JPS58194810A - Coated soft miniature capsule - Google Patents

Coated soft miniature capsule

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Publication number
JPS58194810A
JPS58194810A JP7704482A JP7704482A JPS58194810A JP S58194810 A JPS58194810 A JP S58194810A JP 7704482 A JP7704482 A JP 7704482A JP 7704482 A JP7704482 A JP 7704482A JP S58194810 A JPS58194810 A JP S58194810A
Authority
JP
Japan
Prior art keywords
capsule
soft
coated
coating
minicapsules
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
JP7704482A
Other languages
Japanese (ja)
Inventor
Takashi Morishita
森下 孝
Shinsuke Sonoi
園井 伸輔
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 JP7704482A priority Critical patent/JPS58194810A/en
Publication of JPS58194810A publication Critical patent/JPS58194810A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To prepare the titled soft miniature capsule capable of effectively suppressing the deterioration of the skin and the content of the capsule with time, without lowering the commercial value nor giving unagreeable feeling to the palate, by coating a filled soft miniature capsule with a powder coating layer and an overcoating layer. CONSTITUTION:A soft miniature capsule 2 having a diameter of <=5mm. and containing the content 1, especially a capsule obtained by treating a filled soft miniature capsule having a skin containing (A) gelatin, (B) a water-soluble polyhydric alcohol or its water-soluble derivative and (C) a low methoxyl pectin or sodium alginate with the compound capable of causing gelation of the aqueous solution of the component (C), is coated with the powder coating layer 3 and an overcoating layer 4 to obtain the objective coated soft miniature capsule. The miniaturization of the capsule 2 and the double-layer coating (3, 4) of the capsule result in the above advantages, and accordingly, the capsule is suitable as food, drink, candy or drug.

Description

【発明の詳細な説明】 本発明は複層状コーティング軟ミニカプセルに関する。[Detailed description of the invention] The present invention relates to multilayer coated soft minicapsules.

従来からカプセル化された種々の食品等が広く出回って
いる。特に流体状の比較的飲食しにくい食物や服用しに
くい医薬等はシームレスの軟カプセル化した後、外側に
糖衣等のコーティングを施して口当たりをよくして製品
化している。
BACKGROUND ART Conventionally, various encapsulated foods and the like have been widely available. In particular, liquid foods that are relatively difficult to eat or drink, and medicines that are difficult to take are made into products by encapsulating them into seamless soft capsules and then applying a coating such as sugar coating to the outside to make them more palatable.

しかしながら従前からこの種の食品等に使用されている
軟カプセルは粒径が比較的大きい(約8〜lomyn)
のため(従来のカプセル化技術ではミニカプセル化は困
難であった〕、糖衣等のコーティングを施すとカプセル
全体が更に大きくなり、商品価値を低下さぜたり、摂取
に際して口の中でカプセルが潰れた時に比較的多量の内
容物が口内に一度にひろがるので不快な感触を味う等の
欠点がある。
However, the soft capsules traditionally used for this type of food have a relatively large particle size (approximately 8~lomyn).
(Mini-capsules are difficult to achieve with conventional encapsulation technology); applying a coating such as sugar coating will make the entire capsule even larger, lowering its commercial value and causing the capsule to collapse in the mouth when ingested. There are disadvantages such as a relatively large amount of the contents being spread in the mouth at once, resulting in an unpleasant sensation.

また、従来の軟カプセル化食品等ではカプセルの皮膜自
体が経時的に変質し不溶化したり味が悪くなったりして
糖衣等のコーティング効果を低下または相殺するばかり
でなく、皮膜が軟弱なためにコーティング処理そのもの
がおこないにくい等の難点がある。
In addition, with conventional soft encapsulated foods, the capsule film itself deteriorates over time, becoming insolubilized or having a bad taste, which not only reduces or offsets the coating effect of sugar coating, etc., but also because the film is weak. There are some drawbacks, such as the fact that the coating process itself is difficult to perform.

