CN110651837A - Improved grease composition - Google Patents

Improved grease composition Download PDF

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Publication number
CN110651837A
CN110651837A CN201810697115.9A CN201810697115A CN110651837A CN 110651837 A CN110651837 A CN 110651837A CN 201810697115 A CN201810697115 A CN 201810697115A CN 110651837 A CN110651837 A CN 110651837A
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mass
oil
fat
conjugated linoleic
fatty acid
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CN201810697115.9A
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李德坤
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Individual
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23DEDIBLE OILS OR FATS, e.g. MARGARINES, SHORTENINGS, COOKING OILS
    • A23D9/00Other edible oils or fats, e.g. shortenings, cooking oils
    • A23D9/02Other edible oils or fats, e.g. shortenings, cooking oils characterised by the production or working-up
    • 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
    • A61K31/21Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/22Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
    • A61K31/23Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
    • A61K31/231Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms having one or two double bonds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Organic Chemistry (AREA)
  • Hematology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Food Science & Technology (AREA)
  • Polymers & Plastics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Emergency Medicine (AREA)
  • Fats And Perfumes (AREA)

Abstract

The invention relates to the field of grease, and discloses an improved grease composition which contains A, B, C components as follows: a is 0.5-30% by mass of a glyceride containing conjugated linoleic acid: the oil contains 20-70% by mass of conjugated linoleic acid and 10-60% by mass of medium-chain fatty acid; 68.5 to 99.4% by mass of glyceride containing no conjugated linoleic acid: the oil or fat contains 40 to 90.7 mass% of diglyceride, 9 to 59.5 mass% of triglyceride and 0.1 to 5 mass% of monoglyceride; c is less than or equal to 2 mass percent of free fatty acid; d: stearic acid in an amount of not more than 2% by mass.

