WO2010057852A1 - Poudres d'huile solide - Google Patents
Poudres d'huile solide Download PDFInfo
- Publication number
- WO2010057852A1 WO2010057852A1 PCT/EP2009/065229 EP2009065229W WO2010057852A1 WO 2010057852 A1 WO2010057852 A1 WO 2010057852A1 EP 2009065229 W EP2009065229 W EP 2009065229W WO 2010057852 A1 WO2010057852 A1 WO 2010057852A1
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- Prior art keywords
- oil
- powder
- accordance
- protein
- oils
- Prior art date
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Classifications
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/02—Edible oil or fat compositions containing an aqueous phase, e.g. margarines characterised by the production or working-up
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23D—EDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
- A23D7/00—Edible oil or fat compositions containing an aqueous phase, e.g. margarines
- A23D7/005—Edible oil or fat compositions containing an aqueous phase, e.g. margarines characterised by ingredients other than fatty acid triglycerides
- A23D7/0053—Compositions other than spreads
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/115—Fatty acids or derivatives thereof; Fats or oils
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/16—Inorganic salts, minerals or trace elements
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/17—Amino acids, peptides or proteins
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
- A23P10/00—Shaping or working of foodstuffs characterised by the products
- A23P10/30—Encapsulation of particles, e.g. foodstuff additives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23P—SHAPING OR WORKING OF FOODSTUFFS, NOT FULLY COVERED BY A SINGLE OTHER SUBCLASS
- A23P10/00—Shaping or working of foodstuffs characterised by the products
- A23P10/40—Shaping or working of foodstuffs characterised by the products free-flowing powder or instant powder, i.e. powder which is reconstituted rapidly when liquid is added
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B15/00—Solidifying fatty oils, fats, or waxes by physical processes
Definitions
- the present invention relates in general to the field of oil powders.
- the present invention relates to an oil composition that is in powder form at room temperature.
- One embodiment of the present invention is a solid oil powder that has a very high oil content.
- Solidification of oil-in water emulsions is a technique that is employed in the pharmaceutical, cosmetic and food industry to reduce a liquid-oil base into a so lid- like powder.
- the most diffused method is spray drying the emulsion to rapidly evaporate the water continuous phase (Faldt, P. et al. Food Hydrocolloids, 10, 421 (1996), Vega C. et al. Food Hydrocolloids, 45, 66 (2005), Fuchs, M. et al. J. Food Engineering, 75, 27 (2006), Bruckner, M. et al. European Food, Research. And Technology, 226, 137 (2007), Baranauskiene, R. et al. J. Agric. Food Chem., 55, 3027 (2007)).
- This method is typically used to encapsulate hydrophobic compounds and aroma into the oil droplets or to increase stability of oil against oxidation (Klinkesorn, U. et al. J. Agric. Food Chem., 53, 8365 (2005), Gu, Y. S. et al. J. Agric. Food Chem., 52, 3626 (2004), Shaw, L. A. et al. J. Agric. Food Chem., 55, 3112 (2007)).
- a solid hydrophilic carrier is normally added to the water solution.
- this hydrophilic carrier together with the surfactant used to stabilize the liquid emulsion, constitute the continuous phase of the powder, also referred to as "solid dry base".
- the minimum amount of solid hydrophilic carrier needed varies from study to study but it is in general comprised between 30 and 80 weight-% of the total dry base (Klinkesorn, U. et al. J. Agric. Food Chem., 53, 8365 (2005), Gu, Y. S. et al. J. Agric. Food Chem., 52, 3626 (2004), Jost, R. et al. Food Microstructure, 8, 23 (1989)).
- Typical examples of the constituents of the solid dry base are lactose, glucose, maltodextrin, starch and cellulose.
- This hydrophilic carrier in the formulation alters the composition of the powder with respect the original emulsion, concentrating the solid carrier into the final powder, and thus reducing the amount of liquid dry base (the oil droplets). Without the presence of this solid carrier, however, the emulsion droplets coalesce either during the spray drying processing or afterwards, leading to the collapse of the powder and the leaking of the oil.
- a possible alternative way to the introduction of this solid carrier is the stabilization of the oil droplets interfaces in a physico-chemical way in order to provide enough elasticity to the interfaces to survive the spray drying process.
