JP2009242334A - Liquid composition for soft-capsule filling - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a liquid composition for soft-capsule filling, in which a slightly oil-soluble ingredient is dispersed as an active ingredient in an edible fatty oil, and both the dispersibility of the slightly oil-soluble ingredient in the edible fatty oil and the dispersibility of the slightly oil-soluble ingredient in living bodies are equal to or better than those of conventional liquid compositions using beeswax as a dispersant. <P>SOLUTION: The liquid composition for soft-capsule filling, in which the slightly oil-soluble ingredient is dispersed in the edible fatty oil, contains a reacted monoglyceride, a distilled monoglyceride and a diglycerol fatty acid ester having a monoester content of ≥50%. <P>COPYRIGHT: (C)2010,JPO&INPIT

Description

  The present invention relates to a liquid composition for filling soft capsules.

  Soft capsules containing a hardly oil-soluble or powdery active ingredient are generally produced by filling a capsule having gelatin as a coating with a dispersion prepared by dispersing an active ingredient in edible fats and oils. At that time, glycerin fatty acid esters and beeswax have been conventionally used as dispersants for stably dispersing active ingredients in edible fats and oils (see Patent Document 1).

  However, soft capsules using beeswax as a dispersant are sufficient for the dispersion of active ingredients in edible oils and fats, but when the preparation is ingested, it is difficult to disperse the active ingredients in vivo and is effective. It is known that the effects of components may not be sufficiently exhibited in vivo. Therefore, as means for solving this problem, for example, a composition in which an active ingredient is suspended by a combination of a glycerin fatty acid ester and a hydrogenated oil (see Patent Document 2) has been proposed.

  However, the above technique is not always satisfactory for practical use, and more effective means are required.

Japanese Patent Laid-Open No. 7-138151, paragraph “0019” JP 2005-112753 A, paragraph “0020”

  An object of the present invention is a liquid composition for filling soft capsules in which a hardly oil-soluble component is dispersed as an active ingredient in an edible oil and fat, and the dispersibility of the hardly oil-soluble component in the edible oil and fat and the poorly oil-soluble property in vivo The dispersibility of the components is to provide a liquid composition for filling soft capsules that is equal to or better than that of a conventional formulation using beeswax as a dispersant.

As a result of intensive studies to solve the above problems, the present inventor has obtained the following knowledge.
(I) By using the reaction monoglyceride and the distilled monoglyceride as a dispersion stabilizer for dispersing the hardly oil-soluble component, the hardly oil-soluble component is stably dispersed in the edible oil and fat without using beeswax.
(Ii) Further, when a diglycerin fatty acid ester having a monoester content of 50% or more is used, the dispersibility of the hardly oil-soluble component in the artificial gastric juice is remarkably improved.
The present invention has been completed based on the above findings, and provides the following liquid composition for filling soft capsules.

  That is, the present invention is a composition in which a hardly oil-soluble component is dispersed in an edible fat and oil, and further contains a reaction monoglyceride, a distilled monoglyceride, and a diglycerin fatty acid ester having a monoester content of 50% or more. A liquid composition for filling soft capsules.

The liquid composition for filling soft capsules of the present invention has a dispersion stability of hardly oil-soluble components in edible fats and oils that is equal to or higher than that of conventional products using beeswax as a dispersant.
The liquid composition for filling soft capsules of the present invention has a significantly improved dispersibility of the poorly oil-soluble component in artificial gastric juice compared to conventional products using beeswax as a dispersant.

  The liquid composition for filling soft capsules of the present invention is a composition in which a hardly oil-soluble component is dispersed in an edible fat using a reactive monoglyceride, a distilled monoglyceride, and a diglycerin fatty acid ester having a monoester content of 50% or more. .

Edible fats and oils The edible fats and oils used in the present invention are not particularly limited as long as they are edible fats and oils that can be used as a carrier of poorly oil-soluble components. For example, olive oil, sesame oil, sesame oil, safflower oil, soybean oil, corn oil, Examples include rapeseed oil, palm oil, palm olein, palm kernel oil, sunflower oil, grape oil, cottonseed oil, coconut oil, peanut oil and the like, and neutralized fatty acid triglycerides, squalene, fish oil and the like. As edible fats and oils in this invention, vegetable fats and oils are preferable, salad oils of vegetable fats and oils are especially preferable, and safflower salad oil is especially preferable. In the present invention, one type of edible oil or fat may be used, or two or more types may be used in any combination.

