EP1146798A2 - Modified food products and beverages, and additives for food and beverages - Google Patents

Modified food products and beverages, and additives for food and beverages

Info

Publication number
EP1146798A2
EP1146798A2 EP00900291A EP00900291A EP1146798A2 EP 1146798 A2 EP1146798 A2 EP 1146798A2 EP 00900291 A EP00900291 A EP 00900291A EP 00900291 A EP00900291 A EP 00900291A EP 1146798 A2 EP1146798 A2 EP 1146798A2
Authority
EP
European Patent Office
Prior art keywords
yoghurt
product
plant sterols
food
milk
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP00900291A
Other languages
German (de)
French (fr)
Inventor
Evgeny Naum The Old School House VULFSON
Barry Arnold Law
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nutrahealth Ltd (UK)
Original Assignee
Nutrahealth Ltd (UK)
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GBGB9901892.1A external-priority patent/GB9901892D0/en
Application filed by Nutrahealth Ltd (UK) filed Critical Nutrahealth Ltd (UK)
Publication of EP1146798A2 publication Critical patent/EP1146798A2/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D2/00Treatment of flour or dough by adding materials thereto before or during baking
    • A21D2/08Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
    • A21D2/10Hydrocarbons
    • AHUMAN NECESSITIES
    • A21BAKING; EDIBLE DOUGHS
    • A21DTREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
    • A21D2/00Treatment of flour or dough by adding materials thereto before or during baking
    • A21D2/08Treatment of flour or dough by adding materials thereto before or during baking by adding organic substances
    • A21D2/14Organic oxygen compounds
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
    • A23C9/00Milk preparations; Milk powder or milk powder preparations
    • A23C9/12Fermented milk preparations; Treatment using microorganisms or enzymes
    • A23C9/13Fermented milk preparations; Treatment using microorganisms or enzymes using additives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
    • A23C9/00Milk preparations; Milk powder or milk powder preparations
    • A23C9/12Fermented milk preparations; Treatment using microorganisms or enzymes
    • A23C9/13Fermented milk preparations; Treatment using microorganisms or enzymes using additives
    • A23C9/1307Milk products or derivatives; Fruit or vegetable juices; Sugars, sugar alcohols, sweeteners; Oligosaccharides; Organic acids or salts thereof or acidifying agents; Flavours, dyes or pigments; Inert or aerosol gases; Carbonation methods
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
    • A23C9/00Milk preparations; Milk powder or milk powder preparations
    • A23C9/12Fermented milk preparations; Treatment using microorganisms or enzymes
    • A23C9/13Fermented milk preparations; Treatment using microorganisms or enzymes using additives
    • A23C9/133Fruit or vegetables
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23CDAIRY PRODUCTS, e.g. MILK, BUTTER OR CHEESE; MILK OR CHEESE SUBSTITUTES; MAKING THEREOF
    • A23C9/00Milk preparations; Milk powder or milk powder preparations
    • A23C9/152Milk preparations; Milk powder or milk powder preparations containing additives
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23DEDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
    • A23D7/00Edible oil or fat compositions containing an aqueous phase, e.g. margarines
    • A23D7/005Edible oil or fat compositions containing an aqueous phase, e.g. margarines characterised by ingredients other than fatty acid triglycerides
    • A23D7/0056Spread compositions
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23DEDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
    • A23D7/00Edible oil or fat compositions containing an aqueous phase, e.g. margarines
    • A23D7/015Reducing calorie content; Reducing fat content, e.g. "halvarines"
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, 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
    • A23L33/00Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
    • A23L33/10Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
    • A23L33/105Plant extracts, their artificial duplicates or their derivatives
    • A23L33/11Plant sterols or derivatives thereof, e.g. phytosterols
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23PSHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
    • A23P10/00Shaping or working of foodstuffs characterised by the products
    • A23P10/30Encapsulation of particles, e.g. foodstuff additives

Definitions

  • the present invention relates to modified food products
  • beverages particularly those containing plant sterols, and it relates to
  • additives for food and beverages particularly plant sterol additives.
  • fermented milk products such as yoghurt; emulsified fat
  • hyperlipidaemic manifestations hyperglycaemia as well as anti-proliferative disorders
  • modified sterols such as saponins (US Patents 4 602 003 & 4 242 502),
  • sitosterol has somewhat higher hypocholesterolemic activity than
  • sitosterol and stanol esters when tested in parallel trials, are equally
  • Emulsified low fat spreads, fermented dairy products and some other common foods and beverages described herein satisfy these criteria.
  • Fat spreads and margarine can be prepared with different fat
  • a fat spread is a water-in-oil or oil-in-water
  • plant sterols are used and they are contained predominantly in the
  • these fermented foods typically contain micro ⁇
  • Soybeans for example, are fermented to produce Japanese "miso"
  • milk is also fermented to produce nutritionally valuable products.
  • Examples of these products include yoghurt, sour cream, kefir, ymer as well as fresh cheeses such as quark and fromage frais. Buttermilk, which
  • micro-organisms which are fermented using specific micro-organisms.
  • the micro-organisms which are fermented using specific micro-organisms.
  • micro-organisms used which, depending on the species or strain,
  • flavouring substances such as diacetyl or acetaldehyde and structure
  • constituents such as polysaccharides.
  • bacteria such as Lactobacillus acidophilus in
  • fermented milk products contains an active culture of micro-organisms
  • Yoghurt is generally made by a process that includes the following
  • a starter culture consisting of one or more yoghurt-producing micro-
  • organisms is added (inoculation) and blended in while maintaining the
  • Yoghurt can be prepared with a range of fat contents. For example,
  • a yoghurt can be labelled as “non-fat”, if it contains less than 0.5% milkfat and as “low fat”, if it contains from not less than 0.5% to
  • non-fat or very low fat yoghurt in
  • the UK should also have fat content below 0.5%, whilst in Germany and
  • yoghurt may be prepared in
  • Liquid yoghurt at the other extreme, is
  • yoghurts are classified according to their physical state.
  • serving size cups also known as
  • products are generally made by cooking a fruit and sugar mixture with the
  • cooked fruit product may contain discernible pieces of fruit in it or may be
  • Sundae style fruited yoghurt is generally made in retail containers
  • fruited yoghurt is generally made by mixing a suitable amount of fruit
  • Drinking yoghurt is based on the stirring manufacturing process
  • the shelf life of yoghurt can be increased by the so-called
  • yoghurt collectively be referred to as "yoghurt”.
  • This invention relates to the provision of novel food additives
  • plant sterols and lycopenes such as tomato
  • the method comprises coating the hydrophobic
  • Hydrophobic compounds which can be shown to be beneficial
  • This invention also relates, in one embodiment, to the discovery that
  • hydrophobic compound such as plant sterol or
  • plant sterols are incorporated predominantly into the aqueous phase of the
  • This embodiment also relates to a
  • Another aspect of this invention relates to the discovery that the
  • This invention also relates to food
  • This invention brings to the market a range of novel hydrophobic
  • a food product which is produced by the fermentation of a
  • composition made with no plant sterols added.
  • milk product which is produced by the fermentation of a
  • yoghurts which are produced by fermentation of a mixture of milk and/or
  • composition and fat content as well as yoghurt products are provided
  • Yet another aspect of this invention is to provide a process for the
  • Yet another aspect of this invention is to provide a process for the
  • Still another aspect of this invention is to provide a method for the
  • hydrophobic compounds of benefit to human health
  • fat spread is understood to mean a product containing at least
  • a fat spread or a yoghurt are as defined by legislation or relevant
  • Low fat and “very low fat” spreads may have less
  • organoleptic properties of the modified food product or beverage are
  • lactic acid bacteria is understood to mean micro ⁇
  • edible products in a solid or liquid form, which are produced by contacting a fermentable raw material with a particular micro-organism for the time
  • milk products include
  • milk is understood to mean conventional milk as well as
  • yoghurt products is understood to mean foods and
  • yoghurt products include
  • the invention provides a method for making a composition suitable
  • the hydrophobic compound is any one of a plant sterol
  • carotenoids and poorly water soluble anti-oxidants or a combination
  • the component acceptable as a food additive is any one of
  • polypeptide may conveniently be a milk-derived or soya-derived protein.
  • polysaccharides include, for example, modified cellulose, pectins and
  • the hydrophobic compound is one which is solid at room
  • the hydrophobic compound is a plant sterol or
  • hydrophobic compound is contacted with the component acceptable as a
  • composition suitable for inclusion in a food product or beverage is one
  • hydrophobic compound such as plant sterol or lycopene
  • hydrophobic compound to coating agent is from about 0J to about 0.4
  • the amount of coating agent allows the particles to be
  • composition may be formed in situ in the process of the
  • sterols are biologically active compounds which are present in
  • heating step is used by most manufacturers of fermented milk products
  • resulting yoghurt had a texture, appearance and flavour like the
  • milk preferably milk proteins or other proteins, prior to adding the above
  • the coated sterols to the aqueous phase of a food product or a beverage.
  • the coating can be achieved by stirring a suspension of plant sterols with
  • the coating agent or the coating agent can be added to the suspension as
  • sterols can be
  • milk proteins such as caseins and their salts, whey proteins and milk
  • derived solids such as milk powder, whey or buttermilk are preferably
  • coating agents such as proteins from sources other than milk
  • the added volume may vary from about 1.0
  • the suspension of plant sterols can also be prepared by
  • casein sodium caseinate, whey proteins, whey, milk powder or buttermilk or even milk itself. It is also surprising that a fine suspension of plant
  • sterols in water can be produced in the absence of surfactants such as, for
  • polyoxyethylene sorbitan esters or sodium dodecyl sulphate examples, polyoxyethylene sorbitan esters or sodium dodecyl sulphate, and
  • final admixture with plant sterols can vary from about 0.1 % to about 2.0%
  • the suspension of sterols can be stirred for some time in the
  • the suspension can be any suitable material.
  • the suspension can be any suitable material.
  • the suspension can be any suitable material.
  • the suspension can be any suitable material.
  • ionisable functional groups are employed such as proteins or
  • the pH of the suspension can be altered by adding a
  • dilute acid or base such as to neutralise substantially the net charge in the molecule of the coating agent, preferably to a pH which is near the
  • the pH is typically adjusted with a dilute acid to
  • pH is adjusted back to the preferred values of 6J-6.7.
  • coating can be achieved by precipitating plant sterols into solution
  • sterols can be dissolved in an
  • organic solvent preferably a water-miscible organic solvent
  • coated plant sterols can also be found to be satisfactory.
  • the coated plant sterols can also be found to be satisfactory.
  • non-sterol food additives Such additives can be physiologically active
  • plant sterols prior to the coating as described herein, can be co-
  • the additives can be used in the amount as small as
  • coated plant sterols display properties which are different from that of
  • caseinate coated plant sterols can be suspended in water with relative
  • coating agent is encouraged to adhere to the surface of the plant sterol
  • plant sterol particles can be fruitfully employed.
  • the resulting coated composition is an ability to easily form an aqueous
  • the coating composition should expose functionality.
  • human health also has a functionality which when exposed to an aqueous
  • phase encourages the coated particles to form a suspension in the
  • aqueous phase aqueous phase.
  • coating agents those which have ionisable
  • the coating agents must be approved for food use and be compatible
  • the coating can be accomplished in situ i.e.
  • milk directly in milk, preferably in milk fortified with milk derived solids, as well
  • present invention gives acceptable appearance and organoleptic
  • flavour to, or are substantially indistinguishable from, the corresponding
  • beverage the method comprising the step of combining a plant sterol,
  • additive interacts with the surface of the hydrophobic compound.
  • the invention provides a composition suitable for inclusion
  • a food product or beverage comprising a plant sterol, lycopene or other hydrophobic compound which can be shown to be beneficial for human
  • composition of the invention which is useful in food and
  • casein caseinate
  • whey protein
  • ⁇ -sitosterol are selected from the group comprising ⁇ -sitosterol, ⁇ -campesterol, ⁇ -
  • stigmasterol stigmasterol, ⁇ -sitostanol, ⁇ -campestanol and ⁇ -stigmastanol and their
  • carboxylic acid esters and a mixture thereof.
  • the milk-derived solid and the plant sterol are contacted at
  • the present invention can be any plant sterols. Furthermore, in addition to plant sterols, the present invention can be any plant sterols.
  • additives are sufficiently hydrophobic to enable their coating according to
  • said additives can be coated separately and used in foods and beverages
  • invention provides a method for preparing a food product or beverage
  • composition suitable for inclusion in a food product or beverage the
  • hydrophobic compound which can be shown to be beneficial for human
  • the component which is acceptable as a food additive interacts with the
  • composition eg coated plant sterol
  • composition is a stage where the food additive
  • the hydrophobic compound resides in the aqueous phase
  • the invention also provides a food product or beverage which is
  • the hydrophobic compound is a plant sterol or lycopene
  • a food additive is a milk-derived solid.
  • fermented with lactic acid bacteria preferably fermented milk products
  • present invention are made involves forming a milk base by admixing
  • fermentable dairy product including whole milk, low fat milk, skimmed milk,
  • skim milk condensed milk, evaporated milk, milk powder including non-fat
  • NFDM dry milk powder
  • buttermilk buttermilk, cream and the like, and optionally
  • thickeners and stabilisers and optionally a sweetener, and optionally
  • mixture is optionally homogenised by conventional homogenisation means
  • the mixture is inoculated with a suitable micro-organism
  • cows milk as defined herein or ingredients derived
  • butterfat may also be used. It was found that regardless of whether
  • yoghurts are made from fresh milk or reconstituted milk and whether the
  • milk and milk powder used were skimmed, semi-skimmed or whole, the
  • dry milk and milk powder which contain the coated plant sterols in
  • preparations may contain as li t ⁇ e as about 50% or as much as about 95%
  • organic solvents or an organic solvent-water mixtures preferably with
  • rice bran oil such as cycloartol and 24-methyl-cycloartol, and from
  • sheanut such as amyrin, lupeol and butyrospermol may also be used.
  • the yoghurt according to this invention contains
  • milk solids in quantity from between about 10% to about 25% by weight.
  • the butterfat content may be between less than 0.2-0.5% for
  • non fat or very low fat yoghurt to about 10% for a Greek style yoghurt.
  • primary fat contributing ingredient in yoghurt is generally milk, a low fat
  • butterfat content of less than about 0.4% and preferably less than about
  • thermophilus
  • yoghurts of this invention are made by making the
  • whey proteins in quantity from about 1.0 gram to about 3.0 gram per 100
  • desired amount of plant sterols typically from about 1.5 gram to about 5
  • the acidifying agent may be a food quality acid, for example, lactic or citric
  • supplementary size reduction techniques include, for example, passing the slurry through a colloidal mill, or a two stage homogeniser followed by
  • impeller blender in which the slurry is prepared.
  • the slurry can be passed
  • the ingredients of the fermentation mixture are then treated at high
  • the heat treatment may be carried out at many different temperature and
  • the heat treated and pasteurised mixture is cooled in one or more
  • micro ⁇ inoculated with a micro-organism to initiate the fermentation.
  • organism used in the fermentation is essentially a lactic acid bacterium
  • the micro-organism can be one of several yoghurt producing
  • Lactobacillus bulgaricus a lactic acid
  • micro-organisms producing micro-organisms. These micro-organisms can be used in equal
  • Lactobacillus is Lactobacillus
  • Lactobacillus and Streptococcus which may be used to practice the present invention include Lactobacillus bulgaricus, helveticus, jugurti,
  • lactis or acidophilus lactis or acidophilus and Streptococcus thermophilus, cemorris, lactis or
  • Bifidobacterium sp. for example, Bifidobacterium breve
  • Lactococcus casei can also be optionally added.
  • products including yoghurts, can be prepared with the addition of more
  • fermented milk products such as yoghurt, in addition to plant sterols,
  • the fermentation is continued for an appropriate time until the
  • yoghurt composition reaches a pH in the range of about 3.8 to about 5.0
  • precipitate may sometimes be formed at the bottom of the container.
  • a stabilising or thickening agent can be any suitable stabilising or thickening agent.
  • ingredients such as fruits or flavouring agents. It is preferred to use
  • a thickening agent is preferably water soluble and one that is
  • the amount of the thickening agent used does not exceed about 0.5% to
  • Such stabilising or thickening agents include plant exudates (e.g. gum
  • seaweed extracts e.g. alginates
  • plant and seed gums e.g guar
  • plant extracts e.g. pectin
  • animal derived products e.g gelatin
  • demethylated pectins may be used either on their own or in combination
  • emulsifiers such as mono/diglycerides, lecithin or polysorbates.
  • flavouring which are normally used in conventional yoghurt varieties. It is
  • thickening agents as described herein can be used in the normally
  • the fruit is added in the conventional manner either as a dispersion
  • the fruit can be conventionally
  • fruit preparation at the bottom can, after capping, be inverted to cause the
  • the amount of the fruit added can vary from about 5% to about
  • fruit component may optionally contain, in addition to conventional sugars,
  • compositions of, for example,
  • strawberry fruit products Swiss style fruit product comprising 40-55%
  • agents for agents, acidifiers and preservatives, are suitable.
  • flavouring agent can be optionally added to the pasteurised
  • flavouring agents may be natural or artificial,
  • flavours such as vanilla, chocolate and others which are customarily sweet
  • flavouring agent used in the yoghurt art can all be used.
  • the amount of flavouring agent can all be used.
  • composition on a dry weight basis is used. It may also be desirable or even required when a flavouring agent is
  • a sweetening agent to, for example, offset the taste of
  • sucrose sucrose
  • fructose and synthetic agents such as
  • reducing starch syrup and trehalose may also be employed.
  • Colouring agents may also be used in the preparation of the
  • a colouring agent can be any acceptable
  • flavouring ingredient preferably appropriate to the flavouring agent.
  • the amount of colouring agent may be any suitable colouring agent.
  • yoghurt products can be produced from the yoghurt
  • a yoghurt drink can be any suitable drink.
  • a yoghurt drink can be any suitable drink.
  • a yoghurt drink can be any suitable drink.
  • yoghurt according to this invention is cooled down and water, a food grade
  • compositions which are prepared with no plant sterol added.
  • a yoghurt fruit flavouring can be prepared by adding the plant
  • sterols preferably in a mixture with other solids such as sugar, to a
  • blended fruit at elevated temperature between about 60°C to about 95°C
  • compositions which are made with no plant sterols added. This is an
  • the plant sterols are unesterified
  • the yoghurt fruit they may be free or esterified plant sterols; it is preferred
  • the equipment used in carrying out the present invention is

