JP2984105B2 - Soft capsule manufacturing equipment - Google Patents

Soft capsule manufacturing equipment

Info

Publication number
JP2984105B2
JP2984105B2 JP3236965A JP23696591A JP2984105B2 JP 2984105 B2 JP2984105 B2 JP 2984105B2 JP 3236965 A JP3236965 A JP 3236965A JP 23696591 A JP23696591 A JP 23696591A JP 2984105 B2 JP2984105 B2 JP 2984105B2
Authority
JP
Japan
Prior art keywords
soft capsule
film
bath
main
thickness
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.)
Expired - Lifetime
Application number
JP3236965A
Other languages
Japanese (ja)
Other versions
JPH0551315A (en
Inventor
孝之 深沢
隆 近藤
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.)
FUJI KAPUSERU KK
Original Assignee
FUJI KAPUSERU 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 FUJI KAPUSERU KK filed Critical FUJI KAPUSERU KK
Priority to JP3236965A priority Critical patent/JP2984105B2/en
Publication of JPH0551315A publication Critical patent/JPH0551315A/en
Application granted granted Critical
Publication of JP2984105B2 publication Critical patent/JP2984105B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Medical Preparation Storing Or Oral Administration Devices (AREA)
  • Cosmetics (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の技術分野】本発明は、溶解性の良い軟カプセ
ル型入浴剤を製造可能とする軟カプセル製造装置に関す
るものであり、更に詳しくは溶解性を高める為に、軟カ
プセル型入浴剤の皮膜を薄くしても皮膜の接着部分は厚
く均一な為に製品の強度を損なったり経時的に内容入浴
剤が漏れたりすることがない安定な軟カプセル型入浴剤
を製造可能とする軟カプセル製造装置に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an apparatus for producing a soft capsule-type bath preparation having good solubility, and more particularly to a soft capsule-type bath preparation for improving the solubility. A stable soft capsule-type bath agent that does not impair the strength of the product or leaks out of the bath agent over time because the bonded portion of the film is thick and uniform even if the film is thinned.
The present invention relates to a soft capsule manufacturing apparatus capable of manufacturing a soft capsule.

【0002】[0002]

【従来の技術】一般に、浴槽に1粒〜2粒投入すると浴
湯によりゼラチン等の水溶性高分子を基剤とする皮膜が
溶解し、内容入浴剤を放出し、美肌及び保湿効果をもた
らす処の軟カプセル型入浴剤は、1回の使用量が定量化
し易い点や包装を破らずにそのままの形で浴槽に投入で
きる点、又、ホホバ油、オリ−ブ油、ビタミンE等の美
肌及び保湿効果をもたらす油脂や様々の香料成分を粉末
化せずにそのままの形で配合出来る点で優れており、特
に肌への皮脂補給を期待する高齢者や、芳香効果ボディ
−トリ−トメント効果を期待する女性には根強い人気を
博している。
2. Description of the Related Art Generally, when one or two tablets are put into a bath, a bath based on a water-soluble polymer such as gelatin dissolves in the bath water to release the contents of the bath additive, thereby providing a beautiful skin and a moisturizing effect. The soft capsule type bath preparation of the present invention is characterized in that it is easy to quantify the amount used at one time, that it can be put into a bathtub as it is without breaking the packaging, that it has beautiful skin such as jojoba oil, olive oil, vitamin E, etc. It is excellent in that oils and fats and various fragrance ingredients that provide a moisturizing effect can be blended as they are without powdering, especially for elderly people who expect to supply sebum to the skin, and for the fragrance effect body-treatment effect. Women who expect it are gaining popularity.

