JPS5936540A - Production of microcapsule - Google Patents

Production of microcapsule

Info

Publication number
JPS5936540A
JPS5936540A JP57145652A JP14565282A JPS5936540A JP S5936540 A JPS5936540 A JP S5936540A JP 57145652 A JP57145652 A JP 57145652A JP 14565282 A JP14565282 A JP 14565282A JP S5936540 A JPS5936540 A JP S5936540A
Authority
JP
Japan
Prior art keywords
powder
capsules
capsule
hardening
oil
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.)
Pending
Application number
JP57145652A
Other languages
Japanese (ja)
Inventor
Yoshimi Nagano
永野 由巳
Akira Okada
章 岡田
Koroku Tachibana
橘 孝六
Reiko Ueda
上田 玲子
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.)
Ajinomoto Co Inc
Original Assignee
Ajinomoto Co Inc
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 Ajinomoto Co Inc filed Critical Ajinomoto Co Inc
Priority to JP57145652A priority Critical patent/JPS5936540A/en
Publication of JPS5936540A publication Critical patent/JPS5936540A/en
Pending legal-status Critical Current

Links

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
    • B01J13/20After-treatment of capsule walls, e.g. hardening
    • B01J13/22Coating

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Dispersion Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Manufacturing Of Micro-Capsules (AREA)
  • Grain Derivatives (AREA)
  • General Preparation And Processing Of Foods (AREA)
  • Jellies, Jams, And Syrups (AREA)
  • Medicinal Preparation (AREA)

Abstract

PURPOSE:To make a titled capsule easily soluble in hot water by coating powder on the microcapsules produced by a coacervation method without hardening the same or without hardening thoroughly the same and drying the coated capsules. CONSTITUTION:Powder such as wheat flour is coated as a coating agent for preventing sticking on the microcapsules produced by a coacervation method at the amt. corresponding to 10-250% of the weight of the capsules without hardening the capsules or without hardening thoroughly the same, whereafter the capsules are dried. The powder for peventing sticking to be used is one kind among starch, solid powdered fats, celluloses, protein powder, inorg. salt powder, powder of org. acids and the salts thereof, powder of amino acids and the salts thereof, cane sugar, etc. or their combinations as powder for food. The microcapsules produced by the coacervation method which are heretofore not used so much in food are made easily soluble in water or hot water and are produced inexpensively.

Description

【発明の詳細な説明】 本発明はコアセルベーション法によりゼラチン皮膜のカ
プセルをつくる際に、生成したカプセルを水溶液中より
取出し、当該カプセルを粉末でコーティングし、カプセ
ル同志が直接何着しない状態にしてから所定の水分まで
乾燥させることにより温水で溶解するマイクロカプセル
を製造する方法に関する。
DETAILED DESCRIPTION OF THE INVENTION When producing gelatin-coated capsules by the coacervation method, the present invention takes out the produced capsules from an aqueous solution, coats the capsules with powder, and prevents the capsules from directly adhering to each other. The present invention relates to a method for producing microcapsules that dissolve in hot water by drying the microcapsules to a predetermined moisture content.

従来、コアセルベーション法により製造されたマイクロ
カプセルは水溶液より取出すと、表面の皮膜が不安定で
、そのままでは実用化出来ない。そこで、通常はコアセ
ルベーションで生成したマイクロカプセルに硬化剤例え
ばホルムアルデヒド等のアルデヒド類を作用させてゼラ
チン皮膜を不溶化させてマイクロカプセルを安定化し、
更に乾燥し製品とする方法がとられている。
Conventionally, microcapsules produced by the coacervation method have an unstable surface film when taken out of an aqueous solution, and cannot be put to practical use as is. Therefore, usually a hardening agent such as an aldehyde such as formaldehyde is applied to the microcapsules produced by coacervation to insolubilize the gelatin film and stabilize the microcapsules.
A method of further drying the product is used.