Description

Improved grease composition
Technical Field
The invention relates to the field of grease, in particular to an improved grease composition.
Background
The grease is a daily necessity of people, provides rich nutrition and necessary energy while endowing dishes with good flavor and mouthfeel, and is an important raw material in food processing. In modern society, the intake of oil and fat is increasing day by day, and at present, the average consumption of oil and fat per person per day of urban residents in China is nearly 50 grams, which is twice of the average consumption of oil and fat per person per day recommended by the world health organization. The prevalence rates of rich diseases such as obesity, hyperlipidemia, cardiovascular diseases, fatty liver and the like are increased year by year due to excessively high oil intake and unbalanced nutrition, and the probability that various diseases are gathered and developed into metabolic syndrome patients is higher and higher, so that the health of people is seriously threatened at present. The metabolic syndrome is a syndrome with central obesity as the core, and is a syndrome with elevated blood pressure, blood sugar, blood ester and/or reduced high density lipoprotein cholesterol (HDL-C). It is estimated that in the urban population in china, at least 1 out of 8 adults suffers from metabolic syndrome. Metabolic syndrome has become a new chronic disease and a new public health problem. Metabolic syndrome is the accumulation of multiple risk factors, and comprehensive intervention is the main prevention and treatment means. The reduction of fat intake is an important measure for preventing obesity and metabolic syndrome, however, the flavor of foods lacking fat is affected and the processing process of foods is also affected.
Against a series of side effects associated with fat intake, fat substitutes and fat mimetics have been developed against this background. The fat substitutes are fatty acid-based esters that differ in structure from triglycerides in common edible oils, resulting in their non-accumulative or low-energy profile in the human body. The oil simulant is produced by adopting protein, carbohydrate and glue substances, the reality and the processability of the oil simulant in simulating oil are far lower than those of ester oil substitutes, and the application field of the oil simulant is greatly limited. In the 50 s of the twentieth century, interest was drawn in developed countries, in which sucrose fatty acid polyester is a product that has been commercially used, has a similar taste to fat and is not metabolized by the human body, and thus does not provide heat. However, sucrose fatty acid polyesters can affect the absorption of fat soluble vitamins and cause anal leakage. Medium-chain fatty acids are easily energized and thus accumulate little body fat, but when the amount of triglycerides composed of medium-chain fatty acids is excessively taken, symptoms such as diarrhea, nausea, chest distress, etc. are caused. If the fat or oil composition contains a large amount of medium-chain fatty acids, the smoke point is low and the foaming is remarkable, so that the fat or oil composition has a disadvantage of being unsuitable for deep-fry cooking and the like, and fatty acids essential to the human body cannot be provided. The long and short chain fatty acid triglyceride has the characteristic of low calorie, but has high freezing point and poor universality. Protein and carbohydrate have energy densities of half or less of that of fat, and can provide a fat substitute with low calorie by processing the fat to have physical properties and taste similar to those of fat, but have disadvantages such as being unusable as a heating medium due to lack of heat resistance. HArAK. 1993 reports that diglyceride has the function of reducing blood fat (Ann Nutr MetAb 1993; 37: 185), and researches show that the diglyceride has high general properties and nutritional functions with common edible oil, is a more suitable oil substitute and is widely concerned.
To date, there have been a number of patents on diglycerides. Patent 00811830.2 discloses a fat containing at least 35 wt% of diglycerides and containing phytosterols. The grease composition formula requires diglyceride and phytosterol, and the synergistic effect of the diglyceride and the phytosterol is needed to achieve the function of reducing the arteriosclerosis factor. Due to the solubility problem, the addition of high-content sterol in the oil has certain difficulty in implementation, and because large-scale production and supply of sterol are not available, the oil has certain difficulty in mass production.
Disclosure of Invention
The invention aims to provide a grease composition and application thereof, aiming at the defects in the prior art, wherein the grease composition can be used for preventing and treating metabolic syndrome and is applied to edible oil, fat or oil processing food and pharmaceutical compositions.
The improved grease composition of the invention contains A, B, C components as follows:
0.5 to 30% by mass of a glyceride containing conjugated linoleic acid: the oil contains 20-70% by mass of conjugated linoleic acid and 10-60% by mass of medium-chain fatty acid;
68.5 to 99.4% by mass of a glyceride containing no conjugated linoleic acid: the oil or fat contains 40 to 90.7 mass% of diglyceride, 9 to 59.5 mass% of triglyceride and 0.1 to 5 mass% of monoglyceride;
c, less than or equal to 2 mass percent of free fatty acid;
d: stearic acid in an amount of not more than 2% by mass.
The conjugated linoleic acid is a conjugated linoleic acid isomer.
The medium-chain fatty acid is a saturated fatty acid with 6-12 carbon atoms.
In order to suppress unfavorable crystallization or solidification of the fat and oil composition during storage at a high temperature or a low temperature, the proportion of the long-chain saturated fatty acid in the glyceride not containing the conjugated linoleic acid is 20% by mass or less based on the whole of the long-chain fatty acids constituting the fat and oil composition.
In order to provide the product with better oxidation stability, the grease composition also contains an antioxidant. The antioxidant is one or more of tert-butyl hydroquinone, tert-butyl p-hydroxyanisole, dibutyl hydroxytoluene, ascorbyl palmitate, propyl gallate and vitamin E.
The oil composition of the invention is applied to edible oil, fat or oil processing food and pharmaceutical compositions.
The raw material for producing the edible oil of the invention can be natural animal and vegetable oil, fat and processed oil obtained by transesterification, fractionation and the like, or vegetable oil such as soybean oil, rapeseed oil, corn oil, peanut oil, sunflower seed oil, safflower oil and the like and processed oil obtained by the vegetable oil.
The fat or oil composition of the present invention can be obtained by various methods including hydrolysis of triglyceride, glycerolysis of triglyceride, esterification of fatty acid, transesterification of free fatty acid or fatty acid ester with glyceride, and the like, and these reactions can be catalyzed chemically or enzymatically.
Compared with the prior art, the invention has the following beneficial effects and advantages:
the grease composition obtained by the invention not only provides necessary fatty acid nutrition, but also has physiological functions of preventing and treating metabolic syndrome, and is convenient to produce, low in cost and convenient to popularize and apply; meanwhile, the edible oil has good low-temperature stability, good flavor and excellent oxidation resistance, has good universality as common edible oil, and can be used for various purposes such as cooking, frying, food processing and the like.
Detailed Description
The following embodiments are given for the purpose of describing the practice of the present invention in detail, but the scope of the present invention is not limited by the following examples,
example 1
Putting 200g of commercially available CLA and caprylic capric acid glyceride (CLA: caprylic capric acid glyceride is 3, mol) into a 500ml triangular flask with a plug, preheating to 50 ℃, adding 40g of immobilized lipase (Novo435, Novozymes A/S), placing in a 50 ℃ constant temperature water bath shaking table, carrying out oscillation reaction for 5h under the condition of 200r/min, stopping the reaction, filtering the product to remove immobilized enzyme particles, further separating out fatty acid in the product through molecular distillation, and carrying out decoloration and deodorization on heavy fractions in a conventional manner to obtain the oil composition 1.
Under the conditions of 50% water addition and strong stirring, carrying out hydrolysis reaction on commercially available rapeseed oil at 40 ℃ by using free 1, 3-site specific LipAse as a catalyst (Lipase F-AP15, a product of Amano Enzyme Inc., or a free LipAse product with high hydrolase activity of other companies), stopping the reaction after reaching a certain hydrolysis degree, keeping the temperature at 65 ℃ for 0.5h to inactivate Enzyme activity, standing to remove most of water, removing residual water under the conditions of vacuum and 80 ℃, adding diatomite, stirring for 0.5h, filtering to remove residual Enzyme protein, further separating the residual product by molecular distillation, and decoloring and deodorizing in a conventional manner to obtain an oil composition 2 mainly containing diglyceride and triglyceride and a composition 3 mainly containing free fatty acid.
The oil composition 1 and the oil composition 2 were mixed uniformly at a volume ratio of 20: 80 to obtain an oil composition 4.
Example 2
500g of commercially available CLA ethyl ester and caprylic capric acid glyceride (CLA ethyl ester: caprylic capric acid glyceride is 3, mol) are filled into a constant temperature reactor with a stirrer at 60 ℃ to be uniformly mixed, 10g of immobilized lipase (Lipozyme TL IM, Novozymes A/S) is filled into a packed bed type column type enzyme reactor (with a heat preservation jacket), then a metering pump is adopted to continuously extract a reaction substrate from the reaction vessel and inject the reaction substrate into the enzyme reactor, so that the reaction substrate generates ester exchange reaction under the catalysis of immobilized enzyme, and the reaction product flows out of the enzyme reactor and directly enters the container filled with the substrate, so that continuous cyclic reaction is performed. The flow rate is adjusted to be about 3L/hr, and the reaction is stopped after the grease is continuously circulated in the enzyme reactor for 6 hours. The reaction product was subjected to molecular distillation to further separate ethyl ester, and the heavy fraction was then subjected to decolorization and deodorization in a conventional manner to obtain an oil composition 5.
After uniformly mixing the composition 3 with a certain amount of glycerol (fatty acid group: glycerol ═ 2, mol), adding a commercially available immobilized 1, 3-site specific lipase (lipozyme rmim, novozyme a/S, or other commercially available immobilized lipase), keeping the internal pressure of the system at 5mmHg absolute, reacting the mixture at 60 ℃ while stirring until the free fatty acid content is reduced to 10%, stopping the reaction, filtering to remove the immobilized enzyme particles, further separating the remaining product by molecular distillation, and then decoloring and deodorizing in a conventional manner to obtain a diglyceride-based oil composition 6.
The oil and fat composition 5 and the oil and fat composition 6 were mixed uniformly at a volume ratio of 10: 90 to obtain an oil and fat composition 7.
Example 3
The oil composition 1 and the oil composition 2 were mixed uniformly at a volume ratio of 15: 85 to obtain an oil composition 8.
Example 4
The oil composition 5 and the oil composition 6 were mixed uniformly at a volume ratio of 5: 95 to obtain an oil composition 9.
Example 5
0.2g of t-butylhydroquinone was completely dissolved in 10g of the oil and fat composition 4, and then uniformly mixed with the oil and fat composition 4 at a volume ratio of 10: 990 to obtain the oil and fat composition 10.
Example 6
0.2g of t-butyl p-hydroxyanisole and 0.1g of ascorbyl palmitate were completely dissolved in 10g of the oil and fat composition 9, and then the mixture was uniformly mixed with the oil and fat composition 9 in a volume ratio of 10: 990, so that the oil and fat composition 11 was obtained.

