JPH03232819A - Solid galenical, its production and system therefor - Google Patents

Solid galenical, its production and system therefor

Info

Publication number
JPH03232819A
JPH03232819A JP2026648A JP2664890A JPH03232819A JP H03232819 A JPH03232819 A JP H03232819A JP 2026648 A JP2026648 A JP 2026648A JP 2664890 A JP2664890 A JP 2664890A JP H03232819 A JPH03232819 A JP H03232819A
Authority
JP
Japan
Prior art keywords
galenical
split mold
state
mold
solid
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
JP2026648A
Other languages
Japanese (ja)
Other versions
JP2752493B2 (en
Inventor
Hikoshige Fujii
藤井 彦重
Tomoaki Mori
森 友昭
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.)
TOCHIMOTO TENKAIDOU KK
Original Assignee
TOCHIMOTO TENKAIDOU 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 TOCHIMOTO TENKAIDOU KK filed Critical TOCHIMOTO TENKAIDOU KK
Priority to JP2026648A priority Critical patent/JP2752493B2/en
Publication of JPH03232819A publication Critical patent/JPH03232819A/en
Application granted granted Critical
Publication of JP2752493B2 publication Critical patent/JP2752493B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Medicines Containing Plant Substances (AREA)

Abstract

PURPOSE:To obtain the solid galenical, a uniform compression-molded product excellent in shape retentivity without causing cracks or damages by charging a split mold with moderately dried chopped galenical followed by pressing, opening the mold under a pressed state and then releasing such state. CONSTITUTION:A quantitative feeder 3 is fed, through a belt conveyor 2, with moderately dried chopped galenical 1, and a given amount of the galenical 1 is put, using another quantitative feeder 4, into a split mold 5 brought to a closed state by both left and right cylinders. This galenical is then pressed vertically with a cylinder 6 followed by opening the split mold 5 while maintaining such pressed state and then releasing the pressed state, thus obtaining the objective solid galenical 7 consolidatedly integrated in a block form under uniform compressed state. With the present method, the decocting effect of the present galenical will be markedly improved, leading to increasing extract content and also high decreasing effect on viable cell number in general.

Description

【発明の詳細な説明】 [産業上の利用分野] この発明は固形生薬、及びその製造方法及び装置の改良
に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] This invention relates to solid herbal medicines, and improvements in their manufacturing methods and devices.

[従来の技術] 従来より、固形生薬を製造するため、種々の加圧成型法
が提案されている。
[Prior Art] Conventionally, various pressure molding methods have been proposed for producing solid herbal medicines.

例えば特開昭56−31756号は、両端が開口するシ
リンダー内に切断生薬を詰め、両端から2つのピストン
で圧縮する製造法である。
For example, Japanese Patent Application Laid-Open No. 56-31756 discloses a manufacturing method in which cut herbal medicine is packed in a cylinder with open ends and compressed with two pistons from both ends.

また特公昭63−26653号は、底板上に設けた方形
枠状金型に適度に乾燥した切断生薬を収納し、この収納
された切断生薬をピストン式の金属加圧板により加圧す
る製法を提案している。
In addition, Japanese Patent Publication No. 63-26653 proposed a manufacturing method in which moderately dried cut crude drugs were stored in a rectangular frame-shaped mold provided on the bottom plate, and the stored cut crude drugs were pressurized by a piston-type metal pressure plate. ing.

[発明が解決しようとする課題] しかしながらいずれの方法も、定型の型内に詰め込み圧
縮する方法であるため、加圧成型後の成型品の取り出し
は、型内から強制的に押し出さなければならず、しかも
加圧を解除すると、これに反発する成型品の内部圧力の
かかり方が、枠内壁に直接接触する部分とそうでない部
分とで異なり、成型品の取り出し方いかんでは割れや損
傷する場合もあった。特に加圧の程度が大きければ大き
い程、型内部に成型品が強固に詰まっており、その傾向
は増大し、取り出しは容易でなく、かつまた取り出しの
際、強制的に取り出すことから、成型品の外周部が損傷
し、固形生薬として必要不可欠な保形性に欠ける問題点
があった。従って従来の方法ではその圧縮の程度にも製
法上の点から自ずと限界があるのが実情であった。
[Problem to be solved by the invention] However, since both methods involve packing and compressing the material into a fixed mold, the molded product must be forcibly pushed out of the mold to take it out after pressure molding. Moreover, when the pressure is released, the internal pressure applied to the molded product will differ depending on the part that is in direct contact with the inner wall of the frame and the part that is not, and depending on how the molded product is removed, it may crack or be damaged. there were. In particular, the greater the degree of pressurization, the more firmly the molded product is packed inside the mold, and this tendency increases, making it difficult to take out the mold and forcing it out. There was a problem in that the outer periphery of the drug was damaged and it lacked shape retention, which is essential for solid herbal medicines. Therefore, in the conventional method, there is a limit to the degree of compression due to the manufacturing method.

