JPH0562547B2 - - Google Patents

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Publication number
JPH0562547B2
JPH0562547B2 JP63077751A JP7775188A JPH0562547B2 JP H0562547 B2 JPH0562547 B2 JP H0562547B2 JP 63077751 A JP63077751 A JP 63077751A JP 7775188 A JP7775188 A JP 7775188A JP H0562547 B2 JPH0562547 B2 JP H0562547B2
Authority
JP
Japan
Prior art keywords
surface layer
plastic
container
mouth
infusion
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
JP63077751A
Other languages
Japanese (ja)
Other versions
JPH01249057A (en
Inventor
Takehiko Washimi
Hiroshi Oota
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.)
Kyoraku Co Ltd
Original Assignee
Kyoraku Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kyoraku Co Ltd filed Critical Kyoraku Co Ltd
Priority to JP63077751A priority Critical patent/JPH01249057A/en
Publication of JPH01249057A publication Critical patent/JPH01249057A/en
Publication of JPH0562547B2 publication Critical patent/JPH0562547B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、糖質輸液剤、電解質輸液剤、血漿増
量剤、浸透圧利尿剤、脂肪乳剤、高カロリー輸液
剤などの静脈注射用の輸液等を収容する可撓性の
輸液用プラスチツク容器に関するもので、さらに
詳しくは内部に空気を供給せずとも胴部を変形さ
せて点滴を行う所謂「自然滴下」の際の滴下性が
きわめて良好な輸液用プラスチチツク容器に関す
るものである。 〔従来の技術〕 落としても割れないこと、軽量であるなどの利
点により、近年輸液用容器のプラスチツク化が急
速に進んでる。特にプラスチツク材料の柔軟性を
利用して、胴部を変形させて点滴を行う自然滴下
のタイプのものが多用されている。これは、自然
滴下の場合容器内に空気が供給することなく点滴
が行え、したがつて容器内に雑菌の侵入の心配の
ない衛生上の利点を有するためである。 上記した自然滴下タイプの輸液用プラスチツク
容器には、バツク形式(例えば特公昭61−38705
号)のものと、ボトル形式(例えば特開昭62−
227355号等)のものがある。 〔発明が解決しようとする課題〕 前掲前者のものは、二枚のフイルムやチユーブ
状のフイルムの管状体からなる口部の挿入部分を
除いた全周を高周波加熱により熱シールして袋体
を形成し、次いで硬質の合成樹脂からなる管体を
非シール部に挿入し熱シールにて形成するもので
あるので、製造が煩雑でしかも管体と袋体とのシ
ール部分から滅菌加圧時に破袋するという問題点
を有していた。 前掲後者のものは、底部を有して自立するもの
であり、その胴部の横断面形状を楕円形としその
垂直方向には直線状とすることにより胴部の負圧
時に凹変形しやすく自然滴下に対応できるように
したものである。しかし、このボトル形式のもの
は、滴下が完全に終了したときの滴下率を測定す
ると、元の充填されていた輸液の量の50%下に落
ちてしまうという問題点を有している。本発明は
以上の点に鑑み、以以下の目的を有するものであ
る。 自然滴下性が良好で、最終的に残存する輸液
量を最少に抑えること。 製造が容易で、口部の製造時に一体で形成で
きること。 栓体の口部への溶着が容易でかつ完全である
こと。 耐熱性を有し、滅菌時に劣化しないこと。 内部の異物を検知することのできる透明性を
有すること。 〔課題を解決するための手段〕 上記の目的を達成するために、本発明は次のよ
うに構成した。それはつまり、 横断面形状が楕円形の胴部と他端が栓体にて溶
着密封される口部とをブロー成形にて一体に形成
したプラスチツク容器であつて、該胴部の前面
壁、後面壁及び両側面壁が胴部中心に向けて凸面
状をなすとともに、内表面層と外表面層との少な
くとも2層構造に構成され、内表面層と外表面層
の弾性率比(T×E)の和は5〜12Kg/mmであ
り、外表面層を構成するプラスチツクは流動開始
点が115℃〜170℃でかつ肉厚0.5mmの全光線透過
率が85%以上であり、内表面層を構成するプラス
チツクは流動開始点が、110℃以下であることを
特徴とする輸液用プラスチツク容器としたもので
ある。 本発明の弾性率比とは、引張弾性率(JISK
7113)EKg/mm2と肉厚Tmmとの積であり、その単
位はKg/mmで表されるものである。本発明の輸液
用プラスチツク容器の弾性率比は、内表面層と外
表面層との和が5〜12Kg/mmであり、さらに好し
くは5〜10Kg/mmである。弾性率比が12Kg/mmを
越えると滴下率が低下して自然滴下性が劣り、逆
に5Kg/mm未満であると蒸気滅菌時に変形する。 本発明の流動開始点とは、荷重100Kg、ダイス
1mmφ×10mmの高化式フローテスターで流動が2
mm2/seccになつたときの温度をいう。全光線透過
率とは、JISK6714に規定する420nmの波長の光
の入射光量と全光線透過量との比を表わしたもの
をいう。 本発明の輸液用プラスチツク容器において、内
表面層には流動開始点が110℃未満のプラスチツ
クで構成され、例えばエチレン酢酸ビニル共重合
体、直鎖状低密度ポリエチレン、直鎖状中密度ポ
リエチレン、アイオノマー樹脂等が好適である。
また、外表面層には流動開始点が115〜170℃で肉
厚0.5mmの全光線透過率が85%以上のプラスチツ
クで構成され、例えば2モル%〜20モル%のエチ
レンを含有するエチレンプロピレンランダム共重
合体またはエチレンプロピレンブロツク共重合
体、ポリプロピレンのホモポリマーやコモノマー
を極少量含むプロピレンランダム共重合体が好適
である。 本発明の輸液用プラスチツク容器は内表面層と
外表面層との少なくとも2層構造に構成され、内
表面層と外表面層との間に気体バリア層、接着剤
層あるいはその他の介在層を全体肉厚の20%を越
えない範囲の肉厚で介在させることも可能であ
る。 また、本発明の輸液用プラスチツク容器は、静
脈注射用に特定されるものではなく、液体を皮
下、血管内、腹腔内などに投与するものとして広
範囲に使用できる。 以下、本発明の理解を容易にするために図面を
用いて説明する。1は輸液用プラスチツク容器で
ある。輸液用プラスチツク容器1は、胴部2及び
口部3より形成されている。胴部2は、中空部分
を形成する前面壁4、後面壁5及び側面壁6,6
と上部分を形成する上面壁7、下部分を形成する
下面壁8,8より構成されている。胴部2及び口
部3は、第5図に示すように内表面層2a,3a
と外表面層2b,3bの2層構成である。上面壁
7の中心には口部3が一体に形成されている。口
部3は、その上端にゴム栓を内包する栓体9と互
いのフランジ部3′,9′にて内表面層3aとを加
熱溶着して密封されている。下面壁8の中心に
は、吊り孔10aを備えた吊り具10を一体に有
する。前面壁4、後面壁5及び側面壁6,6は胴
部2の中心に向けて凸面状をなしている。第3図
は、胴部2の中心の横断面の外形形状を示し、第
4図は、第1図のA−A部分の横断面の外形形状
を示す。 上記容器1は、ブロー波形により栓体9を除い
た胴部2及び口部3を一体に形成し、輸液を口部
3から充填し、ついで口部3を栓体9にて密封す