- a typical example is the multi-step deposition onto the droplets surfaces of positively charged polyelectrolytes capable to crosslink by ionic complexation, thus providing to the interfaces the need elasticity (Klinkesorn, U. et al. J. Agric. Food Chem., 53, 8365 (2005), Gu, Y. S. et al. J. Agric. Food Chem., 52, 3626 (2004), Moreau, L.et al. J. Agric. Food Chem., 51, 6612 (2003)).
- a typical example would be to stabilize an oil- in water emulsion by a protein and to adjust the solution pH to acidic enough values to positively charge the protein. Then the emulsion is dialyzed or diluted with another water solution containing a negatively charged polyelectrolyte capable to ionically complex with the positively charged oil droplets interfaces (made positive by the protein layer).
- Another variant is to stabilize the droplets by a low molecular weight anionic surfactant such as lecithin and then expose the emulsion to a polycationic polsaccharide, such as chitosan.
- dried solid oil powders comprising oily compounds that are usually liquid at room temperature are available today only in formulations, which comprise a relatively high weight percentage of non-oily compounds. Having available at room temperature a dry solid oil powder comprising a very high percentage of oily compounds or even consisting essentially of oily compounds would bring about several significant advantages, such as simpler formulations, absence of water- transport layers, increased hydrophobic encapsulation efficiency, etc. Consequently, there is a need in the art for such solid oil powders.
- the inventors have used protein stabilized oil-in-water emulsions, thermal cross- linking and spray drying techniques to achieve, for example, in a one-step process, solid oil powders in which the total amount of oil can be easily made for example as high to 95% by weight, and possibly as high as 99%, without compromising the solid nature of the powder.
- the solid dry base is simply given by the protein cross-linked around the droplet surfaces (typically 1% or less), and the optional presence of salt (typically 5% or less and only if the emulsion is spray dried from a buffer salt solution).
- one embodiment of the present invention is an oil powder that is solid at room temperature and that comprises at least 90 weight-%, preferably at least 95 weight-%, even more preferred at least 99 weight-% oil.
- a powder is a bulk, granular solid composed of a large number of fine particles that may flow freely when shaken or tilted.
- the oil powder of the present invention is preferably a dry powder.
- an oil powder considered as dry if no more than 1 weight-% of oil - and preferably no oil - is leaking out of the oil powder at room temperature, if the oil powder is stored at room temperature for 24 hours without exceeding the normal atmospheric pressure.
- the oil powder of the present invention is considered as solid if the powder particles that comprise the possibly liquid oil retain their individual three-dimensional structure and are not "melting".
- the solid oil powders of the present invention have for example the advantages that they can be produced with a very simple and efficient procedure, for example a one- step-process, that they can be produced with very high oil contents, that they do not require a solid dry base as the powders of the prior art, and that the can be produced with only protein as additive and optionally with salt, which is both skin friendly, natural and generally even food grade.
- a solid oil powder comprising 90 weight-% oil may comprise up to 10 weight-% protein.
- a solid oil powder according to the present invention comprise a maximum of 1 weight-% protein and/or a maximum of 5 weight-% salt.
- the oil powder in accordance with the present invention in particular the individual particles of the powder, may comprise an inner core comprising the oil fraction and an outer shell comprising cross-linked protein.
- the amount of protein and/or salt used may be adjusted to fine tune the stability of the particles.
- the particles are meant to release their oil content under pressure.
- the amount of protein and/or salt used along with the degree of crosslinking of the protein shell of the powder particles will determine the amount of pressure needed to release the oil.
- the particles may also be designed to release their oily content upon application of heat.
- Heat application will cause the oil to expand, which will ultimately lead to a disruption of the protein shell around the oil fraction. The thicker the protein membrane is the more heat will be needed to liberate the oil from the shell.
- oils that can be used in accordance with the present invention are not particularly limited.
- the term "oil” comprises for the purpose of the present invention mineral oils, and/or organic oils (oils produced by plants or animals), in particular food grade oils and/or oils for cosmetic applications.
- Typical mineral oils comprise paraff ⁇ nic oils (based on n-alkanes), naphthenic oils (based on cycloalkanes), and aromatic oils (based on aromatic hydrocarbons).
