JPH05238954A - Carrier suitable for chewing administration - Google Patents

Carrier suitable for chewing administration

Info

Publication number
JPH05238954A
JPH05238954A JP4075149A JP7514992A JPH05238954A JP H05238954 A JPH05238954 A JP H05238954A JP 4075149 A JP4075149 A JP 4075149A JP 7514992 A JP7514992 A JP 7514992A JP H05238954 A JPH05238954 A JP H05238954A
Authority
JP
Japan
Prior art keywords
weight
parts
carrier
chewing
fatty acid
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
JP4075149A
Other languages
Japanese (ja)
Other versions
JP3136310B2 (en
Inventor
Yuka Itou
有香 伊藤
Masahito Takahashi
雅人 高橋
Hiroyuki Mochizuki
弘之 望月
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.)
Toyo Capsule Co Ltd
Original Assignee
Toyo Capsule 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 Toyo Capsule Co Ltd filed Critical Toyo Capsule Co Ltd
Priority to JP04075149A priority Critical patent/JP3136310B2/en
Publication of JPH05238954A publication Critical patent/JPH05238954A/en
Application granted granted Critical
Publication of JP3136310B2 publication Critical patent/JP3136310B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a carrier, capable of being chewed and administered without causing an oily taste or touch and useful for a medicine, etc., sealed in a soft capsule. CONSTITUTION:The objective carrier, useful for a medicine or a food material and suitable for chewing administration is characterized in that it is composed of 50-99 pts.wt. uniformly mixed edible oil and 1-20 pts.wt. surfactant having 1-20HLB.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、医薬品又は食品のため
の、薬物又は食品素材を担持することができ且つ咀嚼し
て服用するに適した担体に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a carrier for medicines or foods, which can carry a drug or food material and is suitable for chewing.

【0002】[0002]

【従来の技術】従来、医薬品の分野において、薬物を服
用するための担体としてソフトカプセルが用いられてい
る。ソフトカプセルは主として、油状の薬物等のよう
な、散剤や錠剤、硬カプセル剤等の通常の剤形には適さ
ずしかも服用毎の定量採取の困難な薬物を所定量服用す
るための担体である。しかし、ソフトカプセルは通常肉
厚であるため寸法が大型になる傾向があり、そのままで
は嚥下しにくく、患者によっては服用が容易でない場合
がある。このため、服用者はソフトカプセルを噛み潰す
ことにより服用を容易化せんと試みる場合があるが、従
来のソフトカプセルは噛み潰すと非常に油っぽい又は苦
い味覚及び感触を与えるため、通常そのまま飲み込まざ
るを得なかった。
2. Description of the Related Art Conventionally, in the field of pharmaceuticals, soft capsules have been used as carriers for taking drugs. Soft capsules are mainly carriers for taking a predetermined amount of a drug, such as an oily drug, which is not suitable for a usual dosage form such as powders, tablets, hard capsules, etc., and which is difficult to quantitatively collect for each dose. However, since soft capsules are usually thick and tend to be large in size, they are difficult to swallow as they are and may not be easy to take depending on the patient. For this reason, the user may try to facilitate the administration by chewing soft capsules, but conventional soft capsules give a very greasy or bitter taste and feel when chewed, and thus they must be swallowed as they are. I didn't get it.

【0003】[0003]

【発明が解決しようとする課題】本発明は、このような
状況に鑑み、薬物又は食品素材のための担体であって、
咀嚼しても油っぽさの等の不快な味覚や感触を与えるこ
とがなく、容易に咀嚼して嚥下することのできる、特に
ソフトカプセル内への封入に適した担体を提供すること
を目的とする。更に本発明は、ソフトカプセルへの封入
を要しない固形の担体の提供をも目的とする。
In view of such a situation, the present invention provides a carrier for a drug or food material,
The object of the present invention is to provide a carrier that does not give an unpleasant taste or feel such as oiliness even when chewed, can be easily chewed and swallowed, and is particularly suitable for encapsulation in a soft capsule. To do. Another object of the present invention is to provide a solid carrier that does not require encapsulation in soft capsules.