The hardly oil-soluble component The hardly oil-soluble component used in the present invention is composed of a substance having low lipophilicity and constitutes an active ingredient of the liquid composition for filling soft capsules of the present invention.
The hardly oil-soluble component in the present invention is in the form of powder, and refers to a substance that does not dissolve within 30 minutes when 1 g of the powder is added to 100 g of edible oil and fat and mixed at 20 ° C.
Examples of such poorly oil-soluble components include vitamins (particularly water-soluble vitamins such as ascorbic acid, vitamins B1, B2, B6, and B12), nutritional supplements such as citric acid, hyaluronic acid, and calcium powder; royal jelly extract Powder (Powder), Propolis Extract Powder, Blueberry Extract Powder, Agaricus Extract Powder, Shark Cartilage Extract Extract Powder, Turmeric Powder, Ginkgo Leaves Extract Powder, Gymnema Extract Powder, Other Animal and Plant Powders, Lactose, Oligosaccharide, Chitosan, Dietary Fiber, etc. Or other medicinal ingredients such as herbal extract powder, Chinese medicine, and pharmaceutical compositions. Of these, blueberry extract powder, ginkgo biloba extract powder and vitamins are preferred. The hardly oil-soluble component can be used alone or in combination of two or more.

Reaction monoglyceride The reaction monoglyceride used in the present invention is obtained by removing unreacted glycerin as much as possible from the esterification product of glycerin and fatty acid or the transesterification product of glycerin and fat (triglyceride). And a mixture containing monoglyceride (glycerin monofatty acid ester), diglyceride (glycerin difatty acid ester) and triglyceride (glycerin trifatty acid ester). The content of monoglyceride in 100% of the reaction monoglyceride is usually about 40 to 60%, preferably about 45 to 55%. Further, the content of diglyceride in 100% of the reaction monoglyceride is usually about 15 to 40%, preferably about 20 to 30%. The content of triglyceride in 100% of the reaction monoglyceride is usually about 1 to 10%, preferably about 1 to 5%.

The composition of the reaction monoglyceride, that is, the contents of monoglyceride, diglyceride and triglyceride in the reaction monoglyceride can be determined by analyzing the reaction monoglyceride by HPLC (high performance liquid chromatography). Specifically, the reaction moglyceride is analyzed under the analysis conditions shown below, and after the analysis, the peak corresponding to each component of the test sample recorded on the chromatogram by the data processor is used with an integrator. Measure the peak area. Based on the measured peak area, the monoglyceride content, the diglyceride content, and the triglyceride content can be obtained as area percentages.
The HPLC analysis conditions are shown below.

(HPLC analysis conditions)
Apparatus: High performance liquid chromatograph (model: LC-10AS; manufactured by Shimadzu Corporation)
Detector: RI detector (model: RID-6A; manufactured by Shimadzu Corporation)
Column: GPC column (model: SHODEX KF-802; manufactured by Showa Denko KK), 2 connected columns Temperature: 40 ° C
Mobile phase: THF
Flow rate: 1.0 mL / min
Test solution injection volume: 15 μL

  The fatty acid constituting the reactive monoglyceride used in the present invention is preferably a linear saturated fatty acid having 6 to 24 carbon atoms derived from edible animal and vegetable oils and fats (for example, caproic acid, caprylic acid, capric acid, lauric acid). , Myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid, lignoceric acid, etc.), more preferably palmitic acid, stearic acid, behenic acid and the like.

  As a manufacturing method of the reaction monoglyceride used by this invention, the manufacturing method by (1) esterification reaction of glycerol and fats and oils and (2) the manufacturing method by esterification reaction of glycerol and a fatty acid are mentioned, for example. The outline of these production methods is shown in the following (1) and (2), respectively.

