WO2010021820A1 - Stable beverage products comprising polyunsaturated fatty acid emulsions - Google Patents

Stable beverage products comprising polyunsaturated fatty acid emulsions Download PDF

Info

Publication number
WO2010021820A1
WO2010021820A1 PCT/US2009/052224 US2009052224W WO2010021820A1 WO 2010021820 A1 WO2010021820 A1 WO 2010021820A1 US 2009052224 W US2009052224 W US 2009052224W WO 2010021820 A1 WO2010021820 A1 WO 2010021820A1
Authority
WO
WIPO (PCT)
Prior art keywords
oil
fold
emulsion
liquid phase
fatty acid
Prior art date
Application number
PCT/US2009/052224
Other languages
French (fr)
Inventor
Youlung Chen
Lihong D'angelo
Shen CHENG
George A. King
Original Assignee
The Coca-Cola Company
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
Application filed by The Coca-Cola Company filed Critical The Coca-Cola Company
Priority to CN2009801328468A priority Critical patent/CN102131406A/en
Priority to EP09790990A priority patent/EP2317876A1/en
Priority to JP2011523851A priority patent/JP2012500628A/en
Publication of WO2010021820A1 publication Critical patent/WO2010021820A1/en

Links

Classifications

    • 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
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • 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
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/385Concentrates of non-alcoholic beverages
    • A23L2/39Dry compositions
    • A23L2/395Dry compositions in a particular shape or form
    • 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
    • A23L29/00Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/03Organic compounds
    • 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
    • A23L29/00Foods or foodstuffs containing additives; Preparation or treatment thereof
    • A23L29/10Foods or foodstuffs containing additives; Preparation or treatment thereof containing emulsifiers
    • 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
    • A23L33/115Fatty acids or derivatives thereof; Fats or oils
    • A23L33/12Fatty acids or derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/045Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates
    • A61K31/047Hydroxy compounds, e.g. alcohols; Salts thereof, e.g. alcoholates having two or more hydroxy groups, e.g. sorbitol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/20Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/20Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • A61K31/202Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids having three or more double bonds, e.g. linolenic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0087Galenical forms not covered by A61K9/02 - A61K9/7023
    • A61K9/0095Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/10Dispersions; Emulsions
    • A61K9/107Emulsions ; Emulsion preconcentrates; Micelles
    • A61K9/1075Microemulsions or submicron emulsions; Preconcentrates or solids thereof; Micelles, e.g. made of phospholipids or block copolymers
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23VINDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
    • A23V2002/00Food compositions, function of food ingredients or processes for food or foodstuffs