しかもこの種の製法では、固定された型内におけるピス
トンの上下動による加圧であるので、加圧を解除すると
、これに反発する成型品の内部圧力が直接上方にのみ逃
げるので、成型後の厚みが厚く、また厚みの変化度合い
が大きいなど厚みの安定性に欠ける問題点があった。従
って従来の製法では、厚みがかなり薄い成型品を得るに
は、かなり加圧しなければならず、或いはまた長時間加
圧する必要があり、生産性の点で問題であった。
Moreover, in this type of manufacturing method, pressure is applied by the vertical movement of a piston within a fixed mold, so when the pressure is released, the internal pressure of the molded product that rebounds against this escapes directly upward, so that the There was a problem in that the thickness was thick and the degree of change in thickness was large, resulting in a lack of stability in thickness. Therefore, in the conventional manufacturing method, in order to obtain a molded product with a fairly thin thickness, it is necessary to apply a considerable amount of pressure, or it is necessary to apply pressure for a long time, which poses a problem in terms of productivity.

一方、この種の加圧成型は、生薬を固形化することが本
来の目的であるが、さらに付随的効果として加圧により
切断生薬の煮出し効果が向上しエキス含量が増える利点
があることが知られている(特公昭6B−26653号
参照)。これは加圧により皮膜に亀裂等が生じ、内部へ
水が浸透性が増すためと考えられている。また加圧は一
般生菌数を減少させる効果も併せ持つ。この点からすれ
ば切断生薬が均一かつ高圧縮化された成型品の提供が望
まれるところではあるが、既述の通り、均一な圧縮成型
品を迅速かつ簡単に成型することが困難であるのが実情
であり、均一な圧縮状態において生薬の煮出し効果と一
般生菌数の減少効果が改良された固形生薬はいまだ提供
されていない。
On the other hand, although the original purpose of this type of pressure molding is to solidify crude drugs, it is also known that pressurization improves the boiling effect of cut crude drugs and increases the extract content. (See Japanese Patent Publication No. 6B-26653). This is thought to be due to the fact that cracks occur in the coating due to pressure, which increases the permeability of water into the interior. Pressurization also has the effect of reducing the number of viable bacteria in general. From this point of view, it would be desirable to provide molded products in which cut crude drugs are uniformly and highly compressed, but as mentioned above, it is difficult to quickly and easily mold uniform compression molded products. This is the current situation, and solid herbal medicines with improved boiling effects and general viable bacteria count reduction effects in a uniformly compressed state have not yet been provided.

この発明の目的は、切断生薬の均一な高圧縮成型品を迅
速かつ簡単に成型することができる製造方法及びその装
置を提供し、また均一に高圧縮成型された固形生薬を提
供する点にある。
An object of the present invention is to provide a manufacturing method and apparatus for quickly and easily molding a cut herbal medicine into a uniform, highly compressed product, and also to provide a solid herbal medicine that is uniformly and highly compressed. .

[課題を解決するための手段] 上記の目的達成のため鋭意検討した結果、割型内に適度
に乾燥した切断生薬を投入し、これを加圧した後、当該
加圧状態下で割型を開き、しかる後加圧状態を解除して
、均一な圧縮成形品を得る製法を開発した。
[Means for solving the problem] As a result of intensive studies to achieve the above objective, we put a moderately dried cut herbal medicine into a split mold, pressurized it, and then opened the split mold under the pressurized state. We developed a manufacturing method in which a uniform compression molded product is obtained by opening the mold, then releasing the pressurized state.

