JPH1128243A - Medical container - Google Patents

Medical container

Info

Publication number
JPH1128243A
JPH1128243A JP9202576A JP20257697A JPH1128243A JP H1128243 A JPH1128243 A JP H1128243A JP 9202576 A JP9202576 A JP 9202576A JP 20257697 A JP20257697 A JP 20257697A JP H1128243 A JPH1128243 A JP H1128243A
Authority
JP
Japan
Prior art keywords
container
needle
cap material
medical
communication
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
JP9202576A
Other languages
Japanese (ja)
Inventor
Soichi Kuroki
宗一 黒木
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.)
Material Engineering Technology Laboratory Inc
Original Assignee
Material Engineering Technology Laboratory Inc
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 Material Engineering Technology Laboratory Inc filed Critical Material Engineering Technology Laboratory Inc
Priority to JP9202576A priority Critical patent/JPH1128243A/en
Publication of JPH1128243A publication Critical patent/JPH1128243A/en
Pending legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To keep a communicating needle sterile before use by providing a connecting part of a container main body for storing a medical liquid, to which a medicine container for mixing is connected at the time of use with a communicating needle pierced through a mouth part of the medicine container, a cap material, and a cylindrical sterilized maintaining room capable of holding the medicine container. SOLUTION: This medical container 1 is so constructed that a container main body 3 which stores a medical liquid and has a flexible wall is provided with a connecting part to which a medicine container for mixing is connected at the time use. In this container, the connecting part is provided with a communicating needle 6 pierced through a mouth part of the medicine container, and a cap material 7 having a pierced wall pierced by the communicating needle 6. A cylindrical sterilized room 8 capable of holding a medicine container is connected in such a manner as to surround the periphery of the cap material 7, and a lid material 9 is removably stuck to the opening of the sterilized maintaining room 8. Thus the communicating needle 6 is disposed in the connecting part, the part is covered with the cap material 7, and the medicine container where to be pierced is held in the sterilized maintaining room 8, whereby the sterilized state can be kept before use.

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、医療用容器に関するも
のであり、より詳細には、使用時に、樹脂容器本体と凍
結乾燥物等の薬剤が収容された薬剤容器とを無菌的に簡
単に連結することができる医療用容器、特に、連結部で
の部材を最小限に抑えて製造上の簡略化と容器自体のコ
ンパクト化を達成した確実に薬剤を薬液に溶解すること
のできる医療用容器に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a medical container, and more particularly, to a method of simply aseptically assembling a resin container body and a drug container containing a drug such as a lyophilized product at the time of use. Medical containers that can be connected, in particular, medical containers that can reliably dissolve a drug in a drug solution by minimizing the number of members at the connecting portion and achieving simplification in manufacturing and downsizing of the container itself. It is about.

【0002】[0002]

【従来の技術】点滴注射に用いられる輸液、透析液、臓
器保存液等のバック、コンテナ等の医療用容器は、一般
に樹脂容器である。また輸液にはその使用時に抗生物質
などが混注、混合された後に点滴注射されるものがあ
る。このような混注、或いは混合には注射器が使用され
る。例えば、抗生物質の入ったバイアルに溶解液が注射
器を介して入れられる。抗生物質と溶解液とが混合さ
れ、混合液は注射器でバイアル内から吸い戻される。そ
して、輸液容器の排出口に注射器が刺通され、その混合
液が輸液容器内に充填される。最近、かかる煩雑操作を
省略するため、医療用容器にバイアル等の連結部を備え
たものが種々提案されている。連結部を備えた医療用容
器としては薬液或いは溶解液を収容した容器本体に連通
手段を設けたものと、容器本体とバイアル等の薬剤容器
とを予め連結部で連結して、使用時まで各容器内同士が
連通されない状態におかれるものとがある。前者はいわ
ゆるハーフキット医療用容器と一般に称され、後者はフ
ルキット医療用容器と称されている。
2. Description of the Related Art Medical containers such as bags and containers for infusions, dialysis solutions, organ preservation solutions and the like used for infusion are generally resin containers. In addition, some infusions are infused with antibiotics or the like at the time of use, and are then injected by infusion after mixing. A syringe is used for such co-injection or mixing. For example, a lysate is placed via a syringe into a vial containing the antibiotic. The antibiotic and the lysis solution are mixed, and the mixture is drawn back out of the vial with a syringe. Then, the syringe is pierced through the outlet of the infusion container, and the mixed solution is filled in the infusion container. Recently, various types of medical containers provided with a connecting portion such as a vial have been proposed in order to eliminate such complicated operations. As a medical container provided with a connecting portion, a container provided with communication means in a container main body containing a drug solution or a solution, and a container main body and a drug container such as a vial are connected in advance by a connecting portion, and each of them is used until use. Some containers are placed in a state where they cannot communicate with each other. The former is commonly referred to as a so-called half-kit medical container, and the latter is referred to as a full-kit medical container.

【0003】ハーフキット医療用容器としては、例え
ば、可撓性容器と、該容器の上端から上方に伸びる筒状
の収容カプセルとから構成され、カプセル内に連通手段
である両頭刺通型の連通針が収容され、使用時に連通針
の一端を薬剤容器の口部のゴム栓に刺通し、連通針の他
端を可撓性容器の上端に設けたゴム栓に刺通して薬剤容
器内と可撓性容器内とを連通させる薬剤容器の連通手段
を備えた溶解液容器が提案されている(特開平7−32
8097号公報)。筒状カプセルの下部開口は可撓性容
器の上端に密封連結され、上部開口は無菌維持シートに
よって密封され、連通針はカプセル内に無菌的に収容さ
れている。また、可撓性容器と、可撓性容器に取り付け
られるカップ材と、カップ材内に配せられる連通針と、
連通針を覆うガスケットとからなる医療用容器が提案さ
れ、カップ材に螺合ネジが形成され、薬剤容器が連通針
に刺通されると確実に薬剤容器内と可撓性容器内とが連
通する構造のものも提案されるている(特表平2−50
3272号公報)。
[0003] A half-kit medical container is composed of, for example, a flexible container and a cylindrical housing capsule extending upward from the upper end of the container. A needle is accommodated, and at the time of use, one end of the communication needle is pierced into a rubber stopper at the mouth of the medicine container, and the other end of the communication needle is pierced through a rubber stopper provided at the upper end of the flexible container. There has been proposed a solution container provided with a communication means of a medicine container for communicating with the inside of the container (Japanese Patent Laid-Open No. 7-32).
No. 8097). The lower opening of the cylindrical capsule is hermetically connected to the upper end of the flexible container, the upper opening is sealed by a sterile maintenance sheet, and the communicating needle is aseptically contained in the capsule. Further, a flexible container, a cup material attached to the flexible container, a communication needle disposed in the cup material,
A medical container comprising a gasket that covers the communication needle has been proposed, a screw thread is formed in the cup material, and when the drug container is pierced through the communication needle, the inside of the drug container and the inside of the flexible container are reliably connected. A structure having the following structure has also been proposed (Table 2-50)
No. 3272).