Definitions

  • the present invention relates to beverage products comprising at least one beverage base and at least one polyunsaturated fatty acid emulsion.
  • Polyunsaturated fatty acids including long chain polyunsaturated fatty acids (LC-PUFAs)), and especially long chain omega-3 fatty acids (e.g., docosahexanoic acid (DHA) and eicosapentaenoic acid (EPA)), are known to enhance cognitive function and maintain cardiovascular health, among other health benefits (See, e.g., von Schacky, C, "Omega-3 Fatty Acids and Cardiovascular Disease,” Current Opinion in Clinical Nutrition and Metabolic Care 7, no. 2 (March 2004): 131-6 and Simopoulos, A.P., "Essential Fatty Acids in Health and Chronic Disease,” American Journal of Clinical Nutrition 79, no.
  • LC-PUFAs long chain polyunsaturated fatty acids
  • omega-3 fatty acids e.g., docosahexanoic acid (DHA) and eicosapentaenoic acid (EPA)
  • omega-3 fatty acids are effective in reducing the risk of coronary heart disease (See “FDA Announces Qualified Health Claims for Omega-3 Fatty Acids," FDA News, September 8, 2004, www.fda.gov/bbs/topics/news/2004/NEW01 115.html).
  • consumer trends indicate demands for products containing polyunsaturated fatty acids are increasing.
  • omega-3 fatty acids are nutrients required in the human diet.
  • omega-3 fatty acids are not synthesized in human body, but are found in natural sources such as the oil of certain plants and animals, including fishes, walnuts, lingonberrys, hemp, flax, chia, perilla, purslane, and algae. Since omega-3 fatty acids are not synthesized by the body, they, and their health benefits, must be obtained through food or dietary supplement. Supplementing a diet with omega-3 fatty acids frequently involves ingestion of supplements which have a fishy odor and/or taste.
  • omega-3 fatty acids are modified to make eicosanoids, which affect inflammation and other cellular functions, endogenous cannabinoids, which affect mood, behavior, and inflammation, resolvins, isofurans, isoprostanes, epoxyeicosatrienoic acids (EETs), and neuroprotectin D.
  • omega-3 fatty acids form lipid rafts affecting cellular signaling and act on DNA to activate or inhibit transcription factors for NFKB, a pro-inflammatory cytokine.
  • polyunsaturated fatty acids can become unstable and degrade.
  • various means of incorporating polyunsaturated fatty acids into functional food and beverage products have been used to try to reduce or eliminate degradation of polyunsaturated fatty acids for delivery to a consumer.
  • products have been produced as bulk oils (for spread and softgel capsules), powdered omega-3 (for cereal bars), microencapsulated omega-3 oils (for cereal bars, yogurt and beverages) and liposome/emulsion concentrates (for beverages).
  • Technology for dispersion of omega-3 fatty acids in food using whey protein as an emulsif ⁇ er and technologies using high oil loading liposome to deliver polyunsaturated fatty acids have also been developed.
  • omega-3 fatty acids are desirable to consumers without the acid becoming unstable or degrading.
  • At least some prior attempts to include omega-3 -fatty acids in beverage products have shown the majority of the nutrients to be present as sediment and thus not entirely available for continuous and complete consumption. For example, milk protein based omega-3 powder settles down quickly in high acid juice. Pectin or other hydrocolloids may be added to keep the powder suspended and protected.
  • Non-milk protein based omega-3 powder may be added in juice without the presence of hydrocolloids, however, heavy sediment has been observed, especially in clear juice and juice drinks. Other developments have been applied to juice but resulted in heavy fishy notes and taste development during process and/or storage. Thus, it would be desirable to provide a nutritious beverage product wherein the omega-3 -fatty acids remain dispersed, aesthetically pleasing, stable after pasteurization and/or offer high bioavailability to consumers.
  • the present invention relates to a beverage product composition
  • a beverage product composition comprising at least one beverage base and at least one polyunsaturated fatty acid emulsion, said emulsion comprising a continuous liquid phase; an emulsif ⁇ er; and a discontinuous liquid phase comprising a blend including a polyunsaturated fatty acid source and a dispersing agent, the polyunsaturated fatty acid source comprising at least one polyunsaturated fatty acid, wherein the weight ratio of the fatty acid source to the dispersing agent in the blend ranges from about 9:1 to about 1 :10.
  • FIG. 1 Effects on plasma phospholipid (PL) DHA content of healthy 4 to 6 and 7 to 12 year old children after consumption of approximately 180 mL of the beverage product of the present invention containing either 50 mg (low dose) or 100 mg (high dose) of DHA daily for about 6 weeks.
  • PL phospholipid
  • this disclosure encompasses beverage product compositions, specifically juice beverages comprising at least one polyunsaturated fatty acid emulsion described herein and a method for making a stable beverage product with an increased bioavailability of polyunsaturated fatty acids.
  • the formation of a stable emulsion according to embodiments of the present invention inhibits, reduces, or suppresses the oxidation, and the associated fishy odor and smell, of the LC-PUFAs. Additionally, the formation of a stable emulsion allows for its inclusion into the beverage product of certain embodiments the present invention in order to deliver an aesthetically
  • the emulsion comprises an emulsion concentrate.
  • beverage emulsion concentrates beverages and the like; polyunsaturated fatty acids, and particularly LC-PUFAs, and their health benefits, may be provided to the consumer in a stable and well dispersed form.
  • At least some embodiments of the present invention provide a beverage product with high bioavailable PUFAs in a non-sedimentary form to allow for more complete consumption of the PUFAs in the beverage by consumers.
  • a beverage product comprising a beverage base supplemented with the emulsion as described herein comprising PUFAs, particularly LC-PUFAs, and
  • the present invention are able to offer a novel method for more complete consumption of PUFAs in the beverage in order to provide an effective increase in the plasma PL DHA content.
  • beverage base refers to the type of fluid or liquid that is included in the beverage of the present invention. Accordingly to embodiments of the present invention, the beverage base may include, but is not limited to, pulp and pulp- free citrus and non-citrus fruit juices, fruit drink, vegetable juice, vegetable drink, milk,
  • beverage base may also be carbonated or non-carbonated.
  • the beverage base may comprise one or more fruit juices or fruit drinks.
  • Fruit juices may include, but
  • 135 are not limited to, orange juice, grapefruit juice, apple juice, red grape juice, white grape juice, pear juice, concord grape juice, pineapple juice, pomegranate juice, cranberry juice, passion fruit juice, lime juice, lemon juice, mango juice, guava juice, banana juice, red and black currant juice, cashew apple juice, cantaloupe melon juice, apricot juice, blackberry juice, lingonberry juice, dewberry juice, gooseberry juice, crabapple juice,
  • the beverage base may comprise one or more vegetable juices or vegetable drinks.
  • Vegetable juices may include, but are not limited to, tomato juice, beet juice, carrot juice, celery juice, or any combination thereof.
  • the beverage base may comprise milk, including but not limited to, whole milk, 2% milk, 1% milk, fat- free milk, or any combination thereof.
  • the beverage base may comprise soy milk, including but not limited to pure soy milk, 4% soy milk, 2%, soy milk, 1% soy milk, fat- free soy milk, any varied fat percent of soy milk, or any combination thereof.
  • the beverage base may comprise tea, including but not limited to green tea, black tea, oolong tea, white tea, red tea, herbal tea,
  • caffeinated tea decaffeinated tea, hot tea, iced tea or any combination thereof.
  • the beverage base may comprise a carbonated beverage, including but not limited to, colas and sodas.
  • the beverage base may comprise coffee, including but not limited to regular caffeinated coffee, partially or totally decaffeinated
  • the beverage base may comprise water, including but not limited to, distilled water, spring water, filtered water, flavored water, and combinations thereof. [0023] According to some embodiments, the beverage base may comprise other
  • beverage products such as smoothies, yogurt drinks, hot chocolate, energy drinks, sports drinks, and combinations thereof.
  • Emulsions such as smoothies, yogurt drinks, hot chocolate, energy drinks, sports drinks, and combinations thereof.
  • emulsion concentrate refers to an emulsion which may be used to produce a final product emulsion having lower concentrations of emulsif ⁇ er and
  • the emulsion concentrate may comprise a beverage emulsion concentrate which can be combined with a beverage base to form the beverage product of the present invention.
  • the emulsion concentrate is easily dispersed within a continuous liquid phase, without further homogenization
  • emulsion concentrates allows for the storage of LC-PUFAs in a stable and compact form for storage as well as transport before being dosed into a final emulsion form and included in a beverage product for consumption by a consumer.
  • homogenization of the emulsion concentrate may be carried out in a smaller scale than homogenization of a final emulsion form to be consumed by a consumer.
  • Embodiments of the emulsion of the present invention comprise a continuous liquid phase, an emulsifier, and a discontinuous liquid phase.
  • emulsion refers to an immiscible mixture of a continuous liquid phase and a discontinuous liquid phase.
  • continuous liquid phase refers to the
  • discontinuous liquid phase refers to the multiplicity of discrete elements dispersed within, and immiscible with, the continuous liquid phase.
  • embodiments of the discontinuous liquid phase include a blend including a dispersing agent and a LC-PUFA source.
  • the LC-PUFA source includes at least one LC-
  • LC-PUFA refers to any polyunsaturated carboxylic acid or organic acid with a long aliphatic tail. It should also be understood by a person of ordinary skill in the
  • emulsifier refers to any substance which increases the
  • the emulsifier may be at least partially soluble in the continuous liquid phase, the discontinuous liquid phase, or both.
  • the continuous liquid phase may be any liquid which is compatible with the LC-PUFA, the discontinuous liquid phase, and the emulsifier.
  • the continuous liquid phase may be, but is not limited to, a consumer product capable of ingestion so as to provide for delivery of the LC-PUFA to a consumer.
  • the continuous liquid phase may include, but is not limited to, water, carbonated water, syrup, diet beverages, carbonated soft drinks, fruit juices, vegetable juices, isotonic beverages, non-isotonic beverages, soft drinks containing fruit juice, coffee, tea, other aqueous liquids, pharmaceutical excipients, natural sweeteners, synthetic sweeteners, caloric sweeteners, non-caloric sweeteners, sodium benzoate,
  • EDTA ethylenediaminetetraacetic acid
  • the continuous liquid phase may be acidic.
  • the continuous liquid phase may have a pH ranging from about 2 to about 7. In another embodiment, the continuous liquid phase may have a pH from about
  • the continuous liquid phase includes at least one polyphenol.
  • the polyphenol may inhibit, suppress, or reduce degradation of the LC- PUFA and prevents lipid oxidation.
  • the polyphenol may also prevent any odor or taste of the LC-PUFA from being perceived by a consumer.
  • polyphenols may inhibit, suppress, or reduce degradation of the LC- PUFA and prevents lipid oxidation.
  • the polyphenol may also prevent any odor or taste of the LC-PUFA from being perceived by a consumer.
  • polyphenols may inhibit, suppress, or reduce degradation of the LC- PUFA and prevents lipid oxidation.
  • polyphenol may also prevent any odor or taste of the LC-PUFA from being perceived by a consumer.
  • polyphenols may also prevent any odor or taste of the LC-PUFA from being perceived by a consumer.
  • polyphenols examples include, but are not limited to, polyphenols found naturally in a variety of foods including
  • the polyphenol may comprise a phenolic acid or a flavonoid.
  • phenolic acids include, but are not limited to, cinnamic acid or benzoic acid.
  • Flavonoids which may be used with embodiments of this invention included flavonols, flavones, flavanones, flavanols, isoflavones, anthocyanidins, tannins, and stilbenes, for example.
  • the polyphenol may comprise a flavonoid such as quercetin, proanthocyanidin, catechin, resveratrol, and procyanidin, for instance.
  • the polyphenol may comprises a catechin selected from the group consisting of (+)-catechin, (-)-epicatechin, (-)-epicatchin gallate, (-)-epigallocatechin, and epigallocatechin gallate.
  • suitable polyphenols may be
  • antioxidants 245 included in the emulsions in commercial available antioxidants such as the antioxidants listed in Table 1 below:
  • the polyphenol may
  • the polyphenol may be present in the emulsion in an amount ranging from about 0.01 % by weight of the emulsion to about 5 % by weight of the emulsion. Still more particularly, the polyphenol may be present in the emulsion in an amount ranging from about 0.1 % by weight of the
  • the continuous liquid phase may additionally include a water dispersible bioactive.
  • water dispersible bioactive refers to materials which are both dispersible in water and soluble in water.
  • Suitable water dispersible bioactives for embodiments of the present invention include, but are not 260 limited to, lutein, ⁇ -carotene, lycopene (e.g., from tomato), astaxanthin, zeaxanthin, enzymes such as papain (e.g., from papaya), carotenoids (e.g., from watercress), eucalyptol (e.g., from basil or rosemary), eugerol (e.g., from basil), gingerol (e.g., from ginger), avenacoside (e.g., from oats), phenolic acids such as gallic acid (e.g., from blueberries) or rosmarinic acid (e.g., from rosemary), flavonoids (e.g.
  • quercetin e.g., from blueberries, grape seeds, grapes, mate, or green tea
  • catechins e.g., from green tea
  • anthocyanins e.g., from grape seeds, grapes, or blueberries
  • phytoestrogen e.g., from red clover
  • naringin e.g., from grapefruit
  • coumarins e.g., from oats
  • proanthocyanidins e.g., from grape seeds, green tea, guarana, or mate
  • curcuminoids e.g., from tumeric
  • caramel coloring vitamins such as
  • Vitamin E e.g., from cucumber
  • Vitamin K e.g., from alfalfa
  • any natural or synthetic food grade colored or uncolored material which absorbs UV light or any other material understood by a person of ordinary skill in the art to be a suitable water dispersible bioactive, for example. Additional water dispersible bioactives which may be used in embodiments of the present invention are found in
  • the water dispersible bioactives may be present in the continuous liquid phase in an amount ranging from about 0% by weight of the continuous liquid phase to about 20 % by weight of the continuous liquid phase. According to other embodiments of the
  • the water dispersible bioactives may be present in the continuous liquid phase in an amount ranging from about 50 mg to about 100 mg.
  • the water dispersible bioactives provide photo-oxidative protection such that the oxidation of the polyunsaturated fatty as is reduced, inhibited or suppressed. It is believed that the water
  • Embodiments of the present invention also include a discontinuous liquid
  • Suitable LC-PUFA sources for embodiments of the present invention include any LC-PUFA source which comprises at least one LC-PUFA capable of being
  • the LC- PUFA source may be a LC-PUFA oil or a LC-PUFA powder, or combinations thereof.
  • Suitable LC-PUFA oils can be derived from algae, fish, animals, plants, or combinations thereof, for example.
  • the blend may be referred to herein as an "oil blend”.
  • LC-PUFA oils for embodiments of the present invention include omega-3 fatty acid oils, omega-6 fatty acid oils and omega- 9 fatty acid oils, for instance.
  • omega-3 fatty acid oils examples include, but are not limited to, alpha-linolenic acid oil, eicosapentaenoic acid oil, docosahexaenoic acid oil, and combinations thereof.
  • the omega-3 fatty acid may be synthesized.
  • Suitable omega-6 fatty acid oils for embodiments of this invention include, but are not limited to, gamma- linolenic acid oil, and arachidonic acid oil.
  • suitable omega-3 fatty acid oils include fish oils, (e.g., menhaden oil, tuna oil, salmon oil, bonito oil, and cod oil), microalgae docosahexaenoic acid oil, microalgae omega-3 oils, and the like, or combinations thereof.
  • fish oils e.g., menhaden oil, tuna oil, salmon oil, bonito oil, and cod oil
  • microalgae docosahexaenoic acid oil e.g., fish oils, and the like, or combinations thereof.
  • the fish oils may be crude or refined and also may be enzyme treated.
  • suitable omega-3 fatty acid oils may include commercially available omega-3 fatty acid oils such as Microalgae DHA oil (from Martek, Columbia, MD), OmegaPure (from Omega Protein, Houston, TX), Marinol C-38 (from Lipid Nutrition, Channahon, IL), Bonito oil and MEG-3 (from Ocean Nutrition, Dartmouth, NS), Evogel (from Symrise, Holzminden, Germany), Marine Oil, from tuna or salmon (from Arista Wilton, CT), OmegaSource 2000, Marine Oil, from menhaden Marine Oil, from cod (from OmegaSource, RTP, NC).
  • the polyunsaturated fatty acids may include marine phospholipids such as krill oil, scallop oil, or other oils including astaxanthin.
  • the LC-PUFA source is present in the emulsion concentrate in an amount ranging from about 0.5 % by weight of the emulsion concentrate to about 35 % by weight of the emulsion concentrate. More particularly, the LC-PUFA source is present in the emulsion concentrate in an amount ranging from about 2 % by weight of the emulsion concentrate to about 30 % by weight of the emulsion concentrate.
  • the LC-PUFA source is present in the emulsion concentrate in an amount ranging from about 5 % by weight of the emulsion concentrate to about 20 % by weight of the emulsion concentrate. Still more particularly, the LC-PUFA source is present in the emulsion concentrate in an amount ranging from about 15 % by weight of the emulsion to about 20 % by weight of the emulsion concentrate.
  • the LC-PUFA source is present in the emulsion in an amount ranging from about 0.002% by weight of the emulsion to about 35 % by weight of the emulsion. More particularly, the LC-PUFA source is present in the emulsion in an amount ranging from about 0.005 % by weight of the emulsion to about 30% by weight of the emulsion. Still more particularly, the LC-PUFA source is present
  • the dispersing agent is selected from vitamin E, ascorbyl palmitate, rosemary extract, a terpene, a flavor oil, a vegetable oil, or an essential oil and the like, and combinations thereof. According to particular embodiments
  • the essential oil may be a citrus oil, leaf oil, spice oil, peel oil, and combinations thereof.
  • suitable essential oils include, but are not limited to, lemon oil, orange oil, lime oil, grapefruit oil, mandarin oil, bitter orange oil, mint oil, peppermint oil, rosemary oil, flax seed oil, cranberry seed oil, bergamot oil, and combinations thereof.
  • the dispersing agent comprises a terpene
  • suitable terpenes include, but are not limited to, d-limonene, 1-limonene, dl-limonene (i.e., greater than 99 wt% dl-limonene), orange distillate oil (i.e., greater than 97 wt% dl- limonene) and combinations thereof.
  • the blend may additionally include a weighing agent.
  • Suitable weighing agents for embodiments of the present invention include
  • the continuous liquid phase further comprises a sugar.
  • suitable sugars for embodiments of the present invention include a monosaccharide, a
  • 355 disaccharide, a trisaccharide, an oligosaccharide, or combinations thereof.
  • continuous liquid phases which include a sugar include carbonated beverages with caloric sweeteners, fruit juices, and combinations thereof.
  • the continuous liquid phase may also include a high- potency sweetener.
  • suitable high-potency sweeteners include dulcoside A,
  • the weighing agent in such embodiments increases the density of the discontinuous liquid phase so that the discontinuous liquid phase does not float to the top of the emulsion and agglomerate.
  • Such functionality is particularly useful in embodiments where the continuous liquid phase contains sugar
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. In other embodiments, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 5% to about 35% of the discontinuous liquid phase.
  • the weighing agent comprises brotmnafed vegetable oil CBVO
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 30% of the discontinuous liquid phase. More specifically, the brorainated vegetable oil ( BVO) weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 20% of the
  • the weighing agent comprises glyceryl ester of wood rosin (i.e., ester gum)
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the glyceryl ester of wood rosin weighing agent may be present in the discontinuous liquid phase in an amount ranging from about
  • the weighing agent comprises sucrose di acetate hexa-isob ⁇ tyrale (SAIB)
  • SAIB sucrose di acetate hexa-isob ⁇ tyrale
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More .specifically, the suc ⁇ xse diacetate hexa-isobutyrate weighing agent may be present in the discontinuous liquid phase in an amount ranging
  • the weighing agent comprises refined gum dar ⁇ ar
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the refined gum damar weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to
  • the weighing agent comprises ganuaba wax
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the ganuaba wax weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 35% of the discontinuous
  • the weighing agent comprises benzyl bcnzoate
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 40% of the discontinuous liquid phase. More specifically, the benzyl bcnzoate weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 30% of the discontinuous liquid phase.
  • the weighing agent comprises polyglyceryi ester
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the polyglyecryl ester weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 35% of the discontinuous liquid phase. In embodiments where the weighing agent comprises polyglyceryi ester, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the polyglyecryl ester weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 35% of the discontinuous liquid phase. In embodiments where the weighing agent
  • the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 30% of the discontinuous liquid phase. More specifically, the glyceryl tribenzoate weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 25% of the discontinuous liquid phase.
  • the amount of dispersing agent in the blend should be sufficient to create a stable emulsion rather than just masking the flavor or smell of the LC-PUFA.
  • the amount of dispersing agent should be sufficient to provide oxidative stability (i.e., inhibit, suppress, or reduce oxidation of the LC-PUFA) and stabilize the resulting emulsion.
  • dispersing agent in the blend can range from about 9:1 to about 1 :10. More particularly, the weight ratio of the LC-PUFA source to the dispersing agent in the blend can range from about 5 : 1 to about 1 :1. Still more particularly, the weight ratio of the LC-PUFA source to the dispersing agent in the blend can range from about 4: 1 to about 3:1. [0046] In particular embodiments wherein the emulsion comprises an emulsion
  • the blend may be present in the emulsion concentrate in an amount ranging from about 0.5 % by weight of the emulsion concentrate to about 35 % by weight of the emulsion concentrate. More particularly, the blend is present in the emulsion in an amount ranging from about 2 % by weight of the emulsion concentrate to about 30 % by weight of the emulsion concentrate. Still more particularly, the blend is present in the
