JPH0278613A - Soft capsule containing essential oil - Google Patents

Soft capsule containing essential oil

Info

Publication number
JPH0278613A
JPH0278613A JP63229538A JP22953888A JPH0278613A JP H0278613 A JPH0278613 A JP H0278613A JP 63229538 A JP63229538 A JP 63229538A JP 22953888 A JP22953888 A JP 22953888A JP H0278613 A JPH0278613 A JP H0278613A
Authority
JP
Japan
Prior art keywords
oil
gelatin
capsule
polypeptide
cinnamon
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
JP63229538A
Other languages
Japanese (ja)
Other versions
JPH07550B2 (en
Inventor
Kazuoki Komata
小俣 一起
Tatsuo Hashimoto
橋本 竜男
Masato Takahashi
正人 高橋
Shinzo Tatematsu
立松 信三
Norikazu Ito
伊藤 典一
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.)
Nitta Gelatin Inc
Taisho Pharmaceutical Co Ltd
Original Assignee
Nitta Gelatin Inc
Taisho Pharmaceutical 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 Nitta Gelatin Inc, Taisho Pharmaceutical Co Ltd filed Critical Nitta Gelatin Inc
Priority to JP63229538A priority Critical patent/JPH07550B2/en
Publication of JPH0278613A publication Critical patent/JPH0278613A/en
Publication of JPH07550B2 publication Critical patent/JPH07550B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Medicinal Preparation (AREA)
  • Medicines Containing Plant Substances (AREA)

Abstract

PURPOSE:To obtain a capsule resistant to the lowering of solubility and discoloration with time, composed of gelatin and a polypeptide and containing an aldehyde-containing natural vegetable oil such as cinnamon oil or anise oil and an essential oil extract reactive to the amino group of gelatin. CONSTITUTION:The soft gelatin capsule is composed of a capsule wall made of gelatin compounded with 15-70wt.% (preferably 20-50wt.%) of a polypeptide and is filled with an oil such as cinnamon oil, anise oil, clove oil, peppermint oil, ginger oil, cardamom oil, lemon oil, citrus oil or l-menthol. Preferably, the polypeptide has a molecular weight of 5,000-10,000 and is used in the form of powder. The gelatin wall of the capsule produced by the above process is resistant to the lowering of solubility and the discoloration with time. The capsule is produced by mixing gelatin with a polypeptide, swelling the mixture with purified water and forming a capsule by a capsule-forming machine using cinnamon oil, etc., as a contact.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、ゼラチン軟カプセルに関する。更に詳しくは
、ゼラチン皮膜の不溶化を防止して、安定した溶解性を
示すゼラチン軟カプセルに関する。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to soft gelatin capsules. More specifically, the present invention relates to soft gelatin capsules that prevent gelatin coatings from becoming insolubilized and exhibit stable solubility.

[従来の技術] 従来、ゼラチン皮膜の不溶化を防止する技術として、ゼ
ラチンに種々の添加剤を配合する方法(特公昭60−9
011号公報、特公昭57−3008号公報、□特開昭
59−39834号公報)とゼラチン分子中のアミノ基
を有機酸で封鎖した所謂モデファイトゼラチンを使用す
る方法(特開昭50−106876号公報)が知られて
いる。
[Prior Art] Conventionally, as a technique for preventing gelatin film from becoming insolubilized, there has been a method of blending various additives with gelatin (Japanese Patent Publication No. 60-9).
No. 011, Japanese Patent Publication No. 57-3008, Japanese Patent Publication No. 59-39834) and a method using so-called modephite gelatin in which the amino groups in gelatin molecules are blocked with organic acids (Japanese Patent Publication No. 50-106876). Publication No.) is known.

[発明が解決しようとする課題] しかしながら、内容物の種類、例えば、ケイヒ油、ウィ
キョウ油、チョウジ油、ハツカ油、ショウキ5つ油、シ
ョウズク油、レモン油、トウヒ油、l−メントールのよ
うにゼラチンのアミノ基と反応しやすい化合物などを含
有した場合、ゼラチン皮膜の溶解性が経時的に劣化した
り、ゼラチン皮膜が変色することがあった。
[Problems to be Solved by the Invention] However, the types of contents, such as cinnamon oil, fennel oil, clove oil, pepper oil, ginger oil, ginger oil, lemon oil, spruce oil, l-menthol, etc. If a compound that easily reacts with the amino groups of gelatin is contained, the solubility of the gelatin film may deteriorate over time or the gelatin film may change color.