Abstract

A method for making a composition suitable for inclusion in a food product or beverage the method comprising the step of combining a hydrophobic compound which can be shown to be beneficial for human health with a component which is acceptable as a food additive, wherein the component which is acceptable as a food additive interacts with the surface of the hydrophobic compound. Preferably, the hydrophobic compound is a plant sterol or lycopene or a combination thereof. Food products and beverages supplemented with plant sterol and other hydrophobic compounds are provided. In particular, the food products or beverages are an emulsifiable spread or ones which are fermented with lactic acid bacteria.

Description

MODIFIED FOOD PRODUCTS AND BEVERAGES, AND ADDITIVES
FOR FOOD AND BEVERAGES
FIELD OF THE INVENTION
The present invention relates to modified food products and
beverages, particularly those containing plant sterols, and it relates to
additives for food and beverages, particularly plant sterol additives.
The application describes novel plant sterol containing additives,
and a method for their preparation and their general use in food products
and beverages; food products which are produced by the fermentation of a
mixture of raw material and plant sterols with lactic acid bacteria and, more
specifically to fermented milk products such as yoghurt; emulsified fat
products, and more specifically, to low fat spreads, which contain the
novel plant sterols additives of this invention; and processes for the
preparation of the above said food products and beverages, which are
supplemented with plant sterols. in addition, the application describes
novel additives which contain other hydrophobic compounds which are
known to benefit human health, such as lycopenes, and their use in food
products and beverages.
BACKGROUND OF THE INVENTION
The medicinally useful properties of plant sterols have been known
or a considerable time. In 1953 Pollak reported the preventive effect of plant sterols on experimental atherosclerosis in rabbits (Circulation, (1953)
7, 696-701 ) and plant sterols-induced reduction of the level of blood serum
cholesterol in man (Circulation (1953) 7, 702-706). Three years later
Farquhar et al (Circulation, (1956) 14, 77-82) demonstrated a significant
reduction of serum cholesterol in young men with atherosclerotic heart
disease. Other therapeutic effects e.g. in the treatment and prevention of
diverse geriatric diseases, hypertrophy of the prostate, rheumatic and
hyperlipidaemic manifestations, hyperglycaemia as well as anti-
inflammatory and haemostatic actions, were also described for various
modified sterols such as saponins (US Patents 4 602 003 & 4 242 502),
dihydrocholanes (US Patent 4 117 121 ) and sterol glycosides and their
derivatives (British Patents 1 298 047 & 1 491 532, US Patents 3 991 186,
4 188 379 & 4 254 111).
The mechanism of action of plant sterols is not completely
understood at present. Also, certain controversy exists with regard to the
relative potency of individual sterols and their derivatives and the most
efficient way of administering them. Thus, Ikeda and Sugano
(Atheroclerosis, (1977) 30, 227-237) basing their conclusion on animal
trials suggested that stanol, which is the 5 -saturated derivative of
sitosterol, has somewhat higher hypocholesterolemic activity than
sitosterol. Miettinen et al (US Patent 5 502 045) reported that stanol esters
are more potent in lowering cholesterol than unesterified stanol and
suggested that the difference was due to better solubility of the former compounds in the oil matrix which was used to administer them. On the
other hand, Mattson et al (Am. J. Clin. Nutr., (1982) 35, 697-700) found
the opposite effect when comparing the efficacy of sitosterol suspension
and oil soluble sitosterol oleate, whilst in another study (J. Nutr. (1977)
107, 1139-1146) no appreciable difference between free sterols and their
esters was found. The recent extensive study by Weststrate and Meijer
(Eur. J. Clin. Nutr., (1998) 52, 334-343) also suggests that the esters of
sitosterol and stanol esters, when tested in parallel trials, are equally
effective in lowering the level of serum cholesterol in humans. However,
irrespective of the relative potency of various plant sterols and their
derivatives, it has been well established in the prior art that these
compounds lower the level of serum cholesterol in humans. It is also clear
that laborious and expensive modifications of plant sterols by, for example,
hydrogenation (WO 98/38206) or esterification (WO 98/01126) are
unnecessary and are not necessarily in the interest of the consumer who
will have to, at the end of the day, pay the costs associated with these
modifications.
Due to their beneficial effects, and the fact that plant sterols are
naturally occurring components of vegetable fats and oils (and hence their
consumption is considered to be safe), plant sterols were also suggested
for use in food formulations by, for example, dissolving sterols in an
effective food-acceptable solubilising agent such as triglycerides,
vegetable oils, tocopherols, polyols and alcohols (US Patent 5 244 887; EP 0 839 458; EP 0 289 636; WO97/42830; WO 98/31372; ). Other
vegetable oil-based products, notably margarine, mayonnaise and fat
spreads which contained plant sterols and their esters, were disclosed in
several patent applications (US Patent 5 502 045; WO 97/42830; WO
98/06405; WO 98/01126; WO 98/19556). At least one of these products
(US Patent 5 502 045) has been approved for human consumption and
margarine supplemented with stanol esters is now available on the market
under the tradename Benecol. Thus, it is generally accepted that plant
sterols and their esters in dosages of about 1 gram per day or more can
reduce the level of blood cholesterol and that they are generally well
tolerated in long term use.
It is well known that plant sterols are very poorly soluble in water
(The Merck index, 11th Edition, 1989, Ed. S. Budavari). Consequently
vegetable oil-based formulations have been often used in the prior art for
the incorporation of plant sterols in food products. However, these foods
are not suitable for those consumers who try to limit their fat intake due to
various health reasons and/or specific dietary requirements. There is
therefore a need in the trade to develop and introduce new products
supplemented with plant sterols, including low fat and non-fat or virtually
fat free products, to satisfy consumer demand. It is also clear from the
prior art that in order to draw the maximum benefit from such products,
they should be consumed on a regular basis and in sufficient quantities.
Emulsified low fat spreads, fermented dairy products and some other common foods and beverages described herein satisfy these criteria.
Fat spreads and margarine can be prepared with different fat
content as legally specified and typically between 10% and 80% fat by
weight and the products can be labelled accordingly as, for example, low
fat or very low fat spreads. The latter are especially appealing to many
health conscious consumers. Generally, depending on the fat content and
other ingredients used, a fat spread is a water-in-oil or oil-in-water
emulsion (or a combination of the two) which has a butter like consistency
and taste and which is spreadable. A number of such spreads which are
supplemented with plant sterols, and methods for their manufacture are
known in the prior art. For example, a pharmaceutically stable emulsion of
finely dispersed plant sterols is disclosed in US 3 085 939; US 4,195,084
and EP 0 289 636. According to these inventions chemically unmodified
plant sterols are used and they are contained predominantly in the
aqueous phase of the product. However, the dispersion according to
these invention is fluid and therefore it does not have a taste and
consistency like butter and is not spreadable. On the other hand, the
products produced according to US 5,502,045, WO 98/06405, WO
98/19556 and WO 98/01126, satisfy the requirements i.e. have a taste
and consistency like butter and are spreadable but they contain plant
sterols which were subjected to chemical modifications and the sterols are
incorporated into the oil phase of the product in the form of esters. Thus,
according to these inventions an expensive and unnecessary chemical modification of plant sterols is required prior to their incorporation into a fat
spread.
Some processes of incorporating unmodified plant sterols into fat
spreads are also known in the prior art. For example, Tianen et al (WO
98/13023) disclosed the process of adding plant sterols to a pre-prepared
(i.e. already emulsified) fat spread by admixing finely ground sterols with
the spread. However, according to this invention an expensive grinding
treatment of plant sterols to reduce the particle size to about 30 micron is
necessary to improve the organoleptic properties of this product.
Generally the poor organoleptic properties of this and similar products
result from a different organoleptic perception of the particulate sterols in
the oil and water phases between which the sterol powder is evenly
distributed by admixing. Also the process of this invention is incompatible
with most modern methods of manufacturing fat spreads which are often
packed into tubs straight after emulsification. The process of this invention
cannot be readily used for the production of low and very low fat spreads
as the texture of these spreads and their appearance will be adversely
affected by blending with particulate material. Therefore there is a need in
the trade to produce a fat spread, and especially a low and a very low fat
spread, which contains plant sterols and have acceptable organoleptic
properties. There is also a need in the trade to develop a suitable sterol-
containing additive which use would be compatible with the current
manufacturing methods for the production of such spreads. These needs are addressed by the present invention.
Yet another group of foods and beverages which since ancient
times have formed an important part of the human diet in many regions of
the world are fermented food products and beverages. Although such
foods vary widely in their appearance, texture and organoleptic properties
in accordance with the raw materials used for their production, they
typically share several common features. Firstly, their production involves
at least three common steps: (1 ) pasteurisation of the raw material; (2)
contacting the pasteurised material with a specific micro-organism or a
mixture of micro-organisms and (3) incubating the mixture of raw material
and micro-organisms for sufficient time to enable the fermentation to
occur. Secondly, these fermented foods typically contain micro¬
organisms, dead or alive, as well as metabolites of their fermentation
which are believed to be beneficial to human health. Thirdly, many of
these foods constitute a substantial part of the diet and are consumed on
a regular basis.
Rice and soybeans are the most common raw materials for the
production of fermented foods in many Eastern countries, including Japan.
Soybeans, for example, are fermented to produce Japanese "miso"
(soybean paste), "tofu" (soybean protein curd) and many others. Soybean
milk is also fermented to produce nutritionally valuable products.
In Western countries fermented milk products are most widely used.
Examples of these products include yoghurt, sour cream, kefir, ymer as well as fresh cheeses such as quark and fromage frais. Buttermilk, which
is obtained as a by-product in the production of butter, can also be
fermented using specific micro-organisms. The micro-organisms which
are used in the production of fermented milk products, are known as
starter cultures or starters. These micro-organisms are often mixtures
containing lactic acid bacteria.
The nature of the product is determined to a considerable extent by
the micro-organisms used which, depending on the species or strain,
contribute to various degree to the formation of acid such as lactic acid,
flavouring substances such as diacetyl or acetaldehyde and structure
forming constituents such as polysaccharides. In some cases, one
particular species of bacteria is used (such as Lactobacillus acidophilus in
the production of acidophilus milk) but usually the product acquires
characteristic properties as a consequence of the action of a mixture of
micro-organisms on the raw material. For example, in kefir various other
bacteria and yeast were detected in addition to Lactobacilli and
Streptococci.
In many countries, notably Europe and USA, yoghurts are the most
popular among fermented milk products. Yoghurt (as well as some other
fermented milk products) contains an active culture of micro-organisms
which can pass unharmed through the stomach. When the yoghurt micro¬
organisms enter into the intestinal area, they are believed to cause a
favourable floral implantation and suppress undesirable bacteria in the human digestive system. Yoghurt has also been found to be acceptable in
the diet of those people who have maladsorption of lactose or an
intolerance to lactose. Yoghurt is also believed to be beneficial to health
due to its relatively high content of vitamins, minerals and other
substances of considerable nutritional value. Consequently, yoghurt is
consumed daily by a large proportion of the population in many countries
as it is considered to be a healthy form of dairy product.
Yoghurt is generally made by a process that includes the following
steps:
(1 ) Yoghurt base mix which contains milk and added milk ingredients is
pasteurised using a high temperature;
(2) The pasteurised mix is then cooled down to a predetermined
temperature;
(3) A starter culture consisting of one or more yoghurt-producing micro-
organisms is added (inoculation) and blended in while maintaining the
lower temperature;
(4) The fermentation is carried out until sufficient acid is produced and a
thickened yoghurt product of the desired consistency (coagulum) is
obtained;
(5) The bacterial growth and metabolism are essentially arrested by
cooling the yoghurt composition, usually to about 0°C-5°C.
Yoghurt can be prepared with a range of fat contents. For example,
according to FDA, a yoghurt can be labelled as "non-fat", if it contains less than 0.5% milkfat and as "low fat", if it contains from not less than 0.5% to
no more than 2.0% milkfat. The standards and labelling practices vary
from country to country. For example, non-fat or very low fat yoghurt in
the UK should also have fat content below 0.5%, whilst in Germany and
Australia the corresponding values are below 0.3% and below 0.2%
respectively.
Depending upon the dairy ingredients employed, other ingredients
and the processing treatment and methods, yoghurt may be prepared in
various forms. Frozen yoghurt, at one extreme, is generally consumed in
hard frozen or soft serve form. Liquid yoghurt, at the other extreme, is
consumed by drinking, either directly or through a straw, rather than using
a spoon. Usually yoghurts are classified according to their physical state.
One of the most common form of yoghurt which is known as "firm" or "set
type" is firm bodied, smooth and viscous, generally having the consistency
of a light gel. Set yoghurt is filled into serving size cups, also known as
retail containers, after the inoculation step and the containers are
incubated at a suitable temperature regime. "Stirred" yoghurt is inoculated
and incubated in a fermentation vessel and, when the fermentation is
completed, the coagulum is broken during the cooling and packaging
steps.
Fruits and flavouring agents are often added to yoghurt to suit
particular tastes. Fruit-flavoured yoghurts are made Sundae style with fruit
product at the bottom, Swiss style with fruit product pre-mixed, or Western style with the fruit product at the bottom and the yoghurt is often
additionally coloured and/or flavoured with natural and/or artificial
colouring and flavouring agents. Fruited yoghurts are conventionally
made with standard fruit products, also referred to as yoghurt fruit. Fruit
products are generally made by cooking a fruit and sugar mixture with the
addition of other agents such as colouring agents and thickeners. The
cooked fruit product may contain discernible pieces of fruit in it or may be
finely divided (puree form).
Sundae style fruited yoghurt is generally made in retail containers,
by filling inoculated yoghurt mix over or under a suitable amount of fruit
product and incubating the filled container for a suitable time. Swiss style
fruited yoghurt is generally made by mixing a suitable amount of fruit
product, after completion of the fermentation step. Fruited yoghurts
typically contain from about 10% to about 30% fruit product by weight of
the fruited yoghurt.
Drinking yoghurt is based on the stirring manufacturing process,
except that a milk with lower solids content is generally used. The
coagulum is broken down before filling into retail containers and fruit juice
may be used instead of fruit product.
The shelf life of yoghurt can be increased by the so-called
thermisation process which requires that the yoghurt is pasteurised and
aseptically filled and the fruit product either added before the yoghurt or
separately in its own container within the overall package. This process is designed to increase the shelf life of the product but it also results in the
destruction of beneficial micro-organisms in the yoghurt.
In the present specification all the described types of yoghurt will
collectively be referred to as "yoghurt".
SUMMARY OF THE INVENTION
This invention relates to the provision of novel food additives
containing hydrophobic compounds which can be shown to be beneficial
to human health, such as plant sterols and lycopenes (such as tomato
lycopenes), and a method for their preparation and their use in various
food products, beverages and processes involved in making food products
and beverages. The method comprises coating the hydrophobic
compound with food additives which are compatible with the above said
products and processes, and in a preferred embodiment with milk-derived
ingredients and proteins. A number of suitable coating agents are
disclosed. Hydrophobic compounds which can be shown to be beneficial
to human health also include carotenoids other than lycopene and poorly
water soluble anti-oxidants.
This invention also relates, in one embodiment, to the discovery that
by combining the hydrophobic compound (such as plant sterol or
lycopene) with milk, milk-derived solids or other proteins in an aqueous
phase of an emulsified fat spread prior to emulsification, the undesirable
sensation in the mouth is substantially reduced or eliminated altogether and a fat spread with good organoleptic properties is produced. According
to this embodiment of the invention the hydrophobic compounds such as
plant sterols are incorporated predominantly into the aqueous phase of the
fat spread in a largely insoluble form. This embodiment also relates to a
process for the preparation of fat spreads with acceptable organoleptic
properties which does not necessarily require expensive chemical or
mechanical treatment of the above said plant sterols. The process
according to this embodiment of the invention is to bring the hydrophobic
compound, such as insoluble plant sterols, and milk derived or other
coating ingredients into contact in the aqueous phase of the fat spread,
preferably at elevated temperature, prior to the emulsification of the above
said aqueous phase with a fat phase to produce the desired emulsified
product which has a taste and appearance similar to butter and which is
spreadable.
A further embodiment of the invention also relates to a method for
the preparation of a dry ingredient containing hydrophobic compound,
such as plant sterol, and milk derived solids which can be used directly in
the production of food products or beverages by conventional
manufacturing methods.
Another aspect of this invention relates to the discovery that the
addition of plant sterols to a fermentable raw material does not interfere
with lactic acid bacteria fermentation. This invention also relates to food