  • the blend in an amount ranging from about 5 % by weight of the emulsion concentrate to about 20 % by weight of the emulsion concentrate. Still more particularly, the blend is present in the emulsion concentrate in an amount ranging from about 10 % by weight of the emulsion concentrate to about 20 % by weight of the emulsion concentrate. [0047] In particular embodiments, the blend may present in the emulsion in an
  • the blend may be present in the emulsion in an amount ranging from about 0.005 % by weight of the emulsion to about 30 % by weight of the emulsion. Still more particularly, the blend may be present in the emulsion in an amount ranging from about 0.01% by weight of the emulsion to about 20 % by weight of
  • the blend may be present in the emulsion in an amount ranging from about 0.02% by weight of the emulsion to about 20 % by weight of the emulsion.
  • the blend may further comprise a folded oil.
  • the folded oils further improve the oxidative stability and
  • Suitable folded oils for embodiments of the present invention include, but are not limited to, 4-fold bergamot oil, bergaptene free bergamot oil, terpeneless grapefruit oil, 4-fold grapefruit oil, 5 -fold grapefruit oil, 6-fold grapefruit oil, 10-fold grapefruit oil, high aldehyde grapefruit oil, 5-fold grapefruit juice extract, 7-fold 460 grapefruit juice extract, terpeneless lemon oil, 2-fold lemon oil, 3 -fold lemon oil, 5 -fold lemon oil, 10-fold lemon oil, 13-fold lemon oil, washed 5-fold lemon oil, 10-fold lemon oil, Sesquiterpeneless lemon oil, FC free lemon oil, distilled 3-fold lime oil, distilled 4- fold lime oil, distilled 5 -fold lime oil, distilled terpeneless lime oil, distilled sesquiterpeneless lime oil, distilled washed 5 fold lime oil, cold pressed 3 -fold lime oil,
  • the discontinuous liquid phase may comprise a terpeneless oil.
  • the folded oil may be present in the discontinuous liquid phase in an amount ranging from about 1 % by
  • the folded oil may be present in the discontinuous liquid phase in an amount ranging from about 7.5 % by weight of the discontinuous liquid phase to about 45 % by weight of the discontinuous liquid phase. Still more particularly, the folded oil may be present in the discontinuous liquid phase in an amount ranging from
  • the emulsion may comprise a continuous liquid phase, an emulsifier, and a discontinuous liquid phase comprising a blend including a polyunsaturated fatty acid source and a folded oil.
  • the emulsion might not include a dispersing agent. Rather, the folded oil helps to form a stable emulsion wherein the degradation of the polyunsaturated fatty acid is inhibited, suppressed, or reduced.
  • the discontinuous liquid phase may also include medium chain triglycerides. In particular embodiments, the medium chain triglycerides
  • the medium chain triglycerides may be present in the discontinuous liquid phase in an amount ranging from about 1 % by weight of the discontinuous liquid phase to about 60 % by weight of the discontinuous liquid phase.
  • the medium chain triglycerides may be present in the discontinuous liquid phase in an amount ranging from about 7.5 % by weight of the discontinuous liquid phase to about 40 % by weight of the discontinuous liquid phase. Still more particularly, the medium chain triglycerides may be present in the discontinuous liquid phase in an amount ranging from about 10 % by weight of the discontinuous liquid phase to about 30
  • the discontinuous liquid phases may also include other components such as oil soluble vitamins (e.g., vitamin A, vitamin D, vitamin E, or Vitamin K), phytochemicals, and other lipid nutrients.
  • the discontinuous liquid phase may additionally include other components such as oil soluble vitamins (e.g., vitamin A, vitamin D, vitamin E, or Vitamin K), phytochemicals, and other lipid nutrients.
  • the discontinuous liquid phase may additionally include other components such as oil soluble vitamins (e.g., vitamin A, vitamin D, vitamin E, or Vitamin K), phytochemicals, and other lipid nutrients.
  • the discontinuous liquid phase may additionally include other components such as oil soluble vitamins (e.g., vitamin A, vitamin D, vitamin E, or Vitamin K), phytochemicals, and other lipid nutrients.
  • the discontinuous liquid phase may additionally include other components such as oil soluble vitamins (e.g., vitamin A, vitamin D, vitamin E, or Vitamin K), phytochemicals, and other lipid nutrients.
  • the discontinuous liquid phase may additionally include other components such as oil soluble vitamins (e.
  • oil dispersible bioactive refers to materials which are both dispersible in oil and soluble in oil.
  • oil dispersible bioactives for embodiments of the present invention include, but are not limited to, oxygenated carotenoids, such as lutein (e.g., from tomato), astaxanthin and non- oxygenated carotenoids, such as ⁇ -carotene and lycopene, and combinations thereof or
  • suitable oil dispersible bioactives may include enzymes such as papain (e.g., from papaya), carotenoids (e.g., from watercress), eucalyptol (e.g., from basil or rosemary), eugerol (e.g., from basil), gingerol (e.g., from ginger), avenacoside (e.g., from oats), phenolic acids such as gallic acid (e.g., from papaya), carotenoids (e.g., from watercress), eucalyptol (e.g., from basil or rosemary), eugerol (e.g., from basil), gingerol (e.g., from ginger), avenacoside (e.g., from oats), phenolic acids such as gallic acid (e.g., from papaya), carotenoids (e.g., from watercress), eucalyptol (e.g., from basil or rosemary), e
  • rosmarinic acid e.g., from rosemary
  • flavonoids e.g., from watercress or willow
  • quercetin e.g., from blueberries, grape seeds, grapes, mate, or green tea
  • catechins e.g., from green tea
  • anthocyanins e.g., from grape seeds, grapes, or blueberries
  • phytoestrogen e.g., from red clover
  • naringin e.g., from grapefruit
  • coumarins e.g., from oats
  • proanthocyanidins e.g., from grape seeds, green tea
  • curcuminoids e.g., from tumeric
  • caramel coloring any other material understood by a person of ordinary skill in the art to be a suitable water dispersible bioactive, for instance.
  • Additional oil dispersible bioactives which may be used in embodiments of the present invention are found in "Lipid Oxidation", by E.N. Frankel, pages 209-298, 2 nd Edition, The Oily Press, 2005. According to particular
  • the oil dispersible bioactives may be present in the discontinuous liquid phase in an amount ranging from about 0% by weight of the discontinuous liquid phase to about 20 % by weight of the discontinuous liquid phase. According to other embodiments of the invention, the oil dispersible bioactives may be present in the discontinuous liquid phase in an amount ranging from about 50 mg to about
  • the oil dispersible bioactives provide photo-oxidative protection such that the oxidation of the polyunsaturated fatty as is reduced, inhibited or suppressed. It is believed that the oil dispersible bioactive absorbs some UV light such that polyunsaturated fatty acid is exposed to less light. In some embodiments of the present in invention which are
  • the oil soluble bioactives may hydrate a portion of the skin of the consumer ingesting the emulsion.
  • the discontinuous liquid phase may also include an oil blend antioxidant.
  • oil blend antioxidants for embodiments of the present invention include, but are not limited to, butylated hydroxytoluene (BHT), butylated
  • the oil blend antioxidant may be present in the discontinuous liquid phase in an amount ranging from about 0 % by weight of the discontinuous liquid phase to about 5 % by weight of the discontinuous liquid phase.
  • Embodiments of the present invention include emulsions in which the discontinuous liquid phase is present in the emulsion in the form of particles.
  • these discontinuous liquid phase particles have an average particle size from about 0.1 ⁇ m to about 1.5 ⁇ m. More particularly, the discontinuous liquid phase particles may have an average particle size from about 0.1 ⁇ m to about l.O ⁇ m. Still more
  • the discontinuous liquid phase particles may have an average particle size from about 0.15 ⁇ m to about 0.7 ⁇ m.
  • Emulsifiers which may be used in the present invention include any emulsifier compatible with the LC -PUFAs and the dispersing agents used in the emulsion. Natural or synthetic emulsifiers may be suitable for embodiments of the
  • the emulsifier may be a modified natural emulsifier. That is, the emulsifier may be chemical modified, enzymatically modified, physically modified, or combinations thereof.
  • the emulsif ⁇ er is a food grade emulsif ⁇ er. Examples of other suitable emulsifiers for
  • 560 embodiments of this invention include, but are not limited to, pectin, ⁇ -pectin, gum ghatti, modified gum arabic (e.g., TicamulsionTM, from TIC Gums, Belcamp, MD), gum acacia (e.g., EficaciaTM, from Colloides Naturels International (CNI), Bridgewater, NJ), Quillaja extract (e.g., Q NaturalelOO from Desert King, San Diego, CA and National Starch Chemical Bridgewater, NJ), modified food starch (e.g., from National Starch &
  • the emulsion comprises a fruit juice or drink containing a fruit juice (e.g., orange juice or grapefruit juice)
  • citrus oil may be present in the continuous liquid phase, which aids in the chemical stability of the emulsion and thus,
  • the emulsifier may comprise a carbohydrate-based macromolecule.
  • suitable carbohydrate-based macromolecules include gum acacia, modified food starch, gum ghatti, pectins (e.g., beta-pectin), modified gum acacia,
  • the emulsifier is present in the emulsion in an amount ranging from about 0.0002% by weight of the emulsion to about 45 % by weight of the emulsion. In other embodiments, the emulsifier is present in the emulsion in an amount ranging from about 0.001 % by weight of the emulsion to about 25 % by weight
  • the emulsifier is present in the emulsion in an amount ranging from about 0.01 % by weight of the emulsion to about 20 % by weight of the emulsion. In still other embodiments, the emulsifier is present in the emulsion in an amount ranging from about 5 % by weight of the emulsion to about 20 % by weight of the emulsion.
  • the emulsion may also include a stabilizing agent to further stabilize the emulsion and also improve the taste profile and/or improve the shelf life of the emulsion.
  • suitable stabilizing agents include, but are not limited to, vitamin C, polyphenols from fruit and vegetable sources, such as rosemary extract, tea polyphenols and grape seed extracts,
  • the stabilizing agent may be at least partially soluble in the continuous liquid phase, the discontinuous liquid phase, or both.
  • an emulsion comprising a stabilizing agent has a shelf life of more than 3 months. As used herein, "shelf-life"
  • 595 refers to a time period within which embodiments of emulsions may be stored and remain suitable for consumer use.
  • the emulsion further comprises a surfactant which further reduces the surface tension between the oil phase and the suspension medium, thereby improving the stability of the emulsion and homogenization of the emulsion.
  • surfactants for embodiments of this invention include, but are not limited to, dioctyl succinate sulfate sodium salt (DSS), medium chain triglyceride (MCT), propylene glycol alginate (PGA) and combinations thereof.
  • the surfactant may be at least partially soluble in the continuous liquid phase, the discontinuous liquid phase, or both.
  • methods for making an emulsion comprise providing a first liquid, providing a second liquid, and combining the first liquid, the second liquid, and an emulsifier so as to form the emulsion.
  • Embodiments of the second liquid comprise a blend that includes a long chain polyunsaturated fatty acid source and a dispersing agent.
  • chain polyunsaturated fatty acid sources include at least one long chain polyunsaturated fatty acid.
  • emulsions comprise a continuous liquid phase including the first liquid and a discontinuous liquid phase including the second liquid.
  • Embodiments of the emulsion may be any of the emulsions described above.
  • the first liquid may be any of the emulsions described above.
  • Embodiments of the second liquid may include dispersing agents similar to any of the dispersing agents above.
  • LC-PUFA sources included in embodiments of the second liquid may be any of the LC-PUFA sources described above.
  • embodiments of the second liquid may comprise the same components
  • Suitable emulsif ⁇ ers may be similar to the emulsif ⁇ ers described above.
  • Embodiments of the present invention include methods wherein the step of combining comprises combining the first liquid, the second liquid, and the emulsifier sequentially or simultaneously.
  • the dispersing 625 agent is combined with the long chain polyunsaturated fatty acid source to form the blend in the second liquid and then the first liquid, the second liquid, and the emulsifier are combined to form the emulsion.
  • the dispersing agent is combined with the LC-PUFA source and emulsifier to form the blend in the second liquid and then the first liquid and the second liquid are combined to form
  • the step of combining comprises mixing the emulsifier into the first liquid, mixing the dispersing agent with the polyunsaturated fatty acid source to form the blend in the second liquid, and then homogenizing the first liquid and the second liquid to form the emulsion.
  • the first liquid and the second liquid are examples of the first liquid and the second liquid.
  • emulsifier may be used to form a mucilage or emulsifier solution. Then, the mucilage comprising the first liquid and the emulsifier may be combined with the second liquid, which includes the dispersing agent mixed with the polyunsaturated fatty acid, to form a pre-emulsion. The pre-emulsion can then be homogenized to form the emulsion.
  • 640 emulsifier may be combined simultaneously by a homogenizing process.
  • the step of combining may comprise forming an emulsion concentrate comprising a portion of the first liquid, the second liquid, and the emulsifier and then adding the remainder portion of the first liquid to the emulsion concentrate to form the emulsion comprising the discontinuous liquid phase and the continuous liquid phase.
  • the present disclosure also provides for a method of making an emulsion comprising providing a first liquid, providing a second liquid, and combining the first liquid, the second liquid, and an emulsifier so as to form an emulsion concentrate.
  • Embodiments of the second liquid comprise a blend that includes a long chain polyunsaturated fatty acid source and a dispersing agent.
  • the emulsion concentrate may
  • Embodiments of the first liquid and third liquid may comprise components of the continuous liquid phase as described above.
  • the emulsion may comprise a beverage, a herbal
  • composition or a pharmaceutical composition, for example.
  • Embodiments of the present invention may also include emulsions which are spray dried, spray dried and coated, or spray dried and agglomerated. It should be understood by a person of ordinary skill in the art that embodiments of the emulsion may be spray dried by any method known in the art for spray drying. In addition, it should be
  • embodiments of the spray dried emulsions may be coated or agglomerated with other components.
  • embodiments of the spray dried emulsions may be coated or agglomerated by sugars and maltodextrin or combinations thereof.
  • embodiments of the spray dried emulsions may be coated or
  • the spray dried, spray dried and coated, and/or spray dried and agglomerated emulsions can be added to liquid compositions wherein the emulsions disperse and form a liquid emulsion.
  • embodiments of spray dried, spray dried and coated, or spray dried and agglomerated may be added to a beverage to form a
  • the emulsions created by embodiments of the method of the present invention are stable and provide protection for the long chain polyunsaturated fatty acid from oxidation.
  • the embodiments of the emulsions of the present invention may improve the bioavailability of the polyunsaturated fatty acids as compared to bulk
  • the discontinuous liquid phase plays a role in determining the effectiveness of the emulsification/homogenization processes. Since LC-PUFA sources, such as LC-PUFA oils, are hydrophobic and viscous, these properties can reduce the effectiveness of homogenization. Therefore, the dispersing agent is included in the discontinuous liquid phase to reduce the viscosity of the discontinuous liquid phase to a viscosity lower than
  • the viscosity of the LC-PUFA source 685 the viscosity of the LC-PUFA source. Inclusion of the dispersing agent in the discontinuous liquid phase also results in the discontinuous liquid phase having a surface tension less than the surface tension of the LC-PUFA source. Consequently, the discontinuous liquid phase, which includes the LC-PUFA source, is more easily dispersed in the emulsion. 690 [0070] Moreover, having smaller discontinuous liquid phase particle size and higher continuous liquid phase viscosity can improve emulsion stability. Addition of the dispersing agent to the emulsion to form the blend having the LC-PUFA source also reduces the discontinous liquid phase particle size to improve homogenization efficiency. [0071] Furthermore, Stokes' law indicates that the discontinuous liquid phase
  • the discontinuous liquid phase density affects emulsion's stability.
  • Stokes' law indicates that emulsion stability can be enhanced by reducing the density difference between the continuous liquid phase and discontinuous liquid phase.
  • the discontinuous liquid phase density can be adjusted.
  • the LC-PUFA has first vicosity and the dispersing agent has a second 700 viscosity less than the first density.
  • a higher percentage of the dispersing agent in the discontinuous liquid phase results in a lower discontinuous liquid phase density.
  • the discontinuous liquid phase density decreases as the percentage of 705 dispersing agent in the blend increases (i.e., the percentage of LC-PUFA oil percentage decreases).
  • PUFA source is that at least a portion of any degradation or oxidation of the LC-PUFA is inhibited, suppressed, or reduced by forming the emulsion having the long chain 710 polyunsaturated fatty acid source.
  • substantially all of the degradation of the long chain polyunsaturated fatty acid is inhibited, suppressed, or reduced by forming the emulsion having the long chain polyunsaturated acid source.
  • forming the emulsion having the at least one the long chain 715 polyunsaturated acid substantially masks the odor or the taste of the at least one long chain polyunsaturated fatty acid source (e.g., a fishy odor).
  • Blending the dispersing agent with the LC-PUFA source also reduces oxidation of the LC-PUFA source. For example, it is believed that dispersing agents which are more polar form a protective layer between the LC-PUFA source and the continuous liquid phase.
  • antioxidant 720 dispersing agents such as vitamin E, ascorbyl palmitate, and rosemary extract help to protect the LC-PUFA from oxidation. Furthermore, the reduction of degradation of the LC-PUFA increases the emulsion shelf-life.
  • embodiments of emulsions of the present invention may be functional in compositions such as beverage product compositions, herbal compositions,
  • the present invention provides for a beverage product comprising a beverage base and the emulsion described herein wherein the LC-PUFA is substantially, completely soluble, undetectable to the taste
  • LC-PUFA particularly omega-3 fatty acids, namely DHA and EPA, can be ingested by a consumer with substantially less undesirable odor, taste, or like property.
  • incorporating the polyunsaturated fatty acid into beverages may be done in a variety of
  • the polyunsaturated fatty acid may be incorporated within the beverage by adding the emulsion to a beverage base in a mixer.
  • Another way may include adding the emulsion to the final beverage product before pasteurization. Either of these methods provides for a final beverage product that provides a nutritious beverage, is aesthetically pleasing, and provides a high bioavailability of desirable polyunsaturated
  • fatty acids such as omega-3-fatty acids
  • a mixer When a mixer is used to incorporate PUFAs or LC-PUFAs into some beverage embodiments of the present invention, known shear mixers may be used.
  • a low shear mixer may be provided to mix the LC-PUFA emulsion with water or another beverage base and other ingredients (e.g. vitamins, etc.).
  • the entire mixture may be passed through a pasteurizer and then filled or packaged.
  • the emulsion may be incorporated into the beverage base before pasteurization.
  • all ingredients except the emulsion may be
  • the emulsion may then be added into the mixture and then the mixture may be pasteurized for filling or packaging.
  • the PUFAs or LC-PUFAs may also be incorporated into a pasteurized beverage base mixture to produce a finalized filled or packaged product.
  • the emulsion of the present invention is water soluble and eases the dispersion of PUFAs or LC-PUFAs into the beverage base without sedimentation. Even
  • the emulsion may maintain its stability over the shelf life of the beverage when homogenized, making the emulsion particles particularly small and dispersible. For example, after 3 weeks, 9 weeks, or 11 weeks of shelf life storage, some embodiments of the beverage products of the present invention exhibited substantially no
  • the emulsions were prepared by first preparing a mucilage by weighting water content for the batch in a 600 ml beaker. The beaker was placed under a propeller 790 based agitator. Sodium benzoate was added to the mixing vortex and the emulsif ⁇ er solution was mixed for 3 minutes. Citric acid was added to the mixing vortex and the emulsif ⁇ er solution was mixed for 3 minutes. Emulsif ⁇ er was slowly added to the mixing vortex and agitation was continued for 1 hour. The emulsif ⁇ er solution was placed on a table overnight to allow foam to separate.
  • a pre-emulsion was prepared by placing the filtered emulsif ⁇ er solution
  • the mucilage was through a 100 mesh screen
  • a propeller based agitator and oil blend of DHA oil and orange distillate, medium chain triglyceride, and/or folded oil was slowly added to the mixing vortex to produce a coarse emulsion.
  • the coarse emulsion solution was transferred to the high shear mixer (Polytron PT3100 or Pri Sci 250).
  • the emulsion was prepared by running DI water through a NanoMizer and adjust the plunger speed to achieve homogenization pressure of 31 MPa (4500 psi). The pre-emulsion was homogenized twice at the desired homogenization pressure. If
  • Tables 6 and 7 summarizes the results of a particle size measurement of the emulsion and shows that addition of orange distillate, medium chain triglycerides and/or folded oils to DHA oils can significantly improve ease of emulsif ⁇ cation of DHA oils.
  • Ticamulsion 2010A, dl-limonene, and 15% Martek DHA oil were prepared using the procedures of EXAMPLE 1.
  • the omega-3 fatty acid oil was supplied by Martek Bioscience and was stabilized with an antioxidant mixture system of tocopherols,
  • the FSA instrument measured oxygen concentration at the headspace of the sample cell ( ⁇ 40 c.c. in volume or -2X10 20 oxygen molecules).
  • the SafTest® system was used to analyze the oxidative degradation of in- house Omega-3 emulsions.
  • the SafTest® system is a colorimetric method (based on the ferric thiocyanate method modified for safety reasons by replacing benzene methanol
  • Green tea polyphenols were used to examine the antioxidant efficacy of GTP in retarding off taste development due to Omega-3 oil oxidation in embodiments of the emulsion.
  • Table 10 shows the ongoing shelf stability evaluation of Fanta Orange Zero fortified with DHA oil and different additives. The results indicate that after 12 weeks of ambient storage the test samples with GTP have not developed
  • the emulsion was prepared by first preparing a mucilage by weighting
  • a pre-emulsion was prepared by placing the emulsifier solution under a propeller based agitator and oil blend of DHA oil, sucrose diacetate hexa-isobutyrate and orange distillate, medium chain triglyceride, and/or folded oil was slowly added to the mixing vortex to produce a coarse emulsion.
  • the coarse emulsion solution was
  • the emulsion was prepared by running DI water through an APV 1000 homogenizer and adjust the homogenization pressure of 4500 psi. The pre-emulsion was homogenized twice at the desired homogenization pressure. If necessary, the plunger

