JPH038435A - Water soluble soft capsule - Google Patents

Water soluble soft capsule

Info

Publication number
JPH038435A
JPH038435A JP1143261A JP14326189A JPH038435A JP H038435 A JPH038435 A JP H038435A JP 1143261 A JP1143261 A JP 1143261A JP 14326189 A JP14326189 A JP 14326189A JP H038435 A JPH038435 A JP H038435A
Authority
JP
Japan
Prior art keywords
gelatin
water
polypeptide
soft capsule
soluble
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.)
Granted
Application number
JP1143261A
Other languages
Japanese (ja)
Other versions
JPH0620534B2 (en
Inventor
Wataru Yanase
梁瀬 渉
Susumu Inoue
進 井上
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.)
RIYOUEI SHOJI KK
Original Assignee
RIYOUEI SHOJI KK
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 RIYOUEI SHOJI KK filed Critical RIYOUEI SHOJI KK
Priority to JP1143261A priority Critical patent/JPH0620534B2/en
Publication of JPH038435A publication Critical patent/JPH038435A/en
Publication of JPH0620534B2 publication Critical patent/JPH0620534B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Fodder In General (AREA)
  • General Preparation And Processing Of Foods (AREA)
  • Medicinal Preparation (AREA)
  • Manufacturing Of Micro-Capsules (AREA)
  • Detergent Compositions (AREA)

Abstract

PURPOSE:To obtain the water soluble soft capsule which dissolves in a cold aq. soln. of <=35 deg.C by mixing polypeptide gelatin and modified gelatin and adding materials which impart resilience and water holdability thereto. CONSTITUTION:The modified gelatin formed by substituting the amino group in the gelatin with an org. acid at about 30 to 100% is used. The polypeptide gelatin which is formed by hydrolyzing the amino group in the gelatin molecule and has <=15000mol.wt. is used. The base material which is soluble in cold water and can be made into soft capsules is obtd. by mixing 90 to 60wt.% modified gelatin and 10 to 40wt.% polypeptide gelatin. About 30 to 60wt.% glycerin, about 5 to 20wt.% sorbit and about 5 to 40wt.% 'Macrogol(R)' (triethylene-glycol-TEG), etc., are added thereto to impart the resilience and water retainability thereto. The water soluble soft capsule which is harmless and is easily soluble in the cold aq. soln. of <=35 deg.C is obtd. in this way.

Description

【発明の詳細な説明】 (産業上の利用分野) この発明は、35℃以下の水溶液で溶解する、例えば液
体或は粉末の洗剤、飼料混入薬剤等の被包に使用する水
溶性軟カプセルに関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) This invention relates to water-soluble soft capsules that dissolve in an aqueous solution at 35° C. or below and are used for encapsulating liquid or powder detergents, feed-mixed drugs, etc. It is something.

(従来の技術) 一般に食品及び医薬品等の被包のために使用される軟カ
プセル剤は、無害であり、しかも易溶性であることを必
要とするところから、ゼラチンを基剤とし、これにグリ
セリン或はソルビットなどを加えて粘性を増加させたも
のが使用されている。
(Prior art) Soft capsules, which are generally used for encapsulating foods and pharmaceuticals, are made of gelatin and glycerin, as they need to be harmless and easily soluble. Alternatively, sorbitol or the like is added to increase the viscosity.

軟カプセル剤の用途は上述の医薬品に限られず、洗剤、
飼料等に拡大する傾向にあるが、これらの用途では軟カ
プセル剤に冷水溶液に易溶性である等の物性が要求され
ている。
The uses of soft capsules are not limited to the pharmaceuticals mentioned above, but also detergents,
There is a tendency to expand its use to feeds, etc., and for these uses, soft capsules are required to have physical properties such as being easily soluble in cold water solutions.

(発明が解決しようとする問題点) しかし、従来のゼラチンを基剤とする軟カプセル剤はゼ
ラチンの物性上、35〜37℃でなければ水溶液に溶解
しないなどの難点がある。
(Problems to be Solved by the Invention) However, conventional gelatin-based soft capsules have the disadvantage that they do not dissolve in an aqueous solution unless the temperature is 35 to 37°C due to the physical properties of gelatin.

