JPS6324652B2 - - Google Patents

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Publication number
JPS6324652B2
JPS6324652B2 JP59130849A JP13084984A JPS6324652B2 JP S6324652 B2 JPS6324652 B2 JP S6324652B2 JP 59130849 A JP59130849 A JP 59130849A JP 13084984 A JP13084984 A JP 13084984A JP S6324652 B2 JPS6324652 B2 JP S6324652B2
Authority
JP
Japan
Prior art keywords
edible
powder
oils
fat
fats
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP59130849A
Other languages
Japanese (ja)
Other versions
JPS6112248A (en
Inventor
Masaharu Nagao
Kazushi Kinoshita
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Takasago International Corp
Original Assignee
Takasago Perfumery Industry Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Takasago Perfumery Industry Co filed Critical Takasago Perfumery Industry Co
Priority to JP59130849A priority Critical patent/JPS6112248A/en
Publication of JPS6112248A publication Critical patent/JPS6112248A/en
Publication of JPS6324652B2 publication Critical patent/JPS6324652B2/ja
Granted legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J13/00Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
    • B01J13/02Making microcapsules or microballoons

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は食用油脂含有カプセルの製造法に関す
る。 (従来の技術) 特公昭34−5600号公報及び米国特許第2809895
号明細書 芳香油をコーンシロツプ(水飴)に分散させた
乳濁液を微粒子状の固体とする方法が開示されて
いる。 米国特許第3041180号明細書 上記発明の関連技述であり、コーンシロツプに
グリセロール、グリコール類及び乳化剤を加える
ことにより乳化を容易にした方法が開示されてい
る。 特開昭58−116652号公報 食用固形油脂を粉末調味料に吸着せしめ、顆粒
を得る方法が開示されている。 (発明が解決しようとする問題点) 近年は飲食品に対する嗜好の変化に対応してそ
の形態も様々に変つてきている。そのため、飲食
品の素材である各種の食用油脂類についても粉末
状乃至顆粒状のものが要望されている。 特定の素材を粉末乃至顆粒化する方法として乳
糖などへの吸着法や噴霧乾燥法、顆粒造粒法など
が知られており、食用油脂類についてもこれらの
方法の適用が試みられている。 しかしながら、多大の努力にも拘らず、市販の
粉末油脂はその被覆が不完全であるため、経時的
に油脂特有の酸化による劣化を受け易く、さらに
比較的吸湿性に富むため、保存性に劣り固化し易
い。しかも、溶解性も不十分であり、ママコにな
り易く、その上溶解した状態でも透明性に欠ける
ものが多い等未だ多くの問題点があり、これら欠
点の解消された粉末状乃至顆粒状の食用油脂の出
現が望まれている。 (問題点を解決するための手段) 本発明者らは、上記問題点を解決すべく鋭意研
究を重ねた結果、シヨ糖と或種の澱粉加水分解物
よりなる混合物を用いて食用油脂をカプセル化す
ると、得られるカプセルは細粒であるにも拘ら
ず、外気との接触はほぼ完全に断たれるため、食
用油脂の酸化による劣化も少なく、極めて安定し
た粉末状乃至顆粒状の製品であることを見出し、
かかる知見に基いて本発明を完成したのである。 すなわち本発明は、食用油脂を、DEが5〜12
である澱粉加水分解物と蔗糖の重量混合比が40:
60〜55:45の糖質混合物にてカプセル化すること
を特徴とする食用油脂含有カプセルの製造法を提
供するものである。 本発明に用いられる食用油脂には特別な制限は
なく、例えば大豆油、コーン油、サフラワー油な
どの精製植物性食用油脂、乳脂、牛脂、豚脂など
の精製動物性油脂、これらの加工油脂類、例えば
バター、マーガリンなどを挙げることができる。 次に、糖質混合物の成分である澱粉加水分解物
としてはDEが5〜12の範囲のものを用い、好ま
しくはDE7〜8のものを使用する。DEの大きい
ものはアモルフアス化は良好であるが、吸湿性が
大きくなり、またDEの小さいものは吸湿性は少
なくなるがアモルフアス化が悪くなり、結晶化し
てカプセルが壊れ易くなる。これら糖質の特徴と
して、純粋なものほど一般的に結晶化し易く、ま
たアモルフアス状態にないと製造時にきれいな糸
状で射出されて来ないので、アモルフアスの良否
が製品化に与える影響が非常に大きい。したがつ
て、混合すべき糖質の種類、混合比率等は重要な
要素である。 本発明では蔗糖と澱粉加水分解物を重量混合比
が40:60〜55:45の範囲で混合して得られる糖質
混合物を用いており、その結果最も良好なカプセ
ルを得ることができる。 食用油脂を糖質混合物の溶液に分散させるにあ
たり乳化剤を加えることが望ましい。乳化剤とし
ては食品添加物として許可されたものを任意に使
用できるが、特に大豆レシチン、蔗糖脂肪酸エス
テルであつてHLBが約4〜12のものが好ましい。
乳化剤の添加量は原料食用油脂の重量に基いて3
〜5%程度で十分である。 そのほか必要に応じて酸化防止剤や他の添加物
を適宜添加することができる。酸化防止剤として
は食品添加物として許容されているもの、例えば
l−ソルビン酸ナトリウム、2,6−ジ−t−ブ
チル−4−メチルフエノール(BHT)、ビタミン
Eなどや天然のローズマリー、セージなどの抽出
物等を用いることができ、特に糖質と食用油脂と
の調和の面からビタミンEが好ましい。なお、酸
化防止剤を用いる場合、その添加量は原料食用油
脂の重量に基いて約2%程度が適当である。その
他の添加物としてはフレーバー、食用色素などの
ほかエイコサペンタエン酸等の栄養物質やグルタ
ミン酸ソーダ等の呈味物質などがある。 本発明の食用油脂含有カプセルは以下の方法に
より製造することができる。 まず、蔗糖と澱粉加水分解物の混合物に少量の
水を加えて加熱溶融する。一方、食用油脂には乳
化剤等の補助成分を適宜加え十分に混合する。 前記糖質混合物の加熱を停止した後、激しく撹
拌しながら必要量の食用油脂を徐々に添加、分散
せしめる。ここで糖質混合物に対する食用油脂の
配合量については0.2〜20重量%とすべきであり、
品質の安定性の面から0.5〜10重量%が好ましい。 糖質混合物に食用油脂を添加した後、若干撹拌
を続ける。このようにして得られた乳化物(マト
リツクス)を加温したエクストルーダーに移す。
一方、冷却槽にアルコールを入れ、約−10℃〜−
20℃に冷却しておく。アルコールは冷却と洗浄を
目的として用いられるものであり、食品衛生上害
を与えないものであればよいが、加温された糖質
混合物と接触することを考慮すると、沸点が低す
ぎるものは不適当である。しかし、再利用のため
に蒸留精製することを考慮すると、低沸点のアル
コールが望ましく、また水分は糖質の流出の原因
となるので出来るだけ無水物として蒸留回収ので
