JPS6230783B2 - - Google Patents

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Publication number
JPS6230783B2
JPS6230783B2 JP53091891A JP9189178A JPS6230783B2 JP S6230783 B2 JPS6230783 B2 JP S6230783B2 JP 53091891 A JP53091891 A JP 53091891A JP 9189178 A JP9189178 A JP 9189178A JP S6230783 B2 JPS6230783 B2 JP S6230783B2
Authority
JP
Japan
Prior art keywords
liquid
chamber
container
drug solution
opening
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
Application number
JP53091891A
Other languages
Japanese (ja)
Other versions
JPS5519135A (en
Inventor
Kazuo Takura
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.)
Terumo Corp
Original Assignee
Terumo Corp
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 Terumo Corp filed Critical Terumo Corp
Priority to JP9189178A priority Critical patent/JPS5519135A/en
Publication of JPS5519135A publication Critical patent/JPS5519135A/en
Publication of JPS6230783B2 publication Critical patent/JPS6230783B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は過型人工腎臓装置に用いうる薬液容
器に関する。詳しく述べると、過型人工腎臓装
置の過器から排出される液量に相当する薬液
を処理液に供給するのに用いうるイコライザーと
薬液容器の機能をも兼ね備えた過型人工腎臓装
置に用いうる薬液容器に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a drug solution container that can be used in an oversized artificial kidney device. To be more specific, it can be used in an oversized artificial kidney device that also has the functions of an equalizer and a drug solution container that can be used to supply a treatment solution with a medical solution equivalent to the amount of liquid discharged from the oversized device of the oversized artificial kidney device. Concerning liquid medicine containers.

過型人工腎臓装置は未だ研究開発の域を脱し
ていない。今までに紹介された過型人工腎臓装
置のうち、血液等の被処理液を過器によつて血
球成分の多い処理液と老廃物を含む血漿の液と
に分離し、前記液を廃液とし、その廃液量相当
分の薬液を補液するものについては、第1図に示
すように、廃液手段中に逆止弁16,17を直列
に2個設け、それらの逆止弁16,17の間に連
結したシリンジ18により廃液を計量し、他方薬
液の瓶19から薬液4を処理液返還手段12に供
給する補液手段11中に逆止弁20,21を2個
直列に設け、それらの逆止弁20,21間に前記
と同タイプのシリンジ22を連結し、2個のシリ
ンジ18,22の作動を同時に行うようシリンジ
のポンプ機構23と連結し、一方のシリンジが
液を吸引するとき、他方のシリンジも薬液4を吸
引し、また逆に一方のシリンジが液を排出した
とき、他方のシリンジも薬液を排出するようにシ
リンジの往復運動に合わせて同一回路中の逆止弁
が交互に開閉するものであつた。
Hypermorphic artificial kidney devices are still in the realm of research and development. Among the oversized artificial kidney devices that have been introduced so far, the liquid to be processed, such as blood, is separated into a processed liquid containing many blood cell components and a plasma liquid containing waste products using a sieving device, and the liquid is used as waste liquid. For those that replenish the chemical solution equivalent to the amount of waste solution, as shown in FIG. 1, two check valves 16 and 17 are installed in series in the waste solution means, and a Two check valves 20 and 21 are installed in series in the liquid replenishing means 11, which measures the waste liquid with a syringe 18 connected to the syringe 18, and supplies the chemical liquid 4 from the chemical liquid bottle 19 to the processing liquid return means 12. A syringe 22 of the same type as described above is connected between the valves 20 and 21, and is connected to a pump mechanism 23 of the syringe so that the two syringes 18 and 22 operate simultaneously, so that when one syringe sucks liquid, the other syringe The check valves in the same circuit alternately open and close according to the reciprocating movement of the syringe so that the syringe also aspirates the drug solution 4, and conversely, when one syringe discharges the solution, the other syringe also discharges the drug solution. It was something to do.

これにより、液は間欠的に吸引と排出が行な
われ、薬液も同様に間欠的に吸引と排出が行なわ
れて処理液返還手段に供給される。
As a result, the liquid is intermittently suctioned and discharged, and the chemical solution is also intermittently suctioned and discharged, and is supplied to the processing liquid return means.