[課題を解決するための手段] 本発明者らは、ゼラチン皮膜の溶解性の劣化とと変色を
防止するために、種々の界面活性剤、可塑剤などの”添
加物をゼラチンに配合して、不溶化と変色の状況を検討
した結果、ポリペプチドを粉末化してゼラチンに配合し
たゼラチン軟カプセルが、該目的を満たすことを見出し
、その知見に基づき本発明を完成するに至った。
[Means for Solving the Problems] In order to prevent deterioration of solubility and discoloration of the gelatin film, the present inventors have incorporated various additives such as surfactants and plasticizers into gelatin. As a result of examining the situation of insolubilization and discoloration, it was discovered that soft gelatin capsules prepared by powdering a polypeptide and blending it with gelatin met the objective, and based on this knowledge, the present invention was completed.

本発明は、ケイヒ油、ウィキョウ油、チョウジ油、ハツ
カ油、ショウキョウ油、ショウズク油、レモン油、トウ
ヒ油、l−メントールからなる群の一種または二種以上
を内容物として含有し、ポリペプチドをゼラチンに対し
て15〜70重量%の割合で配合した皮膜から成るゼラ
チン軟カプセルである。
The present invention contains as contents one or more of the group consisting of cinnamon bark oil, fennel oil, clove oil, mustard oil, ginger oil, ginger oil, lemon oil, spruce oil, l-menthol, and contains polypeptides. It is a soft gelatin capsule consisting of a film containing 15 to 70% by weight of gelatin.

本発明のポリペプチドは、経時的な溶解性の劣化と変色
を防止するために分子量s、 ooo〜to、oooの
ポリペプチドを粉末化して用いることが好ましい、ポリ
ペプチドのゼラチンに対する配合量は、15〜70重量
%であり、更に、好ましくは20〜50重量%である。
In order to prevent deterioration of solubility and discoloration over time, it is preferable to use the polypeptide of the present invention by powdering the polypeptide with a molecular weight of s, ooo to ooo, and the amount of the polypeptide to gelatin is as follows: The content is 15 to 70% by weight, more preferably 20 to 50% by weight.

本発明の製造法は、打抜法、滴下法、浸漬法などの通常
の軟カプセルをの製造方法を用いることができるが、打
抜法のロータリ一方式が好ましい。また、内容物によっ
ては、滴下法による継ぎ目のない所謂シームレスカプセ
ルを製造する方法が好ましい0本発明の製造法の1つを
例示すれば、以下の如くである。
For the production method of the present invention, conventional methods for producing soft capsules such as a punching method, a dropping method, and a dipping method can be used, but a rotary one-type punching method is preferable. Furthermore, depending on the contents, a method of producing a so-called seamless capsule without a seam by a dropping method is preferable.An example of the production method of the present invention is as follows.

ゼラチンとポリペプチドを混合し、精製水を適量加えて
攪拌し、その後10〜20分静置して膨潤許せる。これ
を60°Cの温度に層温して溶解して均一なゼラチン水
溶液とする。このゼラチン水溶液を脱泡し、皮膜組成物
として、これにケイヒ油等のアルデヒド含有天然植物油
及びゼラチンアミノ基と反応しやすい精油抽出物を内容
物としてカプセル製造機によりカプセル化する。こうし
て得られたカプセルを温度23°C1湿度40%に制御
された製造室で16〜60時間乾燥し、成型品とする。
Gelatin and polypeptide are mixed, an appropriate amount of purified water is added and stirred, and then left to stand for 10 to 20 minutes to allow swelling. This is heated to a temperature of 60°C and dissolved to form a uniform aqueous gelatin solution. This gelatin aqueous solution is defoamed, and a film composition is encapsulated using a capsule making machine, with contents of an aldehyde-containing natural vegetable oil such as cinnamon oil and an essential oil extract that easily reacts with gelatin amino groups. The capsules thus obtained are dried for 16 to 60 hours in a production room controlled at a temperature of 23° C. and a humidity of 40% to form a molded product.

また、本発明の軟カプセル剤はゼラチンを主基剤として
いるが、それに、可塑剤として、グリセリンやD−ソル
ビトール、また防腐剤などを適宜添加してゼラチン溶液
を調製し、皮膜組成物を形成することもできる。
In addition, the soft capsules of the present invention have gelatin as the main base, and a gelatin solution is prepared by adding glycerin, D-sorbitol, or a preservative as a plasticizer, as appropriate, to form a film composition. You can also.

[発明の効果] 本発明のゼラチンカプセルは、ケイと油等のアルデヒド
含有天然植物油及びゼラチンのアミノ基と反応しやすい
精油抽出物を内容物としても、不溶化することがない。
[Effects of the Invention] The gelatin capsule of the present invention does not become insolubilized even when it contains aldehyde-containing natural vegetable oils such as silicone oil and essential oil extracts that easily react with the amino groups of gelatin.

また、経時的にも溶解性の劣化と変色がないゼラチンカ
プセルである。
In addition, the gelatin capsules do not deteriorate in solubility or change color over time.

[実施例] 本発明を、更に、実施例、試験例を挙げて具体的に説明
する。
[Example] The present invention will be further specifically explained by giving Examples and Test Examples.