きることが好ましい。これらの要求を満足するア
ルコールとしてはイソプロピルアルコールが最も
好ましいが、エチルアルコールも十分に使用する
ことができる。 乳化物(マトリツクス)を撹拌しながらエクス
トルーダーより前記冷却槽に射出する。この間、
冷却槽内の温度上昇を抑制するため十分に冷却し
ておくことが必要であり、射出された粒子が軟化
しないように約10℃以下に保つべきである。射出
終了後も少し撹拌を続け、十分に破砕、冷却、外
表面の洗浄を行なつた後、遠心分離等の操作でカ
プセルとアルコールを分離する。この分離操作は
食用油脂カプセルとアルコールが分離でき、粒子
の破砕を伴なわないものであれば各種の手段を適
用することができる。 アルコール分離後の食用油脂カプセルは再固結
を防止するため、ケーキング防止剤を添加、混和
することが望ましい。ここでケーキング防止剤と
しては種々のものが使用できるが、第3燐酸カル
シウム、α−乳糖などが好ましく、特にα−乳糖
が好適である。ケーキング防止剤の添加量は適宜
決定すればよいが、α−乳糖の場合は糖質混合物
の重量に基いて1〜5%、好ましくは2〜3%が
適当である。 ケーキング防止剤と混和後、食用油脂カプセル
の乾燥を行なう。乾燥は種々の方法により実施し
うるが、未乾燥粒子が熱のために溶解したり、流
動のために粉末化する等の欠点がない方法が適当
である。また、乾燥は可及的に低温で行なうこと
が望ましい。この目的のためには、真空回転乾燥
機にて加熱温度約30〜35℃、真空度約20〜
50Torrにて静かに回転させながら乾燥すること
が好ましい。 (発明の効果) 本発明により得られる食用油脂含有カプセルは
吸湿に対する保存性にすぐれており、溶解性も良
好である。その上、溶液状にて使用する場合、透
明性にすぐれており、広範囲に及ぶ利用が期待で
きる。 (実施例) 次に、実施例および使用例により本発明を詳し
く説明する。 参考例 1 各種のケーキング防止剤についてその性能を下
記の方法により評価した。結果を第1表に示す。 (1) 溶解性 水または1%クエン酸水溶液100mlにケーキ
ング防止剤1gを入れ、撹拌して溶解せしめ、
肉眼にて判定した。 (2) ケーキング防止効果 前記した本発明の方法によりカプセル化した
食用油脂をアルコールと分離した後、未乾燥の
状態にて湿つた重量に対して所定のケーキング
防止剤3重量%を加えた。 次いで、これをロータリーエバポレーター中
で約40℃の湯浴上で減圧下に乾燥した。乾燥
後、約24時間開放下(または室内)に放置した
のちカプセルの外表面の状態を観察し、以下の
如く判定した。 〇……サラサラした状態のもの △……ややブロツキングを生ずるもの ×……ブロツキングを生ずるもの
(Industrial Application Field) The present invention relates to a method for producing edible oil- and fat-containing capsules. (Prior art) Japanese Patent Publication No. 34-5600 and U.S. Patent No. 2809895
A method is disclosed in which an emulsion in which an aromatic oil is dispersed in corn syrup is made into a finely divided solid. US Patent No. 3,041,180 This is related to the above invention, and discloses a method in which emulsification is facilitated by adding glycerol, glycols, and an emulsifier to corn syrup. JP-A-58-116652 discloses a method for obtaining granules by adsorbing solid edible fats and oils onto powdered seasonings. (Problems to be Solved by the Invention) In recent years, the forms of food and drink have been changing in response to changes in tastes for food and drink. Therefore, there is a demand for various edible oils and fats that are raw materials for food and drink products in powder or granule form. Known methods for powdering or granulating specific materials include lactose adsorption methods, spray drying methods, and granulation methods, and attempts have been made to apply these methods to edible oils and fats as well. However, despite many efforts, commercially available powdered fats and oils have incomplete coatings, so they are susceptible to deterioration over time due to oxidation that is characteristic of fats and oils.Furthermore, they are relatively hygroscopic, resulting in poor shelf life. Easy to solidify. Moreover, there are still many problems such as insufficient solubility, easy to form lumps, and even in the dissolved state, many of them lack transparency. The appearance of fats and oils is desired. (Means for Solving the Problems) As a result of extensive research in order to solve the above problems, the present inventors have found that edible fats and oils are encapsulated using a mixture of sucrose and a certain type of starch hydrolyzate. Although the resulting capsules are fine particles, contact with the outside air is almost completely cut off, so there is little deterioration due to oxidation of edible fats and oils, and the product is extremely stable in the form of powder or granules. I found out that
The present invention was completed based on this knowledge. That is, the present invention uses edible fats and oils with a DE of 5 to 12.
The weight mixing ratio of starch hydrolyzate and sucrose is 40:
