JP3686890B2 - Container stopper - Google Patents

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JP3686890B2
JP3686890B2 JP2002243331A JP2002243331A JP3686890B2 JP 3686890 B2 JP3686890 B2 JP 3686890B2 JP 2002243331 A JP2002243331 A JP 2002243331A JP 2002243331 A JP2002243331 A JP 2002243331A JP 3686890 B2 JP3686890 B2 JP 3686890B2
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stopper
outer cap
needle
plug body
film
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JP2004083028A (en
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一弘 森
和人 塩谷
淳 武藤
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塩谷エムエス株式会社
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Description

【0001】
【発明の属する技術分野】
本発明は、アミノ酸や電解質等の輸液や凍結乾燥製剤の溶解液などを収容した医療用、薬用ボトルやバッグ等の容器の口部に使用する、針刺し用の止栓に関する。
【0002】
【従来の技術】
この種の止栓はブチル系ゴム、イソプレンゴム、ブタジエンゴム、天然ゴム等のゴム製のものが主流であるが、これは加硫、洗浄工程を要するため加工コスト高であり、またゴム製の栓本体とこれを包囲する外キャップとは異材質であるため、分別廃棄処分にも難点がある。
【0003】
近年、このようなゴム製の止栓の欠点を解消するために熱可塑性エラストマー製の医療用、薬用止栓が多々開発されている。例えば、熱可塑性エラストマーで栓本体を成形した後、外キャップをインサート成形して熱可塑性エラストマー製栓本体の内圧を上げる方法にて液漏れを防止するという止栓がある。また、止栓の外キャップを成形した後熱可塑性合成樹脂弾性体の溶融樹脂を500Kg/cm2以上の射出圧力で針刺し部を射出成形して針刺し止栓を製造するというものがある(特開2000−140068号公報)。また、熱可塑性エラストマー製の栓本体と外キャップを各々、別々に成形して組み立てる止栓もある。
【0004】
【発明が解決しようとする課題】
しかし、上記したいずれの熱可塑性エラストマー製止栓も、注射用や点滴用の針等に使用される前に必ず高温・高圧の滅菌処理が行われるが、この滅菌後、止栓が物性の変化から針刺し後液漏れが発生したり、また針刺し時の針保持力を失ったりすることがある。
【0005】
また、この種の止栓を使用する薬用容器において人体に薬液投与するとき輸液セット・カテーテルなど薬用容器に刺された樹脂針から人体に連結管で繋ぎ薬液を投与するが、人体と薬液容器間の距離から連結管とコネクターなどの自重で樹脂針を止栓に刺したときの針保持力が重要視される。従来の熱可塑性エラストマー製止栓は針保持力を上げるため栓本体のエラストマー硬度を上げるか、栓本体を必要以上に厚くして針の保持力を上げているが、エラストマー硬度を上げると針刺し抵抗が強くなり、栓本体の肉厚を厚くすると製造時間と栓本体の材料費がかかり、コスト高にもなる。
【0006】
そこで、本発明の目的は、高温・高圧滅菌後、針を刺した時や抜いた時も液漏れを起こさず、また栓本体の肉厚をそれほど厚くしなくて針刺し抵抗を少なくしても針刺し保持力を十分に確保できる容器の止栓を提供することにある。
【0007】
【課題を解決するための手段】
本発明の容器の止栓は、環形状の外キャップの内径より大きい外径を持ち熱可塑性エラストマーからなる針刺し可能な栓本体が前記外キャップの内部に圧入嵌合されており、前 記外キャップ内の栓本体の下面側にストッパーリングが嵌め込まれ、このストッパーリングの開口上端面に、2枚の50〜350μm厚のフィルムがインサート成形または溶着されており、そのうちの 1 枚のフィルムが前記栓本体の下面に溶着されるとともに、2枚目のフィルムとの間に空気層を形成してなることに特徴を有するものである。
【0008】
【0009】
上記構成のように外キャップの内径より大きい外径を持ち熱可塑性エラストマーからなる栓本体が外キャップに圧入嵌合されていると、栓本体は外キャップにより常時圧縮された内部応力を有した状態にある。したがって、高温・高圧の滅菌処理後も、栓本体に針を刺したとき、この刺しこみ部分が切り裂かれて開口しても圧縮された内部応力による弾性復元力でこれを塞ぐので、内部の液体が漏れることはなく、また針保持力も増大する。また、栓本体から針を抜いた後でもこの部分は圧縮された内部応力による弾性復元力で塞がれるので、内部の液体が漏れることはない。
【0010】
【0011】
【発明の実施の形態】
本発明の好適な実施形態を図面に基づき説明する。図1は一実施例の止栓の断面図、図2は図1の止栓の外キャップと栓本体を分離状態で示す断面図、図3は他の実施例の栓本体の断面図である。
【0012】
図1、図2において、本発明の容器の止栓は、環形状に成形された外キャップ1に、自由状態で該外キャップ1の内径aよりも大きな外径bを持つ熱可塑性エラストマーからなる針刺し可能な栓本体2を圧入嵌合してなる。
【0013】