また、このようなゼラチンを基剤とする軟カプセル剤の
欠点を解消するために、通常のゼラチンにゼラチン分子
中のアミノ基を加水分解したポリペプチドゼラチンを配
合して軟カプセル剤を構成する試み、或は通常のゼラチ
ンにゼラチン分子中のアミノ基を有機酸で封鎖したモデ
ィファイドゼラチンを配合して軟カプセル剤を構成する
試み等があるが、冷水溶液に溶解せず、何れも十分な成
果を納めるに至っていない。
In addition, in order to overcome the drawbacks of soft capsules based on gelatin, an attempt was made to form soft capsules by blending polypeptide gelatin, which is obtained by hydrolyzing the amino groups in the gelatin molecule, with ordinary gelatin. There have also been attempts to form soft capsules by blending regular gelatin with modified gelatin in which the amino groups in the gelatin molecule are blocked with organic acids, but these efforts have failed to dissolve in cold aqueous solutions and have not produced satisfactory results. I haven't been able to pay it yet.

そこで、この発明は35℃以下の冷水溶液に溶解する軟
カプセル剤を提供することを目的とする。
Therefore, an object of the present invention is to provide a soft capsule that dissolves in a cold aqueous solution at 35° C. or lower.

(問題点を解決するための手段) そして、この発明においては以上の目的を達成するため
鋭意研究の結果、ゼラチン分子中のアミノ基を加水分解
したポリペプチドゼラチンとゼラチン分子中のアミノ基
を有li酸で封鎖したモディファイドゼラチンとの混合
割合がモディファイドゼラチン90〜60WtX 、ポ
リペプチドゼラチン10〜40wtXを基剤とし、これ
に柔軟性と保水性とを与えるグリセリン、ソルビット、
マクロゴール等を加えてなる水溶性軟カプセルを提案す
るものである。
(Means for Solving the Problems) In order to achieve the above object, in this invention, as a result of intensive research, we have developed a polypeptide gelatin obtained by hydrolyzing the amino group in the gelatin molecule and a polypeptide gelatin that has the amino group in the gelatin molecule. The mixing ratio of modified gelatin sequestered with lithium acid is 90 to 60 wtX of modified gelatin, 10 to 40 wtX of polypeptide gelatin, and glycerin, sorbitol, which gives flexibility and water retention to this base material.
We propose water-soluble soft capsules containing macrogol and the like.

ここで、モディファイドゼラチンとしてはゼラチン中の
アミノ基を有m酸で30%〜10ozに置換したもの、
好ましくは90X〜100πに置換したものが使用され
る。
Here, modified gelatin includes gelatin in which amino groups are substituted with 30% to 10 oz of m-acid;
Preferably, those substituted with 90X to 100π are used.

ポリペプチドゼラチンとしては分子量15,000以下
、好ましくは1 、000〜2,000のものが使用さ
れる。
The polypeptide gelatin used has a molecular weight of 15,000 or less, preferably 1,000 to 2,000.

また、モディファイドゼラチンの量を90〜60wtX
としたのは、90wtX以上では冷水溶性にはなりに(
(,60wtX以下では軟カプセル化が不可能など等の
難点があるためである。
Also, increase the amount of modified gelatin to 90 to 60wtX.
The reason for this is that above 90wtX, it becomes less soluble in cold water (
(This is because there are drawbacks such as the impossibility of soft encapsulation at 60 wtX or less.

また、ポリペプチドゼラチンの量を10〜40wtXと
したのは、40wtX以上では軟カプセルが不可能とな
り、10wtX以下では冷水溶性になりにくい等の難点
があるためである。
Moreover, the reason why the amount of polypeptide gelatin is set to 10 to 40 wtX is because if it is more than 40 wtX, it becomes impossible to form a soft capsule, and if it is less than 10 wtX, it is difficult to become cold water soluble.

なお、グリセリンの配合量は30WtX〜60wt%程
度であり、またソルビットは可塑剤及び保水性の目的の
ために加えられ、その配合量は5wtX〜20wtX程
度である。
The blending amount of glycerin is about 30wtX to 60wt%, and sorbitol is added for the purpose of plasticizer and water retention, and the blending amount is about 5wtX to 20wtX.

更に、マクロゴールは可塑剤及び保水性の目的で加えら
れ、その配合量は5wtトl0wt%程度である。
Furthermore, macrogol is added for the purpose of plasticizer and water retention, and its blending amount is about 5wt% to 10wt%.

(実施例) 以下、この発明の実施例を示す。(Example) Examples of this invention will be shown below.

実施例1 配合例1 モデファイトゼラチン        90゜ポリペプ
チドゼラチン        1G。
Example 1 Formulation Example 1 Modephite gelatin 90° polypeptide gelatin 1G.