The present invention provides a method for producing edible fat-containing capsules, which is characterized in that the capsules are encapsulated with a carbohydrate mixture of 60 to 55:45. The edible oils and fats used in the present invention are not particularly limited, and include, for example, refined vegetable edible oils such as soybean oil, corn oil, and safflower oil, refined animal fats and oils such as milk fat, beef tallow, and pork fat, and processed oils and fats thereof. Examples include butter, margarine, etc. Next, as the starch hydrolyzate which is a component of the carbohydrate mixture, one having a DE of 5 to 12 is used, preferably one having a DE of 7 to 8. Those with a high DE have good amorphization, but have high hygroscopicity, and those with a low DE have low hygroscopicity, but have poor amorphization, making it easy to crystallize and break the capsule. Characteristics of these carbohydrates are that the purer they are, the easier they are to crystallize, and if they are not in an amorphous state, they will not be injected in the form of clean threads during production, so the quality of the amorphous has a very large effect on the commercialization of the product. Therefore, the types of carbohydrates to be mixed, the mixing ratio, etc. are important factors. In the present invention, a carbohydrate mixture obtained by mixing sucrose and starch hydrolyzate at a weight mixing ratio of 40:60 to 55:45 is used, and as a result, the best capsules can be obtained. It is desirable to add an emulsifier when dispersing the edible fat into the carbohydrate mixture solution. Any emulsifier that is approved as a food additive can be used, but soybean lecithin and sucrose fatty acid esters having an HLB of about 4 to 12 are particularly preferred.
The amount of emulsifier added is 3 based on the weight of the raw edible fat.
~5% is sufficient. In addition, antioxidants and other additives may be added as appropriate. Antioxidants include those permitted as food additives, such as sodium l-sorbate, 2,6-di-t-butyl-4-methylphenol (BHT), vitamin E, natural rosemary, and sage. Vitamin E is particularly preferred from the viewpoint of harmony between carbohydrates and edible fats and oils. In addition, when using an antioxidant, the appropriate amount of addition is about 2% based on the weight of the raw material edible fat. Other additives include flavors, food colors, and other nutritional substances such as eicosapentaenoic acid and taste substances such as monosodium glutamate. The edible fat-containing capsule of the present invention can be produced by the following method. First, a small amount of water is added to a mixture of sucrose and starch hydrolyzate and the mixture is heated and melted. On the other hand, auxiliary components such as emulsifiers are appropriately added to the edible oil and fat and mixed thoroughly. After stopping the heating of the carbohydrate mixture, a required amount of edible oil and fat is gradually added and dispersed while stirring vigorously. Here, the amount of edible oil and fat added to the carbohydrate mixture should be 0.2 to 20% by weight.
From the viewpoint of quality stability, 0.5 to 10% by weight is preferable. After adding the edible fat and oil to the carbohydrate mixture, continue stirring slightly. The emulsion (matrix) thus obtained is transferred to a heated extruder.
Meanwhile, put alcohol in a cooling tank and
