• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
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  • 优先权
    • 专利摘要:
    PURPOSE: A method of producing microcapsules containing fat by gelling fat using a protein-based coating material and transglutaminase enzyme is provided. The produced microcapsules are applied to various fields containing food, storable for a long period of time and easy to handle. CONSTITUTION: Microcapsules containing fat are obtained by the steps of: preparing a protein solution by melting protein-based coating material in distilled water; preparing a enzyme-added protein solution by adding transglutaminase enzyme to the protein solution; preparing an exterior continuous phase by mixing the protein solution and fat and then dissolving the obtained O/W emulsion in corn oil; preparing an O/W/O multiplex emulsion by adding the O/W emulsion to the exterior continuous phase; preparing microcapsules by gelling the O/W/O multiplex emulsion in a thermostatic water bath; and extracting, washing and drying the microcapsules. The fat is selected from the group consisting of fish oil, vegetable oil, medium-chain fatty acid and lipid-soluble nutrition components.
    公开号:KR20040042987A
    申请号:KR1020020070961
    申请日:2002-11-15
    公开日:2004-05-22
    发明作者:박지용；조영희；심현규；이재호；최기현；최성원
    申请人:주식회사 그린바이오텍；
    IPC主号:
    专利说明:

    Method for preparing microcapsule Comprising Oil and Fat}
    [10] The present invention relates to a method for preparing oil-containing microcapsules, and more specifically, to oil-containing oils containing polyunsaturated fatty acids which are unstable to heat and oxidation, for example, O / W / O polyemulsified fish oil, to a protein-based coating material and transgle The present invention relates to a method for microencapsulation by gelation using a transglutaminase enzyme.
    [11] Recently, polyunsaturated fatty acids have been reported to have various physiological effects, and as their nutritional and medical value is revealed, interest in them has increased. In particular, unsaturated fatty acids such as docosahexane (abbreviated as "DHA") and icosapentaenoic acid (abbreviated as "EPA") are constituents of brain cells and are considered as early childhood components from birth. It is known to promote brain development while improving development, memory and learning, as well as promoting growth, reflexes in the nervous system, and cancer prevention.
    [12] Research into the use of fats and fats containing DHA and EPA, which have such excellent functions, in functional foods and medicines has been actively conducted, and it is already being used in products such as infant formula, miso, and canned tuna. High fish oil refined concentrates are used as dietary supplements.
    [13] However, fish oils and vegetable oils containing a large amount of DHA and EPA are unstable to oxygen or light and are easily oxidized during storage, causing undesirable odors. have.
    [14] In other words, to improve stability, methods of adding emulsifiers and pulverization by mixing them with sugars have been studied, and deodorization techniques and masking agents have been studied to remove fishy smells. A method for microencapsulating has been proposed.
    [15] Looking at the prior art for the microencapsulation of the fats and oils, Ahn et al. Improved the oxidation stability of DHA and EPA by adding lecithin to fish oil, but did not improve the sensory properties of fish oil (Korean Journal of Food Science and Technology) , 1991, 23 (5): 578-581).
    [16] In addition, Maruyama et al. (Japanese Patent Laid-Open No. 63-023736) have gelatin and gum arabic as coating materials and can be applied to foods and medicines by encapsulating fish oil containing polyunsaturated fatty acids using coacervation method. Kandor et al. (Japanese Patent Application Laid-Open No. 02-103289) have described enteric coating materials such as ethyl cellulose, cellulose acetate trimellitate and cellulose acetate phthalate. To prepare a tasteless, odorless fish oil-containing microcapsules.
    [17] In addition, Chang and Ha (Korean Journal of Food Science and Technology, 2000, 32 (3): 646-653) describe a method for encapsulating highly refined fish oil using agar and waxy corn starch. Chang and Lim (Korean Patent Laid-Open Publication No. 2000-0026177) proposed a method of preparing a biocompatible capsule using sodium alginate and chitosan.
    [18] However, in the microencapsulation process of fats and oils containing polyunsaturated fatty acids described above, a carbohydrate coating material was mainly used.
    [19] Recently, in consideration of the nutritional and physiological functionalities of the coating material itself, studies have been actively conducted to microencapsulate the protein using the coating material. However, the conventional encapsulation method using protein is a gelation method using thermal denaturation and harmful cross-linking agent, which is not suitable for heat-resistant maintenance and requires a new encapsulation method because it is difficult to use in food. do.