【0004】[0004]

【発明が解決しようとする課題】しかしながら、従来の
ハーフ型医療用容器には未だ以下の問題点がある。医療
用容器における連結部に設けられる連通手段は両頭刺通
型の連通針であるため、カプセル内に無菌状態で、しか
も使用時に移動可能に配する必要がある。特に、その移
動に際しては薬剤容器の口部が可撓性容器のゴム栓より
先に連通針で刺通されなければならないという構成要件
が課せられるため、カプセル内の収容構造が複雑となる
おそれがある。また、単に連結針にガスケットを被せた
のみでは使用時までに接続部が汚染を受け、その都度、
ガスケット部分を殺菌処理して使用しなければならな
い。従って、本発明は、連結部内の連通手段の取付構造
が簡単にでき、また部品点数もできる限り抑えて製造上
の省力化を行うことができ、また使用時まで連結針の無
菌維持が簡単にできる医療用容器を提供することを目的
としている。
However, the conventional half-type medical container still has the following problems. Since the communication means provided at the connection portion of the medical container is a double-headed communication needle, it is necessary to arrange the medical device aseptically in the capsule and to be movable during use. In particular, when moving the medicine container, there is a requirement that the mouth of the medicine container must be pierced with a communication needle before the rubber stopper of the flexible container, so that the accommodation structure in the capsule may be complicated. is there. In addition, if the gasket is simply covered on the connecting needle, the connecting portion will be contaminated by the time of use.
The gasket must be sterilized before use. Therefore, according to the present invention, the connecting structure of the communication means in the connecting portion can be simplified, the number of parts can be reduced as much as possible to save labor in manufacturing, and the aseptic maintenance of the connecting needle can be easily maintained until use. It is intended to provide a medical container that can be used.

【0005】[0005]

【課題を解決するための手段】本発明は、薬液を収容し
た可撓壁を有する樹脂製の容器本体に、使用時に混注用
の薬剤容器が接続される連結部を有する医療用容器にお
いて、上記連結部には上記薬剤容器の口部に刺通する連
通針と、上記連通針による刺通が可能な被刺通壁及び可
撓壁を有するキャップ材と、該キャップ材の周囲を囲み
上記薬剤容器の口部の挿入が可能な筒形状の無菌維持室
と、上記無菌維持室の開口に着脱可能に貼着される蓋材
とが設けられ、上記連通針は上記連結部内に配せられ、
且つ上記キャップ材で覆われ、上記キャップ材は上記連
結部の開口を直接或いは間接的に密封して該連結部に取
付られ、上記無菌維持室は上記連結部に一体に形成さ
れ、或いは別体として取付られ、上記蓋材は蒸気透過性
で且つ菌不透過性の材料で形成され、上記無菌維持室内
は上記容器本体内の薬液と共に蒸気滅菌処理されて使用
時まで無菌的に維持されていることを特徴とする医療用
容器を提供することにより、上記目的を達成したもので
ある。
According to the present invention, there is provided a medical container having a connecting portion for connecting a medicine container for co-infusion at the time of use to a resin container body having a flexible wall for accommodating a chemical solution. The connecting portion has a communication needle penetrating the mouth of the medicine container, a cap material having a pierced wall and a flexible wall that can be pierced by the communication needle, and a medicine material surrounding the cap material and surrounding the cap material. A cylindrical aseptic maintenance room capable of inserting the mouth of the container and a lid material that is detachably attached to the opening of the aseptic maintenance room are provided, and the communication needle is disposed in the connecting portion,
And the cap material is attached to the connection portion by directly or indirectly sealing the opening of the connection portion, and the aseptic maintenance chamber is formed integrally with the connection portion, or is separately formed. The lid material is formed of a vapor-permeable and bacteria-impermeable material, and the sterility-maintaining chamber is steam-sterilized together with the chemical solution in the container body and is aseptically maintained until use. The object has been achieved by providing a medical container characterized by the above-mentioned.

【0006】上記容器本体に収容される薬液は、一般に
電解質液である。例えば、乳酸、酢酸、重炭酸等を含む
リンゲル液、糖、アミノ酸、ペプチド、脂肪等を含む高
カロリー輸液、透析液、臓器保存液等の溶液である。
尚、薬液は凍結乾燥薬剤の単なる溶解液、希釈液でも良
く、かかる薬液は単純な無菌水であっても良い。薬液
は、容器本体内液密に収容された後に蒸気滅菌処理され
るものである。
[0006] The chemical solution contained in the container body is generally an electrolyte solution. Examples thereof include Ringer's solution containing lactic acid, acetic acid, bicarbonate and the like, high calorie infusion containing sugar, amino acid, peptide, fat, etc., dialysate, organ preservation solution and the like.
The chemical may be a simple solution or dilution of the lyophilized drug, and the chemical may be simple sterile water. The chemical solution is subjected to a steam sterilization process after being stored in the container body in a liquid-tight manner.

【0007】上記医療用の容器本体は可撓性壁を有す
る。可撓性壁は撓むことにより容器内の容積が容易に変
化するものであれば良い。また、医療用容器壁は内容物
の確認ができる程度に透明性を有することが望ましい。
容器内での薬剤の状態を確認する上で必要となるからで
ある。上記容器本体は樹脂素材からなり、インフレーシ
ョンフィルム、チューブ、シート及びフィルムから成形
したもの、押出成形、射出成形、又はブロー成形したも
のである。容器本体の樹脂素材としてはポリオレフィン
系樹脂、塩化ビニル、塩化ビニリデン系樹脂、ポリエス
テル系樹脂、ポリビニルアルコール系樹脂、ポリアクリ
ルニトリル系樹脂、ポリアクリル酸系樹脂、ポリアミド
系樹脂等の汎用樹脂である。また樹脂容器は単層又は多
層で形成されていても良い。容器内の薬剤と接触する最
内層は、薬剤に影響を与えない、また溶出物が生じない
樹脂層であることが望ましい。このような樹脂として
は、ポリオレフィン系樹脂が望ましく、例えば、低、
中、高−密度ポリエチレン、ポリプロピレン等の低級オ
レフィン樹脂等が挙げられる。上記容器壁にはガスバリ
アー性層が形成されていることが望ましい。特に、酸素
等を容易に透過しない層であることが望ましい。このよ
うなガスバリアー性層としては、殆ど、又は全くガスを
透過させないアルミニウム等の金属層や酸化珪素、酸化
マグネシウム、酸化チタン等の無機蒸着層であり、また
ポリ塩化ビニリデン、ポリエステル、ナイロン、エチレ
ン−ビニルアルコール共重合体、フッ素系樹脂等のよう
にガスバリアー性の高い樹脂層である。ガスバリアー性
層の酸素透過量は40cc・20μ/m2・day・a
tm(温度:20℃)以下、特に、30cc・20μ/
2・day・atm以下、また好ましくは5cc・2
0μ/m2・day・atm以下、更には1cc・20
μ/m2・day・atm以下であることが望ましい。
[0007] The medical container main body has a flexible wall. The flexible wall may be any as long as the volume in the container is easily changed by bending. Further, it is desirable that the medical container wall has such transparency that the contents can be confirmed.
This is because it is necessary to confirm the state of the medicine in the container. The container body is made of a resin material, and is formed from an inflation film, a tube, a sheet, and a film, or is formed by extrusion, injection, or blow molding. The resin material for the container body is a general-purpose resin such as polyolefin resin, vinyl chloride, vinylidene chloride resin, polyester resin, polyvinyl alcohol resin, polyacrylonitrile resin, polyacrylic acid resin, polyamide resin, and the like. Further, the resin container may be formed in a single layer or a multilayer. The innermost layer that comes into contact with the drug in the container is preferably a resin layer that does not affect the drug and does not generate elutes. As such a resin, a polyolefin-based resin is desirable.
Medium and low-density olefin resins such as high-density polyethylene and polypropylene are exemplified. It is desirable that a gas barrier layer is formed on the container wall. In particular, a layer that does not easily transmit oxygen or the like is desirable. Examples of such a gas barrier layer include a metal layer made of aluminum or the like which hardly transmits gas at all or an inorganic vapor-deposited layer made of silicon oxide, magnesium oxide, titanium oxide, etc., and polyvinylidene chloride, polyester, nylon, ethylene, and the like. -A resin layer having a high gas barrier property, such as a vinyl alcohol copolymer and a fluororesin. The oxygen permeation amount of the gas barrier layer is 40 cc · 20 μ / m 2 · day · a
tm (temperature: 20 ° C.) or less, especially 30 cc · 20 μ /
m 2 · day · atm or less, preferably 5 cc · 2
0 μ / m 2 · day · atm or less, further 1 cc · 20
It is desirably not more than μ / m 2 · day · atm.

