JPS5944096B2 - Method for producing gelatin capsules filled with hydrophilic substances - Google Patents

Method for producing gelatin capsules filled with hydrophilic substances

Info

Publication number
JPS5944096B2
JPS5944096B2 JP54166806A JP16680679A JPS5944096B2 JP S5944096 B2 JPS5944096 B2 JP S5944096B2 JP 54166806 A JP54166806 A JP 54166806A JP 16680679 A JP16680679 A JP 16680679A JP S5944096 B2 JPS5944096 B2 JP S5944096B2
Authority
JP
Japan
Prior art keywords
filling material
coating
coating material
gelatin
hydrophilic
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
JP54166806A
Other languages
Japanese (ja)
Other versions
JPS5689833A (en
Inventor
孝 森下
信彦 八木
正人 荒川
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.)
Morishita Jintan Co Ltd
Original Assignee
Morishita Jintan Co Ltd
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 Morishita Jintan Co Ltd filed Critical Morishita Jintan Co Ltd
Priority to JP54166806A priority Critical patent/JPS5944096B2/en
Publication of JPS5689833A publication Critical patent/JPS5689833A/en
Publication of JPS5944096B2 publication Critical patent/JPS5944096B2/en
Expired 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
    • B01J13/06Making microcapsules or microballoons by phase separation
    • B01J13/08Simple coacervation, i.e. addition of highly hydrophilic material

Description

【発明の詳細な説明】 本発明は充填物が親水性物質からなるゼラチンカプセル
の製造方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing gelatin capsules in which the filling is made of a hydrophilic substance.

充填物質に油性のものを用い、一方被膜物質に水溶性の
物質を用いたカプセルは、従来のカプセル製造装置によ
る製造が可能であった。
Capsules using an oil-based filling material and a water-soluble coating material can be manufactured using conventional capsule manufacturing equipment.

しかしながら、充填物質が油性のものでなくて親水性の
ものである場合には、従来のカプセル製造装置でこの種
のゼラチンカプセルを得ることは相当の制限があった。
However, when the filling material is not oily but hydrophilic, there are considerable limitations in obtaining gelatin capsules of this type with conventional capsule manufacturing equipment.

それは、充填物質も被膜物質も共に親水性のものである
ため、例えば従来法のうちの滴下法という方法で両液を
二重オリフィスより同時に冷却油中に押し出したとする
と、充填物質の浸透圧で被膜物質中に充填物質が移行し
てしまうという現象が生じるため、止むを得ずロータリ
ー法や手技法で極(小量の水を含む親水性物質を充填す
る方法がとられていた。
Because both the filling material and the coating material are hydrophilic, for example, if both liquids were simultaneously pushed into cooling oil through a double orifice using the conventional drip method, the osmotic pressure of the filling material would Because of the phenomenon that the filling material migrates into the coating material, it was unavoidable to use the rotary method or manual techniques to fill the coating with a hydrophilic material containing a small amount of water.

さらに、充填物質、被膜物質が共に親水性のものである
場合に充填物質の液性が酸性であるときは、酸がゼラチ
ンを破壊するためカプセル化が困難で、充填物は酸性以
外のものに限定せざるを得なかった。
Furthermore, if both the filling material and the coating material are hydrophilic and the liquid nature of the filling material is acidic, it will be difficult to encapsulate the gelatin because the acid will destroy the gelatin. I had to limit it.

このように、従来法においてはカプセル化できる充填物
が限定されてしま°うたぬ実用性に乏しく、且つ滴下法
による場合のような直径4罷以下の美しく成型されたカ
プセルを得ることは到底望めず、粒径が小さい場合に連
続量産という体制は全くとれない等の欠点があった。
As described above, in the conventional method, the filler that can be encapsulated is limited, and it is extremely impractical, and it is impossible to obtain beautifully shaped capsules with a diameter of 4 lines or less as in the case of the dropping method. First, there were drawbacks such as the fact that continuous mass production was not possible at all when the particle size was small.

本発明はかかる事情にかんがみてされたものであって、
被膜物質が水溶性ゼラチン物質で、充填物質が親水性物
質であり、且つ酸性のものであっても滴下法により連続
量産することを可能にするものであり、この種のカプセ
ルを迅速に、しかも美しく成型されたカプセルを製造で
きるようにしたものである。
The present invention has been made in view of such circumstances, and includes:
The coating material is a water-soluble gelatin material, the filling material is a hydrophilic material, and even if the filling material is acidic, continuous mass production is possible by the dropping method, and this type of capsule can be produced quickly and efficiently. This makes it possible to produce beautifully shaped capsules.