【0004】[0004]

【課題を解決するための手段】本発明者は、ソフトカプ
セルに封入される担体の有する物性と噛み潰したときに
それが口腔内に与える感触との関係について種々検討し
た。その結果、食用油と所定の界面活性剤との所定の組
合せによって、咀嚼してもかかる味覚・感触を与えるこ
とのない材質であって、医薬品等を担持してソフトカプ
セルに封入するに適し、一層広い製剤形態をも可能にす
る担体が得られることを見出し、更に検討を加えて本発
明を完成した。
Means for Solving the Problems The present inventor has conducted various studies on the relationship between the physical properties of a carrier encapsulated in a soft capsule and the feel it gives to the oral cavity when chewed. As a result, a predetermined combination of edible oil and a predetermined surfactant is a material that does not give such a taste and feel even when chewed, and is suitable for carrying a drug or the like and encapsulating it in a soft capsule. It was found that a carrier that enables a wide range of dosage forms can be obtained, and further studies were conducted to complete the present invention.

【0005】すなわち本発明は、まず、食用油50乃至
99重量部及びHLB(親水性疎水性バランス)が1乃
至20の界面活性剤1乃至20重量部よりなることを特
徴とする、ソフトカプセルに封入して咀嚼服用するに適
した薬物又は食品素材のための半流動性の液状の担体で
ある。該担体はまた、3重量部までの甘味料を含有させ
て味覚を更に改善することができ、それによっても担体
としての能力は維持できる。
That is, according to the present invention, first, 50 to 99 parts by weight of edible oil and 1 to 20 parts by weight of a surfactant having an HLB (hydrophilic / hydrophobic balance) of 1 to 20 are encapsulated in a soft capsule. It is a semi-fluid liquid carrier for a drug or food material suitable for chewing. The carrier may also contain up to 3 parts by weight of sweetener to further improve the taste and thereby maintain its capacity as a carrier.

【0006】更に、本発明の担体はゼラチンを20重量
部まで含有してなることができ、そうすることによっ
て、ゼラチン量に依存して、常温で半流動体乃至固形の
咀嚼服用に適した担体とすることができる。半流動体の
場合にはゼラチンを含まない場合と同様にソフトカプセ
ルに封入することができるほか、チューブに注入した形
態で使用することができ、固形の場合には例えば直方
体、球形等の適宜の形状としてそのまま咀嚼服用するこ
とができる。但し、必ずしもこれらの形態に限定されな
い。
Furthermore, the carrier of the present invention may contain up to 20 parts by weight of gelatin, whereby a carrier suitable for chewing, which is semi-fluid or solid at room temperature, depends on the amount of gelatin. Can be In the case of a semi-liquid, it can be enclosed in a soft capsule as in the case of not containing gelatin, and it can be used in the form of being injected into a tube. It can be taken as it is by chewing. However, it is not necessarily limited to these forms.

【0007】加えて、本発明の担体は、ゼラチン量を適
宜調節して適当な硬さを与えることにより、それ自身カ
プセルを形成することもできる。このカプセルに本発明
の所望の硬さ又は流動性の担体を封入すれば、従来の軟
カプセル及び硬カプセルと類似の形態を有する医薬品で
あってしかも咀嚼服用に適したものを提供することもで
きる。
In addition, the carrier of the present invention can itself form a capsule by appropriately adjusting the amount of gelatin to give an appropriate hardness. By encapsulating the carrier having the desired hardness or fluidity of the present invention in this capsule, it is possible to provide a drug having a form similar to that of conventional soft capsules and hard capsules, which is also suitable for chewing. ..

【0008】本発明の担体に薬物又は食品素材を担持さ
せるには、加熱融解した本発明の担体にこれら薬物等を
単に溶解又は分散させて担持させればよく、それにより
半流動性乃至固形の咀嚼服用に適した混合物を得ること
ができる。これを上述の通り、軟カプセル、チューブ等
に封入し又は所望の形状に成形して医薬品又は食品とす
ることができる。
In order to support the drug or food material on the carrier of the present invention, the drug or the like may be simply dissolved or dispersed and supported on the carrier of the present invention which has been melted by heating. A mixture suitable for chewing can be obtained. As described above, it can be enclosed in a soft capsule, a tube, or the like or molded into a desired shape to prepare a medicine or food.

【0009】本発明において使用し得る食用油の例とし
ては、動植物油、エステル類等があり、このうち、植物
油が好ましく、特に炭素数6乃至12の中鎖脂肪酸トリ
グリセリドが好ましい。
Examples of the edible oil which can be used in the present invention include animal and vegetable oils, esters and the like. Among them, vegetable oil is preferable, and medium chain fatty acid triglyceride having 6 to 12 carbon atoms is particularly preferable.