【0003】ところが、現行の軟カプセル型入浴剤は皮
膜の溶解性が十分でない為に浴湯に投入後、内容入浴剤
を放出してから皮膜が完全に溶解するまでに8〜10分
程度かかり、このことが使用感を阻害する場合があっ
た。従来、軟カプセル型入浴剤は次の如く製造される。
(図11)(特公昭61−12698号)即ち、ゼラチ
ン等を基剤とする皮膜液を加温して溶液状態とし、それ
を冷却ゲル化させ、フィルム状に成形した皮膜1を1対
の噛合回転する円筒型成形金型2の両側より狭間に送る
ように成してある。3は内容液4を貯溜したポンプ器筺
であり、前記円筒型成形金型2と連動するピストン5で
該内容液4を前記両側一対のフィルム状皮膜1の間に圧
入する。しかる時、該ポンプ器筺3によりフィルム状皮
膜1は適温に熱せられる為、円筒型成形金型2の表面に
形成される凸状の歯と歯の圧切によりヒ−トシ−ルされ
カプセル本体6が成形される。
However, since the current soft capsule type bath agent has insufficient solubility of the film, it takes about 8 to 10 minutes from the release of the content bath agent to the complete dissolution of the film after being poured into bath water. However, this sometimes hindered the usability. Conventionally, a soft capsule-type bath agent is produced as follows.
(FIG. 11) (JP-B-61-12698) That is, a coating solution based on gelatin or the like is heated to a solution state, which is cooled and gelled, and a film 1 formed into a film is formed into a pair. The cylindrical molding die 2 that is engaged and rotated is fed in a narrower space than both sides. Reference numeral 3 denotes a pump housing in which the content liquid 4 is stored, and a piston 5 interlocking with the cylindrical molding die 2 presses the content liquid 4 between the pair of film-like films 1 on both sides. At this time, the film-like film 1 is heated to an appropriate temperature by the pump housing 3, so that the capsule body 6 is heat-sealed by pressing the convex teeth formed on the surface of the cylindrical molding die 2 and the teeth. Is molded.

【0004】上記従来の装置で製造される場合、フィル
ム状皮膜1は図12に示すように円筒型成形金型2の回
転方向へ引っぱられながら切断されるため成形後のカプ
セルの接着部は図13に示すように接着部8及び9の厚
みが一定にならず特にカプセル側の接着部ではフィ
ルム状皮膜1が下方へ引っぱられながら切断される為該
接着部が局部的に薄くなる事が多い。これまで経験的
に接着部(8、9)の厚さは乾燥時には最低0.1mm
以上なければ経時的に内容入浴剤の液漏れを招来する可
能性が高い事が知られている為、軟カプセル型入浴剤製
造時、接着部(8、9)の厚さを最低0.1mm以上と
なるようにフィルム状皮膜の厚さを設定する必要があ
り、前述した接着部(8、9)が局部的に薄くなること
を考慮すると充填時におけるフィルム状皮膜1の厚さを
0.9mm以上としなければならず軟カプセル型入浴剤
のカプセル総重量中に占める皮膜重量の割合、即ち、皮
膜率が10%を越えてしまい、又、皮膜厚さは0.2m
mを越えてしまうが、軟カプセル型入浴剤の浴湯への溶
解性を向上せしめる為に単に皮膜を薄くする事はできな
かった。
When manufactured by the above-mentioned conventional apparatus, the film-like film 1 is cut while being pulled in the rotation direction of the cylindrical mold 2 as shown in FIG. adhesive portion 8 for the thickness of the bonding portion 8 and 9 the adhesive portion 8, the film-like coating one particular capsule upper side not fixed is cut while being pulled downwards, as shown in 13 is locally thinned There are many things. Experience has shown that the thickness of the bonded parts (8, 9) is at least 0.1 mm when dry.
Otherwise, it is known that there is a high possibility of causing leakage of the bath salt content with time, so that the thickness of the bonding portion (8, 9) should be at least 0.1 mm at the time of manufacturing the soft capsule bath bath agent. It is necessary to set the thickness of the film-like film so as to be as described above. Considering that the above-mentioned bonded portions (8, 9) are locally thinned, the thickness of the film-like film 1 at the time of filling is set to 0.1. The ratio of the coating weight to the total weight of the capsule of the soft capsule type bath agent, that is, the coating ratio exceeds 10%, and the coating thickness is 0.2 m
m, but the film could not simply be thinned in order to improve the solubility of the soft capsule-type bath agent in the bath water.