products which are produced by the fermentation of a mixture of raw material and plant sterols with lactic acid bacteria. The process of the
invention brings together a raw material such as milk and conventional
milk-derived ingredients and plant sterols, which are virtually insoluble in
the fermentation mixture, to produce a range of fermented food products
that have similar texture, appearance and flavour to, or are substantially
indistinguishable from, the corresponding product compositions which are
made with no plant sterols added. The use of other food ingredients such
as thickeners, sweeteners, flavourings, colouring agent and fruit products
to improve the texture, appearance and flavour of the plant sterol
supplemented yoghurt and other products is also disclosed.
This invention brings to the market a range of novel hydrophobic
compound-supplemented, such as plant sterol-supplemented, fermented
food products which were not previously known.
In accordance with one broad aspect of the present invention there
is provided a food product which is produced by the fermentation of a
mixture of a fermentable raw material and plant sterols using lactic acid
bacteria, and which has a similar texture, appearance and flavour to, or is
substantially indistinguishable from, the corresponding product
composition made with no plant sterols added.
In accordance with another aspect of this invention, a fermented
milk product is provided which is produced by the fermentation of a
mixture of milk and/or conventional milk-derived ingredients and plant
sterols using lactic acid bacteria, and which has a similar texture, appearance and flavour to, or is substantially indistinguishable from, the
corresponding product composition which is made with no plant sterols
added.
In accordance with yet another aspect of this invention, a range of
yoghurts, which are produced by fermentation of a mixture of milk and/or
conventional milk-derived ingredients and plant sterols, of different type,
composition and fat content as well as yoghurt products are provided
where the above said yoghurts and yoghurt products have a similar
texture, appearance and flavour to, or are substantially indistinguishable
from, the corresponding product compositions which are made with no
plant sterols added.
Yet another aspect of this invention is to provide a process for the
preparation of the above said fermented food products, where plant sterols
are added to the fermentation mixture prior to inoculation of a fermentable
raw material with micro-organisms.
Yet another aspect of this invention is to provide a process for the
preparation of the above said fermented milk products and yoghurts and
yoghurt products, where plant sterols are added to the fermentation
mixture prior to and/or during the heat treatment step.
Still another aspect of this invention is to provide a method for the
supplementation of yoghurt and yoghurt products, by their admixture with
plant sterols and their derivatives, where the sterols are added either in
the pre-coated form or as a fine powder, until a homogenous product is obtained and where the above said homogenous product has a similar
texture, appearance and flavour to, or is substantially indistinguishable
from, the corresponding product composition which is made with no plant
sterols added.
DETAILED DESCRIPTION OF THE INVENTION
DEFINITIONS
In the present invention the following terms and definitions are
used:
In the context of the hydrophobic compounds of the invention, the
term "which can be shown to be beneficial to human health" is understood
to mean any physiologically active compound which is not a nutrient and
can be shown to prevent or reduce the risk or ameliorate the conditions or
symptoms of a disease when taken regularly as a part of a diet.
The term "hydrophobic compounds" of benefit to human health is
understood to mean any organic substances which are substantially
insoluble in the aqueous phase of a food product or beverage at or close
to the concentration which is thought to be necessary to provide the above
said health benefit.
The term "emulsified fat products" is understood to mean any
products which comprise oil-in-water or water-in-oil emulsion or a
combination of the two. The term "fat spread" is understood to mean a product containing at
least 5% fat, has a consistency and taste similar to that of butter and
which is spreadable on a surface of solid foods such as a slice of bread.
The definitions of "low fat" and "very low fat" when referring to, for
example, a fat spread or a yoghurt are as defined by legislation or relevant
regulatory authorities. "Low fat" and "very low fat" spreads may have less
than 5% fat.
The term "food acceptable" is understood to mean that a process
and/or a substance which is permitted for use in the manufacturing of food
products and/or beverages or a process and/or a substance for which
such a permission can be obtained.
The term "acceptable organoleptic properties" of a product is
understood to mean that the product may be organoleptically
distinguishable but its overall organoleptic quality is comparable to the
analogous products which are currently on the market. In other words, the
organoleptic properties of the modified food product or beverage are
generally acceptable to the consumer.
The term "lactic acid bacteria" is understood to mean micro¬
organisms which are capable of producing lactic acid in the course of
fermentation.
The term "fermented food products" is understood to mean any
edible products, in a solid or liquid form, which are produced by contacting a fermentable raw material with a particular micro-organism for the time
sufficient for the fermentation to occur.
The term "fermentable raw material" is understood to mean any
material which is or can be fermented by conventional manufacturing
methods.
The term "fermented milk products" is understood to mean the
products which are produced by incubating milk or a fermentable raw
material derived therefrom with a particular micro-organism or a mixture of
micro-organisms. As used herein "fermented milk products" include
various types of regular yoghurt, low fat yoghurt, non fat yoghurt, kefir,
ymer, buttermilk, butterfat, sour cream, sour whipped cream as well as
fresh cheeses such as quark and fromage frais, each with its respective
modifications.
The term "milk" is understood to mean conventional milk as well as
equivalent compositions formed by suitable admixtures of butterfat-
containing milk products and/or milk solids.
The term "yoghurt products" is understood to mean foods and
beverages containing yoghurt or yoghurt derived ingredients in not
insubstantial quantities. As used herein "yoghurt products" include
yoghurt drinks, instant yoghurt compositions, ice creams, frozen desserts
and the like.
The term "substantially indistinguishable products" is understood to
mean products which appear the same when inspected by the naked eye and which cannot be instantly distinguished organoleptically by an
assessor.
PREPARATION OF A COMPOSITION SUITABLE FOR INCLUSION IN A
FOOD PRODUCT OR BEVERAGE WHICH COMPOSITION CONTAINS
PLANT STEROL, LYCOPENE OR OTHER HYDROPHOBIC
COMPOUND
The invention provides a method for making a composition suitable
for inclusion in a food product or beverage the method comprising the step
of combining a plant sterol, lycopene or other hydrophobic compound
which can be shown to be beneficial for human health with a component
which is acceptable as a food additive, wherein the component which is
acceptable as a food additive interacts with the surface of the hydrophobic
compound. Preferably, any undesirable sensation of powderiness in the
mouth due to the plant sterol, lycopene or hydrophobic compound as
defined is masked.
Typically, the hydrophobic compound is any one of a plant sterol
(some of which are described in more detail below), lycopene and other
carotenoids and poorly water soluble anti-oxidants, or a combination
thereof.
Suitably, the component acceptable as a food additive is any one of
a food-acceptable polypeptide, polysaccharide or low molecular weight
substances with similar chemical functionality/functional groups. As is discussed in more detail below, the food-acceptable
polypeptide may conveniently be a milk-derived or soya-derived protein.
Any other food-acceptable polypeptides would be suitable provided
that they can interact with the hydrophobic surface of sterols, lycopenes or
other hydrophobic food compound beneficial to human health. Specific
polysaccharides include, for example, modified cellulose, pectins and
starch.
Typically, the hydrophobic compound is one which is solid at room
temperature; preferably, the hydrophobic compound is a plant sterol or
lycopene or a combination thereof.
As is described in more detail below, it is preferred that the
hydrophobic compound is contacted with the component acceptable as a
food additive in aqueous suspension. It is particularly preferred that the
composition suitable for inclusion in a food product or beverage is one
which allows the hydrophobic compound, such as plant sterol or lycopene,
to be in the aqueous phase once incorporated into the food product or
beverage.
Preferably during the preparation of the composition the ratio of
hydrophobic compound to coating agent is from about 0J to about 0.4
w/w. Preferably the amount of coating agent allows the particles to be
fully coated.
The composition may be formed in situ in the process of the
preparation of a food-product or beverage, or it can be prepared separately and added during the manufacture of the food product or
beverage.
One of the difficulties of incorporating plant sterols, lycopenes and
other hydrophobic compounds which can be shown to be beneficial to
human health, into predominantly aqueous-based food products and
drinks is their extremely poor solubility in water. For example, plant sterols
are hydrophobic substances and, as obtained, do not disperse well in
water. This behaviour is generally attributed to their poor wettability in
aqueous solutions. It was unexpectedly found that plant sterols can be
satisfactorily admixed into milk, preferably at elevated temperatures as
specified herein and that their addition does not interfere significantly with
lactic acid bacteria fermentation. The latter result is especially surprising
because sterols are biologically active compounds which are present in
many type of cells, for example in cell membranes, and are known to
influence metabolic activity and growth of micro-organisms.
It was discovered that the addition of as much as about 5 gram of
plant sterols per 100 gram of milk which was fortified with 1.5 gram of high
protein whey powder has no appreciable effect on the rate of lactic acid
bacteria fermentation as determined, for example, by the time necessary
for the resulting yoghurt to reach a pH of about 4.5. Even more surprising,
there was little difference in the appearance of the resulting yoghurt and
the corresponding conventional product made with no plant sterols added.
This is a surprising finding given that the solid content of fortified skimmed milk used was only about 12 gram of solid per 100 ml.
It was further found that the organoleptic properties of yoghurt are
appreciably dependent on whether plant sterols are added to the
fermentation mixture before, during or after the milk heating step. This
heating step is used by most manufacturers of fermented milk products
such as yoghurts, regardless of the variety, to achieve the denaturation of
milk proteins and to pasteurise the milk. Thus, when the same plant
sterols were added to the milk after cooling but prior to the addition of
starter culture containing lactic acid bacteria, the organoleptic properties of
the product was poor as determined by tasting. Typically, these products
were gritty and left an undesirable sensation in the mouth. However,
when plant sterols were added to milk during or prior to the heating step,
preferably blended in at the stage of homogenisation of the milk, the
resulting yoghurt had a texture, appearance and flavour like the
corresponding product composition which is made with no plant sterols
added.
It was also found after extensive study and research that a product
with even better organoleptic properties i.e. the product which is
substantially indistinguishable from the corresponding composition which
is made with no plant sterols added, can be obtained when plant sterols
are pre-coated with certain food additives, preferably those derived from
milk, preferably milk proteins or other proteins, prior to adding the above
said coated sterols to the aqueous phase of a food product or a beverage. The coating can be achieved by stirring a suspension of plant sterols with
the coating agent or the coating agent can be added to the suspension as
a solid or as a concentrated solution. In addition sterols can be
suspended and homogenised in a solution of the coating agent. Although
milk proteins such as caseins and their salts, whey proteins and milk
derived solids such as milk powder, whey or buttermilk are preferably
used, those skilled in the art will instantly recognise that other food
acceptable coating agents such as proteins from sources other than milk,
and polysaccharides and even low molecular weight substances with
appropriate functionality may also be employed.
Typically, a suspension or slurry of plant sterols in water containing
from about 10% to about 30%, and preferably from about 15% to about
25% of sterol by weight, is prepared by extensive homogenisation using
conventional methods and a small volume of a concentrated aqueous
solution of, for example, sodium caseinate or whey protein or milk powder
is then added. The above said concentrated solution typically has a solid
content from about 8% to about 20% by weight, preferably from about
12% to about 18% by weight. The added volume may vary from about 1.0
to about 10 parts per 10 parts, preferably from about 1.5 to 3 parts per 10
parts of the suspension of sterols.
The suspension of plant sterols can also be prepared by
homogenising the said sterols in a pre-prepared solution of, for example,
casein, sodium caseinate, whey proteins, whey, milk powder or buttermilk or even milk itself. It is also surprising that a fine suspension of plant
sterols in water can be produced in the absence of surfactants such as, for
example, polyoxyethylene sorbitan esters or sodium dodecyl sulphate, and
without grinding plant sterol with admixers e.g. sugars as was previously
practised in the art (see, for example, US 3,085,939; US 4,195,0840;
US3,881 ,005; GB 934,686). The solid content of the coating agent in the
final admixture with plant sterols can vary from about 0.1 % to about 2.0%
by weight, preferably from about 0.5% to about 1.5% by weight.
It was found that the coating can be accomplished by a variety of
treatments. The suspension of sterols can be stirred for some time in the
presence of the coating agent at ambient temperatures, or heated and
then cooled down or treated by changing pH. For example, the plant
sterol suspension prepared by any of the methods described herein, can
be left stirring at ambient temperatures, preferably from about 0°C to about
25°C for a period of time from about 20 minutes to about 16 hours,
preferably from about 1 hour to about 5 hours. Also, the suspension can
be heated to a temperature from about 30°C to about 100°C, preferably
from about 40°C to about 60°C, preferably with stirring. The heating time
may vary from about 15 minutes to about 2 hours, depending on the final
temperature and the rate of heating and cooling. Also, if substances with
ionisable functional groups are employed such as proteins or
polysaccharides, the pH of the suspension can be altered by adding a
dilute acid or base such as to neutralise substantially the net charge in the molecule of the coating agent, preferably to a pH which is near the
isoelectric point of the coating agents present in the suspension. In the
case of sodium caseinate, the pH is typically adjusted with a dilute acid to
a pH of between about 4.0 and about 5.0, preferably to pH 4.5 to
protonate the available carboxyl groups, and the slurry is left stirring for a
period of time from about 1 hour to about 16 hours, after which time the
pH is adjusted back to the preferred values of 6J-6.7. Alternatively the
coating can be achieved by precipitating plant sterols into solution
containing a coating agent. For example, sterols can be dissolved in an
organic solvent, preferably a water-miscible organic solvent, and the
resulting solution is then poured into water containing milk-derived solids
or proteins or other suitable coating agents as described herein. All these
methods were found to be satisfactory. The coated plant sterols can also
be recovered in a dry form using conventional drying techniques,
preferably spray drying.
It was also found that coating according to the present invention
can be successfully obtained when plant sterols are combined with other
non-sterol food additives. Such additives can be physiologically active
food substances known to those skilled in the art or other substances
added to enhance, for example, the bioavailability of plant sterol. For
example, prior to the coating as described herein, plant sterols can be co-
precipitated with lycopenes which are also known to reduce plasma level
cholesterol in humans, but by the mechanism different to that of plant sterols, or lecithin. The additives can be used in the amount as small as
less than 0J part to 1 part of plant sterols (e.g. lycopene) or as high as
0.95 part to 1 part of plant sterols (e.g. lecithin).
The treatments described herein usually result in the coating of
plant sterol particles in the suspension by proteins and/or other
components present in, for example, milk powder. Consequently, the
coated plant sterols display properties which are different from that of
uncoated material. It was observed, for example, that spray dried sodium
caseinate coated plant sterols can be suspended in water with relative
ease and on stirring form a suspension which is rather similar in
appearance to milk. It was found that the separation of plant sterol
particles in this suspension occurs significantly more slowly than in
analogous suspensions made from uncoated sterols.
The formation of the "coat" on the surface of sterol particles can be
directly observed by confocal laser microscopy when proteins, for
example, are labelled with an appropriate fluorescent dye under conditions
similar to those described by Aherne et al (J. Am. Chem. Soc. (1996) 118,
8771-8772). Both the labelling methods and the technique of fluorescent
microscopy are well known in the art.
The common feature of the treatments described herein is that the
coating agent is encouraged to adhere to the surface of the plant sterol
particles. In the case of proteins, this can be achieved, for example, by
substantial neutralisation of the net charge of the protein by adjusting the pH to values close to the protein's isoelectric point or by any other
treatment leading to their partial denaturation, e.g. heating or presence of
organic solvents, or simply by prolonged incubation at ambient
temperatures. Thus, in the case of whey proteins which are known to
denature at relatively low temperature, mild heating is the preferred
treatment. These examples of treatments are not exhaustive and those
skilled in the art will instantly recognise that numerous other treatments
and modifications to the coating procedures disclosed herein can be used
to exercise this aspect of the present invention. It is asserted that in
addition to prolonged incubations, pH adjustment and heat treatment, any
other treatment or conditions which may be reasonably expected to
promote the interaction between the coating agent and the surface of the
plant sterol particles can be fruitfully employed. A desirable property of
the resulting coated composition is an ability to easily form an aqueous
suspension.
Ideally, the coating composition should expose functionality. This
means that the coating component which is acceptable as a food additive,
which when it interacts with the surface of the plant sterol, lycopene or