る。 栓体9と口部3とは密封は、加熱板の接触によ
りフランジ部3a,9aの溶着面を加熱溶融し、
互いに圧縮して溶着するものである。その後、容
器1を115℃の加圧された滅菌槽内に一定時間載
置して、輸液用プラスチツク容器の滅菌槽内に一
定時間載置して、輸液の滅菌処理を行う。 〔作用〕 本発明は以上のように構成したもので、自然滴
下性が良好で、特に最終的に残存する輸液量を最
少に抑えるとともに、口部と胴部とを一体に形成
でき、栓体の溶着も容易にかつ完全にかつ完全に
得られるとともに滅菌による容器の変形もないの
である。 本発明の輸液用プラスチツク容器が、何故良好
が滴下率が得られるのか、詳しいことは不明であ
るが、胴部の前面壁、後面壁及び両側面壁がとも
に胴部中心に向けて凸面状でしかも横断面形状が
楕円形であるという特定形状の容器を、特定の弾
性率比の範囲内であるプラスチツクにて構成した
ことに起因していることは判明している。特に驚
くべきことには、従来広く知られていた胴部の横
断面の諸断面の周囲が実質的にすべて等しくした
胴部形状を有する輸液用プラスチツク容器よりも
はるかに良好な滴下率を得られることが判明し
た。 〔実施例〕 第1表に示すプラスチツク材料を用いて、第1
図から第4図に示した胴部2の前面壁4、後面壁
5及び両側面壁6,6が胴部中心に向けて凸面状
とした第2表に示す構成の実施例1〜実施例4及
び比較例1、比較例2の容器をブロー成形するこ
とにより得た。また、実施例1と同じ層構成に
て、第6図に示す胴部の横断面形状が長円形でそ
の垂直方向に直線状である形状の比較例3の容器
を得た。なお上記各容器は重量が20gであつた。 実施例及び比較例の各容器の中に全容量の75%
に当る500c.c.の輸液を充填し口部を栓体にて密封
し、115℃の加圧された滅菌槽に30分間載置して
滅菌処理し、この容器の全光線透過率
(JISK6714)を測定するとともに、外観の測定及
び下記の滴下試験を行なつた。この結果を第2表
に示す。
[Industrial Field of Application] The present invention provides flexible fluids for accommodating intravenous infusions such as carbohydrate infusions, electrolyte infusions, plasma expanders, osmotic diuretics, fat emulsions, and high-calorie infusions. The present invention relates to a plastic container for infusions, and more specifically, it relates to a plastic container for infusions that has extremely good dripping properties during so-called "natural dripping," in which the body is deformed to inject an infusion without supplying air to the inside. be. [Prior Art] In recent years, the use of plastic containers for infusions has rapidly progressed due to their advantages such as not breaking when dropped and being lightweight. In particular, the natural drip type, which takes advantage of the flexibility of plastic material and deforms the body to administer the drip, is often used. This is because, in the case of natural dripping, dripping can be performed without supplying air into the container, and therefore, there is a sanitary advantage in that there is no fear of germs entering the container. The above-mentioned natural drip type plastic containers for infusions include bag type containers (for example, Japanese Patent Publication No. 61-38705
) and bottle format (e.g. JP-A-62-
227355 etc.). [Problem to be Solved by the Invention] In the former, the bag body is made by heat-sealing the entire circumference except for the insertion part of the mouth part, which is made of two films or a tube-shaped film body, by high-frequency heating. Then, a tube made of hard synthetic resin is inserted into the non-sealed part and heat-sealed, so manufacturing is complicated and the seal between the tube and the bag can be ruptured during sterilization and pressurization. It had the problem of being packaged. The latter has a bottom and stands on its own, and its body has an elliptical cross-sectional shape and is straight in the vertical direction, making it easy to deform concavely when the body is under negative pressure. It is designed to be able to handle dripping. However, this bottle-type bottle has a problem in that when the dripping rate is measured when the dripping is completely completed, it is 50% lower than the amount of the originally filled infusion solution. In view of the above points, the present invention has the following objects. Good natural dripping properties, minimizing the final amount of remaining infusion fluid. It is easy to manufacture and can be formed in one piece when manufacturing the mouth part. Welding of the plug to the mouth part must be easy and complete. It is heat resistant and does not deteriorate during sterilization. Must be transparent enough to detect