【0008】上記薬液に混注される薬剤としては、抗生
物質、生理活性物質などの凍結乾燥物、抽出薬剤、その
他の薬剤等を挙げることができ、通常、輸液、透析液等
に混注されるものである。上記薬剤容器はバイアル等の
ガラス容器、或いは樹脂容器等を挙げることができ、そ
の口部に被刺通用の密封ゴム栓等が設けられているもの
である。医療用容器は薬剤容器が使用時に容器本体の連
結部に連結されるものである。尚、薬剤容器はゴム栓等
の連通針による被刺通部を備えた容器である限り、如何
なる形態の容器であっても適用できる。
[0008] Examples of the drug to be co-injected into the above-mentioned drug solution include lyophilized products such as antibiotics and physiologically active substances, extracted drugs, and other drugs. It is. Examples of the medicine container include a glass container such as a vial, a resin container, and the like, and a sealing rubber stopper or the like for piercing is provided at the mouth. The medical container is one in which the medicine container is connected to the connecting portion of the container body when used. In addition, as long as the medicine container is a container provided with a portion to be pierced by a communication needle such as a rubber stopper, any type of container can be applied.

【0009】上記容器本体の連結部はシート樹脂で本体
が形成される場合には筒状の樹脂ポート成形材などがシ
ートの端部熱溶着シールの際に取り付けられる。上記容
器本体の連結部は本体がブロー成形物の場合にはブロー
エアの吹出口を連結部とすることもでき、また吹出口以
外の部分に連結部を一体成形することもできる。上記連
通針は上記連結部内に配される。連通針は金属製、樹脂
製の成形物からなるが、その加工性、耐腐食性等から樹
脂製成形物が望ましい。連通針には薬剤容器の口部に刺
通する刺通部と連結部に固定する基端部が形成される。
When the main body is formed of sheet resin, the connecting portion of the container main body is attached with a tubular resin port molding material or the like at the time of heat sealing at the end of the sheet. When the main body is a blow-molded product, the connection part of the container main body can be a blow-out port of blow air, or the connection part can be integrally formed with a portion other than the blow-out port. The communication needle is disposed in the connection portion. The communication needle is formed of a metal or resin molded product, but a resin molded product is desirable because of its workability and corrosion resistance. The communicating needle has a piercing portion penetrating the mouth of the medicine container and a base end fixed to the connecting portion.

【0010】上記連通針を覆う上記キャップ材は上記連
結部の開口を直接或いは間接的に密封して連結部に取り
付けられる。即ち、キャップ材は連通針の連通開口を外
界に対して塞ぎ、連通針を容器本体内に確保するように
して連通針を覆っている。キャップ材は連通針の被刺通
壁を有し、また可撓性の壁を有している。このため連通
針が被刺通壁を介して薬剤容器の口部に刺通すると、可
撓性の壁が縮んで被刺通壁が連通針に破封されて口部と
共に移動させられる。このようなキャップ材はゴム製の
弾性部材でも良く樹脂等からなる柔軟な袋状材料でも良
い。上記キャップ材の周囲を囲む無菌維持室は、ほぼ筒
形状に形成され、その基端は容器本体の連結部に取り付
けられるか、或いは容器本体と一体に形成されるもので
ある。そして、無菌維持室の開口は上記薬剤容器の口部
及び胴部の挿入が可能な大きさに形成されている。また
無菌維持室の開口には着脱可能に蓋材が貼着され、蓋材
は蒸気透過性で且つ菌不透過性の材料からなる。このよ
うな蓋材の材料としては紙類に樹脂成分を混ぜて所定の
ポアを形成したシートや撥水性の樹脂をラミネートした
シート等を挙げることができる。このように、蒸気透過
性の蓋材であれば、容器本体内の薬液を高圧蒸気滅菌処
理する際に蒸気が無菌維持室内に充満し、無菌維持室内
及びキャップ材の表面が滅菌される。従って、上記無菌
維持室内は上記容器本体内の薬液と共に蒸気滅菌処理さ
れて使用時まで無菌的に維持されることとなる。
The cap member covering the communication needle is attached to the connecting portion by directly or indirectly sealing the opening of the connecting portion. That is, the cap material covers the communication needle so as to close the communication opening of the communication needle with the outside world and secure the communication needle in the container body. The cap member has a pierced wall of the communication needle and a flexible wall. Therefore, when the communicating needle pierces the mouth of the medicine container through the pierced wall, the flexible wall shrinks, and the pierced wall is broken by the communicating needle and moved together with the mouth. Such a cap material may be a rubber elastic member or a soft bag-like material made of resin or the like. The aseptic maintenance room surrounding the periphery of the cap material is formed in a substantially cylindrical shape, and its base end is attached to a connecting portion of the container body or is formed integrally with the container body. The opening of the sterile maintenance chamber is formed in a size that allows the insertion of the mouth and the trunk of the medicine container. A lid is detachably attached to the opening of the sterility maintenance room, and the lid is made of a vapor-permeable and bacteria-impermeable material. Examples of such a lid material include a sheet in which a resin component is mixed with paper to form a predetermined pore, a sheet in which a water-repellent resin is laminated, and the like. As described above, with the vapor-permeable lid material, when the chemical solution in the container main body is subjected to the high-pressure steam sterilization treatment, the steam fills the aseptic maintenance room, and the surfaces of the aseptic maintenance room and the cap material are sterilized. Therefore, the aseptic maintenance room is subjected to steam sterilization processing together with the chemical solution in the container main body, and is maintained aseptically until use.

