JPS6012941A - Preparation of soft capsule - Google Patents

Preparation of soft capsule

Info

Publication number
JPS6012941A
JPS6012941A JP58121970A JP12197083A JPS6012941A JP S6012941 A JPS6012941 A JP S6012941A JP 58121970 A JP58121970 A JP 58121970A JP 12197083 A JP12197083 A JP 12197083A JP S6012941 A JPS6012941 A JP S6012941A
Authority
JP
Japan
Prior art keywords
capsule
water
filler
capsules
soft
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
JP58121970A
Other languages
Japanese (ja)
Inventor
Koroku Tachibana
橘 孝六
Yoshimi Nagano
永野 由巳
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 JP58121970A priority Critical patent/JPS6012941A/en
Publication of JPS6012941A publication Critical patent/JPS6012941A/en
Pending legal-status Critical Current

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  • Jellies, Jams, And Syrups (AREA)
  • Medical Preparation Storing Or Oral Administration Devices (AREA)

Abstract

PURPOSE:To prevent dissolution of a base of capsule caused by water, and to enable preparation of a soft capsule, by blending a capsule filler with sugaralcohol, sodium lactate, L-proline, etc. without using an oily component. CONSTITUTION:In preparing a solt capsule, a capsule filler is blended with (1) >=150wt% one more more selected from sugaralcohol, sodium lactate, and sodium pyrrolidonecarboxylate based on water contained in the filler and/or (2) >=100wt% L-lysine and/or L-proline based on water contained in the filler. Consequently, dissolution of capsule base caused by water can be prevented without using an oily component, and a stable soft capsule can be prepared. As the result, in the case of a food, uses full of varieties such as capsuled seasoning, dessert, drink, etc. can be expected.

Description

【発明の詳細な説明】 本発明は、軟カプセルの製造法に関し、更に詳しクハ、
糖アルコール、乳酸ナトリウム、ビロリドンカルン1?
ン酸ナトリウム(PCA−Na )、L−リジン又はL
−ゾロリン、をカプセル充填剤中に配合することにより
、油性成分を併用しなくても、水分によるカプセル基剤
(ゼラチン被膜)の溶解が防止されて安定な軟カプセル
の製造法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing soft capsules, and more particularly,
Sugar alcohol, sodium lactate, virolidone carne 1?
Sodium phosphate (PCA-Na), L-lysine or L
The present invention relates to a method for producing stable soft capsules by incorporating Zoroline into a capsule filler, thereby preventing dissolution of the capsule base (gelatin coating) by moisture without using an oily component in combination.

医薬1食品等において通常使用されるカプセルには2つ
の形態、即ち、硬質カプセルと軟質カプセルがある。こ
の内軟質のいわゆる軟カプセルは、一般にゼラチン等の
水溶性の皮膜物質をグリセリン等で可塑化して形成した
カブセルシートにょシ非水性の物質を被覆成型して製造
している。
There are two forms of capsules commonly used in pharmaceutical products, foods, etc.: hard capsules and soft capsules. Among these, soft capsules are generally produced by coating a non-aqueous substance on a capsule sheet formed by plasticizing a water-soluble film material such as gelatin with glycerin or the like.

カプセル基剤は、元来水溶性であるために、充填剤が水
性溶液乃至は懸濁液の形態である場合は、軟カプセルを
形成することは困難であった。
Since the capsule base is originally water-soluble, it has been difficult to form soft capsules when the filler is in the form of an aqueous solution or suspension.

−万、充填剤として使用される物質は必ずしも粉末状等
の非水性の形態で得られる訳ではなく、粉末化によシ品
質が劣化したり、エネルギーコスト的にも不利な場合が
多いのみならず粉末を油性成分に溶解乃至は懸濁化させ
る際の操作上のトラブルも予想される。具体的には、フ
レーバー物質を充填剤に使用する場合、乾燥粉末化工程
でフレーバーの飛散乃至は変質を生じ、乾燥エネルギー
も必要であシ、工程管理も複雑になる。
- However, substances used as fillers are not necessarily obtained in non-aqueous forms such as powders, and powdering often results in poor quality and is disadvantageous in terms of energy costs. Operational troubles are also expected when dissolving or suspending the powder in an oily component. Specifically, when a flavor substance is used as a filler, the flavor may scatter or change in quality during the drying and powdering process, drying energy is required, and process control becomes complicated.