(1) Production method of reaction monoglyceride by transesterification For example, in a normal reaction vessel equipped with a stirrer, a heating jacket, a baffle plate, etc., glycerin and fats and oils are charged at a molar ratio of 2: 1. For example, sodium hydroxide is added and stirred and mixed, and heated in a nitrogen gas atmosphere at, for example, about 180 to 260 ° C., preferably about 200 to 250 ° C., for about 0.5 to 15 hours, preferably about 1 to 3 hours. A transesterification reaction is performed. The reaction pressure condition is preferably normal pressure or reduced pressure. The obtained reaction liquid is a mixture containing glycerin, monoglyceride, diglyceride, triglyceride and the like.
After completion of the reaction, the catalyst remaining in the reaction solution is neutralized, and then the reaction solution is preferably distilled under reduced pressure to distill off the remaining glycerin. If necessary, desalting, decolorization, filtration, etc. Finally, a reaction monoglyceride containing about 40 to 60% of monoglyceride with respect to the whole is obtained.

(2) Method for producing reaction monoglyceride by esterification reaction For example, a normal reaction vessel equipped with a stirrer, a heating jacket, a baffle plate and the like is charged with glycerin and fatty acid at a molar ratio of 1: 1, and an acid or Alkali is added as a catalyst and under any inert gas atmosphere such as nitrogen or carbon dioxide, for example in the range of about 180-260 ° C, preferably about 200-250 ° C for about 0.5-5 hours, preferably about Esterification reaction is performed by heating for 1 to 3 hours. The obtained reaction liquid is a mixture containing glycerin, monoglyceride, diglyceride, triglyceride and the like.
After completion of the reaction, the catalyst remaining in the reaction solution is neutralized, and then the reaction solution is preferably distilled under reduced pressure to distill off the remaining glycerin. If necessary, desalting, decolorization, filtration, etc. Finally, a reaction monoglyceride containing about 40 to 60% of monoglyceride with respect to the whole is obtained.

  Examples of the reactive monoglyceride include Poem P-200 (product name; monoglyceride content of about 52%; manufactured by Riken Vitamin Co., Ltd.), Poem V-200 (product name; monoglyceride content of about 50%; manufactured by Riken Vitamin Co., Ltd.) and poem. B-200 (product name; monoglyceride content: about 47%; manufactured by Riken Vitamin Co., Ltd.) and the like are commercially produced and sold. In the present invention, these commercially available products can be used as the reactive monoglyceride.

Distilled Monoglyceride The distilled monoglyceride used in the present invention is a product obtained by purifying the above-mentioned reaction monoglyceride to increase the monoglyceride content, and the content of monoglyceride in 100% distilled monoglyceride is usually about 90% or more.
The content of monoglyceride in 100% distilled monoglyceride is determined by analyzing the distilled monoglyceride using HPLC under the above analysis conditions. Specifically, after analyzing the distilled monoglyceride under the above HPLC analysis conditions, the peak area corresponding to each component of the test sample recorded on the chromatogram by the data processor is measured using an integrator, Based on the measured peak area, the monoglyceride content can be determined as an area percentage.

  Examples of the method for producing the distilled monoglyceride used in the present invention include a method in which the reaction monoglyceride is vacuum distilled using, for example, a falling film molecular distillation device or a centrifugal molecular distillation device. By refine | purifying using these methods, the distillation monoglyceride which contains about 90% or more of the whole monoglyceride can be obtained. The upper limit of the monoglyceride content in the distilled monoglyceride is usually about 99%.

Diglycerin fatty acid ester The diglycerin fatty acid ester used in the present invention is obtained by purifying diglycerin fatty acid ester, which is an esterification product of diglycerin and fatty acid, by a method known per se. The content is increased to about 50% or more with respect to the whole. Preferably, the monoester content is about 70% or more of the total. The upper limit of the monoester content is usually about 96%.

  Content of the monoester body in diglycerin fatty acid ester is calculated | required by analyzing diglycerin fatty acid ester using HPLC on the said analysis conditions. Specifically, after analyzing diglycerin fatty acid ester under the above HPLC analysis conditions, the peak area corresponding to each component of the test sample recorded on the chromatogram by the data processor is measured using an integrator. And based on the measured peak area, content of a monoester body can be calculated | required as an area percentage.

  As the diglycerin used as a raw material for the diglycerin fatty acid ester used in the present invention, a small amount of acid or alkali is usually added to glycerin as a catalyst, and this is added under any inert gas atmosphere such as nitrogen or carbon dioxide. For example, a diglycerin mixture having an average degree of polymerization of glycerin of about 1.5 to 2.4, preferably an average degree of polymerization of about 2.0, obtained by heating at a temperature of about 180 ° C. or higher and causing a polycondensation reaction. It is done. Further, diglycerin may be obtained using glycidol or epichlorohydrin as a raw material. After completion of the reaction, treatments such as neutralization, desalting, and decolorization may be performed as necessary.

