JP2016131577A - Medical multi-chamber container - Google Patents

Medical multi-chamber container Download PDF

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JP2016131577A
JP2016131577A JP2015006042A JP2015006042A JP2016131577A JP 2016131577 A JP2016131577 A JP 2016131577A JP 2015006042 A JP2015006042 A JP 2015006042A JP 2015006042 A JP2015006042 A JP 2015006042A JP 2016131577 A JP2016131577 A JP 2016131577A
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film
covering
container
medical multi
chamber container
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JP6800560B2 (en
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正英 河内
Masahide Kawachi
正英 河内
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Otsuka Pharmaceutical Factory Inc
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Abstract

PROBLEM TO BE SOLVED: To provide a medical multi-chamber container in which a partition sealing part can be opened reliably and easily, alternatively it is hard to open in transport, etc.SOLUTION: A medical multi-chamber container 10 includes: a container body 12 formed of a partition sealing part 28 for peelably bonding first and second films 12a, 12b, and partitioning the inside into first and second storage parts 24, 26; a medicine ejection part 14 in communication with the second storage part 26; and a covering member 22 for covering up at least a portion of the container body. The covering member comprises first and second coated films 22a, 22b bonded to first and the second films, respectively. The first and the second coated films are bonded to the first and second films on the partition sealing part by the bonding strength not less than the bonding strength of the partition sealing part, and are peelably bonded to the first and second films on the second storage part.SELECTED DRAWING: Figure 1

Description

本発明は、混合すると経時変化を起こすような不安定な各種薬剤(液剤、粉末若しくは固形剤)を個別に収納する複数の収納部を備える医療用複室容器に関する。   The present invention relates to a medical multi-chamber container provided with a plurality of storage units that individually store various unstable drugs (solutions, powders, or solid agents) that change with time when mixed.

静脈注射により患者に投与される薬剤の中には、予め混合すると望ましくない経時的変化を起こすような不安定な薬剤がある。例えば、アミノ酸輸液とブドウ糖輸液の場合には、メイラード反応によって混合液が褐変する。また、脂肪乳剤と電解質溶液の場合には脂肪分が凝集し、リン酸含有液とカルシウム含有液の場合にはリン酸カルシウムの沈殿が生じる。   Among drugs administered to patients by intravenous injection, there are unstable drugs that cause undesirable changes over time when premixed. For example, in the case of an amino acid infusion and a glucose infusion, the mixed solution browns due to the Maillard reaction. In the case of a fat emulsion and an electrolyte solution, fat is aggregated, and in the case of a phosphoric acid-containing solution and a calcium-containing solution, precipitation of calcium phosphate occurs.

これらの薬剤を収納する容器として、混合前の複数種の薬剤成分をそれぞれ個別に収納する医療用複室容器が知られている(特許文献1参照)。かかる複室容器としては、特許文献1に記載のように、各薬剤を個別に収納するための複数の収納部と、複数の収納部を仕切る仕切り用封止部とを備えるものがある。仕切り用封止部の接合強度は低く設定されているため、複数の収納部の一方の外側から圧力を加えると、収容部内の圧力の高まりによって仕切り用封止部が開封し、複数の収納部同士が開通する。これにより、個別に収納されていた薬剤が混合され、経時的変化を生ずる前に患者に投与することが可能となる。   As a container for storing these drugs, there is known a medical multi-chamber container that individually stores a plurality of types of drug components before mixing (see Patent Document 1). As such a multi-chamber container, as disclosed in Patent Document 1, there is a container including a plurality of storage portions for individually storing each medicine and a partition sealing portion for partitioning the plurality of storage portions. Since the bonding strength of the partition sealing portion is set low, when pressure is applied from one outer side of the plurality of storage portions, the partition sealing portion is opened due to an increase in pressure in the storage portion, and the plurality of storage portions Opening each other. As a result, the individually stored medicines are mixed and can be administered to the patient before a change with time occurs.

特開2002−136570号公報JP 2002-136570 A

前述したような従来の医療用複室容器においては、仕切り用封止部を開封させるために収納部へ加える圧力が十分でない場合や、収納部に圧力を加える動作が行われない場合には、仕切り用封止部が開封せず複数の収納部同士も開通しないため、個別に収納された薬剤が混合されないまま患者に投与されてしまう危険性があった。   In the conventional medical multi-chamber container as described above, when the pressure applied to the storage part is not sufficient to open the partition sealing part, or when the operation of applying pressure to the storage part is not performed, Since the partition sealing part is not opened and a plurality of storage parts are not opened, there is a risk that individually stored medicines are administered to the patient without being mixed.

収納部へ加える圧力が十分でない場合に対しては、複数の収納部同士が開通しやすいように仕切り用封止部の接合強度を大幅に低くすることが考えられる。しかしながら、仕切り用弱シール部の接合強度を易開封の面から低くすると、輸送時の衝撃など意図しない場合に仕切り用弱シール部が開封してしまい、薬剤の混合や経時的変化が生じてしまうおそれがある。   In the case where the pressure applied to the storage portion is not sufficient, it is conceivable to significantly reduce the bonding strength of the partition sealing portion so that the plurality of storage portions can be easily opened. However, if the bonding strength of the partition weak seal part is lowered from the easy-opening surface, the partition weak seal part is opened when an impact such as an impact during transportation is not intended, and mixing of the medicine or a change over time occurs. There is a fear.

本発明は、上記問題点に鑑みてなされたものであり、容器本体の仕切り用封止部を確実に且つ容易に開封することができ、その一方で輸送時の衝撃などでは開封しにくい医療用複室容器を提供することを目的とする。   The present invention has been made in view of the above-described problems, and can reliably and easily open the partition sealing portion of the container body, while being difficult to open due to impact during transportation. The object is to provide a multi-chamber container.

本発明者らは、医療用複室容器の構造について鋭意検討した結果、上記課題を解決できる医療用複室容器を創案した。すなわち、本発明による医療用複室容器は、第1のフィルムと該第1のフィルムに対向する第2のフィルムとから構成された袋状の容器本体であり、第1のフィルムと第2のフィルムとを剥離可能に接合することにより内部を第1の収納部と第2の収納部とに仕切る仕切り用封止部が形成されている容器本体と、容器本体に取り付けられ、第2の収納部と連通する薬剤排出部と、少なくとも容器本体の一部を覆う被覆部材とを備えるものであって、被覆部材が、第1のフィルム及び第2のフィルムにそれぞれ接合される第1の被覆フィルム及び第2の被覆フィルムからなり、第1の被覆フィルム及び第2の被覆フィルムが、仕切り用封止部上の第1のフィルム及び第2のフィルムに、仕切り用封止部の接合強度以上の接合強度にて接合されており、第1の被覆フィルム及び第2の被覆フィルムが、第2の収納部上の第1のフィルム及び第2のフィルムに剥離可能に接合されているものである。   As a result of intensive studies on the structure of a medical multi-chamber container, the present inventors have devised a medical multi-chamber container that can solve the above-described problems. That is, the medical multi-chamber container according to the present invention is a bag-like container body composed of a first film and a second film facing the first film, and the first film and the second film A container main body in which a partition sealing portion is formed to partition the inside into a first storage portion and a second storage portion by releasably joining the film, and the second storage is attached to the container main body. The first covering film is provided with a medicine discharge portion communicating with the portion and a covering member that covers at least a part of the container body, and the covering member is bonded to the first film and the second film, respectively. And the second covering film, the first covering film and the second covering film are equal to or higher than the bonding strength of the partition sealing portion to the first film and the second film on the partition sealing portion. Bonded with bonding strength Ri, the first coating film and the second coating film, those which are releasably joined to the first film and second film on the second housing portion.