【0010】本発明においてはHLB1乃至20の界面
活性剤が使用できるが、より好ましくはHLBは3乃至
8である。適当な界面活性剤としては、多価アルコー
ル、ポリエチレングリコール、動植物成分等があるが、
このうち、糖エステル、グリセリンアシルエステル、ソ
ルビタンアシルエステル、ポリオキシエチレンソルビタ
ンアシルエステルが好ましく、特にグリセリン脂肪酸エ
ステル、ショ糖脂肪酸エステルが好ましい。
In the present invention, a surfactant having an HLB of 1 to 20 can be used, and more preferably, the HLB is 3 to 8. Suitable surfactants include polyhydric alcohols, polyethylene glycol, animal and plant components,
Among these, sugar ester, glycerin acyl ester, sorbitan acyl ester, and polyoxyethylene sorbitan acyl ester are preferable, and glycerin fatty acid ester and sucrose fatty acid ester are particularly preferable.

【0011】上記食用油と界面活性剤との使用比率は、
上記食用油50乃至99重量部に対し上記界面活性剤1
乃至20重量部であるが、更に好ましくは、上記食用油
50乃至99重量部に対して上記界面活性剤1乃至15
重量部であり、特に好ましくは、上記食用油70乃至9
9重量部に対して上記界面活性剤5乃至15重量部であ
る。
The use ratio of the above-mentioned edible oil and surfactant is
1 to 50 parts by weight of the edible oil to 1 part of the surfactant
The amount of the surfactant is 1 to 15 parts by weight, more preferably 50 to 99 parts by weight of the edible oil.
Parts by weight, and particularly preferably the edible oils 70 to 9
The amount of the surfactant is 5 to 15 parts by weight based on 9 parts by weight.

【0012】甘味料としては、食品や医薬品に通常使用
されている物である限り特に制限はない。
The sweetener is not particularly limited as long as it is a commonly used sweetener in foods and pharmaceuticals.

【0013】本発明の担体に担持されるべき薬物として
は、本発明の担体との混合によって不安定化等の不都合
を生じないものであり、且つ口中で咀嚼することに問題
のない内服用薬物であれば特に制限されない。また、食
品素材としては、加工食品に含まれうる種々の材料を担
持させることができる。
The drug to be loaded on the carrier of the present invention does not cause instability such as destabilization by mixing with the carrier of the present invention, and is a drug for oral administration which has no problem in chewing in the mouth. If there is no particular limitation. Further, as the food material, various materials that can be included in the processed food can be supported.

【0014】[0014]

【実施例】以下、実施例に基づき本発明を更に詳細に説
明する。 〔実施例1〕 処方 中鎖脂肪酸トリグリセリド 88重量部 グリセリン脂肪酸エステル(HLB3) 8重量部 ショ糖脂肪酸エステル(HLB15) 2重量部 アスパルテーム 1重量部 ハッカ油 1重量部 合 計 100重量部 中鎖脂肪酸トリグリセリドにグリセリン脂肪酸エステル
を加え、60〜70℃の水浴上で加温し溶解する。これ
にショ糖脂肪酸エステル、アスパルテーム及びハッカ油
を加えて攪拌し、カプセル内容液を製する。この液を常
法に従い軟カプセル被膜に充填し軟カプセル剤を得る。
The present invention will be described in more detail based on the following examples. [Example 1] Prescription Medium-chain fatty acid triglyceride 88 parts by weight Glycerine fatty acid ester (HLB3) 8 parts by weight Sucrose fatty acid ester (HLB15) 2 parts by weight Aspartame 1 part by weight Mint oil 1 part by weight Total 100 parts by weight Medium-chain fatty acid triglyceride Glycerin fatty acid ester is added to and heated in a water bath at 60 to 70 ° C. to dissolve. Sucrose fatty acid ester, aspartame and peppermint oil are added to this and stirred to prepare a capsule content liquid. This solution is filled into a soft capsule film according to a conventional method to obtain a soft capsule agent.

【0015】〔実施例2〕 処方 中鎖脂肪酸トリグリセリド 88重量部 グリセリン脂肪酸エステル(HLB6) 10重量部 アスパルテーム 1重量部 ハッカ油 1重量部 合 計 100重量部 中鎖脂肪酸トリグリセリドにグリセリン脂肪酸エステル
を加え、60〜70℃の水浴上で加温し溶解する。これ
にアスパルテーム及びハッカ油を加えて攪拌し、半流動
体の液を製する。この液を常法に従い軟カプセル被膜に
充填し、軟カプセル剤を得る。又は別に、この液をチュ
ーブに充填して製品とする。
Example 2 Formulation Medium chain fatty acid triglyceride 88 parts by weight Glycerine fatty acid ester (HLB6) 10 parts by weight Aspartame 1 part by weight Mint oil 1 part by weight Total 100 parts by weight Glycerin fatty acid ester was added to medium chain fatty acid triglyceride, Dissolve by heating on a water bath at 60 to 70 ° C. Aspartame and peppermint oil are added to this and stirred to prepare a semi-fluid liquid. This solution is filled into a soft capsule film according to a conventional method to obtain a soft capsule. Alternatively, a tube is filled with this liquid to obtain a product.

