WO2019093708A1 - Procédé de production de composition de suppression d'odeur contenant de l'huile insaturée et de l'arginine - Google Patents
Procédé de production de composition de suppression d'odeur contenant de l'huile insaturée et de l'arginine Download PDFInfo
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- WO2019093708A1 WO2019093708A1 PCT/KR2018/013082 KR2018013082W WO2019093708A1 WO 2019093708 A1 WO2019093708 A1 WO 2019093708A1 KR 2018013082 W KR2018013082 W KR 2018013082W WO 2019093708 A1 WO2019093708 A1 WO 2019093708A1
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- arginine
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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 OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- 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
- A23L33/12—Fatty acids or derivatives thereof
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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 OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/20—Removal of unwanted matter, e.g. deodorisation or detoxification
Definitions
- the present invention relates to a method for producing an odor-suppressing biologically-derived unsaturated oil and an arginine-containing composition, and a composition prepared thereby.
- Omega-3 fatty acids have a double bond at the third carbon position from the end of a hydrocarbon chain. They contain a large amount of fatty acids such as fish oil and flaxseed oil, which are refined and used as food additives and health functional foods.
- omega-3s such as EPA (Eicosapentaenoic acid) and DHA (Docosahexaenoic acid) in fish oil and seaweed
- omega-3 fatty acid called ALA (Alpha-linoleic acid)
- This omega-3 fatty acid lowers the levels of triglycerides and cholesterol and inhibits thrombus formation. It also reduces inflammation, helps absorption of calcium, helps calm, improves bone function, and prevents various adult diseases. Therefore, omega-3 fatty acids have been reported to prevent hypertension and arteriosclerosis, prevent Alzheimer's disease, anti-cancer effect and anti-inflammatory effects such as diabetes prevention, vision protection and arthritis.
- omega-3 can not be used as a treatment for cardiovascular disease or Alzheimer's disease.
- omega-3 is present in the membranes of the human body, but it can not be synthesized in the body, so it is an essential fatty acid to be supplied from the outside, so taking or ingesting it is essential. Therefore, omega-3 health functional foods need to be taken to supplement at least essential fatty acids.
- arginine a kind of essential amino acid
- Nitric oxide is a signaling substance and is involved in various physiological activities such as immune function and vasodilation. Therefore, arginine is effective for hypertension and cardiovascular disease, improves blood supply, improves athletic performance, and has been reported to prevent hair loss. It is also known that it facilitates insulin secretion, improves sexual function as a neurotransmitter, and acts as an immune defense.
- omega-3 tends to avoid consumption because of its odor, compared with excellent efficacy.
- Unsaturated fatty acids such as omega-3 fatty acids are oxidized from the moment they are extracted and react with oxygen to form hydroperoxides and free radicals, which are then decomposed into aldehydes and alcohols.
- malodorous odors are caused by the aldehyde compounds such as cis-4-heptenal, octanal, 2,4-octadienal, trans-2 and cis-6-nonadienal.
- Oxidized unsaturated fatty acids do not cause clinical side effects, but about 10% of fishy asians and about 20% of Westerners who take omega-3 fatty acids from fish oil as a raw material cause omega-3 to be avoided. It is the main reason to lower the preference.
- Reference 1 has used a method of mixing a strong fragrance such as lemon fragrance into fish oil or the like in large quantities and then forming a soft capsule to shield the odor.
- Reference 2 of the present invention has developed a food composition containing lemon fragrance.
- Cited Reference 3 used omega-3 coated with corn zein to make confectionery such as chips and cookies. In reference 4, whey and amino acid source were added to foods such as bread containing fat to prevent oxidation of fat, thereby enhancing consumers' taste and prolonging the preservation period.
- Citation 5 has developed a beverage composition in which fish oil and juice are made into an oil-in-water emulsion for cancer treatment and post treatment.
- Reference 6 has developed a method of smelling odor by immersing spice plants such as thyme, log wood and the like in fish oil for at least 20 days at around 20 degrees .
