JPH09206371A - Separation method for blood components - Google Patents

Separation method for blood components

Info

Publication number
JPH09206371A
JPH09206371A JP8016532A JP1653296A JPH09206371A JP H09206371 A JPH09206371 A JP H09206371A JP 8016532 A JP8016532 A JP 8016532A JP 1653296 A JP1653296 A JP 1653296A JP H09206371 A JPH09206371 A JP H09206371A
Authority
JP
Japan
Prior art keywords
blood
container element
bag
plasma
parent bag
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.)
Pending
Application number
JP8016532A
Other languages
Japanese (ja)
Inventor
Jiro Naito
二郎 内藤
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.)
Nissho Corp
Original Assignee
Nissho 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 Nissho Corp filed Critical Nissho Corp
Priority to JP8016532A priority Critical patent/JPH09206371A/en
Publication of JPH09206371A publication Critical patent/JPH09206371A/en
Pending legal-status Critical Current

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  • Medical Preparation Storing Or Oral Administration Devices (AREA)
  • External Artificial Organs (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide a separation method for blood components to obtain plasma without a leucocyte and concentrated erythrocytes. SOLUTION: A parent bag comprises a first container element, a second container element and a guide tube means part. The first container element 101 is filled with the blood plasma and the second container element with the erythrocytes by centrifuge. When each blood component is transported to each child bag, the parent bag is folded in the guide tube means part and the upper layer containing plasma and the lower layer containing erythrocytes are simultaneously transported and the intermediate layer containing leucocyte is remained in the part of guide tube means.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、血液バッグを用い
て全血中の各血液成分をそれぞれに分離する方法に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for separating each blood component in whole blood using a blood bag.

【0002】[0002]

【従来の技術】全血に含まれる多様な血液成分を取り出
して、血液製剤を得るには血液バツグセツトが使用され
る。図3は従来から採用されている血液バツグセツトを
平面的に示した説明図である。血液バツグセツトを使用
した従来からの血液分離方法は以下のとおりである。
2. Description of the Related Art A blood bag set is used to extract various blood components contained in whole blood to obtain a blood product. FIG. 3 is a plan view showing a blood bag set which has been conventionally used. The conventional blood separation method using the blood bag set is as follows.

【0003】採血針3・採血チユーブ2が接続部9と他
に2個又は3個の接続部が備えられた親バツグ1に全血
を採取し、この全血を血漿を含有する上層と白血球を含
有する中間層(以下、バフイーコートと言う。)と赤血
球を含有する下層に遠心分離した後、連通ピース14を
連通状態にして、本体8を押しつけながら接続部12か
らチユーブ16を介して子バツグ4に血液の上層部すな
わち血漿を移送する。
Blood collection needle 3 and blood collection tube 2 are used to collect whole blood in a parent bag 1 provided with two or three connection parts 9 and other connection parts, and the whole blood is collected into an upper layer containing plasma and white blood cells. After centrifuging into an intermediate layer containing (hereinafter, referred to as buffy coat) and a lower layer containing red blood cells, the communication piece 14 is brought into a communication state, and the main body 8 is pressed while the connection portion 12 is pressed through the tube 16 through the probe 16. The upper layer of blood, namely plasma, is transferred to 4.

【0004】次に連通ピース15を連通状態にして、本
体8を押しつけながら接続部13からチユーブ17を介
して子バツグ5に、バフイーコートを移送する。その結
果、血漿部分を収納した子バツグ及びバフイーコートを
収納した子バツグを得る。この際、親バツグ1には赤血
球濃厚液(以下、CRCと言う。)が残る。これを改め
て接続部を介して子バツグに移すことは自由に選択す
る。最近の例ではCRCに赤血球保存液を添加する。こ
れに関する添加方法は別に小型の子バツグ(図示なし)
を用意してCRCに赤血球保存液をチユーブ17内を通
して添加することもあった。
Next, the communication piece 15 is brought into a communication state, and the buffy coat is transferred from the connection portion 13 to the child bag 5 through the tube 17 while pressing the main body 8. As a result, a child bag containing the plasma portion and a child bag containing the buffy coat are obtained. At this time, a concentrated red blood cell liquid (hereinafter referred to as CRC) remains in the parent bag 1. It is freely chosen to transfer it again to the child bag via the connection. In a recent example, a red blood cell preservation solution is added to CRC. Addition method related to this is a small child bag (not shown)
In some cases, the erythrocyte preservative solution was added to the CRC through the tube 17 by preparing.