【0016】〔実施例3〕 処方 中鎖脂肪酸トリグリセリド 78重量部 グリセリン脂肪酸エステル 10重量部 アスパルテーム 1重量部 ハッカ油 1重量部 ゼラチン 10重量部 合 計 100重量部 中鎖脂肪酸トリグリセリドにグリセリン脂肪酸エステル
を加え、60〜70℃の水浴上で加温し溶解する。これ
にアスパルテーム、ハッカ油及び加温溶解したゼラチン
を加えて攪拌する。この液を型に流し込み、成型、乾燥
する。
Example 3 Formulation Medium chain fatty acid triglyceride 78 parts by weight Glycerine fatty acid ester 10 parts by weight Aspartame 1 part by weight Mint oil 1 part by weight Gelatin 10 parts by weight Total 100 parts by weight Glycerin fatty acid ester is added to medium chain fatty acid triglyceride , Warm on a water bath at 60-70 ° C to dissolve. Aspartame, peppermint oil, and warmed and dissolved gelatin are added to this and stirred. This liquid is poured into a mold, molded and dried.

【0017】〔各実施例の製剤の咀嚼適性の評価〕実施
例1乃至3の製剤を口中で咀嚼したところ、清涼感と甘
味が感じられたが、基剤特有の油っぽい味覚及び感触は
感じられず、咀嚼して服用するに適する製剤であること
が確認された。
[Evaluation of Chewing Ability of Preparations of Each Example] When the preparations of Examples 1 to 3 were chewed in the mouth, a refreshing feeling and sweetness were felt, but the oily taste and feel peculiar to the base were It was not felt, and it was confirmed that the preparation was suitable for chewing.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 A61K 47/36 F 7433−4C ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area A61K 47/36 F 7433-4C

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】均一に混合された食用油50乃至99重量
部及びHLBが1乃至20の界面活性剤1乃至20重量
部よりなることを特徴とする、薬物又は食品素材のため
の咀嚼服用に適した担体。
1. A chewable dose for a drug or food material, which comprises 50 to 99 parts by weight of a uniformly mixed edible oil and 1 to 20 parts by weight of a surfactant having an HLB of 1 to 20. Suitable carrier.
【請求項2】均一に混合された食用油50乃至99重量
部、HLBが1乃至20の界面活性剤1乃至20重量部
及び最大で3重量部までの甘味料よりなることを特徴と
する、薬物又は食品素材のための咀嚼服用に適した担
体。
2. A uniform mixture of edible oil 50 to 99 parts by weight, 1 to 20 parts by weight of HLB 1 to 20 parts by weight and up to 3 parts by weight of a sweetener. A chewable carrier suitable for drugs or food materials.
【請求項3】ゼラチンを更に含んでなることを特徴とす
る、請求項1又は2に記載の担体。
3. The carrier according to claim 1, which further comprises gelatin.
【請求項4】固形物であることを特徴とする、請求項3
に記載の担体。
4. A solid material according to claim 3, wherein the solid material is a solid material.
The carrier according to.
【請求項5】薬物又は食品素材を溶解させ又は分散させ
て担持したことを特徴とする、請求項1乃至4のいずれ
かに記載の担体。
5. The carrier according to any one of claims 1 to 4, wherein the drug or food material is dissolved or dispersed and carried.
【請求項6】ソフトカプセルに封入されていることを特
徴とする、請求項1乃至5のいずれかに記載の担体。
6. The carrier according to claim 1, wherein the carrier is encapsulated in a soft capsule.
JP04075149A 1992-02-26 1992-02-26 Carriers suitable for chewing clothing Expired - Fee Related JP3136310B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP04075149A JP3136310B2 (en) 1992-02-26 1992-02-26 Carriers suitable for chewing clothing

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP04075149A JP3136310B2 (en) 1992-02-26 1992-02-26 Carriers suitable for chewing clothing