本発明者は充填物を含有するカプセルを軟ミニカプセル
化し、これを複層状にコーティングする軟誉萱得られる
ことを究明し本発明を完成した。
The present inventor has completed the present invention by discovering that it is possible to obtain a soft capsule by converting a capsule containing a filler into a soft mini-capsule and coating the capsule in a multi-layered manner.

即ぢ本発明は第1図の模式的縦断面図に示すように、充
填物(1)を含有した軟ミニカプセル(2)を覆った粉
末被覆層(3)を上掛は被覆層(4)で覆ったコーティ
ング軟ミニカプセルに関する。
As shown in the schematic longitudinal cross-sectional view of FIG. ) about coated soft minicapsules.

本発明に使用する軟ミニカプセルの皮膜物質は特に限定
的ではないが、好適なものはfa)ゼラチン、(1))
水溶性多価アルコールまたはその水溶性誘導体およびi
c)低メトキシルペクチンまたはアルギン酸ナトリウム
を含有する基材を低メトキシルペクチンまたはアルギン
酸ナトリウムの水溶液をケル化し得る化合物で処理して
得られるもので、以下これについてさらに詳述する。
The coating material for the soft minicapsules used in the present invention is not particularly limited, but preferred ones are fa) gelatin, (1))
Water-soluble polyhydric alcohol or its water-soluble derivative and i
c) It is obtained by treating a base material containing low methoxyl pectin or sodium alginate with a compound capable of kelizing an aqueous solution of low methoxyl pectin or sodium alginate, which will be described in more detail below.

軟ミニカプセルの材料のうち、ゼラチンおよび水溶性多
価アルコールまたはその水溶性誘導体は従来のカプセル
の製造に用いられるグレードのものをそのまま使用すれ
はよい。
Among the materials for the soft minicapsules, gelatin and water-soluble polyhydric alcohols or water-soluble derivatives thereof may be of the same grade as used in the production of conventional capsules.

水溶性多価アルコールまたはその水溶性誘導体としては
グリセリン、ポリグリセリン、ソルビット、エチレング
リコール、ポリエチレングリコール、プロピレングリコ
ール、ポリプロピレングリコーノペ酸化エチレン−酸化
プロピレン共重合イ札オリゴサツカライド、シュガーエ
ステル、グリセリド、ソルビタンエステル類等が例示さ
れるが、これに限定されるものではない。
Examples of water-soluble polyhydric alcohols or their water-soluble derivatives include glycerin, polyglycerin, sorbitol, ethylene glycol, polyethylene glycol, propylene glycol, polypropylene glycol, ethylene oxide-propylene oxide copolymerized oligosaccharide, sugar ester, glyceride, Examples include, but are not limited to, sorbitan esters.

通常ゼラチンの使用量はカプセル皮膜総市匿の60〜9
0重敗%、好ましくは低メi・キシルペクチンを使用す
るときは65〜75重阻%、アルギン酸ナトリウムを使
用するときは65〜85重計%であり、また水溶性多価
アルコールまたはその水溶性誘導体の使用量は皮膜総重
量の10〜30重量%、好ましくは15〜25重量%で
ある。
Normally, the amount of gelatin used is 60 to 9 for the capsule coating.
0 weight percent, preferably 65 to 75 weight percent when using low Me xyl pectin, and 65 to 85 weight percent when using sodium alginate, and water-soluble polyhydric alcohol or its water-soluble The amount of the sexual derivative used is 10 to 30% by weight, preferably 15 to 25% by weight of the total weight of the film.

一方、低メトキシルペクチンは分子量200,000以
」二、メトキシル化度1〜6%、奸才しくは3.5〜5
%のものが好適でこれらは→J−ンキスト社等から入手
し得るものを適宜使用すればよく、その使用量は皮膜総
重量の5〜20重量%、好ましくは10〜15重量%で
、20重量%より多いときは軟カプセル製造そのものが
困難となり、また5重量%より少ないときは耐水性が悪
くなる。
On the other hand, low methoxyl pectin has a molecular weight of 200,000 or more, a degree of methoxylation of 1 to 6%, and a degree of methoxylation of 3.5 to 5.
% is preferable, and those available from →J-Nquist Co., Ltd. may be used as appropriate, and the amount used is 5 to 20% by weight, preferably 10 to 15% by weight, and 20 to 20% by weight of the total weight of the film. When it is more than 5% by weight, it becomes difficult to produce soft capsules, and when it is less than 5% by weight, water resistance becomes poor.