水性成分をそのまま、即ち液状でカプセル充填剤とすれ
ばこのような問題点が克服できるため、従来、油中水型
エマルジョン化して、ゼラチン被膜と水性カプセル充填
剤とが直接に接触するととを防止する等の方法で軟カプ
セル化を実現したシ、或いはゼラチン被膜自体を強化す
る等他方法も試みられている。
These problems can be overcome by using the aqueous component as it is, that is, in liquid form, as a capsule filler. Conventionally, water-in-oil emulsions are used to prevent direct contact between the gelatin coating and the aqueous capsule filler. Other methods have also been attempted, such as achieving soft encapsulation using methods such as oxidation, or strengthening the gelatin coating itself.

しかしながら、上記従来法では、油脂等の加配が必須で
あるため、油脂の使用が好捷しくない場合には不都合で
その適用には制約があり、ゼラチン被膜の強化では、食
品で使用できない硬化剤を使用したり、或い(・よ、被
膜が強固になシすぎて、使用、飲用時に逆に溶は即く、
利用しにくい等の問題が生じる。
However, in the above conventional method, since it is essential to add fats and oils, it is inconvenient and its application is limited when the use of fats and oils is not suitable. Or (・yo, the coating is too strong and it dissolves quickly when using or drinking.
Problems such as difficulty in use arise.

従って、軟カプセルに訃いては、油脂等の非水性物質の
配合なしでは必ずしも満足できる品質のものを製造でき
るとはいえない実情にある。
Therefore, when it comes to soft capsules, it is not always possible to produce soft capsules of satisfactory quality without incorporating non-aqueous substances such as fats and oils.

本発明者らは上記現状に鑑み、油脂等を併用しなくても
安定に水性成分をカプセルに充填する方法を開発すべく
鋭意研究を重ねた結果、水性成分に糖アルコール類、乳
酸ソーダ、PCA−Na 、 L−リジン、L−プロリ
ンを単独又は組合せて添加することにより上記課題が解
決できるとの知見に至った。
In view of the above-mentioned current situation, the present inventors have conducted intensive research to develop a method for stably filling capsules with aqueous ingredients without using oils or fats, etc. As a result, we have found that sugar alcohols, sodium lactate, PCA, It has been found that the above problem can be solved by adding -Na, L-lysine, and L-proline alone or in combination.

本発明は、この知見に基づき完成されたものでアシ、即
ち、軟カプセルの製造に際して、−一一一1−−−■−
−カプセル充填剤として、(1)糖アルコール、乳酸ナ
トリウム及びPCA−Na O中から選ばれた1種以上
を充填剤に含まれる水分の150重量%以上含有せしめ
るか及び/又は(2) L −+Jレジンび/若しくは
L−プロリンを充填剤に含まれる水分の100重量%以
上含有せしめることを特徴トスる軟カプセルの製造方法
である。
The present invention was completed based on this knowledge, and in the production of reeds, that is, soft capsules.
- As a capsule filler, (1) one or more selected from sugar alcohol, sodium lactate, and PCA-NaO is contained at least 150% by weight of the water contained in the filler, and/or (2) L - This is a method for producing soft capsules characterized by containing +J resin/or L-proline in an amount of 100% by weight or more of the water contained in the filler.

以下、本発明を具体的に説明する。The present invention will be explained in detail below.