- the food grade oil and/or oil for cosmetic applications may for example be selected from the group consisting of olive oil, safflower oil, sunflower oil, fish oil, soy bean oil, soy oil, palm kernel oil, palm oil, coconut oil, flaxseed oil, rapeseed oil, primrose oil, essential oils, animal oil, mineral oils, organic oil and combinations thereof.
- An essential oil is a concentrated, hydrophobic liquid containing volatile aroma compounds, for example from plants. They are also known as volatile or ethereal oils.
- An oil is "essential" in the sense that it carries at least one scent, or essence, for example of a plant. Essential oils are often used in cosmetic applications to produce a fragrance.
- the protein that is used to encapsulate the oil to produce the dry powder of the present invention may be any protein.
- the protein is a food grade protein and/or a protein that provides additional benefits to the consumer, for example in terms of taste, texture, and/or anti-allergenicity.
- milk- and/or whey derived proteins are preferred.
- Preferred milk proteins or milk protein fractions in accordance with the present invention comprise whey proteins, ⁇ -lactalbumin, ⁇ -lactoglobulin, bovine serum albumin, acid casein, casemates, ⁇ -casein, ⁇ -casein, ⁇ -casein, for example.
- the protein source may be based on acid whey or sweet whey or mixtures thereof and may include alpha- lactalbumin and beta- lactoglobulin in whatever proportions are desired.
- the proteins may be intact or at least partially hydro lysed. It may be desirable to use partially hydro lysed proteins (for example with a degree of hydrolysis between 2 and 20%), for subjects that are believed to be at risk of developing cows' milk allergy.
- the protein may comprise comprise ⁇ -lactalbumin, ⁇ -lacto globulin, bovine serum albumin, acid casein, casemates, ⁇ -casein, ⁇ -casein, ⁇ -casein,, egg albumen, lyzozyme, soy proteins, gluten, rice proteins, corn proteins, potato proteins, pea proteins, or any kind of globular and random coil proteins or combinations thereof.
- the salt that may be used in accordance with the present invention is equally not particularly limited. Preferred are alkali metal salts or earth alkali metal salts.
- the oil powder may comprise sodium citrate, magnesium citrate, potassium citrate, or combinations thereof.
- the oil powder of the present invention may be used for example as a vehicle to deliver valuable compounds.
- the oil may contain such a valuable compound.
- the oil may contain at least one liposoluble compound, such as for example a plant polyphenols, a fatty acid, such as DHA, n-3 fatty acids such as ⁇ -linolenic acid, stearidonic acid, eicosatrienoic acid, eicosatetraenoic acid, eicosapentaenoic acid, docosapentaenoic acid, clupanodonic acid, docosahexaenoic acid, tetracosapentaenoic acid, or tetracosahexaenoic acid, n-6 fatty acids such as linoleic acid, gamma- lino lenic acid, eicosadienoic acid, dihomo- gamma- lino lenic acid, arachidonic acid, docosadienoic acid, adrenic acid, docosapentaenoic acid
- a fatty acid such as
- the single particles of the oil powder of the present invention may have any size depending only on the intended use of the powder. Larger particles will allow reducing the amount of protein necessary to encapsulate the oil even further. Smaller particles will in general have a greater stability and will allow a more exact dosability. Typical particle diameters of the oil powder in accordance with the present invention may be in the range of about 0,1-100 ⁇ m, for example about 1 to 50 ⁇ m.
- the oil powder of the present invention may be used in a number of different applications.
- the oil powder may be used for the production of a composition, wherein preferably, the composition is selected from the group consisting of a lubricant, a food composition, a food additive, a nutraceutical, a pharmaceutical composition and/or a cosmetic composition.
- Such a composition has the advantage that it may be used to protect the oil and/or the liposoluble compounds contained therein, for example from influences that reduce the quality of the composition such as oxidative damage.
- compositions comprising the oil powder of the present invention will furthermore provide an improved flowability and/or an improved dosability of the oils and/or of the liposoluble compounds that may be contained therein.
- composition and/or the oil powders of the present invention may be used to provide a powder that is re-dispersable in water as a single primary emulsion.