この様にしてつくられたマイクロカプセルは温水に対し
ても不溶でかつ、特に食品では使うことの出来ないアル
デヒド等を使うため、食品用としてはコアセルベーンコ
ン法によるマイクロカプセルは殆んど実用化されていな
いのが実情である。
Microcapsules made in this way are insoluble even in hot water, and use aldehydes that cannot be used in food products, so microcapsules made by the core cell vanecon method are rarely used in food products. The reality is that it has not been standardized.

もし、カプセルが常温の空気中で安定てかつ水中で皮膜
が溶解するようになれば食品への利用も可能で、広い用
途が望める。例えば調理時に添加する、8或いは粉末飲
料やインスタントラーメン等に添加し水或いは湯をそそ
ぐと溶解して内容物が出てくる等の用途がある。また、
口腔や胃の中で溶解可能なものとすれば、医療用途等に
適用できるし、更に他の分野の利用も可能となる。現在
この様な機能を持ったカプセルは例えば、いわゆるソフ
トカプセルと言うゼラチン皮膜をつくって硬化処理行わ
ずに次いてその内容物を入れるカプセルがある。しかし
、これは皮膜をつくってから内容物を入れていく方法で
あるので粒径が大きく(通常数瓢φ以上)生産性があま
り良くなく、高価である。
If the capsules were to be stable in air at room temperature and the film could be dissolved in water, they could be used in foods, and a wide range of applications could be expected. For example, it can be added during cooking, or it can be added to powdered drinks, instant noodles, etc., and when water or hot water is poured over it, it dissolves and the contents come out. Also,
If it can be dissolved in the oral cavity or stomach, it can be applied to medical applications, and can also be used in other fields. Currently, capsules with such functions include so-called soft capsules, which are made with a gelatin coating and the contents are then put into the capsule without hardening. However, since this method involves forming a film and then adding the contents, the particle size is large (usually several diameters or more), and productivity is not very good and it is expensive.

そのため、高価な医薬か特殊な健康食品等に用途が限定
される傾向にある。
Therefore, their use tends to be limited to expensive medicines or special health foods.

この様な事実にもとづき、本発明の目的は主として、従
来食品へあまり使われなかったコアセ)レヘ−ジョン法
によるマイクロ力プセルヲ水、又は温水中で容易にとけ
るようにし、かつ安価に製造する新規な方法を提供する
ことにある。
Based on these facts, the main purpose of the present invention is to develop a new micro-particle that can be easily dissolved in water or hot water and manufactured at low cost by the co-aeration method, which has not been used much in the past for food products. The goal is to provide a method.

本発明者らは、この様な目的を達成すべく種々研究の結
果、溶解性を持たすには硬化処理を行わずにマイクロカ
プセルの乾燥を効率よく行わせることがポイントである
と考え、コアセルベーンコン法によりつくったマイクロ
カプセルを硬化処理を行わずに又は不完全な硬化処理の
段階で、溶液より取り出してカプセルに粉末全付着させ
てお互に(−1着しない状態にすれば、カプセルの乾燥
を容易に必要なだけ行う事が可能であり、硬化処理して
いないので容易に溶解するマイクロカプセルが得られる
ことを見出し、本発明を完成した。以下に本発明を詳し
く述べる。
As a result of various studies to achieve this purpose, the present inventors believe that the key to achieving solubility is to efficiently dry the microcapsules without performing a curing process. If the microcapsules made by the vane-con method are taken out of the solution without curing treatment or during incomplete curing treatment, and the powder is completely attached to the capsules so that they do not stick to each other (-1), the capsules The present invention was completed based on the discovery that microcapsules can be easily dried as much as necessary, and that microcapsules that dissolve easily because they are not subjected to hardening treatment can be obtained.The present invention will be described in detail below.

