extruded nutritional powders of the present
disclosure manufactured by the extrusion processes described herein provide fat
separation (emulsion quality) and dispersibility in water that is at least equivalent to
conventional spray dried nutritional powders; that is, the extruded powders of the
present disclosure have excellent emulsification properties such that upon
reconstitution with a conventional amount of water, the resulting liquid mixture is
substantially stable and there is substantially no fat (oil) separation in the product over
an extended period of time, even up to 24 hours or longer under refrigerated
temperatures, typically -3 degrees C to about 5 degrees C. Additionally, the extruded
nutritional powders show excellent dispersibility upon mixing with water such that
clumping is substantially reduced or eliminated. The extruded nutritional powder thus
provides reconstituted liquids that have substantially no creaming defects over time,
including at 24 hours under refrigerated temperature, typically -3 degrees C to about 5
degrees C.
[0088] The present embodiments are to be considered in all respects as
illustrative and not restrictive and that all changes and equivalents also come within
the description of the present disclosure. The following non-limiting examples will
further illustrate the extruded nutritional powders and methods of the present
disclosure.
EXAMPLES
[0089] The following examples illustrate specific embodiments and/or
features of the extruded nutritional powders of the present disclosure. The examples
are given solely for the purpose of illustration and are not to be construed as
limitations of the present disclosure, as many variations thereof are possible without
departing from the spirit and scope of the disclosure. All exemplified amounts are
weight percentages based upon the total weight of the powder, unless otherwise
specified.
Example 1
[0090] In this Example, an extruded nutritional powder was prepared using
the process set forth in Figure 1. The water rate utilized was 1.6 kg/hour and the
extrudate rate was 10 kg/hour. The extruded nutritional powder was prepared using
the bill of materials of Example 3.
[009 1] The emulsion quality and dispersibility of the extruded nutritional
powder upon reconstitution with water was analyzed and compared to a spray dried
nutritional powder having the same composition.
[0092] The emulsion quality was analyzed by evaluating the fat separation
for both the extruded nutritional powder and the spray dried nutritional powder at
room temperature 30 minutes after reconstitution and at 40°F (4.4°C) 24 hours after
reconstitution. The results are shown in FIGS. 3A and 3B.
[0093] As shown in FIGS. 3A and 3B there was little to no fat separation at
either time point of 30 minutes or 24 hours after reconstitution. That is, the emulsion
quality with respect to fat separation was similar for the extruded nutritional powder
and the spray dried nutritional powder.
Additionally, the dispersibility of the extruded nutritional powder was compared to
the dispersibility of the spray dried nutritional powder. The results are shown in
FIGS. 4A and 4B. As shown in FIGS. 4A and 4B, dispersion of the extruded
nutritional powder was similar to the spray dried nutritional powder.
Example 2
[0094] Example 2 illustrates a pediatric nutritional powder that could be
prepared using the extrusion methods of the present disclosure. The starting
ingredients of Example 2 are listed in the following Table.
Example 3
[0095] Example 3 illustrates an infant nutritional powder that could be
prepared using the extrusion methods of the present disclosure. The starting
ingredients of Example 3 are listed in the following Table.
otass um y rox e o s g
Example 4
[0096] Example 4 illustrates an infant nutritional powder that could be
prepared using the extrusion methods of the present disclosure. The starting
ingredients of Example 4 are listed in the following Table.
Example 5
[0097] Example 5 illustrates an adult nutritional powder that could be
prepared using the extrusion methods of the present disclosure. The starting
ingredients of Example 5 are listed in the following Table.
EXAMPLE 6
[0098] Example 6 illustrates an infant nutritional powder that could be
prepared using the extrusion methods of the present disclosure. The starting
ingredients of Example 5 are listed in the following Table.
EXAMPLE 7
[0099] Example 7 illustrates an infant nutritional powder prepared with heat
labile vitamins.
Ingredient Description kAg/m1,0o0u0ntk,g
NFDM 199
WPC 60.3
Lactose 376
Potassium Citrate 8.05
Calcium Carbonate 4.18
Nucleotide/Choline Premix 2.29
Potassium Chloride 1.52
Sodium Ascorbate 1.44
Vitamin/Mineral Premix 1.09
Magnesium Chloride 0.874
Sodium Chloride 0.781
Ferrous Sulfate 0.442
Choline Chloride 0.421
L-Carnitine 0.0256
Riboflavin 0.00310
Water 101-162
HOSO (High Oleic
Saflower Oil) 112
Soy Oil 83.5
Coconut Oil 76.9
ARA 2.87
Lecithin Ultralec 1.10
DHA 1.08
Vitamin ADEK 0.368
MC Premix 0.182
Beta Carotine 0.000598
GOS 65.5
[00100] The ingredients listed above are extruded to form a nutritional
composition. The protein and lactose blends are introduced into the extruder via a
hopper. Water is added into the extruder to perform hydration. After the composition
has been hydrated, the oil blend is introduced into the extruder. Once the oil blend is
introduced, the composition within the extruder is emulsified (i.e., the composition is
emulsified within the extruder). After emulsification, galactooligosaccharides (GOS)
are introduced into the extruder, wherein dispersive mixing is performed.