    [20] An object of the present invention is to maintain the microencapsulated oil by a gelation reaction using a protein-based coating material and transglutaminase enzyme in order to solve the conventional problems that occur when the microencapsulation using a protein-based coating material It is to provide a method for producing the containing microcapsules.
    [1] 1 is a graph of the change in viscosity of each protein solution after transglutaminase enzyme treatment.
    [2] Figure 2 is a graph of the emulsion stability of oil-in-water (O / W) emulsion according to the protein-based coating material.
    [3] Figure 3 is a manufacturing process of the holding microcapsules according to the present invention.
    [4] Figure 4 is a graph of the stability of the O / W / O type emulsion according to the emulsifier.
    [5] Figure 5 is a graph of the change in water solubility of the microcapsules with temperature.
    [6] Figure 6a is a SEM photograph observing the form of the microcapsules prepared from Example 4.
    [7] Figure 6b is a SEM photograph observing the form of the microcapsules prepared from the comparative example.
    [8] 7 is a graph of the oxidative stability of oil-containing microcapsules.
    [9] 8 is a graph of the controlled release of fats and oils from oil-containing microcapsules in pepsin (pH 2.2).
    [21] In order to achieve the above object, the present invention provides a method for preparing oil-containing microcapsules comprising the following steps.
    [22] (a) dissolving the protein coating material in distilled water to prepare a protein solution;
    [23] (b) adding a transglutaminase enzyme to the protein solution to prepare a protein solution containing the enzyme;
    [24] (c) mixing the resultant and the fat or oil to produce an oil-in-water (O / W type) emulsion, and dissolving an emulsifier in jade oil to prepare an external continuous phase;
    [25] (d) adding the oil-in-water emulsion to the external continuous phase to prepare an O / W / O type emulsion;
    [26] (e) gelling the multiemulsion in a constant temperature water bath to produce microcapsules;
    [27] (f) filtering the resultant to extract microcapsules;
    [28] (g) washing the resultant; And
    [29] (h) drying the resultant.
    [30] The production method according to the present invention comprising the above step is the protein-based coating material is isolated soy protein, whey protein isolate, casein or wheat protein (soluble wheat protein) Wherein the fat or oil is fish oil, vegetable oil, medium chain fatty acid or fat-soluble nutrient, and the content of the protein-based coating material is 4 to 14% by weight, preferably 10% by weight, based on the protein solution. The gelation reaction is carried out for 4 to 20 hours, preferably for 4 hours at a temperature of 37 ℃, the washing of step (g) is characterized in using alcohol.
    [31] Hereinafter, the present invention will be described in detail.
    [32] First, to prepare a protein solution by dissolving a protein-based coating material in distilled water to prepare a microcapsules containing oil according to the present invention, and then add a transglutaminase enzyme to the protein solution to prepare a protein solution added enzyme do.
    [33] In this case, the protein-based coating material is separated soy protein, whey isolate protein, casein or wheat protein, and the content of the protein-based coating material in the prepared protein solution is 4 to 14% by weight, preferably 10% by weight. do.
    [34] In addition, the enzyme is prepared by dissolving the purified powdery transglutaminase enzyme in 0.5M tris-acetic acid buffer (pH 7.0) and converting it into a liquid phase.
    [35] In the present invention, prior to the preparation of oil-containing microcapsules using a transglutaminase enzyme, a protein gel is prepared by using the protein solution and enzyme for the purpose of selecting a coating material and a condition suitable for gel formation. Manufacture.
    [36] This is due to the addition of a liquid transglutaminase enzyme to the protein solution containing the protein-based coating material, and then to a constant temperature in a constant temperature water bath to increase the viscosity and elasticity of the protein solution, which may have been left for a certain time. When protein gels are obtained, it is possible to identify which temperature and protein-based coating material is most suitable for gel formation.
    [37] In this case, when gel formation was observed according to the gelation temperature, it was confirmed that the gel formation was the easiest at 37 ° C., and it was confirmed that the separated soy protein was most suitable as a coating material.
    [38] Next, the resulting oil and fat are mixed to prepare an oil-in-water emulsion, and an external continuous phase is prepared by dissolving an emulsifier in jade oil.
    [39] As the fats and oils, fish oil, vegetable oil, medium-chain fatty acids or fat-soluble nutrients containing polyunsaturated fatty acids such as DHA or EPA are used, and the fats and oils are dispersed phases in which the fats and oils are core materials in order to increase the shelf life of the fats and to remove odors. It is used as, the resulting transglutaminase enzyme is dispersed in a protein solution added to prepare an oil-in-water emulsion. This is prepared by homogenizing with oil homogenizer for 10 minutes while slowly dropping oily fat or oil into aqueous protein solution.