other hydrophobic compound which can be shown to be beneficial to
human health, also has a functionality which when exposed to an aqueous
phase encourages the coated particles to form a suspension in the
aqueous phase. Generally among the coating agents, those which have ionisable
groups, preferably carboxyl groups, with a pKa between about 3.5 and
about 7.5 and/or those whose solubility in water depends strongly on pH
and/or temperature of the aqueous solution or suspension are preferred.
Also, the coating agents must be approved for food use and be compatible
with the process for the preparation of food products and beverages
according to the present invention. Those skilled in the art will recognise
that coating agents others than milk derived proteins such as other
proteins and various functionalised polysaccharides as well as
appropriately functionalised low molecular weight substances, may also be
used. Appropriately functionalised low molecular weight substances
preferably contain at least one carboxyl and at least one hydroxyl group.
It was further found that the coating can be accomplished in situ i.e.
directly in milk, preferably in milk fortified with milk derived solids, as well
as by using the separate coating procedures described herein. The
incubation of plant sterols with milk or reconstituted milk or milk fortified
with whey proteins or any other suitable additives prior to or after
homogenisation of milk, preferably at temperatures between about 40°C
and 95°C is sufficient to achieve the coating which according to the
present invention gives acceptable appearance and organoleptic
properties of the final product.
Although not wishing to advance or be bound by any particular
theory, it is assumed that sterol particles coated with milk proteins, interact during or after the heating stage with casein micelles and whey proteins
and/or other milk components in solution and that these interactions are
important for integrating the coated plant sterols into the product such as,
for example, yoghurt. It is assumed that it is these interactions that lead to
the production of yoghurts which have a similar texture, appearance and
flavour to, or are substantially indistinguishable from, the corresponding
product compositions which are made with no plant sterols added. Those
skilled in the art will instantly recognise that the coated plant sterols
according to this invention may also be used in a variety of other foods
and food products as is described in more detail below, particulariy in the
Examples.
Further details of the method of the invention are given below in
relation to fermented dairy products and emulsified fat products.
It will be appreciated that the invention also provides a composition
suitable for inclusion in a food product or beverage obtainable by the
method for making a composition suitable for inclusion in a food product or
beverage the method comprising the step of combining a plant sterol,
lycopene or other hydrophobic compound which can be shown to be
beneficial for human health with a component which is acceptable as a
food additive, wherein the component which is acceptable as a food
additive interacts with the surface of the hydrophobic compound.
Similarly, the invention provides a composition suitable for inclusion
in a food product or beverage comprising a plant sterol, lycopene or other hydrophobic compound which can be shown to be beneficial for human
health with a component which is acceptable as a food additive coated on
the surface thereof.
A composition of the invention which is useful in food and
pharmaceutical formulations, and one which is particulariy useful in
relation to emulsified fat products, is a dry ingredient which is obtained by
drying, preferably spray drying, of a mixture containing a milk derived solid
and plant sterols, where the milk derived solid and the plant sterols are
contacted in an aqueous suspension, and where the milk derived solid is
selected from the group consisting of casein, caseinate, whey protein,
whey, milk powder, buttermilk and bufferfat, and where the plant sterols
are selected from the group comprising β-sitosterol, β-campesterol, β-
stigmasterol, β-sitostanol, β-campestanol and β-stigmastanol and their
carboxylic acid esters, and a mixture thereof.
Typically, the milk-derived solid and the plant sterol are contacted at
a temperature above 40°C, preferably with stirring. Preferably the contact
is carried out at a temperature and exposure time combination which is
sufficient for pasteurisation.
Furthermore, in addition to plant sterols, the present invention can
also be practised with other food additives which are known to be
beneficial to human health, for example lycopene, provided that these
additives are sufficiently hydrophobic to enable their coating according to
the present invention, preferably with proteins or milk-derived solids or any other coating agent according to the method disclosed herein. The above
said additives can be coated separately and used in foods and beverages
on their own or premixed, or co-precipitated with plant sterols as
exemplified herein.
PRODUCT PREPARATION
The methods and products detailed above are useful in the
preparation of a variety of food products and beverages. Thus, the
invention provides a method for preparing a food product or beverage
which is supplemented with a plant sterol, lycopene or other hydrophobic
compound which can be shown to be beneficial for human health the
method comprising the step of (1 ) carrying out the method for making a
composition suitable for inclusion in a food product or beverage the
method comprising the step of combining a plant sterol, lycopene or other
hydrophobic compound which can be shown to be beneficial for human
health with a component which is acceptable as a food additive, wherein
the component which is acceptable as a food additive interacts with the
surface of the hydrophobic compound in situ during the preparation
process or (2) adding at an appropriate stage during the preparation
process a composition obtainable by the method of step (1 ) above, or a
composition suitable for inclusion in a food product or beverage
comprising a hydrophobic compound which can be shown to be beneficial
for human health with a component which is acceptable as a food additive coated on the surface thereof, or (3) a combination of (1 ) and (2).
The appropriate stage in a manufacturing process for adding the
composition (eg coated plant sterol) is a stage where the food additive
comprising the "coat" material can be added without substantially altering
the overall manufacturing process or the properties of the final product.
For example, in the case of emulsified fat spreads this is a stage of
formulating the aqueous phase of the product prior to emulsification, whilst
in the case of manufacturing a yoghurt this is the stage of fortifying milk
with additional whey solids and in the case of the preparation of yoghurt
fruits this is the stage of heating up the initial pre-mix prior to the addition
of the fruit.
Typically, the hydrophobic compound resides in the aqueous phase
of the final food product or beverage. For example, preferably it resides in
the aqueous phase of an emulsified fat product.
The invention also provides a food product or beverage which is
supplemented with a hydrophobic compound which can be shown to be
beneficial for human health obtainable by the method mentioned
immediately above.
Preferably, the hydrophobic compound is a plant sterol or lycopene
or combination thereof. Preferably, the component which is acceptable as
a food additive is a milk-derived solid.
The following is a description of certain food products and beverages which have been supplemented with the hydrophobic
compound which can be shown to be beneficial to human health. Some of
the processes do not make use of coated hydrophobic compounds but, for
the avoidance of doubt, processes, food products and beverages made
using such processes are part of the invention described herein.
Fermented dairy products
An extensive study and research was carried out on the processing
methods and conditions that are required to produce products which are
fermented with lactic acid bacteria, preferably fermented milk products,
preferably yoghurt and yoghurt products, with acceptable organoleptic
properties, where the above said fermented products are supplemented
with plant sterols, preferably with the plant sterols coated according to the
present invention.
In general, the process by which the fermented milk products of the
present invention are made involves forming a milk base by admixing,
preferably at an elevated temperature of about 30°C or above, a
fermentable dairy product including whole milk, low fat milk, skimmed milk,
skim milk, condensed milk, evaporated milk, milk powder including non-fat
dry milk powder (NFDM), buttermilk, cream and the like, and optionally
thickeners and stabilisers, and optionally a sweetener, and optionally
adding other sweeteners, flavourings and colorants, and optionally adding
vitamins and minerals to the admixture in sufficient quantities to provide a
product which is either similar in texture, appearance and flavour to, or is substantially indistinguishable from, the corresponding product
composition which is made with no plant sterols added. The resulting
mixture is optionally homogenised by conventional homogenisation means
and pasteurised and further heat labile ingredients such as vitamin C are
optionally added. The mixture is inoculated with a suitable micro-organism
or a mixture of micro-organisms which produce lactic acid during the
fermentation and which are suitably chosen for the kind of product to be
made, and the inoculated mixture is maintained under a carefully
controlled temperature regime until the desired flavour, texture and
appearance are achieved.
In making the fermented milk products of this invention, it is
preferred to use cows milk as defined herein or ingredients derived
therefrom. However other milk, for example, ewe milk, goat milk, buffalo
milk and others as well as ingredients derived therefrom such as whey,
whey proteins, caseins, caseinates, milk powder, cream, buttermilk or
butterfat, may also be used. It was found that regardless of whether
yoghurts are made from fresh milk or reconstituted milk and whether the
milk and milk powder used were skimmed, semi-skimmed or whole, the
yoghurt which is supplemented with plant sterol according to the present
invention has a similar texture, appearance and flavour to, and often is
substantially indistinguishable from, the corresponding product
composition which is prepared by the same method using the same
ingredients but with no plant sterol added. Furthermore, it was found that a substantial part of the milk or milk powder, preferably between about
20% to about 70% on a dry weight basis, can be replaced by soymilk.
Also, dry milk and milk powder which contain the coated plant sterols in
accordance with the present invention, may be utilised as one of the
ingredients.
It was further found that yoghurts which have similar texture,
appearance and flavour to, or are substantially indistinguishable from, the
yoghurt of the same composition but with no plant sterol added, can be
prepared using a variety of plant sterol preparations from different
suppliers (Sigma Aldrich Chemical Co (Dorset, UK), Fluka Chemicals
(Dorset, UK) and ICN Biomedicals Inc (Ohio, USA)). The plant sterols
preparations may contain as li t\e as about 50% or as much as about 95%
of a single compound such as β-sitosterol and different quantities of other
plant sterols such as campesterol, stigmasterol and the like. 5α-saturated
derivatives of the above said sterols, for example, β-stanol can also be
used. It was further found that some technical grade sterol preparations,
typically containing about 50% of plant sterol or less desirable for use in
the present invention in the form as obtained from the supplier. These
preparations have a distinct and unpleasant smell and must be further
purified to remove the odorous impurity. This can be accomplished by
conventional methods such as chromatography or precipitation from
organic solvents or an organic solvent-water mixtures, preferably with
organic solvents that are permitted in food processing. It was also found that, in general, yoghurts which are supplemented
with sitosterol have somewhat better organoleptic properties than those
prepared with stanol, both at the same loading. It was also found that
esterification of the free hydroxyl group with a carboxylic acid in the
molecule of stanol results in some improvement in the organoleptic
properties of the product (this esterification can be accomplished by
numerous methods well known in the art) and the yoghurt which has a
similar texture, appearance and flavour can be produced using the above
said esters. It will therefore be obvious to those skilled in the art that plant
sterol preparations with different content of individual components as well
as other derivatives of plant sterols may also be used according to the
present invention. For example, plant sterols which are obtainable from
rice bran oil such as cycloartenol and 24-methyl-cycloartenol, and from
sheanut such as amyrin, lupeol and butyrospermol may also be used.
It was also found that yoghurts with somewhat better organoleptic
properties are obtained when plant sterols are used as a fine powder
rather than in the form of larger particles. In the latter case, it is preferred
to break the particles by high power homogenisation or any other form of
shearing to improve the organoleptic properties of piant-sterol
supplemented fermented products such as yoghurt and the like.
It is preferable that the yoghurt according to this invention contains
milk solids in quantity from between about 10% to about 25% by weight.
Satisfactory results are also obtained when the milk solids content of the yoghurt prior to pasteurisation is about 15%, for example, between 12%
and 21 %. The butterfat content may be between less than 0.2-0.5% for
non fat or very low fat yoghurt to about 10% for a Greek style yoghurt. In
order to prepare a low fat or non fat yoghurt or yoghurt product, the use of
fat contributing ingredients must be carefully controlled. In as much as the
primary fat contributing ingredient in yoghurt is generally milk, a low fat
content may be achieved readily by selecting a skimmed milk with a
butterfat content of less than about 0.4% and preferably less than about
0.2% by weight. Typically, for the production of yoghurt use is made of
starters consisting of Lactobacillus bulgaricus and Streptococcus
thermophilus.
Typically the yoghurts of this invention are made by making the
fermentation mixture by blending the desired amount of milk, to which
whey proteins in quantity from about 1.0 gram to about 3.0 gram per 100
gram of milk, preferably about 1.5 gram per 100 gram of milk, with the
desired amount of plant sterols, typically from about 1.5 gram to about 5
gram per 100 gram of milk. The pH of the mixture is adjusted to the
preferred value of 6J-6.7, if necessary, by adding an acidifying agent.
The acidifying agent may be a food quality acid, for example, lactic or citric
acid. In a commercial scale process it is preferred to employ a
supplemental size reduction step after the slurry preparation but prior to
admixture with the whey containing milk (yoghurt base). Suitable
supplementary size reduction techniques include, for example, passing the slurry through a colloidal mill, or a two stage homogeniser followed by
passing the slurry through mesh screeners, and using a high speed shear
impeller blender in which the slurry is prepared. The slurry can be passed
through the homogeniser for one, two or more passes sufficient to provide
good suspension. Homogenisation prior to pasteurisation is optionally
carried out in order to promote a smooth texture in the yoghurt and aid in
the dispersion. Any prior art homogenisation conditions can be
satisfactorily employed in the present invention.
The ingredients of the fermentation mixture are then treated at high
temperature, preferably at legally specified time and temperature
conditions, using techniques and equipment well known in the art. While
the heat treatment may be carried out at many different temperature and
exposure time combinations, the body and texture of the yoghurt is
generally improved by the application of heat treatment regimes which are
known from the art to be sufficient to cause a substantial denaturation of
whey proteins. Also it is preferred to carry out the heat treatment under
such a combination of temperature and exposure time that is sufficient to
pasteurise the fermentation mixture i.e. to inactivate or deter the
development of undesired micro-organisms. Typically the heat treatment
is performed at a temperature in the range of 60°C to about 110°C,
preferably at about 80°C to 95°C, and optionally under high pressure, and
optionally, with stirring. Care should be exercised not to heat the mixture
longer than necessary as deleterious effects can result. It was generally found that regardless of specific heating regimes, the yoghurts which are
supplemented with plant sterols according to the present invention have a
similar texture, appearance and flavour to, or are substantially
indistinguishable from, the corresponding product compositions which are
prepared by the same method from the same ingredients but with no plant
sterol added.
The heat treated and pasteurised mixture is cooled in one or more
stages, optionally with stirring, to a temperature in the range of about 37°C
to about 50°C, preferably to between about 40°C to about 45°C and it is
inoculated with a micro-organism to initiate the fermentation. The micro¬
organism used in the fermentation is essentially a lactic acid bacterium
which is preferably used in a mixture with other yoghurt producing micro¬
organisms. The micro-organism can be one of several yoghurt producing
cultures. It is preferred to use Lactobacillus bulgaricus, a lactic acid
forming rod-shaped bacterium, and a Streptococcus thermophilus, a
coccoid bacterium, either alone or together with other suitable yoghurt
producing micro-organisms. These micro-organisms can be used in equal
amounts or their relative quantities can be adjusted as desired, in
accordance to the preference of the yoghurt producer. Lactobacillus
acidophilus, or other yoghurt producing micro-organisms can be added to
the Lactobacillus bulgaricus - Streptococcus thermophilus combination
above or in other combinations. Other examples of species of
Lactobacillus and Streptococcus which may be used to practice the present invention include Lactobacillus bulgaricus, helveticus, jugurti,
lactis or acidophilus and Streptococcus thermophilus, cemorris, lactis or
diacetilatis. Bifidobacterium sp., for example, Bifidobacterium breve,
bifidum, infantis, longum, adolescentis and Lactococcus sp., for example,
Lactococcus casei, can also be optionally added. These micro-organisms
can be obtained as starter cultures from commercial sources such as, for
example, Chr. Hansen A/S of Denmark or Gist Brocades NV of the
Netherlands or from public culture collections, or isolated from natural
sources. Species and strains which are selected or genetically modified
for higher resistance to phage infection or to provide yoghurts with
superior properties or under superior manufacturing may also be
employed.
It was generally found that regardless of specific micro-organisms
used and the source of the starter culture, the yoghurts that are
supplemented with plant sterol according to the present invention have a
similar texture, appearance and flavour to, or are substantially
indistinguishable from, the products prepared by the same method from
the same ingredients with the same micro-organisms but with no plant
sterol added.
Those skilled in the art will instantly recognise that fermented milk
products, including yoghurts, can be prepared with the addition of more
specialised cultures such as the above mentioned Bifidus bacteria to