すなわち割型内で加圧された切断生薬が均一な圧縮状態
で固結一体化されている固形生薬を発明したものである
In other words, we have invented a solid herbal medicine in which cut herbal medicines pressurized in a split mold are solidified and integrated in a uniformly compressed state.

かかる固形生薬を製造する上で好ましい装置としては、
底板と、この底板」二で左右両側に開閉可能に対向し、
左右両側から加圧される断面略コ字状の一対の割型と、
この割型内をシリンダー駆動により昇降する加圧プラン
ジャーとを圧縮成形手段とする製造装置が好ましい。
Preferred equipment for producing such solid herbal medicines include:
The bottom plate and this bottom plate 2 face each other so that they can be opened and closed on both the left and right sides,
A pair of split molds with a roughly U-shaped cross section that are pressurized from both the left and right sides,
It is preferable to use a manufacturing apparatus in which the compression molding means is a pressurizing plunger that moves up and down within the split mold by a cylinder drive.

[作用] この発明は上述の通り、従来の如く定型の型内に詰め込
み圧縮するのではなく、割型内で加圧する方法・装置で
あるので、加圧成型後の成型品の取り出しは、割型を開
き、ピストンなどによる加圧を解除すれば容易に取り出
すことができる。しかも加圧状態の解除は、まず割型を
開き、しかる後解除するので、従来の如く一方向から強
制的に押し出すものではないため、内部圧力のかかり方
が全体に均一であり、成型品に割れや損傷が生じる場合
は少なく、保形性にきわめてすぐれている。
[Function] As mentioned above, this invention is a method and device that pressurizes inside a split mold instead of packing and compressing it in a regular mold as in the past, so taking out the molded product after pressure molding is easy. It can be easily taken out by opening the mold and releasing the pressure applied by a piston or the like. Furthermore, the pressurized state is released by first opening the split mold and then releasing it, so it is not forcibly extruded from one direction as in the past, so the internal pressure is applied uniformly throughout the molded product. It rarely cracks or gets damaged, and has excellent shape retention.

この作用効果は加圧の程度が大きければ大きい程顕著で
あり、また強固に詰まった成型品であっても取り出しは
容易である。従ってこの方法・装置によれば軟質のもの
は勿論、特に従来では困難であった超硬質で均一な圧縮
状態でブロック状に固結一体化されている固形生薬も成
形でき、広範囲の均一圧縮成形品を提供することができ
る。
This effect becomes more pronounced as the degree of pressurization increases, and even a tightly packed molded product can be easily removed. Therefore, with this method and equipment, it is possible to mold not only soft medicines, but also solid herbal medicines that are solidified into blocks in a uniformly compressed state that is extremely hard, which was difficult to do in the past. can provide products.

またこの製法によれば、割型を開いた後、加圧を解除す
るので、これに反発する成型品の内部圧力は四方に逃げ
るので、成型後の厚みを薄くでき、また厚みの変化度合
いを押さえることが可能で、厚みの安定性にすぐれてい
る。従って厚みがかなり薄い成型品を得る場合でも、加
圧の程度を落とすことが可能であり、しかも短時間で加
圧することにより薄い成型品を得ることができる。
In addition, according to this manufacturing method, the pressure is released after opening the split mold, so the internal pressure of the molded product that resists this escapes in all directions, making it possible to reduce the thickness after molding and also to reduce the degree of change in thickness. It can be pressed down and has excellent thickness stability. Therefore, even when obtaining a molded product that is quite thin, it is possible to reduce the degree of pressure applied, and moreover, a thin molded product can be obtained by applying pressure in a short time.

またこの方法によれば、既述の通り、高圧縮可能である
ので、切断生薬の煮出し効果が顕著に向上し、エキス含
量を増量することができる。しかも一般生菌数の減少効
果もすぐれている。
Further, according to this method, as mentioned above, since high compression is possible, the effect of boiling the cut herbal medicine is significantly improved, and the extract content can be increased. Moreover, it has an excellent effect of reducing the number of viable bacteria in general.

