JPH02205A - Perfume-containing coating agent for soft capsule - Google Patents

Perfume-containing coating agent for soft capsule

Info

Publication number
JPH02205A
JPH02205A JP63280978A JP28097888A JPH02205A JP H02205 A JPH02205 A JP H02205A JP 63280978 A JP63280978 A JP 63280978A JP 28097888 A JP28097888 A JP 28097888A JP H02205 A JPH02205 A JP H02205A
Authority
JP
Japan
Prior art keywords
perfume
pullulan
coating
weight
coating agent
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
JP63280978A
Other languages
Japanese (ja)
Inventor
Masaru Hineno
日根野 優
Koichi Ohashi
功一 大橋
Masami Nemoto
根本 正美
Hiroshi Yamaguchi
洋 山口
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.)
Taisho Pharmaceutical Co Ltd
Original Assignee
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 Taisho Pharmaceutical Co Ltd filed Critical Taisho Pharmaceutical Co Ltd
Priority to JP63280978A priority Critical patent/JPH02205A/en
Publication of JPH02205A publication Critical patent/JPH02205A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the subject preparation exhibiting high retention of perfume after the lapse of time and capable of keeping stable feeling to the palate the adding a polyhydric alcohol to a pullulan solution containing an oily perfume and a surfactant such as a sugar ester having high HLB. CONSTITUTION:An emulsion of a perfume is prepared by vacuum emulsification of 1pt.wt. of a perfume (e.g. menthol, peppermint oil or cinnamon oil) and 0.1-10 pts.wt. of a surfactant (e.g. sugar ester having an HLB of 15-16). The emulsion is added with a proper amount of water, mixed with pullulan (at a concentration of 8-12wt.% in the whole liquid) and then mixed with 5-30wt.% of a polyhydric alcohol (e.g. glycerol or sorbitol) to obtain the subject coating agent. When the water-content in the soft capsule is 8.0-8.5wt.% after drying, the perfume retainability in the soft capsule coating film is high and the capsule is resistant to coagulation, softening and cracking.

Description

【発明の詳細な説明】 [産業上の利用分!!?] 本発明は、軟カプセル剤のコーティング剤に関するもの
であり、更に詳しくは、ソフトカプセル用コーティング
剤に関する。
[Detailed description of the invention] [Industrial use! ! ? ] The present invention relates to a coating agent for soft capsules, and more particularly to a coating agent for soft capsules.

[従来の・技術] 従来、香料を含有許せたソフトカプセルは知られていな
い、プルランで固形医薬品を被覆した例は特開昭60−
104011号公報に知られている。
[Conventional technology] So far, soft capsules that can contain fragrance have not been known; an example of coating a solid drug with pullulan was disclosed in Japanese Patent Application Laid-Open No. 1986-
It is known from the publication No. 104011.

[発明が解決しようとする課題] 固形製剤には服用感を高める上で香料の添加が一般に汎
用されている。しかし、単に粉末または液状香料を倍散
させたものを添加混合しただけでは経時的な消失は免れ
ず、特にメントール、ケイヒ油などの揮発性精油の場合
などは、その保持が極めて困難であった。
[Problems to be Solved by the Invention] Flavoring agents are generally added to solid preparations to enhance the feeling of taking them. However, simply adding and mixing powdered or liquid fragrances will inevitably cause them to disappear over time, and it is extremely difficult to retain them, especially in the case of volatile essential oils such as menthol and cinnamon oil. .

プルランには、優れた酸素透過の抑制作用、保香性機能
があり、こうした目的に適していると思われるが、実際
、プルランにしかない酸素透過の抑制作用、保香性機能
を失わないようにプルランを高濃度でスプレーコーティ
ングするとプルラン特有の曳糸性により製膜が困難であ
った。この為、プルランの酸素透過の抑制機能、保香性
を失わないようにスプレーコーティングするには、プル
ランの濃度および添加剤の質、量を選ばなければならな
かった。
Pullulan has an excellent oxygen permeation inhibiting effect and aroma-retaining function, and is thought to be suitable for these purposes.However, in reality, pullulan has an excellent oxygen permeation inhibiting effect and aroma-retaining function. When spray coating pullulan at a high concentration, it was difficult to form a film due to pullulan's unique stringiness. For this reason, the concentration of pullulan and the quality and quantity of additives had to be selected in order to perform spray coating without losing pullulan's ability to suppress oxygen permeation and aroma retention.