軟カプセル充填剤に使用する水性成分としては、水溶性
ビタミン、アミノ酸等の溶液、ビーフェキス、ボークエ
キス、チキンエキス、ボーンエキス、魚介類エキス等の
動物質エキス、野菜エキス、キノコエキス等の植物質エ
キスその他の各種エキス類、味噌、圧油、或いはスーブ
の素等のル4味料、コーヒークリーム等のクリーム類、
蜂蜜その他のシロップ類、ゼリー、プリン、即席ホット
チョコレート等のデザート類などが挙げられるが水性の
ものであれば特に種類を問わず使用可能であシ、また、
非水性の油脂等を含んでもよく、これらの中から1種類
又は2種類以上を組合せればよい〇尚、水性成分以外に
、油脂その他の非水性成分を併用する場合、従来法であ
れば油中水型エマルジョン化する必要があったが、本発
明方法では、必ずしも油中水型エマルジョン化する必要
はない。
Aqueous ingredients used in soft capsule fillers include solutions of water-soluble vitamins and amino acids, animal extracts such as Beefex, Bork extract, chicken extract, bone extract, and seafood extract, vegetable extracts, and vegetable extracts such as mushroom extract. Extracts and other various extracts, miso, pressure oil, seasonings such as soup stock, creams such as coffee cream,
Desserts such as honey and other syrups, jellies, puddings, and instant hot chocolate can be used, but any type can be used as long as they are water-based.
Non-aqueous fats and oils may also be included, and one or two or more of these may be used in combination.If oil or other non-aqueous components are used in addition to the aqueous component, conventional methods Although it was necessary to form a water-in-oil emulsion, in the method of the present invention, it is not necessarily necessary to form a water-in-oil emulsion.

従って工程が簡略化でき、乳化安定剤等の加配を省略す
ることが可能とガる。
Therefore, the process can be simplified and the addition of emulsion stabilizers and the like can be omitted.

本発明で使用出来る添加剤はソルビトール、キシリトー
ル、マンニトール、マルチトールナトの糖アルコール、
乳酸ナトリウム、PCA−Na 、 L−リジン、L−
プロリン等の非常に保湿性の高い物質である。これらの
添加剤は単独でも2種以上と組合せても使用出来る。添
加量はカブセル化する物質の種類、濃度及び添加剤の種
類によって異なるが、糖アルコール類、乳酸ナトリウム
、PCA −Naの場合には被カシセル化物質中の含水
量の150係以上、好ましくは200チ以上を、またL
−リジン、L−プロリンの場合は被カシセル化物質中の
含水量の100%以上、好ましくは150チ以上を添加
する。添加量がこれ以下になるとカプセルのゼラチン皮
膜が溶解してしまう。
Additives that can be used in the present invention include sugar alcohols such as sorbitol, xylitol, mannitol, maltitol,
Sodium lactate, PCA-Na, L-lysine, L-
It is a highly moisturizing substance such as proline. These additives can be used alone or in combination of two or more. The amount added varies depending on the type and concentration of the substance to be encapsulated and the type of additive, but in the case of sugar alcohols, sodium lactate, and PCA-Na, it is 150 times or more of the water content in the substance to be encapsulated, preferably 200 times the water content of the substance to be encapsulated. More than C, also L
- In the case of lysine and L-proline, 100% or more of the water content in the substance to be cassicated, preferably 150% or more, is added. If the amount added is less than this, the gelatin coating of the capsule will dissolve.

この様に保湿剤を添加することにより水性物質を軟カプ
セル化する事が出来る理由は明確でないが次の様に推定
される。即ち、内容物中の水分子が保湿剤によシ自山水
の状態からゆるい結合水の状態へ変化し、ゼラチン皮膜
中へ水が移動しにくくなる。
The reason why an aqueous substance can be soft encapsulated by adding a humectant in this way is not clear, but it is presumed to be as follows. That is, the water molecules in the contents change from the state of natural mountain water to the state of loosely bound water due to the humectant, making it difficult for water to move into the gelatin film.