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Nutrition Science (AREA)
  • Food Science & Technology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Polymers & Plastics (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Dispersion Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Mycology (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Abstract

A beverage product comprising at least one beverage base and at least one polyunsaturated fatty acid emulsion, said emulsion comprising a continuous liquid phase; an emulsifϊer; and a discontinuous liquid phase comprising a blend including a polyunsaturated fatty acid source and a dispersing agent, the polyunsaturated fatty acid source comprising at least one polyunsaturated fatty acid, wherein the weight ratio of the fatty acid source to the dispersing agent in the blend ranges from about 9: 1 to about 1 :10.

Description

STABLE BEVERAGE PRODUCTS COMPRISING POLYUNSATURATED
FATTY ACID EMULSIONS
CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application is a continuation in part of U.S. Application No.
11/850,158, filed on September 5, 2007, which claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Patent Application No. 60/824,709, filed on September 6, 2006, U.S. Provisional Patent Application No. 60/888,256, filed on February 5, 2007, and U.S. Provisional Patent Application No. 60/948,338, filed on July 6, 2007, the disclosures of which are expressly incorporated herein by reference.
TECHNICAL FIELD
[0002] The present invention relates to beverage products comprising at least one beverage base and at least one polyunsaturated fatty acid emulsion.
BACKGROUND OF THE INVENTION [0003] Polyunsaturated fatty acids (including long chain polyunsaturated fatty acids (LC-PUFAs)), and especially long chain omega-3 fatty acids (e.g., docosahexanoic acid (DHA) and eicosapentaenoic acid (EPA)), are known to enhance cognitive function and maintain cardiovascular health, among other health benefits (See, e.g., von Schacky, C, "Omega-3 Fatty Acids and Cardiovascular Disease," Current Opinion in Clinical Nutrition and Metabolic Care 7, no. 2 (March 2004): 131-6 and Simopoulos, A.P., "Essential Fatty Acids in Health and Chronic Disease," American Journal of Clinical Nutrition 79, no. 3 (March 2004): 523-4.) Recent qualified studies have also indicated that omega-3 fatty acids are effective in reducing the risk of coronary heart disease (See "FDA Announces Qualified Health Claims for Omega-3 Fatty Acids," FDA News, September 8, 2004, www.fda.gov/bbs/topics/news/2004/NEW01 115.html). In addition, consumer trends indicate demands for products containing polyunsaturated fatty acids are increasing.
[0004] Essential fatty acids such as omega-3 fatty acids are nutrients required in the human diet. However, omega-3 fatty acids are not synthesized in human body, but are found in natural sources such as the oil of certain plants and animals, including fishes, walnuts, lingonberrys, hemp, flax, chia, perilla, purslane, and algae. Since omega-3 fatty acids are not synthesized by the body, they, and their health benefits, must be obtained through food or dietary supplement. Supplementing a diet with omega-3 fatty acids frequently involves ingestion of supplements which have a fishy odor and/or taste. [0005] Within the body, omega-3 fatty acids are modified to make eicosanoids, which affect inflammation and other cellular functions, endogenous cannabinoids, which affect mood, behavior, and inflammation, resolvins, isofurans, isoprostanes, epoxyeicosatrienoic acids (EETs), and neuroprotectin D. In addition, omega-3 fatty acids form lipid rafts affecting cellular signaling and act on DNA to activate or inhibit transcription factors for NFKB, a pro-inflammatory cytokine.
[0006] During storage under certain conditions, polyunsaturated fatty acids can become unstable and degrade. Thus, various means of incorporating polyunsaturated fatty acids into functional food and beverage products have been used to try to reduce or eliminate degradation of polyunsaturated fatty acids for delivery to a consumer. For example, products have been produced as bulk oils (for spread and softgel capsules), powdered omega-3 (for cereal bars), microencapsulated omega-3 oils (for cereal bars, yogurt and beverages) and liposome/emulsion concentrates (for beverages). Technology for dispersion of omega-3 fatty acids in food using whey protein as an emulsifϊer and technologies using high oil loading liposome to deliver polyunsaturated fatty acids have also been developed.
[0007] However, conventional emulsion technology, i.e., homogenizing the omega-3 fatty oils using food grade emulsifϊer (e.g., gum arabic or lecithin), gives unstable emulsions with large oil particle sizes. Maintaining both physical and chemical stability of polyunsaturated fatty acids in compositions such as beverages is particularly difficult because polyunsaturated fatty acids are prone to oxidation, which can adversely impact the organoleptic properties of these compositions. In addition, such oxidation is undesirable according to recent research because consumption of foods containing highly oxidized lipids may have adverse health implications. [0008] Furthermore, processing of typical emulsions by homogenization of the compositions comprising the polyunsaturated fatty acids requires large mixing equipment, storage, and transport requirements to facilitate delivery of these fatty acid emulsions to the consumer. Therefore, it would be desirable to provide omega-3 fatty acids to consumers without the acid becoming unstable or degrading. [0009] In particular, it would be desirable to provide omega-3 -fatty acids to consumers in a convenient beverage product. At least some prior attempts to include omega-3 -fatty acids in beverage products have shown the majority of the nutrients to be present as sediment and thus not entirely available for continuous and complete consumption. For example, milk protein based omega-3 powder settles down quickly in high acid juice. Pectin or other hydrocolloids may be added to keep the powder suspended and protected. The use of hydrocolloids, however, increases the beverage viscosity. Non-milk protein based omega-3 powder may be added in juice without the presence of hydrocolloids, however, heavy sediment has been observed, especially in clear juice and juice drinks. Other developments have been applied to juice but resulted in heavy fishy notes and taste development during process and/or storage. Thus, it would be desirable to provide a nutritious beverage product wherein the omega-3 -fatty acids remain dispersed, aesthetically pleasing, stable after pasteurization and/or offer high bioavailability to consumers.
SUMMARY OF THE INVENTION [0010] The present invention relates to a beverage product composition comprising at least one beverage base and at least one polyunsaturated fatty acid emulsion, said emulsion comprising a continuous liquid phase; an emulsifϊer; and a discontinuous liquid phase comprising a blend including a polyunsaturated fatty acid source and a dispersing agent, the polyunsaturated fatty acid source comprising at least one polyunsaturated fatty acid, wherein the weight ratio of the fatty acid source to the dispersing agent in the blend ranges from about 9:1 to about 1 :10.
BRIEF DESCRIPTION OF THE DRAWINGS
[0011] FIG. 1 Effects on plasma phospholipid (PL) DHA content of healthy 4 to 6 and 7 to 12 year old children after consumption of approximately 180 mL of the beverage product of the present invention containing either 50 mg (low dose) or 100 mg (high dose) of DHA daily for about 6 weeks.
DETAILED DESCRIPTION
[0012] As summarized above, this disclosure encompasses beverage product compositions, specifically juice beverages comprising at least one polyunsaturated fatty acid emulsion described herein and a method for making a stable beverage product with an increased bioavailability of polyunsaturated fatty acids. The formation of a stable emulsion according to embodiments of the present invention inhibits, reduces, or suppresses the oxidation, and the associated fishy odor and smell, of the LC-PUFAs. Additionally, the formation of a stable emulsion allows for its inclusion into the beverage product of certain embodiments the present invention in order to deliver an aesthetically
100 pleasing and more complete health-beneficial drink. In particular embodiments, the emulsion comprises an emulsion concentrate. By producing embodiments of the present invention as beverage emulsion concentrates, beverages and the like; polyunsaturated fatty acids, and particularly LC-PUFAs, and their health benefits, may be provided to the consumer in a stable and well dispersed form.
105 [0013] At least some embodiments of the present invention provide a beverage product with high bioavailable PUFAs in a non-sedimentary form to allow for more complete consumption of the PUFAs in the beverage by consumers. With the consumption of such a product comprising a beverage base supplemented with the emulsion as described herein comprising PUFAs, particularly LC-PUFAs, and
110 specifically omega-3 fatty acids such as DHA, the present inventors have found that plasma phospholipid (PL) DHA content may increase. Such study has been shown in at least healthy 4 to 6 and 7 to 12 year old children consuming about 180 mL. At least some embodiments of the present invention, therefore, are able to provide a product wherein the daily consumption of said product may increase the plasma PL DHA content after 6
115 weeks by at least about 20%, at least about 25%, at least about 32%, at least about 40%, or at least about 47% (mole % of total fatty acids). As shown in FIG. 1, daily consumption of approximately 180 ml of the beverage product of at least some embodiments of the present invention comprising the emulsion described herein containing either 50 mg (low dose) or 100 mg (high dose) of DHA, showed significant
120 increase of plasma PL DHA content after 6 weeks (as shown by mole % of total fatty acid). By incorporating PUFAs within an emulsion that is incorporated into a beverage base, at least some embodiments the present invention are able to offer a novel method for more complete consumption of PUFAs in the beverage in order to provide an effective increase in the plasma PL DHA content.
125 Beverage Base
[0014] As used herein, the term "beverage base" refers to the type of fluid or liquid that is included in the beverage of the present invention. Accordingly to embodiments of the present invention, the beverage base may include, but is not limited to, pulp and pulp- free citrus and non-citrus fruit juices, fruit drink, vegetable juice, vegetable drink, milk,
130 soy milk, tea, water, sports drink, flavored water, energy drink, coffee, smoothies, yogurt drinks, hot chocolate and combinations thereof. The beverage base may also be carbonated or non-carbonated.
[0015] According to certain embodiments of the present invention, the beverage base may comprise one or more fruit juices or fruit drinks. Fruit juices may include, but
135 are not limited to, orange juice, grapefruit juice, apple juice, red grape juice, white grape juice, pear juice, concord grape juice, pineapple juice, pomegranate juice, cranberry juice, passion fruit juice, lime juice, lemon juice, mango juice, guava juice, banana juice, red and black currant juice, cashew apple juice, cantaloupe melon juice, apricot juice, blackberry juice, lingonberry juice, dewberry juice, gooseberry juice, crabapple juice,
140 prune juice, plum juice, kiwi juice, strawberry juice, blueberry juice, red raspberry juice, black raspberry juice, cherry juice, watermelon juice, peach juice, nectarine juice, loganberry juice, honeydew melon juice, papaya juice, boysenberry juice, youngberry juice, rhubarb juice, guanabana juice, acai juice, goji juice, fig juice, elderberry juice, date juice, carambola juice, acerola juice, quince juice, bilberry juice, tangerine juice, or any
145 combination thereof. Fruit drinks provide the flavor of any of the aforementioned fruit juices and contain greater than 0% fruit juice but less than 100% fruit juice. [0016] According to some embodiments, the beverage base may comprise one or more vegetable juices or vegetable drinks. Vegetable juices may include, but are not limited to, tomato juice, beet juice, carrot juice, celery juice, or any combination thereof.
150 Vegetable drinks provide the flavor of any of the aforementioned vegetable juices and contain greater than 0% vegetable juice but less than 100% vegetable juice. [0017] According to some embodiments, the beverage base may comprise milk, including but not limited to, whole milk, 2% milk, 1% milk, fat- free milk, or any combination thereof.
155 [0018] According to some embodiments, the beverage base may comprise soy milk, including but not limited to pure soy milk, 4% soy milk, 2%, soy milk, 1% soy milk, fat- free soy milk, any varied fat percent of soy milk, or any combination thereof. [0019] According to some embodiments, the beverage base may comprise tea, including but not limited to green tea, black tea, oolong tea, white tea, red tea, herbal tea,
160 caffeinated tea, decaffeinated tea, hot tea, iced tea or any combination thereof.
[0020] According to some embodiments, the beverage base may comprise a carbonated beverage, including but not limited to, colas and sodas. [0021] According to some embodiments, the beverage base may comprise coffee, including but not limited to regular caffeinated coffee, partially or totally decaffeinated
165 coffee, iced coffee, espresso, cappuccino, latte, and combinations thereof.
[0022] According to some embodiments, the beverage base may comprise water, including but not limited to, distilled water, spring water, filtered water, flavored water, and combinations thereof. [0023] According to some embodiments, the beverage base may comprise other
170 beverage products such as smoothies, yogurt drinks, hot chocolate, energy drinks, sports drinks, and combinations thereof. Emulsion
[0024] As used herein, "emulsion concentrate" refers to an emulsion which may be used to produce a final product emulsion having lower concentrations of emulsifϊer and
175 discontinuous liquid phase than the concentrations of emulsifier and discontinuous liquid phase in the emulsion concentrate. For example, the emulsion concentrate may comprise a beverage emulsion concentrate which can be combined with a beverage base to form the beverage product of the present invention. In particular, the emulsion concentrate is easily dispersed within a continuous liquid phase, without further homogenization
180 required. The formation of emulsion concentrates allows for the storage of LC-PUFAs in a stable and compact form for storage as well as transport before being dosed into a final emulsion form and included in a beverage product for consumption by a consumer. In addition, homogenization of the emulsion concentrate may be carried out in a smaller scale than homogenization of a final emulsion form to be consumed by a consumer.
185 Thus, lower equipment costs are realized.
[0025] Embodiments of the emulsion of the present invention comprise a continuous liquid phase, an emulsifier, and a discontinuous liquid phase. As used herein, "emulsion" refers to an immiscible mixture of a continuous liquid phase and a discontinuous liquid phase. As used herein, "continuous liquid phase" refers to the
190 portion of the emulsion in which the discontinuous liquid phase is dispersed. Accordingly, "discontinuous liquid phase," as used herein, refers to the multiplicity of discrete elements dispersed within, and immiscible with, the continuous liquid phase. In addition, embodiments of the discontinuous liquid phase include a blend including a dispersing agent and a LC-PUFA source. The LC-PUFA source includes at least one LC-
195 PUFA. As used herein, "dispersing agent" refers to any material which increases the stability of emulsions of the present invention and/or increases the ease of dispersion of discontinuous liquid phases of the present invention within continuous liquid phases. As used herein, "LC-PUFA" refers to any polyunsaturated carboxylic acid or organic acid with a long aliphatic tail. It should also be understood by a person of ordinary skill in the
200 art that though the embodiments described herein which include LC-PUFA may include other polyunsaturated fatty acids such as short chain polyunsaturated fatty acids or medium chain polyunsaturated fatty acids instead of or in combination with the LC- PUFA. [0026] As used herein, "emulsifier" refers to any substance which increases the
205 stability of the emulsion so that the discontinuous liquid phase remains substantially dispersed within the continuous liquid phase once the emulsion is formed. Within particular embodiments of the emulsion of the present invention, the emulsifier may be at least partially soluble in the continuous liquid phase, the discontinuous liquid phase, or both.
210 [0027] In embodiments of the present invention, the continuous liquid phase may be any liquid which is compatible with the LC-PUFA, the discontinuous liquid phase, and the emulsifier. In some embodiments, the continuous liquid phase may be, but is not limited to, a consumer product capable of ingestion so as to provide for delivery of the LC-PUFA to a consumer. Thus, according to particular embodiments of the present
215 invention, the continuous liquid phase may include, but is not limited to, water, carbonated water, syrup, diet beverages, carbonated soft drinks, fruit juices, vegetable juices, isotonic beverages, non-isotonic beverages, soft drinks containing fruit juice, coffee, tea, other aqueous liquids, pharmaceutical excipients, natural sweeteners, synthetic sweeteners, caloric sweeteners, non-caloric sweeteners, sodium benzoate,
220 ethylenediaminetetraacetic acid (EDTA), ascorbic acid, citric acid, dietary fiber, dairy products, soy products, and the like, and combinations thereof.
[0028] In particular embodiments, the continuous liquid phase may be acidic. In one embodiment, the continuous liquid phase may have a pH ranging from about 2 to about 7. In another embodiment, the continuous liquid phase may have a pH from about
225 2.5 to about 5.
[0029] In particular embodiments, the continuous liquid phase includes at least one polyphenol. The polyphenol may inhibit, suppress, or reduce degradation of the LC- PUFA and prevents lipid oxidation. Thus, the polyphenol may also prevent any odor or taste of the LC-PUFA from being perceived by a consumer. In addition, polyphenols
230 have also been noted as being effective in protecting against cardiovascular diseases and cancer (See Arts and Hollman, "Polyphenols and Disease Risk in Epidemiologic Studies," Am J CHn Nutr 2005;Sl (suppl) : 317S-25S).
[0030] Examples of suitable polyphenols for embodiments of this invention include, but are not limited to, polyphenols found naturally in a variety of foods including
235 plants, tea leaves, fruits, vegetables, and cocoa or may be synthesized or synthetic. For example, the polyphenol may comprise a phenolic acid or a flavonoid. Examples of phenolic acids include, but are not limited to, cinnamic acid or benzoic acid. Flavonoids which may be used with embodiments of this invention included flavonols, flavones, flavanones, flavanols, isoflavones, anthocyanidins, tannins, and stilbenes, for example.
240 [0031] In particular embodiments, the polyphenol may comprise a flavonoid such as quercetin, proanthocyanidin, catechin, resveratrol, and procyanidin, for instance. In other embodiments, the polyphenol may comprises a catechin selected from the group consisting of (+)-catechin, (-)-epicatechin, (-)-epicatchin gallate, (-)-epigallocatechin, and epigallocatechin gallate. In particular embodiments, suitable polyphenols may be
245 included in the emulsions in commercial available antioxidants such as the antioxidants listed in Table 1 below:
Table 1
Figure imgf000009_0001
Figure imgf000010_0001
[0032] According to particular embodiments of the invention, the polyphenol may
250 be present in the emulsion in an amount ranging from about 0.01 % by weight of the emulsion to about 10 % by weight of the emulsion. More particularly, the polyphenol may be present in the emulsion in an amount ranging from about 0.01 % by weight of the emulsion to about 5 % by weight of the emulsion. Still more particularly, the polyphenol may be present in the emulsion in an amount ranging from about 0.1 % by weight of the
255 emulsion to about 3 % by weight of the emulsion.
[0033] In particular embodiments, the continuous liquid phase may additionally include a water dispersible bioactive. As used herein, "water dispersible bioactive" refers to materials which are both dispersible in water and soluble in water. Suitable water dispersible bioactives for embodiments of the present invention include, but are not 260 limited to, lutein, β-carotene, lycopene (e.g., from tomato), astaxanthin, zeaxanthin, enzymes such as papain (e.g., from papaya), carotenoids (e.g., from watercress), eucalyptol (e.g., from basil or rosemary), eugerol (e.g., from basil), gingerol (e.g., from ginger), avenacoside (e.g., from oats), phenolic acids such as gallic acid (e.g., from blueberries) or rosmarinic acid (e.g., from rosemary), flavonoids (e.g., from watercress or
265 willow) such as quercetin (e.g., from blueberries, grape seeds, grapes, mate, or green tea), catechins (e.g., from green tea), anthocyanins (e.g., from grape seeds, grapes, or blueberries), phytoestrogen (e.g., from red clover), or naringin (e.g., from grapefruit), coumarins (e.g., from oats), proanthocyanidins (e.g., from grape seeds, green tea, guarana, or mate), curcuminoids (e.g., from tumeric), caramel coloring, vitamins such as
270 Vitamin E (e.g., from cucumber) or Vitamin K (e.g., from alfalfa), and combinations thereof or any natural or synthetic food grade colored or uncolored material which absorbs UV light or any other material understood by a person of ordinary skill in the art to be a suitable water dispersible bioactive, for example. Additional water dispersible bioactives which may be used in embodiments of the present invention are found in
275 "Lipid Oxidation", by E.N. Frankel, pages 209-298, 2nd Edition, The Oily Press, 2005, which is hereby incorporated by reference. According to particular embodiments of the invention, the water dispersible bioactives may be present in the continuous liquid phase in an amount ranging from about 0% by weight of the continuous liquid phase to about 20 % by weight of the continuous liquid phase. According to other embodiments of the
280 invention, the water dispersible bioactives may be present in the continuous liquid phase in an amount ranging from about 50 mg to about 100 mg.
[0034] In some embodiments and without being bound by theory, the water dispersible bioactives provide photo-oxidative protection such that the oxidation of the polyunsaturated fatty as is reduced, inhibited or suppressed. It is believed that the water
285 soluble bioactive absorbs some UV light such that polyunsaturated fatty acid is exposed to less light. In some embodiments of the present in invention which are ingestible, the water soluble bioactives may hydrate a portion of the skin of the consumer ingesting the emulsion. [0035] Embodiments of the present invention also include a discontinuous liquid