本発明の医療用複室容器によれば、被覆部材と仕切り用封止部との接合強度が仕切り用封止部の接合強度以上であるため、複室容器の使用を開始するために被覆部材を少なくとも容器本体の一部から引き離して剥離するとその引張力によって仕切り用封止部も開封され、2つの収納部同士が確実に開通される。これにより、収納部へ加える圧力が十分でない場合や、収納部に圧力を加える動作が行われない場合であっても、個別に収納されていた薬剤が確実に混合され、患者に投与することが可能となる。   According to the medical multi-chamber container of the present invention, since the bonding strength between the covering member and the partition sealing portion is equal to or higher than the bonding strength of the partition sealing portion, the covering member is used to start the use of the multi-chamber container. When the container is separated from at least a part of the container body and peeled, the partition sealing part is also opened by the tensile force, and the two storage parts are reliably opened. Thereby, even when the pressure applied to the storage unit is not sufficient or the operation of applying pressure to the storage unit is not performed, the individually stored medicines can be reliably mixed and administered to the patient. It becomes possible.

また、従来の医療用複室容器は、薬剤排出部がピールシールにより被覆され使用時までの無菌状態が保たれるようになっているが、この複室容器を使用する際、使用者は、仕切り用封止部を開封すると共にピールシールを剥がさなければならず、薬剤投与の作業に手間がかかるという問題もある。   In addition, the conventional medical multi-chamber container is designed so that the medicine discharge part is covered with a peel seal and is kept in a sterile state until use, but when using this multi-chamber container, the user There is also a problem that it takes time and labor to administer the medicine, since the partition sealing portion must be opened and the peel seal must be peeled off.

これに対し、薬剤排出部も被覆部材により被覆されている医療複室容器においては、従来施されていたピールシールが不要となり、被覆部材を剥がすのみで、薬剤排出部の露出と仕切り用封止部の開封とを同時に行うことができ、薬剤投与作業の手間を軽減することができる。   On the other hand, in the medical multi-chamber container in which the medicine discharge part is also covered with the covering member, the peel seal which has been conventionally applied becomes unnecessary, and the exposure of the medicine discharge part and the sealing for partitioning can be performed only by peeling the covering member. The opening of the part can be performed at the same time, and the labor of the drug administration work can be reduced.

被覆部材は省資源の観点から容器本体の一部にのみ設けてもよいが、被覆部材が容器本体の全体を被覆するようにしてもよい。これにより、従来の医療用複室容器に対して施されていた外装を省くことが可能となる。これは、省資源に寄与すると共に、外装の廃棄をも不要とするので薬剤投与作業の手間を軽減することにも繋がる。   The covering member may be provided only on a part of the container body from the viewpoint of resource saving, but the covering member may cover the entire container body. Thereby, it becomes possible to omit the exterior which was provided with respect to the conventional medical multi-chamber container. This contributes to resource saving and also eliminates the need for disposal of the exterior, leading to a reduction in labor for drug administration.

また、第1の被覆フィルム及び第2の被覆フィルムは、仕切り用封止部の接合強度以上の接合強度にて、第2の収納部上の第1のフィルム及び第2のフィルムに剥離可能に接合されていることが好ましい。これにより、被覆部材を第2の収納部から剥離しているときに仕切り用封止部の開封が開始されるため、より一層、開封を確実に行うことができる。   In addition, the first cover film and the second cover film can be peeled off from the first film and the second film on the second storage portion with a bonding strength equal to or higher than the bonding strength of the partition sealing portion. It is preferable that it is joined. Thereby, since the opening of the sealing part for a partition is started when the coating | coated member is peeled from the 2nd accommodating part, it can open more reliably.

第1の被覆フィルム及び第2の被覆フィルムの、薬剤排出部側の端部にフック挿入用の穴を形成してもよい。この穴は、第1の被覆フィルム及び第2の被覆フィルムを薬剤排出部及び容器本体の第2の収納部から剥離し、仕切り用封止部を中心に反対側に折り返した状態において、薬剤排出部とは反対側の容器本体の端部よりも外側に配置されるようになっている。これにより、いわゆる点滴スタンドのフックにこの医療用複室容器を吊すことができる。この構成によれば、被覆部材の剥離から、点滴スタンドに吊るし医療用複室容器の使用を開始するまで一連の動作で行うことが可能となり、簡便に薬剤投与を行うことができる。   You may form the hole for hook insertion in the edge part by the side of a chemical | medical agent discharge part of a 1st coating film and a 2nd coating film. In the state where the first cover film and the second cover film are peeled off from the drug discharge part and the second storage part of the container body and folded back to the opposite side with the partition sealing part as the center, this hole It arrange | positions outside the edge part of the container main body on the opposite side to a part. Thereby, this medical multi-chamber container can be hung on the hook of a so-called drip stand. According to this configuration, it is possible to perform a series of operations from the peeling of the covering member to the start of the use of the medical multi-chamber container suspended from the drip stand, and the drug administration can be easily performed.

第1の被覆フィルム及び第2の被覆フィルムの、第1のフィルム及び第2のフィルムに対する接合方法としては種々考えられるが、各フィルムの表面層が熱可塑性樹脂層である場合又は各フィルムの全体が熱可塑性樹脂からなる場合には、熱融着によることが有効である。熱融着は熱を加えるだけの簡便な方法であり、加熱温度を調整することで接合強度を容易にコントロールすることができるからである。また、熱融着は、医療用複室容器の製造工程の最終段階で通常施される高圧蒸気滅菌の温度を利用して行うことができる。この場合、複室容器の製造工程から被覆部材に係る接合工程を省くことができるという利点がある。また、高圧によって、被覆部材の内面と容器本体の外面とを密に接合させることもできる。   Various bonding methods of the first coated film and the second coated film to the first film and the second film are conceivable. When the surface layer of each film is a thermoplastic resin layer, or the whole of each film. When is made of a thermoplastic resin, it is effective to use heat fusion. This is because heat fusion is a simple method in which only heat is applied, and the bonding strength can be easily controlled by adjusting the heating temperature. Further, the heat fusion can be performed by utilizing the temperature of high-pressure steam sterilization that is usually performed in the final stage of the manufacturing process of the medical multi-chamber container. In this case, there exists an advantage that the joining process which concerns on a coating | coated member can be omitted from the manufacturing process of a multi-chamber container. Further, the inner surface of the covering member and the outer surface of the container body can be tightly joined by high pressure.

なお、第1の被覆フィルム及び第2の被覆フィルムの形態は種々考えられ、例えば医療用複室容器全体を被覆するブリスター包装を構成するものであってもよい。   In addition, the form of the 1st coating film and the 2nd coating film is considered variously, For example, you may comprise the blister packaging which coat | covers the whole medical multi-chamber container.

本発明によれば、容器本体の仕切り用封止部が、医療用複室容器の使用時には開封しやすく、その一方で輸送時の衝撃などでは開封しにくい医療用複室容器を提供することが可能となる。特に、被覆部材が薬剤排出部も被覆する医療用複室容器においては、ピールシールが不要となる。これによって、薬剤排出部の露出から仕切り用封止部の開封まで一連の動作で行うことができ、薬剤投与作業が容易となることから好ましい。   According to the present invention, it is possible to provide a medical multi-chamber container in which the partition sealing portion of the container body is easy to open during use of the medical multi-chamber container, but is difficult to open due to impact during transportation. It becomes possible. In particular, in a medical multi-chamber container in which the covering member also covers the medicine discharge portion, no peel seal is required. This is preferable because it can be performed by a series of operations from the exposure of the medicine discharge section to the opening of the partition sealing section, and the medicine administration work is facilitated.