- Primary emulsions are two-phase systems in which a phase, such as oil, is dispersed in another phase, such as water. These emulsion are referred to as primary oil- in- water emulsions. By dispersing water in an oil matrix, one will refer to these systems as water-in-oil primary emulsions.
- the powder of the present invention may conveniently be used to produce emulsions in hydrophilic solvents, such as water, for example, simply by adding the powder to the hydrophilic solvent and by agitating.
- hydrophilic solvents such as water
- the powder of the present invention has the advantage that it can be used to bring oil into contact, for example, with the skin or with another surface, while it can be avoided that an oil film is left behind, for example, on a device that is used to apply the oil. Further, accidental spills of the powder of the present invention can be easily swept away without the need to use detergents to remove an oil film. Oil is released from the powder of the present invention only by applying stress to the individual particles, so that the protein shell is bursting and the at least one oil is set free.
- the oil powder can release liquid oils for example upon sharing, compression, shaking, squeezing, spreading or combination thereof.
- the present invention further extends to a method to prepare an oil of the present invention.
- Such a method comprises the steps of mixing the oil, the protein and optionally the salt, and/or at least one liposoluble compound to prepare an emulsion, cross-link the protein, - spray dry the emulsion to generate the oil powder.
- the protein may be crosslinked by any method that is known in the art, for example by UV-radiation, chemically, enzymatically or by heat application for example by elevating the temperature to at least 70 0 C for at least 5 minutes.
- Figure 1 shows the parent size distribution of a 10% olive oil- in- water emulsion stabilized by 1% ⁇ -lactoglobulin, prior and after the cross-linking process.
- Figure 2A shows the aspect of the resulting spray dried powder (after 15 minutes at 80 0 C heat denaturation of the protein at the interface) from the emulsion described in Figure 1.
- the spray drying was done in a B ⁇ chi 190 mini spray dryer (temperature inlet 125°C, outlet 84°C).
- Figure 2B shows the same powder of Figure 2A, as observed by Bright field light microscopy.
- Figure 2C shows the same powder of Figure 2A, as observed by UV Light Microscopy (excitation: BP450-490, emission LP 520, Nile Red staining, Mounting agent: glycerol 40%).
- Figure 2D shows the same powder of Figure 2A, as observed by Bright Field Light Microscopy (Protein Staining). Cryofixation: anhydrous Glutaraldehyde/ Osmium tetraoxide in methanol. Embedding: Spurr. Thin sections 1 micron: Staining: Toluidine blue. Figure 2E shows the same powder of Figure 2A, as observed by Bright Field Light Microscopy (Protein Staining). Cryof ⁇ xation: anhydrous Glutaraldehyde/ Osmium tetraoxide in methanol. Embedding: Spurr. Thin sections 1 micron: Staining: Toluidine blue. (Higher magnification compared to Figure 2D).
- Figure 3 shows the aspect of a spray dried powder (after 15 minute at 80 0 C heat denaturation of the protein at the interface) from a 10% olive oil- in- water emulsion stabilized by 4% soy protein (spray drying was done in a B ⁇ chi 190 mini spray dryer (temperature inlet 125°C, outlet 84°C).
- Example 1 Spray dried olive oil powder (with beta-lactoglobulin protein)
- Sol A Prepare a 20 mM of tri-sodium citrate buffer solution (11.764g/21)
- Emulsion Olive oil in 1% Big buffer solution Emulsion Olive oil in 1% Big buffer solution
- Table 1 shows the characteristic of the parent emulsion as studied by a Malvern Mastersizer.
- the obtained dry oil powder was analyzed by
- Glutaraldehyde/ Osmium tetroxide in methanol Embedding: Spurr. Thin sections 1 micron: Staining: Toluidine blue.
- Cryofixation anhydrous Glutaraldehyde/ Osmium tetroxide in methanol.
- Embedding Spurr.
- Thin sections 1 micron Staining: Toluidine blue.