[00101] After the extrusion step, the extrudate is dried in a Merk Vacuum
belt dryer for about 25 minutes of drying time. The dried extrudate product contains
less than about 5% moisture content. Once dried, the extrudate is milled using a
Fitzmill to obtain granules in the range of from about 275 to about 325 microns.
WHAT IS CLAIMED IS:
1. A process for manufacturing an extruded nutritional powder, the process
comprising:
introducing water into an extruder;
introducing a dry blend comprising at least a portion of a protein and,
optionally, a portion of a carbohydrate into the extruder;
introducing an oil blend comprising fat into the extruder;
mixing the dry blend and oil blend to form an emulsified mixture within the
extruder and extruding the emulsified mixture to form an extrudate;
drying the extrudate; and
forming a powder from the dried extrudate.
2. The process of claim 1wherein the dry blend, water, and oil blend are held
within the extruder for a total time period of from about 30 seconds to about 300
seconds.
3. The process of claim 1 further comprising dryblending an optional ingredient
with the dried extrudate subsequent to forming a powder from the dried extrudate.
4. The process of claim 1wherein the extruder is a co-rotating twin screw
extruder.
5. The process of claim 1wherein the drying is done using a vacuum dryer.
6. The process of claim 5 wherein the drying is done using a continuous vacuum
dryer.
7. The process of claim 1wherein the extruded nutritional powder is selected
from the group consisting of a soy based-extruded nutritional powder, a lactose-free
extruded nutritional powder, a rice-starch based extruded nutritional powder, a milk
protein-based extruded nutritional powder, a protein hydrolysate-based extruded
nutritional powder, and combinations thereof.
8. A process for manufacturing an extruded nutritional powder, the process
comprising:
introducing water into an extruder;
introducing a dry blend comprising at least a portion of one protein and
optionally, at least a portion of a carbohydrate into the extruder and hydrating
the dry blend;
introducing an oil blend comprising at least a portion of one fat into the
extruder;
mixing the hydrated dry blend and oil blend to form an emulsified mixture
within the extruder, wherein water comprises less than 22% by weight of total
emulsified mixture;
extruding the emulsified mixture to form an extrudate;
drying the extrudate; and
grinding the dried extrudate into a nutritional powder.
9. The process of claim 8 wherein water comprises less than 14% by weight of
total dry blend, water, and oil blend.
10. The process of claim 1 or 8 wherein the dry blend comprises protein and
carbohydrate.
11. The process of claim 1 or 8 wherein the dry blend further comprises vitamins,
minerals, or both.
12. The process of claim 1 or 8 wherein the dry blend, water, and oil blend are
mixed and emulsified at a temperature range of from about 25°C to about 100°C.
13. The process of claim 8 wherein the dry blend, water, and oil blend are held
within the extruder for a total time period of from about 30 seconds to about 300
seconds.
14. The process of claim 1 or 8 wherein the dry blend additionally includes an
ingredient selected from the group consisting of minerals, citrates, a protein hydration
aid, from 1% to 3% by weight of the total oil, and combinations thereof.
15. A process for manufacturing an extruded nutritional powder, the process
comprising:
introducing water into an extruder;
introducing at least a portion of a protein into the extruder;
introducing an oil blend comprising fat into the extruder;
introducing a carbohydrate into the extruder;
mixing and emulsifying the protein, water, oil blend, and carbohydrate within
the extruder to form an emulsified mixture and extruding the emulsified
mixture to form an extrudate;
drying the extrudate; and
grinding the dried extrudate into a nutritional powder.
16. The process of claim 15, further comprising adding vitamins, minerals, or
both, to the extruder.
17. The process of claim 15 wherein the protein, water, oil blend, and
carbohydrate are mixed and emulsified at a temperature range of from about 25°C to
about 100°C.
18. The process of claim 15 wherein the protein, water, oil blend, and
carbohydrate are held within the extruder for a total time period of from about 30
seconds to about 300 seconds.
19. The process of claim 1, 8, or 15 comprising drying the extrudate at a
temperature of from about 80°C to about 160°C.
20. The process of claim 8 or 15 further comprising dryblending an optional
ingredient with the dried extrudate subsequent to grinding the dried extrudate into a
nutritional powder.