【0005】以上のようにして得られたものが血液製剤
として用いられる。その際、患者に対してバツグに備わ
っているプロテクター10付きポート11から輸血され
る。
The thus obtained product is used as a blood product. At that time, blood is transfused to the patient from the port 11 with the protector 10 provided in the bag.

【0006】[0006]

【発明が解決しようとする課題】上記のような従来から
の血液分離方法は以下のような問題がある。(1)バフ
イーコートを移送した後といえども、本体8の内面の一
部はバフイーコートで汚されている。(2)CRCに赤
血球保存液を添加する際、連結方法にもよるが、チユー
ブ17内に付着・残存するバフイーコートを含んでしま
った赤血球保存液がCRCに添加されることもある。
The conventional blood separation method as described above has the following problems. (1) Even after the buffy coat is transferred, a part of the inner surface of the main body 8 is soiled with the buffy coat. (2) When adding the red blood cell preservative solution to the CRC, the red blood cell preservative solution containing the buffy coat adhering to and remaining in the tube 17 may be added to the CRC, depending on the connecting method.

【0007】(1)や(2)のような状態でCRCを得
ると、僅かではあるがバフイーコートを含有した不純な
CRCしか得られない。このような不純なCRCを人体
に輸血すると副作用として以下の重大な問題が発生す
る。
When the CRC is obtained in the states of (1) and (2), only a small amount of impure CRC containing the buffy coat can be obtained. Blood transfusion of such an impure CRC into the human body causes the following serious problems as a side effect.

【0008】(i)同種抗体(抗HLA)の産生に伴
い、非溶血性輸血副作用(発熱・輸血後肺症状)がおこ
る。(ii)白血球中のリンパ球特にT細胞によって、
移植片対宿主病(GVHD)が発症し、殆どの場合死に
至る。(iii)白血球がサイトメガロウイルス(CM
V)やHTLV−Iのようなウイルスのトランスフアー
となるので、輸血ウイルス感染症がおこる。
(I) Non-hemolytic transfusion side effects (fever / post-transfusion pulmonary symptoms) occur with the production of alloantibodies (anti-HLA). (Ii) by lymphocytes in white blood cells, especially T cells,
Graft-versus-host disease (GVHD) develops and most often results in death. (Iii) White blood cells are cytomegalovirus (CM
V) and HTLV-I are transferors of viruses such as transfusion virus infection.

【0009】本発明は(i)、(ii)、(iii)の
重大な問題を未然に防ぐためにバフイーコートを含まな
いCRCを得るために発明されたものである。
The present invention was invented to obtain a CRC containing no buffy coat in order to obviate the serious problems (i), (ii) and (iii).

【0010】[0010]

【課題を解決するための手段】本発明は、第1容器要素
と第2容器要素と、第1容器要素の底と第2容器要素の
頂部とを流体的に接続する導管手段と、血液を容器要素
へ導入する手段と、容器要素の各々から血液成分を抜き
出す手段とからなり、第1容器要素と第2容器要素とは
全血の赤血球成分の容積と血漿成分の容積との関係と同
じである容積の関係を有する親バッグを使用するもので
あって、上記親バッグに全血で満たし、第1容器要素に
低比重のものを、第2の容器要素に高比重のものを満た
せるように遠心分離し、第1容器要素は血漿で満たし、
第2容器要素は赤血球で満たし、血漿と赤血球とを分割
する表面が導管手段中に位置するようにし、また、白血
球を含有する中間層が導管手段部分に位置させ、各血液
成分を各接続部を介して各子バツグに移送するにあた
り、先ず親バッグを導管手段の部分で折り、血漿と赤血
球を同時に移送し、白血球を含有する中間層を親バック
の導管手段の部分内に残すことを特徴とする血液成分分
離方法を要旨とする。
SUMMARY OF THE INVENTION The present invention provides a first container element and a second container element, conduit means for fluidly connecting the bottom of the first container element and the top of the second container element, and blood. The first container element and the second container element have the same relationship between the volume of the red blood cell component and the volume of the plasma component of the whole blood. Using a parent bag having a certain volume relationship such that the parent bag can be filled with whole blood and the first container element can be filled with low specific gravity and the second container element with high specific gravity. Centrifuge, fill the first container element with plasma,
The second container element is filled with red blood cells such that the surface separating the plasma and red blood cells is located in the conduit means, and an intermediate layer containing white blood cells is located in the conduit means portion, and each blood component is associated with each connection. When transferring to each child bag via the parent bag, first, the parent bag is folded at the part of the conduit means, plasma and erythrocytes are transferred at the same time, and the intermediate layer containing white blood cells is left in the part of the conduit means of the parent bag. The gist is the method for separating blood components.