  In the present invention, the diglycerin mixture is purified using a method known per se such as distillation or column chromatography, and the diglycerin content consisting of two molecules of glycerin is about 50% or more, preferably about 70% of the total. As described above, high-purity diglycerin having a high concentration of about 90% or more is preferably used.

  Examples of the fatty acid used as a raw material for the diglycerin fatty acid ester used in the present invention include linear saturated fatty acids having 6 to 24 carbon atoms (for example, caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid). , Stearic acid, arachidic acid, behenic acid, lignoceric acid, etc.) or unsaturated fatty acids (eg palmitooleic acid, oleic acid, elaidic acid, linoleic acid, γ-linolenic acid, α-linolenic acid, arachidonic acid, ricinoleic acid) , Condensed ricinoleic acid, etc.), preferably capric acid, lauric acid, myristic acid, oleic acid and the like. As the fatty acid, those containing 70% or more of capric acid, lauric acid, myristic acid or oleic acid are commercially available, and it is preferable to use them in the present invention. Examples of the commercially available fatty acids include, for example, trade name (1) NAA-122 (manufactured by NOF Corporation), (2) LUNAC L-98 (manufactured by Kao Corporation), (3) myristic acid 98 (Miyoshi oil and fat (4) NAA-142 (manufactured by NOF Corporation), (5) LUNAC MY-98 (manufactured by Kao Corporation), (6) extra olein (manufactured by NOF Corporation), (7) LUNAC O-V ( Kao), (8) LUNAC OP (manufactured by Kao), and the like.

  The outline of the preferable manufacturing method of the diglycerin fatty acid ester used in the present invention is as follows. For example, in a normal reaction vessel equipped with a stirrer, a heating jacket, a baffle plate and the like, diglycerin and fatty acid in a molar ratio of about 1: 0.8 to 1: 1.2, preferably about 1: 1. Then, sodium hydroxide is added as a catalyst, mixed with stirring, and heated at a predetermined temperature in a nitrogen gas atmosphere while removing water produced by the esterification reaction out of the system. The reaction temperature is usually in the range of about 180 to 260 ° C, preferably in the range of about 200 to 250 ° C. The reaction pressure is under reduced pressure or normal pressure, and the reaction time is about 0.5 to 15 hours, preferably about 1 to 3 hours. The end point of the reaction is usually determined by measuring the acid value of the reaction mixture and using an acid value of about 12 or less. The obtained reaction liquid is a mixture containing unreacted fatty acid, unreacted diglycerin, diglycerin monofatty acid ester, diglycerin difatty acid ester, diglycerin trifatty acid ester, diglycerin tetrafatty acid ester and the like. After completion of the reaction, the resulting reaction solution is cooled to about 120 ° C. or more and less than 180 ° C., preferably about 130 to 150 ° C., then acid is added to neutralize the catalyst, and preferably left for about 15 minutes to 1 hour. When unreacted diglycerin is separated into the lower layer, it is removed to obtain diglycerin fatty acid ester.

  Furthermore, the diglycerin fatty acid ester is molecularly distilled using, for example, a falling film molecular distillation apparatus or a centrifugal molecular distillation apparatus, or purified using a method known per se such as column chromatography or liquid-liquid extraction. As a result, a diglycerin fatty acid ester containing about 50% or more, preferably about 70% or more of the monoester can be obtained.

  Examples of the diglycerin fatty acid ester having a monoester content of 50% or more include Poem DM-100 (trade name; manufactured by Riken Vitamin), Poem DO-100V (trade name; manufactured by Riken Vitamin), and Poem DL-100. (Trade name; manufactured by Riken Vitamin Co., Ltd.) are commercially produced and sold. In the present invention, these commercially available products can be used as diglycerin fatty acid esters having a monoester content of 50% or more.

Other components The liquid composition for filling soft capsules of the present invention has a content of 50% or more of the above edible fats and oils, hardly oil-soluble components, reactive monoglycerides, distilled monoglycerides, and monoesters as necessary as long as the effects of the present invention are exhibited. Ingredients other than the diglycerin fatty acid ester may be included. Examples of other components include antioxidants (for example, extracted tocopherol and ascorbyl palmitate). Other components can be used alone or in combination of two or more.