医療用複室容器の一実施形態を示す概略的平面図である。It is a schematic plan view which shows one Embodiment of a medical multi-chamber container. 図1のII−II線に沿った概略的断面図である。It is a schematic sectional drawing in alignment with the II-II line of FIG. 容器本体から被覆部材を剥離する際の動作を示す概略的断面図である。It is a schematic sectional drawing which shows the operation | movement at the time of peeling a coating | coated member from a container main body. 医療用複室容器の使用時の状態を示す概略的断面図である。It is a schematic sectional drawing which shows the state at the time of use of a medical multi-chamber container. 医療用複室容器の変形例を示す概略的断面図である。It is a schematic sectional drawing which shows the modification of a medical multi-chamber container. 医療用複室容器の変形例を示す概略的断面図である。It is a schematic sectional drawing which shows the modification of a medical multi-chamber container. 医療用複室容器の変形例を示す概略的断面図である。It is a schematic sectional drawing which shows the modification of a medical multi-chamber container. 医療用複室容器の変形例を示す概略的断面図である。It is a schematic sectional drawing which shows the modification of a medical multi-chamber container.

以下、本発明に係る医療用複室容器の実施形態について図面を参照しつつ説明する。   Hereinafter, embodiments of a medical multi-chamber container according to the present invention will be described with reference to the drawings.

図1は、医療用複室容器の一実施形態を示す概略的平面図であり、図2は図1のII−II線に沿った概略断面図である。これらの図に示すように、医療用複室容器10は、矩形形状の容器本体12と、この容器本体12に取り付けられた薬剤排出部14とを備えている。また、医療用複室容器10はさらに被覆部材22を備え、当該被覆部材22は容器本体12及び薬剤排出部14を覆っている。   FIG. 1 is a schematic plan view showing an embodiment of a medical multi-chamber container, and FIG. 2 is a schematic cross-sectional view taken along line II-II in FIG. As shown in these drawings, the medical multi-chamber container 10 includes a rectangular container main body 12 and a medicine discharge section 14 attached to the container main body 12. Further, the medical multi-chamber container 10 further includes a covering member 22 that covers the container main body 12 and the medicine discharge portion 14.

容器本体12は、2枚のフィルム(第1のフィルム12a及び第2のフィルム12b)の周縁部30をその全周にわたり接合することで袋状に構成されている。これにより、容器本体12内に薬剤を収納できる。   The container main body 12 is configured in a bag shape by joining the peripheral portions 30 of two films (the first film 12a and the second film 12b) over the entire circumference. Thereby, a medicine can be stored in the container body 12.

容器本体12を構成するフィルムは、本実施形態では、同一形状かつ同一寸法の2枚の単層又は複層のフィルムであり、容器本体12の内側である内面がポリエチレン、ポリプロピレン、ポリスチレン等の熱可塑性樹脂であることが好ましい。熱可塑性樹脂を用いることにより、熱融着にてフィルム同士を接合することができる。また、容器本体12の外側である外面もポリエチレン、ポリプロピレン、ポリスチレン等の熱可塑性樹脂であることが好ましい。これにより、後述する高圧蒸気滅菌などの手段によって容器本体12の外面と被覆部材22の内面とを熱融着により接合できる。容器本体12を構成するフィルムは、少なくとも内面が耐薬品性を有し、フィルム全体として柔軟性を有することが好ましい。   In this embodiment, the film constituting the container body 12 is a single-layer or multi-layer film having the same shape and the same dimensions, and the inner surface inside the container body 12 is a heat such as polyethylene, polypropylene, polystyrene, or the like. A plastic resin is preferred. By using a thermoplastic resin, the films can be joined by heat fusion. Moreover, it is preferable that the outer surface which is the outer side of the container main body 12 is also thermoplastic resins, such as polyethylene, a polypropylene, a polystyrene. Thereby, the outer surface of the container main body 12 and the inner surface of the covering member 22 can be joined by thermal fusion by means such as high-pressure steam sterilization described later. It is preferable that at least the inner surface of the film constituting the container main body 12 has chemical resistance, and the film as a whole has flexibility.

なお、容器本体12を構成するフィルムとして、熱可塑性を有しない他の材料からなるフィルムを用いることもできる。この場合、接着剤を用いるなど他の手法により周縁部30を接合すればよい。   In addition, as a film which comprises the container main body 12, the film which consists of another material which does not have thermoplasticity can also be used. In this case, what is necessary is just to join the peripheral part 30 by other methods, such as using an adhesive agent.

容器本体12は、本実施形態では矩形形状であり、その長手方向が図1の縦方向(上下方向)となるように配置されている。以下、この図1に示す状態を基準として容器本体12の上下関係を説明する場合がある。   The container main body 12 has a rectangular shape in this embodiment, and is arranged so that the longitudinal direction thereof is the vertical direction (vertical direction) in FIG. Hereinafter, the vertical relationship of the container body 12 may be described based on the state shown in FIG.

容器本体12の上下方向の略中央部には、図1の左右横方向に延びる連通可能な仕切り用封止部28が形成されている。仕切り用封止部28によって、容器本体12の内部空間が上部空間(以下、「第1の収納部24」)と下部空間(以下、「第2の収納部26」)とに仕切られる。これにより、予め混合あるいは溶解することが適しない2種以上の薬剤を容器本体12に収納することが可能となる。例えば、メイラード反応による褐色変化等を起こすため隔離する必要がある各種薬剤をそれぞれ封入することができ、具体的には、一方の収納部24又は26にアミノ酸を含有する溶液、他方の収納部26又は24にブドウ糖を含有する溶液を収納することができる。また、液体状の薬剤だけでなく、固形または粉末状の薬剤を収納してもよい。   A partition sealing portion 28 that extends in the horizontal direction in FIG. 1 and that can communicate is formed at a substantially central portion in the vertical direction of the container body 12. By the partition sealing portion 28, the internal space of the container body 12 is partitioned into an upper space (hereinafter, “first storage portion 24”) and a lower space (hereinafter, “second storage portion 26”). As a result, two or more kinds of drugs that are not suitable to be mixed or dissolved in advance can be stored in the container body 12. For example, various chemicals that need to be isolated in order to cause browning due to the Maillard reaction can be enclosed. Specifically, one of the storage units 24 or 26 contains an amino acid solution, and the other storage unit 26 Alternatively, a solution containing glucose can be stored in 24. Further, not only a liquid drug but also a solid or powder drug may be stored.

仕切り用封止部28は、容器本体12を構成する2枚のフィルム同士を熱融着することで形成される。仕切り用封止部28の接合強度は、融着時間や温度等を調整することによって、周縁部30の接合強度よりも小さくされている。   The partition sealing portion 28 is formed by heat-sealing two films constituting the container body 12. The bonding strength of the partition sealing portion 28 is made smaller than the bonding strength of the peripheral edge portion 30 by adjusting the fusion time, temperature, and the like.

薬剤排出部14は、容器本体12における第2の収納部26側の端部に接続されている。薬剤排出部14は、薬剤が通過する通路を有する薬剤排出管16と、この薬剤排出管16を閉じるゴム栓18とから構成されている。ここで、医療用複室容器10の使用時(仕切り用封止部28の開封後)には、刺栓針をゴム栓18に刺入することにより、容器本体12内の薬剤を患者に投与可能となる。   The medicine discharge unit 14 is connected to the end of the container body 12 on the second storage unit 26 side. The medicine discharge part 14 is composed of a medicine discharge pipe 16 having a passage through which the medicine passes, and a rubber plug 18 that closes the medicine discharge pipe 16. Here, when the medical multi-chamber container 10 is used (after the partition sealing portion 28 is opened), the medicine in the container body 12 is administered to the patient by inserting the piercing needle into the rubber plug 18. It becomes possible.