- the technology has been used to mask odor by using a strong incense or flavor masking method to eliminate rancidity odor, or to smell the odor by mixing proteins such as zein, whey protein and amino acid source.
- proteins such as zein, whey protein and amino acid source.
- zein, whey and amino acid source which are a complex of a wide range of amino acids, are used without specifying the chemical action with the odor source. Therefore, there is a problem that the odor removal efficiency is not high.
- imines produced by reaction with aldehydes, amino acids, proteins and the like, which cause odor are hydrolyzed by gastric acid upon ingestion, resulting in an adverse reaction that generates aldehydes, resulting in odor in the trim.
- an object of the present invention is to provide an unsaturated oil and an arginine-containing composition containing arginine capable of supplementing unsatisfactory action of an unsaturated oil in addition to an unsaturated biological oil including omega-3 fatty acids,
- the present invention provides a composition capable of eliminating or reducing odor caused by an aldehyde compound generated when an unsaturated oil is oxidized, and a method for producing the same.
- a method for producing an odor-suppressing unsaturated oil and an arginine-containing composition which comprises mixing at least one of sulfur compounds capable of generating sulfur dioxide and cysteine with an unsaturated oil to remove an aldehyde compound generated from the unsaturated oil step; And adding arginine or a salt thereof to the composition, and a process for producing an odor-suppressing unsaturated oil and an arginine-containing composition.
- the sulfur compounds capable of generating sulfur dioxide include at least one of sodium sulfite, sodium acid sulfite, sodium metabisulfite, sodium dibasulfite, potassium sulfite, potassium metabisulfite, potassium acid sulfite and calcium hydrogen sulfite Containing unsaturated oil and a method for producing an arginine-containing composition.
- the salt of arginine is at least one of a hydrochloride salt, a sulfate salt, and a nitrate salt, and provides a method of preparing an odor-suppressing unsaturated oil and an arginine-containing composition.
- the method provides a method for preparing an odor-suppressing unsaturated oil and an arginine-containing composition, which further comprises a step of precipitating and removing the sulfite adduct produced after removing the aldehyde compound .
- the method comprises the step of adding a basic amino acid to remove residual sulfur dioxide after the step of removing the aldehyde compound, and a method for producing an odor-suppressing unsaturated oil and an arginine- to provide.
- the method further comprises the step of adding a lipophilic bioactive material after the step of adding arginine or a salt thereof, wherein the lipophilic bioactive material is an anthocyanin, saponin, ginsenoside, quercetin, Containing unsaturated oil and an arginine-containing composition, wherein the composition is at least one or more selected from the group consisting of furitrine, curcumin, cinnamide, lycopene, beta carotene, lutein, vitamin E, polyphenol, tocopherol and terpene.
- the lipophilic bioactive material is an anthocyanin, saponin, ginsenoside, quercetin, Containing unsaturated oil and an arginine-containing composition, wherein the composition is at least one or more selected from the group consisting of furitrine, curcumin, cinnamide, lycopene, beta carotene, lutein, vitamin E, polyphenol, tocopherol and ter
- Another aspect of the present invention provides an odor-suppressing unsaturated oil and an arginine-containing composition produced by any one of the above-described manufacturing methods.
- the odor-suppressing unsaturated oil / arginine composition according to an embodiment of the present invention reacts sulfur compounds in a solid state without using any additional solvent to solidify the odor source caused by the aldehyde compound generated when the unsaturated oil is oxidized, It is very convenient compared to the method by distillation or the like, and it is possible to suppress discoloration due to arginine.
- Figure 2 is a GC analysis chart of Omega 3.
- 3 is a graph showing a change in removal rate according to reaction temperature in the removal reaction of aldehydes using sodium diphosphate.
- first, second, etc. may be used to describe various components, but the components should not be limited by the terms. The terms are used only for the purpose of distinguishing one component from another.
- first component may be referred to as a second component, and similarly, the second component may also be referred to as a first component.
- the singular expressions include plural expressions unless the context clearly dictates otherwise.
- the terms "comprises” or “having” and the like are used to specify that there is a feature, a number, a step, an operation, an element, a component or a combination thereof described in the specification, But do not preclude the presence or addition of one or more other features, integers, steps, operations, components, parts, or combinations thereof.