Preparation method of composition The liquid composition for filling soft capsules of the present invention uniformly disperses these ingredients while mixing and stirring the edible oil and fat, the hardly oil-soluble component, the reactive monoglyceride, the distilled monoglyceride and the diglycerin fatty acid ester. It is manufactured by. Specifically, for example, edible fats and oils, reaction monoglyceride, distilled monoglyceride and diglycerin fatty acid ester are heated to, for example, about 60 to 90 ° C., preferably about 70 to 80 ° C., and uniformly mixed and stirred. For example, by cooling to about 40 to 60 ° C., and further adding a hardly oil-soluble component, and mixing and stirring uniformly. In addition, as reaction monoglyceride, distilled monoglyceride, and diglycerin fatty acid ester, those previously mixed, heated and melted can be used. Although there is no restriction | limiting in particular in the apparatus for mixing and stirring, For example, high-speed stirrers, such as a biomixer and a homojetter, or a high-speed grinder can be used.

Component ratio The content of the edible fat / oil in 100% by mass of the liquid composition for filling soft capsules of the present invention is not particularly limited, but is usually about 20 to 95% by mass, preferably about 25 to 90% by mass, more preferably about 30 to 80% by mass. In the present invention, if the content of the edible oil / fat is in the above range, the hardly oil-soluble component can be sufficiently dispersed in the edible oil / fat, and the dispersion stability of the hardly oil-soluble component in the edible oil / fat is good.

  The content of the poorly oil-soluble component in 100% by mass of the liquid composition for filling soft capsules of the present invention is not particularly limited, but is usually about 1 to 70% by mass, preferably about 3 to 60% by mass, and more preferably. About 10-50 mass%. If content of a hardly oil-soluble component is the said range in this invention, a hardly oil-soluble component can fully be disperse | distributed in edible fats and oils. Moreover, since the dispersion stability of the hardly oil-soluble component in the edible fat is good, the hardly oil-soluble component is not separated in the soft capsule. Furthermore, since the amount of the active ingredient (poor oil-soluble component) in the soft capsule produced using the liquid composition for soft capsule filling is sufficient, the effect of the poor oil-soluble component in vivo when the soft capsule is ingested, for example, , Physiological activity etc. are fully exhibited.

  The content of the reactive monoglyceride in 100% by mass of the liquid composition for filling soft capsules of the present invention is not particularly limited, but is usually about 0.5 to 15% by mass, preferably about 0.5 to 10% by mass, More preferably, it is about 1-8 mass%. In the present invention, if the content of the reactive monoglyceride is in the above range, the dispersion stability of the hardly oil-soluble component in the edible fat is good, so that the hardly oil-soluble component is not separated in the soft capsule. Furthermore, since the amount of the active ingredient (poor oil-soluble component) in the soft capsule becomes sufficient, when the soft capsule is ingested, the effect of the poor oil-soluble component is sufficiently exhibited in vivo.

  The content of distilled monoglyceride in 100% by mass of the liquid composition for filling soft capsules of the present invention is not particularly limited, but is usually about 0.5 to 15% by mass, preferably about 0.5 to 10% by mass. %, More preferably about 1 to 8% by mass. In the present invention, when the content of the distilled monoglyceride is in the above range, the dispersion stability of the hardly oil-soluble component in the edible fat is good, and therefore the hardly oil-soluble component is not separated in the soft capsule. Furthermore, since the amount of the active ingredient (poor oil-soluble component) in the soft capsule becomes sufficient, when the soft capsule is ingested, the effect of the poor oil-soluble component is sufficiently exhibited in vivo.

  The content of the diglycerin fatty acid ester having a monoester content of 50% or more in 100% by mass of the liquid composition for filling soft capsules of the present invention is not particularly limited, but is usually about 0.05 to 1.5% by mass, for example. , Preferably, it is about 0.05-1 mass%, More preferably, it is about 0.1-1 mass%. In the present invention, when the content of the diglycerin fatty acid ester is within the above range, the dispersibility of the hardly oil-soluble component in the artificial gastric juice is good when a dispersibility test in the artificial gastric juice described below is performed. That is, the dispersibility of the hardly oil-soluble component in the living body is sufficient. Moreover, since the amount of the active ingredient (poor oil-soluble component) in the soft capsule becomes sufficient, when the soft capsule is ingested, the effect of the poor oil-soluble component is sufficiently exhibited in vivo.