本願発明者らは被膜物質と充填物質との両者が親水性物
質である場合において、被膜物質である水溶性ゼラチン
に対して、充填物質が酸性でないときはタンニン酸を加
え、他方充填物質が酸性であるときは腸溶性被膜物質を
添加することにより、充填物質の被膜物質への浸透が弱
められ、両者の界面が保持されるので被膜物質中に充填
物質が移行する現象を防止できることを見い出した。
In the case where both the coating material and the filling material are hydrophilic, the inventors added tannic acid to water-soluble gelatin, which is the coating material, when the filling material is not acidic; It has been found that when this is the case, by adding an enteric coating material, the penetration of the filling material into the coating material is weakened and the interface between the two is maintained, thereby preventing the migration of the filling material into the coating material. .

この場合に、充填物質の液性に応じ、それが酸性でない
場合、即ちアルカリ性及び中性であるときはタンニン酸
を用いると、充填物の浸透が抑制できゼラチンの親水性
物質に対する溶解性が弱(なり、被膜を形成保持するこ
とができる。
In this case, depending on the liquid nature of the filling material, if it is not acidic, that is, alkaline or neutral, tannic acid may be used to suppress the penetration of the filling material and weaken gelatin's solubility in hydrophilic substances. (A film can be formed and maintained.)

しかし、充填物が酸性であるときは、被膜物質であるゼ
ラチンと充填物質中の酸との反応によってゼラチンのゲ
/4度が極度に低下することになり、さらに浸透性が高
まる結果になる。
However, when the filling material is acidic, the reaction between gelatin, which is a coating material, and the acid in the filling material causes the Ge/4 degree of the gelatin to be extremely reduced, resulting in a further increase in permeability.

そこで前記タンニン酸に代わり、酸に溶解しない性質を
有するメチルアクリレート、メタアクリル酸、メチルメ
タアクリレートコポリマーの如き腸溶性被膜剤を被膜に
添加することによりゼラチンのゲル強度の低下を抑制で
きると共に、被膜物質中に充填物質が移行する現象を防
止でき被膜の形成保持が可能となる。
Therefore, by adding an enteric coating agent such as methyl acrylate, methacrylic acid, or methyl methacrylate copolymer, which does not dissolve in acids, to the coating instead of the tannic acid, it is possible to suppress the decrease in the gel strength of gelatin and to prevent the coating from decreasing. It is possible to prevent the filling material from migrating into the material and to maintain the formation of a film.

したがって、このように充填物質の液性に応じた組合せ
のもとに被膜物質と充填物質とを二重オリフィスより冷
却油中に押し出し成型することにより、広範囲にわたる
親水拙物質を充填物とするゼラチンカプセルを迅速に製
造することができる。
Therefore, by extruding and molding the coating material and the filling material into cooling oil through a double orifice based on the combination according to the liquid properties of the filling material, gelatin containing a wide range of hydrophilic substances as filling materials can be produced. Capsules can be manufactured rapidly.

以下、本発明の実施例を掲げる。Examples of the present invention are listed below.

実施例 ■ 本例は中性物質を充填物とするいわゆるコーヒーカプセ
ルであって、被膜物質として ゼラチン 15?葡萄糖
60グタンニン酸
1グ水
60グとからなるゾル溶液を70°に加温し
たものを用い、充填物質として 還元麦芽水飴 100′?コーヒー
エキス粉末 11’水
10グこの混液を70°に加温した
ものを用いる。
Example ■ This example is a so-called coffee capsule filled with a neutral substance, and gelatin is used as the coating material. dextrose
60 gtannic acid
1g water
Using a sol solution consisting of 60g and heated to 70°, reduced malt starch syrup and 100g of reduced malt starch syrup were used as the filling material. Coffee extract powder 11' water
Use 10g of this mixture heated to 70°.

上記の両液を二重オリフィスから下降流として流れる冷
却植物油中に押し出し成形する。
Both liquids are extruded into cooled vegetable oil flowing down-flow through dual orifices.

この場合カプセルの造粒径を植物油の流速の調節によっ
て自在に制御して迅速に連続量産する。
In this case, the granulation size of the capsules can be freely controlled by adjusting the flow rate of the vegetable oil to rapidly and continuously mass-produce the capsules.