アルギン酸ナトリウムを用いる場合のその使用線は皮膜
総重量の1〜10重N%、好ましくは3〜5重討%で、
10重量%より多いとき、あるいは1重量%より少ない
ときはそれぞれ低メトキシルペクチンに関して述べたと
同様の欠点があられれる。
When using sodium alginate, its usage range is 1 to 10% by weight, preferably 3 to 5% by weight, based on the total weight of the film.
When the amount is more than 10% by weight or less than 1% by weight, the same drawbacks as mentioned for low methoxyl pectin occur, respectively.

さらに、低メトキシルペクチンまたはアルギン酸カルシ
ウムの水溶液をゲル化し得る化合物としては2価ないし
それ以上の多価金属の塩、特に低メトキシルペクチンの
場合はカルシウム、マグネシウム等の水溶性塩類、アル
ギン酸すトリウムの場合は典型的には水溶性カルシウム
塩、例えば塩化力ルンウム、りん酸カルシウム等を適宜
使用すればよい。
Furthermore, compounds that can gel an aqueous solution of low methoxyl pectin or calcium alginate include salts of divalent or higher polyvalent metals, especially water-soluble salts such as calcium and magnesium in the case of low methoxyl pectin, and water-soluble salts such as sodium alginate. Typically, a water-soluble calcium salt such as chloride, calcium phosphate, etc. may be used as appropriate.

本発明に係わる充填物含有軟ミニカプセルを調製するに
は、先ずゼラチンと水溶性多価アルコールまたはその水
溶性誘導体に低メトキシルペクチンまたはアルギン酸ナ
トリウムを前記の割合で配合し、これで被カプセル化物
である充填物を被覆してシームレス軟ミニカプセルを製
造する。このようなシームレス軟ミニカプセルは従来公
知の軟カプセル製造法に従って製造すればよい。
To prepare the filled soft minicapsules according to the present invention, first, gelatin and a water-soluble polyhydric alcohol or a water-soluble derivative thereof are blended with low methoxyl pectin or sodium alginate in the above ratio, and then the encapsulated material is Seamless soft minicapsules are produced by coating with certain fillings. Such seamless soft minicapsules may be manufactured according to conventionally known soft capsule manufacturing methods.

得られた充填物含有軟ミニカプセルは、低メトキシルペ
クチンまたはアルギン酸ナトリウムの水溶液をゲル化し
得る化合物溶液、典型的には該化合物の水溶液と接触さ
せる。被処理ミニカプセルは通常1〜10重量%、好ま
しくは3〜5重量%の該化合物の水溶液に5〜30℃、
好ましくは10〜15℃で1〜5分間、好ましくは1〜
3分間浸漬する。処理液の接触は浸漬法の外、噴霧法等
の他の方法によっておこなってもよいが、浸漬法が最も
簡便かつ均一に実施し得る方法である。
The resulting filled soft minicapsules are contacted with a solution of a compound capable of gelling, typically an aqueous solution of low methoxyl pectin or sodium alginate. The minicapsules to be treated are usually 1 to 10% by weight, preferably 3 to 5% by weight of an aqueous solution of the compound at 5 to 30°C.
Preferably at 10-15°C for 1-5 minutes, preferably 1-5 minutes.
Soak for 3 minutes. Contact with the treatment liquid may be carried out by other methods such as a spraying method in addition to the immersion method, but the immersion method is the method that can be carried out most easily and uniformly.

上記処理を施した軟ミニカプセルを次いで乾燥し−洗浄
すめことによって本発明に使用する充填物1含有1欺ミ
ニ力プセlしが1与られる。
The soft minicapsules subjected to the above treatment are then dried and washed to give one filler containing one filler used in the present invention.