290 phase which is capable of being dispersed within the continuous liquid phase and which comprises a blend including a LC-PUFA source and a dispersing agent. The discontinuous liquid phase is immiscible in the continuous liquid phase. [0036] Suitable LC-PUFA sources for embodiments of the present invention include any LC-PUFA source which comprises at least one LC-PUFA capable of being
295 dispersed in an emulsion. According to particular embodiments of the invention, the LC- PUFA source may be a LC-PUFA oil or a LC-PUFA powder, or combinations thereof. Suitable LC-PUFA oils can be derived from algae, fish, animals, plants, or combinations thereof, for example. In such embodiments of the emulsion comprising a LC-PUFA oil, the blend may be referred to herein as an "oil blend". LC-PUFA oils for embodiments of the present invention include omega-3 fatty acid oils, omega-6 fatty acid oils and omega- 9 fatty acid oils, for instance. Examples of suitable omega-3 fatty acid oils for embodiments of this invention include, but are not limited to, alpha-linolenic acid oil, eicosapentaenoic acid oil, docosahexaenoic acid oil, and combinations thereof. In particular embodiments, the omega-3 fatty acid may be synthesized. Suitable omega-6 fatty acid oils for embodiments of this invention include, but are not limited to, gamma- linolenic acid oil, and arachidonic acid oil. In some embodiments, suitable omega-3 fatty acid oils include fish oils, (e.g., menhaden oil, tuna oil, salmon oil, bonito oil, and cod oil), microalgae docosahexaenoic acid oil, microalgae omega-3 oils, and the like, or combinations thereof. The fish oils may be crude or refined and also may be enzyme treated. In particular embodiments, suitable omega-3 fatty acid oils may include commercially available omega-3 fatty acid oils such as Microalgae DHA oil (from Martek, Columbia, MD), OmegaPure (from Omega Protein, Houston, TX), Marinol C-38 (from Lipid Nutrition, Channahon, IL), Bonito oil and MEG-3 (from Ocean Nutrition, Dartmouth, NS), Evogel (from Symrise, Holzminden, Germany), Marine Oil, from tuna or salmon (from Arista Wilton, CT), OmegaSource 2000, Marine Oil, from menhaden Marine Oil, from cod (from OmegaSource, RTP, NC). In other embodiments, the polyunsaturated fatty acids may include marine phospholipids such as krill oil, scallop oil, or other oils including astaxanthin. [0037] In particular embodiments wherein the emulsion comprises an emulsion concentrate, the LC-PUFA source is present in the emulsion concentrate in an amount ranging from about 0.5 % by weight of the emulsion concentrate to about 35 % by weight of the emulsion concentrate. More particularly, the LC-PUFA source is present in the emulsion concentrate in an amount ranging from about 2 % by weight of the emulsion concentrate to about 30 % by weight of the emulsion concentrate. Still more particularly, the LC-PUFA source is present in the emulsion concentrate in an amount ranging from about 5 % by weight of the emulsion concentrate to about 20 % by weight of the emulsion concentrate. Still more particularly, the LC-PUFA source is present in the emulsion concentrate in an amount ranging from about 15 % by weight of the emulsion to about 20 % by weight of the emulsion concentrate.
330 [0038] In particular embodiments, the LC-PUFA source is present in the emulsion in an amount ranging from about 0.002% by weight of the emulsion to about 35 % by weight of the emulsion. More particularly, the LC-PUFA source is present in the emulsion in an amount ranging from about 0.005 % by weight of the emulsion to about 30% by weight of the emulsion. Still more particularly, the LC-PUFA source is present
335 in the emulsion in an amount ranging from about 0.01 % by weight of the emulsion to about 20 % by weight of the emulsion.
[0039] In some embodiments, the dispersing agent is selected from vitamin E, ascorbyl palmitate, rosemary extract, a terpene, a flavor oil, a vegetable oil, or an essential oil and the like, and combinations thereof. According to particular embodiments
340 the essential oil may be a citrus oil, leaf oil, spice oil, peel oil, and combinations thereof. Examples of suitable essential oils for embodiments of this invention include, but are not limited to, lemon oil, orange oil, lime oil, grapefruit oil, mandarin oil, bitter orange oil, mint oil, peppermint oil, rosemary oil, flax seed oil, cranberry seed oil, bergamot oil, and combinations thereof. In embodiments where the dispersing agent comprises a terpene,
345 suitable terpenes include, but are not limited to, d-limonene, 1-limonene, dl-limonene (i.e., greater than 99 wt% dl-limonene), orange distillate oil (i.e., greater than 97 wt% dl- limonene) and combinations thereof.
[0040] In some embodiments, the blend may additionally include a weighing agent. Suitable weighing agents for embodiments of the present invention include
350 brominated vegetable oil, ester gum and other wood rosins, sucrose diacetate hexa- isoburtyurate (SAIB), refined gum dammar, ganuaba wax, benzyl benzoate, polyglyceryl ester, glyceryl tribenzoate, and combinations thereof, for example. In particular embodiments, the continuous liquid phase further comprises a sugar. Examples of suitable sugars for embodiments of the present invention include a monosaccharide, a
355 disaccharide, a trisaccharide, an oligosaccharide, or combinations thereof. Examples of continuous liquid phases which include a sugar include carbonated beverages with caloric sweeteners, fruit juices, and combinations thereof.
[0041] In some embodiments, the continuous liquid phase may also include a high- potency sweetener. Examples of suitable high-potency sweeteners include dulcoside A,
360 dulcoside B, rubusoside, stevia, stevioside, mogroside IV, mogroside V, Luo Han Guo sweetener, siamenoside, monatin and its salts (monatin SS, RR, RS, SR), curculin, glycyrrhizic acid and its salts, thaumatin, monellin, mabinlin, brazzein, hernandulcin, phyllodulcin, glycyphyllin, phloridzin, trilobatin, baiyunoside, osladin, polypodoside A, pterocaryoside A, pterocaryoside B, mukurozioside, phlomisoside I, periandrin I,
365 abrusoside A, cyclocarioside I, sucralose, acesulfame potassium or other salts, aspartame, alitame, saccharin, neohesperidin dihydrochalcone, cyclamate, neotame, N-[N-[3-(3- hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1 -methyl ester, N-[N- [3 -(3 -hydroxy-4-methoxyphenyl)-3 -methylbutyl] -L-α-aspartyl] -L-phenylalanine 1 -methyl ester, N-[N-[3-(3-methoxy-4-hydroxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1 -
370 methyl ester, salts thereof, and combinations thereof.
[0042] Without being bound by theory, the weighing agent in such embodiments increases the density of the discontinuous liquid phase so that the discontinuous liquid phase does not float to the top of the emulsion and agglomerate. Such functionality is particularly useful in embodiments where the continuous liquid phase contains sugar,
375 which may increase the density of the continuous liquid phase. Thus, when the density of the continuous liquid phase is increased by the presence of sugar, the disparity of the densities of the continuous and discontinuous liquid phases is increased, resulting in the less dense discontinuous liquid phase having a tendency to rise to the top of the emulsion if the weighing agent is not present.
380 [0043] In particular embodiments, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. In other embodiments, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 5% to about 35% of the discontinuous liquid phase.
385 [0044] In embodiments where the weighing agent comprises brotmnafed vegetable oil CBVO), the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 30% of the discontinuous liquid phase. More specifically, the brorainated vegetable oil ( BVO) weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 20% of the
390 discontinuous liquid phase. In embodiments where the weighing agent comprises glyceryl ester of wood rosin (i.e., ester gum), the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the glyceryl ester of wood rosin weighing agent may be present in the discontinuous liquid phase in an amount ranging from about
395 5% to about 35% of the discontinuous liquid phase. In embodiments where the weighing agent comprises sucrose di acetate hexa-isobαtyrale (SAIB), the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More .specifically, the sucπxse diacetate hexa-isobutyrate weighing agent may be present in the discontinuous liquid phase in an amount ranging
400 from about 5% to about 35% of the discontinuous liquid phase. In embodiments where the weighing agent comprises refined gum darπar, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the refined gum damar weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to
405 about 35% of the discontinuous liquid phase. In embodiments where the weighing agent comprises ganuaba wax, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the ganuaba wax weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 35% of the discontinuous
410 liquid phase. In embodiments where the weighing agent comprises benzyl bcnzoate, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 40% of the discontinuous liquid phase. More specifically, the benzyl bcnzoate weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 30% of the discontinuous liquid phase. In embodiments
415 where the weighing agent comprises polyglyceryi ester, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 50% of the discontinuous liquid phase. More specifically, the polyglyecryl ester weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 35% of the discontinuous liquid phase. In embodiments where the weighing agent
420 comprises glyceryl tribcnzoate, the weighing agent is present in the discontinuous liquid phase in an amount ranging from about 1% to about 30% of the discontinuous liquid phase. More specifically, the glyceryl tribenzoate weighing agent may be present in the discontinuous liquid phase in an amount ranging from about 5% to about 25% of the discontinuous liquid phase.
425 [0045] Generally, the amount of dispersing agent in the blend should be sufficient to create a stable emulsion rather than just masking the flavor or smell of the LC-PUFA. In particular, the amount of dispersing agent should be sufficient to provide oxidative stability (i.e., inhibit, suppress, or reduce oxidation of the LC-PUFA) and stabilize the resulting emulsion. In some embodiments, the weight ratio of the LC-PUFA source to the
430 dispersing agent in the blend can range from about 9:1 to about 1 :10. More particularly, the weight ratio of the LC-PUFA source to the dispersing agent in the blend can range from about 5 : 1 to about 1 :1. Still more particularly, the weight ratio of the LC-PUFA source to the dispersing agent in the blend can range from about 4: 1 to about 3:1. [0046] In particular embodiments wherein the emulsion comprises an emulsion
435 concentrate, the blend may be present in the emulsion concentrate in an amount ranging from about 0.5 % by weight of the emulsion concentrate to about 35 % by weight of the emulsion concentrate. More particularly, the blend is present in the emulsion in an amount ranging from about 2 % by weight of the emulsion concentrate to about 30 % by weight of the emulsion concentrate. Still more particularly, the blend is present in the
440 emulsion concentrate in an amount ranging from about 5 % by weight of the emulsion concentrate to about 20 % by weight of the emulsion concentrate. Still more particularly, the blend is present in the emulsion concentrate in an amount ranging from about 10 % by weight of the emulsion concentrate to about 20 % by weight of the emulsion concentrate. [0047] In particular embodiments, the blend may present in the emulsion in an
445 amount ranging from about 0.001 % by weight of the emulsion to about 35 % by weight of the emulsion. More particularly, the blend may be present in the emulsion in an amount ranging from about 0.005 % by weight of the emulsion to about 30 % by weight of the emulsion. Still more particularly, the blend may be present in the emulsion in an amount ranging from about 0.01% by weight of the emulsion to about 20 % by weight of
450 the emulsion. Still more particularly, the blend may be present in the emulsion in an amount ranging from about 0.02% by weight of the emulsion to about 20 % by weight of the emulsion.
[0048] In some embodiments, the blend may further comprise a folded oil. In particular embodiments, the folded oils further improve the oxidative stability and
455 reduces improves the particle size distribution by reducing the particle size of the discontinuous liquid phase. Suitable folded oils for embodiments of the present invention include, but are not limited to, 4-fold bergamot oil, bergaptene free bergamot oil, terpeneless grapefruit oil, 4-fold grapefruit oil, 5 -fold grapefruit oil, 6-fold grapefruit oil, 10-fold grapefruit oil, high aldehyde grapefruit oil, 5-fold grapefruit juice extract, 7-fold 460 grapefruit juice extract, terpeneless lemon oil, 2-fold lemon oil, 3 -fold lemon oil, 5 -fold lemon oil, 10-fold lemon oil, 13-fold lemon oil, washed 5-fold lemon oil, 10-fold lemon oil, Sesquiterpeneless lemon oil, FC free lemon oil, distilled 3-fold lime oil, distilled 4- fold lime oil, distilled 5 -fold lime oil, distilled terpeneless lime oil, distilled sesquiterpeneless lime oil, distilled washed 5 fold lime oil, cold pressed 3 -fold lime oil,
465 cold pressed 4-fold lime oil, cold pressed 5-fold lime oil, cold pressed 10-fold lime oil, cold pressed terpeneless lime oil, 4-fold mandarin oil, 5-fold mandarin oil, 10-fold mandarin oil, terpeneless orange oil, 2-fold orange oil, 3 -fold orange oil, 4-fold orange oil, 5-fold orange oil, 7-fold orange oil, 8-fold orange oil, 10-fold orange oil, 15-fold orange oil, 20-fold orange oil, 25 -fold orange oil, 30-fold orange oil, 5 -fold orange juice
470 extract, 8 -fold orange juice extract, 3 -fold tangerine oil, 5 -fold tangerine oil, terpeneless tangerine oil, and combinations thereof. Thus, in some embodiments, the discontinuous liquid phase may comprise a terpeneless oil.
[0049] According to particular embodiments of the invention, the folded oil may be present in the discontinuous liquid phase in an amount ranging from about 1 % by
475 weight of the discontinuous liquid phase to about 60 % by weight of the discontinuous liquid phase. More particularly, the folded oil may be present in the discontinuous liquid phase in an amount ranging from about 7.5 % by weight of the discontinuous liquid phase to about 45 % by weight of the discontinuous liquid phase. Still more particularly, the folded oil may be present in the discontinuous liquid phase in an amount ranging from
480 about 10 % by weight of the discontinuous liquid phase to about 40 % by weight of the discontinuous liquid phase.
[0050] In alternate embodiments of the present invention, the emulsion may comprise a continuous liquid phase, an emulsifier, and a discontinuous liquid phase comprising a blend including a polyunsaturated fatty acid source and a folded oil. Thus,
485 in particular alternate embodiments of the present invention, the emulsion might not include a dispersing agent. Rather, the folded oil helps to form a stable emulsion wherein the degradation of the polyunsaturated fatty acid is inhibited, suppressed, or reduced. [0051] In particular embodiment, the discontinuous liquid phase may also include medium chain triglycerides. In particular embodiments, the medium chain triglycerides
490 further improve the oxidative stability and reduces improves the particle size distribution by reducing the particle size of the discontinuous liquid phase. According to particular embodiments of the invention, the medium chain triglycerides may be present in the discontinuous liquid phase in an amount ranging from about 1 % by weight of the discontinuous liquid phase to about 60 % by weight of the discontinuous liquid phase.
495 More particularly, the medium chain triglycerides may be present in the discontinuous liquid phase in an amount ranging from about 7.5 % by weight of the discontinuous liquid phase to about 40 % by weight of the discontinuous liquid phase. Still more particularly, the medium chain triglycerides may be present in the discontinuous liquid phase in an amount ranging from about 10 % by weight of the discontinuous liquid phase to about 30
500 % by weight of the discontinuous liquid phase.
[0052] In some embodiments, the discontinuous liquid phases may also include other components such as oil soluble vitamins (e.g., vitamin A, vitamin D, vitamin E, or Vitamin K), phytochemicals, and other lipid nutrients. [0053] In particular embodiments, the discontinuous liquid phase may additionally
505 include an oil dispersible bioactive. As used herein, "oil dispersible bioactive" refers to materials which are both dispersible in oil and soluble in oil. Suitable oil dispersible bioactives for embodiments of the present invention include, but are not limited to, oxygenated carotenoids, such as lutein (e.g., from tomato), astaxanthin and non- oxygenated carotenoids, such as β-carotene and lycopene, and combinations thereof or
510 any natural or synthetic food grade colored or uncolored material which absorbs UV light, for example. In other embodiments, suitable oil dispersible bioactives may include enzymes such as papain (e.g., from papaya), carotenoids (e.g., from watercress), eucalyptol (e.g., from basil or rosemary), eugerol (e.g., from basil), gingerol (e.g., from ginger), avenacoside (e.g., from oats), phenolic acids such as gallic acid (e.g., from
515 blueberries) or rosmarinic acid (e.g., from rosemary), flavonoids (e.g., from watercress or willow) such as quercetin (e.g., from blueberries, grape seeds, grapes, mate, or green tea), catechins (e.g., from green tea), anthocyanins (e.g., from grape seeds, grapes, or blueberries), phytoestrogen (e.g., from red clover), or naringin (e.g., from grapefruit), coumarins (e.g., from oats), proanthocyanidins (e.g., from grape seeds, green tea,
520 guarana, or mate), curcuminoids (e.g., from tumeric), caramel coloring, and any other material understood by a person of ordinary skill in the art to be a suitable water dispersible bioactive, for instance. Additional oil dispersible bioactives which may be used in embodiments of the present invention are found in "Lipid Oxidation", by E.N. Frankel, pages 209-298, 2nd Edition, The Oily Press, 2005. According to particular
525 embodiments of the invention, the oil dispersible bioactives may be present in the discontinuous liquid phase in an amount ranging from about 0% by weight of the discontinuous liquid phase to about 20 % by weight of the discontinuous liquid phase. According to other embodiments of the invention, the oil dispersible bioactives may be present in the discontinuous liquid phase in an amount ranging from about 50 mg to about
530 100 mg. In some embodiments and without being bound by theory, the oil dispersible bioactives provide photo-oxidative protection such that the oxidation of the polyunsaturated fatty as is reduced, inhibited or suppressed. It is believed that the oil dispersible bioactive absorbs some UV light such that polyunsaturated fatty acid is exposed to less light. In some embodiments of the present in invention which are
535 ingestible, the oil soluble bioactives may hydrate a portion of the skin of the consumer ingesting the emulsion.
[0054] In other embodiments, the discontinuous liquid phase may also include an oil blend antioxidant. Suitable oil blend antioxidants for embodiments of the present invention include, but are not limited to, butylated hydroxytoluene (BHT), butylated
540 hydroxyanisole (BHA), tert-butylhydroquinone (TBHQ), and combinations thereof. According to particular embodiments of the invention, the oil blend antioxidant may be present in the discontinuous liquid phase in an amount ranging from about 0 % by weight of the discontinuous liquid phase to about 5 % by weight of the discontinuous liquid phase.
545 [0055] Embodiments of the present invention include emulsions in which the discontinuous liquid phase is present in the emulsion in the form of particles. In some embodiments, these discontinuous liquid phase particles have an average particle size from about 0.1 μm to about 1.5 μm. More particularly, the discontinuous liquid phase particles may have an average particle size from about 0.1 μm to about l.Oμm. Still more
550 particularly, the discontinuous liquid phase particles may have an average particle size from about 0.15 μm to about 0.7 μm.
[0056] Emulsifiers which may be used in the present invention include any emulsifier compatible with the LC -PUFAs and the dispersing agents used in the emulsion. Natural or synthetic emulsifiers may be suitable for embodiments of the
555 present invention. According to particular embodiments of the present invention, the emulsifier may be a modified natural emulsifier. That is, the emulsifier may be chemical modified, enzymatically modified, physically modified, or combinations thereof. In embodiments where the emulsion is used in a consumer composition such as a beverage, the emulsifϊer is a food grade emulsifϊer. Examples of other suitable emulsifiers for
560 embodiments of this invention include, but are not limited to, pectin, β-pectin, gum ghatti, modified gum arabic (e.g., Ticamulsion™, from TIC Gums, Belcamp, MD), gum acacia (e.g., Eficacia™, from Colloides Naturels International (CNI), Bridgewater, NJ), Quillaja extract (e.g., Q NaturalelOO from Desert King, San Diego, CA and National Starch Chemical Bridgewater, NJ), modified food starch (e.g., from National Starch &
565 Chemical, Bridgewater, NJ), polysorbates (i.e., tweens), co-emulsifϊers such as propylene glycol alginate (PGA), and combinations thereof.
[0057] In embodiments where the emulsion comprises a fruit juice or drink containing a fruit juice (e.g., orange juice or grapefruit juice), citrus oil may be present in the continuous liquid phase, which aids in the chemical stability of the emulsion and thus,
570 a dispersing agent need not be additionally added to the emulsion. In particular embodiments wherein the continuous liquid phase comprises an acidic composition, such as a carbonated beverage, the emulsifier may comprise a carbohydrate-based macromolecule. Examples of suitable carbohydrate-based macromolecules include gum acacia, modified food starch, gum ghatti, pectins (e.g., beta-pectin), modified gum acacia,
575 and combinations thereof.
[0058] In particular embodiments, the emulsifier is present in the emulsion in an amount ranging from about 0.0002% by weight of the emulsion to about 45 % by weight of the emulsion. In other embodiments, the emulsifier is present in the emulsion in an amount ranging from about 0.001 % by weight of the emulsion to about 25 % by weight
580 of the emulsion. In still other embodiments, the emulsifier is present in the emulsion in an amount ranging from about 0.01 % by weight of the emulsion to about 20 % by weight of the emulsion. In still other embodiments, the emulsifier is present in the emulsion in an amount ranging from about 5 % by weight of the emulsion to about 20 % by weight of the emulsion.