そのため、内容物中に水分があってもゼラチン皮膜が溶
解しなくなるものと推定される。この水の結合している
度合については高分解能岡を使用して測定することが出
来るが、例えば固形分50%、食塩12チのビーフェキ
スとこれにソルビット50係を添加したものを比較する
とソルビットを加えたものの万が3〜4倍も水が拘束さ
れているということが判る。
Therefore, it is presumed that even if there is water in the contents, the gelatin film will not dissolve. The degree to which this water is bound can be measured using a high-resolution Oka, but for example, when comparing Beefex with a solid content of 50% and 12 parts of common salt to which 50 parts of sorbitol has been added, it is possible to measure the amount of sorbitol. It can be seen that 3 to 4 times more water is being restrained than what was added.

軟カプセルの基剤としては、ゼラチンにグリセリン、D
−ソルビトール等の可塑剤を混合したものを用いるが、
使用するゼラチンのゼリー強度や可塑剤の種類、組成比
等は、目的とするカプセルの大きさ、形状に応じて被膜
の厚さ等を設定し、カプセルの硬さ、融点等を考慮して
決定するようにする。具体例としては、(ゼリー強度1
50〜250プルームの)ゼラチンに、その20〜10
0チのグリセリン等の可塑剤を添加し、70〜80℃に
加熱溶解混合したものを製膜すればよい。
The base of soft capsules is gelatin, glycerin, D
- A mixture of plasticizers such as sorbitol is used, but
The jelly strength of the gelatin used, the type of plasticizer, the composition ratio, etc. are determined by setting the thickness of the coating according to the size and shape of the intended capsule, and taking into consideration the hardness, melting point, etc. of the capsule. I'll do what I do. As a specific example, (jelly strength 1
50-250 plumes) of gelatin, 20-10
A film may be formed by adding a plasticizer such as 0% glycerin, heating and melting the mixture at 70 to 80°C.

カプセルの形成は、常法に従って行えばよく、その条件
を特に限定されるものではなく、使用する装置等に応じ
、最適条件を適宜設定するようにする。具体的には、例
えば、ロータリ一式ソフトカプセル成型機(Lelne
r &Song社鯛)を用いる場合、第1図に示すよう
に1対の円筒型成型ダイロール1の両側から模状セグメ
ント2に密着して送シ込せれたゼラチン膜3が、ダイロ
ール1の回転により成型されながらポンフ04にょシカ
プセルの内容物が充填され、セグメント2にょシ冷却さ
れた(30〜35℃)ゼラチン膜がダイロール1により
押圧されて圧着し、カプセルが形成された後、空気乾燥
によシ、被膜水分を2oチ以下、好ましくは10%以下
捷で乾燥する。
Capsules may be formed according to a conventional method, and the conditions are not particularly limited, and the optimum conditions may be set as appropriate depending on the equipment used. Specifically, for example, a rotary set soft capsule molding machine (Lelne
When using the gelatin film 3, which is fed in close contact with the pattern segment 2 from both sides of a pair of cylindrical molding die rolls 1, as shown in FIG. While being molded, the contents of the Pomfu 04 capsule are filled, and the cooled (30-35°C) gelatin membrane of the segment 2 is pressed and crimped by the die roll 1, and after the capsule is formed, it is air-dried. The film is dried by sieving to reduce the moisture content to 20% or less, preferably 10% or less.

カプセルの形状は、球形、卵形2円柱形、その他所型の
形状を選択する。
The shape of the capsule is selected from spherical, oval, bicylindrical, and other shapes.

本発明方法による軟カプセルの典型的用途としては、医
薬、食品等が挙げられるが、医薬の場合粉末に比べて吸
収効率のよい軟カプセルの形態で、しかも水性の成分を
油脂等の混在なしに提供できるし、食品の場合において
も、フレーバーが良好で分散性、溶解性に優れた軟カプ
セルが油脂無添加でも製造できるため、カプセル化され
た調味料デザート、飲料等極めてバラエティに富んだ用
途が期待できる。
Typical uses of the soft capsules produced by the method of the present invention include pharmaceuticals, foods, etc. In the case of pharmaceuticals, the soft capsules have better absorption efficiency than powders, and water-based ingredients are not mixed with fats and oils. In the case of foods, soft capsules with good flavor and excellent dispersibility and solubility can be produced without the addition of fat or oil, so they can be used in a wide variety of applications such as encapsulated seasonings, desserts, and beverages. You can expect it.