21. The process of claim 1, 8 or 15 further comprising dryblending at least one
ingredient.
22. The process of claim 2 1 wherein the at least one ingredient is selected from
the group consisting of probiotics, encapsulated PUFAs, and combinations thereof.
23. An extruded powder comprising fat, carbohydrate, and protein, wherein the
extruded powder, upon reconstitution with water, shows substantially no fat
separation at 24 hours.
24. An extruded powder comprising fat, carbohydrate, and protein, wherein the
extruded powder, upon reconstitution with water, shows substantially no creaming
defect at 24 hours.
25. The process of claim 1, 8, or 15 wherein the extrudate is dried to a moisture
content of between about 0.75% to about 5%.
26. The process of claim 25, wherein a vacuum belt dryer is used in the drying
step.
27. The process of claim 26, wherein the extrudate is dried for a period of about 5
to about 45 minutes.
28. The process of claim 25, wherein a vacuum drum dryer is used in the drying
step.
29. The process of claim 28, wherein the extrudate is dried for a period of about
15 to about 90 seconds.
30. The process of claim 25, wherein a continuous microwave dryer is used in the
drying step.
31. The process of claim 30, wherein the extrudate is dried for a period of about 5
to about 20 minutes.
32. The process of claim 25, further comprising reconstituting the powder to a
ready-to-feed state.
33. The process of claim 3 1, wherein said powder, when reconstituted, forms a
stable emulsion.
34. The process of claim 1, 8, or 15 wherein the extrudate is dried for a period of
about 5 minutes to about 45 minutes using a vacuum belt dryer to produce a
nutritional composition, wherein said nutritional composition forms a stable emulsion
upon reconstitution.
35. The process of claim 34, wherein the drying step is performed at a pressure of
about 20 mbar to about 50 mbar.
36. The process of claim 34, wherein the drying step is performed at a temperature
of about 100°C to about 170°C.
37. A nutritional composition comprising at least one of a fat, protein, and
carbohydrate, and at least one vitamin, mineral, or other nutrient, or combination
thereof, made according to the process of claim 25.
38. The nutritional composition of claim 37, wherein said composition comprises
from about 10% to about 18% protein; from about 30% to about 54% carbohydrate;
and from about 24% to about 50% fat.
39. The nutritional composition of claim 37, wherein said composition comprises
from about 54 to about 140 gm/1 of carbohydrate, from about 20 to about 54 gm/1 of
fat, and from about 7 to about 40 gm/1 of protein.
40. The nutritional composition of claim 37, wherein said composition is
reconstituted to a ready-to-feed state and wherein said composition forms a stable
emulsion upon reconstitution.
4 1. The nutritional composition of claim 37, wherein the composition is prepared
by forming an emulsion within the extruder and then extruding the mixture.
42. The nutritional composition of claim 37, wherein the composition is dried
using a vacuum belt dryer.
43. The nutritional composition of claim 42, wherein the composition is dried for
a period of about 25 minutes, at a pressure of about 20 mbar to about 50 mbar, and at
a temperature of about 100°C to about 170°C.
| # | Name | Date |
|---|---|---|
| 1 | Power of Attorney [22-04-2015(online)].pdf | 2015-04-22 |
| 2 | Form 5 [22-04-2015(online)].pdf | 2015-04-22 |
| 3 | Form 3 [22-04-2015(online)].pdf | 2015-04-22 |
| 4 | Description(Complete) [22-04-2015(online)].pdf | 2015-04-22 |
| 5 | 3418-DELNP-2015.pdf | 2015-05-20 |
| 6 | 3418-delnp-2015-Correspondence Others-(27-05-2015).pdf | 2015-05-27 |
| 7 | 3418-delnp-2015-Assignment-(27-05-2015).pdf | 2015-05-27 |
| 8 | 3418-delnp-2015-GPA-(10-06-2015).pdf | 2015-06-10 |
| 9 | 3418-delnp-2015-Correspondence Others-(10-06-2015).pdf | 2015-06-10 |
| 10 | 3418-delnp-2015-Form-3-(11-06-2015).pdf | 2015-06-11 |
| 11 | 3418-delnp-2015-Correspondence Others-(11-06-2015).pdf | 2015-06-11 |
| 12 | 3418-delnp-2015-Form-3-(11-12-2015).pdf | 2015-12-11 |
| 13 | 3418-delnp-2015-Correspondence Others-(11-12-2015).pdf | 2015-12-11 |
| 14 | 3418-delnp-2015-Form-3-(05-04-2016).pdf | 2016-04-05 |
| 15 | 3418-delnp-2015-Correspondence Others-(05-04-2016).pdf | 2016-04-05 |