Publications (2)

Publication Number Publication Date
JPH05238954A true JPH05238954A (en) 1993-09-17
JP3136310B2 JP3136310B2 (en) 2001-02-19

Family

ID=13567858

Family Applications (1)

Application Number Title Priority Date Filing Date
JP04075149A Expired - Fee Related JP3136310B2 (en) 1992-02-26 1992-02-26 Carriers suitable for chewing clothing

Country Status (1)

Country Link
JP (1) JP3136310B2 (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000051570A1 (en) * 1999-02-26 2000-09-08 Shionogi & Co., Ltd. Chewable soft capsules having improved administration properties and process for producing the same
FR2850275A1 (en) * 2003-01-24 2004-07-30 Scherer Technologies Inc R P Chewable soft capsules for oral administration of unpleasant tasting active agents, e.g. ibuprofen, comprise dispersion of coated active agent in lipophilic carrier contained in capsule shell
JP2005082594A (en) * 2003-09-04 2005-03-31 Boehringer Ingelheim Internatl Gmbh Pharmacological composition for masking bitterness
JP2005529128A (en) * 2002-04-25 2005-09-29 バナー ファーマキャップス, インコーポレーテッド Chewable soft capsule
JP2007051115A (en) * 2005-08-19 2007-03-01 Riken Vitamin Co Ltd Liposoluble medicament composition
JP2015155384A (en) * 2014-02-20 2015-08-27 アリメント工業株式会社 Composition to be filled in soft capsule and soft capsule filled with composition to be filled in soft capsule
US9539205B2 (en) 2006-01-25 2017-01-10 Ayanda Group As Emulsion
US9724296B2 (en) 2008-10-08 2017-08-08 Vitux Group As Chewable gelled emulsions

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7763276B1 (en) 1999-02-26 2010-07-27 Shionogi & Co., Ltd. Chewable soft capsules having improved administration properties and process for producing the same
WO2000051570A1 (en) * 1999-02-26 2000-09-08 Shionogi & Co., Ltd. Chewable soft capsules having improved administration properties and process for producing the same
US8372428B2 (en) 1999-02-26 2013-02-12 Shionogi & Co., Ltd. Chewable soft capsule having improved ingestion property and method for producing same
US9072677B2 (en) 2002-04-25 2015-07-07 Banner Life Sciences Llc Chewable soft capsules
US8414916B2 (en) 2002-04-25 2013-04-09 Banner Pharma Caps, Inc. Chewable soft capsule
US9861586B2 (en) 2002-04-25 2018-01-09 Patheon Softgels, LLC Chewable soft capsules
JP2005529128A (en) * 2002-04-25 2005-09-29 バナー ファーマキャップス, インコーポレーテッド Chewable soft capsule
US8097279B2 (en) 2002-04-25 2012-01-17 Banner Pharmacaps Inc. Chewable soft capsule
US8241665B2 (en) 2002-04-25 2012-08-14 Banner Pharmacaps, Inc. Chewable soft capsule
US9668976B2 (en) 2002-04-25 2017-06-06 Banner Life Sciences, LLC Chewable soft capsules
US8765174B2 (en) 2002-04-25 2014-07-01 Banner Pharmacaps Inc. Chewable soft capsule
FR2850275A1 (en) * 2003-01-24 2004-07-30 Scherer Technologies Inc R P Chewable soft capsules for oral administration of unpleasant tasting active agents, e.g. ibuprofen, comprise dispersion of coated active agent in lipophilic carrier contained in capsule shell
EP1592402A4 (en) * 2003-01-24 2009-01-14 Scherer Technologies Inc R P Dispersion of taste masked crystals or granules of active substances, chewable soft capsules filled with said dispersion, and process for preparing same
JP2005082594A (en) * 2003-09-04 2005-03-31 Boehringer Ingelheim Internatl Gmbh Pharmacological composition for masking bitterness
JP2007051115A (en) * 2005-08-19 2007-03-01 Riken Vitamin Co Ltd Liposoluble medicament composition
US9539205B2 (en) 2006-01-25 2017-01-10 Ayanda Group As Emulsion
US9724296B2 (en) 2008-10-08 2017-08-08 Vitux Group As Chewable gelled emulsions
JP2015155384A (en) * 2014-02-20 2015-08-27 アリメント工業株式会社 Composition to be filled in soft capsule and soft capsule filled with composition to be filled in soft capsule

Also Published As

Publication number Publication date
JP3136310B2 (en) 2001-02-19

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