【0005】又、医薬品や健康食品の軟カプセル剤の溶
解性を高める技術としては、様々な方法が提案されてい
る。例えば皮膜を形成するゼラチンにポリぺプチドを添
加する方法(特公昭60−9011)や同様にゼラチン
に対し酒石酸やクエン酸等の有機酸を添加する方法であ
る。しかし、これ等の技術はいずれも軟カプセル型入浴
剤には採用できない。なぜなら、前者の方法はゲル化能
がないポリぺプチドを皮膜の成分として添加する点で、
又、後者の方法はゼラチンが酸により加水分解されてし
まう点で共に製造された軟カプセル剤の強度が低下して
しまうからである。軟カプセル型入浴剤は医薬品、健康
食品等の経口目的の軟カプセルに比べ大型な製品が多く
カプセルの総重量が2g〜10gと重い為、強度的に不
十分である事は該軟カプセル型入浴剤の製造中あるいは
輸送中等におけるカプセルの割れ及び内容物の漏れ等を
誘発する可能性が高くなるため、これ等の通常の軟カプ
セル剤について提案された従来の技術は採用出来ないの
である。
Various techniques have been proposed as a technique for improving the solubility of soft capsules for pharmaceuticals and health foods. For example, a method of adding a polypeptide to gelatin for forming a film (Japanese Patent Publication No. 60-9011) or a method of similarly adding an organic acid such as tartaric acid or citric acid to gelatin. However, none of these techniques can be adopted for soft capsule type bath salts. This is because the former method adds a non-gelling polypeptide as a component of the film.
Also, in the latter method, the strength of the soft capsules produced together decreases because gelatin is hydrolyzed by acid. Soft capsule type baths are often large in size compared to soft capsules intended for oral use such as pharmaceuticals and health foods, and the total weight of the capsules is as heavy as 2 g to 10 g. Since the possibility of inducing capsule breakage and leakage of contents during the production or transportation of the capsule becomes high, conventional techniques proposed for these ordinary soft capsules cannot be adopted.

【0006】[0006]

【発明が解決しようとする課題】本発明が解決しようと
する課題は、軟カプセル型入浴剤に於いて、強度的に十
分であり、製造中又は輸送中等におけるカプセルの割れ
及び内容物の漏れ等の心配がなく、浴湯に投入した時の
溶解性を従来の製品よりも格段に向上させる点にある。
The problem to be solved by the present invention is to provide a soft capsule-type bath preparation which has sufficient strength and is capable of cracking capsules and leaking contents during production or transportation. There is no concern about this, and the point is that the solubility when poured into bath water is significantly improved as compared with conventional products.

【0007】[0007]

【課題を解決するための手段】尚、以下に説明する本発
明のカプセル製造装置は、軟カプセル型入浴剤の製造に
のみ限定使用されるものではなく、それ以外の他の充填
内容物を有する軟カプセルの製造にも使用されるもので
あることは勿論である。先ず、図1〜図5に基づいて説
明する。Pは本発明に係わるロ−タリ−式自動軟カプセ
ル製造機本体であり、円筒型成形金型20の表面には、
軟カプセル打抜き用の凹状型11を有する複数の独立し
た環状の主歯体12が縦横に適宜配設してある。11A
は貫通孔である。13は前記主歯体12と主歯体12と
の間に凸状に形成した副歯体(連続状態)で、その歯高
hは、主歯体12の歯高Hの50%〜100%程度が好
ましい。即ち、h=50〜100×H(%)である。通
常、この歯高hは歯高H以下であれば特に制限はない
が、均一な厚さの接着部を得るために上記の数値が良
い。
The capsule manufacturing apparatus of the present invention described below is not limited to the use of a soft capsule type bath preparation, but has other filling contents. Of course, it is also used for the production of soft capsules. First, a description will be given based on FIGS. P is a rotary-type automatic soft capsule manufacturing machine main body according to the present invention.
A plurality of independent annular main teeth 12 having concave molds 11 for punching soft capsules are appropriately arranged vertically and horizontally. 11A
Is a through hole. Reference numeral 13 denotes a sub-tooth body (continuous state) formed between the main tooth body 12 and the main tooth body 12 in a convex shape. The tooth height h is 50% to 100% of the tooth height H of the main tooth body 12. The degree is preferred. That is, h = 50-100 × H (%). Usually, the tooth height h is not particularly limited as long as it is equal to or less than the tooth height H, but the above numerical values are good in order to obtain a bonded portion having a uniform thickness.