この過型人工腎臓装置においては、逆止弁、
シリンジ等により回路中の気泡が除去しにくいこ
と、シリンジは吸引時の減圧によりガスケツトと
外筒の密着部より気泡を混入しやすく、気泡の混
入があつた場合、計量された液と薬液は等価で
はなく、このため累積誤差を生じ、過量と薬液
量に差異を生ずる欠点があつた。
In this oversized artificial kidney device, a check valve,
It is difficult to remove air bubbles in the circuit with a syringe, etc., and air bubbles are easily mixed in with the syringe from the close contact between the gasket and the outer cylinder due to the reduced pressure during suction, and if air bubbles are mixed in, the measured liquid and drug solution are equivalent. Instead, this resulted in an accumulated error and a disadvantage in that there was a difference between an overdose and the amount of drug solution.

また、シリンジは往復による回分操作であるの
で気泡の混入がなくとも2個のシリンジ及びその
運動が全く同一でない限り累積誤差を生ずるもの
であつた。
Further, since the syringe is operated in batches by reciprocating, even if there is no air bubbles mixed in, unless the two syringes and their movements are exactly the same, cumulative errors will occur.

また、薬液のシリンジからの排出、処理液への
供給が間欠的であるので、薬液によつて希釈され
た処理液は血球濃度が経時的に不均一になる欠点
がある。
Furthermore, since the chemical solution is discharged from the syringe and supplied to the processing liquid intermittently, the processing liquid diluted with the chemical liquid has the disadvantage that the blood cell concentration becomes uneven over time.

また、気泡のシリンジ内部への混入は回路内の
汚染または空気栓塞の危険性を有するものであつ
た。
In addition, the introduction of air bubbles into the syringe poses a risk of contamination or air blockage within the circuit.

さらに、補液瓶、逆止弁、シリンジ、動力機構
を必要とし、構造が複雑、かつ、これに伴うトラ
ブルの発生など欠点を有するものであつた。
Furthermore, it requires a replenishing fluid bottle, a check valve, a syringe, and a power mechanism, resulting in a complicated structure and associated troubles.

本発明の目的は、これらの欠点を解決し、装置
を簡略化でき、トラブルの発生を防止した過型
人工腎臓装置に用いうる薬液容器を提供するもの
である。
An object of the present invention is to provide a drug solution container that can be used in an oversized artificial kidney device that solves these drawbacks, simplifies the device, and prevents troubles from occurring.

上記目的を達成するものは、過型人工腎臓装
置の過器から排出される過量に相当する薬液
を処理液に供給するのに用いうる薬液容器におい
て、該容器は、3枚の軟質プラスチツク製シート
を積層し、一部を残し、他の周囲を封止して形成
した開口部を有し、内圧の上昇に対して内容積が
変化しないプラスチツク製中空体であり、前記3
枚のシートの中間に位置するシートが該中空体内
を前記薬液が収納される第1室と前記液が導入
される第2室とに区画するとともに、変形可能な
隔膜を形成し、さらに前記中空体の開口部は前記
第1室および第2室の各室の開口部を形成し、該
各室のそれぞれの開口部に少なくとも1つの口部
を設けた過型人工腎臓装置に用いうる薬液容器
である。
What achieves the above object is a drug solution container that can be used to supply a treatment solution with a drug solution equivalent to the excess amount discharged from the oversized artificial kidney device, the container being made of three soft plastic sheets. It is a hollow plastic body having an opening formed by laminating the above three layers, leaving one part and sealing the other, and whose internal volume does not change due to an increase in internal pressure.
A sheet located between the two sheets divides the hollow body into a first chamber in which the chemical liquid is stored and a second chamber into which the liquid is introduced, and forms a deformable diaphragm. The opening of the body forms the opening of each of the first chamber and the second chamber, and each opening of each chamber is provided with at least one mouth. It is.