【0011】本発明に係る医療用容器では部品点数が極
めて少なく、使用時までキャップ材及び連通針の表面が
無菌に維持される。製造時で製造工程が簡単となり、ま
た連通部に於ける滅菌も容器本体と共に行うことができ
る。また両頭針型連通針等のように連結部内で連通針を
移動可能な構造としないため極めて簡単な構造にでき
る。その使用時にあっては、先ず、蓋材を無菌維持室か
ら剥がし、薬剤容器の口部を無菌維持室内に挿入し、キ
ャップ材の先端に口部を当接させる。かかる状態で薬剤
容器を更に押し込めば、キャップ材が破封され口部内に
連通針の刺通部が口部に挿通される。そして、薬剤容器
内と容器本体内とが連通針を介して連通され、薬剤容器
内の薬剤の薬液への混注が可能となる。従って、使用時
の医療用容器の操作も極めて簡単となる。
In the medical container according to the present invention, the number of parts is extremely small, and the surfaces of the cap material and the communication needle are maintained aseptically until use. The manufacturing process is simplified at the time of manufacturing, and sterilization in the communication portion can be performed together with the container body. Further, since the communication needle is not configured to be movable in the connecting portion unlike a double-ended needle communication needle, the structure can be made extremely simple. At the time of use, first, the lid material is peeled off from the sterility maintenance room, the mouth of the medicine container is inserted into the sterility maintenance room, and the mouth is brought into contact with the tip of the cap material. If the medicine container is further pushed in in this state, the cap material is broken and the piercing portion of the communication needle is inserted into the mouth. Then, the inside of the medicine container and the inside of the container main body are communicated via the communication needle, and the medicine in the medicine container can be co-injected into the medicine solution. Therefore, the operation of the medical container at the time of use becomes extremely simple.

【0012】本発明に係る請求項2記載の医療用容器
は、請求項1記載の医療用容器において、上記連通針は
刺通部と、基端フランジ部と、挿入スカート部とが形成
され、上記挿入スカート部を上記連結部に挿入すること
により上記連結針が上記容器本体に位置決め固定され
る。本発明に係る連通針には刺通部及び取付フランジ部
等の基本的な部分以外に挿入スカート部が設けられる。
かかる挿入スカート部により容器組立時に連通針を連結
部の開口に容易に挿入固定できる。また、本発明に係る
請求項3記載の医療用容器は、請求項2記載の医療用容
器において、上記基端フランジ部に上記キャップ材の基
端部を巻き付けて上記キャップ材が上記連通針に位置決
め固定されることを特徴とする。上記キャップ材を最初
から連通針に被せて、連通針のフランジに巻き付けて固
定しておけば、連通針を連結部に挿入するだけて上記キ
ャップ材も容易に連結部に位置決め固定できる。
A medical container according to a second aspect of the present invention is the medical container according to the first aspect, wherein the communication needle has a piercing portion, a base flange portion, and an insertion skirt portion, By inserting the insertion skirt portion into the connection portion, the connection needle is positioned and fixed to the container body. The communication needle according to the present invention is provided with an insertion skirt portion in addition to the basic portions such as the piercing portion and the mounting flange portion.
With the insertion skirt portion, the communication needle can be easily inserted and fixed into the opening of the connection portion when assembling the container. Further, the medical container according to claim 3 of the present invention is the medical container according to claim 2, wherein the base end of the cap material is wound around the base flange portion so that the cap material is attached to the communication needle. It is characterized by being positioned and fixed. If the cap material is put on the communication needle from the beginning and wound around and fixed to the flange of the communication needle, the cap material can be easily positioned and fixed to the connection portion simply by inserting the communication needle into the connection portion.

【0013】本発明に係る請求項4の医療用容器は、請
求項2記載の医療用容器において、上記連通針に形成さ
れている薬剤容器との連通開口以外に、上記連通針に上
記キャップ材内と上記本体内とを連通する液抜き孔を上
記基端フランジ部或いは刺通部の基端に形成することを
特徴とする。本発明に係る医療用容器において、通常、
上記連通針の外側とキャップ材内との間に液が高圧蒸気
滅菌処理時に残留するおそれがある。かかる残留液は使
用時にキャップ材の被刺通壁を破封したとき噴出するお
それがある。即ち、使用時に薬剤容器の口部をキャップ
材に向けて押圧した時に、キャップ材壁は撓み、キャッ
プ材内が収縮して残留液が行き場を失い、その結果、キ
ャップ材の被刺通壁の破封部から吹き出すおそれが生じ
る。この場合、キャップ材をゴム製の弾性材で形成すれ
ばある程度防ぐことができ、キャップ材を弾性材で形成
することが望ましい。しかし、医療用容器には更に安全
性が求められることから、上記連通針の基端フランジ部
或いは刺通部の基端に液抜き孔が形成してあれば、かか
る液抜き孔から液が容器本体内に戻るため上記のような
残留液の噴出は殆ど防止される。
The medical container according to a fourth aspect of the present invention is the medical container according to the second aspect, wherein the cap is provided on the communication needle in addition to the communication opening with the medicine container formed in the communication needle. A drain hole for communicating the inside with the inside of the main body is formed at the base end of the base end flange portion or the piercing portion. In the medical container according to the present invention, usually,
The liquid may remain between the outside of the communication needle and the inside of the cap material during high-pressure steam sterilization. Such a residual liquid may squirt when the punctured wall of the cap material is opened during use. That is, when the mouth portion of the medicine container is pressed toward the cap material during use, the cap material wall bends, the inside of the cap material shrinks, and the residual liquid loses a place to go. There is a risk of blowing out from the puncture. In this case, it can be prevented to some extent by forming the cap material with a rubber elastic material, and it is desirable to form the cap material with an elastic material. However, since further safety is required for the medical container, if a liquid draining hole is formed in the proximal end flange portion of the communication needle or the proximal end of the piercing portion, the liquid is discharged from the container through the liquid draining hole. Since it returns to the main body, the ejection of the residual liquid as described above is almost prevented.

【0014】本発明に係る請求項5記載の医療用容器は
請求項1記載の医療用容器において、上記連通針に形成
されている薬剤容器との連通開口を該薬剤容器の口部の
刺通時まで弾性材で液密に閉じることを特徴とする。上
記連通針の連通開口を弾性材で閉じることにより、高圧
蒸気滅菌処理中に連通針の外側とキャップ材内との間に
液残留を生じないようにすることができる。このような
弾性材としてキャップ材自体を弾性材としても良く、ま
たキャップ材の他に弾性材を連通開口に配してもよい。
弾性材はゴム、エラストマー等である。本発明に係る請
求項6記載の医療用容器は請求項1〜5の何れかに記載
の医療用容器において、上記無菌維持室には外壁面から
突起した指掛け部が形成されていることを特徴とする。
無菌維持室に指掛け部を形成しておけば、薬剤容器を連
結する際に片手で薬剤容器を無菌維持室内に押し込み、
容器本体と容易に連結させることができる。親指で薬剤
容器の底部を当てる一方、指掛け部に人差し指及び中指
を掛けて薬剤容器を押し込むことができる。
A medical container according to a fifth aspect of the present invention is the medical container according to the first aspect, wherein the communication opening formed in the communication needle with the medicine container is pierced through the mouth of the medicine container. It is characterized by being closed liquid-tight with an elastic material until time. By closing the communication opening of the communication needle with the elastic material, it is possible to prevent liquid from remaining between the outside of the communication needle and the inside of the cap material during the high-pressure steam sterilization. As such an elastic material, the cap material itself may be an elastic material, and an elastic material other than the cap material may be disposed in the communication opening.
The elastic material is rubber, elastomer, or the like. The medical container according to claim 6 of the present invention is characterized in that, in the medical container according to any one of claims 1 to 5, a finger hook protruding from an outer wall surface is formed in the sterility maintenance room. And
If a finger hook is formed in the sterility maintenance room, the medicine container is pushed into the sterility maintenance room with one hand when connecting the drug containers,
It can be easily connected to the container body. While touching the bottom of the medicine container with the thumb, the index finger and the middle finger can be hung on the finger hook to push the medicine container.