- a portion such as a layer, film, region, plate, or the like is referred to as being “on” another portion, this includes not only the case where it is “directly on” another portion, but also the case where there is another portion in between.
- a part such as a layer, film, region, plate or the like is referred to as being "under” another part, it includes not only the case where it is “directly underneath” another part but also another part in the middle.
- the odor-suppressing unsaturated oil / arginine complex composition according to an embodiment of the present invention includes a step of removing odors using sulfur compounds.
- arginine used in the present invention is an amine compound
- a very small amount of arginine is dissolved with an unsaturated oil at room temperature, and a Schiff base reaction with an aldehyde, which is an omega-3 malodorous substance, occurs to form an imine compound to alleviate odor .
- an aldehyde which is an omega-3 malodorous substance
- the aldehyde is formed by the gastric acid and the odor is felt in the trim.
- the arginine / unsaturated oil complex exhibits pink-red color due to the resulting imine compound.
- the amount of the imine compound is increased due to oxidation, thereby causing discoloration of the epidermis of the capsule preparation such as soft and hard capsules .
- the present invention has developed a technique for removing aldehydes from unsaturated oils.
- Aldehydes are generally reactive and can react with various materials.
- Removal efficiency was calculated from the relative area of the main peak of omega-3 and the octanal peak as follows.
- aldehyde compounds such as heptenal, octanal, nonadienal, etc.
- omega - 3 1% of aldehyde compounds such as heptenal, octanal, nonadienal, etc.
- sodium dithiosulfate was used in an amount of 5 wt% relative to the omega-3 solution, and the reaction temperature was maintained at room temperature, 60, 80, and 100 o C for 24 hours, and GC analysis was performed to examine the aldehyde removal rate. Respectively.
- the aldehyde removal rate was improved with increasing the reaction temperature.
- 60 o C almost 100% of the nonadienal and heptenal were removed, and the octanal removal rate was about 50%.
- 80 ° C and above the removal rate of all compounds was almost 100%.
- cysteine containing sulfur showed some performance for aldehyde removal.
- cysteine is not highly reactive but its cysteine is very toxic and very safe for use.
- sulfur compounds such as acidic sodium sulfite and sodium dibasic sulfate showed excellent aldehyde removal rate.
- the common feature of these sulfur compounds is that sulfur dioxide is considered to be involved in the aldehyde removal reaction as a substance capable of generating sulfur dioxide gas.
- Sulfur compounds that can generate sulfur dioxide used as a food additive include sodium sulfite, sodium bisulfite, sodium metabisulfite, sodium hydrosulfite, potassium sulfite, Potassium metabisulfite, potassium hydrogen sulfite, calcium hydrogen sulfite, etc., can be used for the purpose of removing the aldehyde of the present invention. Since the compound produced by the addition reaction of the sulfites is a salt compound, it is insoluble in unsaturated oil. Therefore, when the compound is left at room temperature or low temperature, it is separated by precipitation and is removed by filtration.
- This technology is applicable not only to unsaturated fatty acids such as omega-3 but also to unsaturated oils such as squalene extracted from shark and cod liver oil produced from cod liver.
- the preparation of the odor-suppressing unsaturated oil-containing composition comprises: 1) a step of removing aldehydes; 2) precipitation and filtration steps; 3) arginine mixing and grinding steps; 4) mixing step; 5) capsule manufacturing step.
- the sulfite salt or cysteine in the fine powder state is added to omega-3 and dispersed by stirring. At this time, it is effective to mix a small amount of an antioxidant such as vitamin E to prevent the oxidation of the unsaturated oil.
- the sulfites include sodium sulfite, acidic sodium sulfite, sodium metabisulfite, sodium dibasulfate, potassium sulfite, potassium metabisulfite, acidic sodium sulfite and calcium hydrogen sulfite, which are used as food additives.
- the particle size of these particles is preferably not more than 50 ⁇ m. And if it is more than 50 ⁇ m, the surface area is small and the reactivity is low.