さらに、上記目的を達成するものを詳しく述べ
ると、3枚の軟質プラスチツク製シートを積層
し、一部を残し、他の周囲を封止して形成した開
口部を有し、内圧の上昇に対して内容積が変化し
ないプラスチツク製中空体であり、前記3枚のシ
ートの中間に位置するシートが該中空体内を前記
薬液が収納される第1室と前記液が導入される
第2室とに区画するとともに、変形可能な隔膜を
形成し、さらに前記中空体の開口部は前記第1室
および第2室の各室の開口部を形成し、該各室の
それぞれの開口部に少なくとも1つの口部を設け
た薬液容器と、該容器の第1室に充填された薬液
と、該第1室の口部を被処理液導入手段、処理液
返還手段および液の廃液手段を連結した過器
の該処理液返還手段に連結する補液手段と、第2
室の口部を該過器の廃液手段に連結し、第2室
に液を導入したとき、液の導入量に相当する
薬液の排出を行う過型人工腎臓装置である。
Furthermore, to explain in detail what achieves the above purpose, it has an opening formed by laminating three soft plastic sheets, leaving one part open and sealing the other, and is able to withstand increases in internal pressure. It is a hollow body made of plastic whose internal volume does not change, and the sheet located between the three sheets divides the hollow body into a first chamber in which the medicinal solution is stored and a second chamber into which the liquid is introduced. partitioning and forming a deformable diaphragm; further, the opening of the hollow body forms an opening of each of the first and second chambers, and at least one A filtration vessel comprising a chemical liquid container provided with a mouth, a chemical liquid filled in a first chamber of the container, and a mouth of the first chamber connected to a means for introducing a liquid to be treated, a means for returning a treated liquid, and a means for discharging the liquid. a second liquid replenishing means connected to the processing liquid return means;
This is an oversized artificial kidney device in which the mouth of the chamber is connected to the waste liquid means of the overflow device, and when the liquid is introduced into the second chamber, a medicinal solution corresponding to the amount of introduced liquid is discharged.

プラスチツク製中空体の材質はポリエチレン、
ポリプロピレン、ポリ塩化ビニル、エチレン−酢
酸ビニル共重合体等の熱可塑性プラスチツクによ
り形成される。
The material of the plastic hollow body is polyethylene,
It is formed from thermoplastics such as polypropylene, polyvinyl chloride, and ethylene-vinyl acetate copolymer.

この中空体は上記プラスチツクの特性、厚みに
よつて中空体の内容積が内圧の上昇に対して変化
しなければそのまま、内圧の上昇に対して膨張す
るような柔軟なバツグであればその外側にバツグ
の膨張に対して内容積が変化しないようにしたシ
エルを設けたものでもよい。
Depending on the characteristics and thickness of the plastic mentioned above, if the internal volume of the hollow body does not change in response to an increase in internal pressure, the hollow body will remain as it is, but if it is a flexible bag that expands in response to an increase in internal pressure, it will expand to the outside. It may also be provided with a shell whose internal volume does not change as the bag expands.

隔膜の材質は、変形可能な材質であり、例えば
ポリエチレン、ポリプロピレン、ポリ塩化ビニ
ル、エチレン−酢酸ビニル共重合体等の柔軟な熱
可塑性プラスチツクまたはゴム、ラテツクス等の
薄膜形成性の弾性体でもよい。薬液は、例えば生
理食塩液、電界質液、電界質−ブドウ糖液等の細
胞外液補充液、精製された血漿等である。
The material of the diaphragm is a deformable material, such as a flexible thermoplastic such as polyethylene, polypropylene, polyvinyl chloride, or ethylene-vinyl acetate copolymer, or a thin film-forming elastic material such as rubber or latex. The drug solution is, for example, a physiological saline solution, an electrolyte solution, an extracellular fluid replenisher such as an electrolyte-glucose solution, purified plasma, or the like.

口部の材質は、前記中空体の熱可塑性プラスチ
ツクと同質でよく、望ましくは加工適性上中空体
の少なくとも内側材質と同質のものである。
The material of the mouth portion may be the same as the thermoplastic of the hollow body, and is preferably the same as at least the inner material of the hollow body in view of processability.