[課題を解決するための手段] 本発明者らは、鋭意研究した結果、香料を含有させたプ
ルランおよび水溶性プルラン誘導体溶液に5〜30%の
多価アルコールを配合したことを特徴としたコーティン
グ基剤が上記の課題を有利に解決すること、すなわち、
プルランおよび水溶性プルラン誘導体溶液に香料を含有
させた被覆液を用いてソフトカプセルにフィルムを施す
と経時的に安定な保香性ソフトカプセルが得られること
を見出し、本発明を完成した。
[Means for Solving the Problems] As a result of intensive research, the present inventors have developed a coating characterized in that 5 to 30% polyhydric alcohol is blended into pullulan containing a fragrance and a water-soluble pullulan derivative solution. The base material advantageously solves the above problems, namely:
The present invention was completed based on the discovery that a fragrance-retaining soft capsule that is stable over time can be obtained by applying a film to a soft capsule using a coating liquid containing a fragrance in a solution of pullulan and a water-soluble pullulan derivative.

本発明に用いられるプルランとは、グルコースの3量体
であるマルトトリオースを単位として、α−1,6結合
により反復結合した天然高分子状重合体である。また水
溶性プルラン誘導体とは天然プルランを原料として合成
される誘導体で、かつ、水溶性を消失していないもので
あれば良いが、好ましくは水溶性プルランエーテルまた
は水溶性プルランエステルである。
The pullulan used in the present invention is a natural polymer in which maltotriose, which is a trimer of glucose, is repeatedly bonded through α-1,6 bonds. Further, the water-soluble pullulan derivative is a derivative synthesized using natural pullulan as a raw material and may be one that has not lost its water solubility, but preferably water-soluble pullulan ether or water-soluble pullulan ester.

プルランの全液中濃度は、5〜20重量%であり、8〜
12重量%が特に好ましい、プルランの全液中濃度が5
重量%未滴の場合、コーティング乾燥時の香料の消失が
起こり、また20重量%を超えるとフィルム液の粘度が
高まりコーティングが困難となる。特に、スプレーコー
ティングでは、プルランの全液中濃度が12%を超える
とコーテイング液の粘度が高くスプレーが困難になる。
The concentration of pullulan in the total liquid is 5 to 20% by weight, and 8 to 20% by weight.
The concentration of pullulan in the total liquid is 5, particularly preferably 12% by weight.
If the weight percentage is not dropped, the fragrance will disappear when the coating dries, and if it exceeds 20 weight percent, the viscosity of the film liquid will increase, making coating difficult. In particular, in spray coating, if the concentration of pullulan in the total liquid exceeds 12%, the viscosity of the coating liquid becomes high and spraying becomes difficult.

 本発明の香料とはメントール、ハツカ油、ケイヒ油、
スペアミント、ペパーミント、ハープ、シナモン、焼肉
フレーバー、果汁フレーバーなどが挙げられるが、特に
、香料がメントール、ハツカ油、ケイヒ油などの揮発性
精油である場合、本発明のコーティング剤は、保香性の
効果が顕著である。
The fragrances of the present invention include menthol, peppermint oil, cinnamon bark oil,
Examples include spearmint, peppermint, harp, cinnamon, yakiniku flavor, fruit juice flavor, etc., but especially when the flavor is a volatile essential oil such as menthol, peppermint oil, cinnamon bark oil, etc., the coating agent of the present invention has aroma-retaining properties. The effect is remarkable.

また、上記の揮発性精油のごとき油性香料を使用する場
合、それらを効率良く均一に分散させるために各種界面
活性剤の配合が必要である。中でもHLB値が11以上
のシュガーエステルが好ましく、更に、HLB値が15
〜16であるシュガーエステルが最も好ましい、これら
の界面活性剤の配合量は、油性香料1重量部に対し、界
面活性剤0.1〜10重量部を配合することが好ましい
、界面活性剤の配合量が0.1重量部未満だと乳化が完
全にできなくなる。また、10重量部以上添加すれば香
料の乳化、保持がなされており、これ以上添加する必要
はない。
Furthermore, when using oily fragrances such as the above-mentioned volatile essential oils, it is necessary to incorporate various surfactants in order to efficiently and uniformly disperse them. Among them, sugar esters with an HLB value of 11 or more are preferable, and sugar esters with an HLB value of 15 or more are preferable.
-16 sugar esters are most preferred.The blending amount of these surfactants is preferably 0.1 to 10 parts by weight per 1 part by weight of the oily fragrance. If the amount is less than 0.1 part by weight, emulsification will not be complete. Further, if 10 parts by weight or more is added, the fragrance is emulsified and retained, and there is no need to add more.