[実施例] 以下この発明の方法及び装置の具体例について説明する
が、必ずしも限定されるものではない。
[Example] Specific examples of the method and apparatus of the present invention will be described below, but the invention is not necessarily limited thereto.

第1図(A)〜(E)は固形生薬の製造方法の概略工程
図であり、(A)は供給工程、(B)は割型への投入工
程、(C)は加圧工程、(D)は割型の解除工程、(E
)は加圧解除工程を示している。なお太線の矢印は工程
の進行方向を示し、細線の矢印は圧縮方向を示す。
Figures 1 (A) to (E) are schematic process diagrams of the method for producing solid herbal medicines, in which (A) is the feeding process, (B) is the charging process into split molds, (C) is the pressurizing process, ( D) is the split mold release process, (E
) indicates the pressure release process. Note that thick arrows indicate the direction of progress of the process, and thin arrows indicate the direction of compression.

まず適度に乾燥した切断生薬1をベルトコンベア2によ
り定量フィーダー3に供給する(第1図(A))。次に
一定量の切断生薬1を、定量供給装置4によって割型5
内に投入する(第1図(B))。割型5はこの時左右両
方からシリンダーによって閉塞状態としておく。続いて
、垂直方向にシリンダー6により加圧する(第1図(C
))。その後シリンダー6による加圧状態を維持しなが
ら、閉塞状態にある割型5を開く(第1図(D))。
First, appropriately dried cut crude drug 1 is fed to quantitative feeder 3 by belt conveyor 2 (FIG. 1(A)). Next, a certain amount of the cut crude drug 1 is fed into the split mold 5 by the metered supply device 4.
(Figure 1 (B)). At this time, the split mold 5 is closed by cylinders from both the left and right sides. Subsequently, pressure is applied in the vertical direction by the cylinder 6 (see Fig. 1 (C).
)). Thereafter, while maintaining the pressurized state by the cylinder 6, the split mold 5 in the closed state is opened (FIG. 1(D)).

割型5を開いた後は、シリンダー6の加圧状態を解除し
て(第1図(E)) 、均一な圧縮状態でブロック状に
固結一体化されている固形生薬7を得る。続いてスクレ
ーパー8により押出し、ベルトコンベアー9上に乗せ、
搬出する。なおこの例では固形生薬はブロック状に成形
されているが、凹凸状に成形しても差し支えなく、また
真空パック等のパッキング工程を後続して組み込む方法
も採用できる。
After opening the split mold 5, the pressurized state of the cylinder 6 is released (FIG. 1(E)) to obtain a solid crude drug 7 that is solidified and integrated into a block shape under a uniformly compressed state. Next, it is extruded by a scraper 8 and placed on a belt conveyor 9.
Carry it out. In this example, the solid crude drug is formed into a block shape, but it may be formed into an uneven shape, and a method of subsequently incorporating a packing process such as a vacuum pack can also be adopted.

ところで第2図はこの方法を実施する上で好ましい装置
の一例を示す概略図である。前記と同符号で3は定量フ
ィーダー、4は定量供給装置、5は割型、6はシリンダ
ー、8はスクレーパー、9はベルトコンベアーである。
By the way, FIG. 2 is a schematic diagram showing an example of a preferable apparatus for carrying out this method. With the same reference numerals as above, 3 is a quantitative feeder, 4 is a quantitative feeding device, 5 is a split mold, 6 is a cylinder, 8 is a scraper, and 9 is a belt conveyor.

なお、10は底板である。In addition, 10 is a bottom plate.

一方割型5は、この実施例では第3図に示す如く、底板
10上で左右両側に対向した一対の断面略コ字状体5a
、5bからなり、その上部はそれぞれ左右両方向に円弧
を描きながら開閉可能に軸支されている。11はシリン
ダー6に取付けられた加圧プランジャー、12a、12
bは断面略コ字状体5a、5bの各下方部に両側に取付
けられたシリンダーである。
On the other hand, in this embodiment, the split mold 5 consists of a pair of substantially U-shaped cross-sectional bodies 5a facing each other on both left and right sides on the bottom plate 10, as shown in FIG.
, 5b, each of which is pivotally supported at its upper part so that it can be opened and closed while drawing a circular arc in both left and right directions. 11 is a pressurizing plunger attached to the cylinder 6, 12a, 12
Reference numeral b designates cylinders attached to both sides of the lower portions of the U-shaped bodies 5a and 5b.

