JPH0319877Y2 - - Google Patents
Info
- Publication number
- JPH0319877Y2 JPH0319877Y2 JP1987032554U JP3255487U JPH0319877Y2 JP H0319877 Y2 JPH0319877 Y2 JP H0319877Y2 JP 1987032554 U JP1987032554 U JP 1987032554U JP 3255487 U JP3255487 U JP 3255487U JP H0319877 Y2 JPH0319877 Y2 JP H0319877Y2
- Authority
- JP
- Japan
- Prior art keywords
- cap
- sealing membrane
- needle
- resin
- molded
- 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
Links
Landscapes
- Infusion, Injection, And Reservoir Apparatuses (AREA)
Description
〔産業上の利用分野〕
この考案は医療用途等に使用される合成樹製の
輸液用のキヤツプにおいて、特に封口膜部の改良
に関するものである。
〔従来の技術〕
通常、封口膜部は、例えばキヤツプ本体内部に
内設されたゴム栓等の下面において配設され、ボ
トルの封口的役割を果すとともに、外部から注射
針等を突刺した際、容器内部に針刺し可能とする
ために設けられている。そして従来のこの種の封
口膜部は、加工性の見地からすべて、キヤツプ本
体とともに一律に同時成形された射出成形品等が
通常で、いわばキヤツプ本体部と同質の連続成形
体で構成されていた。
〔考案が解決しようとする問題点〕
しかしながら従来の当該構成に係るキヤツプで
は、加工性の点ではもち論好ましいものの、封口
膜部自体が、キヤツプ本体部と射出成形等で同時
に一体成形されているため、成形時において、封
口膜部の中央に位置するゲート部分相当部たる樹
脂溜りを中心に、樹脂結晶が周囲に向つて配向
し、この配向によつて樹脂自体が本来的に具備す
るべきはずの物理的強度をいたずらに減殺する欠
点が見出された。すなわち従来のキヤツプに針刺
しを行なうと、樹脂の配向方向にクラツクが発生
し、場合によつてはこれが進行すると陥没するに
至り、上部に位置するゴム栓等がボトル内に脱落
する事態を生じることがあつたが、いずれも当該
配向に起因することを見出したものである。特に
医薬用の輸液キヤツプでは、滅菌処理を施すこと
が通常であることが多いため、この傾向はさらに
顕著であつた。また素材的にみれば、例えばポリ
プロピレン(PP)を使用した場合では、コポリ
マーよりもホモポリマーにその傾向がはなはだし
く、このことはクラツク防止を図る上で、素材上
の選択において制限されることにもなり、好まし
くなかつた。さらにまた完全な同時一体的な連続
成形体であつたことから、当該成形条件に支配さ
れ、自ずと膜厚は0.3m/m程度が限界となり、
薄ければ薄い程針刺しの点で好ましい封口膜部で
あるにも拘らず、薄肉化の点においては十分なも
のとは必ずしもいえなかつた。また射出成形品の
場合では特に、ゲート部分に相当する樹脂溜りが
封口膜部の中心部にくることから、この部分につ
いては針刺しは事実上困難となり、使用にあたつ
てはこの部分を回避して使用しなければならず、
特に、内容液に他の薬液を混注する際に使用する
いわゆるトランスフアーニードルでは、針刺しに
おけるトラブル発生はさらに顕著で、作業性の点
でも決して好ましいものではなかつた。
そこでこの考案の目的とするところは、針刺し
時におけるクラツク発生を確実に防止し得るとと
もに、素材選択の自由度を保有させることがで
き、さらには封口膜部の薄肉化を可及的に達成す
ることができる外、コアリングトラブルを回避し
て作業性の向上を一段と図り得る輸液用のキヤツ
プを提供しようとするものである。
〔問題点を解決するための手段〕
この考案は上記問題点を解決するため、キヤツ
プ本体の内側に、注射針等を突刺す封口膜部を有
する合成樹脂製の輸液用のキヤツプにおいて、上
記封口膜部を、樹脂の結晶が無配向である独立成
形体からなるフイルムもしくはシートで構成し、
このフイルムもしくはシートとキヤツプ本体部と
を成形一体化して輸液用のキヤツプとしたもので
ある。
〔作用〕
従つて封口膜部が、キヤツプ本体とは別個に成
形されたフイルムもしくはシートであることか
ら、従来のごとく樹脂結晶が成形機のゲート部に
当たる樹脂溜りを中心に、周囲に配向することは
構造上あり得ず、また樹脂の結晶自体が無配向で
あるので、針刺し時におけるクラツク発生は確実
に阻止することができるとともに、また素材上の
選択も自由で、薄肉化も何らの制約もなく達成で
きる。しかも樹脂溜り自体が構造上ないので、針
刺しが困難な部分はなくなり、トラブルは解消さ
れ、作業上の飛躍的な向上が図られる。
〔実施例〕
図面はこの考案に係る輸液用のキヤツプの一実
施例を示す断面図で、1はキヤツプ本体部、2は
キヤツプ本体部の内側において配設された樹脂自
体が無配向である肉厚0.1m/mのフイルム状封
口膜部である。また3はキヤツプ本体部1内に内
設されたゴム栓で、封口膜部2の面上に設けられ
ている。封口膜部2は、射出成形等で成形された
キヤツプ本体部1とは別個の独立成形体からな
り、同時に成形されておらず、インサート成形あ
るいは多色成形等で、この独立成形体たる封口膜
部2をキヤツプ本体部1に貼り合せる構造を採用
している。
従つて注射針をゴム栓より突き刺しても、封口
膜部2は、好ましくない配向組織が皆無で、かつ
また樹脂溜り部分もないので、封口膜部全面に任
意にかつ迅速に針刺しができ、しかもクラツクの
発生を防止できる。
ところでこの実施例では、封口膜部2はインサ
ート成形によつてキヤツプ本体部1と貼合せ、成
形一体化されているが、多色成形等を利用して成
形一体化してもよく、限定されるものではない。
また膜厚も限定されず、0.3m/m以下のシート