【0008】次に図6〜図8について説明する。この実
施例の円筒型成形金型20の場合は副歯体13Aは1個
1個の主歯体12を独立して環状に取り囲んでいる(独
立状態)。この環状の副歯体13Aは主歯体12を一重
に囲撓しているが二重、三重・・・に取り囲んでも良
く、又環状が円形以外の他の形状でも良い。しかして、
前記した図3の場合は副歯体13は主歯体12と主歯体
12との間に単数しか形成されないが、図7の場合には
副歯体13Aが複数個形成されることとなる。
Next, FIGS. 6 to 8 will be described. In the case of the cylindrical molding die 20 of this embodiment, the sub-tooth bodies 13A independently surround each of the main tooth bodies 12 in an annular manner (independent state). The annular sub-tooth body 13A wraps around the main tooth body 12 in a single manner, but may surround the main tooth body 12 in a double, triple,..., Or the annular shape may be other than circular. Then
In the case of FIG. 3 described above, only one auxiliary tooth body 13 is formed between the main tooth body 12 and the main tooth body 12, but in the case of FIG. 7, a plurality of auxiliary tooth bodies 13A are formed. .

【0009】本発明に於いて円筒型成形金型20により
回転方向に引っぱられるフィルム状皮膜Fは、図4及び
図8に示す如く主歯体12間に形成した凸状を成す副歯
体(13、13A)によって接着面に押し入れられなが
ら打ち抜き用の凸状の主歯体12によって圧切されるた
め、従来の方法にみられた接着部が局部的に薄くなる事
がなく、均一な厚さの接着部(図9に示される14、1
5)が得られる。このため、従来の方法では接着厚さが
0.1mm以上となるように充填時に於いて、0.9m
m以上に設定されたフィルム状皮膜厚さが本発明では
0.9mm未満の任意の厚さに設定できる様になった。
In the present invention, the film-like film F which is pulled in the rotational direction by the cylindrical molding die 20 has a convex sub-tooth (formed between the main teeth 12 as shown in FIGS. 4 and 8). 13, 13A), while being pressed into the bonding surface by the convex main tooth body 12 for punching, the bonding portion seen in the conventional method is not locally thinned, and has a uniform thickness. Bonding portions (14, 1 shown in FIG. 9)
5) is obtained. For this reason, in the conventional method, at the time of filling, the bonding thickness becomes 0.9 mm or more.
In the present invention, the thickness of the film-like film set to m or more can be set to an arbitrary thickness of less than 0.9 mm.