【0015】[0015]

【実施例】以下、本発明に係る医療用容器の好ましい実
施例を添付図面を参照しながら詳述する。図1は本発明
に係る医療用容器の第一実施例の正面図である。図2は
第一実施例の医療用容器の要部断面図である。図3は第
一実施例の医療用容器の使用時における要部断面図であ
る。図4は第二実施例の医療用容器における要部断面図
である。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Preferred embodiments of the medical container according to the present invention will be described below in detail with reference to the accompanying drawings. FIG. 1 is a front view of a first embodiment of the medical container according to the present invention. FIG. 2 is a sectional view of a main part of the medical container of the first embodiment. FIG. 3 is a sectional view of a main part when the medical container of the first embodiment is used. FIG. 4 is a sectional view of a main part of the medical container of the second embodiment.

【0016】図1乃至図3に示す如く、本実施例の医療
用容器1は薬液2が収容され可撓壁を有する樹脂製の容
器本体3に、使用時に混注用の薬剤容器4が接続される
連結ポート(連結部)5を有するハーフ型キットであ
る。医療用容器1において、連結ポート5には薬剤容器
4の口部4Aに刺通する連通針6と、連通針6による刺
通が可能な被刺通壁7A及び可撓壁7Bを有するキャッ
プ材7と、キャップ材7の周囲を囲み上記薬剤容器4の
口部4Aの挿入が可能な筒形状の無菌維持室8と、無菌
維持室8の開口8Aに着脱可能に貼着される蓋材9とが
設けられ、連通針6は連結ポート5内に配せられ、且つ
キャップ材7で覆われ、キャップ材7は連結ポート5の
開口を直接或いは間接的に密封して連結ポート5に取付
られ、蓋材9は蒸気透過性で且つ菌不透過性の材料で形
成され、無菌維持室8内は容器本体3内の薬液2と共に
蒸気滅菌処理されて使用時まで無菌的に維持されてい
る。上記連通針6は刺通部6Aと、基端フランジ部6B
と、挿入スカート部6Cとが形成され、挿入スカート部
6Cを連結ポート5に挿入することにより連結針6が容
器本体3に位置決め固定される。上記基端フランジ部6
Bにキャップ材7の基端部7Cを巻き付けてキャップ材
7が連通針6に位置決め固定される。
As shown in FIGS. 1 to 3, a medical container 1 according to the present embodiment has a medicine container 2 containing a chemical solution 2 and a flexible resin wall. This is a half-type kit having a connection port (connection portion) 5. In the medical container 1, the connection port 5 has a communication needle 6 penetrating the mouth 4A of the medicine container 4, and a cap material having a pierced wall 7A and a flexible wall 7B through which the communication needle 6 can penetrate. 7, a cylindrical aseptic maintenance room 8 surrounding the cap member 7 and into which the mouth 4A of the medicine container 4 can be inserted, and a lid member 9 detachably attached to the opening 8A of the aseptic maintenance room 8. The communication needle 6 is disposed in the connection port 5 and is covered with the cap material 7. The cap material 7 is attached to the connection port 5 by directly or indirectly sealing the opening of the connection port 5. The lid 9 is made of a vapor-permeable and bacteria-impermeable material, and the inside of the aseptic maintenance room 8 is steam-sterilized together with the chemical solution 2 in the container body 3 and is maintained aseptically until use. The communication needle 6 has a piercing portion 6A and a proximal flange portion 6B.
And an insertion skirt portion 6C are formed. By inserting the insertion skirt portion 6C into the connection port 5, the connection needle 6 is positioned and fixed to the container body 3. The base end flange 6
The base member 7C of the cap member 7 is wound around B, and the cap member 7 is positioned and fixed to the communication needle 6.

【0017】本実施例の医療用容器1を更に詳しく説明
すると、医療用容器1の容器本体3はブロー成形物から
なる。ブロー成形物の胴壁の厚みは250μmで、その
容量は160mlで、長さが150mmで、幅が80m
mである。ブロー成形物は直鎖状低密度ポリエチレン
(密度:0.935g/cm3、MI:2、融点:12
1℃)からなる。ブロー成形物はブロー成形時のブロー
吹出口が医療用容器における排出ポート12として形成
され、また端部に連結ポート5が形成されている。容器
本体3内には薬液2が充填され、薬液2は薬剤容器内の
凍結乾燥品を溶解する生理食塩水であり、生理食塩水は
除菌フィルタを通して容器本体3に充填されている。
尚、薬液2は容器本体3と共にオートクレーブ滅菌処理
されている。
The medical container 1 of this embodiment will be described in more detail. The container main body 3 of the medical container 1 is made of a blow molded product. The thickness of the body wall of the blow molded product is 250 μm, the capacity is 160 ml, the length is 150 mm, and the width is 80 m.
m. The blow molded product was a linear low density polyethylene (density: 0.935 g / cm 3 , MI: 2, melting point: 12
1 ° C.). The blow molded product has a blow outlet at the time of blow molding formed as a discharge port 12 in a medical container, and a connection port 5 formed at an end. The medical solution 2 is filled in the container body 3, and the medical solution 2 is a physiological saline solution for dissolving the freeze-dried product in the medical container, and the physiological saline solution is filled in the container body 3 through a sterilizing filter.
The chemical solution 2 has been sterilized in an autoclave together with the container body 3.