1欧ミニカプセルの右t、を子は飼犬する光墳物−扮木
破復1曽および上長1け仮覆層の種類や用途等によって
変ILきぜてもよいが一5朋以−を−奸ましくは1〜5
mξ特に2〜411mとするのが一般的であるゎ包含す
るので一献ミニカプセルに封入する充填物のm=m1z
特に限定的ではlぐ一広範囲の飲俊物−1,1i7I2
1品−医薬等およr月二成分糸の反応性接看剤等」工業
的用途に応じて適宜選定すれはよい。
1. The right side of the European mini-capsule, the light tomb that the child keeps as a pet - the 15th anniversary of the 15th anniversary, which can be changed depending on the type and purpose of the temporary covering layer. - Preferably 1 to 5
In particular, mξ is generally set to 2 to 411 m.Since it includes mξ, m = m1z of the filling to be enclosed in the Ikken mini capsule.
Particularly limited to a wide range of drinks - 1,1i7I2
Items 1 - Pharmaceuticals, etc., reactive adhesives for bicomponent threads, etc. may be selected as appropriate depending on the industrial application.

」二記のようにして得られる充填物1含有軟ミニカプセ
ルの表面には一通常のパンコーチインク法又は流動層萌
粒法等の方法によって粉木破覆暦全設は−次いで常法に
よって該粉末破擦暦を糖衣寺の七IIけコーチインクす
ることによって本発明によるコー ティンク軟ミニカプ
セルが調製ヒれる。
The surface of the soft minicapsules containing the filler 1 obtained as described in Section 2 is coated with powder by a conventional method such as the pancoach ink method or the fluidized bed seeding method, and then by a conventional method. Coated soft minicapsules according to the present invention are prepared by coating the powdered powder with Koiji's Seven II Coated Ink.

ミニ II管管上セル被檀する粉末かまひ上用けの種類および
組合せも全く任意であり−カプセル充填物1と同様に広
範囲の飲食物、嗜好品、医薬等から用途に応じて適宜選
定すれはよい。
The type and combination of the powder to be used in the mini-II tube cell is completely arbitrary; similarly to capsule filling 1, it can be appropriately selected from a wide range of foods, drinks, luxury goods, medicines, etc. according to the purpose. Yes.

特に好適な態様として、カプセル内に油溶性成分を含有
させ、該カプセルを非油溶性粉末成分もしくはカプセル
内の成分と反応性の粉末成分で被覆し、該粉末被覆層を
上掛はコーティングすることによって摂取が容易で経時
的な変質の少ない種々の複合的な栄養価の高い飲食物、
嗜好性に富んだ嗜好品、薬効の優れた医薬等が調製され
る。
As a particularly preferred embodiment, an oil-soluble component is contained in a capsule, the capsule is coated with an oil-insoluble powder component or a powder component reactive with the component in the capsule, and the powder coating layer is coated as an overcoat. various complex nutritious foods and drinks that are easy to ingest and have little deterioration over time;
Luxury items with rich palatability, medicines with excellent medicinal effects, etc. are prepared.

例えばカプセル内に小麦胚芽油を含有させ、カプセルを
粉末状のビタミンCで被覆し、砂糖又は低カロリーンユ
ガ−で上掛はコーティングするこトニヨって健康食品が
得られ、カプセル内に香料を含有させ、カプセルを粉糖
で被覆し、砂糖で上掛はコーティングすることによって
香気に富んだ嗜好品が得られ、カプセル内に香料を含有
させ、カプセルを粉糖で被覆し、チョコレートで」−掛
はコーティングすることによって菓子が得られ、また、
カプセルビ」にビタミンAやビタミンE等の油溶性ビタ
ミンを含有させ、カプセルを粉末状のビタミンCで被覆
し、ショ糖又は低カロリーソユガーで」−掛はコーティ
ングすることによって複合ビタミン剤が得られる。
For example, a health food can be obtained by containing wheat germ oil in the capsule, coating the capsule with powdered vitamin C, and coating the top with sugar or low-calorie sugar, and containing flavoring in the capsule. By coating the capsule with powdered sugar and coating the top with sugar, a luxurious item rich in aroma can be obtained. Confectionery is obtained by coating, and
A multivitamin preparation can be obtained by adding oil-soluble vitamins such as vitamin A and vitamin E to capsules, coating the capsules with powdered vitamin C, and coating them with sucrose or low-calorie soyugat. .