- the amount of the aldehyde compound contained in the purified unsaturated oil used as a health functional food is very difficult to be analyzed by GC, so that the amount of the sulfite compound used in the elimination reaction may be small. And 0.5% by weight or less based on the unsaturated oil is suitable for controlling the residual sulfur dioxide according to the standard of the phytosanitary standard. There is a problem in that the sulfur dioxide generated can exceed the standards of the pharmacy.
- the reaction temperature is suitably from -10 ° C to 80 ° C.
- Unsaturated oil can be oxidized at 80 ° C or higher, and the reaction is frozen at -10 ° C or lower, so that sufficient reaction may not occur.
- the aldehyde compound in the purified unsaturated oil is very small, so it is not necessary to add a high temperature for the purpose of increasing the reaction efficiency.
- the reaction time is suitably 4 to 48 hours. The reaction may not be completed in less than 4 hours, and the reaction is terminated in 48 hours or more, so that there is no need to react further.
- Basic amino acids include lysine, histidine, and arginine.
- the molar ratio of the sulfite compound used in the reaction is 1-20 times. Under 1x, complete reaction may not occur, and 20 times or more may cause waste.
- Cysteine may be cysteine itself and salts thereof such as hydrochloride, sulfate, and acetate.
- the particle size of these particles is preferably not more than 50 ⁇ m. When the thickness is 50 m or more, there is a problem that the surface area is small and the reactivity is low.
- the amount of cysteine is suitably from 1 to 10% by weight based on the unsaturated oil. At least 10% by weight may be wasted, and at 1% by weight or less, the reactivity is low and sufficient removal may not occur.
- the reaction temperature is in the range of 20 to 80 ° C. Omega-3 can be oxidized at a temperature higher than 80 ° C.
- the reaction time is suitably from 6 to 48 hours. The reaction may not be completed for less than 6 hours, and the reaction is terminated for longer than 48 hours, so that no further reaction is required.
- a sulfur compound such as a sulfite or cysteine is dissolved in a solvent and reacted in a solid state without being reacted, thereby avoiding a troublesome process of removing the solvent.
- a powder such as aronia, ginseng, bellflower, capers, onion, turmeric, cinnamon, tomato, carrot, kale, nuts, green tea,
- the lipid-soluble physiologically active substance can be extracted.
- the reaction product is allowed to stand at room temperature to -20 ° C. for at least 12 hours to precipitate the resulting sulfurous acid addition compound, followed by centrifugation or filtration to remove the impurities.
- This method is very economical and convenient in comparison with distillation which is a purification method commonly used in chemical processes.
- Cysteine is not toxic and can be left alone, but should be removed if it can affect the doses of the main unsaturated oils and arginine.
- Arginine or its salt hydrochloride, sulphate, acetate and the like are added to the unsaturated oil and mixed and pulverized with a homomix, a colloid mill or a ball mill.
- the amount of arginine is 0-80% by weight and can be adjusted according to the desired function. That is, arginine may not be used only for the function of omega-3, and the amount of addition of up to 80% by weight may be increased to emphasize the function of arginine.
- a physiologically active substance such as vitamin E, beta-carotene, lycopene, quercetin, saponin, polyphenol or lutein is added as needed.
- beeswax, lecithin and the like are added to increase the viscosity.
- the raw material thus prepared is removed from the bubbles under vacuum and made into soft or hard capsules or the like to be used as a health functional food.
- a method for producing an odor-suppressing unsaturated oil and an arginine-containing composition which comprises mixing at least one of sulfur compounds capable of generating sulfur dioxide and cysteine with an unsaturated oil to remove an aldehyde compound generated from the unsaturated oil step; And adding arginine or a salt thereof to the composition, and a process for producing an odor-suppressing unsaturated oil and an arginine-containing composition.
- the unsaturated oil is linoleic acid (ALA) derived from plant seeds such as flax, hemp, and the like; Omega-3 from fish such as salmon, krill, sardines, and the like; Omega-3 fatty acids derived from seaweeds; Squalene, cod liver oil or the like.