585 [0059] In some embodiments, the emulsion may also include a stabilizing agent to further stabilize the emulsion and also improve the taste profile and/or improve the shelf life of the emulsion. Examples of suitable stabilizing agents for embodiments of this invention include, but are not limited to, vitamin C, polyphenols from fruit and vegetable sources, such as rosemary extract, tea polyphenols and grape seed extracts,
590 ethylenediaminetetraacetic acid (EDTA), ethylenediaminetetraacetic acid disodium salt, and combinations thereof. Within particular embodiments of the present invention, the stabilizing agent may be at least partially soluble in the continuous liquid phase, the discontinuous liquid phase, or both. In one embodiment, an emulsion comprising a stabilizing agent has a shelf life of more than 3 months. As used herein, "shelf-life"
595 refers to a time period within which embodiments of emulsions may be stored and remain suitable for consumer use.
[0060] In other embodiments, the emulsion further comprises a surfactant which further reduces the surface tension between the oil phase and the suspension medium, thereby improving the stability of the emulsion and homogenization of the emulsion.
600 Examples of suitable surfactants for embodiments of this invention include, but are not limited to, dioctyl succinate sulfate sodium salt (DSS), medium chain triglyceride (MCT), propylene glycol alginate (PGA) and combinations thereof. Within particular embodiments of the present invention, the surfactant may be at least partially soluble in the continuous liquid phase, the discontinuous liquid phase, or both.
605 [0061] According to particular embodiments of the invention, methods for making an emulsion comprise providing a first liquid, providing a second liquid, and combining the first liquid, the second liquid, and an emulsifier so as to form the emulsion. Embodiments of the second liquid comprise a blend that includes a long chain polyunsaturated fatty acid source and a dispersing agent. Particular embodiments of long
610 chain polyunsaturated fatty acid sources include at least one long chain polyunsaturated fatty acid. In particular embodiments, emulsions comprise a continuous liquid phase including the first liquid and a discontinuous liquid phase including the second liquid. Embodiments of the emulsion may be any of the emulsions described above. [0062] In particular embodiments of the present invention, the first liquid may
615 comprise the same components suitable for embodiments of the continuous liquid phases described above. Embodiments of the second liquid may include dispersing agents similar to any of the dispersing agents above. In addition, LC-PUFA sources included in embodiments of the second liquid may be any of the LC-PUFA sources described above. Furthermore, embodiments of the second liquid may comprise the same components
620 suitable for embodiments of the discontinuous liquid phases described above. Suitable emulsifϊers may be similar to the emulsifϊers described above.
[0063] Embodiments of the present invention include methods wherein the step of combining comprises combining the first liquid, the second liquid, and the emulsifier sequentially or simultaneously. For example, in particular embodiments, the dispersing 625 agent is combined with the long chain polyunsaturated fatty acid source to form the blend in the second liquid and then the first liquid, the second liquid, and the emulsifier are combined to form the emulsion. For another example, in particular embodiments, the dispersing agent is combined with the LC-PUFA source and emulsifier to form the blend in the second liquid and then the first liquid and the second liquid are combined to form
630 the emulsion.
[0064] In particular embodiments, the step of combining comprises mixing the emulsifier into the first liquid, mixing the dispersing agent with the polyunsaturated fatty acid source to form the blend in the second liquid, and then homogenizing the first liquid and the second liquid to form the emulsion. For example, the first liquid and the
635 emulsifier may be used to form a mucilage or emulsifier solution. Then, the mucilage comprising the first liquid and the emulsifier may be combined with the second liquid, which includes the dispersing agent mixed with the polyunsaturated fatty acid, to form a pre-emulsion. The pre-emulsion can then be homogenized to form the emulsion. [0065] Also, in some embodiments, the first liquid, the second liquid, and the
640 emulsifier may be combined simultaneously by a homogenizing process. In yet other embodiments, the step of combining may comprise forming an emulsion concentrate comprising a portion of the first liquid, the second liquid, and the emulsifier and then adding the remainder portion of the first liquid to the emulsion concentrate to form the emulsion comprising the discontinuous liquid phase and the continuous liquid phase.
645 [0066] The present disclosure also provides for a method of making an emulsion comprising providing a first liquid, providing a second liquid, and combining the first liquid, the second liquid, and an emulsifier so as to form an emulsion concentrate. Embodiments of the second liquid comprise a blend that includes a long chain polyunsaturated fatty acid source and a dispersing agent. The emulsion concentrate may
650 be dosed into a third liquid where the emulsion concentrate disperses quickly to form an emulsion. In particular embodiments, homogenization of the emulsion concentrate with the third liquid is not required to form a stable emulsion. Embodiments of the first liquid and third liquid may comprise components of the continuous liquid phase as described above. In particular embodiments, the emulsion may comprise a beverage, a herbal
655 composition, or a pharmaceutical composition, for example.
[0067] Embodiments of the present invention may also include emulsions which are spray dried, spray dried and coated, or spray dried and agglomerated. It should be understood by a person of ordinary skill in the art that embodiments of the emulsion may be spray dried by any method known in the art for spray drying. In addition, it should be
660 understood by a person of ordinary skill in the art that embodiments of the spray dried emulsions may be coated or agglomerated with other components. For example, embodiments of the spray dried emulsions may be coated or agglomerated by sugars and maltodextrin or combinations thereof. Furthermore, understood by a person of ordinary skill in the art that embodiments of the spray dried emulsions may be coated or
665 agglomerated by any method known in the art for coating or agglomerating. In particular embodiments, the spray dried, spray dried and coated, and/or spray dried and agglomerated emulsions can be added to liquid compositions wherein the emulsions disperse and form a liquid emulsion. For example, embodiments of spray dried, spray dried and coated, or spray dried and agglomerated may be added to a beverage to form a
670 beverage emulsion.
[0068] The emulsions created by embodiments of the method of the present invention are stable and provide protection for the long chain polyunsaturated fatty acid from oxidation. In addition, the embodiments of the emulsions of the present invention may improve the bioavailability of the polyunsaturated fatty acids as compared to bulk
675 oil.
[0069] Without being bound by theory, it is believed that in particular embodiments a sufficient amount of the dispersing agent reduces the viscosity and surface tension of the discontinuous liquid phase such that homogenization efficiency of the emulsion is improved. Thus, the viscosity difference between the continuous liquid phase
680 and the discontinuous liquid phase plays a role in determining the effectiveness of the emulsification/homogenization processes. Since LC-PUFA sources, such as LC-PUFA oils, are hydrophobic and viscous, these properties can reduce the effectiveness of homogenization. Therefore, the dispersing agent is included in the discontinuous liquid phase to reduce the viscosity of the discontinuous liquid phase to a viscosity lower than
685 the viscosity of the LC-PUFA source. Inclusion of the dispersing agent in the discontinuous liquid phase also results in the discontinuous liquid phase having a surface tension less than the surface tension of the LC-PUFA source. Consequently, the discontinuous liquid phase, which includes the LC-PUFA source, is more easily dispersed in the emulsion. 690 [0070] Moreover, having smaller discontinuous liquid phase particle size and higher continuous liquid phase viscosity can improve emulsion stability. Addition of the dispersing agent to the emulsion to form the blend having the LC-PUFA source also reduces the discontinous liquid phase particle size to improve homogenization efficiency. [0071] Furthermore, Stokes' law indicates that the discontinuous liquid phase
695 density affects emulsion's stability. In particular, Stokes' law indicates that emulsion stability can be enhanced by reducing the density difference between the continuous liquid phase and discontinuous liquid phase. By adding a dispersing agent to the discontinuous liquid phase, the discontinuous liquid phase density can be adjusted. In some embodiments, the LC-PUFA has first vicosity and the dispersing agent has a second 700 viscosity less than the first density. Thus, in particular embodiments, a higher percentage of the dispersing agent in the discontinuous liquid phase results in a lower discontinuous liquid phase density. For example, in embodiments where substantially all of the discontinuous liquid phase comprises a second liquid having a blend of a dispersing agent and a LC-PUFA oil, the discontinuous liquid phase density decreases as the percentage of 705 dispersing agent in the blend increases (i.e., the percentage of LC-PUFA oil percentage decreases).
[0072] An additional benefit of producing a stable emulsion comprising the LC-
PUFA source is that at least a portion of any degradation or oxidation of the LC-PUFA is inhibited, suppressed, or reduced by forming the emulsion having the long chain 710 polyunsaturated fatty acid source. In particular embodiments, substantially all of the degradation of the long chain polyunsaturated fatty acid is inhibited, suppressed, or reduced by forming the emulsion having the long chain polyunsaturated acid source. Thus, without being bound by theory, it is believed that in embodiments where the LC- PUFA has an odor or taste, forming the emulsion having the at least one the long chain 715 polyunsaturated acid substantially masks the odor or the taste of the at least one long chain polyunsaturated fatty acid source (e.g., a fishy odor). Blending the dispersing agent with the LC-PUFA source also reduces oxidation of the LC-PUFA source. For example, it is believed that dispersing agents which are more polar form a protective layer between the LC-PUFA source and the continuous liquid phase. Also, it is believed that antioxidant 720 dispersing agents such as vitamin E, ascorbyl palmitate, and rosemary extract help to protect the LC-PUFA from oxidation. Furthermore, the reduction of degradation of the LC-PUFA increases the emulsion shelf-life. [0073] In use, embodiments of emulsions of the present invention may be functional in compositions such as beverage product compositions, herbal compositions,
725 pharmaceutical compositions, or the like, which may be ingested or otherwise introduced in to a consumer such that the LC-PUFA, and its beneficial properties offer high bioavailability. In embodiments wherein the emulsion is ingested, the present invention provides for a beverage product comprising a beverage base and the emulsion described herein wherein the LC-PUFA is substantially, completely soluble, undetectable to the taste
730 or smell of the consumer, and available for complete consumption. Thus, LC-PUFA, particularly omega-3 fatty acids, namely DHA and EPA, can be ingested by a consumer with substantially less undesirable odor, taste, or like property.
[0074] In accordance with some embodiments of the present invention, incorporating the polyunsaturated fatty acid into beverages may be done in a variety of
735 ways. Most notably, the polyunsaturated fatty acid may be incorporated within the beverage by adding the emulsion to a beverage base in a mixer. Another way may include adding the emulsion to the final beverage product before pasteurization. Either of these methods provides for a final beverage product that provides a nutritious beverage, is aesthetically pleasing, and provides a high bioavailability of desirable polyunsaturated
740 fatty acids, such as omega-3-fatty acids, to consumers.
[0075] When a mixer is used to incorporate PUFAs or LC-PUFAs into some beverage embodiments of the present invention, known shear mixers may be used. For example, a low shear mixer may be provided to mix the LC-PUFA emulsion with water or another beverage base and other ingredients (e.g. vitamins, etc.). Once all of the
745 ingredients are mixed together, the entire mixture may be passed through a pasteurizer and then filled or packaged.
[0076] In certain embodiments, if a mixture is not used to incorporate the PUFAs or LC-PUFAs into beverage product, the emulsion may be incorporated into the beverage base before pasteurization. In other words, all ingredients except the emulsion may be
750 mixed. The emulsion may then be added into the mixture and then the mixture may be pasteurized for filling or packaging. The PUFAs or LC-PUFAs may also be incorporated into a pasteurized beverage base mixture to produce a finalized filled or packaged product. [0077] The emulsion of the present invention is water soluble and eases the dispersion of PUFAs or LC-PUFAs into the beverage base without sedimentation. Even
755 when high acidic beverages (e.g orange juice, pomegranate juice, and the like) are used as the beverage base, the emulsion may maintain its stability over the shelf life of the beverage when homogenized, making the emulsion particles particularly small and dispersible. For example, after 3 weeks, 9 weeks, or 11 weeks of shelf life storage, some embodiments of the beverage products of the present invention exhibited substantially no
760 loss of the PUFAs or LC-PUFAs incorporated therein as shown by the following tables:
765 Table 2: DHA content in Orange Juice
Figure imgf000026_0001
Table 3: DHA content in Pomegranate Blueberry Juice
Figure imgf000026_0002
EXAMPLES
770 [0078] Other embodiments are further illustrated below in the examples which are not to be construed in any way as imposing limitations upon the scope of this disclosure. On the contrary, it is to be clearly understood that resort may be had to various other embodiments, modifications, and equivalents thereof which, after reading the description therein, may suggest themselves to those skilled in the art without departing from the
775 scope of this disclosure and the appended claims. [0079] EXAMPLE 1 : Effect of oil additive on mean particle size distribution of
DHA emulsions
[0080] Two 250 g emulsions were produced using the formulation of Tables 4 and
780 5 below, where MCT is medium chain triglyceride and OD is orange distillate:
Table 4
785
Figure imgf000027_0001
[0081] The emulsions were prepared by first preparing a mucilage by weighting water content for the batch in a 600 ml beaker. The beaker was placed under a propeller 790 based agitator. Sodium benzoate was added to the mixing vortex and the emulsifϊer solution was mixed for 3 minutes. Citric acid was added to the mixing vortex and the emulsifϊer solution was mixed for 3 minutes. Emulsifϊer was slowly added to the mixing vortex and agitation was continued for 1 hour. The emulsifϊer solution was placed on a table overnight to allow foam to separate.
795 [0082] A pre-emulsion was prepared by placing the filtered emulsifϊer solution
(the mucilage was through a 100 mesh screen) under a propeller based agitator and oil blend of DHA oil and orange distillate, medium chain triglyceride, and/or folded oil was slowly added to the mixing vortex to produce a coarse emulsion. The coarse emulsion solution was transferred to the high shear mixer (Polytron PT3100 or Pri Sci 250). The
800 mixer speed was set at 4 and the emulsifϊer solution was mixed for 2 minutes to yield a pre-emulsion.
[0083] The emulsion was prepared by running DI water through a NanoMizer and adjust the plunger speed to achieve homogenization pressure of 31 MPa (4500 psi). The pre-emulsion was homogenized twice at the desired homogenization pressure. If
805 necessary, the plunger speed was adjusted to achieve the desired homogenization pressure. The emulsion was then packaged and stored in chilled conditions. Tables 6 and 7 summarizes the results of a particle size measurement of the emulsion and shows that addition of orange distillate, medium chain triglycerides and/or folded oils to DHA oils can significantly improve ease of emulsifϊcation of DHA oils.
810 Table 6:
Figure imgf000028_0001
Table 7:
Figure imgf000028_0002
EXAMPLE 2
815
[0084] Omega-3 fatty acid oil-in-water emulsions with 17.5% Eficacia or 17.5%
Ticamulsion 2010A, dl-limonene, and 15% Martek DHA oil were prepared using the procedures of EXAMPLE 1. The omega-3 fatty acid oil was supplied by Martek Bioscience and was stabilized with an antioxidant mixture system of tocopherols,
820 ascorbyl palmitate, soy lecithin and rosemary extract. Eficacia, a special grade of gum arabic, was provided by CNI. Ticamulsion 2010A, a modified gum aracia, was supplied by TIC Gum. All the components were used without further purification. [0085] Omnion's Food Stability Analyzer (FSA) was been employed to determine antioxidant efficacy in retarding lipid oxidation of the omega-3 fatty emulsions. FSA
825 conducted accelerated oxidation studies using the combination of elevated temperature (up to 1500C) and catalysis, a proprietary heavy metal complex. The degree of oxidation acceleration for the combination was on an order of several hundred times faster than the real shelf life study. The FSA instrument measured oxygen concentration at the headspace of the sample cell (~40 c.c. in volume or -2X1020 oxygen molecules). The
830 FSA method was significantly more sensitive than the conventional oxygen bomb method in which high pressure pure oxygen and elevated temperature. The end point determination of the FSA for the oxidative stability analysis was determined by the inflection point (sharp slope change) of the oxygen concentration versus time curve where the added antioxidants are consumed and the lipid auto-oxidation starts to accelerate. In
835 addition, the end point typically indicated the time that it takes ~5% of headspace oxygen or ~1019 oxygen molecules to be consumed by the substrate studied. [0086] The SafTest® system was used to analyze the oxidative degradation of in- house Omega-3 emulsions. The SafTest® system is a colorimetric method (based on the ferric thiocyanate method modified for safety reasons by replacing benzene methanol
840 with isopropanal) and is AOAC certified. The SafTest® system provided a rapid determination of peroxide values of the emulsion studied and the results are summarized in Tables 8 and 9. Thus, the result indicated that addition of the oils and polyphenols to the DHA emulsions reduced oxidative degradation.
845
Table 8: Effect of addition of orange distillate and MCT on the oxidative stability
Figure imgf000029_0001
Figure imgf000030_0001
Table 9: Peroxide value (PV) of Aged In-house Omega-3 emulsions
Figure imgf000030_0002
850 [0087] Green tea polyphenols (GTP) were used to examine the antioxidant efficacy of GTP in retarding off taste development due to Omega-3 oil oxidation in embodiments of the emulsion. Table 10 shows the ongoing shelf stability evaluation of Fanta Orange Zero fortified with DHA oil and different additives. The results indicate that after 12 weeks of ambient storage the test samples with GTP have not developed
855 fishy smell and taste. However, the test sample with vitamin C only did develop fishy taste and smell after 3 weeks of ambient storage. In addition, sensory results of 100 people consumer study show after 12 weeks of ambient storage Fanta Zero Orange fortified with DHA oil and vitamin C/EDTA develops slight fishy smell and taste although the off taste can be masked by the use of cooling agents. Hence, green tea
860 polyphenols should be able to replace vitamin C and EDTA in Omega-3 emulsions and Omega-3 fortified beverages to retard lipid oxidation and ensure shelf stability.
865
870 875
880
885
890
895
900 Table 10: Sensor Evaluation of Fanta Oran e Zero with different additives
Figure imgf000031_0001
Figure imgf000032_0001
RT: Room Temperature (-23 0C)
EXAMPLE 3
[0088] A 200 kg omega-3 fatty acid oil-in-water stable emulsion was made according to the formulation of Table 11 using the procedures of EXAMPLE 1.
Table 11
Unit wt% kg
Ticamulsion 17.5 35
Martek DHA oils 15 30
CP Orange Oils 5 10
Sodium Benzoate 0.13 0.26
Citric Acid 0.2 0.4
Green Tea Extract 0.3 0.6
EDTA 0.1 0.2
Processed Water 61.77 123.54
Total 100 200
EXAMPLE 4 [0089] An omega-3 fatty acid oil-in- water emulsion with 17.5% Ticamulsion
910 2010A was prepared using the formula in Table 12 below. Sucrose diacetate hexa- isobutyrate was used as the weight agent. Table 12
Figure imgf000033_0001
[0090] The emulsion was prepared by first preparing a mucilage by weighting
915 water content for the batch in a 2000 ml beaker. The beaker was placed under a propeller based agitator. Sodium benzoate was added to the mixing vortex and the emulsifier solution was mixed for 3 minutes. Citric acid was added to the mixing vortex and the emulsifier solution was mixed for 3 minutes. Emulsifier was slowly added to the mixing vortex and agitation was continued for 1 hour. The emulsifier solution was placed on a
920 table overnight to allow foam to separate.
[0091] A pre-emulsion was prepared by placing the emulsifier solution under a propeller based agitator and oil blend of DHA oil, sucrose diacetate hexa-isobutyrate and orange distillate, medium chain triglyceride, and/or folded oil was slowly added to the mixing vortex to produce a coarse emulsion. The coarse emulsion solution was
925 transferred to the high shear mixer, Polytron PT3100. The mixer speed was set at 410,000 rpm and the emulsifier solution was mixed for 2 minutes to yield a pre-emulsion. [0092] The emulsion was prepared by running DI water through an APV 1000 homogenizer and adjust the homogenization pressure of 4500 psi. The pre-emulsion was homogenized twice at the desired homogenization pressure. If necessary, the plunger
930 speed was adjusted to achieve the desired homogenization pressure. The emulsion was then packaged and stored in chilled conditions. The resulting emulsion had a discontinuous liquid phase with a mean particle size of 0.173 μm. [0093] It should be understood that the foregoing relates to particular embodiments of the present invention, and that numerous changes may be made therein without departing from the scope of the invention as defined from the following claims.