【0010】しかし、本発明で示される適正な製造時の
フィルム状皮膜厚さtは0.4mm〜0.7mmであ
る。いわゆる皮膜率が4%〜8%であり、この場合、フ
ィルム状皮膜厚さが0.4mm以下、換言すれば製品時
の皮膜率が4%以下であってもカプセル化は可能である
が、製品の強度や保存安定性が損なわれる可能性があり
又皮膜厚さが0.8mm〜0.9mmでは本発明者らが
目的とするところの溶解性の向上が十分に達成出来ない
からである。製造時、フィルム状皮膜厚さを0.4mm
〜0.7mmに調整された軟カプセル型入浴剤は、製品
時の皮膜率が4%〜8%であり、本発明製品Qたる軟カ
プセル型入浴剤の皮膜厚さは0.2mm以下とすること
ができる。
However, the appropriate film thickness t at the time of production shown in the present invention is 0.4 mm to 0.7 mm. The so-called film ratio is 4% to 8%. In this case, encapsulation is possible even if the film-like film thickness is 0.4 mm or less, in other words, the film ratio at the time of the product is 4% or less. This is because the strength and storage stability of the product may be impaired, and if the film thickness is 0.8 mm to 0.9 mm, the improvement in solubility intended by the present inventors cannot be sufficiently achieved. . At the time of manufacture, the thickness of the film-like film is 0.4 mm
The soft capsule type bath agent adjusted to ~ 0.7 mm has a coating rate of 4% to 8% at the time of the product, and the film thickness of the soft capsule type bath agent as the product Q of the present invention is 0.2 mm or less. be able to.

【0011】[0011]

【実施例】次に、実施例、比較例、評価例によって本発
明を具体的に説明する。 実施例 (1)ゼラチン100kg,グリセリン30kg,精製
水95kgを70℃で3時間加熱撹拌して水溶液とし、
真空脱気した後60℃に保った保温釜に入れ、軟カプセ
ル型入浴剤用の皮膜剤とした。 (2)前述の図1〜図5で示した本発明のロータリー式
自動軟カプセル製造機本体Pを用いて(1)の皮膜剤を
冷却ゲル化させ0.5mm厚のフィルム状皮膜とした
後、常法により界面活性剤を主成分とするバスオイルを
被包成形し、内容量8gのラウンド160型軟カプセル
型入浴剤を得た。
Next, the present invention will be specifically described with reference to examples, comparative examples, and evaluation examples. Example (1) 100 kg of gelatin, 30 kg of glycerin, and 95 kg of purified water were heated and stirred at 70 ° C. for 3 hours to form an aqueous solution.
After deaeration in vacuum, the mixture was placed in a heat-retaining pot maintained at 60 ° C. to obtain a film for a soft capsule type bath agent. (2) Using the rotary automatic soft capsule manufacturing machine main body P of the present invention shown in FIGS. 1 to 5, the coating agent of (1) is cooled and gelled to form a 0.5 mm thick film-like film. A bath oil containing a surfactant as a main component was encapsulated and formed by a conventional method to obtain a round 160-type soft capsule-type bath agent having an internal capacity of 8 g.

【0012】比較例 (1)実施例(1)の精製水を70kgとする他は実施
例(1)と同様な処方、方法にて皮膜剤を調整した。 (2)前述の図11で示した特公昭61−12698号
ロータリー式自動軟カプセル製造装置を用いて比較例
(1)の皮膜剤を冷却ゲル化させ0.9mm厚のフィル
ム状皮膜とした後、常法により実施例(2)と同様なバ
スオイルを被包成型し、内容量8gのラウンド160型
入浴剤を得た。
Comparative Example (1) A coating agent was prepared in the same manner as in Example (1) except that the amount of purified water in Example (1) was changed to 70 kg. (2) JP-B-61-12698 shown in FIG.
The gelling agent of Comparative Example (1) was cooled and gelled to form a film having a thickness of 0.9 mm using a rotary type automatic soft capsule manufacturing apparatus of (1), and the same bath oil as in Example (2) was applied by a conventional method. Encapsulation molding was performed to obtain a round 160 type bath agent having an internal capacity of 8 g.

