JPH0357238Y2 - - Google Patents
Info
- Publication number
- JPH0357238Y2 JPH0357238Y2 JP11464487U JP11464487U JPH0357238Y2 JP H0357238 Y2 JPH0357238 Y2 JP H0357238Y2 JP 11464487 U JP11464487 U JP 11464487U JP 11464487 U JP11464487 U JP 11464487U JP H0357238 Y2 JPH0357238 Y2 JP H0357238Y2
- Authority
- JP
- Japan
- Prior art keywords
- plasma
- storage container
- component storage
- plasma component
- components
- 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
Links
- 239000012503 blood component Substances 0.000 claims description 7
- 210000002381 plasma Anatomy 0.000 description 60
- 239000000306 component Substances 0.000 description 55
- 238000003860 storage Methods 0.000 description 37
- 238000005520 cutting process Methods 0.000 description 8
- 238000003466 welding Methods 0.000 description 8
- 210000004369 blood Anatomy 0.000 description 5
- 239000008280 blood Substances 0.000 description 5
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 210000000601 blood cell Anatomy 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 206010052428 Wound Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000001012 protector Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 230000009385 viral infection Effects 0.000 description 1
Landscapes
- Medical Preparation Storing Or Oral Administration Devices (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
Description
【考案の詳細な説明】
(産業上の利用分野)
本考案は、供給者から採取した血液を遠心分離
機等により血球成分と血漿成分に分離した後、主
に血漿成分を保存するための血液成分保存用容器
の改良に関するものである。[Detailed description of the invention] (Industrial application field) This invention is designed to separate blood collected from a supplier into blood cell components and plasma components using a centrifuge, etc., and then to store the blood plasma components. This invention relates to improvements in containers for storing ingredients.
(従来の技術)
従来から使用されている血漿成分保存用容器を
第7図に示す。(Prior Art) A conventionally used plasma component storage container is shown in FIG.
図中、20は血漿成分保存用容器、21は導入
チユ−ブ、22,23は混注口、24はプロテク
ター、25は導入針を示す。 In the figure, 20 is a plasma component storage container, 21 is an introduction tube, 22 and 23 are mixed injection ports, 24 is a protector, and 25 is an introduction needle.
血漿成分保存用容器20はポリ塩化ビニル、エ
チレン酢酸ビニルアセテート、テトラフルオロエ
チレン−エチレン共重合体等のポリオレフイン系
樹脂で低温に耐えるうる合成樹脂からなるものが
用いられている。 The plasma component storage container 20 is made of a synthetic resin that can withstand low temperatures, such as polyolefin resin such as polyvinyl chloride, ethylene vinyl acetate, or tetrafluoroethylene-ethylene copolymer.
供血者から採血した血液は、遠心分離機等によ
り血球成分と血漿成分に分離される。血漿成分
は、血液成分保存用容器にプールされ−20℃以下
で凍結し、長期間保存される。 Blood collected from a blood donor is separated into blood cell components and plasma components using a centrifuge or the like. Plasma components are pooled in blood component storage containers, frozen at -20°C or lower, and stored for long periods of time.
保存された血漿成分は、アルブミン製剤等の各
種分画製剤の原料となる。 The preserved plasma components serve as raw materials for various fractionated preparations such as albumin preparations.
−20℃以下で凍結保存されている血漿入り血液
成分保存用容器20の表面を蒸留水とアルコール
水溶液で内面の血漿が少し溶けた状態になるまで
洗浄し、血漿成分保存用容器の一部をカツターナ
イフ等で切断し、血漿成分を血漿プールタンクに
落とし各種分画製剤に加工している。 Wash the surface of the plasma-containing blood component storage container 20, which is stored frozen at -20°C or lower, with distilled water and an alcohol aqueous solution until the plasma inside is slightly dissolved. The plasma is cut with a cutter knife, etc., and the plasma components are dropped into a plasma pool tank and processed into various fractionated preparations.
(本考案が解決しようとする問題点)
以上説明したような従来の方法では、血漿成分
保存用容器の切断をひとつひとつ人の手により血
漿成分保存用容器の端部を切断しなくてはならず
大変手間のかかる作業で自動化のさまたげになつ
ている。(Problems to be solved by the present invention) In the conventional method as explained above, each end of the plasma component storage container must be cut manually one by one. This is a very time-consuming process that is hindering automation.