栓本体2の素材である熱可塑性エラストマーとしては、スチレン系エラストマー、オレフィン系エラストマー、ポリエステル系エラストマーのうちの少なくとも1種を選択し、単独、複合又は混合して使用する。熱可塑性エラストマー製の栓本体2はエラストマー硬度(JISK6301)が15〜70度、より好ましくは25〜45度の柔らかさを持つ熱可塑性エラストマーで成形される。
【0014】
図2において、外キャップ1の内径aと栓本体2の外径bの比率はa:b=1:1.05〜1.25であることが好ましい。栓本体2の外径bが外キャップ1の内径aの1.25倍を超えると、外キャップ1に栓本体2を圧入することが困難になる。具体的には、例えば、外キャップ1の内径aは23.18mm、栓本体2の外径bは27.0mmである。
【0015】
図2において、栓本体2は針刺領域の外周部の肉厚t1は中心部の肉厚t2よりも厚く形成するとともに、外周部より中心部に向かって漸次薄くなる断面両凹レンズ形状に形成されている。栓本体2の針刺領域の上面中心部及び該中心部付近には針刺し位置を設定する針刺し指定部8が適数個凹設される。栓本体2の下面には針刺し指定部8に対向して凹部9が形成される。
自由状態での栓本体2の針刺領域の外周部肉厚t1と中心部肉厚t2との比率は1:0.3〜0.95とすることが好ましい。具体的には、例えば、栓本体2の針刺領域の外周部肉厚t1を5.5〜6.5mm、中心部肉厚t2を2.4〜5.2mmに設定する。この場合、針刺し指定部8の肉厚t3は0.25〜0.45mmに設定する。
【0016】
外キャップ1の天面開口部はプルタブ5付きの天板(プルトップ)3で引き開け可能に塞がれる。天板3は外キャップ1に薄肉状の引きちぎり部(スコア)4を介して一体に成形されるとともに、天板3の上面にリング状のプルタブ5を一体に成形している。プルタブ5に指を掛けて引き上げることで天板3の引きちぎり部4が引きちぎられて外キャップ1の天面を引き開けることができる。この場合、プルタブ5に加える引きちぎり力は4.5Kg以下、より好ましくは3.5Kg(20mm/60秒移動)で、天板3が容易に引きちぎれるように設定している。
【0017】
外キャップ1内の栓本体2の下面側には、図1に示すごとく50〜350μm厚のフィルム(メンブラン)6を持つストッパーリング7を嵌め込まれるが、その際、図2に示すように、予め、50〜350μmのフィルム6を持つストッパーリング7は栓本体2の下面にインサート成形により一体成形し、そのうえで外キャップ1にこれの開放底から栓本体2ごと嵌め込まれる。その際、外キャップ1の内面の数箇所に上下縦方向の溝10を設けておき、栓本体2の圧入嵌合時に内側の空気が溝10から抜けるようにしてあると、栓本体2を圧入し易い。ストッパーリング7の嵌め込みに際しては、ストッパーリング7の外周に環状の凸条11を設け、この凸条11を外キャップ1の下部内周に設けた凹溝12に嵌め込まれる。
【0018】
上記構成の止栓は外キャップ1の下端部を医療用、薬用のボトルやバッグ等の容器の口部に溶着して使用される。その際、分別廃棄の必要がなく、リサイクルに有利となるように、容器の素材には上記止栓の外キャップ1、栓本体2、ストッパーリング7と同一種の樹脂材が使用される。
【0019】
ストッパーリング7に付ける上記フィルム6としては50〜350μm厚の薄いフィルムを選択することが次の理由により好ましい。
ストッパーリング7にフィルム6を付ける目的は、針刺しや針抜き時に栓本体2の一部が欠損するコアリング現象により生じやすい欠損片の脱落防止や高温滅菌処理時における内圧上昇に伴う薬液漏れの防止のためである。このフィルム6はストッパーリング7の開口上端面にインサート成形により一体に成形されるが、このときフィルム6の成形材料として選ぶ材料がポリプロピレン(PP)で350μm厚のもの、またはポリエチレン(PE)で450μm厚のものがフィルム成形時に樹脂流れを可能にする最小限の肉厚である。しかし、350μm厚を超えるフィルム6では、予め、このフィルム6が一体成形されたストッパーリング7に、栓本体2をインサート成形して止栓として組み立てると、針刺し強度が6.0Kg以上となる。これでは医療現場で樹脂針を刺す時、強い力が必要で看護婦等婦女子では使用し難いという欠点がある。
【0020】
また、フィルム6付きストッパーリング7に栓本体2をインサート成形する場合、栓本体2のエラストマーの収縮度とストッパーリング7の成形樹脂の収縮度との違いから、滅菌後、熱可塑性エラストマー製栓本体2がストッパーリング7の成形樹脂に引っ張られて液漏れを起こす。たとえば、栓本体2の成形材料であるスチレン系エラストマーの収縮率は25〜35/1000%であり、ストッパーリングの成形樹脂であるポリプロピレン系樹脂の収縮率は8〜16/1000%であるため、針刺しにより栓本体2が切り裂かれるとこの切り裂かれた箇所がストッパーリング7の開口上端面に張り付けられた350μm厚よりも厚いフィルム6により外側に引っ張られて開き、当該箇所から液漏れを起こす。
【0021】
しかるに、ストッパーリング7にインサート成形又は溶着するフィルム6として、50〜350μm厚のフィルム6を使用すると、針刺し抵抗は4.5Kg以下に抑えられ、薄いフィルム6全体が熱可塑性エラストマー製栓本体2の下面に沿って一体化するため液漏れ防止にも有利となる。
【0022】
栓本体2の素材の熱可塑性エラストマーには軟化剤等の添加物が含有されているが、この栓本体2を外キャップ1に圧入嵌合するとき前記添加物がにじみ出たり、圧入嵌合後経時的に溶出したりするため、熱可塑性エラストマーの材質の選択範囲が制約される。そこで、熱可塑性エラストマーの材質選択の自由度を持たせるために、ストッパーリング7に付ける50〜350μm厚のフィルム6としては、図3に示すように、2枚の第1,2フィルム6a,6bを使用する。そして、第2フィルム6bは栓本体2の下面に一体に溶着して第1フィルム6aとの間に空気層13を形成する。このように第1,2フィルム6a,6b間に空気層13を形成しておくと、栓本体2からにじみ出たり、溶出したりする添加物は空気層13により効果的に遮断されるバリヤー機能が発揮され、薬液への混入を防止できる。したがって、熱可塑性エラストマーの材質選択の自由度が得られる。なお、フィルム6は3枚以上であってもよい。