次に実施例により本発明を更に説明する。Next, the present invention will be further explained with reference to Examples.

実施例1 ビーフェキス(水分40重量係)50重置部に対し、D
−ソルビトール50重量部、乳酸ナトリウム50重量部
、PCA−Na50重量部、L−リジン30重量部又は
L−プロリン30重量部を添加混合して、混合物をゼラ
チン及びグリセリンから成るゼラチン膜によシ、ローメ
リ一式ソフトカプセル成型機(Leiner & 5o
ns社製)を使用して25%(全重引:10.8g、内
容量10.9.被膜厚0.8%)の球形カプセルに成形
し、20℃乾燥空気で被膜水分10チ捷で乾燥して本発
明のビーフェキスカプセルを得た。
Example 1 D
- adding and mixing 50 parts by weight of sorbitol, 50 parts by weight of sodium lactate, 50 parts by weight of PCA-Na, 30 parts by weight of L-lysine or 30 parts by weight of L-proline, and applying the mixture to a gelatin membrane consisting of gelatin and glycerin; Loemer complete soft capsule molding machine (Leiner & 5o
(manufactured by NS) to form a spherical capsule of 25% (total weight: 10.8 g, content: 10.9, coating thickness 0.8%), and the coating was dried with dry air at 20°C to remove 10% of the coating moisture. After drying, the Beefex capsules of the present invention were obtained.

これらのビーフェキスカプセルを温度4071)湿度6
0チの恒温恒湿槽で120日間保存したところ、いずれ
のカプセルもゼラチン被膜の崩壊は生じなかった。また
これらのカプセルを80℃の温湯に投入したところ30
秒間で完全に溶解し、良質なビーフフレーバーを有する
調味液が得られた。
These Beefex Capsules have temperature 4071) humidity 6
When the capsules were stored for 120 days in a constant temperature and humidity chamber at 0°C, the gelatin coating did not disintegrate in any of the capsules. Also, when these capsules were put into hot water at 80℃, the temperature was 30℃.
A seasoning liquid was obtained which completely dissolved in seconds and had a good quality beef flavor.

実施例2 濃縮、1′−り、チキンエキス(水分50%)13.?
lc部濃縮醤油 17 食 塩 22 M5G 、 IMi)、こしょう 15ガーリック波−
スト 3.0 ラ − ド 1 コ゛ −渭1 4 乳酸ナトリウム 25 上記配合に従い、原料を均質乳化し、次いで、実施例1
の方法により、即席麺用のスープカプセルを調製し、実
施例1と同一の条件下で保存したところ、カプセルの崩
壊はみられず、熱湯に対する溶解性も良好であった。
Example 2 Concentrated, 1'-ri, chicken extract (50% water) 13. ?
lc part Concentrated soy sauce 17 Salt 22 M5G, IMi), Pepper 15 Garlic waves
St 3.0 Rad 1 Cod 1 4 Sodium lactate 25 According to the above formulation, the raw materials were homogeneously emulsified, and then Example 1
When soup capsules for instant noodles were prepared by the method described above and stored under the same conditions as in Example 1, the capsules did not disintegrate and had good solubility in hot water.

実施例3 コーヒー抽出液(水分60%) 45重量部D−マンニ
トール 55 〃 上記原料を混合し、実施例1の方法でカプセル化し、内
容物6gのコーヒーカプセルを調製した。
Example 3 Coffee extract (60% water) 45 parts by weight D-mannitol 55 The above raw materials were mixed and encapsulated by the method of Example 1 to prepare coffee capsules with a content of 6 g.