Cool to 20℃. Alcohol is used for cooling and cleaning purposes, so long as it does not pose a food hygiene hazard, alcohol is fine, but alcohol with a boiling point that is too low should not be used, considering that it will come into contact with the heated carbohydrate mixture. Appropriate. However, in consideration of distillation and purification for reuse, it is desirable to use an alcohol with a low boiling point, and since water causes the outflow of carbohydrates, it is preferable that the alcohol can be distilled and recovered as an anhydride as much as possible. Isopropyl alcohol is the most preferred alcohol that satisfies these requirements, but ethyl alcohol can also be used satisfactorily. The emulsion (matrix) is injected into the cooling tank from the extruder while stirring. During this time,
Sufficient cooling is necessary to suppress the temperature rise in the cooling tank, and the temperature should be kept below about 10°C to prevent the injected particles from softening. After the injection is completed, stirring is continued for a while to thoroughly crush, cool, and wash the outer surface, and then the capsules and alcohol are separated by centrifugation or other operations. Various means can be used for this separation operation as long as the edible fat capsule and the alcohol can be separated and the separation does not involve crushing the particles. In order to prevent re-solidification of the edible oil/fat capsules after alcohol separation, it is desirable to add and mix an anti-caking agent. Various anti-caking agents can be used here, but tertiary calcium phosphate, α-lactose and the like are preferred, with α-lactose being particularly preferred. The amount of the anti-caking agent to be added may be determined as appropriate, but in the case of α-lactose, an appropriate amount is 1 to 5%, preferably 2 to 3%, based on the weight of the carbohydrate mixture. After mixing with the anti-caking agent, the edible oil/fat capsules are dried. Drying can be carried out by various methods, but a method that does not have disadvantages such as melting of undried particles due to heat or pulverization due to flowability is suitable. Further, it is desirable that the drying be performed at as low a temperature as possible. For this purpose, use a vacuum rotary dryer at a heating temperature of approximately 30-35℃ and a vacuum degree of approximately 20-35℃.
It is preferable to dry while rotating gently at 50 Torr. (Effects of the Invention) The edible oil-containing capsules obtained by the present invention have excellent preservability against moisture absorption and good solubility. Moreover, when used in the form of a solution, it has excellent transparency and can be expected to be used over a wide range of areas. (Example) Next, the present invention will be explained in detail with reference to Examples and Usage Examples. Reference Example 1 The performance of various anti-caking agents was evaluated by the following method. The results are shown in Table 1. (1) Solubility Add 1 g of anti-caking agent to 100 ml of water or 1% citric acid aqueous solution, stir to dissolve,
Judgment was made with the naked eye. (2) Anti-caking effect After separating the edible fats and oils encapsulated by the method of the present invention from alcohol, 3% by weight of a predetermined anti-caking agent was added to the wet weight of the oil in an undried state. This was then dried under reduced pressure in a rotary evaporator over a water bath at about 40°C. After drying, the capsule was left in the open (or indoors) for about 24 hours, and then the condition of the outer surface of the capsule was observed and judged as follows. 〇...Smooth condition△...Those that cause some blotching ×...Those that cause blotching