【0023】
熱可塑性エラストマー製栓本体2と外キャップ1の材料選択も高温滅菌処理時の液漏れと滅菌後の針刺し保持力に大きく影響する。
外キャップ1にこれの内径より大きな外径を持つ栓本体2を圧入嵌合してなる止栓は、ボトルまたはバッグ等の容器の口部に溶着して、これを高温・高圧滅菌処理(121°C30分)する。すると、外キャップ1が栓本体2の膨張圧に負けて膨張し、その後栓本体2の収縮により栓本体外径と外キャップ内径の寸法差が無くなり、そのため液漏れ防止と針保持力が失われる。したがって、外キャップ1は高温滅菌時に栓本体2の膨張圧に負けない曲げ弾性率の樹脂材料で成形しておくことが必要である。
【0024】
そこで、本発明は熱可塑性エラストマー製栓本体2のエラストマー硬度(JISK6301)と外キャップ1の曲げ弾性率(K7203)の相関関係を規定することにより液漏れ防止と針保持力の確保を可能にした。すなわち、栓本体2のエラストマー硬度(スチレン系エラストマーとして三菱化学株式会社製のラバロン(登録商標)の使用)と、ポリプロピレン製の外キャツプ2の曲げ弾性率との関係は、図8の表に示すように、曲げ弾性率(K7203)で300Mpa以上、より好ましくは350〜700Mpaがよい。これは、図8の表中に示すごとき高温滅菌時の液漏れ状況から明らかに理解されるであろう。
【0025】
外キャップ1がプルタブ5付きキャップである場合、天板3の引きちぎり強度が問題となる。通常、プルタブ5の引きちぎり強度は、婦女子でも容易に引き開けられるように、3.5Kg(20mm/l分移動)以下が望ましい。しかるに、プルタブ5付き外キャップ1成形品の薄肉の引きちぎり部4の肉厚は成形するうえにおいて最低限度0.35mm厚を必要とする。成形品の肉厚が0.35mm以下になると、成形時、樹脂が成形品全体に回らず成形不良となるからである。引きちぎり部4の肉厚が0.35mm以上で上記した曲げ弾性率(K7203)が350Mpaを満足する樹脂製のプルタブ付き外キャップ1であると、引きちぎり強度が6Kg以上となり、引きちぎり部4を引きちぎり難くなる。
【0026】
そのため、曲げ弾性率(K7203)が350Mpa以上の樹脂を使用し、プルタブ5付き天板3の引きちぎり強度を下げるには引きちぎり部4の肉厚を0.1〜0.25mmにすることが好ましい。引きちぎり部4の肉厚を0.1〜0.25mmとするプルタブ5付き外キャップ1を得るには、成形充填し溶融軟化時に、図4に示すように、金型の突き出しコア14を0.1〜0.25mmまで圧縮してプルタブ5付き外キャップ1を成形する。また、その際、突き出しコア14の頂面14a全体を凸円弧面に形成しておくことで、突き出しコア14の突き出し時に外キャップ成形用キャビティ内の天面側の樹脂を突き出しコア14の外周下方に向けて容易に流動させることができるため、外キャップ1の成形が容易になる。
【0027】
また、このように成形されたプルタブ5付きの天板3の内面は凹円弧面3aに形成され、この凹円弧面3aと栓本体2の針刺領域の凹円弧面2aとの間には、図1に示すごとく空間15が形成される。この空間15によって、高温・高圧滅菌時にも熱可塑性エラストマー製栓本体2の針刺領域とプルタブ5付きの天板3の内面3aとが滅菌温度により溶融一体化するのを防止できるため、プルタブ5付き天板3を小さい引き開け操作力で容易に引きちぎることに役立つ。
【0028】
熱可塑性エラストマー製栓本体2の成形時には肉厚のエラストマーの流動性から栓本体2に気泡を巻き込むことが多い。その気泡部に針を刺すと、これを抜くとき液漏れの原因になる。そこで、本発明は、図5に示すように、予め薄いフィルム6をつけたストッパーリング7をコア16に保持してキャビティ20内で栓本体2を同時成形するとき、図6に示すごとくストッパーリング7の外周と金型17との間に0.05mm以内のガス抜穴18を円周方向に所定間隔で設けておくとエアー・ガスのみが抜けるため、気泡の無い熱可塑性エラストマー製栓本体2が得られる。
【0029】
以上のようにして得られたプルタブ付き外キャップ7内にキャップ内径より大きな外径を持つ熱可塑性エラストマー製栓本体2を圧入嵌合した本発明の止栓によれば、高温滅菌後樹脂針を刺したときにも十分な針保持力が得られ、1時間以上経過後に針を抜いた時も液漏れを起こさぬという好結果が得られた。
【0030】
本発明は外キャップ1としては上記のようなプルタブ付きのものに限られず、図7に示すように外キャップ1の天面開口部が外部気密保持用のフィルム19で塞がれるイージーピールフィルム付きの外キャップにも同様に適用できる。この場合、外部気密保持用のフィルム19は外キャップ1にこれの天面開口部を塞ぐように溶着される。
【0031】
【実施例】
実施例1
ポリプロピレン製の外キャップ1の内径は23.18mm、スチレン系エラストマー(三菱化学株式会社製の、ラバロン(登録商標)T331C 28硬度(JISK6301)製の栓本体2の自由状態での最大外径は27.0mmとし、栓本体2の針刺領域の外周部肉厚t1は5.8mm、中心部肉厚t2は3.8mmとするとともに、前記外周部より中心部に向かって漸次薄くなる断面両凹レンズ形状に形成し、外キャップ1にこの寸法形状の栓本体2を圧入嵌合すると共にストッパーリング7を嵌め込んで組み立てた。
【0032】
比較例1
外キャップの内径と、自由状態での栓本体の外径とは共に23.18mmとした以外は、実施例1の場合と同様である。
【0033】
比較例2
栓本体の全体の肉厚が均一な5.8mmで上下両面が平行なフラットな断面形状に形成した以外は、実施例1の場合と同様である。