本発明の多価アルコール類とは、グリセリン、ソルビト
ール、マンニトール、プロピレングリコールなどである
The polyhydric alcohols of the present invention include glycerin, sorbitol, mannitol, propylene glycol, and the like.

これら多価アルコールの配合量は、プルランの5〜30
重量%が好ましく、10〜25重量%が更に好ましい、
この範囲の濃度で多価アルコールを用いるとプルランの
曳糸性を抑え、スプレーコーティングに適したフィルム
液の粘度を得ることができる。
The blending amount of these polyhydric alcohols is 5 to 30% of pullulan.
% by weight is preferred, and 10 to 25% by weight is more preferred.
When a polyhydric alcohol is used in a concentration within this range, the stringiness of pullulan can be suppressed and the viscosity of the film solution suitable for spray coating can be obtained.

本発明のコーティング剤を調製するには、例えば、下記
の方法による。
The coating agent of the present invention can be prepared, for example, by the following method.

すなわち、シュガーエステルの水分散液に香料を混合攪
拌後、真空乳化により香料の乳化液を調製する。さらに
、適当量の水を加え、プルランを混合後、多価アルコー
ルを添加攪拌して本発明のコーティング剤を得る。
That is, after mixing and stirring a fragrance into an aqueous dispersion of sugar ester, an emulsion of the fragrance is prepared by vacuum emulsification. Furthermore, after adding an appropriate amount of water and mixing pullulan, a polyhydric alcohol is added and stirred to obtain the coating agent of the present invention.

このようにして調製されたコーティング剤を用いてソフ
トカプセル剤をコーティングするには、従来公知の装置
たとえばパンコーティング装置、流動コーティング装置
、通気乾燥機構を備えた各種装置、真空造粒装置などを
用いて行なうことができる。
In order to coat soft capsules with the coating agent prepared in this way, conventionally known equipment such as a pan coating equipment, a fluid coating equipment, various equipment equipped with an aeration drying mechanism, a vacuum granulation equipment, etc. are used. can be done.

しかし、被膜中に残存する水分によって香料の経時的残
存量は変化する。即ち、乾燥終了後のソフトカプセル被
膜中の水分含量が8.0〜8.5重量%である場合、ソ
フトカプセル被膜中の香料の残存量は高い。
However, the amount of fragrance remaining over time changes depending on the moisture remaining in the coating. That is, when the moisture content in the soft capsule coating after drying is 8.0 to 8.5% by weight, the amount of fragrance remaining in the soft capsule coating is high.

また、被膜中に残存する水分の含量が10重量%より多
いとカプセルが凝集し、軟化する。また、逆に被膜中に
残存する水分の含量が、8.0重量%より低いと、被膜
が硬すぎて、ソフトカプセルに亀裂を生じてくる。この
ため乾燥終了後にはソフトカプセル被膜中の水分含量を
8.0〜8.5重量%にすることが好ましい。
Furthermore, if the water content remaining in the coating is more than 10% by weight, the capsules will aggregate and soften. On the other hand, if the water content remaining in the coating is lower than 8.0% by weight, the coating will be too hard and cracks will occur in the soft capsule. For this reason, it is preferable that the water content in the soft capsule coating after drying is 8.0 to 8.5% by weight.

[発明の効果] 本発明のコーティング剤を用いて、コーティングしたソ
フトカプセルは、香料の経時的残存量高い、また、香料
を効率良く均一に分散できるため、安定した服用感が保
てる。更に、ソフトカプセルの内容物主剤に鎮痛抗炎症
剤などを用いた場合には、清涼感のある香料を選べば、
服用感の向上がある。
[Effects of the Invention] Soft capsules coated with the coating agent of the present invention have a high residual amount of flavor over time, and can efficiently and uniformly disperse the flavor, thereby maintaining a stable feeling when taking the capsule. Furthermore, if you use an analgesic and anti-inflammatory agent as the main ingredient in the soft capsule, choose a refreshing fragrance.
There is an improvement in the feeling of taking it.

[実施例] 以下、実施例を挙げて本発明を具体的に説明する。[Example] The present invention will be specifically described below with reference to Examples.