    [40] At this time, since the protein solution itself has a function of stabilizing the emulsion, it is possible to prepare a relatively stable emulsion without using a separate emulsifier.
    [41] In addition, 1-3 wt% of an emulsifier is added to the jade oil to prepare an external continuous phase.
    [42] Next, the oil-in-water emulsion is added to the external continuous phase to prepare a multi-emulsion, and the multi-emulsion is gelled in a constant temperature water bath to generate microcapsules. That is, after preparing the oil-in-water emulsion as in the above-described method, first to prepare a multi-emulsion solution to encapsulate it. This is prepared by dropping the oil-in-water emulsion into jade oil and homogenizing for 10 minutes with a homogenizer. Next, the microemulsion was left in a 37 ° C. constant temperature water bath for 4 hours to induce gelation of proteins to prepare microcapsules.
    [43] Then, the resultant is filtered to extract the microcapsules, and then the preparation of the microcapsules containing oil through washing and drying. This is to separate the microcapsules and jade oil through filtration, and then wash the jade oil remaining on the surface of the separated microcapsules with alcohol, preferably ethanol, and then lyophilize. The alcohol immobilizes the wet gel into a harder gel and provides the effect of removing residual jade oil remaining on the outside of the gel.
    [44] The present invention will be described in detail through the following examples. However, these examples are for illustrative purposes only and the present invention is not limited thereto.
    [45] Example 1: Preparation of Protein Solution and Enzyme
    [46] The isolated soy protein, casein, whey isolate protein and wheat protein were dissolved in distilled water, respectively, to prepare 5 wt% and 10 wt% protein solution, i.e., all 8 protein solutions for each protein.
    [47] In addition, the enzyme was converted into a liquid phase by dissolving 4 mg of purified Streptoverticillium mobaraense- derived transglutaminase enzyme (Ajinomoto, Japan) in 1 mL of 0.5 M tris-acetic acid buffer solution (pH 7.0).
    [48] Example 2 Selection of Concentration of Protein-Based Coatings Suitable for Capsules and Proteins Suitable for Gel Formation (1)
    [49] Protein gels were prepared to select protein concentrations suitable for capsules and protein concentrations suitable for gel formation. First, 5 mL of liquid transglutaminase (4 × 10 3 units / g) was added to 200 mL of each 5 wt% protein solution prepared in Example 1, and then mixed with a homogenizer at a low speed of 100 rpm for 10 minutes. The degree of viscosity increase of each protein solution was observed while standing in a constant temperature bath at 37 ° C. In addition, after the oil-in-water emulsion was prepared using fish oil as a dispersed phase, the emulsion stability was observed.
    [50] Example 3 Selection of Concentration of Protein-Based Coatings Suitable for Capsules and Proteins Suitable for Gel Formation (2)
    [51] To select a protein-based coating material suitable for capsules and a protein concentration suitable for gel formation, first, 5 mL of liquid transglutaminase was added to 200 mL of each 10 wt% protein solution prepared in Example 1 (4 × 10). 3 units / g), and mixed with a homogenizer at a low speed of 100 rpm for 10 minutes, and then standing in a 37 ℃ constant temperature water bath to observe the degree of viscosity increase of each protein solution. In addition, after the oil-in-water emulsion was prepared using fish oil as a dispersed phase, the emulsion stability was observed.
    [52] In the results observed from Examples 2 and 3, the increase in viscosity was the highest in the separated soy protein solution in the case of viscosity increase, and the wheat protein solution and the whey separated protein solution were viscous up to 60 minutes of treatment. There was no change. In the case of kesin solution, after 30 minutes of treatment, the increase in viscosity increased to about 60 cps, but there was no significant change thereafter (see FIG. 1).
    [53] In addition, the emulsion stability was excellent in the emulsion stability in the order of soy protein, kesin, whey isolate protein, wheat protein (see Figure 2).
    [54] From the above results, it was found that the isolated soy protein is the most suitable coating material for preparing microcapsules using transglutaminase enzyme, and the concentration of protein solution suitable for gel formation is 10% by weight.
    [55] Example 4 Preparation of Oil-Containing Microcapsules According to the Present Invention
    [56] First, 5 mL of liquid transglutaminase (4 × 10 3 units / g) was added to 200 mL of the 10% by weight separated soy protein solution prepared in Example 1 according to the attached FIG. 3, followed by a homogenizer of 100 rpm. The mixture was mixed at low speed for 10 minutes to prepare a protein solution containing enzyme.