図1及び図2に示すように、被覆部材22は、容器本体12及び薬剤排出部14の全体を被覆している。本実施形態においては、被覆部材22は単層又は複層の被覆フィルムからなっており、これを2つに折り曲げて表側の第1の被覆フィルム22a及び裏側の第2の被覆フィルム22bとして用いられている。これらの被覆フィルム22a、22bは、容器本体12よりも大きな矩形形状で実質的に同一寸法となっている。これらの被覆フィルム22a、22bの間に容器本体12及び薬剤排出部14を挟み、該被覆フィルム22a、22bの周縁部32の全周にわたり接合することで、容器本体12及び薬剤排出部14は密封されている。   As shown in FIGS. 1 and 2, the covering member 22 covers the entire container body 12 and the medicine discharge part 14. In the present embodiment, the covering member 22 is composed of a single-layer or multi-layer cover film, and is folded into two to be used as a front-side first cover film 22a and a back-side second cover film 22b. ing. These covering films 22a and 22b have a rectangular shape larger than the container body 12 and have substantially the same dimensions. The container main body 12 and the medicine discharge part 14 are sealed by sandwiching the container main body 12 and the drug discharge part 14 between these coating films 22a and 22b and joining them all around the peripheral part 32 of the cover films 22a and 22b. Has been.

図示実施形態では、被覆部材22は、柔軟性を有し、被覆部材22と容器本体12との間の空気を吸引する真空包装により、容器本体12及び薬剤排出部14の外面に対して密着している。また、被覆部材22は容器本体12の略全体(第1の収納部24、仕切り用封止部28及び第2の収納部26の外面)に接合されている。各部位における接合強度については後述する。   In the illustrated embodiment, the covering member 22 has flexibility and is in close contact with the outer surfaces of the container main body 12 and the medicine discharge section 14 by vacuum packaging that sucks air between the covering member 22 and the container main body 12. ing. The covering member 22 is joined to substantially the entire container body 12 (the outer surfaces of the first storage portion 24, the partition sealing portion 28, and the second storage portion 26). The bonding strength at each part will be described later.

接合は、接着剤等によってもよいが、熱融着によることが好ましい。したがって、被覆部材22を構成するフィルム22a、22bは、その少なくとも内面が、容器本体12の樹脂と熱によって融着しやすい、ポリエチレン、ポリプロピレン、ポリスチレン等の熱可塑性樹脂からなることが好ましい。特に、容器本体12を構成するフィルム12a、12bの外面に使用する樹脂と、被覆部材22を構成する被覆フィルム22a、22bの内面に使用する樹脂とを、比較的融点が低い樹脂とすることが好ましい。これにより、医療用複室容器10に対し、製造工程の最終段階で通常施される高圧蒸気滅菌の熱によって、容器本体12を構成するフィルム12a、12bの外面と、被覆部材22を構成する被覆フィルム22a、22bの内面とを接合させることも可能となる。   The bonding may be performed using an adhesive or the like, but is preferably performed by heat fusion. Therefore, it is preferable that at least the inner surfaces of the films 22a and 22b constituting the covering member 22 are made of a thermoplastic resin such as polyethylene, polypropylene, or polystyrene, which is easily fused with the resin of the container body 12 by heat. In particular, the resin used on the outer surfaces of the films 12a and 12b constituting the container body 12 and the resin used on the inner surfaces of the covering films 22a and 22b constituting the covering member 22 may be resins having a relatively low melting point. preferable. Thereby, the outer surface of the films 12a and 12b constituting the container main body 12 and the covering constituting the covering member 22 are applied to the medical multi-chamber container 10 by heat of high-pressure steam sterilization usually applied at the final stage of the manufacturing process. It is also possible to join the inner surfaces of the films 22a and 22b.

本実施形態の医療用複室容器10においては、被覆部材22の内面を構成する被覆フィルム22a、22bに含まれる熱可塑性樹脂と、容器本体12を構成するフィルム12a、12bの外面に含まれる熱可塑性樹脂とがポリエチレンなど同一の樹脂で共通し、一方、容器本体12を構成するフィルム12a、12bの内面に含まれる熱可塑性樹脂はポリプロピレンとポリエチレンとの混合物であることも好ましい。医療用複室容器10の製造工程の最終段階で通常施される高圧蒸気滅菌の温度をポリエチレンの融点より高く、ポリプロピレンの融点よりも低く設定することによって、高圧蒸気滅菌により、ポリエチレンなど同一の樹脂である被覆部材22の内面と容器本体12の外面とを密に接合させることができ、ポリプロピレンとポリエチレンとの混合物により接合強度が低くなる仕切り用封止部28よりも、接合強度を高くすることができる。   In the medical multi-chamber container 10 of the present embodiment, the thermoplastic resin contained in the coating films 22a and 22b constituting the inner surface of the covering member 22 and the heat contained in the outer surfaces of the films 12a and 12b constituting the container body 12 are used. It is also preferred that the plastic resin is common to the same resin such as polyethylene, while the thermoplastic resin contained in the inner surfaces of the films 12a and 12b constituting the container body 12 is a mixture of polypropylene and polyethylene. By setting the temperature of high-pressure steam sterilization usually applied in the final stage of the manufacturing process of the medical multi-chamber container 10 to be higher than the melting point of polyethylene and lower than the melting point of polypropylene, the same resin such as polyethylene can be obtained by high-pressure steam sterilization. The inner surface of the covering member 22 and the outer surface of the container body 12 can be tightly bonded, and the bonding strength is made higher than that of the partition sealing portion 28 in which the bonding strength is lowered by a mixture of polypropylene and polyethylene. Can do.

本実施形態の医療用複室容器10においては、被覆部材22を用いて薬剤排出部14も被覆していることから、薬剤排出部14のゴム栓18の上面を衛生上の観点から被覆するために通常用いられるピールシールが不要となる。また、使用前の段階で薬剤排出部14が被覆部材22で覆われているため、複数の収納部24、26の開通前の使用を防止することが可能となる。   In the medical multi-chamber container 10 of the present embodiment, since the medicine discharge portion 14 is also covered with the covering member 22, the upper surface of the rubber plug 18 of the medicine discharge portion 14 is covered from the viewpoint of hygiene. The peel seal normally used in the case is not necessary. In addition, since the medicine discharge portion 14 is covered with the covering member 22 before use, it is possible to prevent the use of the plurality of storage portions 24 and 26 before opening.

なお、被覆部材22のフィルム22a、22bは、遮光性やガスバリア性、水蒸気バリア性を有することが好ましい。また、図2から理解される通り、容器本体12及び薬剤排出部14の形状、及び、被覆部材22のフィルム22a、22bの性状によっては、被覆部材22と容器本体12や薬剤排出部14との間に空間が形成される場合がある。このような場合には、この空間に酸素吸収剤や水分吸収剤が封入されていてもよい。これらにより、容器本体12内の薬剤が酸素や水分によって劣化する成分の場合でも、劣化を抑制できる。   In addition, it is preferable that the films 22a and 22b of the covering member 22 have light shielding properties, gas barrier properties, and water vapor barrier properties. Further, as understood from FIG. 2, depending on the shape of the container main body 12 and the drug discharge portion 14 and the properties of the films 22 a and 22 b of the cover member 22, the cover member 22 and the container main body 12 and the drug discharge portion 14 A space may be formed between them. In such a case, an oxygen absorbent or a moisture absorbent may be enclosed in this space. Accordingly, even when the drug in the container body 12 is a component that deteriorates due to oxygen or moisture, deterioration can be suppressed.

次に、本実施形態の医療用複室容器の使用方法について説明する。   Next, the usage method of the medical multi-chamber container of this embodiment is demonstrated.