すなわち、本発明は先ずゼラチン−アラビアガム或いは
アルギン酸ソーダ、カラギナン等の系ニヨルコアセルペ
ーション法により食用油、フレーバー油、油溶性ビタミ
ン含有油等のカプセル化物質のマイクロカプセルをつく
る。次に、このカプセルをそのまま、又はカプセルが取
扱イニくイ場合は一旦エタノール、タンニン酸、カリミ
ョウバン等の食品に使用可能な硬化剤を使用してカプセ
ル皮膜の不完全な硬化処理を行った後、溶液中より取出
して、澱粉等の付着防止用の粉末を付着させ、カプセル
同志がお互に何着しない状態にしてから品温40℃以下
になるようにして乾燥する。乾燥后、篩分を行い、余分
な付着していない粉末を除去して製品とするものである
That is, in the present invention, first, microcapsules of encapsulated substances such as edible oils, flavor oils, oils containing oil-soluble vitamins, etc. are made by a coacerpation method based on gelatin-gum arabic, sodium alginate, carrageenan, etc. Next, either use the capsule as it is, or if the capsule is not suitable for handling, after partially curing the capsule film using a food-grade curing agent such as ethanol, tannic acid, or potassium alum. The capsules are taken out of the solution, coated with powder to prevent adhesion such as starch, and dried to a temperature of 40° C. or less after ensuring that the capsules do not stick to each other. After drying, it is sieved to remove excess powder that has not adhered to the product.

使用する付着防止用粉末はカプセルの表面に付着し、カ
プセル同志が付着しないようにすることが出来るもので
あればよいが、食品用の粉末としては、大豆蛋白、ゼラ
チン、カゼイン等の蛋白類、食塩等の無機塩類、アミノ
酸及びその塩類、酒石酸、クエン酸等の有機酸及びその
塩類、穀粉、澱粉その他の多糖類、結晶セルロース等の
セルロース類、水添植物脂等の固型脂等の粉−5− 末が使用可能である。
The adhesion prevention powder to be used may be any powder that can adhere to the surface of the capsules and prevent the capsules from adhering to each other, but food-grade powders include proteins such as soybean protein, gelatin, casein, etc. Powders such as inorganic salts such as table salt, amino acids and their salts, organic acids such as tartaric acid and citric acid and their salts, grain flour, starch and other polysaccharides, celluloses such as crystalline cellulose, and solid fats such as hydrogenated vegetable fats. -5- end can be used.

特に、水に溶は難い物質、例えば固型脂粉末、セルロー
ス粉末、小麦粉などはカプセル同志の付着防止効果が大
で、他の粉末に比して、添加量が少なくて乾燥が可能で
ある。使用する粉末は付着防止効果と同時に用途によっ
て使い分ける方が望ましい。特にカプセルか゛−使用さ
れる系に添加されている物質を利用することが一番好ま
しい。例えば油脂を使う系では粉末固型脂を使用する等
が考えられる。
In particular, substances that are difficult to dissolve in water, such as solid fat powder, cellulose powder, and wheat flour, have a great effect of preventing capsules from adhering to each other, and can be dried with a small amount added compared to other powders. It is preferable to use different powders depending on the purpose and the adhesion prevention effect. In particular, it is most preferable to use substances added to the system used in capsules. For example, in systems that use fats and oils, it is conceivable to use powdered solid fats.

付着粉末量は使用する粉末の種類、カプセルの大きさに
よって異るがカプセル重量の好ましくは10〜250%
更に望ましくは20〜50%が良い。
The amount of adhering powder varies depending on the type of powder used and the size of the capsule, but is preferably 10 to 250% of the capsule weight.
More preferably, it is 20 to 50%.

カプセルを溶液より取出し粉末をイ」着させる方法には
特に限定された方法はないが、例えばカプセルの水を切
り攪拌している粉末中に少量づつ滴下して粉末を付着さ
せていく方法、或いは逆に水切りしたカプセルに粉末を
まぶして混合していく方法があるが、前者の方がやり易
い。
There is no particular method for removing the capsule from the solution and depositing the powder on it, but for example, there is a method in which the water in the capsule is drained and the powder is dropped little by little into the powder that is being stirred, or On the other hand, there is a method of sprinkling powder on drained capsules and mixing them, but the former method is easier.