【0034】
(試験方法)
満容量600ml収納できるボトル又はバッグの容器に電解水(薬液)を500ml充填し、上記の実施例1、比較例1及び比較例2の各止栓をそれぞれ前記容器の口部に熱溶着し、総重量を計測する。実施例1、比較例1及び比較例2の各止栓の溶着された前記容器を121°Cの蒸気熱で30分間滅菌を行い、Φ4.5の樹脂製針を針刺し指定部8に刺し1時間経過後、針を抜き、4.5Kgで3分間の加圧を行った後、再度前記容器の総重量を計測し、針刺し前と針刺し抜き後の重量を比較して液漏れ量を調べた。
【0035】
(試験結果)
上記比較試験の結果は図9の図表に示す通りである。実施例1の止栓を使用し高温滅菌処理した容器の止栓からの液漏れの発生は平均で0.003g(1滴は0.035g)で、1滴も漏れが無かった。即ち121°Cの蒸気熱で30分間滅菌しても実施例1の止栓の液漏れ試験では問題の無いことが判明した。
これに対し、比較例1の止栓は平均で31.61g、最大で80.31g、最小で3.0gと液漏れが激しく、比較例2の止栓も平均で9.27g、最大で21.26g、最小で1.03gであって、いずれも液漏れを防止することができなかった。
【0036】
【発明の効果】
本発明の容器の止栓によれば、高温・高圧滅菌後も針刺し時や針抜き出し時の液漏れをよく防止でき、また栓本体の肉厚をさほど厚くしなくて針刺し抵抗を少なくしても針刺し保持力を十分に確保できるという利点がある。
【図面の簡単な説明】
【図1】 本発明の一実施例の止栓の断面図である。
【図2】 図1の止栓の外キャップと栓本体を分離状態で示す断面図である。
【図3】 他の実施例の栓本体の断面図である。
【図4】 プルタブ付き外キャップの成形態様を示す断面図である。
【図5】 栓本体の成形金型にストッパーリングを保持した態様を示す金型の半欠截断面図である。
【図6】 図5におけるA−A線断面図である。
【図7】 他の実施例の止栓の断面図である。
【図8】 熱可塑性エラストマー製栓本体のエラストマー硬度と外キャップの曲げ弾性率の相関関係を示す図表である。
【図9】 実施例1と比較例1,2の液漏れ試験の比較結果を示す図表である。
【符号の説明】
1 外キャップ
2 栓本体
3 天板
4 引きちぎり部
5 プルタブ
6 フィルム
6a 第1フィルム
6b 第2フィルム
7 ストッパーリング
8 針刺し指定部
13 空気層
15 空間
19 フィルム
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a stopper for needle stick used in a mouth of a container such as a medical or medicinal bottle or bag containing an infusion such as an amino acid or an electrolyte or a solution of a freeze-dried preparation.
[0002]
[Prior art]
This type of stopcock is mainly made of rubber such as butyl rubber, isoprene rubber, butadiene rubber, natural rubber, etc., but this requires a vulcanization and cleaning process, and is expensive to process. Since the stopper main body and the outer cap surrounding the stopper main body are made of different materials, there is also a difficulty in separating and disposal.
[0003]
In recent years, in order to eliminate such drawbacks of rubber stoppers, many medical and medical stoppers made of thermoplastic elastomer have been developed. For example, there is a stopper that prevents liquid leakage by molding a plug body with a thermoplastic elastomer and then insert molding an outer cap to increase the internal pressure of the thermoplastic elastomer plug body. Also, there is a method of manufacturing a needle stick stopper by molding an outer cap of a stopper and injection molding a needle stick portion of a thermoplastic synthetic resin elastic body with an injection pressure of 500 kg / cm 2 or more (Japanese Patent Laid-Open No. 2000). -140068). There is also a stopcock in which a plug body made of a thermoplastic elastomer and an outer cap are separately molded and assembled.