図3は、容器本体12から被覆部材22を剥離する際の動作を示す概略的断面図である。図3に示すように、医療用複室容器10の使用を開始する際には、薬剤排出部14側から薬剤排出部14に隣接していない第1の収納部24側へ、被覆部材22の両側の被覆フィルム22a、22bを剥離していく。なお、図1、図2に示すように、被覆部材22の被覆フィルム(表側、22a)の周縁部32につまみ部34が形成されている。このため、被覆フィルム(裏側、22b)の端部36とつまみ部34をそれぞれ把持することにより、被覆部材22を剥離しやすくなる。   FIG. 3 is a schematic cross-sectional view showing the operation when the covering member 22 is peeled from the container body 12. As shown in FIG. 3, when the use of the medical multi-chamber container 10 is started, the covering member 22 is moved from the medicine discharge section 14 side to the first storage section 24 side not adjacent to the medicine discharge section 14. The covering films 22a and 22b on both sides are peeled off. In addition, as shown in FIG. 1, FIG. 2, the knob part 34 is formed in the peripheral part 32 of the coating film (front side, 22a) of the coating | coated member 22. As shown in FIG. For this reason, it becomes easy to peel the covering member 22 by gripping the end portion 36 and the knob portion 34 of the covering film (back side, 22b).

ここで、被覆部材22と容器本体12との間の接合強度について詳細に説明する。被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bは、仕切り用封止部28上の第1のフィルム12a及び第2のフィルム12bに、仕切り用封止部28の第1のフィルム12aと第2のフィルム12bとの接合強度以上の接合強度にて接合されている。図3に示すように、複室容器10の使用を開始するために被覆部材22を薬剤排出部14及び容器本体12から引き離して剥離すると、その引張力F,Fによって仕切り用封止部28も開封され、2つの収納部24、26同士が確実に開通される。このため、2つの収納部24、26に個別に収納されていた薬剤が確実に混合された後に、患者に投与することが可能となる。なお、第1の被覆フィルム22a及び第2の被覆フィルム22bは、仕切り用封止部28上の第1のフィルム12a及び第2のフィルム12bに、仕切り用封止部28の接合強度よりも高い接合強度にて接合されていることが、仕切り用封止部28の開封をより確実に行う観点から好ましい。   Here, the bonding strength between the covering member 22 and the container body 12 will be described in detail. The first covering film 22a and the second covering film 22b of the covering member 22 are formed on the first film 12a and the second film 12b on the partition sealing portion 28 by the first sealing portion 28. The film 12a and the second film 12b are bonded with a bonding strength equal to or higher than the bonding strength. As shown in FIG. 3, when the covering member 22 is pulled away from the medicine discharge portion 14 and the container body 12 to start using the multi-chamber container 10, the partition sealing portion 28 is also caused by the tensile forces F and F. The container is opened and the two storage portions 24 and 26 are reliably opened. For this reason, it becomes possible to administer to the patient after the medicines individually stored in the two storage portions 24 and 26 are reliably mixed. The first covering film 22a and the second covering film 22b are higher than the bonding strength of the partition sealing portion 28 to the first film 12a and the second film 12b on the partition sealing portion 28. Bonding with bonding strength is preferable from the viewpoint of more reliably opening the partition sealing portion 28.

また、被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bは、第2の収納部26上の第1のフィルム12a及び第2のフィルム12bに剥離可能に接合されており、剥離可能であればその接合強度はどのような強度であってもよい。しかし、被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bは、仕切り用封止部28の接合強度以上の接合強度にて、第2の収納部26上の第1のフィルム12a及び第2のフィルム12bに剥離可能に接合されていることが好ましい。これにより、被覆部材22を第2の収納部26から剥離する動作によって仕切り用封止部28の開封が開始されるため、より一層、開封を確実に行うことが可能となる。なお、第1の被覆フィルム22a及び第2の被覆フィルム22bは、第2の収納部26上の第1のフィルム12a及び第2のフィルム12bに、仕切り用封止部28の接合強度よりも高い接合強度で接合されていることがより好ましい。   Moreover, the 1st coating film 22a and the 2nd coating film 22b of the coating | coated member 22 are joined to the 1st film 12a and the 2nd film 12b on the 2nd accommodating part 26 so that peeling is possible, and peeling If possible, the bonding strength may be any strength. However, the first covering film 22a and the second covering film 22b of the covering member 22 have a bonding strength equal to or higher than the bonding strength of the partition sealing portion 28, and the first film 12a on the second storage portion 26. And it is preferable that it is joined to the 2nd film 12b so that peeling is possible. Thereby, since the opening of the partition sealing portion 28 is started by the operation of peeling the covering member 22 from the second storage portion 26, the opening can be further reliably performed. In addition, the 1st coating film 22a and the 2nd coating film 22b are higher than the joint strength of the partition sealing part 28 to the 1st film 12a and the 2nd film 12b on the 2nd accommodating part 26. It is more preferable that they are bonded with bonding strength.

また、被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bと、第1の収納部24上の第1のフィルム12a及び第2のフィルム12bとの接合強度は、仕切り用封止部28の開封の観点からは特に制限されない。しかし、複室容器10が点滴スタンドに吊るされている際に、薬剤などの荷重によって容器本体12が被覆部材22から剥がれて落下するのを防止する観点から、被覆部材22の被覆フィルム22a、22bと第1の収納部24上のフィルム12a、12bとが薬剤などの荷重によって剥離しない接合強度で接合されていることが好ましく、剥離不可能なように接合されていてもよい。   Further, the bonding strength between the first coating film 22a and the second coating film 22b of the coating member 22 and the first film 12a and the second film 12b on the first storage portion 24 is determined by the partition sealing. From the viewpoint of opening the portion 28, there is no particular limitation. However, when the multi-chamber container 10 is suspended from the drip stand, the covering films 22a and 22b of the covering member 22 are prevented from preventing the container body 12 from being peeled off from the covering member 22 due to a load such as a medicine. And the films 12a and 12b on the first storage unit 24 are preferably bonded with a bonding strength that does not peel off due to a load such as a drug, and may be bonded so that they cannot be peeled off.

図3に示すように、被覆部材22の両側の第1の被覆フィルム22a、第2の被覆フィルム22bは、容器本体12から全て剥離しないようにすることもできる。医療機関においては、医療廃棄物の処理は厳格であり分別も徹底されているところ、本実施形態の複室容器10であれば、容器本体12と被覆部材22が一体であることから、一回で廃棄処理することができ、分別処理の手間が軽減される点においても利便性が高い。   As shown in FIG. 3, the first covering film 22 a and the second covering film 22 b on both sides of the covering member 22 may not be peeled from the container body 12. In a medical institution, treatment of medical waste is strict and thorough separation is performed. In the case of the multi-chamber container 10 of the present embodiment, the container body 12 and the covering member 22 are integrated. Therefore, it can be disposed of in a convenient manner, and the convenience of separation processing is reduced.

図4は、医療用複室容器の使用時の状態を示す概略的断面図である。図4に示すように、薬剤排出部14側から剥離した被覆部材22の第1の被覆フィルム22a、第2の被覆フィルム22bは、容器本体12の被覆時に容器本体12の外面側と接合していた内面が、仕切り用封止部28を中心に折り返されることによって反転し外面となる。また、容器本体12の被覆時の外面は、同様に折り返されることによって反転し内面となり、第1の収納部24側を被覆している第1の被覆フィルム22a及び第2の被覆フィルム22bの外面と重なり合う。   FIG. 4 is a schematic cross-sectional view showing a state in use of the medical multi-chamber container. As shown in FIG. 4, the first covering film 22 a and the second covering film 22 b of the covering member 22 peeled from the medicine discharge section 14 side are joined to the outer surface side of the container body 12 when the container body 12 is covered. The inner surface is inverted by turning back around the partition sealing portion 28 and becomes the outer surface. In addition, the outer surface of the container body 12 when covered is similarly reversed to be reversed to become the inner surface, and the outer surfaces of the first covering film 22a and the second covering film 22b covering the first storage portion 24 side. And overlap.