以下、本発明の一実施例を図面によつて詳述す
る。
Hereinafter, one embodiment of the present invention will be described in detail with reference to the drawings.

薬液容器1は、例えば伸縮性の小さい材質ポリ
塩化ビニル製シートを3枚2,3,2積層し、一
端を開口し他の周囲を高周波融着して両側シート
からなる中空体2,2とその中間シートの隔膜3
により2室を有する袋とし、第1室に薬液4を充
填し、両室とも空気を排除し、次に述べる手段に
連結しやすい例えば断面H字型のポリ塩化ビニル
製筒状口部5,6を各室の開口端に1個づつ挾持
し、袋2,3,2と口部5,6を高周波融着す
る。
The drug solution container 1 is made by laminating three sheets 2, 3, 2 made of polyvinyl chloride, which is a material with low elasticity, for example, and opening one end and high-frequency welding the other periphery to form a hollow body 2, 2 made of sheets on both sides. Diaphragm 3 of the intermediate sheet
The bag is made into a bag having two chambers, the first chamber is filled with a chemical solution 4, air is excluded from both chambers, and a cylindrical opening 5 made of polyvinyl chloride with an H-shaped cross section, for example, is easily connected to the means described below. 6 is held one by one at the open end of each chamber, and the bags 2, 3, 2 and the openings 5, 6 are welded together by high frequency.

この薬液容器1は、望ましくは高圧加熱水蒸気
により容器とともに薬液4を滅菌してもよいが、
エチレンキサイドガスにより滅菌した容器に薬液
を無菌分注してもよい。
The drug solution container 1 may be desirably sterilized together with the drug solution 4 using high-pressure heated steam.
The drug solution may be aseptically dispensed into containers sterilized with ethylene oxide gas.

被処理液導入手段13は、プラスチツク製チユ
ーブの一端にカヌラを有し、他端は過器7に連
結され、該チユーブ中程に被処理液を圧送するロ
ーラーポンプ14が設けられている。処理液返還
手段12は、プラスチツク製チユーブの一端にカ
ヌラを有し、他端は過器7に連結されている。
The liquid to be treated introduction means 13 has a cannula at one end of a plastic tube, the other end of which is connected to the strainer 7, and a roller pump 14 for pumping the liquid to be treated is provided in the middle of the tube. The processing liquid return means 12 has a cannula at one end of a plastic tube, and the other end is connected to the strainer 7.

廃液手段8は、プラスチツク製チユーブの一端
を過器7に連結し、他端は薬液容器1の口部6
に連結され、該チユーブの中程にローラポンプ9
を設けている。
The liquid waste means 8 has one end of a plastic tube connected to the strainer 7, and the other end connected to the opening 6 of the chemical liquid container 1.
roller pump 9 in the middle of the tube.
has been established.

また、除水手段10は、プラスチツク製チユー
ブの一端を該廃液手段8に連結し、このチユーブ
中程に除水用ローラーポンプ15を設けられてい
る。
Further, the water removal means 10 has one end of a plastic tube connected to the liquid waste means 8, and a water removal roller pump 15 is provided in the middle of this tube.

補液手段11は、プラスチツク製チユーブから
なり、一端を薬液容器1の口部5に連結し、他端
を処理液返還手段12に連結している。この手段
11は必要に応じて該チユーブ中程に点滴筒を設
け補液量測定をしてもよい。
The liquid replacement means 11 is made of a plastic tube, and one end is connected to the opening 5 of the chemical solution container 1, and the other end is connected to the processing liquid return means 12. This means 11 may include a drip tube installed in the middle of the tube to measure the amount of replacement fluid, if necessary.

血液等の被処理液は被処理液導入手段13のカ
ヌラから供給され、ローラーポンプ14により加
圧される過器7へ送られる。
The liquid to be treated, such as blood, is supplied from the cannula of the liquid to be treated introduction means 13 and sent to the overflow vessel 7 which is pressurized by a roller pump 14 .