以−にのように本発明によるコーティング軟ミニカプセ
ルは、カプセル自体がミニ化されているためにカプセル
表面上にさらに被覆層を設けても全体が大きくなって商
品価値を低下させたりすることはなく、また摂取に際し
て不快な感触を与えることも少なく、しかも、カプセル
が複層で被覆されるのでカプセル皮膜およびカプセル充
填物の経時的変質を効果的に抑制する等前記問題点を悉
く解消する。
As described above, since the coated soft minicapsules according to the present invention are miniaturized, even if an additional coating layer is provided on the capsule surface, the overall size will not increase and the commercial value will not be reduced. Furthermore, since the capsule is coated with multiple layers, it effectively suppresses deterioration of the capsule film and capsule filling over time, and all of the above problems are solved.

本発明は飲食物、嗜好品および医薬等において単一カプ
セル内に同時に封入できない成分あるいはカプセル化が
困難な成分とカプセル化成分を複合単一化する場合に特
に有効であり、これらの分野において多数の新規な形態
の摂取物を提供する。
The present invention is particularly effective when combining and unifying ingredients that cannot be encapsulated at the same time in a single capsule or ingredients that are difficult to encapsulate and encapsulated ingredients in foods, drinks, luxury goods, medicines, etc. A novel form of ingestion is provided.

以下、実施例によって本発明を説明する。The present invention will be explained below with reference to Examples.

実施例1 次の配合成分によって被覆液を調製した。Example 1 A coating solution was prepared using the following ingredients.

」L:L                重債部ゼラ
チン               14グリセリン 
             3低メトキンルペクチン 
         3゜精製水           
     8゜この被覆液を特開昭51−8875号公
報に記載の方法に従い、環状孔から押し出すと同時に環
状孔の同側に同心円状に設けられた内孔口から被カプセ
ル化物としてかんきつ系オイルと植物油の混合物(重り
比10ニア5)を押し出し、この複合ジェットを冷却液
(植物油、流動パラフィン等)中に放出し、粒径4wn
に造粒した(重量3oTng/P;充填物85重量%;
皮膜15重量%〕。
”L:L Heavy part gelatin 14 glycerin
3 low metquinlupectin
3゜purified water
8゜According to the method described in JP-A No. 51-8875, this coating liquid is extruded through the annular hole, and at the same time, citrus oil and citrus oil as the encapsulated material are extruded through the inner hole opening provided concentrically on the same side of the annular hole. A mixture of vegetable oils (weight ratio 10 nia 5) is extruded and this composite jet is ejected into a cooling liquid (vegetable oil, liquid paraffin, etc.) with a particle size of 4wn.
(weight 3oTng/P; filler 85% by weight;
Film: 15% by weight].

得られた充填物含有軟ミニカプセルを5%塩化カルシウ
ム水溶液(15℃〕に3分間浸漬し、次いで乾燥、洗浄
した。
The obtained filled soft minicapsules were immersed in a 5% aqueous calcium chloride solution (15° C.) for 3 minutes, then dried and washed.

このカプセル表面を、ビタミンC25重量%、粉糖25
重量%、香料1重量%、砂糖455重量およびアラビT
ゴム4重磁%がら成る混合物で厚さ2咽に被覆した(重
置240”’f/P)。
The surface of this capsule was coated with 25% by weight of vitamin C and 25% of powdered sugar.
% by weight, 1% by weight of flavoring, 455% by weight of sugar and Arabi T
It was coated to a thickness of 2 mm with a mixture consisting of 4% rubber (superposition 240''f/P).

この被覆カプセル上にさらに砂糖を厚さ0.5 mmに
上掛はコーティングすることによって複層状軟ミニカプ
セル化食品を調製した。
A multilayer soft mini-encapsulated food was prepared by further coating the coated capsules with sugar to a thickness of 0.5 mm.