foreign objects inside. [Means for Solving the Problems] In order to achieve the above object, the present invention is configured as follows. In other words, it is a plastic container in which a body with an elliptical cross-sectional shape and a mouth portion whose other end is welded and sealed with a stopper are integrally formed by blow molding. The face wall and both side walls have a convex shape toward the center of the body, and are configured with at least a two-layer structure of an inner surface layer and an outer surface layer, and the elastic modulus ratio (T × E) of the inner surface layer and the outer surface layer. The plastic forming the outer surface layer has a flow start point of 115℃ to 170℃ and a total light transmittance of 85% or more with a wall thickness of 0.5mm. The plastic container for infusions is characterized by a flow start point of 110°C or lower. The elastic modulus ratio in the present invention refers to tensile elastic modulus (JISK
7113) It is the product of EKg/mm 2 and wall thickness Tmm, and its unit is expressed in Kg/mm. The elastic modulus ratio of the plastic container for infusion of the present invention is such that the sum of the inner surface layer and the outer surface layer is 5 to 12 kg/mm, more preferably 5 to 10 kg/mm. If the elastic modulus ratio exceeds 12 Kg/mm, the dripping rate will decrease and the natural dripping properties will be poor, whereas if it is less than 5 Kg/mm, it will deform during steam sterilization. In the present invention, the flow starting point is the point at which the flow is 2.
It refers to the temperature when the temperature reaches mm 2 /scc. The total light transmittance refers to the ratio between the amount of incident light and the total amount of light transmitted at a wavelength of 420 nm as defined in JISK6714. In the plastic container for infusions of the present invention, the inner surface layer is composed of a plastic whose flow initiation point is less than 110°C, such as ethylene vinyl acetate copolymer, linear low density polyethylene, linear medium density polyethylene, ionomer, etc. Resin etc. are suitable.
In addition, the outer surface layer is made of plastic with a flow initiation point of 115 to 170°C, a wall thickness of 0.5 mm, and a total light transmittance of 85% or more, such as ethylene propylene containing 2 mol% to 20 mol% ethylene. Random copolymers, ethylene-propylene block copolymers, polypropylene homopolymers, and propylene random copolymers containing very small amounts of comonomers are suitable. The plastic container for infusion according to the present invention has a structure of at least two layers, an inner surface layer and an outer surface layer, and a gas barrier layer, adhesive layer, or other intervening layer is disposed between the inner surface layer and the outer surface layer. It is also possible to intervene with a thickness not exceeding 20% of the wall thickness. Furthermore, the plastic container for infusion of the present invention is not limited to intravenous injection, but can be used in a wide range of applications for administering liquid subcutaneously, intravascularly, intraperitoneally, etc. DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be explained below using drawings to facilitate understanding of the present invention. 1 is a plastic container for infusion. A plastic container 1 for infusion is formed of a body 2 and a mouth 3. The body portion 2 includes a front wall 4, a rear wall 5, and side walls 6, 6 forming a hollow portion.