またカツターナイフ等による切断では、カツタ
ーナイフと血漿成分が接触し衛生的にも問題が指
摘されている。さらにカツターナイフ等の鋭利な
切断器具を利用しているとその作業に従事する人
を傷つけ各種ウイルスに感染する恐れがあり大変
危険なものであつた。 Furthermore, when cutting with a cutter knife or the like, it has been pointed out that there is a sanitary problem because the cutter knife comes into contact with plasma components. Furthermore, the use of sharp cutting tools such as cutter knives was extremely dangerous as they could injure the people working on them and could potentially infect them with various viruses.
そこで本考案は、上述したような問題点を解決
するために検討した結果提案されたものである。 Therefore, the present invention was proposed as a result of studies to solve the above-mentioned problems.
(問題点を解決するための手段)
以上の問題点を解決するために本考案では、血
液成分保存用容器本体の内面又は外面のどちらか
一方に少なくとも1本以上のカツト溝又は脆弱部
を設けた血液成分保存用容器を提供するものであ
る。(Means for Solving the Problems) In order to solve the above problems, the present invention provides at least one cut groove or fragile portion on either the inner or outer surface of the blood component storage container body. The present invention provides a container for storing blood components.
(作用)
混注口2,3、導入チユーブ4、導入針5係止
溝6,7,8,9から成る血液成分保存用容器の
端部を持ち、カツト溝10に対して垂直方向に力
を加えることにより血液成分保存用容器を引き裂
き、凍結している血漿成分を取り出すものであ
る。(Function) Hold the end of the blood component storage container consisting of the mixed injection ports 2, 3, the introduction tube 4, the introduction needle 5 and the locking grooves 6, 7, 8, 9, and apply force in the vertical direction to the cut groove 10. By adding this, the blood component storage container is torn open and the frozen plasma components are taken out.
(実施例)
第1図に本考案の血漿成分保存用容器1の実施
例を示す。(Example) FIG. 1 shows an example of the plasma component storage container 1 of the present invention.
血漿成分保存用容器1は、混注口2,3、導入
チユーブ4、導入針5、カツト溝10又は脆弱部
10′から構成されている。 The plasma component storage container 1 is composed of mixed injection ports 2, 3, an introduction tube 4, an introduction needle 5, a cut groove 10, or a weakened portion 10'.
カツト溝10又は脆弱部10′の構造について
その具体的な実施例を第2図〜第5図に示す。 Specific examples of the structure of the cut groove 10 or the weakened portion 10' are shown in FIGS. 2 to 5.
第2図は、二枚のシート31,32の内面にカ
ツト溝10を血漿成分保存用容器1の長さ方向に
設け、シート端部33,34を高周波溶着、超音
波溶着などの接着手段により袋状に形成した所の
第1図のA−A断面図を示す。 In FIG. 2, cut grooves 10 are provided on the inner surfaces of two sheets 31 and 32 in the length direction of the plasma component storage container 1, and sheet ends 33 and 34 are bonded by bonding means such as high frequency welding and ultrasonic welding. A sectional view taken along line A-A in FIG. 1 of the bag-shaped structure is shown.
第3図は、二枚のシート31,32の外面にカ
ツト溝10を血漿成分保存用容器1の長さ方向に
設けシート端部33,34を高周波溶着、高周波
溶着等の接着手段により袋状に形成した第1図の
A−A断面図を示す。 In FIG. 3, cut grooves 10 are formed on the outer surfaces of two sheets 31 and 32 in the longitudinal direction of the plasma component storage container 1, and the sheet ends 33 and 34 are bonded by high-frequency welding or high-frequency welding to form a bag. 1 is a cross-sectional view taken along line A-A in FIG. 1.
又第2図、第3図に示すカツト溝10は、例え
ば、押出成形により形成することができる。 Further, the cut grooves 10 shown in FIGS. 2 and 3 can be formed by extrusion molding, for example.
第4図は、二枚のシート31,32の端部3
3,34を高周波溶着、超音波溶着等により袋状
に形成する際に生じる脆弱部10′を血漿成分保
存用容器1の外面中央部に設けた所の断面図を示
す。 FIG. 4 shows the end portion 3 of two sheets 31 and 32.
3 and 34 into a bag shape by high frequency welding, ultrasonic welding, etc., is shown in a cross-sectional view of a place where a fragile portion 10', which is generated when forming parts 3 and 34 into a bag shape by high frequency welding, ultrasonic welding, etc., is provided at the center of the outer surface of the plasma component storage container 1.