【表】 参考例 2 各種の糖質混合物についてその性能を下記の方
法により評価した。結果を第2表に示す。 (1) 混和状態、アモルフアス構成要素及び射出状
態混合物を肉眼で観察し、以下の如く判定し
た。 ◎……良好、〇……やや良、×……不良 (2) 耐吸湿性 20メツシユ(篩上)グラニユー糖20g中に20
メツシユ(篩上)の試料1gを混和し、RH80
%、25℃の恒温恒湿器内に1時間放置した後、
下記の如く判定した。 〇……サラサラした状態のもの ×……一部ブロツキングを起しているもの ××……ほとんどブロツキングを起しているも
[Table] Reference Example 2 The performance of various carbohydrate mixtures was evaluated by the following method. The results are shown in Table 2. (1) The mixture state, amorphous component, and injection state were observed with the naked eye and judged as follows. ◎...Good, 〇...Slightly good, ×...Poor (2) Moisture absorption resistance 20 mesh (on sieve) 20 g of granulated sugar
Mix 1 g of the mesh sample (on the sieve) and
%, after leaving it in a constant temperature and humidity chamber at 25℃ for 1 hour,
It was determined as follows. 〇……Things that are in a smooth condition×……Those with some blotching ××……Those with mostly blotching

【表】 * 焦結
実施例 1 煮詰釜内に水3を入れ沸騰させた。これに精
製グラニユー糖11Kgと澱粉加水分解物(「パイン
デツクス#1(DE7〜8)」、松谷化学工業(株)製)
9Kgを加えて加熱溶解せしめ、さらに内温117〜
120℃に達するまで煮詰めた。 一方、精製ヘツド1Kgを加温溶解し、これに大
豆レシチン40g、ビタミンE(「イーミツクス−
80」、エーザイ(株)製)20g及びバターフレーバー
(高砂香料工業(株)製)20gを加え、撹拌混合して
溶解せしめ、液状食用油脂を調製した。 前記糖質混合液は加熱を停止し、高速撹拌(約
2000rpm)しながら液状食用油脂を徐々に添加し
た。添加終了後、約1〜2分間撹拌を続け十分に
分散、乳化せしめた。 この乳化液を加温したエクストルーダーに移し
た。また、破砕用撹拌機付の冷却槽に約50のイ
ソプロパノールを入れ約−10℃に冷却しておく。
このイソプロパノールを冷却、撹拌をしながらエ
クストルーダーの押し出し口径0.7mmφの孔より
約2Kg/cm2Gの圧力で前記乳化液を押出した。押
出し終了後の液温は約2℃であつた。 次いで、遠心分離機を用いてアルコールを分離
して得た食用油脂含有カプセルを予めα−乳糖
600gを入れてある真空回転乾燥機へ仕込み、加
熱温度30〜35℃、真空度20〜30Torrで約5時間
乾燥し、製品18.8Kgを得た。本カプセルは乳白
色、ほとんど無臭に近い微粒状粒体であり、20〜
60メツシユのもの13.2Kgであつた。 実施例 2〜6 第3表に示した各成分を所定の割合で使用し、
実施例1と同様にして食用油脂含有カプセルを得
た。 各カプセルの色調は実施例2(乳白色)、実施例
3(褐色)、実施例4(黄色)、実施例5(淡黄色)、
実施例6(乳白色)であつた。
[Table] * Scorching Example 1 Water 3 was placed in a boiling pot and brought to a boil. Add to this 11 kg of purified granulated sugar and starch hydrolyzate ("Pinedex #1 (DE7-8)", manufactured by Matsutani Chemical Industry Co., Ltd.)
Add 9 kg and heat to dissolve, further increasing the internal temperature to 117 ~
It was boiled down until it reached 120℃. On the other hand, heat and dissolve 1 kg of purified head, add 40 g of soybean lecithin, and vitamin E ("Emix").
80 (manufactured by Eisai Co., Ltd.) and 20 g of Butter Flavor (manufactured by Takasago International Corporation) were added and stirred and mixed to dissolve, thereby preparing a liquid edible fat. Stop heating the carbohydrate mixture and stir at high speed (approx.
2000 rpm), liquid edible oil and fat were gradually added. After the addition was completed, stirring was continued for about 1 to 2 minutes to sufficiently disperse and emulsify. This emulsion was transferred to a heated extruder. In addition, about 50 g of isopropanol is placed in a cooling tank equipped with a crushing stirrer and cooled to about -10°C.
While cooling and stirring the isopropanol, the emulsion was extruded through a hole having an extrusion diameter of 0.7 mm in an extruder at a pressure of about 2 kg/cm 2 G. The liquid temperature after extrusion was about 2°C. Next, the edible oil-containing capsules obtained by separating alcohol using a centrifuge are pre-mixed with α-lactose.
600 g of the product was placed in a vacuum rotary dryer and dried at a heating temperature of 30 to 35°C and a vacuum of 20 to 30 Torr for about 5 hours to obtain 18.8 kg of product. This capsule is a milky white, almost odorless, fine granular substance with a
The weight of 60 pieces was 13.2 kg. Examples 2 to 6 Each component shown in Table 3 was used in a predetermined ratio,
Edible oil-containing capsules were obtained in the same manner as in Example 1. The color tone of each capsule is Example 2 (milky white), Example 3 (brown), Example 4 (yellow), Example 5 (light yellow),
Example 6 (milky white).