- Example 2 Spray dried olive oil powder with soy proteins
- Sol A Prepare a 20 mM of tri-sodium citrate buffer solution ( 11.764g/21)
- Sol B Prepare a solution of 4% soy protein (Solpro 958 90%) in the buffer (17.6g Blg/382.4g buffer) by controlling the pH at 8 with NaOH 1 M
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Abstract
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2738986A CA2738986C (fr) | 2008-11-19 | 2009-11-16 | Poudres d'huile solide |
AU2009317352A AU2009317352B2 (en) | 2008-11-19 | 2009-11-16 | Solid oil powders |
BRPI0922051A BRPI0922051B1 (pt) | 2008-11-19 | 2009-11-16 | óleo em pó, seu uso e seu método de preparação |
UAA201107617A UA105506C2 (uk) | 2008-11-19 | 2009-11-16 | Тверда олія в порошку |
US13/125,230 US8609118B2 (en) | 2008-11-19 | 2009-11-16 | Solid oil powders |
NZ591660A NZ591660A (en) | 2008-11-19 | 2009-11-16 | Solid oil powders |
RU2011124935/13A RU2523297C2 (ru) | 2008-11-19 | 2009-11-16 | Твердые масляные порошки |
CN200980145614.6A CN102215697B (zh) | 2008-11-19 | 2009-11-16 | 固体油粉末 |
IL211538A IL211538A (en) | 2008-11-19 | 2011-03-03 | Solid oil powders |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08169434.1 | 2008-11-19 | ||
EP08169434A EP2191730B1 (fr) | 2008-11-19 | 2008-11-19 | Poudres d'huile solides |
Publications (1)
Publication Number | Publication Date |
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WO2010057852A1 true WO2010057852A1 (fr) | 2010-05-27 |
Family
ID=40512492
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/EP2009/065229 WO2010057852A1 (fr) | 2008-11-19 | 2009-11-16 | Poudres d'huile solide |
Country Status (16)
Country | Link |
---|---|
US (1) | US8609118B2 (fr) |
EP (1) | EP2191730B1 (fr) |
CN (1) | CN102215697B (fr) |
AT (1) | ATE509529T1 (fr) |
AU (1) | AU2009317352B2 (fr) |
BR (1) | BRPI0922051B1 (fr) |
CA (1) | CA2738986C (fr) |
ES (1) | ES2364443T3 (fr) |
IL (1) | IL211538A (fr) |
MY (1) | MY155476A (fr) |
NZ (1) | NZ591660A (fr) |
PL (1) | PL2191730T3 (fr) |
PT (1) | PT2191730E (fr) |
RU (1) | RU2523297C2 (fr) |
UA (1) | UA105506C2 (fr) |
WO (1) | WO2010057852A1 (fr) |
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WO2014006084A1 (fr) | 2012-07-03 | 2014-01-09 | Nestec S.A. | Produit de confiserie comprenant une poudre d'huile agglomérée |
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WO2017126668A1 (fr) * | 2016-01-21 | 2017-07-27 | 日清オイリオグループ株式会社 | Épaississant de composant liquide |
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WO2019081398A1 (fr) | 2017-10-26 | 2019-05-02 | Nestec S.A. | Procédé de fabrication permettant de produire une poudre de fibres lipidiques |
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CN113040229B (zh) * | 2019-12-26 | 2024-05-24 | 丰益(上海)生物技术研发中心有限公司 | 一种油脂组合物及其制备方法 |
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EP1925211A1 (fr) * | 2006-11-27 | 2008-05-28 | Friesland Brands B.V. | Procédé de préparation d'huiles poudrées |
WO2009084205A1 (fr) * | 2007-12-28 | 2009-07-09 | Kao Corporation | Procédé de production d'une préparation cosmétique |
-
2008
- 2008-11-19 EP EP08169434A patent/EP2191730B1/fr not_active Not-in-force
- 2008-11-19 PT PT08169434T patent/PT2191730E/pt unknown
- 2008-11-19 ES ES08169434T patent/ES2364443T3/es active Active