[0004]
[Problems to be solved by the invention]
However, any of the above-mentioned thermoplastic elastomer stoppers must be sterilized at a high temperature and high pressure before being used for injection or infusion needles. May leak after needle sticking, and may lose the needle holding force during needle sticking.
[0005]
In addition, when a chemical solution is administered to the human body in a medicinal container using this kind of stopper, the chemical solution is connected to the human body through a connecting tube from a resin needle stuck in the medicinal container such as an infusion set or catheter, but between the human body and the chemical solution container. From the distance, importance is attached to the needle holding force when a plastic needle is inserted into a stopcock by its own weight such as a connecting tube and a connector. Conventional stopper plugs made of thermoplastic elastomer increase the hardness of the plug body to increase the needle holding force, or increase the holding force of the needle by making the plug body thicker than necessary. If the wall thickness of the plug body is increased, the manufacturing time and the material cost of the plug body are increased, and the cost is increased.
[0006]
Therefore, the object of the present invention is to prevent needle leakage even when a needle is inserted or removed after sterilization at high temperature and high pressure, and even if the resistance of needle insertion is reduced without increasing the wall thickness of the stopper body. An object of the present invention is to provide a stopper for a container that can sufficiently secure a holding force.
[0007]
[Means for Solving the Problems]
Stopcock of the container of the present invention, needle sticks can plug body made has thermoplastic elastomer inner diameter larger than the outer diameter of the outer cap ring shape are press-fitted to the inside of the outer cap, before Kigai cap stopper ring is fitted on the lower surface side of the plug body of the inner, the open top surface of the stopper ring, the two 50~350μm thick film are insert-molded or welded, one film is the plug of which It is characterized in that it is welded to the lower surface of the main body and an air layer is formed between the second film .
[0008]
[0009]
When a plug body made of a thermoplastic elastomer having an outer diameter larger than the inner diameter of the outer cap is press-fitted into the outer cap as in the above configuration, the plug body has an internal stress that is constantly compressed by the outer cap. It is in. Therefore, even after sterilization at high temperature and high pressure, when the needle is inserted into the stopper body, even if the pierced part is cut and opened, it is closed by the elastic restoring force due to the compressed internal stress. Does not leak, and the needle holding force increases. Further, even after the needle is removed from the stopper body, this portion is closed by the elastic restoring force due to the compressed internal stress, so that the liquid inside does not leak.
[0010]
[0011]
DETAILED DESCRIPTION OF THE INVENTION
A preferred embodiment of the present invention will be described with reference to the drawings. FIG. 1 is a sectional view of a stopper plug according to one embodiment, FIG. 2 is a sectional view showing an outer cap and a stopper body of the stopper stopper of FIG. 1 in a separated state, and FIG. 3 is a sectional view of a stopper body according to another embodiment. .
[0012]
1 and 2, the stopper of the container of the present invention is made of a thermoplastic elastomer having an outer diameter b larger than an inner diameter a of the outer cap 1 in a free state on an outer cap 1 formed in an annular shape. It is formed by press-fitting a plug body 2 that can be needle-punctured.
[0013]
As the thermoplastic elastomer that is the material of the plug body 2, at least one of a styrene elastomer, an olefin elastomer, and a polyester elastomer is selected and used alone, in combination, or mixed. The plug body 2 made of a thermoplastic elastomer is molded from a thermoplastic elastomer having an elastomer hardness (JISK6301) of 15 to 70 degrees, more preferably 25 to 45 degrees.
[0014]
In FIG. 2, the ratio of the inner diameter a of the outer cap 1 to the outer diameter b of the plug body 2 is preferably a: b = 1: 1.05-1.25. When the outer diameter b of the plug body 2 exceeds 1.25 times the inner diameter a of the outer cap 1, it is difficult to press-fit the plug body 2 into the outer cap 1. Specifically, for example, the inner diameter a of the outer cap 1 is 23.18 mm, and the outer diameter b of the plug body 2 is 27.0 mm.
[0015]
In FIG. 2, the plug body 2 is formed in a biconcave lens shape having a cross section that is thicker at the outer peripheral portion of the needle stick region than the thickness t2 of the central portion and gradually becomes thinner from the outer peripheral portion toward the central portion. ing. An appropriate number of needle puncture designating portions 8 for setting a needle puncture position are recessed in the central portion of the upper surface of the needle puncture region of the stopper body 2 and in the vicinity of the central portion. A concave portion 9 is formed on the lower surface of the stopper body 2 so as to face the needle puncture designation portion 8.
The ratio between the outer peripheral wall thickness t1 and the central wall thickness t2 of the needle stick region of the stopper main body 2 in the free state is preferably 1: 0.3 to 0.95. Specifically, for example, the outer peripheral wall thickness t1 of the needle stick region of the stopper main body 2 is set to 5.5 to 6.5 mm, and the central wall thickness t2 is set to 2.4 to 5.2 mm. In this case, the thickness t3 of the needle stick designation portion 8 is set to 0.25 to 0.45 mm.