実施例2 被覆液を次の配合処方によって調製する以外は実施例1
と同様にして複層状軟ミニカプセル化食品を調製した。
Example 2 Example 1 except that the coating liquid was prepared according to the following formulation.
A multi-layered soft mini-encapsulated food was prepared in the same manner as above.

成 分              重量部ゼラチン 
              13.3グリセリン  
           5.7アルギン酸ナトリウム 
        1精製水             
  80
Ingredients Part by weight Gelatin
13.3 Glycerin
5.7 Sodium alginate
1 purified water
80

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明による複層状のコーティング軟ミニカプ
セル〆の模式的縦断面図である。 (1)はカプセル充填物、(2)はカプセル皮膜、(3
)は粉末被覆層、(4)は上掛はコーティング層を示す
。 特許出願人練下仁丹株式会社 代理人弁理士青山葆ほか1名 第1図 58−
FIG. 1 is a schematic longitudinal cross-sectional view of a multilayer coated soft minicapsule according to the present invention. (1) is capsule filling, (2) is capsule membrane, (3
) indicates a powder coating layer, and (4) indicates a coating layer. Patent applicant Renshita Jintan Co., Ltd. Representative patent attorney Aoyama Hao and one other person Figure 1 58-

Claims (1)

【特許請求の範囲】 1、充填物(1)を含有した軟ミニカプセル(2)を、
粉末被覆層(3)および上掛は被覆層(4)で覆ったコ
ーティング軟ミニカプセル。 2、充填物を含有した軟ミニカプセルが、(a)ゼラチ
ン、(b)水溶性多価アルコールまたはその水溶性誘導
体および(C1低メトキシルペクチンまたはアルギン酸
す) IJウムを含有する皮膜を有する充填物含有軟ミ
ニカプセルを低メトキシルペクチンまたはアルギン酸ナ
トリウムの水溶液をゲル化し得る化合物で処理して得ら
れる充填物含有軟ミニカプセルである第1項記載のコー
ティング軟ミニカプセル。 3、軟ミニカプセルの粒径が5+o+以下である第1項
記載のコーティング軟ミニカプセル。 4、 コーチインク款ミニカプセルが飲食物、嗜好品ま
たは医薬である第1項記載のコーティング軟ミニカプセ
ル。
[Claims] 1. A soft minicapsule (2) containing a filler (1),
Coated soft minicapsules covered with a powder coating layer (3) and a coating layer (4). 2. A soft minicapsule containing a filling having a film containing (a) gelatin, (b) a water-soluble polyhydric alcohol or a water-soluble derivative thereof, and (C1 low methoxyl pectin or alginate) IJium. 2. The coated soft minicapsules according to claim 1, which are filled soft minicapsules obtained by treating the filled soft minicapsules with a compound capable of gelling an aqueous solution of low methoxyl pectin or sodium alginate. 3. The coated soft minicapsule according to item 1, wherein the soft minicapsule has a particle size of 5+o+ or less. 4. The coated soft minicapsule according to item 1, wherein the coach ink minicapsule is a food or drink, a luxury item, or a medicine.
JP7704482A 1982-05-07 1982-05-07 Coated soft miniature capsule Pending JPS58194810A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7704482A JPS58194810A (en) 1982-05-07 1982-05-07 Coated soft miniature capsule

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7704482A JPS58194810A (en) 1982-05-07 1982-05-07 Coated soft miniature capsule

Publications (1)

Publication Number Publication Date
JPS58194810A true JPS58194810A (en) 1983-11-12

Family

ID=13622772

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7704482A Pending JPS58194810A (en) 1982-05-07 1982-05-07 Coated soft miniature capsule

Country Status (1)