ないしフイルムはもち論、少なくとも30μ程度ま
でのフイルムまで薄肉化できるが、加工性との関
係で0.1〜0.2m/m程度が最も好ましい範囲であ
る。また素材としてはキヤツプ本体と同じく、ポ
リプロピレンのコポリマーを使用しているが、ホ
モコポリマーを使用することもでき、その他適切
な素材を自由に選択できる。
またこの実施例はゴム栓3を内設した構造のも
のであるが、これに限定されず、例えばゴム栓が
ない、封口膜部のみの構造のものも採用できる。
次に前記実施例のキヤツプについて針刺しによ
るコアリング発生試験を行なつた。なお比較のた
め従来の射出成形による成形膜についても試験し
た。サンプルは115℃、30分の条件で蒸気滅菌し
たものを用い、検体数は20個とした。針刺し角度
は垂直90゜及び斜め60゜の両条件で行なつた。テス
ト針はメーカーの異なる18GRB針(使用針A,
B,C)、200型プラスチツク針(使用針D)、200
型金属針(使用針E)及び500型プラスチツク針
(使用針F)を用いた。
第1表はコアリングの発生個数を示す。
[Industrial Field of Application] This invention relates to an improvement in the sealing membrane portion of a synthetic resin infusion cap used for medical purposes. [Prior Art] Normally, a sealing membrane is disposed on the bottom surface of a rubber stopper or the like installed inside the cap body, and serves to seal the bottle, and when a syringe needle or the like is inserted from the outside. It is provided to allow needle insertion into the inside of the container. From the viewpoint of processability, conventional sealing membranes of this type were generally injection molded products that were uniformly molded together with the cap main body, so to speak, they were composed of a continuous molded product of the same quality as the cap main body. . [Problems to be solved by the invention] However, in conventional caps with this configuration, although it is preferable in terms of processability, the sealing membrane part itself is simultaneously molded integrally with the cap main body by injection molding, etc. Therefore, during molding, the resin crystals are oriented toward the periphery around the resin reservoir, which is located in the center of the sealing membrane and corresponds to the gate part. A drawback was discovered that unnecessarily reduced the physical strength of the material. In other words, when a conventional cap is punctured with a needle, a crack occurs in the orientation direction of the resin, and in some cases, this progresses to the point where it collapses, causing a situation where the rubber stopper located at the top falls out into the bottle. However, it was discovered that all of these results were caused by the orientation. In particular, this tendency was even more pronounced for pharmaceutical infusion caps, which are often sterilized. In terms of materials, for example, when polypropylene (PP) is used, homopolymers tend to be more prone to this than copolymers, and this can lead to restrictions on material selection in order to prevent cracks. I didn't like it. Furthermore, since it was a completely simultaneous and integral continuous molded product, the film thickness was naturally limited to about 0.3 m/m due to the molding conditions.