[0016]
The top opening of the outer cap 1 is closed by a top plate (pull top) 3 with a pull tab 5 so that it can be pulled open. The top plate 3 is integrally formed with the outer cap 1 through a thin tear-off part (score) 4, and a ring-shaped pull tab 5 is integrally formed on the top surface of the top plate 3. By pulling the pull tab 5 with a finger, the tearing portion 4 of the top plate 3 is torn off and the top surface of the outer cap 1 can be pulled open. In this case, the tearing force applied to the pull tab 5 is 4.5 kg or less, more preferably 3.5 kg (20 mm / 60 seconds movement), and the top plate 3 is set to be easily torn.
[0017]
A stopper ring 7 having a film (membrane) 6 having a thickness of 50 to 350 μm as shown in FIG. 1 is fitted on the lower surface side of the plug body 2 in the outer cap 1. In this case, as shown in FIG. The stopper ring 7 having a film 6 having a thickness of 50 to 350 μm is integrally formed on the lower surface of the plug body 2 by insert molding, and then fitted to the outer cap 1 together with the plug body 2 from the open bottom thereof. At that time, if vertical grooves 10 are provided at several locations on the inner surface of the outer cap 1 so that the inner air can be removed from the grooves 10 when the plug body 2 is press-fitted, the plug body 2 is press-fitted. Easy to do. When the stopper ring 7 is fitted, an annular ridge 11 is provided on the outer periphery of the stopper ring 7, and the ridge 11 is fitted in a groove 12 provided on the lower inner circumference of the outer cap 1.
[0018]
The stopper having the above structure is used by welding the lower end of the outer cap 1 to the mouth of a container such as a medical or medicinal bottle or bag. In this case, the same kind of resin material as the outer cap 1 of the stopper, the stopper body 2 and the stopper ring 7 is used as the material of the container so that there is no need for separate disposal and it is advantageous for recycling.
[0019]
As the film 6 to be attached to the stopper ring 7, it is preferable to select a thin film having a thickness of 50 to 350 μm for the following reason.
The purpose of attaching the film 6 to the stopper ring 7 is to prevent the missing piece from falling off due to a coring phenomenon in which a part of the plug body 2 is lost during needle sticking or needle removal, and to prevent leakage of chemicals due to an increase in internal pressure during high temperature sterilization. For. The film 6 is integrally formed on the upper end surface of the stopper ring 7 by insert molding. At this time, the material selected as the molding material for the film 6 is polypropylene (PP) having a thickness of 350 μm, or polyethylene (PE) having a thickness of 450 μm. The thickness is the minimum wall thickness that allows resin flow during film formation. However, in the film 6 having a thickness of more than 350 μm, when the stopper body 7 is integrally molded with the stopper body 7 in which the film 6 is integrally formed and assembled as a stopper, the needle stick strength becomes 6.0 kg or more. This has the disadvantage that a strong force is required when a plastic needle is stabbed at a medical site, making it difficult for nurses and other women to use.
[0020]
Further, when the plug body 2 is insert-molded in the stopper ring 7 with the film 6, the plug body made of thermoplastic elastomer after sterilization due to the difference between the shrinkage degree of the elastomer of the stopper body 2 and the shrinkage degree of the molding resin of the stopper ring 7 2 is pulled by the molding resin of the stopper ring 7 to cause liquid leakage. For example, the shrinkage rate of the styrene elastomer that is the molding material of the plug body 2 is 25 to 35/1000%, and the shrinkage rate of the polypropylene resin that is the molding resin of the stopper ring is 8 to 16/1000%. When the stopper main body 2 is torn by needle puncture, the torn portion is pulled outward by a film 6 thicker than 350 μm thick attached to the upper end surface of the stopper ring 7 and causes liquid leakage from the portion.
[0021]
However, when the film 6 having a thickness of 50 to 350 μm is used as the film 6 to be insert-molded or welded to the stopper ring 7, the needle stick resistance is suppressed to 4.5 kg or less, and the entire thin film 6 is made of the thermoplastic elastomer plug body 2. Since it is integrated along the lower surface, it is advantageous for preventing liquid leakage.
[0022]
The thermoplastic elastomer of the material of the plug body 2 contains additives such as a softening agent. However, when the plug body 2 is press-fitted to the outer cap 1, the additive oozes out or has elapsed after the press-fitting. The range of selection of the thermoplastic elastomer material is limited. Therefore, as shown in FIG. 3, two first and second films 6a and 6b are used as the film 6 having a thickness of 50 to 350 μm to be attached to the stopper ring 7 in order to give a degree of freedom in selecting the material of the thermoplastic elastomer. Is used. The second film 6b is integrally welded to the lower surface of the plug body 2 to form an air layer 13 between the second film 6b and the first film 6a. When the air layer 13 is formed between the first and second films 6a and 6b as described above, the barrier function that the air layer 13 effectively blocks the additive that oozes or elutes from the plug body 2 is obtained. Demonstrated and can be prevented from mixing into chemicals. Therefore, the degree of freedom in selecting the material of the thermoplastic elastomer can be obtained. The film 6 may be three or more.
[0023]
The material selection of the thermoplastic elastomer plug body 2 and the outer cap 1 also greatly affects the liquid leakage during the high temperature sterilization treatment and the needle stick holding force after sterilization.