【0013】評価例 (1)接着厚さ測定 実施例及び比較例の軟カプセル型入浴剤の中心部を図1
0の如く切断し、実体顕微鏡にてA〜D各々の部位の厚
さを測定した。このとき、A及びBは接着部を示し、C
及びDは皮膜部を示す。上記結果を表1に示す。n=1
0の意味は同一種類のカプセル剤を10個採用し、各々
1回づつ延べ10回の試験を行ったことである。
Evaluation Examples (1) Measurement of Adhesive Thickness FIG. 1 shows the center part of the soft capsule-type bath preparations of Examples and Comparative Examples.
It cut | disconnected like 0, and measured the thickness of each part of A-D with a stereoscopic microscope. At this time, A and B indicate the bonding parts, and C
And D indicate a film portion. The results are shown in Table 1. n = 1
The meaning of 0 means that ten capsules of the same kind were employed, and each test was performed ten times in total.

【0014】[0014]

【表1】 [Table 1]

【0015】表1により示された如く実施例の軟カプセ
ル型入浴剤は比較例のそれに比べ接着部は厚く皮膜部は
薄かった。
As shown in Table 1, the soft capsule type bath preparation of the example had a thicker adhesive portion and a thinner film portion as compared with the comparative example.

【0016】(2)溶解試験 1リットルのビ−カ−に800mlの湯を入れ37±1
℃に保ち、その中に実施例及び比較例の軟カプセル型入
浴剤を入れヤマト化学(株)製のマグネチックスタ−ラ
−M41にて直径8mmφ長さ2.5cmの攪拌子を最
高回転(約1000rpm)にして攪拌した。この時、
該軟カプセル型入浴剤が内容入浴剤を放出し始める時間
を開口時間、皮膜が完全に溶解するまでの時間を溶解時
間として測定した。上記結果を表2に示す。
(2) Dissolution test Pour 800 ml of hot water into a 1 liter beaker, 37 ± 1
C., and the soft capsule-type bathing agents of Examples and Comparative Examples were placed therein, and the magnetic stirrer having a diameter of 8 mm and a length of 2.5 cm with a magnetic stirrer M41 manufactured by Yamato Chemical Co., Ltd. was rotated at the maximum speed ( (About 1000 rpm) and stirred. At this time,
The time when the soft capsule type bathing agent began to release the content bathing agent was measured as the opening time, and the time until the film was completely dissolved was measured as the dissolving time. Table 2 shows the results.

【0017】[0017]

【表2】 [Table 2]

【0018】表2に示した様に実施例の軟カプセル型入
浴剤は比較例のそれに比べ開口時間は同等であったが溶
解に要する時間は1/3以下であった。
As shown in Table 2, the opening time of the soft capsule type bathing agent of the example was equivalent to that of the comparative example, but the time required for dissolution was 1/3 or less.

【0019】(3)強度測定 木屋式硬度計を用いて実施例及び比較例の軟カプセル型
入浴剤を圧縮して破裂した時の該入浴剤に加わった圧力
を破戒強度(kg)として測定した結果を表3に示す。
(3) Strength Measurement The pressure applied to the soft-capsule type bath preparations of Examples and Comparative Examples when the bath preparations were compressed and ruptured was measured as breaking strength (kg) using a Kiya type hardness tester. Table 3 shows the results.

【0020】[0020]

【表3】 [Table 3]

【0021】以上の評価例によって、本発明の軟カプセ
ル型入浴剤は従来の軟カプセル型入浴剤に比べて3倍以
上速く溶解するにも拘らず強度的に劣る事はなかった。
又、経時的に内容液の漏れの原因になる接着部の局部的
な薄さがみられない為、保存安定性が従来品に比べて向
上する事が示唆された。
According to the above evaluation examples, the soft capsule-type bath preparation of the present invention was not inferior in strength in spite of dissolving more than three times faster than the conventional soft capsule-type bath preparation.
In addition, it was suggested that the storage stability was improved as compared with the conventional product because the local thinness of the adhesive portion causing the leakage of the liquid content with time was not observed.

【0022】[0022]

【発明の効果】以上説明したように、本発明では従来の
軟カプセル型入浴剤に比べて、製品の強度や保存安定性
を損なう事なく浴湯に投入した時の溶解性を格段に向上
させることができた。
As described above, in the present invention, as compared with the conventional soft capsule-type bath preparation, the solubility when the product is put into bath water without significantly impairing the strength and storage stability of the product is remarkably improved. I was able to.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明に係わるカプセル製造機本体の概略全体
図である。
FIG. 1 is a schematic overall view of a capsule manufacturing machine main body according to the present invention.