Although the thinner the sealing membrane is, the better it is in terms of needle stickability, it cannot necessarily be said that it is sufficient in terms of thinning. In addition, especially in the case of injection molded products, the resin pool corresponding to the gate part is located in the center of the sealing membrane part, so it is virtually difficult to puncture this part with a needle, so avoid this part when using it. must be used with
In particular, with so-called transfer needles used when co-injecting other medicinal solutions with the liquid content, troubles caused by needle sticks are even more noticeable, and this is by no means preferable in terms of workability. Therefore, the purpose of this invention is to reliably prevent the occurrence of cracks during needle pricking, maintain flexibility in material selection, and furthermore achieve as thin a sealing membrane as possible. The present invention aims to provide an infusion cap that can avoid coring troubles and further improve workability. [Means for Solving the Problems] In order to solve the above-mentioned problems, this invention provides a cap for infusions made of synthetic resin, which has a sealing membrane portion on the inside of the cap body into which a syringe needle or the like can be pierced. The membrane part is composed of a film or sheet made of an independent molded body in which resin crystals are non-oriented,
This film or sheet and the cap body are integrally molded to form a cap for infusion. [Function] Therefore, since the sealing membrane part is a film or sheet formed separately from the cap body, the resin crystals are not oriented around the resin pool that corresponds to the gate part of the molding machine, as in the conventional case. This is structurally impossible, and since the resin crystal itself is non-oriented, it is possible to reliably prevent cracks from occurring during needle insertion, and there is also freedom in material selection, and there are no restrictions on thinning. It can be achieved without any problem. Moreover, since there is no resin pool in the structure, there are no difficult parts to stick with a needle, which eliminates troubles and dramatically improves work efficiency. [Example] The drawings are cross-sectional views showing one embodiment of the cap for infusion according to the present invention, in which 1 is a cap main body, and 2 is a cap in which the resin itself disposed inside the cap main body is non-oriented. It is a film-like sealing membrane part with a thickness of 0.1m/m. Further, reference numeral 3 denotes a rubber plug installed inside the cap main body 1, and is provided on the surface of the sealing membrane 2. The sealing membrane part 2 is an independent molded body separate from the cap body part 1 molded by injection molding or the like, and is not molded at the same time, but is formed by insert molding or multicolor molding, etc. A structure is adopted in which the part 2 is bonded to the cap main body part 1. Therefore, even if a syringe needle is inserted through a rubber stopper, the sealing membrane part 2 has no unfavorably oriented tissue and there is no resin pool, so the needle can be inserted arbitrarily and quickly over the entire surface of the sealing membrane part. This can prevent cracks from occurring. Incidentally, in this embodiment, the sealing membrane part 2 is bonded to the cap main body part 1 by insert molding and is integrally molded, but it may be integrally molded using multicolor molding or the like, but there are limitations. It's not a thing.