A stopper formed by press-fitting a stopper body 2 having an outer diameter larger than the inner diameter of the outer cap 1 is welded to the mouth of a container such as a bottle or a bag, and this is subjected to high-temperature and high-pressure sterilization treatment (121 ° C for 30 minutes). Then, the outer cap 1 expands against the expansion pressure of the plug body 2, and then the plug body 2 contracts to eliminate the dimensional difference between the outer diameter of the plug body and the inner diameter of the outer cap. . Therefore, it is necessary to mold the outer cap 1 with a resin material having a bending elastic modulus that does not lose the expansion pressure of the plug body 2 during high temperature sterilization.
[0024]
Therefore, the present invention makes it possible to prevent liquid leakage and secure the needle holding force by defining the correlation between the elastomer hardness (JISK6301) of the thermoplastic elastomer plug body 2 and the bending elastic modulus (K7203) of the outer cap 1. . That is, the relationship between the elastomer hardness of the plug body 2 (use of Lavalon (registered trademark) manufactured by Mitsubishi Chemical Corporation as a styrene elastomer) and the flexural modulus of the outer cap 2 made of polypropylene is shown in the table of FIG. Thus, the flexural modulus (K7203) is 300 Mpa or more, more preferably 350 to 700 Mpa. This will be clearly understood from the situation of liquid leakage during high temperature sterilization as shown in the table of FIG.
[0025]
When the outer cap 1 is a cap with a pull tab 5, the tear strength of the top plate 3 becomes a problem. Usually, the tearing strength of the pull tab 5 is preferably 3.5 kg (20 mm / l movement) or less so that women and girls can easily pull it apart. However, the thickness of the thin tearing portion 4 of the molded product of the outer cap 1 with the pull tab 5 requires a minimum thickness of 0.35 mm for molding. This is because when the thickness of the molded product is 0.35 mm or less, the resin does not rotate around the entire molded product during molding, resulting in molding failure. If the outer cap 1 with a pull tab made of resin satisfying the above-mentioned bending elastic modulus (K7203) of 350 Mpa when the thickness of the tearing portion 4 is 0.35 mm or more, the tearing strength is 6 kg or more, and the tearing portion 4 It becomes difficult to tear off.
[0026]
Therefore, using a resin having a flexural modulus (K7203) of 350 MPa or more and reducing the tear strength of the top plate 3 with the pull tab 5, the thickness of the tear portion 4 should be 0.1 to 0.25 mm. preferable. In order to obtain the outer cap 1 with the pull tab 5 in which the thickness of the tear-off portion 4 is 0.1 to 0.25 mm, as shown in FIG. Compress to 1 to 0.25 mm to form the outer cap 1 with the pull tab 5. At that time, the entire top surface 14a of the protruding core 14 is formed in a convex arcuate surface, so that the resin on the top surface side in the outer cap molding cavity is protruded when the protruding core 14 is protruded. Therefore, the outer cap 1 can be easily molded.
[0027]
Moreover, the inner surface of the top plate 3 with the pull tab 5 formed in this way is formed in a concave arc surface 3a, and between the concave arc surface 3a and the concave arc surface 2a of the needle stick region of the stopper body 2, A space 15 is formed as shown in FIG. This space 15 prevents the needle stick region of the thermoplastic elastomer plug body 2 and the inner surface 3a of the top plate 3 with the pull tab 5 from being melted and integrated due to the sterilization temperature even during high temperature and high pressure sterilization. This is useful for easily tearing the attached top plate 3 with a small pulling operation force.
[0028]
When molding the plug body 2 made of thermoplastic elastomer, air bubbles are often involved in the plug body 2 due to the fluidity of the thick elastomer. If a needle is pierced into the bubble, liquid leakage may occur when the needle is removed. Therefore, in the present invention, as shown in FIG. 6, when the stopper body 7 with the thin film 6 previously attached is held on the core 16 and the plug body 2 is simultaneously formed in the cavity 20, as shown in FIG. 7 is provided with a gas vent hole 18 of 0.05 mm or less between the outer periphery of the die 7 and the die 17 at a predetermined interval in the circumferential direction, so that only air gas is released. Is obtained.
[0029]
According to the stopper of the present invention in which the plug body 2 made of a thermoplastic elastomer having an outer diameter larger than the inner diameter of the cap is press-fitted into the outer cap 7 with a pull tab obtained as described above, the resin needle after high-temperature sterilization is A sufficient needle holding force was obtained even when stabbed, and a good result was obtained that no liquid leakage occurred even when the needle was removed after 1 hour or more had elapsed.
[0030]
In the present invention, the outer cap 1 is not limited to the one having the pull tab as described above, and has an easy peel film in which the top surface opening of the outer cap 1 is closed by an external airtight film 19 as shown in FIG. The same applies to the outer cap. In this case, the outer airtight film 19 is welded to the outer cap 1 so as to close the opening on the top surface.
[0031]
【Example】
Example 1
The outer diameter of the outer cap 1 made of polypropylene is 23.18 mm, and the maximum outer diameter in the free state of the plug body 2 made of styrene-based elastomer (manufactured by Mitsubishi Chemical Corporation, Lavalon (registered trademark) T331C 28 hardness (JISK6301)) is 27. 0.02 mm, the outer peripheral wall thickness t1 of the needle stick region of the stopper body 2 is 5.8 mm, the central wall thickness t2 is 3.8 mm, and the cross-concave biconcave lens gradually becomes thinner from the outer peripheral portion toward the central portion. The stopper body 7 was press-fitted and assembled into the outer cap 1 and assembled with the stopper ring 7.