図4に示すように、第1の被覆フィルム22a及び第2の被覆フィルム22bを薬剤排出部14及び容器本体12の第2の収納部26上の第1のフィルム12a及び第2のフィルム12bから剥離し、仕切り用封止部28を中心に反対側に折り返した状態において、薬剤排出部14とは反対側の容器本体12の端部よりも外側に、フック挿入用の穴38が形成されており、フック40が穴38に挿入される。この穴38は、図1に示すように、被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bの、薬剤排出部14側の端部に形成されたものである。これにより、いわゆる点滴スタンドのフック40に本医療用複室容器10を吊すことができる。このように、本実施形態の医療用複室容器10によれば、被覆部材22の剥離から、点滴スタンドに吊るし使用を開始するまで一連の動作で行うことが可能となり、簡便に薬剤投与を行うことができる。なお、従来の複室容器では、例えば仕切り用封止部の開封作業中に放置されてしまうと、仕切り封止部が開封され薬剤の混合や経時変化が生じてしまうが、本実施形態の複室容器によれば一連の動作で使用開始できるため、開封作業中或いは開封作業後に放置されることを防止しやすくなる。   As shown in FIG. 4, the first coating film 22 a and the second coating film 22 b are separated from the first film 12 a and the second film 12 b on the drug discharge unit 14 and the second storage unit 26 of the container body 12. In the state of peeling and folding back to the opposite side with the partition sealing portion 28 as the center, a hook insertion hole 38 is formed on the outer side of the end portion of the container body 12 on the side opposite to the medicine discharge portion 14. The hook 40 is inserted into the hole 38. As shown in FIG. 1, the hole 38 is formed at the end of the first covering film 22 a and the second covering film 22 b of the covering member 22 on the side of the medicine discharge section 14. Thereby, the medical multi-chamber container 10 can be suspended from the hook 40 of a so-called drip stand. As described above, according to the medical multi-chamber container 10 of the present embodiment, it is possible to perform a series of operations from peeling of the covering member 22 until it is hung on the drip stand and starts to be used. be able to. In the case of a conventional multi-chamber container, for example, if the container is left during the opening operation of the partition sealing portion, the partition sealing portion is unsealed, resulting in mixing of the medicines and changes over time. According to the chamber container, use can be started by a series of operations, so that it is easy to prevent the chamber container from being left during or after the opening operation.

図5は、医療用複室容器10bの変形例を示す概略的断面図である。図5に示す通り、被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bは、容器本体12の仕切り用封止部28上及び第2の収納部26上の第1のフィルム12a及び第2のフィルム12bと接合しているだけでもよく、仕切り用封止部28上の第1のフィルム12a及び第2のフィルム12bのみと接合しているだけでもよい。例えば、高圧蒸気滅菌済みの容器本体12に被覆部材22を接合させる場合には、両者の接合部分が少ない方が接着剤使用量も削減できる。なお、このような変形例の医療用複室容器10bにおいては、図2で示す医療用複室容器10と比べ、被覆部材22と容器本体12や薬剤排出部14との間の空間が広くなる傾向にあることから、容器本体12内の薬剤の劣化を抑制するために、酸素吸収剤又は水分吸収剤Aを封入することが好ましい。また、図5の医療用複室容器10bを点滴スタンドに吊るす際の落下防止の観点から、被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bと、仕切り用封止部28上の第1のフィルム12a及び第2のフィルム12bとの接合部分は、薬剤などの荷重によって剥離しない接合強度で接合されていることが好ましく、剥離不可能に接合されていてもよい。   FIG. 5 is a schematic cross-sectional view showing a modified example of the medical multi-chamber container 10b. As shown in FIG. 5, the first covering film 22 a and the second covering film 22 b of the covering member 22 are the first film 12 a on the partition sealing portion 28 and the second storage portion 26 of the container body 12. And only the first film 12a and the second film 12b on the partition sealing portion 28 may be bonded. For example, when the covering member 22 is joined to the container body 12 that has been subjected to high-pressure steam sterilization, the amount of adhesive used can be reduced when the joint portion between the two is small. In addition, in the medical multi-chamber container 10b of such a modification, the space between the covering member 22 and the container main body 12 or the medicine discharge part 14 becomes wider than the medical multi-chamber container 10 shown in FIG. Because of this tendency, it is preferable to enclose the oxygen absorbent or the water absorbent A in order to suppress the deterioration of the medicine in the container body 12. Further, from the viewpoint of preventing the drop when the medical multi-chamber container 10b of FIG. 5 is hung on the drip stand, the first covering film 22a and the second covering film 22b of the covering member 22 and the partition sealing portion 28 are also provided. The joint portion between the first film 12a and the second film 12b is preferably joined with a joining strength that does not peel off due to a load such as a drug, and may be joined so as not to peel off.

図6は、医療用複室容器10cの変形例を示す概略的断面図である。図6に示す通り、被覆部材22は、第2の収納部26及び仕切り用封止部28までを被覆しており、第1の収納部24は被覆していない。このように、省資源の観点から被覆部材22は容器本体12の一部にのみ設けてもよい。また、酸素や水分によって劣化しやすい薬剤を収納する場合には、被覆部材22として酸素や水分の透過を抑制する素材を用い、当該薬剤を被覆部材22で覆われた第2の収納部26へ収納してもよい。なお、医療用複室容器10cについても医療用複室容器10bと同様に、点滴スタンドに吊るす際の落下防止の観点から、被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bと、仕切り用封止部28上の第1のフィルム12a及び第2のフィルム12bとの接合部分が、薬剤などの荷重によって剥離しない接合強度で接合されていることが好ましく、剥離不可能に接合されていてもよい。   FIG. 6 is a schematic cross-sectional view showing a modification of the medical multi-chamber container 10c. As shown in FIG. 6, the covering member 22 covers up to the second storage portion 26 and the partition sealing portion 28, and does not cover the first storage portion 24. Thus, from the viewpoint of resource saving, the covering member 22 may be provided only on a part of the container body 12. Further, when storing a drug that easily deteriorates due to oxygen or moisture, a material that suppresses permeation of oxygen or moisture is used as the covering member 22, and the drug is supplied to the second storage portion 26 covered with the covering member 22. It may be stored. The medical multi-chamber container 10c is similar to the medical multi-chamber container 10b in that the first covering film 22a and the second covering film 22b of the covering member 22 are prevented from being dropped when hung on the drip stand. In addition, it is preferable that the joining portions of the first film 12a and the second film 12b on the partition sealing portion 28 are joined with a joining strength that does not peel off due to a load such as a drug, and are joined so as not to be peeled off. It may be.

図7は、医療用複室容器の変形例を示す概略的断面図である。図7に示す通り、容器本体12及び薬剤排出部14はブリスター包装によって被覆されていてもよい。例えば、被覆部材22の第2の被覆フィルム22b上に、容器本体12の第2のフィルム12bが接するように容器本体12を配置する。続いて、被覆部材22の第1の被覆フィルム22aを容器本体1の第1のフィルム12a上に配置し、容器本体12及び薬剤排出部14を覆う。次に、第1の被覆フィルム22a及び第2の被覆フィルム22bの周縁部32を接合することで、容器本体12及び薬剤排出部14を密封できる。さらに、被覆部材22と容器本体12との間の空気を吸引し真空包装することによって、容器本体12と被覆部材22とを密着させることができる。   FIG. 7 is a schematic cross-sectional view showing a modification of the medical multi-chamber container. As shown in FIG. 7, the container body 12 and the medicine discharge part 14 may be covered with blister packaging. For example, the container body 12 is disposed on the second covering film 22b of the covering member 22 so that the second film 12b of the container body 12 is in contact therewith. Subsequently, the first covering film 22 a of the covering member 22 is disposed on the first film 12 a of the container main body 1 to cover the container main body 12 and the medicine discharge unit 14. Next, the container main body 12 and the chemical | medical agent discharge part 14 can be sealed by joining the peripheral part 32 of the 1st coating film 22a and the 2nd coating film 22b. Furthermore, the container body 12 and the covering member 22 can be brought into close contact with each other by sucking the air between the covering member 22 and the container body 12 and vacuum-packaging it.