=  6 − この際、カプセルは軟かいのてつぶさない様に取扱いに
は十分注意する必要がある。この取扱いを容易にするた
め、食品に使える硬化剤例えばタンニン酸、カリ明ばん
、エタノール等の溶液中に浸して半硬化の状態にしてカ
プセルの強度を増してから水切りして粉末と混合すれば
、硬化工程が増えるが取扱い易く又乾燥もし易くなる。
= 6 - At this time, the capsules are soft and must be handled with great care so as not to crush them. To facilitate this handling, the capsules are strengthened by soaking them in a solution of a food-grade hardening agent, such as tannic acid, potassium alum, or ethanol, to a semi-hardened state, and then draining and mixing with the powder. Although the curing process is increased, it is easier to handle and dry.

食用以外の用途では、例えば上述のアルデヒド等の溶液
中に浸漬し、表面が少し硬化した状態のものを粉末と混
合することも可能である。
For uses other than food, for example, it is possible to immerse it in a solution of the above-mentioned aldehyde, etc., and mix it with a powder in a state where the surface is slightly hardened.

なお半硬化であるので温水溶解性はそのまま保持される
Note that since it is semi-cured, its solubility in hot water is maintained as it is.

粉末でコーティングされたカプセルの乾燥は品温が高温
となってカプセルを溶解しないよウニ出来るだけ低温で
好ましくは品温40℃以下になるように乾燥できればど
の様な方法でもよい。
Any method may be used for drying the powder-coated capsules as long as it can be dried at a temperature as low as possible, preferably below 40°C, so that the capsules do not dissolve due to high temperatures.

例えば脱湿空気による冷風乾燥、温風乾燥、真空乾燥等
がよい。乾燥品の水分は5%以下が好ましい。
For example, cold air drying using dehumidified air, hot air drying, vacuum drying, etc. are preferable. The moisture content of the dried product is preferably 5% or less.

水分が高すぎると保存中にカプセルが溶解し内容物が出
ることがあるので乾燥は十分行う必要がある。
If the moisture content is too high, the capsules may dissolve during storage and the contents may come out, so they must be thoroughly dried.

マタ、複合コアセルベーションをつ<6場合、多くはゼ
ラチン−アラビアガム系を使用スるが本発明ではアラビ
アガムの代りにアルギン酸ナトリウム、カラギナン、カ
ルボキシメチルセルロース、寒天、ポリビニルベンゼン
スルホン酸等を使つコアセルベーション法によるカルブ
セルにも適用可能である。
When complex coacervation is <6, gelatin-gum arabic is often used, but in the present invention, sodium alginate, carrageenan, carboxymethyl cellulose, agar, polyvinylbenzenesulfonic acid, etc. are used instead of gum arabic. It is also applicable to carbucel by coacervation method.

次に本発明の実施例を示すが、本発明はこれに限定され
るものではない。
Next, examples of the present invention will be shown, but the present invention is not limited thereto.

7を60℃に加熱混合し、その后酢酸を添加してpH=
4.1  に調整し冷却層レモンのフレーバーオイル+
oomlを攪拌しながら添加してオイルのカプセル化を
行った。カプセル化完了后、アラビアガム、酢酸、余剰
のゼラチンを違才して、直径500μ程度のオイルカプ
セルを得た。
7 was heated and mixed at 60°C, and then acetic acid was added to adjust the pH to
4. Adjust to 1 and add cooling layer lemon flavor oil +
The oil was encapsulated by adding ooml with stirring. After the encapsulation was completed, gum arabic, acetic acid, and excess gelatin were mixed to obtain oil capsules with a diameter of about 500 μm.