実施例1〜10 表1(皮膜組成) ゼラチン(分子量的100.000 )とポリペプチド
の粉末[商品名;水溶性ゼラチンU(新田ゼラチン株式
会社)コを表1の割合で配合した合計1kgを容量2に
のポリエチレン製袋中で振とうして混合後、容量101
の脱泡装置付の溶解タンクに入れ、精製水(25℃)を
2500g加えて攪拌し、その後、60℃で10分静置
して溶解し、タンク内を減圧しながら攪拌し均一な水溶
液とした。 この水溶液を皮膜基剤として、皮膜組成物
を調製した。
Examples 1 to 10 Table 1 (Film composition) Gelatin (molecular weight 100.000) and polypeptide powder [trade name: water-soluble gelatin U (Nitta Gelatin Co., Ltd.)] were blended in the proportions shown in Table 1, totaling 1 kg. After shaking and mixing in a polyethylene bag with a capacity of 2,
Add 2,500 g of purified water (25°C) to the solution tank equipped with a defoaming device, stir, then let stand at 60°C for 10 minutes to dissolve, and stir while reducing the pressure inside the tank to form a homogeneous aqueous solution. did. A film composition was prepared using this aqueous solution as a film base.

表2 この皮膜組成物に、予め調製しておいた表2の処方の内
容液(基剤に精油成分を生薬として入れ均一に攪拌して
調製したもの)を使用してカプセル製造機(特開昭61
−14915〜14954号公報)によりカプセルを製
造した。
Table 2 This film composition was prepared using a capsule making machine (unexamined Japanese Patent Application Publication No. 2003-100000) using the contents of the formulation shown in Table 2 prepared in advance (prepared by adding essential oil components as crude drugs to the base and stirring uniformly). 1986
-14915 to 14954).

こうして得られたカプセルを温度23℃、湿度40%に
制御された製造室で約6時間乾燥し、その後棚型除湿乾
燥機(温度23°C1湿度40%以下)で48時間乾燥
し成形品とした。
The capsules thus obtained are dried for about 6 hours in a manufacturing room controlled at a temperature of 23°C and a humidity of 40%, and then dried for 48 hours in a shelf-type dehumidifying dryer (temperature of 23°C and humidity of 40% or less) to form a molded product. did.

試験例1(崩壊試験、変色状況、皮膜強度)(検体) 検体1〜10;実施例1〜10のカプセル各々20個。Test example 1 (disintegration test, discoloration status, film strength) (sample) Specimens 1 to 10: 20 capsules each of Examples 1 to 10.

対照検体フ実施例と内容物、使用したカプセル製造機お
よび乾燥条件が同じでゼラチン1kgと精製水2.5k
gの組成の皮膜のカプセル20個。
Control sample: Same contents, same capsule manufacturing machine and drying conditions as Example, 1 kg of gelatin and 2.5 kg of purified water.
20 capsules with a film composition of g.

(試験法) 製造直後の崩壊試験は、第11改正日本薬局方、一般試
験法38、崩壊試験法の(0カプセル剤の操作法に準じ
て測定した。
(Test method) The disintegration test immediately after manufacture was carried out in accordance with the 11th edition of the Japanese Pharmacopoeia, General Test Method 38, Disintegration Test Method (Operating method for capsules).

1力月後の崩壊度は、検体をガラス瓶(キャップ付)に
入れ、温度40℃、湿度75%の状態で1力月放置した
後、検体を取り出し、製造直後の崩壊度と同様に測定し
た。
The degree of disintegration after one month was determined by placing the sample in a glass bottle (with a cap) and leaving it for one month at a temperature of 40°C and humidity of 75%, then removing the sample and measuring the degree of disintegration immediately after manufacture. .

皮膜強度は、レオメータ−(NMR−2030D−D型
、不動工業株式会社製)を使用し、1分間6〔の早さで
押し潰した時の破壊強度を平均値で示す、尚、この測定
に用いたカプセル20個は、製造直後量の内直径s、o
nn、、皮膜の厚き0.211Hのものを用いた。
The film strength is expressed as the average breaking strength when crushed at a rate of 6 [for 1 minute] using a rheometer (NMR-2030D-D model, manufactured by Fudo Kogyo Co., Ltd.). The 20 capsules used had an inner diameter of s, o immediately after production.
A film with a film thickness of 0.211H was used.

(結果) 表3に示す。(result) It is shown in Table 3.

試験例2(崩壊試験および変色試験) (検体) 実施例と同じ内容物と表4の皮膜組成のカプセル620
個。
Test Example 2 (Disintegration test and discoloration test) (Sample) Capsule 620 with the same contents as in Example and the film composition shown in Table 4
Individual.

(試験法) 試験例1と同様である。(Test method) Same as Test Example 1.