【0018】図2に示す如く容器本体3の連結ポート5
には連通針6が取り付けられ、連通針6はポリプロピレ
ンの樹脂成形物で刺通部6A、基端フランジ部6B及び
挿入スカート部6Cが形成されている。挿入スカート部
6Cは中心方向に弾性変形して折れ曲がり、連通針6は
挿入スカート部6Cを介して連結ポート5に位置決めさ
れている。連通針6はキャップ材7に覆われ、キャップ
材7はシリコンゴムからなる弾性材で形成されている。
キャップ材7は天面が連通針6の刺通可能な被刺通壁7
Aと側面が柔軟な可撓性壁7Bと基端部7Cとからな
り、基端部7Cは連通針6の基端フランジ6Bを巻き付
けて連通針6と共に連結ポート5に固定されている。連
通針6の基端フランジ6Bには液抜き孔13が形成さ
れ、蒸気滅菌処理等で連通針6とキャップ材7との間に
残留する僅かな薬液2は液抜き孔13を介して排出され
る。また連通針6には返し部6Dが形成され、一旦、刺
通されたゴム栓16から連通針6が外れるのを防止し、
確実なポンピングができるようにしている。
As shown in FIG. 2, the connection port 5 of the container body 3
A communication needle 6 is attached to the communication needle 6, and the communication needle 6 is formed of a polypropylene resin molding and has a piercing portion 6A, a proximal flange portion 6B, and an insertion skirt portion 6C. The insertion skirt 6C is elastically deformed and bent in the center direction, and the communication needle 6 is positioned at the connection port 5 via the insertion skirt 6C. The communication needle 6 is covered with a cap material 7, and the cap material 7 is formed of an elastic material made of silicone rubber.
The cap member 7 has a ceiling surface on which the communication needle 6 can pierce.
A and a flexible wall 7B having a flexible side surface and a base end portion 7C. The base end portion 7C is fixed to the connection port 5 together with the communication needle 6 by winding the base end flange 6B of the communication needle 6. A liquid draining hole 13 is formed in the proximal end flange 6B of the communication needle 6, and a small amount of the chemical solution 2 remaining between the communication needle 6 and the cap member 7 due to steam sterilization or the like is discharged through the liquid draining hole 13. You. A return portion 6D is formed on the communication needle 6 to prevent the communication needle 6 from coming off the rubber stopper 16 once pierced,
Ensures reliable pumping.

【0019】連結ポート5には無菌維持室8が熱溶着に
より固定され、無菌維持室8はポリエチレンの筒状樹脂
成形物からなる。無菌維持室8には押さえ顎部8Bが形
成され、無菌維持室8を連結ポート5に熱溶着する際
に、連通針6の基端フランジ部6B及びキャップ材7の
基端部7Cを顎部8Bは押さえている。これにより、連
通針6は容器本体3内に配せられた状態で連結ポート5
がキャップ材7により密封されている。無菌維持室8の
開口8Aは薬剤容器4の胴部及び口部の挿入が可能に形
成され、開口8Aには蓋材9が着脱可能に貼着されてい
る。蓋材9は天然パルプ及び合成樹脂パルプが積層さ
れ、蒸気透過性で菌不通過性の径孔が形成される。この
ため、容器本体3内の薬液2と共に無菌維持室8内が高
圧蒸気滅菌され、無菌維持室8は無菌に維持される。ま
た無菌維持室8の外面には半径方向に突起させた指掛け
部14が形成される。
The aseptic maintenance chamber 8 is fixed to the connection port 5 by heat welding, and the aseptic maintenance chamber 8 is made of a polyethylene resin molded article. A holding jaw 8B is formed in the aseptic maintenance room 8, and when the aseptic maintenance room 8 is thermally welded to the connection port 5, the proximal flange 6B of the communication needle 6 and the proximal end 7C of the cap material 7 are jawed. 8B is holding down. As a result, the communication needle 6 is placed in the container
Are sealed by the cap material 7. An opening 8A of the sterile maintenance room 8 is formed so that the body and the mouth of the medicine container 4 can be inserted, and a lid 9 is detachably attached to the opening 8A. The cover member 9 is formed by laminating natural pulp and synthetic resin pulp, and has a vapor-permeable and bacteria-impermeable diameter hole. Therefore, the inside of the aseptic maintenance room 8 together with the chemical solution 2 in the container body 3 is subjected to high-pressure steam sterilization, and the aseptic maintenance room 8 is maintained aseptically. A finger hook 14 is formed on the outer surface of the aseptic maintenance room 8 so as to protrude in the radial direction.

【0020】次に、第一実施例の医療容器1について説
明する。先ず、連結ポート5及び排出ポート12が形成
された医療用容器の本体3をブロー成形により製造し、
これの内部を洗滌して乾燥する。また、連通針6、キャ
ップ材7及び無菌維持室8を洗滌して乾燥する。そし
て、連通針6にキャップ材7を被せ、キャップ材7の基
端部7Cを連通針6の基端フランジ部6Bに取り付け
る。次に、キャップ材7を取り付けた連通針6の挿入ス
カート部6Cを容器本体3の連結ポート5内に挿入し、
連通針6の位置決めを行う。かかる状態で無菌維持室8
を連結ポート5に熱溶着して取付け、その取付の際に顎
部8Aで連通針6及びキャップ材7の基端フランジ部6
B及び基端部7Cを押さえて液密に連結ポート5を閉じ
る。無菌維持室8の開口8Aに蓋材9を液密に貼り付け
る。次に、排出ポート12から薬液2を所定量充填し、
排出ポート12をゴム栓15で液密に閉じる。薬液を収
容した容器本体3を温度110℃で高圧蒸気滅菌処理
し、無菌維持室8内を乾燥した後、医療用容器1とす
る。
Next, the medical container 1 of the first embodiment will be described. First, the body 3 of the medical container in which the connection port 5 and the discharge port 12 are formed is manufactured by blow molding.
The inside of this is washed and dried. Further, the communication needle 6, the cap material 7, and the sterility maintenance room 8 are washed and dried. Then, the cap material 7 is put on the communication needle 6, and the base end 7 </ b> C of the cap material 7 is attached to the base flange 6 </ b> B of the communication needle 6. Next, the insertion skirt 6C of the communication needle 6 to which the cap member 7 is attached is inserted into the connection port 5 of the container body 3, and
The communication needle 6 is positioned. In such a state, the aseptic maintenance room 8
Is attached to the connection port 5 by heat welding, and at the time of the attachment, the communication needle 6 and the base flange 6 of the cap 7 are attached by the jaw 8A.
B and the base end 7C are pressed to close the connection port 5 in a liquid-tight manner. The lid 9 is stuck to the opening 8A of the aseptic maintenance room 8 in a liquid-tight manner. Next, a predetermined amount of the drug solution 2 is filled from the discharge port 12,
The discharge port 12 is closed liquid-tight with a rubber stopper 15. The container body 3 containing the drug solution is subjected to high-pressure steam sterilization at a temperature of 110 ° C., and the inside of the aseptic maintenance room 8 is dried.