obtain products with health benefits in addition to those provided by plant sterol. It is assumed to be obvious that such cultures as well as other food
additives of proven benefit to human health can be added to the
fermented milk products such as yoghurt, in addition to plant sterols,
provided that the above said additives do not interfere with sterols
chemically and do not interfere with the process of making yoghurts and
other fermented milk products.
The fermentation is continued for an appropriate time until the
yoghurt composition reaches a pH in the range of about 3.8 to about 5.0,
preferably from about 4.0 to about 4.7, a pH about 4.3-4.6 being preferred.
At this time the consistency of the yoghurt is denominated as firm as is
understood in the yoghurt art. Appropriate time for fermentation is
generally in the range of about 3 hours to about 20 hours, preferably from
about 4 hours to about 6 hours. Longer and shorter times may be used
but generally are unnecessary. Fermentation is carried out in the
fermentation vessel or in yoghurt containers.
It was also found that at a higher loading of plant sterols, typically in
excess of about 3.0 gram per 100 gram of milk, a certain amount of
precipitate may sometimes be formed at the bottom of the container. It
was further found that this precipitation can be reduced considerably or
avoided altogether by, for example, increasing the initial amount of micro¬
organisms used in fermentation or by increasing the fermentation
temperature or by the combination of the above or by any other method
which reduces the fermentation time. In general a lower fermentation time is preferred for the preparation of set type yoghurts with higher sterol
loading as specified herein. It was also found that the formation of
precipitate can be substantially reduced or even avoided altogether by
using a continuous or semi-continuos fermentation techniques which are
well known to those skilled in the art, with the use of pre-fermenting and
coagulation tanks being preferred. It was further found that the quantity of
precipitate can be reduced or avoided and the organoleptic properties of
the product improved by the use of an appropriate stabilising or thickening
agents.
According to the yoghurt art, a stabilising or thickening agent can
be optionally added in a suitable quantity to retard any whey separation
during storage and transportation (the process known as syneresis).
These agents are also known in the art to offset the influence of added
ingredients such as fruits or flavouring agents. It is preferred to use
stabilising and/or thickening agents with low fat and non fat yoghurts that
are supplemented with plant sterols in accordance with this invention. It is
also preferred to use stabilising or thickening agents with yoghurts
according to the present invention which are supplemented with higher
quantities of plant sterol from about 2.0 gram to about 5.0 gram by weight
per 100 gram of the final product, regardless of the fat content. It was
found that the use of the above said stabilising and thickening agents
improves the texture and the mouthfeel of the yoghurts, often producing a
yoghurt which is substantially indistinguishable from the composition which is prepared by the same method from the same ingredients but with no
plant sterol added.
Conventional stabilising and thickening agents can be used in the
normally required quantity to retain the desired consistency and texture of
the yoghurt. A thickening agent is preferably water soluble and one that is
approved for use in fermented food products such as yoghurt. Generally
the amount of the thickening agent used does not exceed about 0.5% to
about 1.0%, depending on yoghurt composition, the other additives used
and, in particular, the type of thickening or stabilising agent employed.
Such stabilising or thickening agents include plant exudates (e.g. gum
arabic), seaweed extracts (e.g. alginates), plant and seed gums (e.g guar
gum), plant extracts (e.g. pectin) and animal derived products (e.g gelatin).
These commercial thickeners and stabilisers are soluble in water and milk
and therefore can be incorporated into the yoghurt mix prior to the
fermentation process or added at a later stage in the preparation of
conventional stirred yoghurt. Also, other polysaccharides such as xanthan
gum, locust gum and carrageenan and pectin derivatives such as partially
demethylated pectins, may be used either on their own or in combination
with emulsifiers such as mono/diglycerides, lecithin or polysorbates.
It was further found that the even when the above mentioned
precipitate was formed after fermentation, it can be blended into the
yoghurt by conventional stirring to produce stirred yoghurts. Once stirred
in, no further precipitation was observed during a storage period of several weeks. However, some powderiness was still noted in the organoleptic
assessment of the stirred yoghurts when prepared at loadings in excess of
about 2.5 gram of sterol per 100 gram of milk and especially at levels
exceeding 3 gram per 100 gram of the final product. It was then
discovered that this sensation of powderiness can be greatly reduced and
in most cases eliminated completely by the additional of a fruit and/or a
flavouring which are normally used in conventional yoghurt varieties. It is
sometimes advantageous to add to the yoghurt an amount of thickening
agent to offset the influence of such added fruits or flavouring agents. The
thickening agents as described herein can be used in the normally
required amount to retain the desired texture and consistency and to
improve the organoleptic properties of the final yoghurt.
The fruit is added in the conventional manner either as a dispersion
in the pasteurised fermentation mix or it can be added aseptically in the
form of a pasteurised fruit preparation. The fruit can be conventionally
added to the bottom of the container in which yoghurt is sold before
adding the yoghurt or it can be packed in a separate compartment to be
mixed with yoghurt prior to consumption. The yoghurt container, with the
fruit preparation at the bottom can, after capping, be inverted to cause the
fruit preparation to come to the top of the yoghurt surface. The fruit
preparation can also be mixed into the yoghurt if stirred or Swiss style
yoghurt is desired. The amount of the fruit added can vary from about 5% to about
40%, preferably from about 10% to about 35% by weight of yoghurt. The
fruit component may optionally contain, in addition to conventional sugars,
monosaccharide sugars having a high sweetening effect. For example, it
is well known in the art that the syrup for the fruit pieces can be
advantageously prepared using a combination of fructose and sucrose as
the sweetener. Generally, the following compositions of, for example,
strawberry fruit products: Swiss style fruit product comprising 40-55%
strawberries, 30-40% sugar, 1-3% modified starch and Sundae style fruit
product comprising 35-45% strawberries, 15-25% sugar, 15-20% com
syrup, 2-4% modified starch, both with optional flavouring and colouring
agents, acidifiers and preservatives, are suitable.
The flavouring agent can be optionally added to the pasteurised
fermentation mixture. The flavouring agents may be natural or artificial,
and it is preferable to use those which impart a fruit flavour such as
strawberry, blueberry, peach, cherry, lemon, mango, banana and the like.
Other flavours such as vanilla, chocolate and others which are customarily
used in the yoghurt art can all be used. The amount of flavouring agent
used may vary widely according to the taste, but generally an amount from
about 0.1 % to about 5.0%, typically from about 0.3% to about 3.0% and
preferably from about 0.5% to about 1 % by weight based upon the total
composition on a dry weight basis, is used. It may also be desirable or even required when a flavouring agent is
employed, to use a sweetening agent to, for example, offset the taste of
added compounds. Conventional sweetening agents can be used for this
purpose, such as sucrose, fructose, and synthetic agents such as
aspartame, saccharin and the like. Other sweet substances, for example,
palatinose, palatinite, maltose, maltitol, mesoerythritol, starch syrup,
reducing starch syrup and trehalose may also be employed.
Colouring agents may also be used in the preparation of the
yoghurt of this invention. A colouring agent can be any acceptable
colouring ingredient, preferably appropriate to the flavouring agent. For
example, it is preferred to use an appropriate approved red colouring in
the case of strawberry flavour and an appropriate approved yellow
colouring with banana flavouring. The amount of colouring agent may
vary widely but an amount generally from about 0.001 % to about 1.0%,
typically from about 0.02% to about 0.5% and preferably from about 0.05%
to about 0.2% by weight of the total yoghurt composition may be used
based on dry weight of the yoghurt composition.
Various yoghurt products can be produced from the yoghurt
according to the present invention. For example, a yoghurt drink can be
prepared using standard methods well known in the art. Typically, the
yoghurt according to this invention is cooled down and water, a food grade
acid to adjust pH, stabilisers and flavourings are added and the mixture is
homogenised, preferably at elevated temperature, preferably under pressure. It was generally found that yoghurt products such as yoghurt
drinks which are supplemented with plant sterols according to the present
invention have a similar texture, appearance and flavour to, or are
substantially indistinguishable from, the corresponding product
compositions which are prepared with no plant sterol added.
It was also found after extensive study that plant sterols can be
added to fruit yoghurts in a powdered form without significantly impairing
the taste of the product when, for example, the said sterols are
incorporated into the fruit. It is preferred to use the plant sterols which are
coated in accordance with the present invention, preferably plants sterol
coated with milk proteins, and recovered by drying, preferably by spray
drying. It was found, for example, that plant sterols, coated with sodium
caseins and recovered by drying, when added to water form a fine
suspension on stirring at elevated temperature. In appearance this
suspension resembles milk. It was further found that this suspension can
be used in place of water for the preparation of fruit products as
exemplified in the present invention. For a large scale production it is
desirable to subject the above said suspension of plant sterols to a particle
size reduction procedure carried out by methods described herein or other
methods well known in the art.
It was also found that even non-coated plant sterols in a powdered
form may be used for the production of yoghurt fruit, if ground and sieved
to a particle size of about 50 micron, and preferably below about 30 micron, to give a yoghurt with acceptable organoleptic properties. For
example, a yoghurt fruit flavouring can be prepared by adding the plant
sterols, preferably in a mixture with other solids such as sugar, to a
blended fruit at elevated temperature between about 60°C to about 95°C,
under conditions of vigorous agitation.
It was further found that fruited yoghurts can be prepared by
incorporating plant sterols both into the yoghurt and the yoghurt fruit, to
provide products which have a similar texture, appearance and flavour to,
or are substantially indistinguishable from, the corresponding product
compositions which are made with no plant sterols added. This is an
important finding because it enables the production of yoghurts which
have a significantly higher loading of plant sterols and acceptable
organoleptic properties. Preferably, the plant sterols are unesterified
(free) plant sterols: when the plant sterols are added to, or are present in,
the yoghurt fruit they may be free or esterified plant sterols; it is preferred
that they are free plant sterols.
The equipment used in carrying out the present invention is
available commercially and can be conventionally used by those skilled in
the art. The equipment utilised must permit the preparation of plant sterol
suspensions and slurries, pH adjustments, stirring, homogenisation,
controlled heating and cooling, drying and spray-drying, carrying out a
fermentation process without contamination and with suitable control of fermentation temperatures, breaking yoghurt gels, preparing and admixing
additional ingredients and final packaging of yoghurts.
Although the present invention is illustrated mainly by the
production of yoghurt, those skilled in the art will appreciate that it can be
practised successfully in connection with other fermented products and,
especially fermented milk products such sour cream, kefir, ymer,
buttermilk and the like as well as fresh cheeses, all with their respective
modifications. Also, yoghurt products such as instant yoghurt
compositions, frozen yoghurt, frozen desserts and the like as defined ,
herein can be produced from the yoghurt in accordance with the present
invention.
Emulsified fat products.
This embodiment of the invention relates to the discovery that when
plant sterols are combined with milk derived solids in a suspension to
obtain the coated sterols according to this invention, this suspension can
be used as an aqueous phase for the manufacture of emulsified fat
spreads and, preferably low and very low fat spreads with acceptable
organoleptic properties. This is a surprising finding because it is well
known in the art that organoleptic properties of emulsified low fat spreads
are very sensitive to the composition of the aqueous phase. Although not wishing to be bound by or advance any particular
theory, it is assumed that milk derived solids interact with hydrophobic
surface of plant sterol particles and this interaction is sufficient to mask the
undesirable sensation in the mouth as well as to enable one to use
conventional manufacturing methods for the incorporation of plant sterols
in emulsified fat spreads, preferably low fat spreads. Furthermore when
the contact between plant sterol particles and milk derived solids in an
aqueous suspension is made according to this invention, the water can be
evaporated and the recovered solid can be used directly in the production
of emulsified fat spreads, preferably by adding the said solid to the
aqueous phase of the spread prior to emulsification.
According to the present invention, the process for the production of
the above said emulsified fat spread involves contacting plant sterols and
milk derived solids in an aqueous suspension, preferably at elevated
temperatures, preferably above 40°C. Higher temperatures can also be
used and, in this case it is preferred to use the combination of temperature
and time exposure which is sufficient to pasteurise the aqueous phase. It
is preferred to use milk solids containing a relatively high proportion of
proteins such as, for example, sodium caseinate and high protein whey
powder but other milk derived solids such as, for example, milk powder
and buttermilk may all be satisfactorily employed. The aqueous phase
may contain additional ingredients such as stabilisers, flavouring agents,
salts, food grade acids such as lactic and citric acid and preservatives to increase the shelf life of the product and reduce the risk of microbial
contamination.
It was also unexpectedly found that when plant sterols are added to
the aqueous phase of fat spreads in the absence of milk derived solids,
the emulsification sometimes cannot be carried out satisfactorily, with the
emulsion turning into a soft gel. This often happens when emulsification is
carried out at too high a temperature and more so when lecithin or
polyglycerol esters are used as emulsifiers. The addition of milk derived
solids offset this undesirable change in the structure of the emulsion.
However, it was also found that the order of addition of milk derived solids
and other ingredients such as, for example, gelatine is important. Thus,
no gelling was observed on emulsification when plant sterols were
contacted with milk solids in the aqueous phase of a fat spread prior to the
addition of gelatine or even when plant sterols were contacted with a
mixture of gelatine and whey powder for a reasonable time. However,
when whey powder is added to plant sterols suspension in gelatine
immediately prior to emulsification, the gelling often occurs. Once again,
without wishing to be bound by or advance any particular theory it is
assumed that the interaction between milk derived solids and plant sterol
particles is responsible for this effect.
An extensive study and research was done to elucidate the above
said phenomenon and it was found that the addition of lecithin (E322)
and/or polyglycerol esters (e.g. E476) to a vegetable oil, even in quantities as low as 1 % by weight or below, increases substantially the solubility of
plant sterols in the said oil. Thus, for example the addition of 1 % w/w of
soy lecithin to sunflower oil increases the solubility of β-sitosterol to about
7% at 60°C, whilst in the absence of lecithin the solubility of β-sitosterol is
known to be significantly lower. A similar effect is observed with β-stanol.
The addition of polyglycerol esters to oils also increases the solubility of β-
sitosterol substantially but glycerol esters (monoglycerides, E471) are
relatively inefficient. It was further found that the above said plant sterols
solution rapidly turned into a gel on cooling or when a small amount of
water is added. A similar observation was made by Ritter et al (WO
97/42830) who disclosed the formation of organogels on mixing two
sterols of plant origin. However according to the invention of Ritter et al at
least two different sterols, one of which is esterified, are necessary to
achieve the formation of organogels. The gels produced according to the
present invention by dissolving plant sterols in an oil matrix containing
lecithin and (poly)glycerol esters or the like can be fruitfully exploited for
the preparation of cosmetic and food products such as spreads,
squeezable margarines and dressing using manufacturing methods that
are well established in the art. It was found however that no formation of
the gel occurred in the process of the preparation of fat spread, even when
a substantially higher amount of lecithin was present in the aqueous phase
prior to emulsification, if the mixture of plant sterols and lecithin was
coated according to this invention. When producing low and very low fat spreads according to this
invention it is preferred to use stabilisers. The stabilisers which can be
used to practice the present invention include gelatine, maltodextrins,
starch and modified starch, cellulose and its derivatives and pectins and
their derivatives and other polysaccharides of plant or seaweed origin.
However, this is not an exhaustive list and those skilled in the art will
instantly recognise that other stabilisers as well as various mixtures
thereof can also be successfully employed.
The fat spreads according to this invention can be made with a
different fat content, preferably with fat content below 40%. Conventional
fat phases containing vegetable oils such as, for example, sunflower oil,
soybean oil, rapeseed oil and the like can all be used as obtained or after
hardening or any other chemical or physical treatment as known and
acceptable in the art. Animal fats, preferably butter fat, may also be used.
Other ingredients can be optionally added to the fat phase. Examples of
the above said ingredients include flavouring and colouring agents and
vitamins, preferably those which are conventionally used in the
manufacture of fat spreads.
Conventional emulsifiers, preferably mono/di-glycerides (E471 ),
lecithin (E322) and polyglycerol esters (E476), can be used to produce the
fat spreads according to this invention, preferably using the process of this
invention. The above said emulsifiers can be used on their own or as a
mixture or any combination thereof or in conjunction with other suitable emulsifiers which are known in the art. The emulsifier can be added to the
oil phase or to a part of the oil phase or to the aqueous phase, preferably