【図2】本発明の円筒型成形金型の斜視図である。FIG. 2 is a perspective view of a cylindrical mold according to the present invention.

【図3】図2のX−X線部分の拡大断面図である。FIG. 3 is an enlarged cross-sectional view taken along a line XX of FIG. 2;

【図4】本発明の図3の主歯体と副歯体との関係を示す
要部の拡大縦断正面図である。
FIG. 4 is an enlarged longitudinal sectional front view of a main part showing a relationship between a main tooth body and an auxiliary tooth body of FIG. 3 of the present invention.

【図5】主歯体と副歯体との歯高の関係を示す拡大説明
図である。
FIG. 5 is an enlarged explanatory view showing a relationship between tooth heights of a main tooth body and an auxiliary tooth body.

【図6】他の実施例の円筒型成型金型の斜視図である。FIG. 6 is a perspective view of a cylindrical mold according to another embodiment.

【図7】図6のY−Y線部分の拡大断面図である。FIG. 7 is an enlarged sectional view taken along line YY of FIG. 6;

【図8】図7に於ける主歯体と副歯体との関係を示す要
部の拡大縦断正面図である。
FIG. 8 is an enlarged longitudinal sectional front view of a main part showing a relationship between a main tooth body and an auxiliary tooth body in FIG. 7;

【図9】本願品の拡大縦断正面図である。FIG. 9 is an enlarged vertical sectional front view of the product of the present application.

【図10】本願品の拡大縦断正面図であって接着厚さ及
び皮膜厚さを測定する部位を示してある。
FIG. 10 is an enlarged vertical sectional front view of the product of the present application, showing a portion for measuring an adhesive thickness and a film thickness.

【図11】従来装置の説明図である。FIG. 11 is an explanatory diagram of a conventional device.

【図12】従来装置の要部の拡大縦断正面図である。FIG. 12 is an enlarged vertical sectional front view of a main part of a conventional device.

【図13】従来品の拡大縦断正面図である。FIG. 13 is an enlarged vertical sectional front view of a conventional product.

【符号の説明】[Explanation of symbols]

20・・・円筒型成形金型 11・・・凹状型 12・・・主歯体 13・・・副歯体 13A・・・副歯体 Q・・・本発明製品 20 ... Cylindrical molding die 11 ... Concave mold 12 ... Main tooth body 13 ... Secondary tooth body 13A ... Secondary tooth body Q: Product of the present invention

Claims (4)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 円筒型成形金型の表面に、複数の主歯体
を形成すると共に、該主歯体間に副歯体を連続状態に形
成した軟カプセル製造装置。
1. A soft capsule manufacturing apparatus in which a plurality of main teeth are formed on the surface of a cylindrical molding die, and sub-teeth are continuously formed between the main teeth.
【請求項2】 円筒型成形金型の表面に、複数の主歯体
を形成すると共に、該主歯体を取り囲んで副歯体を独立
状態に形成した軟カプセル製造装置。
2. A soft capsule manufacturing apparatus in which a plurality of main teeth are formed on a surface of a cylindrical molding die, and auxiliary teeth are formed independently around the main teeth.
【請求項3】 請求項1又は2の記載に於いて、副歯体
の歯高hを主歯体の歯高Hの50〜100%に成した軟
カプセル製造装置。
3. The soft capsule manufacturing apparatus according to claim 1 , wherein the tooth height h of the sub-tooth is 50 to 100% of the tooth height H of the main tooth.
【請求項4】 請求項の記載に於いて副歯体を二重三
重…に取り巻いて形成した軟カプセル製造装置。
4. An apparatus for producing a soft capsule according to claim 2 , wherein said auxiliary teeth are formed in a double triple.
JP3236965A 1991-08-23 1991-08-23 Soft capsule manufacturing equipment Expired - Lifetime JP2984105B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3236965A JP2984105B2 (en) 1991-08-23 1991-08-23 Soft capsule manufacturing equipment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP3236965A JP2984105B2 (en) 1991-08-23 1991-08-23 Soft capsule manufacturing equipment