【0021】このように製造された医療用容器1におい
て、部品点数が少ないため、その加工、洗滌の手間が極
めて少ない。また、組立に際しても、各部品の取付精度
を厳しく設定することもなく、連通針6及びキャップ材
7の取付けが極めて簡単に連結ポート5に位置決め固定
できる。また従来のように連通針6を容器本体3に相対
移動させ、薬剤容器4の口部4Aと容器本体3との刺通
順序を構成上考慮することもない。無菌維持室8内の無
菌的維持には、容器本体3内の薬液2の滅菌処理と同時
に滅菌がなされ、使用時まで無菌的に維持されるので、
医療用容器1としての安全性が高い。医療用容器1を使
用する場合には無菌維持室8の蓋材9を剥がし、薬剤容
器4の口部4Aを挿入し、先ず、口部4Aのゴム栓16
をキャップ材7の被刺通壁7Aに当接させる。かかる口
部4Aの挿入移動は、薬剤容器4の底部を親指等で押圧
する一方、無菌維持室8の指掛かり部14に人差し指及
び中指を添えることにより無菌維持室8を保持する。か
かる操作により口部4Aが連通針6に相対的に移動し、
キャップ材7の被刺通壁7Aが破封され、連通針6の刺
通部6Aが薬剤容器4のゴム栓16を刺通する。これに
より、薬剤容器4内と容器本体3内とが連通する。ま
た、キャップ材7が被刺通壁7Aを破封する際に、キャ
ップ材7内が縮み内部残留水がその破封部から吹き出そ
うとするが、連通針6の基端フランジ部6Aの液抜き孔
13から容器本体3内に排出されるためそのような吹き
出しの危険性は回避される。薬剤容器4と医療用容器1
とは連通状態となる。また、連通針6には返し部6Dが
あるいため、薬剤容器4のゴム栓16と連通針6との刺
通関係が不用意に解除されるおそれがない。
In the medical container 1 manufactured as described above, since the number of parts is small, the labor for processing and cleaning is extremely small. Also, at the time of assembling, the mounting of the communication needle 6 and the cap member 7 can be positioned and fixed to the connection port 5 extremely easily without setting the mounting accuracy of each part strictly. Further, unlike the related art, the communication needle 6 is relatively moved to the container main body 3, and the piercing order between the mouth 4A of the medicine container 4 and the container main body 3 is not considered in the configuration. Aseptic maintenance in the aseptic maintenance room 8 is performed at the same time as sterilization of the chemical solution 2 in the container body 3 and is maintained aseptically until use.
The safety as the medical container 1 is high. When the medical container 1 is used, the lid 9 of the sterile maintenance room 8 is peeled off, and the mouth 4A of the medicine container 4 is inserted.
Is brought into contact with the pierced wall 7A of the cap member 7. In the insertion movement of the mouth 4A, the bottom of the medicine container 4 is pressed with a thumb or the like, while the index finger and the middle finger are attached to the finger hook 14 of the sterility maintenance chamber 8 to hold the sterility maintenance chamber 8. With this operation, the mouth 4A moves relatively to the communication needle 6, and
The punctured wall 7A of the cap member 7 is opened, and the piercing portion 6A of the communication needle 6 pierces the rubber stopper 16 of the medicine container 4. Thereby, the inside of the medicine container 4 and the inside of the container body 3 communicate with each other. Further, when the cap material 7 breaks the punctured wall 7A, the inside of the cap material 7 shrinks and water remaining inside tries to blow out from the broken portion. Since the gas is discharged from the hole 13 into the container body 3, such a risk of blowing is avoided. Drug container 4 and medical container 1
Becomes a communication state. Further, since the communication needle 6 has the return portion 6D, the piercing relationship between the rubber stopper 16 of the medicine container 4 and the communication needle 6 is not inadvertently released.

【0022】次に、本発明に係る医療用容器の第二実施
例を添付図面の図4に従って説明する。図4に示す医療
用容器21が第一実施例の医療用容器1とほぼ同様であ
るが以下の点が相違する。医療用容器21の無菌維持室
部材22は容器本体の連結ポート23と一体成形されて
いる。連通針24の刺通部24Aの連通開口25は弾性
ゴム材26に液密に覆われ、連通針24及び弾性ゴム材
26は可撓性壁を有した樹脂製のキャップ材27で液密
に覆われている。連通針24の基端フランジ部24Bは
連結ポート23の口部の周縁とリング状の止め材28と
の間に保持され、止め材28は連結ポート23の口部の
周縁に液密に熱溶着固定されている。止め材28の上面
には薬剤容器の口部の受け入れ突周条部28Aが設けら
れ、また、キャップ材27の基端フランジ27Aが熱溶
着されている。その他はほぼ同様な構造を採っている。
このような構成された医療用容器21においても、第一
実施例の医療用容器1と同様な作用効果を奏する以外
に、弾性ゴム材26が高圧蒸気滅菌時に連通針24の刺
通部24Aの連通開口25を液密に覆っているため、キ
ャップ材27内と連通針24の外側に液が溜まるおそれ
が少ない。
Next, a second embodiment of the medical container according to the present invention will be described with reference to FIG. 4 of the accompanying drawings. The medical container 21 shown in FIG. 4 is almost the same as the medical container 1 of the first embodiment, except for the following points. The sterile maintenance room member 22 of the medical container 21 is integrally formed with the connection port 23 of the container body. The communication opening 25 of the piercing portion 24A of the communication needle 24 is liquid-tightly covered with an elastic rubber material 26, and the communication needle 24 and the elastic rubber material 26 are liquid-tightly covered by a resin cap material 27 having a flexible wall. Covered. The proximal end flange portion 24B of the communication needle 24 is held between the periphery of the mouth of the connection port 23 and the ring-shaped stopper 28, and the stopper 28 is heat-sealed liquid-tight to the periphery of the mouth of the connection port 23. Fixed. On the upper surface of the stopper member 28, a receiving protruding peripheral ridge portion 28A at the mouth of the medicine container is provided, and a base flange 27A of the cap member 27 is thermally welded. Others have almost the same structure.
In the medical container 21 configured as described above, in addition to having the same operation and effect as the medical container 1 of the first embodiment, the elastic rubber material 26 is used for the piercing portion 24A of the communication needle 24 during high-pressure steam sterilization. Since the communication opening 25 is liquid-tightly covered, there is little possibility that liquid will accumulate inside the cap material 27 and outside the communication needle 24.

【0023】[0023]

【発明の効果】以上説明したように本発明に係る医療用
容器においては、上記連結部には上記薬剤容器の口部に
刺通する連通針と、上記連通針による刺通が可能な被刺
通壁及び可撓壁を有するキャップ材と、該キャップ材の
周囲を囲み上記薬剤容器の口部の挿入が可能な筒形状の
無菌維持室と、上記無菌維持室の開口に着脱可能に貼着
される蓋材とが設けられ、上記連通針は上記連結部内に
配せられ、且つ上記キャップ材で覆われ、上記キャップ
材は上記連結部の開口を直接或いは間接的に密封して該
連結部に取付られ、上記無菌維持室は上記連結部に一体
に形成され、或いは別体として取付られ、上記蓋材は蒸
気透過性で且つ菌不透過性の材料で形成され、上記無菌
維持室内は上記容器本体内の薬液と共に蒸気滅菌処理さ
れて使用時まで無菌的に維持されているので、連結部内
の連通手段の取付構造が簡単にでき、また部品点数もで
きる限り抑えて製造上の省力化を行うことができ、また
使用時まで連結針の無菌維持が簡単にできる。
As described above, in the medical container according to the present invention, the connecting portion has a communicating needle penetrating the mouth of the medicine container, and a puncturing object capable of penetrating with the communicating needle. A cap material having a passage wall and a flexible wall, a tubular sterile maintenance room surrounding the cap material and into which the mouth of the medicine container can be inserted, and a detachably adhered to an opening of the sterile maintenance room The communication needle is disposed in the connection portion and covered with the cap material, and the cap material directly or indirectly seals the opening of the connection portion. Attached to the above, the aseptic maintenance room is formed integrally with the connecting portion, or is attached separately, the lid member is formed of a vapor-permeable and bacteria-impermeable material, and the aseptic maintenance room is Steam sterilized together with the drug solution in the container body, , The connecting means in the connecting part can be easily attached, the number of parts can be reduced as much as possible to save labor in manufacturing, and the sterilization of the connecting needle can be maintained until use. Easy to do.