after contacting plant sterols with milk derived solids.
The spreads according to this invention can be prepared to contain
vitamins, such as vitamins A and D, which are conventionally included into
fat spreads or are required to be added by legislation. In addition the
spreads according to this invention can be further fortified with additives
which are known to be beneficial to human health and preferably those
which enhance the desired effect of plant sterols. For example,
antioxidants such α-tocopherol and/or ascorbic acid can be included into
the fat phase or aqueous phase as appropriate. The fat phase can be
further supplemented with plant sterols and their derivatives to, for
example, increase the overall content of the active ingredient in the final
product. Thus, stanol and sterol esters can be included, if desired.
Similarly water soluble additives such as, for example vitamins or
minerals, can be included into the aqueous phase, preferably prior to
contacting plant sterols with milk derived solids according to this invention.
Other food products and beverages
Those skilled in the art would instantly recognise that the
hydrophobic compound-containing composition (such as the sterol-
containing additive) described herein can be used in a large number of
other food products and beverages such as, for example, alcoholic and non-alcoholic drinks, soups, sauces, dips, salad dressings, mayonnaise,
non-fat spreads, confectionery, bread, cakes, biscuits, breakfast cereals,
and non-fermented dairy and non-dairy products.
Additional supplementation
The food products and beverages according to this invention can
also be additionally supplemented with other physiologically active
compounds of known benefit to human health. The above said
physiologically active compounds do not have to be coated or modified in
any other way, if they are sufficiently soluble in the food product or
beverage of the present invention. For example, for low fat products and
drinks it is preferred to use those compounds which are soluble in water
e.g. soya isoflavones, which are known in the prior art to deter the
development of certain cancer and positively influence human health in
many other respects.
EXAMPLES
Example 1.
A standard yoghurt base was prepared by adding 1.5% by weight of
high protein whey powder to pasteurised skimmed milk. The mixture was
homogenised, heated to 80°C and held at this temperature for 30 minutes.
The mixture was then cooled to 45°C and finely divided pasteurised
powder of plant sterols (approximately 60% sitosterol and 40% campesterol and stigmasterol) in the amount of 0, 1.7, 3.5 and 5J gram
per 100 gram of yoghurt mix was added under aseptic conditions. After
admixing plant sterol, the yoghurt mix was inoculated with starter culture
containing 1 :1 Lactobacillus bulgaricus and Streptococcus
thermophilis.(0.5-0.8% w/v), distributed into containers and incubated at
43°C until pH 4.5 was reached. Typically, the fermentation took about 5
hours. No significant difference between the time required to reach the
desired pH was noted between the samples. The organoleptic properties
of the yoghurt supplemented with plant sterols was poor. On storage,
particles of plant sterol powder were found in the whey, on syneresis.
Example 2.
The yoghurt was made as described in Example 1 but plant sterols
(1.7 gram) were added to whey proteins-fortified milk prior to
homogenisation, the resulting suspension was homogenised, heated up to
55°C and left at this temperature for 2 hours. The yoghurt produced had a
texture, appearance and flavour like the corresponding product
composition prepared with no plant sterols added.
Example 3.
A 20 % by weight suspension of plant sterols was prepared by
intensive homogenisation of finely divided sterol powder in water. 1
volume of 10% (w/w) sodium caseinate solution was added and after stirring for 1 hour, the pH of the resulting suspension was adjusted to 4.5
with dilute HCI. The stirring was continued for 5 hours and the pH was
adjusted to 6.4.
Example 4.
Plant sterols suspension was prepared as described in Example 3
but a 9% (w/w) solution of high protein whey powder was used instead of
sodium caseinate. The resulting suspension was heated to 55°C and
incubated at this temperature for 2 hours with stirring.
Example 5.
Plant sterols suspension was prepared as described in Example 3
but a 20% (w/w) solution of semi skimmed milk powder was used instead
of sodium caseinate. The resulting suspension was incubated at room
temperature for 16 hours, with stirring.
Example 6
Plant sterol suspension was prepared as described in Example 3
but instead of pH adjustment, it was stirred for 1 hour and then spray-
dried. Example 7.
Plant sterol suspension was prepared as described in Example 4
and spray-dried.
Example 8.
The yoghurt was made as described in Example 2 by admixing 1
volume of sterol suspension prepared as described in Examples 3, 4 and
5 with 10 volumes of milk prior to homogenisation. The yoghurts obtained
had a similar texture, appearance and flavour to, or were substantially
indistinguishable from, the corresponding product compositions which
were made with no plant sterols added.
Example 9.
The yoghurt was made as described in Example 8 but using 75
parts of soymilk (3.5% protein) fortified with high protein whey powder and
25 parts of pasteurised skimmed milk. The yoghurts obtained had a
similar texture, appearance and flavour to, or were substantially
indistinguishable from, the corresponding product compositions which
were made with no plant sterols added.
Example 10.
The yoghurt base for Swiss style yoghurt was made as described in
Example 8 but 0.75% of a standard premixed stabiliser containing modified food starch, pectin and gelatine, and 3.5 % sugar was added.
The stirred yoghurt was produced by breaking the coagulum and a
standard fruit product (40-50% strawberry or raspberry; 30-40% sugar, 2-
3% modified starch) was mixed in. The yoghurts obtained had a similar
texture, appearance and flavour to, or were substantially indistinguishable
from, the corresponding product compositions which were made with no
plant sterols added.
Example 11.
Swiss style yoghurt was made as described in Example 10, but 2
volumes of sterol suspension prepared as described in Examples 3, 4 and
5 was mixed with 10 volumes of milk prior to homogenisation. The stirred
yoghurt was produced by breaking the coagulum and a fruit product (40-
50% strawberry or raspberry; 30-40% sugar, 2-3% modified starch) was
mixed in. The yoghurts obtained had a texture, appearance and flavour
like the product compositions which were made with no plant sterols
added.
Example 12.
The yoghurt was made as described in Example 10 but 3 volumes
of sterol suspension prepared as described in Examples 3, 4 and 5 was
used. The yoghurts obtained had a similar texture and appearance to the
corresponding product compositions which were made with no plant sterols added but assessors commented on the sensation of powderiness
in the mouth.
Example 13. The yoghurt was made as described in Example 10 but 1.7 gram of
plant sterols prepared as described in Examples 6 and 7 was added to
milk prior to homogenisation. The yoghurts obtained had a similar texture,
appearance and flavour to, or were substantially indistinguishable from,
the corresponding product compositions which were made with no plant
sterols added.
Example 14.
The yoghurt was made as described in Example 13 but using stanol
(>95% purity) and a technical grade preparation (approximately 50%
stanol) which was purified by re-crystallisation from ethanol, instead of the
plant sterol mixture of Example 1. Stanol was subjected to intensive
homogenisation to reduce the crystal size, typically to about 50 micron.
The yoghurts obtained had a texture and appearance like the
corresponding product compositions which were made with no stanol
added, although the assessors noted an aftertaste. Example 15.
Stanol acetate was prepared by esterification of the stanol with
acetic anhydride under standard conditions. The yoghurts were made as
described in Examples 10 and 14. The yoghurts obtained had a texture,
appearance and flavour like the corresponding product compositions
which were made with no stanol acetate added.
Example 16.
A very low fat Swiss style yoghurt was prepared as described in
Example 10 but using yoghurt base made from HTST skimmed milk (9%
solids and less than 0.1 % by weight butterfat) to which 0.75% of a
standard premixed stabiliser containing modified food starch, pectin and
gelatine, 6% of non heat non fat dry solids and 5 % sugar was added.
After blending 1 part of fruit was added per 5 parts of yoghurt. The fat
content of the yoghurt was about 0.2%.
Example 17.
The yoghurt was prepared as described in Example 10 but a
standard Sundae style fruit (35-45% of strawberry or raspberry; 15-20%
sugar 10-20% corn syrup, 2-4% modified starch and remaining % water)
was placed on the bottom of the containers. The inoculated mixture of
ingredients prepared as described in Example 10 was poured on top.
Approximately 1 part of fruit product for 5 parts of yoghurt was used. The products which were assessed after mixing the yoghurt with the fruit had a
similar texture, appearance and flavour to, or were substantially
indistinguishable from, the corresponding product compositions which
were made with no plant sterols added.
Example 18.
A yoghurt base was prepared as described in Example 8. The
product was cooled down to 15°C, and 3% of water and food grade citric
acid was added to adjust the pH to about 4.0. 1.9% by weight of citric
pectin and 4J % by weight of orange essence was added and, after
intensive stirring, the mixture was homogenised under pressure and
heated to about 50°C and cooled down to 3-5°C. The yoghurt drinks
obtained had a similar texture, appearance and flavour to, or were
substantially indistinguishable from, the corresponding product
compositions which were made with no plant sterols added.
Example 19.
Yoghurt fruit was prepared by blending 35 parts strawberries, 5
parts water and 3 parts starch under constant agitation with heating. The
resulting mixture was held at 89-95°C for about 10 minutes until it
thickened and then 30 parts of 3:1 mixture of sugar and plant sterol
prepared as described in Examples 6 and 7 was added with vigorous
agitation together with additional 5 parts of sugar, 15 parts of corn syrup, 4 parts of natural flavouring, 1 part of preservative (potassium sorbate), 0.5
parts of colouring agent and 0.5 parts of citric acid. Vigorous agitation was
continued on cooling.
Example 20.
Yoghurt fruit was prepared as described in Example 19 but finely
divided plant sterol powder with a particle size around 30-50 micron or
below, as assessed by microscopy, was used.
Example 21.
Yoghurt fruit was prepared as follows: Plant sterols prepared as
described in Examples 6 and 7 were added to water and the resulting 20%
(w/w) suspension was homogenised at 50°C. 12 parts of this suspension
was then blended with 45 parts strawberries and 3 parts modified starch
under constant agitation with heating. The resulting mixture was held at
89-95°C for about 10 minutes and then 40 parts of sugar and other
ingredients as described in Example 19 were added with vigorous
agitation which continued on cooling.
Example 22.
Yoghurts were made as described in Examples 11 and 17 with and
without the addition of plant sterols but using the fruit products prepared
as described in Examples 19, 20 and 21. The products which were assessed after mixing the yoghurt with the fruit had a similar texture,
appearance and flavour to, or were substantially indistinguishable from,
the corresponding product compositions which were made with no plant
sterols added.
Example 23.
Plant sterol suspension was prepared as described in Example 4
but Soya bean protein was used as a coating agent.
Example 24.
A 12 % by weight suspension of plant sterols was prepared by
intensive homogenisation of finely divided sterol powder in cow's milk.
The resulting suspension was pasteurised by heating up to 80°C, re-
homogenised and used for the preparation of a beverage as described in
Example 30.
Example 25.
Sterol suspension was prepared as described in Example 24 but
Soya milk was used instead of cow's milk.
Example 26.
A 10% suspension of coated lycopene was prepared as described
in Examples 24 and 25 but using lycopene crystals instead of plant sterols. Example 27.
Plant sterols (10 g) and lecithin (9.5 g) were dissolved in boiling
ethanol (100 mL) and the resulting solution was added to 100 mL of water.
After ethanol was removed the coating of plant sterols was accomplished
by adding 1 volume of 9% whey protein to 10 volumes of the sterol-lecithin
suspension ( as described in Example 4).
Example 28.
Plant sterols (10 g) and lycopene-containing solids (effective concentration
of lycopene 0.5 g) were dissolved in boiling ethanol (100 mL) and the
resulting solution was added to 80 mL of water. After ethanol was
removed the coating of plant sterols was accomplished by adding 1
volume of 9% whey protein to 10 volumes of the sterol-lycopene
suspension.
Example 29.
The yoghurt drink was made as described in Example 18 but 50 mg
of soya isoflavons per helping was added to the product together with
other prior to the homogenisation. Example 30.
A milk shake was prepared to contain the sterol suspension
prepared as described in Example 24 (15%) and non-fat dry milk (6%),
whey concentrate (5%), sugar (9%) fructose-dextrose syrup (12%), corn
syrup (3%), whey (5%), butter (7.2%), flavouring (0.5%), emulsifiers
(0.3%) and water (37%). The syrups and flavouring were added to water
combined with the sterol suspension and mixed under high sheer with
heating up to the pasteurising temperature. Other components were
added and, when the sugar dissolved, the mixture was homogenised and
cooled directly into a heat-exchanger until the temperature of the product
reached about 35°C. The product was stored overnight and then whipped.
Example 31
A milk shake was prepared as described in Example 30 but using
the coated lycopene suspension (see Example 26) instead of coated plant
sterols to give the effective concentration of 10 mg of lycopene per
helping.
Example 32
A dough for bread was prepared to contain (in baker percentage):
flour (100%), water and plant sterol suspension prepared as in Example 4
(66%), compressed yeast (2%), yeast food (0.5%), sucrose (4%), no-fat
milk solids (4%), sucrose (4%), salts including sodium propionate (2.3%), shortening and surfactants (2%). All ingredients were mixed in a Hobart
mixer. The dough was proofed, scaled, hand-rounded and given a rest at
room temperature. The rested dough was sheeted, moulded, placed in a
lightly greased pans and proofed at high humidity. The bread was baked
for 20 min at 215°C in a rotary rack oven. The amount of plant sterol used
was sufficient to give 1.4% of plant sterols per dry weight of the final
bread.
Example 33.
A suspension (18% w/w) of plant sterols was prepared by intensive
homogenisation of finely divided sterol powder in 2% (w/w) solution of milk
powder, heated to 60°C and maintained at this temperature for 30
minutes. Salt (5%) was added and 30 parts of the resulting mixture was
emulsified with 70 parts of a mixture consisting of sunflower oil (79%) and
hydrogenated vegetable oil (21 %). Emulsifiers E471 and E322 (0.5%), fat
soluble butter flavours (0.035%) and colouring (0.04%) were included in
the oil.
Example 34.
A suspension (18% w/w) of plant sterols in water was prepared as
described in Example 33 and 1 part of a 10% solution of whey powder was
added to 5 parts of this suspension. After stirring for 30 minutes the
resulting mixture was spray dried. Example 35.
A fat spread was made as described in Example 33 but plant
sterols prepared as described in Example 34 were used to make a
suspension (18% w/w) of plant sterols in 5% salt solution which was used
to prepare the aqueous phase of the spread.
Example 36.
A fat spread was made as described in Example 35 but the spray
dried plant sterols were added to the oil phase (8.5% w/w). Substantial
thickening was observed during homogenization which hampered
processing. The texture and organoleptic properties of the product were
inferior.
Example 37.
A fat spread was made as described in Example 33 but plant sterol
suspension was prepared in buttermilk (6% w/w protein).
Example 38.
A suspension (18% w/w) of plant sterols in water was prepared by
intensive homogenisation and 1 part of a 10% solution of whey powder
was added to 5 parts of this suspension. The resulting mixture was
heated to 60°C and maintained at this temperature for 90 minutes. Salt (5%) was added and a fat spread was prepared as described in Example
33.
Example 39.
A fat spread was made as described in Example 38 but the oil
phase of the spread contained 20% (w/w) of butterfat.
Example 40.
A fat spread was made as described in Example 38 but the oil
phase of the spread contained 7% of stanol esters which were prepared
as described in US 5,502,045.
Example 41.
A fat spread was prepared as described in Example 38 but 0.06%
α-tocopherol (E307) was added to the oil phase and Soya bean
isoflavones (0.1% w/v) were added to the aqueous phase prior to
emulsification.
Example 42.
A suspension of plant sterols was prepared with whey powder as
described in Example 35. The resulting mixture was homogenised,
heated to 55°C and incubated at this temperature for 30 min. Gelatine
(3%) and salt (2.5%) were added and pH was adjusted to 5.8 by addition of citric acid. 62 parts of this suspension was emulsified with 38 parts of
oil using E471 and E322 (1 %) as emulsifiers.
Example 43. A suspension (15% w/w) of plant sterols was prepared in an
aqueous solution containing gelatine (3%) and salt (2.5%). The resulting
mixture was homogenised, heated to 55°C and incubated at this
temperature for 30 min. The suspension was emulsified with oil as
described in Example 42. No satisfactory product was obtained as the
emulsion gelled.
Example 44.
A fat spread was made as described in Example 43 but using the
plant sterols prepared as described in Example 34. Emulsification
proceeded normally.
Example 45.
380 mg of β-sitosterol was added to 5.0ml of sunflower oil
containing either 1 % lecithin or 0.4% E476. Both samples gave a clear
solution at 60°C which gelled within 10-15 min if cooled down at room
temperature or instantly on the addition of water. At the same
concentration β-sitosterol was not soluble in sunflower oil in the absence
of the emulsifiers. The experiment was repeated with 300 mg of stanol and sunflower oil containing 1 % lecithin (the same amount of stanol was
not soluble in the oil in the absence of lecithin). The stanol/lecithin
solution gelled on cooling or on the addition of water.
Example 46.
A suspension (18% w/w) of plant sterols was prepared by intensive
homogenisation of finely divided sterol powder in water. 1 part of 10%
(w/w) sodium caseinate solution was added per 5 parts of the sterol
suspension and the pH of the resulting suspension was adjusted to 4.6
with citric acid. The suspension was heated up to 90°C with stirring and
incubated at this temperature for 1 h, then gelatine (3%), modified starch
(3%) and salt (2%) were added and, after the added ingredients dissolved,
the mixture was pasteurised at this temperature, cooled down to 50°C and
used as an aqueous phase for the preparation of fat spread. The fat
spread was prepared as described in Example 42 but using 71 parts and
29 parts of the above aqueous suspension and oil phase respectively.
Example 47.
A suspension of plant sterols was prepared as described in
Example 46, and after stirring for 1 hour, spay-dried. An aqueous phase
of fat spread was prepared to contain gelatine (3%), low DE maltodextrin
(15%) and salt (2%) and citric acid (0.5%). Spray dried plant sterols (15% w/w) were admixed into the aqueous solution above, the pH adjusted to
5.8 and a fat spread was made as described in Example 46.
Example 48.
A fat spread was made as described in Example 43 but using plant
sterols prepared as described in Example 27. Emulsification proceeded
normally.