第5図を示す血漿成分保存用容器1の端部3
3,34を血漿成分保存用容器1の内面中央部に
設けた所の断面図を示す。 End portion 3 of plasma component storage container 1 shown in FIG.
3 and 34 are provided at the center of the inner surface of the plasma component storage container 1.
以上血漿成分保存用容器の内面又は外面にカツ
ト溝10、脆弱部10′を設けた所の具体例を示
したが本考案が示すカツト溝10、脆弱部10′
以外にも血漿成分保存用容器1が容易に引き裂く
ことができる構造であれば良い。 Above, a specific example was shown in which the cut groove 10 and the fragile portion 10' were provided on the inner or outer surface of the plasma component storage container.
Any other structure may be used as long as the plasma component storage container 1 can be easily torn apart.
次に本考案による血漿成分保存用容器1の使用
方法について簡単に説明する。 Next, a method of using the plasma component storage container 1 according to the present invention will be briefly explained.
各供血者から採取し分離された血漿成分は、導
入針5を介し導入チユーブ4を通り血漿成分保存
用容器1内に集められる。 Plasma components collected and separated from each blood donor are collected in the plasma component storage container 1 through the introduction tube 4 via the introduction needle 5.
供血者から得られた血漿成分1〜3を血漿
成分保存用容器1内に集め、すみやかに−20℃以
下で凍結され保存する。 Plasma components 1 to 3 obtained from blood donors are collected in a plasma component storage container 1, and immediately frozen and stored at -20°C or lower.
保存された血漿成分は、長期間保存可能であり各
種分画製剤に加工処理する。The preserved plasma components can be stored for a long period of time and are processed into various fractionated preparations.
血漿成分保存用容器1から血漿成分を取り出す
場合、血漿成分保存用容器1の表面に蒸留水、ア
ルコール水溶液等をかけて洗浄すると共に血漿成
分の表面を解凍する。 When taking out the plasma component from the plasma component storage container 1, the surface of the plasma component storage container 1 is washed by pouring distilled water, an aqueous alcohol solution, etc., and the surface of the plasma component is thawed.
次に、機械的に血漿成分保存用容器1を引き裂
く場合について第6図に沿つて説明する。 Next, the case of mechanically tearing the plasma component storage container 1 will be explained with reference to FIG. 6.
第6図には、切断装置11の概略図を示し図
中、12a,12bは上下にスライド可能な血漿
成分保存用容器保持板、13,14,15,16
は血漿成分保存用容器係止ピン、17は保持板1
2a,12bを横方向に広げる為の固定ガイド、
18は支点、19は血漿プールタンクを示してい
る。 FIG. 6 shows a schematic diagram of the cutting device 11, in which 12a and 12b are vertically slidable plasma component storage container holding plates 13, 14, 15, 16.
17 is the retaining plate 1 for the plasma component storage container.
Fixed guide for expanding 2a and 12b laterally,
18 indicates a fulcrum, and 19 indicates a plasma pool tank.
保持板12a,12bに設けてある係止ピン1
3,14,15,16に血漿成分保存用容器の係
止溝6,7,8,9を係止させる。固定された保
持板12a,12bを下方に移動すると保持板1
2a,12bは、固定ガイド17により保持板1
2a,12bの下端部はそれぞれ支点18を中心
として外方向に移動して保持板12a,12bに
固定された血漿成分保存用容器1には、12a,
12b側に分れようとする外方向への力が加わ
り、12a,12bにカツト溝10又は脆弱部1
0′に沿つて引き裂かれる。 Locking pin 1 provided on retaining plates 12a and 12b
3, 14, 15, and 16 are engaged with the engagement grooves 6, 7, 8, and 9 of the plasma component storage container. When the fixed holding plates 12a and 12b are moved downward, the holding plate 1
2a and 12b are attached to the holding plate 1 by the fixed guide 17.
The plasma component storage container 1, whose lower ends 2a and 12b are moved outward about the fulcrum 18 and fixed to the holding plates 12a and 12b, has 12a and 12b, respectively.
An outward force is applied to the 12b side to separate the cut groove 10 or the weak portion 1 to the 12a and 12b.
It is torn along 0'.
血漿成分保存用容器1内にある血漿成分は、あ
らかじめ切断装置11の下方に設けられた血漿プ
ールタンク19内に落下する。 The plasma component in the plasma component storage container 1 falls into a plasma pool tank 19 provided in advance below the cutting device 11.