[0032]
Comparative Example 1
The inner diameter of the outer cap and the outer diameter of the plug body in the free state are both the same as in the case of Example 1 except that the inner diameter is 23.18 mm.
[0033]
Comparative Example 2
The same as in the case of Example 1, except that the plug body has a uniform overall thickness of 5.8 mm and a flat cross-sectional shape in which the upper and lower surfaces are parallel.
[0034]
(Test method)
A bottle or bag container capable of storing a full capacity of 600 ml is filled with 500 ml of electrolyzed water (chemical solution), and the stoppers of Example 1, Comparative Example 1 and Comparative Example 2 are thermally welded to the mouths of the containers, respectively. Measure the total weight. The containers in which the stoppers of Example 1, Comparative Example 1 and Comparative Example 2 were welded were sterilized with steam heat of 121 ° C. for 30 minutes, and a Φ4.5 resin needle was stabbed into the needle stab designation portion 8. After the elapse of time, the needle was removed, and after pressurizing at 4.5 kg for 3 minutes, the total weight of the container was measured again, and the amount of liquid leakage was examined by comparing the weight before needle penetration and after needle penetration. .
[0035]
(Test results)
The results of the comparative test are as shown in the chart of FIG. Occurrence of liquid leakage from the stoppers of containers sterilized at high temperature using the stopper of Example 1 was 0.003 g (one drop was 0.035 g) on average, and no one drop was leaked. That is, even if sterilized with steam heat at 121 ° C. for 30 minutes, it was found that there was no problem in the leak test of the stopper plug of Example 1.
In contrast, the stoppers of Comparative Example 1 averaged 31.61 g, the maximum was 80.31 g, the minimum was 3.0 g, and the leakage was severe, and the stoppers of Comparative Example 2 were 9.27 g on average and 21 at maximum. .26 g and a minimum of 1.03 g, neither of which could prevent liquid leakage.
[0036]
【The invention's effect】
According to the stopper of the container of the present invention, it is possible to well prevent liquid leakage at the time of needle sticking and needle withdrawal even after high temperature and high pressure sterilization, and even if the thickness of the stopper body is not so thick, the needle stick resistance can be reduced. There is an advantage that a sufficient needle-stick holding force can be secured.
[Brief description of the drawings]
FIG. 1 is a cross-sectional view of a stopcock according to an embodiment of the present invention.
FIG. 2 is a cross-sectional view showing an outer cap and a plug body of the stopper plug of FIG. 1 in a separated state.
FIG. 3 is a cross-sectional view of a plug body of another embodiment.
FIG. 4 is a cross-sectional view showing a molding aspect of an outer cap with a pull tab.
FIG. 5 is a half cutaway cross-sectional view of a mold showing an embodiment in which a stopper ring is held in a molding die of a stopper main body.
6 is a cross-sectional view taken along line AA in FIG.
FIG. 7 is a cross-sectional view of a stopper plug according to another embodiment.
FIG. 8 is a chart showing the correlation between the elastomer hardness of the thermoplastic elastomer plug body and the bending elastic modulus of the outer cap.
FIG. 9 is a chart showing a comparison result of a liquid leakage test between Example 1 and Comparative Examples 1 and 2;
[Explanation of symbols]
DESCRIPTION OF SYMBOLS 1 Outer cap 2 Plug body 3 Top plate 4 Tearing part 5 Pull tab 6 Film 6a 1st film 6b 2nd film 7 Stopper ring 8 Needle stick designation | designated part 13 Air layer 15 Space 19 Film

Claims (1)

環形状の外キャップの内径より大きい外径を持ち熱可塑性エラストマーからなる針刺し可能な栓本体が前記外キャップの内部に圧入嵌合されており、前記外キャップ内の栓本体の下面側にストッパーリングが嵌め込まれ、このストッパーリングの開口上端面に、2枚の50〜350μm厚のフィルムがインサート成形または溶着されており、そのうちの 1 枚のフィルムが前記栓本体の下面に溶着されるとともに、2枚目のフィルムとの間に空気層を形成してなることを特徴とする容器の止栓。A needle pierceable stopper body made of a thermoplastic elastomer having an outer diameter larger than the inner diameter of the ring-shaped outer cap is press-fitted into the outer cap, and a stopper ring is provided on the lower surface side of the stopper body inside the outer cap. Are inserted and welded to the upper end surface of the opening of the stopper ring, and one of the films is welded to the lower surface of the stopper body, and 2 A stopper for a container, wherein an air layer is formed between the first film and the film .
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JP5270064B2 (en) * 2005-08-19 2013-08-21 アロン化成株式会社 Medical rubber stopper composition
JP4526091B2 (en) * 2006-04-25 2010-08-18 内外化成株式会社 Manufacturing method of medical cap
TW200808293A (en) 2006-04-25 2008-02-16 Naigai Kasei Co Ltd A medical cap and a producing method thereof
JP4526092B2 (en) * 2007-09-19 2010-08-18 内外化成株式会社 Manufacturing method of medical cap
JP5235476B2 (en) * 2008-04-08 2013-07-10 内外化成株式会社 Medical cap and method for manufacturing the same
JP5204049B2 (en) * 2009-07-02 2013-06-05 奈良県 Plastic cap
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