本実施形態のブリスター包装による医療用複室容器10dにおいても、被覆部材22としてポリエチレンやポリプロピレンなどの熱可塑性樹脂を使用できるため、高圧蒸気滅菌時の熱により、容器本体12の外面と被覆部材22の内面とを接合することができる。被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bは、仕切り用封止部28上の第1のフィルム12a及び第2のフィルム12bに、仕切り用封止部28の第1のフィルム12aと第2のフィルム12bとの接合強度以上の接合強度にて接合される。本実施形態のブリスター包装による医療用複室容器10dは、耐衝撃性に優れる。このため、通常の医療用複室容器の輸送時には、衝撃により仕切り用封止部が開封しないよう2つに折りたたむダブルバック方式を採用する場合があるが、本実施形態の医療用複室容器10dによれば、輸送時に2つに折りたたむ必要がなくなり、包装工程時の作業を簡略化することが可能となる。なお、第1の被覆フィルム22a及び第2の被覆フィルム22bは、仕切り用封止部28上の第1のフィルム12a及び第2のフィルム12bに、仕切り用封止部28の接合強度よりも高い接合強度にて接合されていることが、仕切り用封止部28の開封をより確実に行う観点から好ましい。   Also in the medical multi-chamber container 10d by the blister packaging of the present embodiment, since the thermoplastic resin such as polyethylene or polypropylene can be used as the covering member 22, the outer surface of the container body 12 and the covering member 22 are heated by heat during high-pressure steam sterilization. Can be joined to the inner surface. The first covering film 22a and the second covering film 22b of the covering member 22 are formed on the first film 12a and the second film 12b on the partition sealing portion 28 by the first sealing portion 28. The film 12a and the second film 12b are bonded with a bonding strength equal to or higher than the bonding strength. The medical multi-chamber container 10d by the blister packaging of this embodiment is excellent in impact resistance. For this reason, when transporting a normal medical multi-chamber container, there is a case where a double back method is adopted in which the partition sealing portion is folded in two so as not to open due to an impact, but the medical multi-chamber container 10d of this embodiment is used. According to this, it is not necessary to fold it into two at the time of transportation, and it becomes possible to simplify the work at the time of a packaging process. The first covering film 22a and the second covering film 22b are higher than the bonding strength of the partition sealing portion 28 to the first film 12a and the second film 12b on the partition sealing portion 28. Bonding with bonding strength is preferable from the viewpoint of more reliably opening the partition sealing portion 28.

図8は、医療用複室容器の変形例を示す概略的断面図である。図8に示す医療用複室容器10eは、被覆部材22の第2の被覆フィルム22bが仕切り用封止部28上の第2のフィルム12bと接合していない点で、図7に示す医療用複室容器10dと形状が相違する。ここで、被覆部材22の第1の被覆フィルム22aは、仕切り用封止部28上の第1のフィルム12aに、仕切り用封止部28の第1のフィルム12aと第2のフィルム12bとの接合強度以上の接合強度にて接合され、かつ、被覆部材22の第2の被覆フィルム22bは、第2の収納部26上及び第1の収納部24上の第2のフィルム12bに、仕切り用封止部28の第1のフィルム12aと第2のフィルム12bとの接合強度以上の接合強度で接合されている。医療用複室容器10eによれば、被覆部材22の第1の被覆フィルム22a及び第2の被覆フィルム22bを剥離する際に仕切り用封止部28が容易に開封される。なお、第1の被覆フィルム22aは仕切り用封止部28上の第1のフィルム12aに、又、第2の被覆フィルム22bは第2の収納部26上及び第1の収納部24上の第2のフィルム12bに、仕切り用封止部28の接合強度よりも高い接合強度にて接合されていることが、仕切り用封止部28の開封をより確実に行う観点から好ましい。   FIG. 8 is a schematic cross-sectional view showing a modification of the medical multi-chamber container. The medical multi-chamber container 10e shown in FIG. 8 has the medical cover shown in FIG. 7 in that the second covering film 22b of the covering member 22 is not joined to the second film 12b on the partition sealing portion. The shape is different from the multi-chamber container 10d. Here, the first covering film 22a of the covering member 22 is formed on the first film 12a on the partition sealing portion 28 by the first film 12a and the second film 12b of the partition sealing portion 28. The second covering film 22b of the covering member 22 is bonded to the second film 12b on the second storage portion 26 and the first storage portion 24 for partitioning with a bonding strength higher than the bonding strength. The first film 12a and the second film 12b of the sealing portion 28 are bonded with a bonding strength equal to or higher than the bonding strength. According to the medical multi-chamber container 10e, the partition sealing portion 28 is easily opened when the first covering film 22a and the second covering film 22b of the covering member 22 are peeled off. The first covering film 22a is on the first film 12a on the partition sealing portion 28, and the second covering film 22b is on the second storage portion 26 and on the first storage portion 24. It is preferable from the viewpoint of more reliably opening the partition sealing portion 28 that the second film 12b is bonded with a bonding strength higher than the bonding strength of the partition sealing portion 28.

10(10b,10c,10d,10e)…医療用複室容器
12…容器本体
12a…第1のフィルム
12b…第2のフィルム
14…薬剤排出部
16…薬剤排出管
18…ゴム栓
22…被覆部材
22a…第1の被覆フィルム
22b…第2の被覆フィルム
24…第1の収納部
26…第2の収納部
28…仕切り用封止部
30…(容器本体の)周縁部
32…(被覆部材の)周縁部
34…(第1の被覆フィルムの)つまみ部
36…(第2の被覆フィルムの)端部
38…穴
A…酸素吸収剤又は水分吸収剤。


10 (10b, 10c, 10d, 10e) ... medical multi-chamber container 12 ... container main body 12a ... first film 12b ... second film 14 ... drug discharge section 16 ... drug discharge pipe 18 ... rubber plug 22 ... covering member 22a ... 1st coating film 22b ... 2nd coating film 24 ... 1st accommodating part 26 ... 2nd accommodating part 28 ... Sealing part 30 for partitions (of container main body) 32 ... (of covering member) ) Peripheral part 34 ... knob part 36 (of the first covering film) 36 ... end part (of the second covering film) 38 ... hole A ... oxygen absorbent or moisture absorbent.