Claims

1. A method for making a composition suitable for inclusion in a food
product or beverage the method comprising the step of combining a plant
sterol, lycopene or other hydrophobic compound which can be shown to
be beneficial for human health with a component which is acceptable as a
food additive, wherein the component which is acceptable as a food
additive interacts with the surface of the hydrophobic compound.
2. A method according to Claim 1 wherein the hydrophobic compound
is any one of a plant sterol, lycopene (such as tomato lycopene), other
carotenoids and poorly water soluble anti-oxidants or a combination
thereof.
3. A method according to Claim 1 or 2 wherein the component which
is acceptable as a food additive is any one of a food-acceptable
polypeptide, polysaccharide or low molecular weight substance with
similar chemical functionality/functional groups.
4. A method according to any one of Claims 1 to 3 wherein the
component acceptable as a food additive is a coating agent which is
encouraged to adhere to the surface of the plant sterol, lycopene or other
hydrophobic compound.
5. A method according to any one of Claims 1 to 4 wherein the plant
sterol, lycopene or other hydrophobic compound is contacted with the
component acceptable as a food additive in aqueous suspension.
6. A method according to any one of Claims 1 to 5 which comprises
coating the plant sterol, lycopene or other hydrophobic compound with a
food additive by combining the hydrophobic compound and the food
additive in an aqueous suspension and incubating the resulting mixture,
with stirring, at a temperature between 18°C and 50°C.
7. A method as claimed in Claim 6, where the suspension containing
the plant sterol, lycopene or other hydrophobic compound, and a food
additive is heat-treated at a temperature above 50°C.
8. A method as claimed in any of the Claims 6 and 7, where the pH of
the suspension containing the plant sterol, lycopene or other hydrophobic
compound, and a food additive is adjusted to substantially neutralise the
net charge on the molecule of the food additive and, preferably close to
the isoelectric point of the food additive.
9. A method as claimed in any one of Claims 6 to 8, where the coated
plant sterol, lycopene, or other hydrophobic compound, is recovered in dry
form.
10. A method as claimed in any of the Claims 1 to 9, where the food
additive is a multifunctional substance and contains at least one carboxyl
group and at least one hydroxyl group.
11. A method as claimed in any of the Claims 1 to 9, where the food
additive is a protein.
12. A method as claimed in any of the claims 1 to 9, where the food
additive is derived from milk.
13. A method as claimed in Claim 12, where the food additive is
selected from the group comprising casein, caseinate, whey protein, whey,
milk powder, buttermilk and butterfat.
14. A method as claimed in any of the Claims 1 to 13, where the
hydrophobic compound is a plant sterol selected from the group
comprising β-sitosterol, β-campesterol, β-stigmasterol, β-sitostanol, β-
campestanol and β-stigmastanol and their carboxyiic acid esters, and
mixtures thereof.
15. A method according to any one of Claims 1 to 14 wherein lecithin is
additionally combined with the plant sterol, lycopene or other hydrophobic
compound and the component which is acceptable as a food additive.
16. A method according to Claim 15 wherein the lecithin and
hydrophobic compound are combined prior to combination with the
component which is acceptable as a food additive.
17. A method according to Claim 15 or 16 wherein there is more
hydrophobic compound than lecithin by weight.
18. A method according to any one of Claims 15 to 17 where the
hydrophobic compound and lecithin are combined by dissolving them in a
common solvent and then precipitated prior to combining them with a
component which is acceptable as a food additive.
19. A method according to any one of Claims 1 to 17 wherein the
composition is formed in situ in the preparation of the food product or
beverage.
20. A composition suitable for inclusion in a food product or beverage
obtainable by the method of any one of Claims 1 to 18.
21. A composition suitable for inclusion in a food product or beverage
comprising a plant sterol, lycopene or other hydrophobic compound which
can be shown to be beneficial for human health with a component which is
acceptable as a food additive coated on the surface thereof.
22. A composition according to Claim 20 or 21 wherein the hydrophobic
compound is a plant sterol, lycopene or other carotenoid and pooriy water
soluble anti-oxidants or a combination thereof.
23. A composition according to any one of Claims 20 to 22 wherein the
component acceptable as a food additive is a food-acceptable
polypeptide, polysaccharide or low molecular weight substance with
similar chemical functionality/functional groups.
24. A dry ingredient which is obtained by drying, preferably spray-drying
of a mixture containing a milk derived solid and plant sterols, where the
milk derived solid and the plant sterols are combined in a process wherein
the milk derived solid and the plant sterols are contacted in an aqueous
suspension, and where the milk derived solid is selected from the group
consisting of casein, caseinate, whey protein, whey, milk powder,
buttermilk and butterfat, and where the plant sterols are selected from the
group comprising β-sitosterol, β-campesterol, β-stigmasterol, β-sitostanol, β-campestanol and β-stigmastanol and their carboxylic acid esters, and a
mixture thereof.
25. A dry ingredient according to Claim 24 wherein the contact is
carried out at a temperature above 40°C and preferably with stirring.
26. A dry ingredient according to Claim 24 or 25 wherein the contact is
carried out at a temperature and exposure time combination which is
sufficient for pasteurisation.
27. A composition suitable for inclusion in a food product or beverage
consisting essentially of a plant sterol, lycopene or other hydrophobic
compound which can be shown to be beneficial to human health and
lecithin wherein there is more hydrophobic compound than lecithin by
weight.
28. A composition suitable for inclusion in a food product or beverage
according to Claim 27 wherein the plant sterol, lycopene or other
hydrophobic compound is coated with a component which is acceptable
as a food additive.
29. A method for preparing a food product or beverage which is
suplemented with a plant sterol, lycopene or other hydrophobic compound which can be shown to be beneficial for human health the method
comprising the step of (1 ) carrying out the method of any one of Claims 1
to 17 and 19 in situ during the preparation process or (2) adding at an
appropriate stage during the preparation process a composition according
to any one of Claims 20 to 28 or (3) a combination of (1 ) and (2).
30. A food product or beverage which is supplemented with a plant
sterol, lycopene or other hydrophobic compound which can be shown to
be beneficial for human health obtainable by the method of Claim 29.
31. A food product or beverage according to Claim 30 which is any one
of a fermented or non-fermented dairy product, an emulsified fat product, a
non-dairy product, alcoholic and non-alcoholic drinks, soups, sauces, dips,
salad dressings, mayonnaise, non-fat spreads, confectionery, bread,
cakes, biscuits, and breakfast cereals.
32. A food product or beverage according to Claim 30 which is
produced by the fermentation of a mixture consisting of a fermentable raw
material and plant sterols with lactic acid bacteria, and which has a similar
texture, appearance and flavour to, or is substantially indistinguishable
from, the corresponding product composition which is made with no plant
sterols added.
33. A product as claimed in Claim 32, where the fermented food
product is a fermented milk product.
34. A product as claimed in Claim 33, where the fermented milk
product is selected from the group comprising of yoghurt, yoghurt product,
kefir, ymer, buttermilk, butterfat, sour cream, sour whipped cream and
fresh cheese.
35. A product as claimed in any of the Claims 32 to 34, where the
fermentation is carried out with more than one micro-organism.
36. A product as claimed in any of the Claims 32 to 35, where the
micro-organism is selected from the group comprising Lactobaccilus sp.,
Streptococcus sp., Lactococcus sp., Bifidobacterium sp., and mixtures
thereof.
37. A product as claimed in any of the Claims 32 to 36, which contains
less than 2% fat.
38. A product as claimed in any of the Claims 32 to 37, where plant
sterols are selected from the group comprising β-sitosterol, β-campesterol,
β-stigmasterol, β-sitostanol, β-campestanol and β-stigmastanol and their
carboxylic acid esters, and mixtures thereof.
39. A food product which is produced by the fermentation of a mixture
consisting of a fermentable raw material and plant sterols with lactic acid
bacteria, and which has a similar texture, appearance and flavour to, or is
substantially indistinguishable from, the corresponding product
composition which is made with no plant sterols added.
40. A process for the preparation of the products as claimed in Claim
39, where plant sterols are added to a fermentable raw material prior to
inoculation with micro-organisms.
41. A process for the preparation of the products as claimed in Claim
39, where plant sterols are added to a fermentable raw material prior to
pasteurisation.
42. A process for the preparation of the products as claimed in Claim
39, where the mixture of a fermentable raw material and plant sterols is
heat treated at a temperature above 50°C prior to inoculation with a micro¬
organism.
43. A process as claimed in any of the Claims 40 to 42, where the raw
material is milk or is derived from milk.
44. A process as claimed in any of the Claims 40 to 43 where the plant
sterols used are coated with food additives as claimed in any of the Claims
6 to 18.
45. A product as claimed in any of the Claims 32 to 38, which is
prepared in the process as claimed in any of the Claims 40 to 43 where
the plant sterols used are coated with food additives as claimed in any of
the Claims 6 to 18.
46. An emulsified fat spread according to Claim 30 which is
supplemented with plant sterols, where the plant sterols are included into
the aqueous phase of the product composition in a largely insoluble form.
47. An emulsified fat spread as claimed in Claim 46, which contains
milk derived solids.
48. An emulsified fat spread as claimed in any of the Claims 46 to 47,
where milk derived solids are selected from the group consisting of casein,
caseinate, whey protein, whey, milk powder, buttermilk and butterfat.
49. An emulsified fat spread as claimed in any of the Claims 46 to 48,
which contains at least one additional dietary supplement in addition to
those required by legislation.
50. An emulsified fat spread as claimed in any of the Claims 46 to 49,
which contains less than 40% fat.
51. An emulsified fat spread as claimed in any of the Claims 46 to 50,
where the fat phase is supplemented with oil-soluble plant sterols.
52. An emulsified fat spread as claimed in any of the Claims 46 to 51 ,
where the fat soluble plant sterols are different from the plant sterols
included in the aqueous phase.
53. An emulsified fat spread as claimed in any of the Claims 46 to 52,
where the plant sterols are selected from the group comprising β-
sitosterol, β-campesterol, β-stigmasterol, β-sitostanol, β-campestanol and
β-stigmastanol and their carboxylic acid esters, and a mixture thereof.
54. An emulsified fat spread which is supplemented with plant sterols,
where the plant sterols are included into the aqueous phase of the product
composition in a largely insoluble form.
55. A process for the production of products as claimed in Claim 54,
comprising of contacting milk derived solids and plant sterols in the
aqueous phase of the product composition prior to emulsification.
56. A process as claimed in Claim 55, where the contact is carried out
at a temperature above 40°C and, preferably with stirring.
57. A process as claimed in any of the Claims 55 and 56, where the
contact is carried out at a temperature and exposure time combination
which is sufficient for pasteurisation.
58. A yoghurt which is prepared by (i) admixing milk and milk derived
solids with plant sterols, and heating the mixture to a temperature above
60°C, and (ii) cooling the mixture down, and (iii) adding a starter culture
containing micro-organisms selected from the group comprising
Lactobaccilus sp., Streptococcus sp., Lactococcus sp. and Bifidobacterium
sp., and mixtures thereof and (iv) incubating the resulting mixture until the
milk coagulates.
59. A yoghurt as claimed in Claim 58, which is prepared with non-milk
derived ingredients selected from the group comprising fruit products,
stabilisers, thickeners, sweeteners, flavouring and colouring agents, and a
mixture thereof.
60. A yoghurt as claimed in any of the Claims 58 and 59, which
contains less than 2% fat.
61. A yoghurt as claimed in any of the Claims 58 to 60, where the plant
sterols used are coated with food additives as claimed in any of the Claims
6 to 18.
62. A yoghurt product prepared from the yoghurt as claimed in any of
the Claims 58 to 61.
63. A process for the preparation of stirred yoghurt and yoghurt
products which contain (i) plant sterols and (ii) non-milk derived
ingredients selected from the group comprising fruit products, stabilisers,
thickeners, sweeteners, flavouring and colouring agents, and mixtures
thereof, by admixing the plant sterol into the yoghurt or the yoghurt
product during or after breaking the coagulum.
64. A yoghurt and a yoghurt product which are prepared by the process
as claimed in Claim 63, where the plant sterols are prepared by the
method as claimed in any of the Claims 6 to 18.
65. A process for the preparation of yoghurt fruit containing plant
sterols which comprises (i) blending a mixture of fruit and water and plant
sterols and ingredients selected from the group consisting of stabilisers,
thickeners, sweeteners, flavouring and colouring agents and preservatives and (ii) heating up the mixture to a temperature sufficient to pasteurise the
mixture and (iii) holding the mixture at elevated temperature until it
thickens and (iv) cooling the mixture down, with agitation.
66. A process as claimed in Claim 65, where plant sterols used are
prepared by the method as claimed in any of the Claims 6 to 18.
67. A yoghurt composition which consists of three essential ingredients:
(i) yoghurt base; (ii) yoghurt fruit and (iii) free (unesterified) plant sterols.
68. A yoghurt composition which consists of four essential ingredients:
(i) yoghurt base; (ii) yoghurt fruit, (iii) free (unesterified) plant sterols and
(iv) a non-milk derived ingredient selected from the group comprising
stabilisers, thickeners, sweeteners, flavouring and colouring agents, and
mixtures thereof.
69. A yoghurt composition as claimed in any of the Claims 67 and 68,
where plant sterols used are coated with food additives as claimed in any
of the Claims 6 to 18.
70. A yoghurt composition as claimed in any of the Claims 67 and 68,
where the yoghurt fruit is prepared as claimed in any of the Claims 59 and
60.
71. A yoghurt composition as claimed in any of the Claims 67 to 70,
where plant sterols are incorporated both into the yoghurt base and the
yoghurt fruit.
72. A yoghurt composition as claimed in any of the Claims 67 to 71 ,
which contains less than 2% fat.
73. A yoghurt, a yoghurt product and a yoghurt composition as claimed
in any of the Claims 58 to 62, 63 and 67 to 72, where plant sterols are
selected from the group comprising β-sitosterol, β-campesterol, β-
stigmasterol, β-sitostanol, β-campestanol and β-stigmastanol and mixtures
thereof.
74. An organogel composition consisting of (i) a liquid fat component,
(ii) at least one emulsifying agent and (iii) at least one sterol selected from
the group comprising β-sitosterol, β-campesterol, β-stigmasterol, β-
sitostanol, β-campestanol and β-stigmastanol.
75. An organogel composition as claimed in Claim 74, where the
emulsifying agent is selected from the group comprising lecithin and
polyglycerol esters and mixtures thereof.
76. The use of the organogel compositions as claimed in any of the
Claims 74 and 75 in food and cosmetic products.
77. The use of a dry ingredient as claimed in Claim 24 in food and
pharmaceutical compositions.
78. The use of a composition according to any one of Claims 20 to 28
in food, food products or beverages.
79. The use according to Claim 78 wherein the food is an emulsified
fat spread.
80. A method, product or use according to any one of the preceding
claims wherein a further additive which can be shown to be beneficial to
human health is used.
81. A method, product or use according to Claim 80 wherein the
further additive is a further hydrophobic compound which can be shown to
be beneficial for human health, such as a different plant sterol or lycopene.
82. A method, product or use according to Claim 80 or 81 wherein the
further additive is soluble in aqueous phase of food product or beverage.
83. A method, product or use according to Claim 81 wherein the
further additive is a soya bean isoflavone.
EP00900291A 1999-01-15 2000-01-17 Modified food products and beverages, and additives for food and beverages Withdrawn EP1146798A2 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
GB9900748 1999-01-15
GB9900748 1999-01-15
GB9901892 1999-01-29
GBGB9901892.1A GB9901892D0 (en) 1999-01-29 1999-01-29 Emulsifed spreadable fat product and process for the preparation thereof
PCT/GB2000/000096 WO2000041491A2 (en) 1999-01-15 2000-01-17 Modified food products and beverages, and additives for food and beverages