このカプセルは軟かく破壊し易いので水切りした後、澱
粉3007をビーカーにとり攪拌しながらカプセルを徐
々に滴下混合し、カプセルの周囲に澱粉をコーティング
した。コーティング后30℃の除湿空気による通風乾燥
で約12時間乾燥を行い、次いで篩分けを行い余分の粉
末全除去し約1502のレモンフレーバーオイルカプセ
ルを得た。このカプセルを70℃の温水に添加したとこ
ろ約3秒で溶解し、レモンフレーバーのする温水が得ら
れた。
Since the capsules are soft and easy to break, after draining the water, starch 3007 was placed in a beaker and the capsules were gradually mixed dropwise with stirring to coat the capsules with starch. After coating, it was dried by ventilation drying with dehumidified air at 30° C. for about 12 hours, and then sieved to remove all excess powder to obtain about 1502 lemon flavor oil capsules. When this capsule was added to hot water at 70°C, it dissolved in about 3 seconds, giving hot water with a lemon flavor.

実施例2 実施例1のカプセル調製においてレモンフレーバーオイ
ルの代りに大豆油を使用して大豆油カプセルをつくった
。このカプセルを水切りした后にライスワックス粉末+
504i’の中にゆっくり攪拌しながら徐々に滴下混合
した。カプセル表面にワックス粉末が付着し、カプセル
同志が付着しない状態になってから、30℃の脱湿 9
− 空気で32時間乾燥を行い、水分5%に下げた。
Example 2 Soybean oil capsules were made by substituting soybean oil for the lemon flavor oil in the capsule preparation of Example 1. After draining this capsule, add rice wax powder +
504i' while stirring slowly. After the wax powder adheres to the capsule surface and the capsules do not adhere to each other, dehumidify at 30℃ 9
- Dry with air for 32 hours to reduce moisture content to 5%.

最后に20メツツユの篩で余分のワックス粉末を除去し
約1307のオイルカプセルが得られた。
Finally, excess wax powder was removed using a 20-mesh sieve to obtain about 1307 oil capsules.

このオイルカプセルと調味料及びパン粉を混合し、生の
トリ肉にこの混合調味料をまぶしてオーブントースタ−
180℃、7分間加熱を行うとオイルカプセルが溶解し
てオイルが出て、揚げたてのチキンフライ様のものが得
られた。
Mix this oil capsule with seasonings and bread crumbs, sprinkle this mixed seasoning on raw chicken meat, and put it in the oven toaster.
When heated at 180° C. for 7 minutes, the oil capsules dissolved and oil came out, yielding something resembling freshly fried chicken.

実施例3 実施例1て得られたオイルカプセルを水切りした后、老
化澱粉粉末1507中に徐々に滴下しながらゆっくり攪
拌し、カプセル表面に老化澱粉−粉末を付着させ、実施
例2と同様に乾燥篩分な行い1357のカプセルを得た
。このカプセルは70℃の温水で3秒で溶解した。
Example 3 After draining the oil capsule obtained in Example 1, it was slowly stirred while gradually dropping into aged starch powder 1507 to adhere the aged starch powder to the capsule surface, and dried in the same manner as in Example 2. After sieving, 1357 capsules were obtained. This capsule was dissolved in 70°C hot water in 3 seconds.

−10− 実施例4 実施列1で得られたオイルカプセルを一旦水切りした后
に、5%のタンニン酸溶液booml中に分散させ15
分間放置し表面の硬化を少し行った。これをとりあげ水
洗を1回行い、2002の粉末グルタミン酸ソーダ中に
滴下しながらゆっくり攪拌しカプセル表向にグルタミン
酸ソーダ粉末を付着させ、次いで冷風(30℃脱湿空気
)にて通風乾燥を行い、余剰の粉末を除去して1507
のオイルカプセルが得られた。
-10- Example 4 After draining the oil capsules obtained in Example 1, they were dispersed in 5% tannic acid solution booml.
The surface was allowed to harden a little by leaving it for a minute. Take this, wash it once with water, drop it into 2002 powdered sodium glutamate while stirring slowly to adhere the sodium glutamate powder to the surface of the capsule, and then dry it with cold air (30℃ dehumidified air) to remove excess 1507 by removing the powder of
oil capsules were obtained.