本例の場合造粒径4mmの濃縮コーヒーカプセルが得ら
れた。
In this example, concentrated coffee capsules with a granulation diameter of 4 mm were obtained.

実施例 ■ 本例は中性物質を充填したいわゆるミルクカプセルであ
り、被膜物質は上記実施例■と同一である。
Example (2) This example is a so-called milk capsule filled with a neutral substance, and the coating material is the same as in Example (2) above.

充填物は練乳を700に加温したものを用いる。The filling used was condensed milk heated to 700℃.

実施例■と同じ(二重オリフィスより下降する冷却植物
油中に押し出し成形すると造粒径4框の濃縮ミルクカプ
セルが得られる。
Same as Example ① (extrusion molding into cooled vegetable oil descending from a double orifice yields concentrated milk capsules with a granulation size of 4 squares).

これらのカプセルは水溶性のゼラチン被膜を用いている
ために、日中で容易に溶ける。
These capsules have a water-soluble gelatin coating that easily dissolves during the day.

また充填物質が親水性のものであるから呈味性がよく、
充分に新鮮な香味を味わうことができる。
In addition, since the filling material is hydrophilic, it has good taste.
You can enjoy the fresh flavor.

実施例 ■ 本例では充填物に酸性のものを入れたみかん果汁カプセ
ルである。
Example 1 This example is a tangerine juice capsule containing an acidic filling.

被膜物質として ゼラチン 15 グD−ソ
ルビトール 60 グメチルアクリ
レート、メタアクリル酸、 ■、5クメチルメタアク
リレートコポリマー 炭酸ナトリウム 1,8グ水
65 グこの被
膜溶液の調製は次の如くする。
Gelatin as coating material 15 g D-sorbitol 60 g Methyl acrylate, methacrylic acid, ■, 5 cu methyl methacrylate copolymer Sodium carbonate 1.8 g Water
65 The coating solution is prepared as follows.

まず炭酸ナトリウム1.82と水15fとメチルアクリ
レート、メタアクリル酸、メチルメタアクリレートコポ
リマー1.52とを混じたA液をつくり、次に別途にゼ
ラチン15グ、D−ソルビトール60グ、水50グを混
じて70°に加熱して、これをB液とする。
First, make Solution A by mixing 1.82 g of sodium carbonate, 15 g of water, and 1.52 g of methyl acrylate, methacrylic acid, and methyl methacrylate copolymer, then separately add 15 g of gelatin, 60 g of D-sorbitol, and 50 g of water. Mix and heat to 70°, and use this as liquid B.

このB液に前者のA液を合して70°に加温し、これを
被膜溶液とする。
This B solution and the former A solution are combined and heated to 70°, and this is used as a coating solution.

次に本例の充填物質について述べると、 みかん果汁 95I?無水クエ
ン酸 5グ香料 微
量 これらを混じて70°に加温する。
Next, let's talk about the filling material in this example: Mandarin orange juice 95I? 5 grams of anhydrous citric acid, a small amount of fragrance Mix these together and heat to 70°.

上記の如き被膜溶液と充填溶液を二重オリフィスより下
降流となって流れる冷却植物油中に押し出し成形する。
The coating solution and fill solution as described above are extruded into cooled vegetable oil flowing downwardly through a dual orifice.

本例の場合、カプセルの造粒径を植物油の流速の調節に
よって制御して造粒径4mmのみかん果汁カプセルを得
た。
In this example, the granulation size of the capsules was controlled by adjusting the flow rate of the vegetable oil to obtain mandarin orange juice capsules with a granulation size of 4 mm.

実施例 ■ 本例の場合は、被膜物質は実施例■と同一で充填物質が
次の如き酸性の強い海内エキスカプセルである。
Example (2) In this example, the coating material was the same as in Example (2), and the filling material was a highly acidic marine extract capsule as shown below.

蜂蜜 80グ 梅肉エキス 10グ水
10グこれらを混じて
70°に加温する。
Honey 80g Plum extract 10g Water
Mix 10 grams of these and heat to 70°.

同様にカプセルの造粒径を植物油の流速の調節によって
制御して、両液を二重オリフィスより下降流となって流
れる冷却植物油中に押し出し成形すると、造粒径4罷の
酸性の強い梅肉エキスカプセルが得られた。
Similarly, by controlling the granulation size of the capsule by adjusting the flow rate of the vegetable oil and extruding both liquids into the cooled vegetable oil flowing downward from the double orifice, highly acidic plum meat with a granulation size of 4 lines is produced. Extract capsules were obtained.