このような切断装置11も使用可能となり、血
漿成分にカツターナイフ等の異物を接触させるこ
となく血漿成分保存用容器1内に集められている
血漿成分を取り出すことができた。 Such a cutting device 11 can also be used, and the plasma components collected in the plasma component storage container 1 can be taken out without bringing foreign objects such as a cutter knife into contact with the plasma components.
またより少ない力で血漿成分保存用容器を引き
裂くことが可能であり、自動化による血漿成分の
大量処理ができるようになつた。 In addition, it is now possible to tear the plasma component storage container with less force, and it has become possible to process large quantities of plasma components through automation.
(効果)
以上説明したように本考案によれば、
機械的に処理が可能となり短時間に大量の処
理が行なえる。(Effects) As explained above, according to the present invention, it is possible to process mechanically, and a large amount of processing can be performed in a short time.
血漿成分にカツターナイフ等の異物を接触さ
せずに血漿成分取り出せ大変衛生的である。 It is very hygienic as plasma components can be removed without bringing foreign objects such as a cutter knife into contact with the plasma components.
カツターナイフ等の鋭利な刃物を必要としな
い為、作業者を傷つけることなく傷口からのウ
イルスの感染を防止することが可能になつた。 Since it does not require a sharp knife such as a cutter knife, it has become possible to prevent virus infection from wounds without injuring the worker.
等の優れた効果を有するものである。It has excellent effects such as.
第1図は、本考案の血漿成分保存用容器1を示
す平面図、第2図は、血漿成分保存用容器の内面
にカツト溝を設けた所の断面図、第3図は、血漿
成分保存用容器の外面にカツト溝を設けた所の断
面図、第4図は、血漿成分保存用容器の外面に脆
弱部を設けた所の断面図、第5図は、血漿成分保
存用容器の内面に脆弱部を設けた所の断面図、第
6図は、本考案により血漿成分保存用容器を切断
する時に用いる切断装置を示す平面図、第7図
は、従来型の血漿成分保存用容器を示す。
図中、1は血漿成分保存用容器、2,3は混注
口、4は導入チユーブ、5は導入針、6,7,
8,9は係止溝、10はカツト溝、11は切断装
置、12a,12bは保持板、13,14,1
5,16は係止ピン、17は固定ガイド、18は
支点、19は血漿プールタンク、31,32はシ
ート、33,34はシート端部を示す。
Fig. 1 is a plan view showing a plasma component storage container 1 of the present invention, Fig. 2 is a cross-sectional view of a place where cut grooves are provided on the inner surface of the plasma component storage container, and Fig. 3 is a plan view showing a plasma component storage container 1 of the present invention. Fig. 4 is a sectional view of a place where a cut groove is provided on the outer surface of a container for storing plasma components, and Fig. 5 is a sectional view of a place where a fragile portion is provided on the outer surface of a container for storing plasma components. 6 is a plan view showing a cutting device used to cut a plasma component storage container according to the present invention, and FIG. 7 is a cross-sectional view of a conventional plasma component storage container. show. In the figure, 1 is a plasma component storage container, 2 and 3 are mixed injection ports, 4 is an introduction tube, 5 is an introduction needle, 6, 7,
8, 9 are locking grooves, 10 is a cutting groove, 11 is a cutting device, 12a, 12b is a holding plate, 13, 14, 1
5 and 16 are locking pins, 17 is a fixed guide, 18 is a fulcrum, 19 is a plasma pool tank, 31 and 32 are seats, and 33 and 34 are seat ends.
Claims (1)
本体の内面又は外面のどちらか一方に少なくとも
一本以上のカツト溝又は脆弱部を設けた事を特徴
とする血液成分保存用容器。 1. A container for storing blood components, characterized in that the container body is provided with at least one cut groove or fragile portion on either the inner or outer surface of the container body.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11464487U JPH0357238Y2 (en) | 1987-07-28 | 1987-07-28 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11464487U JPH0357238Y2 (en) | 1987-07-28 | 1987-07-28 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6420847U JPS6420847U (en) | 1989-02-01 |
| JPH0357238Y2 true JPH0357238Y2 (en) | 1991-12-26 |
Family
ID=31355581
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11464487U Expired JPH0357238Y2 (en) | 1987-07-28 | 1987-07-28 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0357238Y2 (en) |
-
1987
- 1987-07-28 JP JP11464487U patent/JPH0357238Y2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6420847U (en) | 1989-02-01 |
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