過器7内の血液は該過器7内に設けられた
フイルターを介して血球成分の多い処理液と老廃
物を含む血漿の液とに分離され、それぞれ過
器7から処理液返還手段12および廃液手段8に
送られる。
The blood in the filtration device 7 is separated through a filter provided in the filtration device 7 into a treatment liquid containing many blood cell components and a plasma liquid containing waste products. The liquid is sent to waste liquid means 8.

廃液手段8の液はローラーポンプ9により薬
液容器1へ圧送される。
The liquid in the waste liquid means 8 is pumped to the chemical liquid container 1 by a roller pump 9.

該薬液容器1内に圧送された液は隔膜3を押
し変形させ、液量と同量の薬液4を補液手段1
1を通して処理液返還手段12へ供給する。処理
液返還手段12は血球成分の多い処理液と薬液を
混合し、カヌラから混合液を排出する。この場
合、排出される処理液と薬液の混合液は被処理液
と同量であり、かつ血球濃度も等しい。
The liquid force-fed into the drug solution container 1 pushes and deforms the diaphragm 3, and the same amount of drug solution 4 as the amount of the liquid is transferred to the fluid replacement means 1.
1 to the processing liquid return means 12. The treatment liquid return means 12 mixes the treatment liquid containing many blood cell components and the medical solution, and discharges the mixed liquid from the cannula. In this case, the amount of the mixed liquid of the processing liquid and the chemical liquid discharged is the same as that of the liquid to be treated, and the blood cell concentration is also the same.

また、この系から必要量除水する場合は除水手
段10のローラポンプ15を駆動することにより
行なわれる。
Further, when a necessary amount of water is removed from this system, the roller pump 15 of the water removal means 10 is driven.

除水及び補液を同時に行う場合はローラーポン
プを除水用と補液用とに分けることにより行なわ
れる。
When removing water and replacing fluid at the same time, the roller pump is divided into two parts: one for water removal and one for fluid replacement.

したがつて、除水手段10が作動したとき、返
還混合液量は被処理液量より除水量分だけ減少
し、かつ、その血球濃度は増加する。
Therefore, when the water removal means 10 operates, the amount of the returned mixed liquid decreases by the amount of water removed from the amount of the liquid to be treated, and the blood cell concentration increases.

すなわち、各手段の液量の式は (被処理液量)=(処理液量)+(液量) (液量)=(除水量)+(補液用液量) (補液用液量)=(補液用薬液量) (返還混合液量)=(処理液量)+(補液用液
量)で表わされるから、 よつて、 (返還混合液量)=(被処理液量)−(除水量)が
成り立つ。
In other words, the formula for the amount of liquid for each means is (Amount of liquid to be treated) = (Amount of liquid to be treated) + (Amount of liquid) (Amount of liquid) = (Amount of water removed) + (Amount of fluid for replacement fluid) (Amount of fluid for replacement fluid) = (Amount of chemical solution for replacement fluid) (Amount of returned mixed fluid) = (Amount of treated fluid) + (Amount of fluid for replacement fluid) Therefore, (Amount of returned mixed fluid) = (Amount of treated fluid) - (Amount of water removed) ) holds true.

このように除水回路の作動により自由に返還混
合液量およびその血球濃度を制御できる。次に、
薬液容器1の他の実施例を第3図に示す。
In this manner, the amount of returned mixed liquid and its blood cell concentration can be freely controlled by operating the water removal circuit. next,
Another embodiment of the chemical liquid container 1 is shown in FIG.

この薬液容器1の薬液と接触する容器が内圧に
より内容積を変化しやすい、すなわち伸縮性のあ
るプラスチツク製バツグ2aである場合、硬質プ
ラスチツク製シエル2bによつてバツグの外容積
を固定してバツグ内容積の変化を防止してもよ
い。
When the container that comes into contact with the chemical solution in the drug solution container 1 is a stretchable plastic bag 2a whose internal volume is likely to change due to internal pressure, the outer volume of the bag is fixed by the hard plastic shell 2b. Changes in internal volume may be prevented.