It is composed of an upper wall 7 forming an upper portion, and lower walls 8, 8 forming a lower portion. The body part 2 and the mouth part 3 have inner surface layers 2a and 3a as shown in FIG.
It has a two-layer structure including outer surface layers 2b and 3b. A mouth portion 3 is integrally formed in the center of the upper wall 7. The mouth portion 3 is sealed by heat-welding a plug body 9 containing a rubber stopper at its upper end and an inner surface layer 3a at the flanges 3' and 9'. At the center of the lower wall 8, a hanging tool 10 having a hanging hole 10a is integrally provided. The front wall 4, the rear wall 5, and the side walls 6, 6 are convex toward the center of the body 2. 3 shows the outer shape of a cross section at the center of the body 2, and FIG. 4 shows the outer shape of a cross section taken along the line AA in FIG. The container 1 has a body part 2 and a mouth part 3 which are integrally formed by blow waveforms, except for a stopper 9, and an infusion solution is filled from the mouth part 3, and then the mouth part 3 is sealed with a stopper 9. The plug body 9 and the mouth part 3 are sealed by heating and melting the welded surfaces of the flange parts 3a and 9a by contact with a heating plate.
They are compressed and welded together. Thereafter, the container 1 is placed in a pressurized sterilization tank at 115° C. for a certain period of time, and the container 1 is placed in a sterilization tank for a plastic container for infusion for a certain period of time to sterilize the infusion. [Function] The present invention, constructed as described above, has good natural dripping properties, particularly minimizes the amount of infusion remaining at the end, and also allows the mouth and body to be integrally formed, making the stopper Welding can be easily and completely achieved, and there is no deformation of the container due to sterilization. The details of why the plastic container for infusion according to the present invention achieves a good dripping rate are not known, but the reason is that the front wall, rear wall, and both side walls of the body are all convex toward the center of the body. It has been found that this is due to the fact that the container, which has a specific shape with an elliptical cross-sectional shape, is made of plastic having a specific elastic modulus ratio. Particularly surprising is that a much better dripping rate can be obtained than in the conventionally known plastic containers for infusions, which have a body shape in which the circumferences of the cross-sections of the body are substantially all the same. It has been found. [Example] Using the plastic materials shown in Table 1, the first
Examples 1 to 4 of the structure shown in Table 2, in which the front wall 4, rear wall 5, and both side walls 6, 6 of the body section 2 shown in FIGS. 4 to 4 are convex toward the center of the body section. It was obtained by blow molding the containers of Comparative Example 1 and Comparative Example 2. In addition, a container of Comparative Example 3 was obtained with the same layer structure as in Example 1, but whose body had an oval cross-sectional shape as shown in FIG. 6 and was linear in the vertical direction. Note that each of the above containers weighed 20 g. 75% of the total capacity in each container of Examples and Comparative Examples
The container was filled with 500 c.c. of infusion solution, the mouth was sealed with a stopper, and the container was sterilized by placing it in a pressurized sterilization tank at 115°C for 30 minutes. ), the appearance was measured, and the following drip test was conducted. The results are shown in Table 2.