- ALA linoleic acid
- the sulfur compounds capable of generating sulfur dioxide include at least one of sodium sulfite, sodium acid sulfite, sodium metabisulfite, sodium dibasulfite, potassium sulfite, potassium metabisulfite, potassium acid sulfite and calcium hydrogen sulfite Containing unsaturated oil and a method for producing an arginine-containing composition.
- the method comprises the step of adding a basic amino acid to remove residual sulfur dioxide after the step of removing the aldehyde compound, and a method for producing an odor-suppressing unsaturated oil and an arginine- to provide.
- a method for preparing an odor-suppressing unsaturated oil and an arginine-containing composition further comprising the step of precipitating and removing an amino acid and a sulfite adduct produced after removing the aldehyde compound, to provide.
- the salt of arginine is at least one of a hydrochloride salt, a sulfate salt, and a nitrate salt, and provides a method of preparing an odor-suppressing unsaturated oil and an arginine-containing composition.
- the arginine or a salt thereof may be 0-80 wt%.
- the method further comprises the step of adding a lipophilic bioactive material after the step of adding arginine or a salt thereof, wherein the lipophilic bioactive material is an anthocyanin, saponin, ginsenoside, quercetin, Containing unsaturated oil and an arginine-containing composition, wherein the composition is at least one or more selected from the group consisting of furitrine, curcumin, cinnamide, lycopene, beta carotene, lutein, vitamin E, polyphenol, tocopherol and terpene.
- the lipophilic bioactive material is an anthocyanin, saponin, ginsenoside, quercetin, Containing unsaturated oil and an arginine-containing composition, wherein the composition is at least one or more selected from the group consisting of furitrine, curcumin, cinnamide, lycopene, beta carotene, lutein, vitamin E, polyphenol, tocopherol and ter
- Fat or fatty acid dissolves in the digestive organ lipophilic vitamins such as lipid-soluble physiologically active substances to microemulsify to promote the absorption of the body.
- Unsaturated oil-containing fat or composition is also a kind of fat, so it will work the same.
- a physiologically active substance in a plant is extracted using an unsaturated oil-containing oil or composition as an extraction solvent to promote the absorption of the lipophilic bioactive substance contained in the plant to improve the bioavailability, Unsaturated oil-containing compositions and methods for their preparation have been developed. Plants include water-soluble substances that dissolve in water, amphoteric substances that dissolve in both water and oil, and oil-soluble substances that dissolve in oil.
- plant-derived physiologically active substances which can be dissolved in unsaturated oils include various known substances as shown in Table 1 below.
- anthocyanins which are a kind of flavonoids such as Aronia
- Ginsenoside a ginseng saponin
- Curcumin in curcumin has been reported to prevent heart attack and inhibit cancer metastasis.
- Excreted carotene, lutein, terpene, etc. prevent antioxidant damage to cells, promote the regeneration of already damaged cells, prevent aging, relieve eye fatigue and prevent night blindness.
- Table 4 is an example of a plant-derived lipid-soluble physiologically active substance.
- an unsaturated oil-containing composition containing a plant-derived physiologically active substance As a method for producing an unsaturated oil-containing composition containing a plant-derived physiologically active substance, a method of extracting a physiologically active substance using alcohol or an organic solvent can be used. However, in this method, since the solvent used for extraction is removed by a method such as vacuum distillation and the extracted physiologically active substance is mixed with unsaturated oil, the process is troublesome and the loss of the extract is severe, resulting in low productivity and uneconomical problems. Therefore, in the present invention, productivity and economical efficiency are improved by using the unsaturated oil-containing oil or the composition as a direct extraction solvent and using a manufacturing process which does not require a solvent removal process.
- Another aspect of the present invention is a process for producing The present invention provides a malodor-suppressing unsaturated oil and an arginine-containing composition.
- the malodor-suppressing unsaturated oil and arginine-containing composition according to an embodiment of the present invention can be used as a health functional food after being formulated with a soft capsule.
- the odor-suppressing unsaturated oil and the arginine-containing composition according to an embodiment of the present invention can be manufactured as an oil-in-water emulsion and used as a composition of juice or beverage.