Country Link
JP (1) JPS58194810A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59157018A (en) * 1983-02-27 1984-09-06 Furointo Sangyo Kk Novel oil-containing coated capsule pperaration
JPH01313421A (en) * 1988-06-13 1989-12-18 Arimento Kogyo Kk Soft film capsule mixed with alginic acid and production thereof
EP0882449A1 (en) * 1997-06-03 1998-12-09 Uni Colloid Kabushiki Kaisha Sustained release capsule and method for preparing the same
WO2007075475A3 (en) * 2005-12-22 2007-12-13 Banner Pharmacaps Inc Gastric reflux resistant dosage forms
WO2009115446A1 (en) * 2008-03-20 2009-09-24 Gelita Ag Use of gelatin particles in powdered coating processes
WO2013031949A1 (en) * 2011-09-02 2013-03-07 富士フイルム株式会社 Soft capsule pharmaceutical preparation, composition for soft capsule pharmaceutical preparation, and method for producing soft capsule pharmaceutical preparation
WO2013093630A2 (en) 2011-12-22 2013-06-27 Pronova Biopharma Norge As Gelatin/alginate delayed release capsules comprising omega-3 fatty acids, and methods and uses thereof
WO2014034548A1 (en) * 2012-08-29 2014-03-06 フロイント産業株式会社 Method for producing seamless capsule
US9782374B2 (en) 2014-06-23 2017-10-10 Patheon Softgels Inc. All-natural enteric soft capsules

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59157018A (en) * 1983-02-27 1984-09-06 Furointo Sangyo Kk Novel oil-containing coated capsule pperaration
JPH01313421A (en) * 1988-06-13 1989-12-18 Arimento Kogyo Kk Soft film capsule mixed with alginic acid and production thereof
EP0882449A1 (en) * 1997-06-03 1998-12-09 Uni Colloid Kabushiki Kaisha Sustained release capsule and method for preparing the same
US6030641A (en) * 1997-06-03 2000-02-29 Uni Colloid Kabushiki Kaisha Sustained release capsule and method for preparing the same
US9693966B2 (en) 2005-12-22 2017-07-04 Banner Life Sciences Llc Gastric reflux resistant dosage forms
WO2007075475A3 (en) * 2005-12-22 2007-12-13 Banner Pharmacaps Inc Gastric reflux resistant dosage forms
US10182990B2 (en) 2005-12-22 2019-01-22 Patheon Softgels Inc. Gastric reflux resistant dosage forms
EP2716283A1 (en) * 2005-12-22 2014-04-09 Banner Pharmacaps Inc. Gastric reflux resistant dosage forms
US8962005B2 (en) 2005-12-22 2015-02-24 Banner Life Sciences Llc Gastric reflux resistant dosage forms
EP2923696A1 (en) * 2005-12-22 2015-09-30 Banner Life Sciences LLC Gastric reflux resistant dosage forms
US9192582B2 (en) 2005-12-22 2015-11-24 Banner Life Sciences Llc Gastric reflux resistant dosage forms
US8367147B2 (en) 2008-03-20 2013-02-05 Gelita Ag Use of gelatin particles in powdered coating processes
WO2009115446A1 (en) * 2008-03-20 2009-09-24 Gelita Ag Use of gelatin particles in powdered coating processes
WO2013031949A1 (en) * 2011-09-02 2013-03-07 富士フイルム株式会社 Soft capsule pharmaceutical preparation, composition for soft capsule pharmaceutical preparation, and method for producing soft capsule pharmaceutical preparation
WO2013093630A2 (en) 2011-12-22 2013-06-27 Pronova Biopharma Norge As Gelatin/alginate delayed release capsules comprising omega-3 fatty acids, and methods and uses thereof
US9456991B2 (en) 2011-12-22 2016-10-04 Erik Baes Gelatin/alginate delayed release capsules comprising omega-3 fatty acids, and methods and uses thereof
WO2014034548A1 (en) * 2012-08-29 2014-03-06 フロイント産業株式会社 Method for producing seamless capsule
US9782374B2 (en) 2014-06-23 2017-10-10 Patheon Softgels Inc. All-natural enteric soft capsules
US9987240B2 (en) 2014-06-23 2018-06-05 Patheon Softgels, Inc. All-natural enteric soft capsules
US10357467B2 (en) 2014-06-23 2019-07-23 Patheon Softgels, Inc. All-natural enteric soft capsules

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