【表】 の。
[Table] of.

〔発明の効果〕〔Effect of the invention〕

本発明は以上のように構成したので、自然滴下
性が良好で、特に最終的に残存する輸液量を最少
を抑えることができるとともに、口部と胴部とを
一体に形成でき栓体の溶着も容易にかつ完全に得
られかつ滅菌による容器の変形もないのである。
Since the present invention is constructed as described above, the natural dripping property is good, and in particular, the amount of infusion remaining at the end can be minimized, and the mouth part and the body part can be formed integrally, and the stopper can be welded. can be easily and completely obtained, and there is no deformation of the container due to sterilization.

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

第1図は本発明の輸液用プラスチツク容器の正
面図、第2図は同上側面図、第3図は第1図のB
−B部の外形形状を示す図、第4図は第1図のA
−A部の外形形状を示す図、第5図は第1図のC
部の拡大断面図、第6図は従来例を示す斜視図で
ある。 1…輸液用プラスチツク容器、2…胴部、2a
…胴部内表面層、2b…胴部外表面層、3…口
部、3a…口部内表面層、3b…口部外表面層、
4…前面壁、5…後面壁、6…側面壁。
Fig. 1 is a front view of the plastic container for infusion according to the present invention, Fig. 2 is a side view of the same, and Fig. 3 is B of Fig. 1.
- A diagram showing the external shape of part B, Figure 4 is A of Figure 1
- A diagram showing the external shape of part A, Figure 5 is C in Figure 1.
FIG. 6 is a perspective view showing a conventional example. 1... Plastic container for infusion, 2... Body, 2a
... trunk inner surface layer, 2b... trunk outer surface layer, 3... mouth, 3a... mouth inner surface layer, 3b... mouth outer surface layer,
4...Front wall, 5...Back wall, 6...Side wall.

Claims (1)

【特許請求の範囲】[Claims] 1 横断面形状が楕円形の胴部と他端が栓体にて
溶着密封される口部とをブロー成形にて一体に形
成した輸液用プラスチツク容器において、該胴部
は前面壁、後面壁及び両側面壁が胴部中心に向け
て凸面状をなすとともに、内表面層と外表面層と
の少なくとも2層構造に構成され、内表面層と外
表面層の弾性率比(T×E)の和は5〜12Kg/mm
であり、外表面層を構成するプラスチツクは流動
開始点が115℃〜170℃でかつ肉厚0.5mmの全光線
透過率が85%以上であり、内表面層を構成するプ
ラスチツクは流動開始点が110℃以下であること
を特徴とする輸液用プラスチツク容器。
1. A plastic container for infusions in which a body having an elliptical cross-sectional shape and a mouth whose other end is welded and sealed with a stopper are integrally formed by blow molding, and the body has a front wall, a rear wall, and a mouth. Both side walls have a convex shape toward the center of the body, and are configured with at least a two-layer structure of an inner surface layer and an outer surface layer, and the sum of the elastic modulus ratios (T x E) of the inner surface layer and the outer surface layer. is 5~12Kg/mm
The plastic that makes up the outer surface layer has a flow start point of 115℃ to 170℃ and a total light transmittance of 85% or more at a wall thickness of 0.5 mm, and the plastic that makes up the inner surface layer has a flow start point of 115℃ to 170℃. A plastic container for infusion that is characterized by a temperature of 110°C or less.
JP63077751A 1988-03-30 1988-03-30 Plastic container for infusion Granted JPH01249057A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63077751A JPH01249057A (en) 1988-03-30 1988-03-30 Plastic container for infusion

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63077751A JPH01249057A (en) 1988-03-30 1988-03-30 Plastic container for infusion

Publications (2)

Publication Number Publication Date
JPH01249057A JPH01249057A (en) 1989-10-04
JPH0562547B2 true JPH0562547B2 (en) 1993-09-08

Family

ID=13642628

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63077751A Granted JPH01249057A (en) 1988-03-30 1988-03-30 Plastic container for infusion

Country Status (1)

Country Link
JP (1) JPH01249057A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101157397A (en) * 2006-01-16 2008-04-09 东莞佳鸿机械制造有限公司 Transfusion container for blow molding shaping as well as its preparing method and material
JP6480915B2 (en) * 2014-03-27 2019-03-13 テルモ株式会社 Medical liquid container body, medicine-filled medical container, medical liquid container body manufacturing method, and drug-filled medical container manufacturing method

Also Published As

Publication number Publication date
JPH01249057A (en) 1989-10-04

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