- the odor-suppressing unsaturated oil and arginine-containing composition according to an embodiment of the present invention can inhibit fishy smell and odor, and can be used as a food additive having a high flavor and nutritional supply source.
- the odor-suppressing unsaturated oil and arginine-containing composition according to an embodiment of the present invention can remove or reduce malodors caused by aldehyde compounds generated by oxidation of unsaturated oils stored and distributed by arginine.
- the active ingredient of plants and animals can be absorbed at the same time by taking one dose, thereby providing convenient convenience and providing a wider and more effective physiological health function.
- Sodium sulphate was added to the oval-shaped bowl to obtain particles having a size of 50 ⁇ m or less. Then, 0.05 g of ointment was added to 200 g of omega-3, and 0.5 g of vitamin E was added. The mixture was stirred at -10 ° C. for 12 hours, Lt; / RTI > Then, 0.5 g of histidine is added to the reaction mixture, which is then stirred for 1 hour. The reaction mixture is placed in a refrigerator for 24 hours, and centrifuged to remove the precipitate.
- Sodium dithionite was poured into a mortar to obtain particles having a size of 50 ⁇ m or less. Then, 0.5 g of the mixture was added to 200 g of omega-3 and stirred at 40 ° C. for 8 hours under nitrogen atmosphere. The reaction mixture is placed in a refrigerator, left for 24 hours, and centrifuged to remove the precipitate. To 100 g of omega-3 from which the aldehyde compound had been removed, 40 g of arginine hydrochloride and 0.5 g of each of vitamin E, beta carotene, lycopene, quercetin, saponin, polyphenol and the like were added. 10 g of lecithin was added and sufficiently pulverized and mixed with a colloid mill The resultant was put in a vacuum oven and vacuum was applied to remove the bubbles, and a soft capsule was prepared by a soft capsule machine.
- Potassium sulfite was added to a mortar to obtain particles having a size of 50 ⁇ m or less. Then, 1 g was added to 200 g of omega-3, and the mixture was reacted at room temperature for 8 hours under nitrogen atmosphere. The reaction mixture is placed in a refrigerator, left for 24 hours, and centrifuged to remove the precipitate. 30 g of arginine hydrochloride and 0.5 g of vitamin E, beta-carotene, lycopene, quercetin, saponin, polyphenol and the like were added to 100 g of omega-3 from which the aldehyde compound had been removed, and 5 g of beeswax was added thereto. The mixture was thoroughly pulverized and mixed with a colloid mill The resultant was put in a vacuum oven and vacuum was applied to remove the bubbles, and a soft capsule was prepared by a soft capsule machine.
- the potassium metabisulfite was added to the mortar to obtain particles having a size of 38 ⁇ m or less. Then, 0.01 g of the potassium metabisulfite was added to 200 g of omega-3 and the mixture was reacted under nitrogen atmosphere with stirring at 80 ° C. for 8 hours. The reaction mixture is placed in a refrigerator, left for 24 hours, and centrifuged to remove the precipitate. To 100 g of Omega-3, 100 g of the aldehyde compound, 30 g of arginine, 5 g of vitamin E, saponin, and lutein were added, and 5 g of beeswax was added. The mixture was thoroughly pulverized and mixed with a colloid mill, And soft capsules were prepared with a soft capsule maker.
- Cysteine hydrochloride was added to a mortar to obtain particles having a size of 50 ⁇ m or less. Then, 20 g of ointment was added to 200 g of omega-3, 2 g of vitamin was added, and the mixture was reacted under nitrogen atmosphere with stirring at 80 ° C. for 24 hours. 10 g of lecithin was added to omega-3 from which the aldehyde compound had been removed, and a soft capsule was prepared using a soft capsule machine.
- Cysteine was sufficiently introduced into a mortar to obtain particles having a particle size of 50 ⁇ m or less. Then, 10 g of the mixture was placed in 200 g of omega-3, and the mixture was reacted under nitrogen atmosphere with stirring at 60 ° C. for 48 hours. To 100 g of omega-3, from which the aldehyde compound had been removed, 40 g of arginine, 2 g of vitamin E and 3 g of beeswax were added and mixed with a homomixer. The mixture was thoroughly mixed and placed in a vacuum oven. Vacuum was removed to remove air bubbles. Capsules were prepared.