- 2008-11-19 PL PL08169434T patent/PL2191730T3/pl unknown
- 2008-11-19 AT AT08169434T patent/ATE509529T1/de active
-
2009
- 2009-11-16 UA UAA201107617A patent/UA105506C2/uk unknown
- 2009-11-16 MY MYPI2011001004A patent/MY155476A/en unknown
- 2009-11-16 AU AU2009317352A patent/AU2009317352B2/en not_active Ceased
- 2009-11-16 CN CN200980145614.6A patent/CN102215697B/zh not_active Expired - Fee Related
- 2009-11-16 BR BRPI0922051A patent/BRPI0922051B1/pt not_active IP Right Cessation
- 2009-11-16 WO PCT/EP2009/065229 patent/WO2010057852A1/fr active Application Filing
- 2009-11-16 NZ NZ591660A patent/NZ591660A/xx not_active IP Right Cessation
- 2009-11-16 CA CA2738986A patent/CA2738986C/fr not_active Expired - Fee Related
- 2009-11-16 RU RU2011124935/13A patent/RU2523297C2/ru not_active IP Right Cessation
- 2009-11-16 US US13/125,230 patent/US8609118B2/en not_active Expired - Fee Related
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2011
- 2011-03-03 IL IL211538A patent/IL211538A/en not_active IP Right Cessation
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EP0372669A1 (fr) * | 1988-12-07 | 1990-06-13 | Asama Chemical Co., Ltd. | Poudre d'huile ou graisse stabilisée |
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US5776490A (en) * | 1996-01-26 | 1998-07-07 | The Center For Innovative Technology | Complex protein-walled microcapsules containing lipid-walled microcapsules and method for producing same |
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012089676A1 (fr) * | 2010-12-29 | 2012-07-05 | Nestec S.A. | Composition de garniture comportant une huile encapsulée |
CN103281913A (zh) * | 2010-12-29 | 2013-09-04 | 雀巢产品技术援助有限公司 | 包含团聚的油粉的糖果产品 |
CN103281906A (zh) * | 2010-12-29 | 2013-09-04 | 雀巢产品技术援助有限公司 | 包含包封油的填充物组合物 |
CN103281908A (zh) * | 2010-12-29 | 2013-09-04 | 雀巢产品技术援助有限公司 | 包封的油在面团制品中的用途 |
JP2014501115A (ja) * | 2010-12-29 | 2014-01-20 | ネステク ソシエテ アノニム | カプセル化油を含むフィリング用組成物 |
US9504265B2 (en) | 2010-12-29 | 2016-11-29 | Nestec S.A. | Filling composition comprising an encapsulated oil |
RU2615481C2 (ru) * | 2010-12-29 | 2017-04-04 | Нестек С.А. | Композиция наполнителя, содержащая инкапсулированное масло |
CN107251956A (zh) * | 2010-12-29 | 2017-10-17 | 雀巢产品技术援助有限公司 | 包含包封油的填充物组合物 |
WO2014006084A1 (fr) | 2012-07-03 | 2014-01-09 | Nestec S.A. | Produit de confiserie comprenant une poudre d'huile agglomérée |
CN104582492A (zh) * | 2012-07-03 | 2015-04-29 | 雀巢产品技术援助有限公司 | 包含团聚油粉末的甜食产品 |
Also Published As
Publication number | Publication date |
---|---|
RU2011124935A (ru) | 2012-12-27 |
CA2738986C (fr) | 2017-08-22 |
PL2191730T3 (pl) | 2011-10-31 |
US20110223225A1 (en) | 2011-09-15 |
CN102215697B (zh) | 2014-05-21 |
ATE509529T1 (de) | 2011-06-15 |
BRPI0922051A2 (pt) | 2015-08-04 |
ES2364443T3 (es) | 2011-09-02 |
US8609118B2 (en) | 2013-12-17 |
CA2738986A1 (fr) | 2010-05-27 |
IL211538A (en) | 2015-06-30 |
NZ591660A (en) | 2013-05-31 |
CN102215697A (zh) | 2011-10-12 |
BRPI0922051B1 (pt) | 2020-02-04 |
RU2523297C2 (ru) | 2014-07-20 |
EP2191730B1 (fr) | 2011-05-18 |
AU2009317352A1 (en) | 2010-05-27 |
UA105506C2 (uk) | 2014-05-26 |
MY155476A (en) | 2015-10-30 |
IL211538A0 (en) | 2011-05-31 |
AU2009317352B2 (en) | 2014-10-16 |
PT2191730E (pt) | 2011-05-30 |
EP2191730A1 (fr) | 2010-06-02 |
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