Publications (1)

Publication Number Publication Date
EP1146798A2 true EP1146798A2 (en) 2001-10-24

Family

ID=26314984

Family Applications (1)

Application Number Title Priority Date Filing Date
EP00900291A Withdrawn EP1146798A2 (en) 1999-01-15 2000-01-17 Modified food products and beverages, and additives for food and beverages

Country Status (3)

Country Link
EP (1) EP1146798A2 (en)
AU (1) AU1995400A (en)
WO (1) WO2000041491A2 (en)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020122865A1 (en) * 2000-12-07 2002-09-05 Marie Boyer Dairy-based beverages fortified with cholesterol-lowering agents
US6660775B2 (en) 2002-02-19 2003-12-09 Biosensory, Inc. Method and compositions for inhibiting the scent tracking ability of biting midges
US6623780B1 (en) 2002-03-26 2003-09-23 Cargill, Inc. Aqueous dispersible sterol product
WO2003092394A1 (en) * 2002-05-03 2003-11-13 Unilever N.V. Food product comprising a phytosterol
RU2329734C2 (en) 2002-06-12 2008-07-27 Дзе Кока-Кола Компани Method of dispersion production, beverage and composition
US7306819B2 (en) 2002-06-12 2007-12-11 The Coca-Cola Company Beverages containing plant sterols
US9173866B2 (en) 2002-07-24 2015-11-03 Children's Hospital Medical Center Compositions and products containing R-equol, and methods for their making
US8668914B2 (en) 2002-07-24 2014-03-11 Brigham Young University Use of equol for treating skin diseases
AU2003249894B2 (en) * 2002-07-26 2007-05-24 Unilever Plc Phytosterols or phytostanols and their use in food products
US8580846B2 (en) 2002-10-29 2013-11-12 Brigham Young University Use of equol for ameliorating or preventing neuropsychiatric and neurodegenerative diseases or disorders
EP1569636B1 (en) 2002-10-29 2017-12-13 Colorado State University Research Foundation Use of equol for treating androgen mediated diseases
FI20030610A0 (en) 2003-04-22 2003-04-22 Raisio Benecol Oy Edible product
PT1651338E (en) 2003-07-17 2011-06-14 Unilever Nv Process for the preparation of an edible dispersion comprising oil and structuring agent
ES2350203T3 (en) * 2003-10-24 2011-01-20 The Coca-Cola Company PROCESS TO PREPARE DISPERSIONS OF FITOSTEROL FOR BEVERAGE APPLICATIONS.
EP1742545A1 (en) * 2004-04-16 2007-01-17 Unilever N.V. Water continuous product comprising sterol or stanolester and a tocopherol
US20050281932A1 (en) * 2004-06-18 2005-12-22 Good Humor - Breyers Ice Cream Frozen confection
CA2595281A1 (en) 2005-02-17 2006-08-24 Unilever Plc Process for the preparation of a spreadable dispersion comprising sterol
DE102005039836A1 (en) 2005-08-23 2007-03-01 Cognis Ip Management Gmbh Sterolesterpulver
US7601380B2 (en) 2005-11-17 2009-10-13 Pepsico, Inc. Beverage clouding system and method
US8309156B2 (en) 2005-12-20 2012-11-13 Pharmachem Laboratories, Inc. Compositions comprising one or more phytosterols and/or phytostanols, or derivatives thereof, and high HLB emulsifiers
DE102006010663A1 (en) * 2006-03-08 2007-09-13 Cognis Ip Management Gmbh Process for the preparation of sterol-containing powders
EP1929885A1 (en) * 2006-12-04 2008-06-11 Cognis IP Management GmbH Process for the manufacture of sterol preparations
CN101902927A (en) * 2007-10-18 2010-12-01 荷兰联合利华有限公司 The liquid edible composition that comprises osajin
EP2070429A1 (en) 2007-12-13 2009-06-17 Cognis IP Management GmbH Oxidative stabilisation of sterols and sterol esters
CA2658440C (en) 2008-04-04 2016-08-23 Kraft Foods Global Brands Llc Dairy composition with probiotics and anti-microbial system
US8865245B2 (en) 2008-12-19 2014-10-21 Conopco, Inc. Edible fat powders
FI20090023A0 (en) 2009-01-26 2009-01-26 Ravintoraisio Oy New food
FI20095146A (en) * 2009-02-18 2010-08-19 Valio Oy Procedure for improving the taste of a food preparation
WO2010104375A1 (en) * 2009-03-12 2010-09-16 N.V. Nutricia Stigmasterol for the treatment of alzheimer's disease
WO2011144405A1 (en) 2010-05-18 2011-11-24 Unilever Nv Edible fat continuous spreads
EA024216B1 (en) 2010-06-22 2016-08-31 Юнилевер Н.В. Edible fat powders
US20130266715A1 (en) 2010-12-17 2013-10-10 René Joachim Buter Process of compacting a microporous fat powder and compacted fat powder so obtained
WO2012079957A1 (en) 2010-12-17 2012-06-21 Unilever Nv Edible water in oil emulsion
FI123374B (en) 2011-03-25 2013-03-15 Ravintoraisio Oy New edible composition
FI125947B (en) 2013-07-05 2016-04-29 Ravintoraisio Oy Blood cholesterol lowering composition
SG10201807499RA (en) * 2014-03-03 2018-09-27 Raisio Nutrition Ltd Serum cholesterol lowering edible product
CN106031389A (en) * 2015-03-17 2016-10-19 张跃华 Lycopene yoghourt and preparation method thereof
JP2019510487A (en) * 2016-03-02 2019-04-18 インターナショナル フレーバーズ アンド フラグランシズ インコーポレイテッド Novel composition for flavor enhancement
FI130459B (en) * 2017-12-29 2023-09-08 Myllyn Paras Oy Konserni Food composition containing plant sterols and/or stanols, its production and use
CN116076640A (en) * 2021-11-08 2023-05-09 莒南和信食品有限公司 Application and process of beta-sitosterol in beverage

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL276700A (en) * 1961-04-05
US3881005A (en) * 1973-08-13 1975-04-29 Lilly Co Eli Pharmaceutical dispersible powder of sitosterols and a method for the preparation thereof
US6846507B1 (en) * 1996-05-10 2005-01-25 Lipton, Division Of Conopco, Inc. Liquid fatty component containing composition
TW360501B (en) * 1996-06-27 1999-06-11 Nestle Sa Dietetically balanced milk product
FI105887B (en) * 1996-09-27 2000-10-31 Suomen Sokeri Oy Products containing plant sterol for use in food and therapeutic applications, process for their preparation and their use
US6423363B1 (en) * 1997-08-22 2002-07-23 Lipton, Division Of Conopco, Inc. Aqueous dispersion
FR2775620B1 (en) * 1998-03-05 2002-04-19 Gervais Danone Sa STABLE HOMOGENEOUS SUSPENSION WITHOUT EMULSIFIER, PROCESS FOR PREPARING SAME, AND USE THEREOF IN FOOD COMPOSITIONS
US5932562A (en) * 1998-05-26 1999-08-03 Washington University Sitostanol formulation to reduce cholesterol absorption and method for preparing and use of same
EP1082026A1 (en) * 1998-06-05 2001-03-14 Forbes Medi-Tech Inc. Compositions comprising phytosterol and/or phytostanol having enhenced solubility and dispersa

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO0041491A2 *

Also Published As

Publication number Publication date
WO2000041491A2 (en) 2000-07-20
WO2000041491A3 (en) 2000-12-07
AU1995400A (en) 2000-08-01

Similar Documents

Publication Publication Date Title
WO2000041491A2 (en) Modified food products and beverages, and additives for food and beverages
US7635492B2 (en) Edible fungi
AU2002352305B2 (en) Protein hydrolysate and plant sterol containing composition for improving serum lipid profile and preventing atherosclerosis
AU2006212485B2 (en) Food products comprising hydrolysed milk solids with improved taste
EP3542635B1 (en) Whey protein-based, high protein, yoghurt-like product, ingredient suitable for its production, and method of production
US8309156B2 (en) Compositions comprising one or more phytosterols and/or phytostanols, or derivatives thereof, and high HLB emulsifiers
CN105792667A (en) High protein, fruit flavoured beverage; high protein, fruit and vegetable preparation; and related methods and food products
CN105792659A (en) High protein denatured whey protein composition, related products, method of production and uses thereof
CN105792663A (en) CMP-containing, high protein denatured whey protein compositions, products containing them, and uses thereof
CA2570334A1 (en) Frozen confection
JPH02286039A (en) Instant yogurt composition and preparation thereof
EP1973427A2 (en) Compositions comprising one or more phytosterols and/or phytostanols, or derivatives thereof, and high hlb emulsifiers
Pimentel et al. Brazilian yogurt-like products
EP1732401A2 (en) Soy sour cream compositions and methods of preparation
EP2645868B1 (en) Set-style fruit yoghurts
EP0853889A2 (en) Amylaceous dairy-like food product
WO2009003932A1 (en) Stable fruit preparation with high acacia gum concentration
JP2003274852A (en) Yogurt
JP2890746B2 (en) Foods containing highly stable intestinal useful bacteria
EP1175156A1 (en) Cereal product
AU2005232369A1 (en) Water continuous product comprising sterol or stanolester and a tocopherol
JPH06113799A (en) Sour cheese drink and its production

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

17P Request for examination filed

Effective date: 20010807

R17P Request for examination filed (corrected)

Effective date: 20010831

17Q First examination report despatched

Effective date: 20020403

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: NUTRAHEALTH LTD. (UK)

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20021203