Claims (8)

第1のフィルムと該第1のフィルムに対向する第2のフィルムとから構成された袋状の容器本体であり、前記第1のフィルムと前記第2のフィルムとを剥離可能に接合することにより内部を第1の収納部と第2の収納部とに仕切る仕切り用封止部が形成されている容器本体、
前記容器本体に取り付けられ、前記第2の収納部と連通する薬剤排出部、及び、
少なくとも前記容器本体の一部を覆う被覆部材、
を備える医療用複室容器であって、
前記被覆部材が、前記第1のフィルム及び前記第2のフィルムにそれぞれ接合される第1の被覆フィルム及び第2の被覆フィルムからなり、
前記第1の被覆フィルム及び前記第2の被覆フィルムが、前記仕切り用封止部上の前記第1のフィルム及び前記第2のフィルムに、前記仕切り用封止部の接合強度以上の接合強度にて接合されており、
前記第1の被覆フィルム及び前記第2の被覆フィルムが、前記第2の収納部上の前記第1のフィルム及び前記第2のフィルムに剥離可能に接合されている、医療用複室容器。
A bag-like container body composed of a first film and a second film facing the first film, and by joining the first film and the second film in a peelable manner. A container body in which a partition sealing portion that partitions the interior into a first storage portion and a second storage portion is formed;
A medicine discharge part attached to the container body and communicating with the second storage part; and
A covering member covering at least a part of the container body;
A medical multi-chamber container comprising:
The covering member comprises a first covering film and a second covering film that are bonded to the first film and the second film, respectively.
The first covering film and the second covering film have a bonding strength equal to or higher than the bonding strength of the partition sealing portion on the first film and the second film on the partition sealing portion. Are joined together.
A medical multi-chamber container in which the first covering film and the second covering film are detachably joined to the first film and the second film on the second storage portion.
第1のフィルムと該第1のフィルムに対向する第2のフィルムとから構成された袋状の容器本体であり、前記第1のフィルムと前記第2のフィルムとを剥離可能に接合することにより内部を第1の収納部と第2の収納部とに仕切る仕切り用封止部が形成されている容器本体、
前記容器本体に取り付けられ、前記第2の収納部と連通する薬剤排出部、及び、
少なくとも前記容器本体の一部を覆う被覆部材、
を備える医療用複室容器であって、
前記被覆部材が、前記第1のフィルム及び前記第2のフィルムにそれぞれ接合される第1の被覆フィルム及び第2の被覆フィルムからなり、
前記第1の被覆フィルムが、前記仕切り用封止部上の前記第1のフィルムに、前記仕切り用封止部の接合強度以上の接合強度にて接合されており、
前記第2の被覆フィルムが、前記第1の収納部上及び第2の収納部上の前記第2のフィルムに、前記仕切り用封止部の接合強度以上の接合強度にて接合されている、医療用複室容器。
A bag-like container body composed of a first film and a second film facing the first film, and by joining the first film and the second film in a peelable manner. A container body in which a partition sealing portion that partitions the interior into a first storage portion and a second storage portion is formed;
A medicine discharge part attached to the container body and communicating with the second storage part; and
A covering member covering at least a part of the container body;
A medical multi-chamber container comprising:
The covering member comprises a first covering film and a second covering film that are bonded to the first film and the second film, respectively.
The first covering film is bonded to the first film on the partition sealing portion with a bonding strength equal to or higher than the bonding strength of the partition sealing portion,
The second covering film is bonded to the second film on the first storage portion and the second storage portion with a bonding strength equal to or higher than the bonding strength of the partition sealing portion. Medical multi-chamber container.
前記被覆部材が、少なくとも前記仕切り用封止部から前記薬剤排出部にかけて前記容器本体の少なくとも一部及び前記薬剤排出部を被覆している、請求項1又は2に記載の医療用複室容器。   The medical multi-chamber container according to claim 1 or 2, wherein the covering member covers at least a part of the container main body and the medicine discharge portion from at least the partition sealing portion to the medicine discharge portion. 前記被覆部材が前記容器本体の全体を被覆している、請求項1〜3のいずれか一項に記載の医療用複室容器。   The medical multi-chamber container according to any one of claims 1 to 3, wherein the covering member covers the entire container body. 前記第1の被覆フィルム及び前記第2の被覆フィルムが、前記仕切り用封止部の接合強度以上の接合強度にて、前記第2の収納部上の前記第1のフィルム及び前記第2のフィルムに剥離可能に接合されている、請求項1〜4のいずれか一項に記載の医療用複室容器。   The first film and the second film on the second storage portion have a bonding strength equal to or higher than the bonding strength of the partition sealing portion. The medical multi-chamber container according to any one of claims 1 to 4, wherein the medical multi-chamber container is detachably bonded to the medical container. 前記第1の被覆フィルム及び前記第2の被覆フィルムの、前記薬剤排出部側の端部にフック挿入用の穴が形成されており、
前記第1の被覆フィルム及び前記第2の被覆フィルムを前記薬剤排出部及び前記容器本体の前記第2の収納部から剥離し、前記仕切り用封止部を中心に反対側に折り返した状態において、前記穴が、前記薬剤排出部とは反対側の前記容器本体の端部よりも外側に配置されるようになっている、請求項3〜5のいずれか一項に記載の医療用複室容器。
A hole for hook insertion is formed at an end of the first covering film and the second covering film on the side of the medicine discharge part,
In the state where the first cover film and the second cover film are peeled off from the second storage part of the medicine discharge part and the container body, and folded back to the opposite side around the partition sealing part, The medical multi-chamber container according to any one of claims 3 to 5, wherein the hole is arranged outside an end portion of the container body opposite to the medicine discharge portion. .
前記第1の被覆フィルム及び前記第2の被覆フィルムが前記第1のフィルム及び前記第2のフィルムに熱融着により接合される、請求項1〜6のいずれか一項に記載の医療用複室容器。   The medical composite according to any one of claims 1 to 6, wherein the first cover film and the second cover film are bonded to the first film and the second film by heat fusion. Chamber container. 前記第1の被覆フィルム及び前記第2の被覆フィルムが当該医療用複室容器全体を被覆するブリスター包装を構成する、請求項1〜7のいずれか一項に記載の医療用複室容器。
The medical multi-chamber container according to any one of claims 1 to 7, wherein the first covering film and the second covering film constitute a blister package that covers the entire medical multi-chamber container.
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Cited By (2)

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Publication number Priority date Publication date Assignee Title
WO2021084869A1 (en) 2019-10-29 2021-05-06 学校法人 愛知医科大学 Manufacturing method for microbubble-containing electrolyte and manufacturing method for microbubble-containing solvent for use in preparing microbubble-containing electrolyte
WO2021161811A1 (en) 2020-02-12 2021-08-19 学校法人 愛知医科大学 Vasodilator composition, vasodilator composition kit, pharmaceutical composition for diseases caused by blood vessel constriction or obstructive impairment, and pharmaceutical composition kit for diseases caused by blood vessel constriction or obstructive impairment

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US20030116452A1 (en) * 2001-11-26 2003-06-26 Jerko Saric Trigger mechanism for self-heating/cooling packages or containers universally applied to both rigid and non-rigid packages and containers
JP2007135933A (en) * 2005-11-18 2007-06-07 Otsuka Pharmaceut Factory Inc Medical multi-chamber container
JP2007175442A (en) * 2005-12-28 2007-07-12 Nipro Corp Medical dual chamber container

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JPH024671A (en) * 1988-06-10 1990-01-09 Material Eng Tech Lab Inc Container with contents
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JP2007135933A (en) * 2005-11-18 2007-06-07 Otsuka Pharmaceut Factory Inc Medical multi-chamber container
JP2007175442A (en) * 2005-12-28 2007-07-12 Nipro Corp Medical dual chamber container

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021084869A1 (en) 2019-10-29 2021-05-06 学校法人 愛知医科大学 Manufacturing method for microbubble-containing electrolyte and manufacturing method for microbubble-containing solvent for use in preparing microbubble-containing electrolyte
JP2021069973A (en) * 2019-10-29 2021-05-06 学校法人 愛知医科大学 Production method of minute bubble-containing electrolyte liquid and production method of minute bubble-containing solvent used for preparing the minute bubble-containing electrolyte liquid
US20220387333A1 (en) * 2019-10-29 2022-12-08 Aichi Medical University Manufacturing Method for Microbubble-Containing Electrolyte and Manufacturing Method for Microbubble-Containing Solvent for Use in Preparing Microbubble-Containing Electrolyte
WO2021161811A1 (en) 2020-02-12 2021-08-19 学校法人 愛知医科大学 Vasodilator composition, vasodilator composition kit, pharmaceutical composition for diseases caused by blood vessel constriction or obstructive impairment, and pharmaceutical composition kit for diseases caused by blood vessel constriction or obstructive impairment

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