Claims

CLAIMSWhat is claimed is: 940
1. A beverage product comprising at least one beverage base and at least one polyunsaturated fatty acid emulsion, said emulsion comprising a continuous liquid phase; an emulsifϊer; and a discontinuous liquid phase comprising a blend including a polyunsaturated fatty acid source and a dispersing agent, the
945 polyunsaturated fatty acid source comprising at least one polyunsaturated fatty acid, wherein the weight ratio of the fatty acid source to the dispersing agent in the blend ranges from about 9: 1 to about 1 :10.
2. The beverage product of claim 1, wherein the dispersing agent is selected from the 950 group consisting of vitamin E, ascorbyl palmitate, rosemary extract, a terpene, a flavor oil, vegetable oil, an essential oil, and combinations thereof.
3. The beverage product of claim 1, wherein the dispersing agent comprises a terpene selected from the group consisting of d-limonene, 1-limonene, dl-limonene, orange
955 distillate oil, and combinations thereof.
4. The beverage product of claim 1, wherein the emulsifϊer comprises a carbohydrate- based macromolecule.
960 5. The beverage product of claim 4, wherein the carbohydrate-based macromolecule is selected from the group consisting of gum acacia, modified food starch, gum ghatti, pectin, beta-pectin, modified gum acacia, and combinations thereof.
6. The beverage product of claim 1, wherein the emulsifϊer comprises Quillaja 965 extract.
7. The beverage product of claim 1, wherein the continuous liquid phase has a pH from about 2 to about 7.
970 8. The beverage product of claim 1, wherein the discontinuous liquid phase further comprises at least one folded oil selected from the group consisting of 4-fold bergamot oil, bergaptene free bergamot oil, terpeneless grapefruit oil, 4-fold grapefruit oil, 5-fold grapefruit oil, 6-fold grapefruit oil, 10-fold grapefruit oil, high aldehyde grapefruit oil, 5 -fold grapefruit juice extract, 7-fold grapefruit juice
975 extract, terpeneless lemon oil, 2-fold lemon oil, 3 -fold lemon oil, 5 -fold lemon oil,
10-fold lemon oil, 13 -fold lemon oil, washed 5 -fold lemon oil, 10-fold lemon oil, Sesquiterpeneless lemon oil, FC free lemon oil, distilled 3-fold lime oil, distilled 4- fold lime oil, distilled 5 -fold lime oil, distilled terpeneless lime oil, distilled sesquiterpeneless lime oil, d istilled washed 5 fold lime oil, cold pressed 3 -fold
980 lime oil, cold pressed 4-fold lime oil, cold pressed 5-fold lime oil, cold pressed 10- fold lime oil, cold pressed terpeneless lime oil, 4-fold mandarin oil, 5 -fold mandarin oil, 10-fold mandarin oil, terpeneless orange oil, 2-fold orange oil, 3-fold orange oil, 4-fold orange oil, 5-fold orange oil, 7-fold orange oil, 8-fold orange oil, 10-fold orange oil, 15-fold orange oil, 20-fold orange oil, 25-fold orange oil, 30-
985 fold orange oil, 5-fold orange juice extract, 8-fold orange juice extract, 3-fold tangerine oil, 5 -fold tangerine oil, terpeneless tangerine oil, and combinations thereof.
9. The beverage product of claim 1, wherein the discontinuous liquid phase further 990 comprises a medium chain triglyceride.
10. The beverage product of claim 1, wherein the continuous liquid phase further comprises at least one polyphenol.
995 11. The beverage product of claim 1 , wherein the at least one polyphenol comprises green tea extract.
12. The beverage product of claim 1, wherein the polyunsaturated fatty acid source comprises an omega-3 fatty acid oil selected from the group consisting of alpha- 1000 linolenic acid oil, eicosapentaenoic acid oil, docosahexaenoic acid oil, and combinations thereof.
13. The beverage product of claim 1, wherein after consumption of said product, the plasma phospholipid DHA content increases by at least about 20 mole% of total
1005 fatty acids.
14. The beverage product of claim 1, wherein said product exhibits a shelf life of at least about 3 weeks.
1010 15. A method for improving bioavailability of a polyunsaturated fatty acid within a beverage product comprising: providing at least one beverage base; and providing an emulsion comprising: a continuous liquid phase; an emulsifier; and a discontinuous liquid phase comprising a blend including a
1015 polyunsaturated fatty acid source and a dispersing agent, the polyunsaturated fatty acid source comprising the polyunsaturated fatty acid, the polyunsaturated fatty acid source comprising at least one polyunsaturated fatty acid, wherein the weight ratio of the fatty acid source to the dispersing agent in the blend ranges from about 9:1 to about 1 :10.
1020
16. The method of claim 15, wherein the emulsion further comprises β-carotene, enzymes, carotenoids, eucalyptol, eugerol, gingerol, avenacoside, phenolic acids, flavonoids, coumarins, proanthocyanidins, curcuminoids, Vitamin E , Vitamin K, or combinations thereof.
1025
17. The method of claim 15, wherein the discontinuous liquid phase further comprises an oil dispersible bioactive comprising lutein.
18. A method for increasing the plasma phospholipid DHA content in a consumer by 1030 providing the beverage product of claim 1.
19. The method of claim 18, wherein said consumer consumes at least about 180 mL per day for at least about 6 weeks.
1035 20. The method of claim 18, wherein said plasma phospholipid DHA content increases by at least about 20 mole% of total fatty acids.
PCT/US2009/052224 2008-08-22 2009-07-30 Stable beverage products comprising polyunsaturated fatty acid emulsions WO2010021820A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CN2009801328468A CN102131406A (en) 2008-08-22 2009-07-30 Stable beverage products comprising polyunsaturated fatty acid emulsions
EP09790990A EP2317876A1 (en) 2008-08-22 2009-07-30 Stable beverage products comprising polyunsaturated fatty acid emulsions
JP2011523851A JP2012500628A (en) 2008-08-22 2009-07-30 Stable beverage products containing polyunsaturated fatty acid emulsions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US12/196,484 US20090018186A1 (en) 2006-09-06 2008-08-22 Stable beverage products comprising polyunsaturated fatty acid emulsions
US12/196,484 2008-08-22

Publications (1)

Publication Number Publication Date
WO2010021820A1 true WO2010021820A1 (en) 2010-02-25

Family

ID=41327616

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2009/052224 WO2010021820A1 (en) 2008-08-22 2009-07-30 Stable beverage products comprising polyunsaturated fatty acid emulsions

Country Status (5)

Country Link
US (1) US20090018186A1 (en)
EP (1) EP2317876A1 (en)
JP (1) JP2012500628A (en)
CN (1) CN102131406A (en)
WO (1) WO2010021820A1 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011154407A1 (en) * 2010-06-11 2011-12-15 Sensient Food Colors Germany Gmbh Dye emulsion
WO2013120025A1 (en) 2012-02-10 2013-08-15 Virun, Inc. Beverage compositions containing non-polar compounds
WO2013167644A1 (en) * 2012-05-11 2013-11-14 Chr. Hansen A/S A composition comprising chlorophyllin as a green pigment
CN107410819A (en) * 2011-04-04 2017-12-01 帝斯曼知识产权资产管理有限公司 Emulsion oil-in-water comprising polyunsaturated fatty acid with and preparation method thereof
US9861611B2 (en) 2014-09-18 2018-01-09 Virun, Inc. Formulations of water-soluble derivatives of vitamin E and soft gel compositions, concentrates and powders containing same
US10016363B2 (en) 2014-09-18 2018-07-10 Virun, Inc. Pre-spray emulsions and powders containing non-polar compounds

Families Citing this family (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090162524A1 (en) * 2007-12-21 2009-06-25 Tropicana Products, Inc. Food product including one or more omega-3 fatty acids and one or more fruit flavors
US20090162525A1 (en) * 2007-12-21 2009-06-25 Tropicana Products, Inc. Food product including one or more encapsulated omega-3 fatty acids and one or more fruit flavors
WO2009111685A1 (en) 2008-03-06 2009-09-11 Sensient Flavors Llc Herbal extracts and flavor systems for oral products and methods of making the same
EP2268274B1 (en) 2008-03-20 2012-05-16 Virun, Inc. Vitamin e derivatives and their uses
MX2010010050A (en) 2008-03-20 2011-03-15 Virun Inc Star Emulsions including a peg-derivative of tocopherol.
US8337931B2 (en) * 2008-06-23 2012-12-25 Virun, Inc. Compositions containing non-polar compounds
KR20120065276A (en) * 2009-05-29 2012-06-20 뉴 챕터, 인코포레이티드. Compositions and methods for modulating lipid composition
US20100332419A1 (en) * 2009-06-24 2010-12-30 The Coca-Cola Company Product integrated fiber based package
CN102469816A (en) * 2009-08-10 2012-05-23 斯托克里-丰康普公司 Method for suspending a flavonoid in a beverage
WO2011029077A2 (en) * 2009-09-04 2011-03-10 Sensient Flavors Llc Botanical extracts and flavor systems and methods of making and using the same
US8293299B2 (en) 2009-09-11 2012-10-23 Kraft Foods Global Brands Llc Containers and methods for dispensing multiple doses of a concentrated liquid, and shelf stable Concentrated liquids
TWI492744B (en) * 2009-12-04 2015-07-21 Abbott Lab Methods of modulating inflammation in preterm infants using carotenoids
EP2563164B1 (en) * 2010-03-23 2016-06-29 Virun, Inc. Nanoemulsion including sucrose fatty acid ester
US8741373B2 (en) * 2010-06-21 2014-06-03 Virun, Inc. Compositions containing non-polar compounds
US20120040076A1 (en) * 2010-08-11 2012-02-16 E. I. Du Pont De Nemours And Company Aquaculture feed compositions
CN103429100B (en) 2010-09-07 2015-09-02 帝斯曼营养品股份公司 Edible emulsion
EP2635134A1 (en) * 2010-11-03 2013-09-11 DSM IP Assets B.V. Carotenoid compositions containing octenyl succinate anhydride-modified gum acacia
DE102011056111B4 (en) * 2011-12-06 2013-08-14 Sensient Colors Europe Gmbh emulsion
GB201204377D0 (en) * 2012-03-13 2012-04-25 Givaudan Sa Composition
US11013248B2 (en) 2012-05-25 2021-05-25 Kraft Foods Group Brands Llc Shelf stable, concentrated, liquid flavorings and methods of preparing beverages with the concentrated liquid flavorings
US9351517B2 (en) 2013-03-15 2016-05-31 Virun, Inc. Formulations of water-soluble derivatives of vitamin E and compositions containing same
US9693574B2 (en) 2013-08-08 2017-07-04 Virun, Inc. Compositions containing water-soluble derivatives of vitamin E mixtures and modified food starch
CN104642835A (en) * 2013-11-19 2015-05-27 丰益(上海)生物技术研发中心有限公司 Composition containing polyunsaturated fatty acid source and preparation thereof
CA2962900C (en) * 2014-09-29 2021-08-24 Barrie Tan Non-synthetic emulsion-based lipid formulations and methods of use
GB201418848D0 (en) * 2014-10-23 2014-12-03 Givaudan Sa Beverage
CN104366508A (en) * 2014-11-13 2015-02-25 天津禹王生物医药科技有限公司 Lutein ester or lutein emulsion and preparation method of lutein ester or lutein emulsion
CN104489823A (en) * 2015-01-12 2015-04-08 中国海洋大学 Fish oil beverage and production method thereof
WO2016167008A1 (en) * 2015-04-13 2016-10-20 アサヒビール株式会社 Limonene-containing product, scented composition, and method for suppressing generation of deterioration odor
JP6829935B2 (en) * 2015-04-13 2021-02-17 アサヒビール株式会社 Alcoholic beverage
US10537123B2 (en) 2015-04-30 2020-01-21 Kraft Foods Group Brands Llc Quillaja-stabilized liquid beverage concentrates and methods of making same
US10441621B2 (en) 2015-09-23 2019-10-15 Reoxcyn, Llc Flavonoid compositions and methods of use
AU2016326523B2 (en) * 2015-09-23 2019-04-04 Berkley, Llc Flavonoid compositions and methods of use
CN105410566A (en) * 2015-11-30 2016-03-23 杭州鑫伟低碳技术研发有限公司 Method for producing edible oil beverage by using polysaccharide and polysaccharide polymer
CN108260820A (en) * 2016-12-30 2018-07-10 内蒙古蒙牛乳业(集团)股份有限公司 A kind of method of vitamin E online-emulsification
CA3081963A1 (en) 2019-05-31 2020-11-30 American River Nutrition, Llc Compositions comprising quillaja extract and methods of preparations and use thereof
CN111084235B (en) * 2019-12-07 2023-11-03 杭州九阳豆业有限公司 Use of Quillaja saponaria extract for reducing air bubble levels in instant soy flour
CN111264863B (en) * 2020-03-04 2022-09-30 中国热带农业科学院农产品加工研究所 Procyanidine-beta-glucan compound emulsion and preparation method thereof