このカプセルを80℃の温湯100ccに投入したとこ
ろ、約30秒で完全に分散溶解し、良質なコーヒー7に
一バーを有するtA前のホットコーヒーが得られた。
When this capsule was poured into 100 cc of 80° C. hot water, it was completely dispersed and dissolved in about 30 seconds, yielding high-quality pre-tA hot coffee having a concentration of 7 to 1 bar.

実施例4 赤ワイン 1.5 CC ワインフレーバー 7グ D−マンニトール 25g 上記原料を混合し、実施例1の方次◇ンチン皮膜のカプ
セル化を即席デザートカプセルを4&。
Example 4 Red wine 1.5 CC Wine flavor 7g D-Mannitol 25g Mix the above raw materials and prepare instant dessert capsules according to the method of Example 1 ◇ Encapsulation of chintin film into instant dessert capsules.

このカプセル4個を温湯約8Qmlに溶解攪拌し、型に
入れて冷蔵庫で1時間冷却したところ、味。
I dissolved and stirred these 4 capsules in about 8Qml of warm water, put it in a mold, and cooled it in the refrigerator for 1 hour.

風味が良好で低カロリーのワインゼリーが得られた。A wine jelly with good flavor and low calories was obtained.

実施例5 75%D−マンニトール液を実施例1と同様の方法でカ
プセル化し、1個当やD−マンニトール500〜を含有
する甘味料カプセルを調製した。
Example 5 A 75% D-mannitol solution was encapsulated in the same manner as in Example 1 to prepare sweetener capsules containing 500 or more D-mannitol per capsule.

このカプセルをホットコーヒー80℃に溶解したところ
30秒間で完全に溶解し、従来にない簡便な形態の低カ
ロリー甘味料として満足できる品質であるとの評価が得
られた。
When this capsule was dissolved in hot coffee at 80°C, it completely dissolved in 30 seconds, and was evaluated as having satisfactory quality as a low-calorie sweetener in an unprecedented and simple form.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、本発明の軟カプセル製造工程の一例を示す模
式図である。 特許出願人 味の素株式会社
FIG. 1 is a schematic diagram showing an example of the soft capsule manufacturing process of the present invention. Patent applicant Ajinomoto Co., Inc.

Claims (1)

【特許請求の範囲】[Claims] 軟カプセルの製造に際し、カプセル充填剤中に、(1)
糖アルコール、乳酸ナトリウム及びピロリドンカルボン
酸ナトリウムの中から選ばれた1種以上を充填剤に含ま
れる水分の150重量重量上含有せしめるか及び/又は
(2)L−リジン及び/若しくはL−ゾロリンを充填剤
に含まれる水分のIOQ重景爪形上含有せしめることを
特徴とする軟カプセルの製造方法。
When producing soft capsules, (1) is added to the capsule filler.
One or more selected from sugar alcohol, sodium lactate, and sodium pyrrolidonecarboxylate is contained in an amount equal to 150% by weight of water contained in the filler, and/or (2) L-lysine and/or L-zoroline is contained. A method for producing a soft capsule, characterized in that water contained in a filler is contained in an IOQ layered shape.
JP58121970A 1983-07-05 1983-07-05 Preparation of soft capsule Pending JPS6012941A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58121970A JPS6012941A (en) 1983-07-05 1983-07-05 Preparation of soft capsule

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58121970A JPS6012941A (en) 1983-07-05 1983-07-05 Preparation of soft capsule

Publications (1)

Publication Number Publication Date
JPS6012941A true JPS6012941A (en) 1985-01-23

Family

ID=14824370

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58121970A Pending JPS6012941A (en) 1983-07-05 1983-07-05 Preparation of soft capsule

Country Status (1)

Country Link
JP (1) JPS6012941A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63164858A (en) * 1986-12-27 1988-07-08 Unie Koroido Kk Outer coat of soft capsule

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63164858A (en) * 1986-12-27 1988-07-08 Unie Koroido Kk Outer coat of soft capsule
JPH0457305B2 (en) * 1986-12-27 1992-09-11 Unie Colloid Kk

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