The film thickness is also not limited, and it is possible to make sheets or films with a thickness of 0.3 m/m or less, or at least 30 μm, but the most preferable range is 0.1 to 0.2 m/m in terms of processability. It is. The material used is polypropylene copolymer, just like the cap itself, but homocopolymers can also be used, and other suitable materials can be freely selected. Further, although this embodiment has a structure in which a rubber stopper 3 is provided, the present invention is not limited to this, and for example, a structure having only a sealing membrane portion without a rubber stopper may also be adopted. Next, a coring generation test by needle pricking was conducted on the cap of the above example. For comparison, a film formed by conventional injection molding was also tested. The samples were steam sterilized at 115°C for 30 minutes, and the number of specimens was 20. The needle insertion angle was 90° vertically and 60° diagonally. The test needles were 18GRB needles from different manufacturers (needle A,
B, C), 200 type plastic needle (used needle D), 200
A type metal needle (used needle E) and a type 500 plastic needle (used needle F) were used. Table 1 shows the number of occurrences of coring.
【表】【table】
以上のごとくこの考案は、完全な同時成形体で
あることが通常であつた従来のキヤツプとは異な
り、封口膜部をキヤツプ本体とは別個の独立成形
体で構成し、しかも樹脂が無配向であるので、封
口膜部をキヤツプ本体に貼り合せて成形一体化し
た構成とすると、封口膜部におけるクラツクの発
生は確実に防止され、素材の選択も自由となり、
しかも薄肉化を可及的に達成可能とし、加えてコ
アリングトラブルを未然に阻止して作業性の向上
を一段と図り得た。
As described above, unlike conventional caps, which are usually completely molded at the same time, this design consists of a sealing membrane part that is an independent molded body separate from the cap body, and the resin is not oriented. Therefore, if the sealing membrane part is bonded to the cap body and integrally molded, the occurrence of cracks in the sealing membrane part will be reliably prevented, and the material selection will be free.
In addition, it has been possible to achieve as thin a wall as possible, and in addition, it has been possible to prevent coring troubles and further improve workability.
図面はこの考案に係るキヤツプの一実施例を示
す断面図である。
1……キヤツプ、2……封口膜部。
The drawing is a sectional view showing an embodiment of the cap according to the invention. 1... Cap, 2... Sealing membrane part.
Claims (1)
口膜部を有する合成樹脂製の輸液用キヤツプにお
いて、上記封口膜部を、樹脂の配向が無配向であ
る独立成形体からなるフイルムもしくはシートで
構成し、キヤツプ本体部と成形一体化したことを
特徴とする輸液用のキヤツプ。 In a synthetic resin infusion cap that has a sealing membrane part into which a syringe needle or the like is pierced inside the cap body, the sealing membrane part is a film or sheet made of an independent molded body in which the orientation of the resin is non-oriented. An infusion cap characterized by being integrally molded with the cap body.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1987032554U JPH0319877Y2 (en) | 1987-03-04 | 1987-03-04 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1987032554U JPH0319877Y2 (en) | 1987-03-04 | 1987-03-04 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS63140953U JPS63140953U (en) | 1988-09-16 |
| JPH0319877Y2 true JPH0319877Y2 (en) | 1991-04-26 |
Family
ID=30839341
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP1987032554U Expired JPH0319877Y2 (en) | 1987-03-04 | 1987-03-04 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0319877Y2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2579969B2 (en) * | 1987-11-11 | 1997-02-12 | 扶桑薬品工業株式会社 | Portion closing member for synthetic resin container for infusion and method therefor |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5559640U (en) * | 1978-10-20 | 1980-04-23 | ||
| JPS6314849Y2 (en) * | 1979-04-20 | 1988-04-26 | ||
| JPS5837396U (en) * | 1981-09-04 | 1983-03-11 | 鈴木シヤツタ−工業株式会社 | Operating device for shutter opening/closing device |
-
1987
- 1987-03-04 JP JP1987032554U patent/JPH0319877Y2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS63140953U (en) | 1988-09-16 |
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