【0011】本発明に使用する容器を含む血液バッグセ
ットは透明又は半透明の合成樹脂製であることが好まし
い。例えば親バッグや子バッグは、ポリ塩化ビニルなど
の合成樹脂製の2枚のシートから構成され、これらシー
トの周囲が熱融着で接着されて作られる。
The blood bag set including the container used in the present invention is preferably made of transparent or translucent synthetic resin. For example, the parent bag and the child bag are composed of two sheets made of synthetic resin such as polyvinyl chloride, and the peripheries of these sheets are bonded by heat fusion.

【0012】本発明の親バッグでは、第1容器要素と第
2容器要素とは全血の赤血球成分の容積と血漿成分の容
積との関係と同じである容積の関係を有するのであっ
て、具体的には親バッグ全体の容量を128ml、25
6ml、512ml等とし、その60%近くを第1容器
要素の容量とし、40%近くを第2容器要素の容量とす
る。本発明では第1容器要素の底と第2容器要素の頂部
とを流体的に接続する導管手段があり、これはバフィー
コートを収容できるだけの容量を必要とし、かつ、この
箇所で親バッグを折れることが必要である。更にこの箇
所にクランプを付け得るのも好ましい。このような親バ
ッグは特開昭53−38189号公報や米国特許391
1918号公報により公知である。
In the parent bag of the present invention, the first container element and the second container element have a volume relationship which is the same as the relationship between the volume of the red blood cell component and the volume of the plasma component of whole blood. The total volume of the parent bag is 128 ml, 25
6 ml, 512 ml, etc., of which 60% is the capacity of the first container element and 40% is the capacity of the second container element. In the present invention, there is a conduit means for fluidly connecting the bottom of the first container element and the top of the second container element, which requires a volume to contain the buffy coat and at which point the parent bag is folded. It is necessary. It is also preferable that a clamp can be attached at this point. Such a parent bag is disclosed in JP-A-53-38189 and U.S. Pat. No. 391.
It is known from Japanese Patent No. 1918.

【0013】本発明の親バッグの上端部には、採血チュ
ーブが直接接続されるか、又はそのための接続部があ
り、更に血漿移送用チューブが直接接続されるか、又は
そのための接続部があり、本発明の親バッグの下端部に
は、CRC移送用チューブが直接接続されるか、又はそ
のための接続部がある。その他プロテクタ付きの輸血口
が備えられていることもある。
At the upper end of the parent bag of the present invention, a blood collection tube is directly connected or has a connection therefor, and further a plasma transfer tube is directly connected or has a connection therefor. At the lower end of the parent bag of the present invention, a CRC transfer tube is directly connected or has a connection therefor. Others may have a blood transfusion port with a protector.

【0014】血漿移送用接続部やCRC移送用接続部
は、周知のように、ポリ塩化ビニルなどの合成樹脂製の
軟質チューブで構成されており、親バッグの2枚のシー
トの周縁を接着する際に両シート間に挟み込まれて固定
される。
As is well known, the plasma transfer connection part and the CRC transfer connection part are made of soft tubes made of synthetic resin such as polyvinyl chloride, and adhere the peripheral edges of the two sheets of the parent bag. At that time, it is fixed by being sandwiched between both seats.