このカプセルを塩、コシヨー、パン粉と混合しトリ肉に
まぶしオーブント−スターで180℃5分間加熱したと
ころカプセルがブレーク゛レオイルが出てチキンフライ
様のものを得た。
When this capsule was mixed with salt, koshiyo, and bread crumbs and sprinkled on chicken meat and heated in an oven toaster at 180°C for 5 minutes, the capsule broke down and oil came out, giving something similar to fried chicken.

実施例5 実施例Iで得たオイルカプセルを一旦水切りした后、9
5%エタノール中に浸漬し、15分間放置し、表面を半
硬化した。
Example 5 After draining the oil capsule obtained in Example I, 9
It was immersed in 5% ethanol and left for 15 minutes to semi-cure the surface.

これをとり出し、粉末大豆蛋白中に滴下しながらゆっく
り攪拌し、カプセル表面に大豆蛋白粉末を付着させ、次
いで通風乾燥(30℃脱湿空気)を行って余剰の粉末を
除去し、120Fのオイルカプセルを得た。
Take this out and slowly stir it while dropping it into powdered soybean protein to make the soybean protein powder adhere to the capsule surface, then perform ventilation drying (30℃ dehumidified air) to remove excess powder, and add it to the powdered soybean protein at 120F. Got the capsule.

このオイルカプセルを70℃温水に投入したところ、約
5秒で溶解した。
When this oil capsule was put into 70°C warm water, it dissolved in about 5 seconds.

実施例6 実施例1のカプセル調製において、レモンフレーバーオ
イル中に油溶性ビタミンを溶解したものを用いて大豆油
カプセルをつくり、このカプセルを水切りした后、アス
コルビン酸粉末、アスパルテーム粉末及びデキスh ’
Jン粉末を均一に混合したものをゆっくり攪拌している
中に徐々に滴下混合し、アスコルビン酸−アスパルテー
ム−デキストリン粉末がカプセル表面に何着し、カプセ
ル同志が付着しない状態になってから30℃の脱湿空気
で12時間乾燥を行い、水分を5%に低下した。
Example 6 In the capsule preparation of Example 1, soybean oil capsules were made using oil-soluble vitamins dissolved in lemon flavored oil, and after draining the capsules, ascorbic acid powder, aspartame powder and dex h'
A homogeneous mixture of J-N powder was gradually mixed dropwise while stirring slowly, and after the ascorbic acid-aspartame-dextrin powder had adhered to the capsule surface and the capsules did not adhere to each other, it was heated to 30°C. Drying was performed for 12 hours using dehumidified air to reduce the moisture content to 5%.

次いで、余分の粉末を除去した。Excess powder was then removed.

このオイルカプセルを37℃温水中に投入したところ約
1分間で溶解した。
When this oil capsule was put into 37°C warm water, it dissolved in about 1 minute.

特許出願人 味の素株式会社  13−Patent applicant: Ajinomoto Co., Inc. 13-

Claims (1)