(結果) 表5に示す。(result) It is shown in Table 5.

ゼラチン皮膜の溶解性の劣化と変色を防止するために、
モデファイトゼラチン及び抗酸化剤、界面活性剤、可塑
剤を配合したが十分に満足できるカプセルは得られなか
った。
In order to prevent deterioration of solubility and discoloration of gelatin film,
Although modephite gelatin, an antioxidant, a surfactant, and a plasticizer were mixed, a fully satisfactory capsule could not be obtained.

表5Table 5

Claims (1)

【特許請求の範囲】[Claims] 1)ケイヒ油、ウイキョウ油、チョウジ油、ハッカ油、
ショウキョウ油、ショウズク油、レモン油、トウヒ油、
l−メントールからなる群の一種または二種以上を内容
物として含有し、ポリペプチドをゼラチンに対して15
〜70重量%の割合で配合した皮膜から成るゼラチン軟
カプセル。
1) Cinnamon oil, fennel oil, clove oil, peppermint oil,
Ginger oil, ginger oil, lemon oil, spruce oil,
Contains one or more members of the group consisting of l-menthol, and contains polypeptide at a ratio of 15% to gelatin.
Soft gelatin capsules consisting of a film containing ~70% by weight.
JP63229538A 1988-09-13 1988-09-13 Essential oil containing soft capsule Expired - Lifetime JPH07550B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63229538A JPH07550B2 (en) 1988-09-13 1988-09-13 Essential oil containing soft capsule

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63229538A JPH07550B2 (en) 1988-09-13 1988-09-13 Essential oil containing soft capsule

Publications (2)

Publication Number Publication Date
JPH0278613A true JPH0278613A (en) 1990-03-19
JPH07550B2 JPH07550B2 (en) 1995-01-11

Family

ID=16893739

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63229538A Expired - Lifetime JPH07550B2 (en) 1988-09-13 1988-09-13 Essential oil containing soft capsule

Country Status (1)

Country Link
JP (1) JPH07550B2 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5631024A (en) * 1995-05-22 1997-05-20 Enviroquest, Ltd. Medicaments for beneficial insects and method
GB2338186A (en) * 1998-06-10 1999-12-15 Reckitt & Colmann Prod Ltd Compositions for treating gastric and oesophageal complaints
JP2010260812A (en) * 2009-05-01 2010-11-18 Nakanihon Capsule Co Ltd Soft capsule
JP2011094438A (en) * 2009-11-02 2011-05-12 Ibicon:Kk Connected boundary block
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
CN109430885A (en) * 2018-12-27 2019-03-08 陈莉 It is a kind of using oligopeptide as nutritional agents of carrier and preparation method thereof
WO2020137694A1 (en) * 2018-12-28 2020-07-02 小林製薬株式会社 Capsule
CN113208085A (en) * 2021-05-31 2021-08-06 四川天味食品集团股份有限公司 Low-temperature stir-frying-free beef tallow hotpot condiment and preparation method thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107027899B (en) * 2017-04-25 2020-08-21 郑州雪麦龙食品香料有限公司 Chili lemon oil, caramel lemon fish and preparation method thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5862120A (en) * 1981-10-09 1983-04-13 Fuji Kapuseru Kk Soft capsule film

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5862120A (en) * 1981-10-09 1983-04-13 Fuji Kapuseru Kk Soft capsule film

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5631024A (en) * 1995-05-22 1997-05-20 Enviroquest, Ltd. Medicaments for beneficial insects and method
GB2338186A (en) * 1998-06-10 1999-12-15 Reckitt & Colmann Prod Ltd Compositions for treating gastric and oesophageal complaints
US6348502B1 (en) 1998-06-10 2002-02-19 Reckitt & Colman Products Limited Formulations for the treatment of gastro-oesophageal reflux
JP2010260812A (en) * 2009-05-01 2010-11-18 Nakanihon Capsule Co Ltd Soft capsule
JP2011094438A (en) * 2009-11-02 2011-05-12 Ibicon:Kk Connected boundary block
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
CN109430885A (en) * 2018-12-27 2019-03-08 陈莉 It is a kind of using oligopeptide as nutritional agents of carrier and preparation method thereof
WO2020137694A1 (en) * 2018-12-28 2020-07-02 小林製薬株式会社 Capsule
JP2020105140A (en) * 2018-12-28 2020-07-09 小林製薬株式会社 Capsule
CN113208085A (en) * 2021-05-31 2021-08-06 四川天味食品集团股份有限公司 Low-temperature stir-frying-free beef tallow hotpot condiment and preparation method thereof
CN113208085B (en) * 2021-05-31 2023-08-18 四川天味食品集团股份有限公司 Low-temperature stir-frying-free beef tallow hotpot condiment and preparation method thereof

Also Published As

Publication number Publication date
JPH07550B2 (en) 1995-01-11

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