Production of Soft Capsule Soft capsules can be produced by wrapping the thus obtained liquid composition for filling soft capsules with a film mainly composed of gelatin according to a conventional method. Specifically, for example, a soft capsule can be produced by a method of injecting and punching out a predetermined amount of a liquid composition for filling a soft capsule between two gelatin sheets.

Dispersion method of poorly oil-soluble component: By mixing and stirring a composition containing edible fats and oils, poorly oil-soluble component, reactive monoglyceride, distilled monoglyceride, and diglycerin fatty acid ester having a monoester content of 50% or more, it is hardly oil-soluble. Ingredients can be well dispersed in edible fats and oils. A method for dispersing such a hardly oil-soluble component in edible fat is also one aspect of the present invention.

  In the dispersion method of the present invention, the edible oil and fat, the hardly oil-soluble component, the reactive monoglyceride, the distilled monoglyceride, the diglycerin fatty acid ester having a monoester content of 50% or more, and preferred embodiments thereof are described in the above-mentioned liquid composition for soft capsule filling. It is the same. As a method of mixing and stirring the composition containing these components, in the production of a soft capsule filling liquid composition, edible fats and oils, hardly oil-soluble components, reactive monoglycerides, distilled monoglycerides, and diesters having a monoester content of 50% or more. This is the same as the method of mixing and stirring the glycerin fatty acid ester. For example, cooking oil and fat, reaction monoglyceride, distilled monoglyceride, and diglycerin fatty acid ester having a monoester content of 50% or more are heated to, for example, about 60 to 90 ° C., preferably about 70 to 80 ° C., and uniformly mixed and stirred After that, it is preferable to cool this to, for example, about 40 to 60 ° C., add a hardly oil-soluble component, and mix and stir uniformly.

  Hereinafter, the present invention will be described more specifically based on examples, but the present invention is not limited thereto.

[Preparation of liquid composition for soft capsule filling]
(1) Raw materials for preparing liquid composition for soft capsule filling 1) Saflower salad oil (manufactured by Cargill Japan)
2) Riboflavin (manufactured by Riken Vitamin)
3) L-ascorbic acid (manufactured by BASF Japan)
4) Reactive monoglyceride (trade name: Poem B-200; monoglyceride content: about 47%; manufactured by Riken Vitamin Co., Ltd.)
5) Reactive monoglyceride (trade name: Poem P-200; monoglyceride content: about 52%; manufactured by Riken Vitamin Co., Ltd.)
6) Distilled monoglyceride (trade name: Poem S-100; monoglyceride content: about 98%; manufactured by Riken Vitamin Co., Ltd.)
7) Distilled monoglyceride (trade name: Poem P-100; monoglyceride content: about 98%; manufactured by Riken Vitamin Co., Ltd.)
8) Diglycerin fatty acid ester (trade name: Poem DM-100; monoester content: about 81%; manufactured by Riken Vitamin Co., Ltd.)
9) Diglycerin fatty acid ester (trade name: Poem DO-100V; monoester content: about 88%; manufactured by Riken Vitamin Co., Ltd.)
10) Diglycerin fatty acid ester (trade name: Poem DL-100; monoester content: about 77%; manufactured by Riken Vitamin Co., Ltd.)
11) Diglycerin fatty acid ester (trade name: Poem J-2081V; monoester content: about 38%; manufactured by Riken Vitamin Co., Ltd.)
12) Diglycerin fatty acid ester (trade name: Poem O-71-DE; monoester content: about 38%; manufactured by Riken Vitamin Co., Ltd.)
13) Beeswax (trade name; deodorized and refined beeswax high acid; made by Celalica Noda)

(2) Composition of raw materials Table 1 shows the composition of raw materials used for the preparation of soft capsule filling liquid compositions (Examples 1 to 4 and Comparative products 1 to 5). Of these, Examples 1 to 4 are examples according to the present invention, and Comparative Examples 1 to 5 are comparative examples for them.