Publications (2)

Publication Number Publication Date
JPH0551315A JPH0551315A (en) 1993-03-02
JP2984105B2 true JP2984105B2 (en) 1999-11-29

Family

ID=17008393

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3236965A Expired - Lifetime JP2984105B2 (en) 1991-08-23 1991-08-23 Soft capsule manufacturing equipment

Country Status (1)

Country Link
JP (1) JP2984105B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19642872C1 (en) 1996-10-17 1998-02-12 Henkel Kgaa Use of sterol sulphate compounds to inhibit serine protease
KR100459853B1 (en) * 2002-01-21 2004-12-04 주식회사 보창 Apparatus for supplying a medicine of manufacturing device for soft gelatine capsule
JPWO2013100013A1 (en) * 2011-12-28 2015-05-11 富士カプセル株式会社 Soft capsule film
KR20170076675A (en) 2014-10-31 2017-07-04 발린스 오르개닉 오일스, 엘.엘.씨. Method and apparatus for the manufacture of softgels

Also Published As

Publication number Publication date
JPH0551315A (en) 1993-03-02

Similar Documents

Publication Publication Date Title
US6197338B1 (en) Effervescent bath tablet, method of preparing it, and the use thereof
US6623751B2 (en) Cosmetic, pharmaceutical, or dermatological patch
AU2006322282B2 (en) Foam wafer containing a polyvinyl alcohol-polyethyleneglycol-graft copolymer
US4260596A (en) Edible unit dosage form consisting of outer mannitol shell and inner liquid or gel center and method for manufacturing the same
JP4870386B2 (en) Rapidly degradable administrable dosage forms for release of active ingredients in the oral cavity or body cavity
JP4969728B2 (en) Low friability mouth-scattering tablet and preparation method thereof
CA2567830C (en) Process for formulating fast dispersing dosage forms comprising at least one fish gelatin selected on the basis of molecular weight
US5827535A (en) Graphically impressed softgel and method for making same
JPH0579048B2 (en)
JPS61246120A (en) Floating long life releasable therapeutical composition
JPH09506268A (en) Method for labeling rapidly dissolving dosage forms
WO1998001113A1 (en) Lubrication assistant and process for the preparation of ethyl stearate used therein
RU2168980C2 (en) Solid pharmaceutical compositions containing (s)-2-(4-iso-butylphenyl)-propionic acid as active component and microcrystalline cellulose and colloidal silicon oxide
HU230033B1 (en) Composition containing n-acetyl-p-aminophenol
JP2984105B2 (en) Soft capsule manufacturing equipment
US20150140113A1 (en) Gelling agent-based dosage form
JPS5813510A (en) Solid medicine for oral administration
EP0330435A2 (en) Solid shampoo composition
JPH0713012B2 (en) Acetaminophen / gelatin capsule
JPH08333243A (en) Tablet having excellent touch in oral cavity
WO2011133911A1 (en) An effervescent carrier, a method of changing the flavor of milk, and an effervescent tablet for changing the flavor of milk
EP0227050B1 (en) Process for the preparation of single dosage administration forms, and administration forms thus obtained
KR20010075711A (en) Process for the manufacture of liquid filled capsules
US5888540A (en) Pharmaceutical products
CN100544709C (en) Antithrombotic chemical compound can be in mouth dispersive pharmaceutical composition

Legal Events

Date Code Title Description
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 19990914

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20080924

Year of fee payment: 9

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090924

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20090924

Year of fee payment: 10

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20100924

Year of fee payment: 11

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20110924

Year of fee payment: 12

EXPY Cancellation because of completion of term