- Potassium sulfite was poured into a mortar to obtain particles having a size of 38 ⁇ m or less. Then, 1 g was added to 200 g of squalene, 1 g of vitamin E was added, and the mixture was reacted under nitrogen atmosphere at room temperature for 12 hours with stirring. The reaction mixture is placed in a refrigerator, left for 24 hours, and centrifuged to remove the precipitate. Then, the resultant was placed in a vacuum oven, a vacuum was applied to remove air bubbles, and a soft capsule was prepared with a soft capsule maker.
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Abstract
La présente invention concerne un procédé de production d'une composition de suppression d'odeur contenant une huile insaturée et de l'arginine, et une composition ainsi produite. Un composé soufré peut être utilisé pour éliminer ou réduire l'odeur générée par un composé aldéhyde qui est généré lorsque l'huile insaturée est oxydée, et supprimer la décoloration provoquée par l'arginine.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR10-2017-0147781 | 2017-11-08 | ||
| KR20170147781 | 2017-11-08 | ||
| KR1020180131056A KR102172036B1 (ko) | 2017-11-08 | 2018-10-30 | 악취 억제형 불포화오일 및 아르기닌 함유 조성물의 제조 방법 |
| KR10-2018-0131056 | 2018-10-30 |
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| WO2019093708A1 true WO2019093708A1 (fr) | 2019-05-16 |
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| PCT/KR2018/013082 Ceased WO2019093708A1 (fr) | 2017-11-08 | 2018-10-31 | Procédé de production de composition de suppression d'odeur contenant de l'huile insaturée et de l'arginine |
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| WO (1) | WO2019093708A1 (fr) |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5750572A (en) * | 1993-12-14 | 1998-05-12 | Prospa B.V. | Salts of a polyunsaturated fatty acid and pharmaceutical formulations containing them |
| KR100901518B1 (ko) * | 2001-01-17 | 2009-06-08 | 알.피.쉐러 테크놀러지즈 인코포레이티드 | 방향성 오일을 함유하는 섭취가능한 조성물 |
| US20100104730A1 (en) * | 2006-06-23 | 2010-04-29 | Haile Mehansho | Concentrated omega-3 fatty acids and mixtures containing them |
| US8173160B2 (en) * | 2004-05-20 | 2012-05-08 | Pbm Pharmaceuticals, Inc. | Compositions comprising edible oils and vitamins and/or minerals and methods for making the compositions |
| KR20170094789A (ko) * | 2014-12-23 | 2017-08-21 | 에보니크 데구사 게엠베하 | 다중불포화 오메가-6 지방산을 포함하는 조성물의 안정성을 증가시키는 방법 |
-
2018
- 2018-10-31 WO PCT/KR2018/013082 patent/WO2019093708A1/fr not_active Ceased
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5750572A (en) * | 1993-12-14 | 1998-05-12 | Prospa B.V. | Salts of a polyunsaturated fatty acid and pharmaceutical formulations containing them |
| KR100901518B1 (ko) * | 2001-01-17 | 2009-06-08 | 알.피.쉐러 테크놀러지즈 인코포레이티드 | 방향성 오일을 함유하는 섭취가능한 조성물 |
| US8173160B2 (en) * | 2004-05-20 | 2012-05-08 | Pbm Pharmaceuticals, Inc. | Compositions comprising edible oils and vitamins and/or minerals and methods for making the compositions |
| US20100104730A1 (en) * | 2006-06-23 | 2010-04-29 | Haile Mehansho | Concentrated omega-3 fatty acids and mixtures containing them |
| KR20170094789A (ko) * | 2014-12-23 | 2017-08-21 | 에보니크 데구사 게엠베하 | 다중불포화 오메가-6 지방산을 포함하는 조성물의 안정성을 증가시키는 방법 |
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