実施例1 塩酸ジフェンヒドラミン67gとプロムワレリル尿素2
78gを大豆油350gに真空乳化機で均一に分散させ
たものをゼラチンとグリセリン混合物(重量比; 10
:3) 305 gを、その倍量の熱湯に溶かして脱気
し、平面上に薄く伸ばした膜で包み込んだ長径13.Q
llm、短径7.5ms、1力プセル重量180m+の
ソフトカプセル1kgを富士産業(株)製ドリアコータ
ーに仕込んだ、80℃の熱水90m1にシュガーエステ
ル31670を5g分散させ、攪拌しながら冷却させ、
常温にした。そこに温水で液状にしたd!−メントール
5gを加えながら攪拌、乳化させてメントール乳化液を
得た。
Example 1 67 g of diphenhydramine hydrochloride and 2 ml of promvalerylurea
A mixture of gelatin and glycerin (weight ratio: 10
:3) 305 g was dissolved in twice the amount of boiling water, degassed, and wrapped in a thin film stretched on a flat surface with a length of 13. Q
llm, minor axis 7.5 ms, and 1 kg of soft capsules with a single force weight of 180 m+ were placed in a doria coater manufactured by Fuji Sangyo Co., Ltd., 5 g of sugar ester 31670 was dispersed in 90 ml of 80° C. hot water, and the mixture was cooled while stirring.
I kept it at room temperature. I liquefied it with warm water d! - A menthol emulsion was obtained by stirring and emulsifying while adding 5 g of menthol.

このメントール乳化液20gに精製水69Kを加え、こ
れにプルラン[井原化学(株)製のPI−20]10g
を溶かし、更にグリセリン1gを加えてプルラン−メン
トールコーティング組成物を得た。このコーティング組
成物を用いて、それぞれ1カプセル当り固形分で5■の
コーテイング量に達するまでコーティングを行なった。
Add 69K purified water to 20g of this menthol emulsion, and add 10g of pullulan [PI-20 manufactured by Ibara Chemical Co., Ltd.].
was dissolved, and 1 g of glycerin was further added to obtain a pullulan-menthol coating composition. Using this coating composition, coating was carried out until a coating weight of 5 μm solids per capsule was reached.

 コーテイング後は、40℃、40%で3日間静置乾燥
させた。
After coating, it was left to dry at 40° C. and 40% for 3 days.

実施例2〜7 表1の処方のプルラン−メントールコーティング組成物
を用いたほかは実施例1と同様にして、ソフトカプセル
のコーティングを行なった。
Examples 2 to 7 Soft capsules were coated in the same manner as in Example 1, except that a pullulan-menthol coating composition having the formulation shown in Table 1 was used.

表1 七の結果、外観的に光沢感を失わない均一なフィルムコ
ーティングが可能となった。
As a result of Table 1, it became possible to achieve a uniform film coating that did not lose its glossy appearance.

崩壊時間は17〜18分であり、日周の基準に適合して
いた。
The disintegration time was 17-18 minutes, meeting diurnal standards.

試験例1[経時変化試験] (検体) 検体1;実施例2で得られたソフトカプセルを20個使
用した。
Test Example 1 [Temporal Change Test] (Sample) Sample 1: 20 soft capsules obtained in Example 2 were used.

検体2;対照品として下記の処方のコーテイング液を用
いてコーティングしたソフトカプセルを20個使用した
Specimen 2: As a control product, 20 soft capsules coated with a coating liquid having the following formulation were used.

(処方) PC−L メントール シュガーエステルS グリセリン 精製水 10重量% 1!!量% 70 1重量% 1重量% 87重量% (試験方法) 検体1,2を8kgビンに入れ、40℃75%RHに3
ケ月保存し、各検体の外観、崩壊およびメントールの残
存率を測定した。
(Formulation) PC-L Menthol Sugar Ester S Glycerin Purified Water 10% by weight 1! ! Amount% 70 1% by weight 1% by weight 87% by weight (Test method) Samples 1 and 2 were placed in an 8kg bottle and heated to 40°C and 75%RH.
The samples were stored for several months, and the appearance, disintegration, and menthol residual rate of each sample were measured.

(結果) 1、外観 凝集、軟化、光沢感の劣化は認められなかった。(result) 1. Appearance No aggregation, softening, or deterioration of glossiness was observed.

2、崩壊性 直後品と変わらない崩壊性を示した。2. Disintegrability It showed the same disintegration properties as the freshly prepared product.

3、メントールの安定性 メントールの定量は、水素炎式のガスクロマトグラフィ
ーにより行なった。その結果は、表2に示す通り、直後
品とかわらない安定性を保持していた。
3. Stability of menthol Menthol was determined by hydrogen flame gas chromatography. As shown in Table 2, the results showed that the product maintained the same stability as the product immediately after use.