なおこの実施例の装置では、第4図に示す如く、底板1
0は両側が段差部13.13で、またこれに対応して割
型5の断面略コ字状体5a、5bの内奥部も段差部13
.13と嵌合する段差形状となっており、閉塞状態の位
置決めを確実なものとしている。
In addition, in the apparatus of this embodiment, as shown in FIG.
0 has stepped portions 13.13 on both sides, and correspondingly, the inner deep portions of the roughly U-shaped cross sections 5a and 5b of the split mold 5 also have stepped portions 13.
.. 13, which ensures reliable positioning in the closed state.

なおこの装置は常温加圧型としているが、加熱加圧タイ
プとしても差し支えない。この場合は、例えば割型5の
各コ字状体にヒーターを埋め込んで加熱する手段が採用
できるが、加熱手段も必ずしも限定されない。
Although this device is of a room temperature pressurization type, it may also be a heating pressurization type. In this case, for example, heating may be performed by embedding a heater in each U-shaped body of the split mold 5, but the heating means is not necessarily limited.

因みに常法により適度に乾燥し、細かく切截粉砕等しだ
十薬を用いて、この装置により、固形生薬を種々の条件
下で製造し、一般生菌数と、大腸菌群の陰陽性、エキス
含量について比較試験した。
By the way, using this equipment, solid herbal medicines are produced under various conditions by properly drying them in a conventional manner, cutting them into small pieces, and crushing them. Comparative tests were conducted on content.

第1表はその結果を示す。Table 1 shows the results.

以下余白 第1表 なお、一般生菌数の試験方法及び大腸菌群の陰陽性試験
は、食品衛生法に準拠して行なった。またエキス含量の
測定は、日本薬局方に準する。
Table 1 is shown in the margin below.The general viable bacteria count test method and the negative/positive test for coliform bacteria were conducted in accordance with the Food Sanitation Act. Furthermore, the extract content is measured in accordance with the Japanese Pharmacopoeia.

第1表から、加圧が大きくなるにつれて、一般生菌数が
減少しており、しかもエキス含量が増大していることが
認められる。また加熱加圧条件で一層この傾向が大きい
ことが認められ、加熱条件下で高加圧することにより、
従来と比べて、一般生菌数が少なく、かつ多量のエキス
含量を含有する固形生薬が得られることが期待できる。
From Table 1, it can be seen that as the pressurization increases, the number of viable bacteria in general decreases, and the extract content increases. It was also observed that this tendency was even greater under heating and pressurizing conditions, and by applying high pressure under heating conditions,
Compared to conventional methods, it is expected that solid herbal medicines with a lower number of viable bacteria and a higher extract content can be obtained.

0 なお原料としてはこの発明では特に硬質の原料には好適
であるが、十薬に限らず、ゲンノショウコ、センナ等各
種のものが使用でき、特に限定されない。
0 In this invention, the raw material is particularly suitable as a hard raw material, but it is not limited to tenyaku, and various kinds such as Gennoshoko and senna can be used, and are not particularly limited.

[発明の効果] 以上の通りこの発明は、割型を使用した製法及び装置で
あるので、切断生薬の均一な高圧縮成型品を迅速かつ簡
単に成型することができ、均一に高圧縮成型された固形
生薬を提供することができるものである。
[Effects of the Invention] As described above, the present invention is a manufacturing method and apparatus that use split molds, so it is possible to quickly and easily mold cut herbal medicines into uniformly high-compression molded products, and it is possible to quickly and easily mold cut herbal medicines into uniformly high-compression molded products. It is possible to provide solid herbal medicines.