このように親水性物質を充填物とするゼラチンカプセル
が従来の装置による方法で迅速且つ連続的に量産できる
In this way, gelatin capsules filled with hydrophilic substances can be rapidly and continuously mass-produced using conventional equipment.

したがって、従来の方法による場合の如く充填物の水含
有量が低く、酸性のもの以外に限定され、且つ粒径4r
IL7rL以下のものを得ることは不可能であるという
欠点が除かれたことになり、本発明によってカプセル化
できる充填物の液性の範囲がより広(なり、粒径0.5
〜4mm中のミニカプセルの成形も可能となった。
Therefore, the water content of the filler is low and limited to non-acidic materials as in the case of conventional methods, and the particle size is 4r.
The drawback that it is impossible to obtain an IL of less than 7 rL has been eliminated, and the range of liquid properties of the filler that can be encapsulated by the present invention is wider (and particle size 0.5
It has also become possible to mold minicapsules of ~4 mm.

これはカプセルという剤形のもつメリットを更に一段と
高めるものであり、嗜好物、食品医薬品、化粧品等その
他種々の分野にわたってその利用範囲を広めるものであ
る。
This will further enhance the advantages of the capsule dosage form, and will expand its range of use to various other fields such as luxury foods, foods and drugs, and cosmetics.

Claims (1)

【特許請求の範囲】[Claims] 1 充填物質が親水性物質であり、且つ被膜物質がゼラ
チン及び糖アルコール、又は葡萄糖などの糖類で構成さ
れた水溶性物質である場合において、充填物質が酸性で
ない場合には被膜物質にタンニン酸を加え、他方充填物
質が酸性である場合は被膜物質に腸溶性被膜剤を添加し
て、このような組合せからなる充填物質と被膜物質の両
液を、別々に二重オリフィスよりジェット流として冷却
油流中に押し出し成形することを特徴とする親水性物質
を充填物とするゼラチンカプセルの製造方法。
1. When the filling material is a hydrophilic material and the coating material is a water-soluble substance composed of gelatin and sugar alcohols or sugars such as glucose, if the filling material is not acidic, tannic acid is added to the coating material. In addition, if the filling material is acidic, an enteric coating agent may be added to the coating material, and both the filling material and coating material made of such a combination may be separately jetted into the cooling oil through a double orifice. A method for producing gelatin capsules filled with a hydrophilic substance, characterized by extrusion molding in a flowing stream.
JP54166806A 1979-12-24 1979-12-24 Method for producing gelatin capsules filled with hydrophilic substances Expired JPS5944096B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP54166806A JPS5944096B2 (en) 1979-12-24 1979-12-24 Method for producing gelatin capsules filled with hydrophilic substances

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP54166806A JPS5944096B2 (en) 1979-12-24 1979-12-24 Method for producing gelatin capsules filled with hydrophilic substances

Publications (2)

Publication Number Publication Date
JPS5689833A JPS5689833A (en) 1981-07-21
JPS5944096B2 true JPS5944096B2 (en) 1984-10-26

Family

ID=15838017

Family Applications (1)

Application Number Title Priority Date Filing Date
JP54166806A Expired JPS5944096B2 (en) 1979-12-24 1979-12-24 Method for producing gelatin capsules filled with hydrophilic substances

Country Status (1)

Country Link
JP (1) JPS5944096B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9072677B2 (en) 2002-04-25 2015-07-07 Banner Life Sciences Llc Chewable soft capsules

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63276451A (en) * 1987-05-09 1988-11-14 Kanebo Ltd Jelly and production thereof
JP3405746B2 (en) * 1992-10-28 2003-05-12 フロイント産業株式会社 Manufacturing method of seamless capsule
JP3625940B2 (en) * 1996-01-29 2005-03-02 信越化学工業株式会社 Aqueous liquid capsule and method for producing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9072677B2 (en) 2002-04-25 2015-07-07 Banner Life Sciences Llc Chewable soft capsules
US9668976B2 (en) 2002-04-25 2017-06-06 Banner Life Sciences, LLC Chewable soft capsules

Also Published As

Publication number Publication date
JPS5689833A (en) 1981-07-21

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