【特許請求の範囲】 1 コアセルベーション法により製造したマイクロカプ
セルを硬化処理せずに又は硬化処理を完全には行わずに
、粉末をコーティングして乾燥することを特徴とする水
中溶解性マイクロカプセルの製造法。 2 付着防止用コーティング剤として、小麦粉、澱粉、
粉末固型脂、セルロース類、蛋白粉末、無機塩粉末、有
機酸及びその塩の粉末、アミノ酸及びその塩の粉末、蔗
糖粉末の内から1種又は組合せて使用することを特徴と
する特許請求の範囲第1項記載のマイクロカプセルの製
造法。 3 コーティング粉末の量がカプセル重量の10〜25
096であることを特徴とする特許請求の範囲第1項記
載のマイクロカプセルの製造法。
[Claims] 1. Water-soluble microcapsules produced by a coacervation method, which are coated with powder and dried without being subjected to hardening treatment or without being completely hardened. manufacturing method. 2. As a coating agent for preventing adhesion, wheat flour, starch,
A patent claim characterized in that one or a combination of powdered solid fat, celluloses, protein powder, inorganic salt powder, organic acid and its salt powder, amino acid and its salt powder, and sucrose powder is used. A method for producing microcapsules according to scope 1. 3. The amount of coating powder is 10-25% of the capsule weight.
096, the method for producing microcapsules according to claim 1.
JP57145652A 1982-08-23 1982-08-23 Production of microcapsule Pending JPS5936540A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57145652A JPS5936540A (en) 1982-08-23 1982-08-23 Production of microcapsule

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57145652A JPS5936540A (en) 1982-08-23 1982-08-23 Production of microcapsule

Publications (1)

Publication Number Publication Date
JPS5936540A true JPS5936540A (en) 1984-02-28

Family

ID=15389959

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57145652A Pending JPS5936540A (en) 1982-08-23 1982-08-23 Production of microcapsule

Country Status (1)

Country Link
JP (1) JPS5936540A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6198148U (en) * 1984-11-30 1986-06-24
JPS63197540A (en) * 1986-12-18 1988-08-16 メロ・ルセロ・サチア Gelatin-polysaccharide micro-capsule and manufacture thereof
US5690990A (en) * 1994-03-04 1997-11-25 Arnhem, Inc. Process for encapsulating the flavor with colloid gel matrix
US5759599A (en) * 1992-03-30 1998-06-02 Givaudan Roure Flavors Corporation Method of flavoring and mechanically processing foods with polymer encapsulated flavor oils
JPH11196779A (en) * 1998-01-07 1999-07-27 Nonogawa Shoji Kk Granular composition for food
JP2002326030A (en) * 2001-05-02 2002-11-12 Ogawa & Co Ltd Method for preventing crosslinking of coating film of noncrosslinked gelatin capsule
KR100495027B1 (en) * 1997-05-06 2005-09-16 주식회사 엘지생활건강 Powder detergent composition with microencapsulated fragrance
CN111918714A (en) * 2018-06-21 2020-11-10 弗门尼舍有限公司 Method for preparing microcapsules

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6198148U (en) * 1984-11-30 1986-06-24
JPH0242844Y2 (en) * 1984-11-30 1990-11-15
JPS63197540A (en) * 1986-12-18 1988-08-16 メロ・ルセロ・サチア Gelatin-polysaccharide micro-capsule and manufacture thereof
US5759599A (en) * 1992-03-30 1998-06-02 Givaudan Roure Flavors Corporation Method of flavoring and mechanically processing foods with polymer encapsulated flavor oils
US5690990A (en) * 1994-03-04 1997-11-25 Arnhem, Inc. Process for encapsulating the flavor with colloid gel matrix
KR100495027B1 (en) * 1997-05-06 2005-09-16 주식회사 엘지생활건강 Powder detergent composition with microencapsulated fragrance
JPH11196779A (en) * 1998-01-07 1999-07-27 Nonogawa Shoji Kk Granular composition for food
JP2002326030A (en) * 2001-05-02 2002-11-12 Ogawa & Co Ltd Method for preventing crosslinking of coating film of noncrosslinked gelatin capsule
CN111918714A (en) * 2018-06-21 2020-11-10 弗门尼舍有限公司 Method for preparing microcapsules
CN111918714B (en) * 2018-06-21 2023-08-11 弗门尼舍有限公司 Method for preparing microcapsules

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