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994010291A1 (en) * 1992-10-30 1994-05-11 Seed Capital Investment (Sci) B.V. CULTURE CELLS OF $i(QUILLAJA SP.)
EP0659347A1 (en) * 1993-12-20 1995-06-28 San-Ei Gen F.F.I., Inc. Stable emulsified compositions and foods containing the same
WO2001047377A2 (en) * 1999-12-28 2001-07-05 Pronova Biocare As Drinkable omega 3-preparation and storage stabilization
WO2003003849A2 (en) * 2001-07-02 2003-01-16 The Procter & Gamble Company Compositions comprising fatty acids having superior stability and flavour properties
WO2007061804A2 (en) * 2005-11-23 2007-05-31 The Coca-Cola Company High-potency sweetener composition with fatty acid and compositions sweetened therewith
WO2007149590A2 (en) * 2006-06-23 2007-12-27 The Procter & Gamble Company Concentrated omega-3 fatty acids and mixtures containing them
WO2008030949A2 (en) * 2006-09-06 2008-03-13 The Coca-Cola Company Stable polyunsaturated fatty acid emulsions and methods for inhibitintg, suppressing, or reducing degradation of polyunsaturated fatty acids in an emulsion
WO2008075062A1 (en) * 2006-12-18 2008-06-26 Nutraceuticals Limited Compositions comprising polyunsaturated fatty acids
WO2009117152A1 (en) * 2008-03-20 2009-09-24 Virun, Inc. Emulsions including a peg-derivative of tocopherol

Family Cites Families (60)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LU66093A1 (en) * 1972-09-15 1974-03-25
US4368213A (en) * 1981-06-23 1983-01-11 The Procter & Gamble Company Emulsion concentrate for palatable polyester beverage
JPS5916749B2 (en) * 1981-08-20 1984-04-17 日本油脂株式会社 oil-in-water emulsion
EP0092076B1 (en) * 1982-04-16 1986-12-17 Societe Des Produits Nestle S.A. Lipid composition for oral, enteral or parenteral feeding
US4871768A (en) * 1984-07-12 1989-10-03 New England Deaconess Hospital Corporation Dietary supplement utilizing ω-3/medium chain trigylceride mixtures
US4705691A (en) * 1985-11-18 1987-11-10 The Procter & Gamble Co. Beverage opacifier
US4705690A (en) * 1985-11-18 1987-11-10 The Procter & Gamble Co. Weighting oil substitutes
US4780309A (en) * 1987-06-16 1988-10-25 Warner-Lambert Company Edible aerosol foam compositions and method of preparing same
US4843095A (en) * 1987-08-07 1989-06-27 Century Laboratories, Inc. Free fatty acids for treatment or propyhlaxis of rheumatoid arthritis arthritis
US4913921A (en) * 1987-09-11 1990-04-03 General Mills, Inc. Food products containing fish oils stabilized with fructose
US4963380A (en) * 1987-11-30 1990-10-16 General Mills, Inc. Beverages containing fish oils stabilized with fructose
GB8729153D0 (en) * 1987-12-14 1988-01-27 Efamol Ltd Fatty acid compositions
CH681343A5 (en) * 1990-10-26 1993-03-15 Nestle Sa
US5587190A (en) * 1991-10-15 1996-12-24 Pernod Ricard Dietary drink intended to enable sustained activity
US5503846A (en) * 1993-03-17 1996-04-02 Cima Labs, Inc. Base coated acid particles and effervescent formulation incorporating same
CN1098681C (en) * 1994-02-04 2003-01-15 施科舍里皮技术有限公司 Oil-in-water emulsions
WO1996000510A1 (en) * 1994-06-28 1996-01-11 The Procter & Gamble Company Stable beverage fountain syrups containing oil phase and method of stabilizing fountain syrup oil phase
US5607697A (en) * 1995-06-07 1997-03-04 Cima Labs, Incorporated Taste masking microparticles for oral dosage forms
AU721754B2 (en) * 1995-10-17 2000-07-13 Unilever Plc Food dressing
DE69831674T2 (en) * 1997-08-01 2006-06-22 Martek Biosciences Corp. DHA-CONTAINING NEEDLE COMPOSITIONS AND METHOD FOR THE PRODUCTION THEREOF
JPH1160980A (en) * 1997-08-13 1999-03-05 Kagome Co Ltd Water-dispersible carotenoid pigment preparation
JP4761093B2 (en) * 1997-12-10 2011-08-31 シクロスポリン セラポイティクス リミテッド Pharmaceutical composition comprising omega-3 fatty acid oil
US20030059471A1 (en) * 1997-12-15 2003-03-27 Compton Bruce Jon Oral delivery formulation
IL123702A (en) * 1998-03-17 2000-07-16 Adumim Chem Ltd Method for obtaining totally natural super-cloud compositions
US6190680B1 (en) * 1998-04-01 2001-02-20 The Nisshin Oil Mills, Ltd. Oily composition and process for producing the same
NZ500703A (en) * 1998-11-04 2001-06-29 F Preparation of food-grade marine edible oils by treatment with silica, vacuum steam deodorisation and addition of a herb extract
US6740341B1 (en) * 1998-11-25 2004-05-25 Cima Labs Inc. Taste masking rapid release coating system
BR9915963B1 (en) * 1998-12-05 2012-07-24 oil or water care emulsion in the form of milk or cream, dry mix emulsion, dry mix emulsion, and use of a polysaccharide combination, a xanthan polysaccharide and a polyglucomannan polysaccharide.
US6241472B1 (en) * 1999-03-22 2001-06-05 Charles Ross & Son Company High shear rotors and stators for mixers and emulsifiers
EP1194111B1 (en) * 1999-07-13 2006-09-06 CLR Chemisches Laboratorium Dr. Kurt Richter GmbH Uv radiation reflecting or absorbing agents, protecting against harmful uv radiation and reinforcing the natural skin barrier
US6248832B1 (en) * 1999-12-10 2001-06-19 Exxon Mobile Chemical Patents Inc. Crosslinked blends of amorphous and crystalline polymers and their applications
US20020004074A1 (en) * 2000-01-18 2002-01-10 Bakal Abraham I. Food composition containing fish oil and a fish oil stabilizing agent
BR0113105A (en) * 2000-08-08 2003-07-08 Kao Corp Oil / fat composition
JP4391673B2 (en) * 2000-08-08 2009-12-24 花王株式会社 Oil composition
US20020044988A1 (en) * 2000-08-22 2002-04-18 Fuchs Eileen C. Nutritional composition and method for improving protein deposition
US20020188024A1 (en) * 2000-08-23 2002-12-12 Chilton Floyd H. Fatty acid-containing emulsion with increased bioavailability
US6576253B2 (en) * 2000-12-05 2003-06-10 Pbm Pharmaceuticals, Inc. Food bars containing nutritional supplements
JP3735070B2 (en) * 2001-03-26 2006-01-11 花王株式会社 Container-packed emulsified beverage
DE10134660A1 (en) * 2001-07-20 2003-02-06 Basf Plant Science Gmbh New isolated nucleic acid encoding desaturase enzymes from pomegranate, useful for recombinant production of unsaturated fatty acids, for e.g. the production of food, animal feeds and pharmaceuticals
US6635293B2 (en) * 2001-10-23 2003-10-21 Kemin Foods, L.C. Finely dispersed carotenoid suspensions for use in foods and a process for their preparation
JP2003258119A (en) * 2002-03-07 2003-09-12 Seiko Epson Corp Method for manufacturing semiconductor device
AU2003236052A1 (en) * 2002-04-11 2003-10-20 Kyowa Hakko Kogyo Co., Ltd. Liquid food/drink containing fat-soluble vitamin and method of stabilizing fat-soluble vitamin
JP4841140B2 (en) * 2002-06-17 2011-12-21 サントリーホールディングス株式会社 Foam retaining agent and use thereof
EP2368445A1 (en) * 2002-06-18 2011-09-28 Martek Biosciences Corporation Stable Emulsions of Oils in Aqueous Solutions and Methods for Producing Same
WO2004016720A2 (en) * 2002-08-14 2004-02-26 E.I. Du Pont De Nemours And Company Coated polyunsaturated fatty acid-containing particles and coated liquid pharmaceutical-containing particles
EP1585965A4 (en) * 2002-08-29 2009-05-13 Univ Massachusetts Utilization of emulsion interface engineering to produce oxidatively stable lipid delivery systems
DE20220081U1 (en) * 2002-12-23 2003-04-30 Unilever Nv Edible emulsion that contains highly unsaturated fats
WO2004064805A1 (en) * 2003-01-15 2004-08-05 Biodelivery Sciences International, Inc. Cochleate preparations of fragile nutrients
NO317310B1 (en) * 2003-02-28 2004-10-04 Bioli Innovation As Oil-in-water emulsion concentrate for nutritional formula and its use.
ATE418540T1 (en) * 2003-05-30 2009-01-15 Astellas Pharma Inc GALLOYL PEPTIDES
JP4276265B2 (en) * 2003-08-07 2009-06-10 ザ プロクター アンド ギャンブル カンパニー Concentrated oil-in-water emulsion
MXPA06001475A (en) * 2003-08-07 2006-05-15 Procter & Gamble Emulsions with a concentrated internal oil phase.
WO2005016292A1 (en) * 2003-08-07 2005-02-24 The Procter & Gamble Company Oil emulsions
US20050233051A1 (en) * 2004-04-15 2005-10-20 Solae, Llc Acid beverage composition utilizing a protein and a vegetable oil and process for making same
US7232585B2 (en) * 2004-06-24 2007-06-19 Xel Herbaceuticals, Inc. Green tea formulations and methods of preparation
US20060088574A1 (en) * 2004-10-25 2006-04-27 Manning Paul B Nutritional supplements
JP5050322B2 (en) * 2005-06-21 2012-10-17 三菱化学株式会社 Oil-containing solid and method for producing the same
US8153180B2 (en) * 2005-09-06 2012-04-10 Pepsico, Inc. Method and apparatus for making beverages
US9743680B2 (en) * 2005-10-14 2017-08-29 Wild Flavors, Inc. Microemulsions for use in food and beverage products
US20070298079A1 (en) * 2006-06-26 2007-12-27 Tropicana Products, Inc. Food fortified with omega-3 fatty acids

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994010291A1 (en) * 1992-10-30 1994-05-11 Seed Capital Investment (Sci) B.V. CULTURE CELLS OF $i(QUILLAJA SP.)
EP0659347A1 (en) * 1993-12-20 1995-06-28 San-Ei Gen F.F.I., Inc. Stable emulsified compositions and foods containing the same
WO2001047377A2 (en) * 1999-12-28 2001-07-05 Pronova Biocare As Drinkable omega 3-preparation and storage stabilization
WO2003003849A2 (en) * 2001-07-02 2003-01-16 The Procter & Gamble Company Compositions comprising fatty acids having superior stability and flavour properties
WO2007061804A2 (en) * 2005-11-23 2007-05-31 The Coca-Cola Company High-potency sweetener composition with fatty acid and compositions sweetened therewith
WO2007149590A2 (en) * 2006-06-23 2007-12-27 The Procter & Gamble Company Concentrated omega-3 fatty acids and mixtures containing them
WO2008030949A2 (en) * 2006-09-06 2008-03-13 The Coca-Cola Company Stable polyunsaturated fatty acid emulsions and methods for inhibitintg, suppressing, or reducing degradation of polyunsaturated fatty acids in an emulsion
WO2008075062A1 (en) * 2006-12-18 2008-06-26 Nutraceuticals Limited Compositions comprising polyunsaturated fatty acids
WO2009117152A1 (en) * 2008-03-20 2009-09-24 Virun, Inc. Emulsions including a peg-derivative of tocopherol

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011154407A1 (en) * 2010-06-11 2011-12-15 Sensient Food Colors Germany Gmbh Dye emulsion
CN107410819A (en) * 2011-04-04 2017-12-01 帝斯曼知识产权资产管理有限公司 Emulsion oil-in-water comprising polyunsaturated fatty acid with and preparation method thereof
WO2013120025A1 (en) 2012-02-10 2013-08-15 Virun, Inc. Beverage compositions containing non-polar compounds
US10874122B2 (en) 2012-02-10 2020-12-29 Virun, Inc. Beverage compositions containing non-polar compounds
WO2013167644A1 (en) * 2012-05-11 2013-11-14 Chr. Hansen A/S A composition comprising chlorophyllin as a green pigment
US9861611B2 (en) 2014-09-18 2018-01-09 Virun, Inc. Formulations of water-soluble derivatives of vitamin E and soft gel compositions, concentrates and powders containing same
US10016363B2 (en) 2014-09-18 2018-07-10 Virun, Inc. Pre-spray emulsions and powders containing non-polar compounds
US10285971B2 (en) 2014-09-18 2019-05-14 Virun, Inc. Formulations of water-soluble derivatives of vitamin E and soft gel compositions, concentrates and powders containing same

Also Published As

Publication number Publication date
US20090018186A1 (en) 2009-01-15
CN102131406A (en) 2011-07-20
JP2012500628A (en) 2012-01-12
EP2317876A1 (en) 2011-05-11

Similar Documents

Publication Publication Date Title
US20090018186A1 (en) Stable beverage products comprising polyunsaturated fatty acid emulsions
US20080058418A1 (en) Stable polyunsaturated fatty acid emulsions and methods for inhibiting, suppressing, or reducing degradation of polyunsaturated fatty acids in an emulsion
EP2555761B1 (en) Thermally stable oil-in-water emulsions containing an oil that contains polyunsaturated fatty acids
EP2696839B1 (en) Methods of making oil-in-water emulsions
US20170064984A1 (en) Oil-in-water emulsions comprising a polyunsaturated fatty acid and methods of making the same
AU2014235283B2 (en) Formulations of water-soluble derivatives of vitamin E and compositions containing same
AU2007212412B2 (en) Dietary supplement composition for blood lipid health
CN101553136A (en) Stable polyunsaturated fatty acid emulsions and methods for inhibitintg, suppressing, or reducing degradation of polyunsaturated fatty acids in an emulsion
US20140271593A1 (en) Formulations of water-soluble derivatives of vitamin e and compositions containing same
US20210251894A1 (en) Functional beverage compositions and methods of using and making same
Md et al. Nanoemulsions to preserve/process bioactive and nutritional food compounds: contemporary research and applications
CA3135250C (en) Stable emulsified vitamin and omega fatty acid compositions and process for preparing same
JP2013509888A (en) Composition containing lipids suitable for edible use

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200980132846.8

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 09790990

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2011523851

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 2009790990

Country of ref document: EP

NENP Non-entry into the national phase

Ref country code: DE