Claims (7)

1. An improved fat composition, characterized in that said fat composition comprises A, B, C components:
a:0.5 to 30 mass% of glyceride containing conjugated linoleic acid: the oil contains 20-70% by mass of conjugated linoleic acid and 10-60% by mass of medium-chain fatty acid;
b:68.5 to 99.4% by mass of a glyceride containing no conjugated linoleic acid: the oil or fat contains 40 to 90.7 mass% of diglyceride, 9 to 59.5 mass% of triglyceride and 0.1 to 5 mass% of monoglyceride;
c: free fatty acid of not more than 2 mass%;
d: stearic acid in an amount of not more than 2% by mass.
2. The improved fat and oil composition of claim 1, wherein the conjugated linoleic acid is an isomer of conjugated linoleic acid.
3. The improved oil and fat composition according to claim 1, wherein the medium-chain fatty acid is a saturated fatty acid having 6 to 12 carbon atoms.
4. The improved fat and oil composition according to claim 1, wherein the proportion of the long-chain saturated fatty acid in the glyceride containing no conjugated linoleic acid is 20% by mass or less based on the total long-chain fatty acids constituting the fat and oil composition.
5. The improved fat composition according to any one of claims 1 to 4, wherein the fat composition further comprises an antioxidant.
6. The improved grease composition according to claim 5, wherein the antioxidant is one or more of tert-butyl hydroquinone, tert-butyl p-hydroxyanisole, dibutyl hydroxytoluene, propyl gallate, ascorbyl palmitate, propyl gallate and vitamin E.
7. Use of the improved fat composition of any one of claims 1 to 6 in edible oils, fats or oil processed foods, pharmaceutical compositions.
CN201810697115.9A 2018-06-29 2018-06-29 Improved grease composition Withdrawn CN110651837A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810697115.9A CN110651837A (en) 2018-06-29 2018-06-29 Improved grease composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810697115.9A CN110651837A (en) 2018-06-29 2018-06-29 Improved grease composition

Publications (1)

Publication Number Publication Date
CN110651837A true CN110651837A (en) 2020-01-07

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Country Status (1)

Country Link
CN (1) CN110651837A (en)

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Application publication date: 20200107