【表】 使用例 1 コンソメスープ粉末 食 塩 70g 砂 糖 16 リンゴ酸 0.3 オニオン末 1 セロリ末 0.2 ガーリツク末 0.2 ホワイトペツパー末 0.4 粉末正油 1.2 実施例1の製品 10.7 上記処方の粉末スープ3gを湯100mlに添加し
たところ、速やかに溶解し、濁りも生じなかつ
た。 使用例 2 粉末ビーフスープ 食 塩 42.7g グルタミン酸ソーダ 10 キヤロツト末 1.5 オニオン末 2.6 ガーリツク末 0.3 ホワイトペツパー末 0.5 セージ末 0.03 タイム末 0.03 実施例2の製品 12.34 上記処方の粉末スープ2.5gを湯100mlに添加し
たところ、速やかに溶解し、濁りも生じなかつ
た。 使用例 3 粉末中華スープ ビーフエキスパウダー 3.5g ゼラチン 0.2 食 塩 19.0 ホワイトペツパー末 0.5 オニオン末 1.0 キヤロツト末 0.3 ガーリツク末 0.2 グルタミン酸ソーダ 2.8 実施例3の製品 12.5 上記処方の粉末スープ4.0gを湯100mlに添加し
たところ、速やかに溶解し、濁りも生ぜず、適度
の油が浮いた。 使用例 4 ケーキミツクス 小麦粉 100重量部 粉 糖 40 脱脂粉乳 10 ベーキングパウダー 3 実施例6の製品 5 食 塩 0.2 上記処方にしたがい各成分を混合してケーキミ
ツクスを作つた。これを約同量の水でといてフラ
イパンにて焼きあげ、チーズ風味のホツトケーキ
を得た。
[Table] Usage example 1 Consomme soup powder Salt 70g Sugar 16 Malic acid 0.3 Onion powder 1 Celery powder 0.2 Garlic powder 0.2 White pepper powder 0.4 Powdered soybean oil 1.2 Product of Example 1 10.7 Add 3g of powdered soup of the above formulation to hot water When added to 100 ml, it dissolved quickly and did not become cloudy. Usage example 2 Powdered beef soup Salt 42.7g Sodium glutamate 10 Carrot powder 1.5 Onion powder 2.6 Garlic powder 0.3 White pepper powder 0.5 Sage powder 0.03 Thyme powder 0.03 Product of Example 2 12.34 Add 2.5g of powdered soup of the above recipe to 100ml of hot water. When added, it quickly dissolved and did not become cloudy. Usage example 3 Powdered Chinese soup beef extract powder 3.5g Gelatin 0.2 Salt 19.0 White pepper powder 0.5 Onion powder 1.0 Carrot powder 0.3 Garlic powder 0.2 Sodium glutamate 2.8 Product of Example 3 12.5 Add 4.0g of powdered soup of the above formulation to 100ml of hot water As a result, it dissolved quickly, did not become cloudy, and a moderate amount of oil floated on top. Usage Example 4 Cake Mix Flour 100 parts by weight Powder Sugar 40 Skimmed Milk Powder 10 Baking Powder 3 Product of Example 6 5 Salt 0.2 Cake mix was prepared by mixing each component according to the above recipe. This was mixed with about the same amount of water and baked in a frying pan to obtain a cheese-flavored hot cake.