【0015】本発明の親バッグは、血漿採取用子バッグ
とCRC採取用子バッグに、又は赤血球保存液(例え
ば、赤血球の有効期間を42日間に延ばすことができる
マニトールとアデニンを主成分とするMAP液)入りバ
ッグにチューブで連通できる状態で接続されて使用する
のが普通である。ここで連通できる状態とは接続部内に
曲げ折ることにより親バッグ内部と外部、すなわち、親
バッグ内部と子バッグの内部を連通させる連通ピース
(折れ棒とも言う。)を備えていることである。このよ
うな接続は周知である。なお親バッグ内部にCPD液・
ACD−A液などの血液保存液が封入されることが多
い。
The parent bag of the present invention is used as a blood bag for collecting plasma and a bag for collecting CRC, or is mainly composed of erythrocyte preservation solution (for example, mannitol and adenine which can extend the effective period of erythrocytes to 42 days). It is usually used by being connected to a bag containing a MAP liquid) in a state of being able to communicate with a tube. Here, the state of being able to communicate means that a connecting piece (also referred to as a folding rod) is provided in the connecting portion that allows the inside and outside of the parent bag to communicate with each other, that is, the inside of the parent bag and the inside of the child bag. Such connections are well known. In addition, CPD liquid in the parent bag
A blood preservation solution such as ACD-A solution is often enclosed.

【0016】本発明の親バッグ内に血液が採取されると
周知の方法によって遠心分離がなされ、血漿部分・バフ
ィーコート・CRCの層に分ける。例えば、遠心分離の
条件は通常3000〜4500×g、6〜10分、好ま
しくは4400×g、6分である。
When blood is collected in the parent bag of the present invention, it is centrifuged by a well-known method to divide it into a plasma portion, a buffy coat and a CRC layer. For example, the conditions for centrifugation are usually 3000 to 4500 xg for 6 to 10 minutes, preferably 4400 xg for 6 minutes.

【0017】この各血液成分を各接続部を介して各子バ
ツグに移送するにあたり、本発明では先ず親バッグを導
管手段の部分で二つ折りにし、第1と第2の容器要素の
各々から血液成分を抜き出す口がいずれも上方又は下方
の同じ方向に向けるのが特徴である。
In transferring each blood component to each child bag via each connecting portion, in the present invention, the parent bag is first folded in two at the conduit means portion, and blood is supplied from each of the first and second container elements. The feature is that all the outlets for extracting the components are directed in the same direction upward or downward.

【0018】連通ピースを折り、接続部とチューブを介
して、親バッグ内と各子バッグ内を連通させてから、親
バッグの第1と第2の容器要素内の血液を圧することに
より、CRCはCRC採取用子バッグへ、同時に血漿は
血漿採取用子バッグに移行させる。この子バッグへの移
行は同時に行う。バフィーコートは親バックの導管手段
の部分内に可能な限り残すこととする。
By folding the communicating piece and connecting the inside of the parent bag with the inside of each child bag through the connecting portion and the tube, the blood in the first and second container elements of the parent bag is pressed to thereby form the CRC. Is transferred to the CRC collection bag, and plasma is simultaneously transferred to the plasma collection bag. The transfer to this child bag is done at the same time. The buffy coat should be left as much as possible within the conduit means of the parent bag.

【0019】本発明において、親バッグから血漿部分・
CRC部分の各層をそれぞれの子バッグに移行させ、親
バッグにバフィーコートのみを残留させる際、目視で管
理してもよく、ホォトセンサなど光学的に管理してもよ
い。
In the present invention, the plasma portion from the parent bag is
When each layer of the CRC part is transferred to each child bag and only the buffy coat remains in the parent bag, it may be visually controlled or optically controlled by a photo sensor or the like.

【0020】[0020]

【発明の実施の形態】以下、図面に基づいて本発明の実
施例を詳細に説明する。図1は本発明の方法に採用され
る親バッグの一例を示す平面図、図2は本発明の方法で
採用される親バッグの他の一例を示す立面図である。
BEST MODE FOR CARRYING OUT THE INVENTION Embodiments of the present invention will be described in detail below with reference to the drawings. FIG. 1 is a plan view showing an example of a parent bag used in the method of the present invention, and FIG. 2 is an elevation view showing another example of a parent bag used in the method of the present invention.

【0021】図1では、第1容器要素101と第2容器
要素102と、第1容器要素101の底と第2容器要素
102の頂部とを流体的に接続する導管手段103と、
血液を容器要素へ導入する手段2、9と、容器要素の各
々から血液成分を抜き出す手段(ポート)6、7とから
なり、第1容器要素101と第2容器要素102とは全
血の赤血球成分の容積と血漿成分の容積との関係と同じ
である容積の関係を有する親バッグ1を示している。
In FIG. 1, a first container element 101 and a second container element 102, conduit means 103 fluidly connecting the bottom of the first container element 101 and the top of the second container element 102,
It comprises means 2, 9 for introducing blood into the container elements and means (ports) 6, 7 for withdrawing blood components from each of the container elements, wherein the first container element 101 and the second container element 102 are red blood cells of whole blood. 1 shows a parent bag 1 having a volume relationship which is the same as the volume relationship between the component volume and the plasma component volume.