以上説明したように、本発明の薬液容器は内圧
の上昇に対して内容積が変化しないようにした中
空体内に2室を有するよう隔膜を設け、第1室に
薬液を充填すれば、薬液容器およびイコライザー
として機能する。
As explained above, the drug solution container of the present invention is provided with a diaphragm so as to have two chambers in the hollow body whose internal volume does not change due to an increase in internal pressure, and if the first chamber is filled with a drug solution, the drug solution container and act as an equalizer.

また、薬液容器は密閉されているので従来のシ
リンジのように気泡を回路内に導入することもな
く、補液手段を汚染せず。液と薬液の交換にお
いても交換誤差を生じない。また、液と薬液の
交換が、従来のようなシリンジの往復運動による
回分操作でなく、液積算量に対して薬液を等量
排出することができるので、累積誤差は生じない
ものであり、かつ連続的に補液でき、返還混合液
の血球濃度は常に均一である。
In addition, since the drug solution container is sealed, unlike conventional syringes, air bubbles are not introduced into the circuit, and the fluid replacement means is not contaminated. No exchange errors occur when exchanging liquids and chemicals. In addition, the exchange of liquid and drug solution is not a batch operation using the reciprocating movement of a syringe as in the past, but the same amount of drug solution can be discharged based on the cumulative amount of liquid, so no cumulative error occurs. Fluid replacement is possible continuously, and the blood cell concentration in the returned mixed fluid is always uniform.

また、隔膜は液圧と薬液圧をバランスする方
向に変形するので破損の心配もない。
Furthermore, since the diaphragm deforms in a direction that balances the liquid pressure and chemical liquid pressure, there is no need to worry about damage.

さらに、本発明では、プラスチツク製中空体
を、平膜状の隔膜で二分して、2室を形成し、そ
の一方(第2室)に液が流入するようにしたの
で、外から液の流入を容易に確認できる。さら
に、隔膜は、伸張する必要なく、変形のみを行
い、液の流入に比例して第2室を拡大させ、そ
れに合わせて第1室の薬液を流出させるので破損
のおそれが少なく、また第2室が破損したとして
も破損の可能性が高いのは、3枚のシートを融着
した周縁部であり、よつて、液は、外部に流出
し第1室の薬液内に混入する危険性が少ない。ま
た、容器全体が軟質であるため、薬液を第1室に
充填したのち容器内部に付着した気泡を容器外側
から押圧することおよびたたくなどすることによ
り比較的容易に気泡を除去することができる。
Furthermore, in the present invention, the plastic hollow body is divided into two by a flat membrane-like diaphragm to form two chambers, and the liquid flows into one of the chambers (the second chamber), so that the liquid can flow in from the outside. can be easily confirmed. Furthermore, the diaphragm only deforms without needing to stretch, expanding the second chamber in proportion to the inflow of liquid, and causing the chemical liquid in the first chamber to flow out accordingly, so there is little risk of damage to the second chamber. Even if the chamber is damaged, the area most likely to be damaged is the periphery where the three sheets are fused together, so there is a risk that the liquid will leak outside and mix into the chemical solution in the first chamber. few. In addition, since the entire container is soft, air bubbles attached to the inside of the container after filling the first chamber with the chemical solution can be removed relatively easily by pressing or tapping from the outside of the container.

また、何等かの原因(例えば、液流入チユー
ブの閉塞、チユーブ接合部からの漏れ)により容
器内に液が流入しない場合には、容器を外側か
ら押圧することにより容易に薬液を送り出すこと
ができる。
In addition, if the liquid does not flow into the container due to some reason (for example, blockage of the liquid inflow tube or leakage from the tube joint), the liquid can be easily delivered by pressing the container from the outside. .

また、薬液容器が容器とイコライザーの働きを
するので、過型人工腎臓装置が従来にくらべ簡
素化でき、故障する度合も少ない。さらに、容器
内に蓄積された液は臨床検査用資料液として利
用でき、保存することもできる。
In addition, since the drug solution container functions as a container and an equalizer, the oversized artificial kidney device can be made simpler and less likely to malfunction than in the past. Furthermore, the liquid accumulated in the container can be used as a material liquid for clinical tests, and can also be stored.