表2Table 2

Claims (1)

【特許請求の範囲】 1)香料を含有させたプルラン溶液に5〜30重量%の
多価アルコールを含有することを特徴としたソフトカプ
セル用コーティング剤。 2)プルランをコーティング基剤中に8〜12重量%配
合した請求項1に記載のソフトカプセル用コーティング
剤。 3)香料が油性香料であり、油性香料1重量部に対し、
界面活性剤0.1〜10重量部を配合した請求項1また
は請求項2に記載のソフトカプセル用コーティング剤。 4)界面活性剤が、高HLBのシュガーエステルである
請求項3に記載のソフトカプセル用コーティング剤。
[Scope of Claims] 1) A coating agent for soft capsules, characterized in that a pullulan solution containing a fragrance contains 5 to 30% by weight of polyhydric alcohol. 2) The coating agent for soft capsules according to claim 1, wherein 8 to 12% by weight of pullulan is blended into the coating base. 3) The fragrance is an oily fragrance, and for 1 part by weight of the oily fragrance,
The coating agent for soft capsules according to claim 1 or 2, which contains 0.1 to 10 parts by weight of a surfactant. 4) The coating agent for soft capsules according to claim 3, wherein the surfactant is a high HLB sugar ester.
JP63280978A 1987-11-09 1988-11-07 Perfume-containing coating agent for soft capsule Pending JPH02205A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63280978A JPH02205A (en) 1987-11-09 1988-11-07 Perfume-containing coating agent for soft capsule

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP28283187 1987-11-09
JP62-282831 1987-11-09
JP63280978A JPH02205A (en) 1987-11-09 1988-11-07 Perfume-containing coating agent for soft capsule

Publications (1)

Publication Number Publication Date
JPH02205A true JPH02205A (en) 1990-01-05

Family

ID=26554009

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63280978A Pending JPH02205A (en) 1987-11-09 1988-11-07 Perfume-containing coating agent for soft capsule

Country Status (1)

Country Link
JP (1) JPH02205A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998001134A1 (en) * 1996-07-10 1998-01-15 Novartis Consumer Health S.A. Oral pharmaceutical combinations of antihistaminic compounds and terpenoids
US6165615A (en) * 1997-07-30 2000-12-26 Takasago International Corporation Gradual-releasing capsule and method for manufacturing the same
JP2002012541A (en) * 2000-06-29 2002-01-15 Taiyo Yakuhin Kogyo Kk Film coating composition and odorproof solid preparation using the same
US6887307B1 (en) 1999-07-22 2005-05-03 Warner-Lambert Company, Llc Pullulan film compositions
DE10138990B4 (en) * 2001-08-15 2005-07-28 Simon Kara cane
KR100832740B1 (en) * 2007-01-17 2008-05-27 한국과학기술원 Mutant microorganism with improved productivity of branched amino acid and method for preparing it using the same
WO2008069262A1 (en) * 2006-12-07 2008-06-12 Daiichi Sankyo Company, Limited Film-coated preparation having improved stability

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55104212A (en) * 1979-02-01 1980-08-09 Heumann Ludwig & Co Gmbh Method of thermally stabilizing and improving size uniformity of soft gelatine capsule containing medicine active ingredient in shell

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55104212A (en) * 1979-02-01 1980-08-09 Heumann Ludwig & Co Gmbh Method of thermally stabilizing and improving size uniformity of soft gelatine capsule containing medicine active ingredient in shell

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998001134A1 (en) * 1996-07-10 1998-01-15 Novartis Consumer Health S.A. Oral pharmaceutical combinations of antihistaminic compounds and terpenoids
US6165615A (en) * 1997-07-30 2000-12-26 Takasago International Corporation Gradual-releasing capsule and method for manufacturing the same
US6887307B1 (en) 1999-07-22 2005-05-03 Warner-Lambert Company, Llc Pullulan film compositions
US7267718B2 (en) 1999-07-22 2007-09-11 Warner-Lambert Company, Llc Pullulan film compositions
JP2002012541A (en) * 2000-06-29 2002-01-15 Taiyo Yakuhin Kogyo Kk Film coating composition and odorproof solid preparation using the same
JP4681713B2 (en) * 2000-06-29 2011-05-11 大洋薬品工業株式会社 Film coating composition and deodorant solid preparation using the same
DE10138990B4 (en) * 2001-08-15 2005-07-28 Simon Kara cane
WO2008069262A1 (en) * 2006-12-07 2008-06-12 Daiichi Sankyo Company, Limited Film-coated preparation having improved stability
JPWO2008069262A1 (en) * 2006-12-07 2010-03-25 第一三共株式会社 Film coating formulation with improved stability
KR100832740B1 (en) * 2007-01-17 2008-05-27 한국과학기술원 Mutant microorganism with improved productivity of branched amino acid and method for preparing it using the same

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