【0022】図2では、第1容器要素101’と第2容
器要素102’と、第1容器要素101’の底と第2容
器要素102’の頂部とを流体的に接続する導管手段1
03’と、血液を容器要素へ導入する手段2’、9’
と、容器要素の各々から血液成分を抜き出す手段(ポー
ト)6’、7’とからなり、第1容器要素101’と第
2容器要素102’とは全血の赤血球成分の容積と血漿
成分の容積との関係と同じである容積の関係を有する親
バッグ1’を示している。
In FIG. 2, a conduit means 1 for fluidly connecting the first container element 101 ', the second container element 102', the bottom of the first container element 101 'and the top of the second container element 102'.
03 'and means 2', 9'for introducing blood into the container element
And means (ports) 6 ', 7'for extracting blood components from each of the container elements. The first container element 101' and the second container element 102 'are composed of the volume of red blood cell component of whole blood and the plasma component. 1 shows a parent bag 1'having a volume relationship which is the same as the volume relationship.

【0023】親バッグ1、1’を全血で満たし、第1容
器要素101、101’に低比重のもの、すなわち、血
漿を、第2の容器要素102、102’に高比重のも
の、すなわち、CRCを満たせるように遠心分離し、血
漿と赤血球とを分割する表面が導管手段103、10
3’中に位置するようにし、また、バフィーコートを導
管手段部分103、103’に位置させ、各血液成分を
各接続部を介して各子バツグ(図示されていない。)に
移送する。先ず親バッグ1、1’を導管手段の部分10
3、103’で二つ折りにし、第1容器要素101、1
01’と第2の容器要素102、102’を押しつけな
がら血漿とCRCを同時に各子バッグに移送し、バフィ
ーコートを親バック1、1’の導管手段の部分103、
103’内に残す。
The parent bags 1, 1'are filled with whole blood and the first container element 101, 101 'is of low specific gravity, ie plasma, and the second container element 102, 102' is of high specific gravity, ie , The surface that divides plasma and red blood cells by centrifuging to fill the CRC is conduit means 103, 10.
3'and the buffy coat is located on the conduit means portions 103, 103 'to transfer each blood component via each connection to each child bag (not shown). First, the parent bag 1, 1'is attached to the portion 10 of the conduit means.
First, the first container element 101, 1
01 'and the second container element 102, 102' are pressed and plasma and CRC are simultaneously transferred to each child bag, and the buffy coat is part 103 of the conduit means of the parent bag 1, 1 '.
Leave in 103 '.

【0024】本発明の方法で血液を5回にわたり採取
し、それを各血液成分に遠心分離し、成分の平均値を求
めた結果、親バッグ1中の赤血球のうち94%をCRC
採取用子バッグに移行させることができ、親バッグ1中
に存在していた白血球のうち、その81%を親バッグ
1、すなわち、導管手段103内に残すことができた。
Blood was collected 5 times by the method of the present invention, and the blood components were centrifuged to obtain the average value of the components. As a result, 94% of the red blood cells in the parent bag 1 were CRC.
It was possible to transfer to the collection child bag, and 81% of the white blood cells existing in the parent bag 1 could be left in the parent bag 1, that is, the conduit means 103.

【0025】比較例として、図3に示す方法で血液を5
回にわたり採取し、遠心分離し、血液各成分の平均値を
求めた結果、親バッグ1中の赤血球のうち88%しかC
RC採取用子バッグに移行させることができず、親バッ
グ1中に存在していた白血球のうち65%しか親バッグ
1に残らなかった。
As a comparative example, blood was removed by the method shown in FIG.
As a result of collecting the blood repeatedly, centrifuging, and obtaining the average value of each blood component, only 88% of the red blood cells in the parent bag 1 were C
It could not be transferred to the RC collection child bag, and only 65% of the white blood cells existing in the parent bag 1 remained in the parent bag 1.