グリセリン            50z水    
                    8G。
glycerin 50z water
8G.

配合例2 モデファイトゼラチン        70tポリペプ
チドゼラチン        30゜グリセリン   
        40tマクロゴール 400    
     10゜水                
         80g配合例3 モデファイトゼラチン        60srボリベ
グチドゼラチン        40゜グリセリン  
          3G。
Formulation example 2 Modephite gelatin 70t polypeptide gelatin 30° glycerin
40t macro goal 400
10゜water
80g formulation example 3 Modephite gelatin 60sr voribegtide gelatin 40°glycerin
3G.

マクロゴール 40G          1G。Macro goal 40G 1G.

配合例1〜3をそれぞれ充分に混合し、次いでゼラチン
溶解タンクにて約60〜80℃の温度にて加熱し、完全
に溶解させた後、軟カプセル成型機にて軟カプセルを成
型した。
Formulation Examples 1 to 3 were thoroughly mixed, and then heated in a gelatin dissolving tank at a temperature of about 60 to 80°C to completely dissolve them, and then molded into soft capsules using a soft capsule molding machine.

実施例2 配合例1〜3の皮膜に内容液として7tの洗剤を入れて
カプセルを製造し、通常の電気洗濯機を用いて洗濯時間
10分、すすぎ時間8分の洗濯を行なったところ水に溶
解した。
Example 2 Capsules were manufactured by adding 7 tons of detergent as the liquid content to the films of Formulation Examples 1 to 3, and when washed using a normal electric washing machine for 10 minutes and 8 minutes for rinsing, the capsules were washed with water. Dissolved.

比較例 比較配合例1 ゼラチン              901rモデフ
アイトゼラチン        10゜グリセリン  
          50g水           
              aO。
Comparative Example Comparative Formulation Example 1 Gelatin 901r modephite gelatin 10°glycerin
50g water
aO.

比較配合例2 ゼラチン             90gポリペプチ
ドゼラチン        10tグリセリン    
        50g水             
            80g比較比較例1.2につ
いて実施例2と同様に、電気洗濯機における溶解度試験
を行った。その結果、カプセルの溶解性がみられなかっ
た。
Comparative formulation example 2 Gelatin 90g polypeptide gelatin 10t glycerin
50g water
A solubility test in an electric washing machine was conducted on 80 g Comparative Example 1.2 in the same manner as in Example 2. As a result, no solubility of the capsule was observed.

(発明の効果) 以上要するに、この発明に係る軟カプセルは無害で、し
かも35℃以下の冷水溶液に易溶性であるので、 液体乃至粉末の洗剤、 或は飼料混入薬剤の 被包にi&適である。
(Effects of the Invention) In summary, the soft capsules according to the present invention are harmless and are easily soluble in cold water solutions at temperatures below 35°C, so they are suitable for encapsulating liquid or powder detergents or drugs mixed in feed. be.

特 許 出 願 人 株式会社 梁永商事Special permission Out wish Man Co., Ltd. Liangei Shoji

Claims (1)

【特許請求の範囲】[Claims] ゼラチン分子中のアミノ基を加水分解したポリプペチド
ゼラチンとゼラチン分子中のアミノ基を有機酸で封鎖し
たモディファイドゼラチンとの混合割合がモディファイ
ドゼラチン90〜60wt%、ポリペプチドゼラチン1
0〜40wt%を基剤とし、これに柔軟性と保水性とを
与えるグリセリン、ソルビット、マクロゴール等を加え
て軟カプセルを形成し、該カプセルの水溶解を可能とし
たことを特徴とする水溶性軟カプセル。
The mixing ratio of polypeptide gelatin in which the amino groups in the gelatin molecule are hydrolyzed and modified gelatin in which the amino groups in the gelatin molecule are blocked with an organic acid is 90 to 60 wt% of modified gelatin and 1 part of polypeptide gelatin.
0 to 40 wt% as a base, to which glycerin, sorbitol, macrogol, etc. that give flexibility and water retention are added to form soft capsules, and the capsules can be dissolved in water. Soft capsule.
JP1143261A 1989-06-06 1989-06-06 Water-soluble soft capsule Expired - Lifetime JPH0620534B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1143261A JPH0620534B2 (en) 1989-06-06 1989-06-06 Water-soluble soft capsule

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1143261A JPH0620534B2 (en) 1989-06-06 1989-06-06 Water-soluble soft capsule

Publications (2)