Claims (1)

【特許請求の範囲】 1 食用油脂を、DEが5〜12である澱粉加水分
解物と蔗糖の重量混合比が40:60〜55:45の糖質
混合物にてカプセル化することを特徴とする食用
油脂含有カプセルの製造法。 2 糖質混合物に対する食用油脂の配合量が0.2
〜20重量%である特許請求の範囲第1項記載の製
造法。
[Claims] 1. Edible fats and oils are encapsulated in a carbohydrate mixture of starch hydrolyzate with a DE of 5 to 12 and sucrose in a weight mixing ratio of 40:60 to 55:45. Method for producing edible oil-containing capsules. 2 The amount of edible oil and fat added to the carbohydrate mixture is 0.2
20% by weight of the manufacturing method according to claim 1.
JP59130849A 1984-06-27 1984-06-27 Production of capsule containing edible fat or oil Granted JPS6112248A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59130849A JPS6112248A (en) 1984-06-27 1984-06-27 Production of capsule containing edible fat or oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59130849A JPS6112248A (en) 1984-06-27 1984-06-27 Production of capsule containing edible fat or oil

Publications (2)

Publication Number Publication Date
JPS6112248A JPS6112248A (en) 1986-01-20
JPS6324652B2 true JPS6324652B2 (en) 1988-05-21

Family

ID=15044126

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59130849A Granted JPS6112248A (en) 1984-06-27 1984-06-27 Production of capsule containing edible fat or oil

Country Status (1)

Country Link
JP (1) JPS6112248A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016049105A (en) * 2014-08-29 2016-04-11 花王株式会社 Method for producing solid dispersion containing difficult-to-dissolve polyphenol

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5011532A (en) * 1988-03-18 1991-04-30 Fuisz Pharmaceutical Ltd. Dispersed systems and method of manufacture
US5709895A (en) * 1994-05-31 1998-01-20 Takasago International Corporation Usa Process for producing flavor-containing capsule
JP2007254339A (en) 2006-03-22 2007-10-04 Takasago Internatl Corp Lock-in type powder
CN113768005B (en) * 2021-09-13 2022-12-20 吉林大学 Macadamia nut tea and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016049105A (en) * 2014-08-29 2016-04-11 花王株式会社 Method for producing solid dispersion containing difficult-to-dissolve polyphenol
US10894058B2 (en) 2014-08-29 2021-01-19 Kao Corporation Method for producing solid dispersion containing hardly soluble polyphenol

Also Published As

Publication number Publication date
JPS6112248A (en) 1986-01-20

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