    [57] Next, the resultant and fish oil containing 40% by weight of DHA was mixed at a weight ratio of 1: 2, and then homogenized at 9,500 rpm for 10 minutes using a homogenizer to prepare an oil-in-water emulsion.
    [58] Next, three kinds of emulsifiers Span 80, Span 60 and PGPR having different HLB values were prepared, and the Span 80 / PGPR mixture (Span 80: PGPR = 1: 1, weight ratio), Span 60 / PGPR mixture (Span 60: PGPR = 1: 1, weight ratio) was prepared, and 2.5 wt% of these were respectively added to the jade oil to prepare an external continuous phase, and then oil-in-water type The oil-in-water emulsion was slowly added dropwise to the external continuous phase for 10 minutes at 9,500 rpm using a homogenizer so that the emulsion and each external continuous phase were mixed in a weight ratio of 1: 4.
    [59] Here, the emulsion stability of the multiemulsion was very excellent in the mixed use of the emulsifier, it was confirmed that the most stable multi-emulsion was prepared when using Span 80 (see Fig. 4).
    [60] Then, the polyemulsion was left in a 37 ° C. constant temperature water bath for 4 hours to induce gelation of the protein to generate microcapsules. The microcapsules were separated from jade oil through filtration and the jade oil remaining on the surface of the capsule was After washing with ethanol, lyophilized to prepare a microcapsules according to the present invention.
    [61] As a result, the capsules were not produced at all when the emulsifier was mixed and PGPR alone was used. The yield was the highest at 79.6 ± 3.4g / 450mL using Span 80, and the lower Span 60 was 52.8 ± 4.25. Yield of g / 450 mL was obtained.
    [62] Comparative Example: Preparation of Oil-Containing Microcapsules Using Heat Modification
    [63] First, 200 mL of the 10 wt% separated soy protein solution prepared in Example 1 and fish oil containing 40 wt% DHA were mixed at a weight ratio of 1: 2, and then homogenized at 9,500 rpm using a homogenizer for 10 minutes in water. A oily emulsion was prepared.
    [64] Next, 2.5 wt% of the emulsifier Span 80 was added to the jade oil to prepare an external continuous phase, and then the oil-in-water emulsion was slowly added dropwise to the external continuous phase so that the oil-in-water emulsion and the external continuous phase were mixed at a weight ratio of 1: 4. A homogenizer was used to homogenize at 9,500 rpm for 10 minutes to prepare a multiemulsion solution.
    [65] Then, while raising the temperature of the multi-emulsification to 85 ℃ heated for 40 minutes to induce thermal denaturation of the separated soy protein to produce a microcapsule, the prepared microcapsules are separated from the jade oil through filtration and on the surface of the capsule The remaining jade oil was washed with ethanol and then lyophilized to prepare microcapsules.
    [66] Example 5 Measurement of Physical Properties of Prepared Microcapsules
    [67] In order to investigate the storage stability of the prepared microcapsules and the controlled release of the internal material of the capsule, physical properties such as shape, size and water solubility of the microcapsules prepared in Example 4 and Comparative Example were measured.
    [68] As a result, the microcapsules prepared in Example 4 were 23.4 ± 2.27µm, and the microcapsules prepared in Comparative Example did not show a large difference of 24.6 ± 2.18µm. In addition, as a result of comparing the water solubility of the microcapsules according to the temperature, the microcapsules prepared in Example 4 showed very low water solubility and were not significantly affected by the temperature of water, whereas the microcapsules prepared from the comparative example were very It showed high water solubility and the water solubility increased with increasing water temperature (see FIG. 5).
    [69] In addition, the shape of the microcapsules observed by electron microscopy was observed to form both spherical form, the difference between the microcapsules prepared from Example 4 showed a stable form that the surface is smooth and tightly bonded (Fig. 6a) In the microcapsules prepared from the comparative example, the surface of the microcapsules was very rough, and fine pores formed during water removal were found in various places of the surface (see FIG. 6B).
    [70] Example 6 Measurement of Oxidation Stability of Prepared Microcapsules
    [71] In order to measure the oxidative stability of the prepared microcapsules, using the ρ-anisidine reagent, the microcapsules prepared in Example 4 and the comparative example were kept without a capsule for 16 days at 50 ° C. at a 2-day interval of ρ−. The change in anisidine value was measured.
    [72] The ρ-anisidine reagent becomes yellow when reacted with an oxide such as aldehyde. An increase in ρ-anisidine value indicates an increase in oxide content.