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

第1図(A)〜(E)は固形生薬の製造方法の概略工程
図であり、(A)は供給工程、(B)は割型への投入工
程、(C)は加圧工程、(D)は割型の解除工程、(E
)は加圧解除工程を示し、第2図はこの発明に係る製造
装置の一実施例を示す概略全体図、第3図は割型の一例
を示す正面図、第4図は同割型の開いた状態を示す概略
図である。 1・・・切断生薬    5・・・割型6・・・シリン
ダー   7・・・固形生薬1 10・・・底板 11・・・プランジャー
Figures 1 (A) to (E) are schematic process diagrams of the method for producing solid herbal medicines, in which (A) is the feeding process, (B) is the charging process into split molds, (C) is the pressurizing process, ( D) is the split mold release process, (E
) shows the pressure release process, FIG. 2 is a schematic overall view showing one embodiment of the manufacturing apparatus according to the present invention, FIG. 3 is a front view showing an example of a split mold, and FIG. 4 is a diagram of the same split mold. It is a schematic diagram showing an open state. 1... Cut crude drug 5... Split mold 6... Cylinder 7... Solid crude drug 1 10... Bottom plate 11... Plunger

Claims (3)

【特許請求の範囲】[Claims] (1)割型内に適度に乾燥した切断生薬を投入し、これ
を加圧した後、当該加圧状態下で割型を開き、しかる後
加圧状態を解除して、均一な圧縮成形品を得ることを特
徴とする固形生薬の製造方法。
(1) After putting moderately dried cut herbal medicine into the split mold and pressurizing it, open the split mold under the pressurized state, and then release the pressurized state to create a uniform compression-molded product. A method for producing a solid crude drug, characterized in that it obtains.
(2)割型内で加圧された切断生薬が均一な圧縮状態で
固結一体化されていることを特徴とする固形生薬。
(2) A solid crude drug characterized in that the cut crude drug pressurized in a split mold is solidified and integrated in a uniformly compressed state.
(3)底板と、この底板上で左右両側に開閉可能に対向
し、左右両側から加圧される断面略コ字状の一対の割型
と、この割型内をシリンダー駆動により昇降するプラン
ジャーとを圧縮成形手段とすることを特徴とする固形生
薬の製造装置。
(3) A bottom plate, a pair of split molds with a substantially U-shaped cross section that face each other on the bottom plate so that they can be opened and closed on both the left and right sides, and are pressurized from both the left and right sides, and a plunger that moves up and down inside the split molds by a cylinder drive. An apparatus for manufacturing solid herbal medicines, characterized in that said is used as a compression molding means.
JP2026648A 1990-02-06 1990-02-06 Solid crude drug and method and apparatus for producing the same Expired - Fee Related JP2752493B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2026648A JP2752493B2 (en) 1990-02-06 1990-02-06 Solid crude drug and method and apparatus for producing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2026648A JP2752493B2 (en) 1990-02-06 1990-02-06 Solid crude drug and method and apparatus for producing the same

Publications (2)

Publication Number Publication Date
JPH03232819A true JPH03232819A (en) 1991-10-16
JP2752493B2 JP2752493B2 (en) 1998-05-18

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Country Status (1)

Country Link
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06339513A (en) * 1992-12-23 1994-12-13 Hugemann Bernhard Solidified storage chemical to mechanically develop active substance fine particle which can be inhaled, and its preparation
JP5199893B2 (en) * 2007-02-16 2013-05-15 帝人ファーマ株式会社 Compression tablet machine

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5631756A (en) * 1979-08-25 1981-03-31 Nagakura Seiyaku Kk Manufacture of solid herb medicine
JPS6169232U (en) * 1984-10-15 1986-05-12
JPS6326653A (en) * 1986-07-21 1988-02-04 Tosoh Corp Photoresist material

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5631756A (en) * 1979-08-25 1981-03-31 Nagakura Seiyaku Kk Manufacture of solid herb medicine
JPS6169232U (en) * 1984-10-15 1986-05-12
JPS6326653A (en) * 1986-07-21 1988-02-04 Tosoh Corp Photoresist material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06339513A (en) * 1992-12-23 1994-12-13 Hugemann Bernhard Solidified storage chemical to mechanically develop active substance fine particle which can be inhaled, and its preparation
JP5199893B2 (en) * 2007-02-16 2013-05-15 帝人ファーマ株式会社 Compression tablet machine
US9078807B2 (en) 2007-02-16 2015-07-14 Teijin Pharma Limited Tablet compression machine

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Publication number Publication date
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