Publication Number Publication Date
JPH038435A true JPH038435A (en) 1991-01-16
JPH0620534B2 JPH0620534B2 (en) 1994-03-23

Family

ID=15334631

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1143261A Expired - Lifetime JPH0620534B2 (en) 1989-06-06 1989-06-06 Water-soluble soft capsule

Country Status (1)

Country Link
JP (1) JPH0620534B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004021800A1 (en) * 2002-09-06 2004-03-18 Nippon Suisan Kaisha, Ltd. Bound feed and process for producing the same
WO2006128685A3 (en) * 2005-05-31 2007-04-19 Gelita Ag Process for making a low molecular weight gelatine hydrolysate and gelatine hydrolysate compositions
KR100770858B1 (en) * 2006-09-08 2007-10-26 삼성전자주식회사 Portable folding cradle
WO2012002464A1 (en) * 2010-06-30 2012-01-05 持田製薬株式会社 ω3 FATTY ACID COMPOUND PREPARATION
JP2013515715A (en) * 2009-12-28 2013-05-09 カプスゲル・ベルギウム・ナムローゼ・フェンノートシャップ Gelatin capsule and gelatin composition for forming capsule film

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1043390A1 (en) * 1999-04-09 2000-10-11 The Procter & Gamble Company Detergent tablet

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5532382B2 (en) 2008-05-09 2014-06-25 株式会社リコー Image forming apparatus

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004021800A1 (en) * 2002-09-06 2004-03-18 Nippon Suisan Kaisha, Ltd. Bound feed and process for producing the same
WO2006128685A3 (en) * 2005-05-31 2007-04-19 Gelita Ag Process for making a low molecular weight gelatine hydrolysate and gelatine hydrolysate compositions
JP2008541743A (en) * 2005-05-31 2008-11-27 ゲリタ アクチェンゲゼルシャフト Process for producing low molecular weight gelatin hydrolyzate and gelatin hydrolyzate composition
US7897728B2 (en) 2005-05-31 2011-03-01 Gelita Ag Process for making a low molecular weight gelatine hydrolysate
KR100770858B1 (en) * 2006-09-08 2007-10-26 삼성전자주식회사 Portable folding cradle
JP2013515715A (en) * 2009-12-28 2013-05-09 カプスゲル・ベルギウム・ナムローゼ・フェンノートシャップ Gelatin capsule and gelatin composition for forming capsule film
WO2012002464A1 (en) * 2010-06-30 2012-01-05 持田製薬株式会社 ω3 FATTY ACID COMPOUND PREPARATION
US8609138B2 (en) 2010-06-30 2013-12-17 Mochida Pharmaceutical Co., Ltd. ω3 fatty acid compound preparation

Also Published As

Publication number Publication date
JPH0620534B2 (en) 1994-03-23

Similar Documents

Publication Publication Date Title
TWI472323B (en) Aqueous composition for enteric hard capsule, method of preparing enteric hard capsule,and enteric hard capsule prepared using the method
AU738231B2 (en) Detergent
BRPI0708996B1 (en) fabric treatment composition and preparation process
BR112016018327B1 (en) PARTICLE, AND, DETERGENT PRODUCT
JP3879941B2 (en) Seamless soft capsule
JPH038435A (en) Water soluble soft capsule
JP2004507579A (en) Water-soluble package containing liquid composition
JP2002500680A (en) pH-sensitive modified cellulose ester
CN103087208A (en) Carrageenan modified by ion-exchange process
EP0808161B1 (en) Solid substances comprising valproic acid and sodium valproate
JP2003511392A (en) Foams and compositions containing these foams
JPS61176519A (en) Production of tablet
JPH0278613A (en) Soft capsules containing essential oils
JP2634448B2 (en) Silk fibroin aqueous solution excellent in storage safety and method for producing the same
JPS59501016A (en) detergent
JP2696230B2 (en) Enzyme granules and granulation method
CN104937091B (en) Soluble aqueous gels with high chelating agent loading
JPH02127496A (en) Solid fuel with corrosion-proofing performance
JPH03255024A (en) Soft capsule readily meltable in mouth
JPS5869299A (en) Body containing detergent unit use quantity, manufacture and use
US12252667B2 (en) Laundry detergent composition
WO2003063855A1 (en) Chewable tablet containing branched amino acids
JPS62138596A (en) bar soap composition
JPH05339874A (en) Fade suppressing agent for oxygen-type bleaching agent
SU329949A1 (en) MODEL COMPOSITION