    [73] As a result, the ρ-anisidine value rapidly increased from the second day of storage in the non-capsulated fat, and continued to increase during the storage period, but the microcapsules prepared in Example 4 and Comparative Example were all changed in the ρ-anisidine value during the storage period. There was little (see FIG. 7).
    [74] Example 7 Controlled Release Measurement of Prepared Microcapsules
    [75] As can be seen from the results measured in Example 5, the microcapsules prepared in Example 4 have high storage stability because of very low water solubility, but if the outer wall of the capsule is not broken, the utilization rate of the nutrients collected in the capsule is lowered. . Therefore, in order to determine the utilization rate of the prepared microcapsules in the state of gastric fluid was measured the degree of release of fats and oils from the inside of the microcapsules prepared in Example 4 and Comparative Example.
    [76] First, 10 g of the microcapsules prepared in Example 4 and Comparative Example were added to 20 mL of pepsin solution (pH 2.2), and then left to stand at 37 ° C. for 4 hours. Next, the treated samples were taken out at 30-minute intervals to measure the amount of oil released from the capsules.
    [77] As a result, in the microcapsules prepared in Comparative Example, the fat was rapidly released up to 2 hours, but in the microcapsules prepared in Example 4, the fat was gradually released during the treatment time (see FIG. 8).
    [78] As described above, the oil-containing microcapsules prepared by the gelling reaction using the protein-based coating material and the transglutaminase enzyme according to the present invention can be applied to various fields including foods, and are collected in the protein-based coating material. Oxidation stability of the polyunsaturated fatty acid can be secured for long-term storage and easy handling. In addition, controlled release from the digestive system may increase the utilization of nutrients in the body.
    权利要求:
    Claims (8)
    [1" claim-type="Currently amended] (a) dissolving the protein coating material in distilled water to prepare a protein solution;
    (b) adding a transglutaminase enzyme to the protein solution to prepare a protein solution containing the enzyme;
    (c) mixing the resultant and the fat or oil to produce an oil-in-water (O / W type) emulsion, and dissolving an emulsifier in jade oil to prepare an external continuous phase;
    (d) adding the oil-in-water emulsion to the external continuous phase to prepare an O / W / O type emulsion;
    (e) gelling the multiemulsion in a constant temperature water bath to produce microcapsules;
    (f) filtering the resultant to extract microcapsules;
    (g) washing the resultant; And
    (H) a method for manufacturing a fat-containing capsule, characterized in that it comprises the step of drying the resultant.
    [2" claim-type="Currently amended] The method of claim 1,
    The protein-based coating material is an oil-containing microorganism characterized in that it is selected from the group consisting of isolated soy protein, whey protein isolate, casein or soluble wheat protein. Capsule manufacturing method.
    [3" claim-type="Currently amended] The method of claim 1,
    The fat and oil is a fat or oil-containing microcapsules manufacturing method, characterized in that selected from the group consisting of fish oil, vegetable oil, medium chain fatty acids and fat-soluble nutrients.
    [4" claim-type="Currently amended] The method of claim 1,
    The content of the protein-based coating material is a fat-containing microcapsules manufacturing method, characterized in that 4 to 14% by weight based on the protein solution.
    [5" claim-type="Currently amended] The method of claim 4, wherein
    The content of the protein-based coating material is a fat-containing microcapsules manufacturing method, characterized in that 10% by weight based on the protein solution.
    [6" claim-type="Currently amended] The method of claim 1,
    The gelation reaction of the step (e) is maintained for 4 to 20 hours at a temperature of 37 ℃ characterized in that the holding microcapsules manufacturing method.
    [7" claim-type="Currently amended] The method of claim 6,
    The gelation reaction of the step (e) is characterized in that the oil-containing microcapsules manufacturing method characterized in that made for 4 hours at a temperature of 37 ℃.
    [8" claim-type="Currently amended] The method of claim 1,
    The washing of step (g) is a method for producing a microcapsules containing oil, characterized in that using alcohol.
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    同族专利:
    公开号 | 公开日
    KR100616133B1|2006-08-28|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2002-11-15|Application filed by 주식회사 그린바이오텍
    2002-11-15|Priority to KR1020020070961A
    2004-05-22|Publication of KR20040042987A
    2006-08-28|Application granted
    2006-08-28|Publication of KR100616133B1
    优先权:
    申请号 | 申请日 | 专利标题
    KR1020020070961A|KR100616133B1|2002-11-15|2002-11-15|Method for preparing of Microcapsule Comprising Oil and Fat|
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