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

第1図は、過型人工腎臓装置の従来例を示す
回路図である、第2図は、本発明の過型人工腎
臓装置に用いうる薬液容器の断面図を含む過型
人工腎臓装置の回路図である、第3図は本発明の
薬液容器の他の実施例を示す斜視図である。 1……薬液容器、2……プラスチツク製中空
体、3……隔膜、4……薬液、5,6……口部。
FIG. 1 is a circuit diagram showing a conventional example of an oversized artificial kidney device. FIG. 2 is a circuit diagram of an oversized artificial kidney device including a sectional view of a drug solution container that can be used in the oversized artificial kidney device of the present invention. FIG. 3 is a perspective view showing another embodiment of the drug solution container of the present invention. 1... Chemical solution container, 2... Plastic hollow body, 3... Diaphragm, 4... Chemical solution, 5, 6... Mouth part.

Claims (1)

【特許請求の範囲】 1 過型人工腎臓装置の過器から排出される
過量に相当する薬液を処理液に供給するのに用
いうる薬液容器において、 該容器は、3枚の軟質プラスチツク製シートを
積層し、一部を残し、他の周囲を封止して形成し
た開口部を有し、内圧の上昇に対して内容積が変
化しないプラスチツク製中空体であり、前記3枚
のシートの中間に位置するシートが該中空体内を
前記薬液が収納される第1室と前記液が導入さ
れる第2室とに区画するとともに、変形可能な隔
膜を形成し、さらに前記中空体の開口部は前記第
1室および第2室の各室の開口部を形成し、該各
室のそれぞれの開口部に少なくとも1つの口部を
設けたことを特徴とする過型人工腎臓装置に用
いうる薬液容器。
[Scope of Claims] 1. A drug solution container that can be used to supply a treatment solution with a drug solution equivalent to the excess amount discharged from the oversized artificial kidney device, the container comprising three soft plastic sheets. It is a hollow body made of plastic that has an opening formed by stacking the sheets, leaving one part open and sealing the other, and whose internal volume does not change due to an increase in internal pressure. The sheet located in the hollow body divides the hollow body into a first chamber in which the medicinal solution is stored and a second chamber into which the liquid is introduced, and forms a deformable diaphragm, and furthermore, the opening of the hollow body is formed into a deformable membrane. 1. A drug solution container that can be used in an oversized artificial kidney device, characterized in that an opening is formed in each of a first chamber and a second chamber, and at least one opening is provided in each opening of each chamber.
JP9189178A 1978-07-27 1978-07-27 Vessel of chemicals* etc* used for filtration type artificial kidney device Granted JPS5519135A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9189178A JPS5519135A (en) 1978-07-27 1978-07-27 Vessel of chemicals* etc* used for filtration type artificial kidney device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9189178A JPS5519135A (en) 1978-07-27 1978-07-27 Vessel of chemicals* etc* used for filtration type artificial kidney device

Publications (2)

Publication Number Publication Date
JPS5519135A JPS5519135A (en) 1980-02-09
JPS6230783B2 true JPS6230783B2 (en) 1987-07-04

Family

ID=14039172

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9189178A Granted JPS5519135A (en) 1978-07-27 1978-07-27 Vessel of chemicals* etc* used for filtration type artificial kidney device

Country Status (1)

Country Link
JP (1) JPS5519135A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3213390A1 (en) * 1982-04-10 1983-10-20 Dieter 3000 Hannover Biela DEVICE FOR ACCOUNTING FOR LIQUID EXCHANGE IN HAEMOFILTRATIONS

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52139298A (en) * 1976-05-17 1977-11-21 Pinkaaton Harii Blood dialyzing system
JPS54105898A (en) * 1978-02-07 1979-08-20 Toray Industries Device for purifying blood

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5727524Y2 (en) * 1976-11-12 1982-06-16

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52139298A (en) * 1976-05-17 1977-11-21 Pinkaaton Harii Blood dialyzing system
JPS54105898A (en) * 1978-02-07 1979-08-20 Toray Industries Device for purifying blood

Also Published As

Publication number Publication date
JPS5519135A (en) 1980-02-09

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