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

【図1】図1は本発明に係る医療用容器の第一実施例の
正断面図である。
FIG. 1 is a front sectional view of a first embodiment of a medical container according to the present invention.

【図2】図2は第一実施例の医療用容器の要部断面図で
ある。
FIG. 2 is a sectional view of a main part of the medical container of the first embodiment.

【図3】図3は第一実施例の医療用容器における使用時
の要部断面図である。
FIG. 3 is a sectional view of a main part of the medical container of the first embodiment when used.

【図4】図4は第二実施例の医療用容器における要部断
面図である。
FIG. 4 is a sectional view of a main part of the medical container of the second embodiment.

【符号の説明】[Explanation of symbols]

1 医療用容器 2 薬液 3 容器本体 4 薬剤容器 5 連結ポート 6 連結針 7 キャップ材 8 無菌維持室 9 蓋材 DESCRIPTION OF SYMBOLS 1 Medical container 2 Chemical liquid 3 Container main body 4 Drug container 5 Connecting port 6 Connecting needle 7 Cap material 8 Sterility maintenance room 9 Lid material

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 薬液を収容した可撓壁を有する樹脂製の
容器本体に、使用時に混注用の薬剤容器が接続される連
結部を有する医療用容器において、 上記連結部には上記薬剤容器の口部に刺通する連通針
と、上記連通針による刺通が可能な被刺通壁及び可撓壁
を有するキャップ材と、該キャップ材の周囲を囲み上記
薬剤容器の口部の挿入が可能な筒形状の無菌維持室と、
上記無菌維持室の開口に着脱可能に貼着される蓋材とが
設けられ、上記連通針は上記連結部内に配せられ、且つ
上記キャップ材で覆われ、上記キャップ材は上記連結部
の開口を直接或いは間接的に密封して該連結部に取付ら
れ、上記無菌維持室は上記連結部に一体に形成され、或
いは別体として取付られ、上記蓋材は蒸気透過性で且つ
菌不透過性の材料で形成され、上記無菌維持室内は上記
容器本体内の薬液と共に蒸気滅菌処理されて使用時まで
無菌的に維持されていることを特徴とする医療用容器。
1. A medical container having a connecting portion in which a medicine container for co-infusion is connected to a resin container main body having a flexible wall for accommodating a drug solution at the time of use, wherein the connecting portion includes the medicine container. A communication needle penetrating the mouth, a cap material having a pierced wall and a flexible wall that can be pierced by the communication needle, and a periphery of the cap material allowing insertion of the mouth of the medicine container; Aseptic maintenance room with a cylindrical shape,
A lid member detachably attached to an opening of the aseptic maintenance room, the communication needle is disposed in the connection portion, and is covered with the cap material, and the cap material is an opening of the connection portion; Is directly or indirectly sealed and attached to the connection part, the aseptic maintenance chamber is formed integrally with the connection part or attached separately, and the lid is vapor-permeable and bacteria-impermeable A medical container characterized by being sterilized by steam sterilization together with the chemical solution in the container main body and used aseptically until the time of use.
【請求項2】 上記連通針は刺通部と、基端フランジ部
と、挿入スカート部とが形成され、上記挿入スカート部
を上記連結部に挿入することにより上記連結針が上記容
器本体に位置決め固定されることを特徴とする請求項1
記載の医療用容器。
2. The communication needle has a piercing portion, a base flange portion, and an insertion skirt portion, and the connection needle is positioned on the container body by inserting the insertion skirt portion into the connection portion. 2. The device according to claim 1, wherein the device is fixed.
The medical container according to any one of the preceding claims.
【請求項3】 上記基端フランジ部に上記キャップ材の
基端部を巻き付けて上記キャップ材が上記連通針に位置
決め固定されることを特徴とする請求項2記載の医療用
容器。
3. The medical container according to claim 2, wherein a base end portion of the cap material is wound around the base end flange portion, and the cap material is positioned and fixed to the communication needle.
【請求項4】 上記連通針に形成されている薬剤容器と
の連通開口以外に、上記連通針に上記キャップ材内と上
記容器本体内とを連通する液抜き孔を上記基端フランジ
部或いは刺通部の基端に形成することを特徴とする請求
項2記載の医療用容器。
4. In addition to the communication opening formed in the communication needle with the medicine container, a liquid drain hole for communicating the inside of the cap material and the inside of the container body with the communication needle is provided in the base flange portion or the puncture hole. 3. The medical container according to claim 2, wherein the medical container is formed at a base end of the passage portion.
【請求項5】 上記連通針に形成されている薬剤容器と
の連通開口を該薬剤容器の口部の刺通時まで弾性材で液
密に閉じることを特徴とする請求項1記載の医療用容
器。
5. The medical device according to claim 1, wherein a communication opening formed in the communication needle with the medicine container is liquid-tightly closed with an elastic material until the opening of the medicine container is pierced. container.
【請求項6】 上記無菌維持室には外壁面から突起した
指掛け部が形成されていることを特徴とする請求項1〜
5の何れかに記載の医療用容器。
6. The aseptic maintenance room is formed with a finger hook protruding from an outer wall surface.
6. The medical container according to any one of 5 above.
JP9202576A 1997-07-10 1997-07-10 Medical container Pending JPH1128243A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9202576A JPH1128243A (en) 1997-07-10 1997-07-10 Medical container

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9202576A JPH1128243A (en) 1997-07-10 1997-07-10 Medical container

Publications (1)

Publication Number Publication Date
JPH1128243A true JPH1128243A (en) 1999-02-02

Family

ID=16459786

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9202576A Pending JPH1128243A (en) 1997-07-10 1997-07-10 Medical container

Country Status (1)

Country Link
JP (1) JPH1128243A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014108323A (en) * 2012-12-04 2014-06-12 Otsuka Pharmaceut Factory Inc Medicine discharge member and medical double-chamber container
JPWO2013172449A1 (en) * 2012-05-17 2016-01-12 味の素製薬株式会社 Connecting member with needle, drug dissolution kit
KR20160010112A (en) * 2014-07-18 2016-01-27 대한약품공업 주식회사 Security connector having vial changing check function and medical solution product with the connector

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2013172449A1 (en) * 2012-05-17 2016-01-12 味の素製薬株式会社 Connecting member with needle, drug dissolution kit
JP2014108323A (en) * 2012-12-04 2014-06-12 Otsuka Pharmaceut Factory Inc Medicine discharge member and medical double-chamber container
KR20160010112A (en) * 2014-07-18 2016-01-27 대한약품공업 주식회사 Security connector having vial changing check function and medical solution product with the connector

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