(3) Preparation of liquid composition for filling soft capsule Based on the formulation shown in Table 1, a liquid composition for filling soft capsule was prepared. That is, reactive monoglyceride, distilled monoglyceride and / or diglycerin fatty acid ester, or beeswax was added to safflower salad oil, which was heated to 80 ° C. and stirred to dissolve the dispersant in the salad oil. This solution was cooled to 50 ° C. at room temperature, and riboflavin (manufactured by Riken Vitamin Co., Ltd.) and L-ascorbic acid (manufactured by BASF Japan Co., Ltd.) were added thereto, and a mixer (model Ultra Turrax T-25 Basic; manufactured by IKA Japan Co., Ltd.) was added. ) And further mixed and stirred at 8000 rpm for 10 minutes. The obtained dispersion was vacuum defoamed and then cooled to room temperature to obtain about 100 g of liquid compositions for filling soft capsules (Examples 1 to 4 and Comparatives 1 to 5).

(4) Evaluation of liquid composition for filling soft capsules The following tests were carried out for each of the liquid compositions for filling soft capsules (Examples 1 to 4 and Comparative Examples 1 to 5) prepared by the method described above. The results are shown in Table 2.

[Evaluation of separation of hardly oil-soluble components]
30 g of each of the liquid compositions for filling soft capsules (implemented products 1 to 4 and comparative products 1 to 5) was placed in a centrifuge tube (capacity 50 ml, with a stopper), and this was centrifuged (model: SL-05; Sakuma Seisakusho Co., Ltd.) For 20 minutes at a rotational speed of 1500 rpm. Thereafter, the centrifuge tube was taken out from the centrifuge, and the presence or absence of separation of the hardly oil-soluble components (riboflavin and L-ascorbic acid) was visually observed in the centrifuge tube sample.

[Evaluation of dispersibility of poorly oil-soluble components in artificial gastric juice]
1 g of liquid composition for filling soft capsules (Examples 1 to 4 and Comparative products 1 to 5) and artificial gastric fluid at about 36 ° C. (prepared so that the mass ratio of hydrochloric acid / NaCl / ion-exchanged water is 7/2/991) 1) 99 g into a 200 ml glass beaker and about 36 using a stirrer (product name; three-one motor; model: BL-600; manufactured by Shinto Kagaku; one 5 cm diameter 4-blade type stirring blade) The mixture was stirred for 30 minutes in a warm water bath at 0 ° C., and the liquid composition for filling soft capsules was dispersed in the artificial gastric juice. The obtained dispersion liquid was analyzed using filter paper No. 2 (diameter 125 mm; manufactured by Advantech Co., Ltd.), and naturally filtered, and fractionated into a residue and a filtrate remaining on the filter paper. 10 g of the obtained filtrate was weighed into a petri dish (diameter 70 mm, height 50 mm) and dried with hot air in a 100 ° C. incubator for 1 hour, and then the mass of the dried material remaining on the petri dish was measured. Based on the measured dry mass and the following formula, the elution rate (%) of the hardly oil-soluble component was determined. Moreover, the same evaluation test was implemented about what made the stirring time by the said stirrer 60 minutes, and the elution rate (%) was calculated | required.

  Of the numerical values in the above formula, “198 (mg)” corresponds to the mass of NaCl contained in 99 g of artificial gastric juice, and “320 (mg)” is difficult to contain in 1 g of the liquid composition for soft capsule filling. It corresponds to the mass of the oil-soluble component.

  As is apparent from the results in Table 2, none of the Examples 1 to 4 caused separation of the hardly oil-soluble component, and the elution rate of the hardly oil-soluble component into the artificial gastric juice was better than beeswax in the dispersant. Compared with the one used (Comparative Example 5), it was significantly improved. On the other hand, those using diglycerin fatty acid esters whose monoester content is not 50% or more (Comparative Examples 1 and 2) do not cause separation, but the elution rate is poor, and either distilled monoglyceride or reaction monoglyceride is used. In those not used (Comparative Products 3 and 4), the separation of the hardly oil-soluble component occurred.

Claims (1)

  A composition in which a hardly oil-soluble component is dispersed in an edible fat and oil, and further contains a reactive monoglyceride, a distilled monoglyceride, and a diglycerin fatty acid ester having a monoester content of 50% or more, for filling soft capsules Liquid composition.