【0026】[0026]

【発明の効果】本発明の方法で血液成分を分離すれば、
親バッグの外部の圧搾状態を工夫するだけで、赤血球や
血漿がバフィーコートで汚されていない箇所を通過し
て、各々の子バッグに移行させ得るので、白血球を含む
ことの少ないCRCや血漿の製剤を得ることができる。
By separating blood components by the method of the present invention,
Only by devising the squeezed condition outside the parent bag, red blood cells and plasma can pass through the area not stained by the buffy coat and be transferred to each child bag, so that CRC and plasma containing little white blood cells can be transferred. A formulation can be obtained.

【0027】本発明の血液分離方法は従来と殆ど同じ血
液バツグセツトを使用するので、血液バツグセツトの製
造工程を殆ど踏襲でき、血液製剤を得る操作においても
従来と殆ど同じ方法が踏襲できる。
Since the blood separating method of the present invention uses almost the same blood bag set as in the conventional method, almost all the steps of manufacturing the blood bag set can be followed, and the operation of obtaining a blood product can be carried out in almost the same manner as the conventional method.

【0028】また赤血球保存液を添加する場合、従来は
別に子バツグを用意し、バフイコートで内壁が汚された
チユーブ内に該保存液を通して添加する方法も行われて
いたが、本発明の方法ではCRCを収納する子バツグに
予め赤血球保存液が添加されておればよいわけであり、
このように赤血球保存液の添加操作が不要となる。
In addition, in the case of adding a red blood cell preservative solution, conventionally, a method has been used in which a child bag is separately prepared and added through the preservative solution into a tube whose inner wall is soiled with a buffy coat. It is only necessary to add the red blood cell preservation solution to the child bag that stores the CRC in advance.
Thus, the operation of adding the red blood cell preservation solution is unnecessary.

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

【図1】本発明に採用される血液バッグの一例を示す平
面図。
FIG. 1 is a plan view showing an example of a blood bag adopted in the present invention.

【図2】本発明に採用される血液バッグの一例を示す立
面図。
FIG. 2 is an elevation view showing an example of a blood bag adopted in the present invention.

【図3】従来の血液バッグセットの平面図。FIG. 3 is a plan view of a conventional blood bag set.

【符号の説明】[Explanation of symbols]

1 親バッグ 2 採血チユーブ 3 採血針 4 血漿採取用子バッグ 5 CRC採取用子バッグ 6 血液成分を抜き出すポート 7 血液成分を抜き出すポート 8 本体 9 接続部 10 プロテクター 11 ポート 12 接続部 13 接続部 14 連通ピース 15 連通ピース 16 チューブ 17 チューブ 101 第1容器要素 102 第2容器要素 103 導管手段部分 1 Parent Bag 2 Blood Collection Tube 3 Blood Collection Needle 4 Plasma Collection Child Bag 5 CRC Collection Child Bag 6 Blood Component Extraction Port 7 Blood Component Extraction Port 8 Main Body 9 Connection Part 10 Protector 11 Port 12 Connection Part 13 Connection Part 14 Communication Piece 15 Communication piece 16 Tube 17 Tube 101 First container element 102 Second container element 103 Conduit means part

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 第1容器要素と第2容器要素と、第1容
器要素の底と第2容器要素の頂部とを流体的に接続する
導管手段と、血液を容器要素へ導入する手段と、容器要
素の各々から血液成分を抜き出す手段とからなり、第1
容器要素と第2容器要素とは全血の赤血球成分の容積と
血漿成分の容積との関係と同じである容積の関係を有す
る親バッグを使用するものであって、 上記親バッグに全血で満たし、第1容器要素に低比重の
ものを、第2の容器要素に高比重のものを満たせるよう
に遠心分離し、第1容器要素は血漿で満たし、第2容器
要素は赤血球で満たし、血漿と赤血球とを分割する表面
が導管手段中に位置するようにし、また、白血球を含有
する中間層が導管手段部分に位置させ、各血液成分を各
接続部を介して各子バツグに移送するにあたり、 先ず親バッグを導管手段の部分で折り、血漿と赤血球を
同時に移送し、白血球を含有する中間層を親バックの導
管手段の部分内に残すことを特徴とする血液成分分離方
法。
1. A conduit means for fluidly connecting a first container element and a second container element, a bottom of the first container element and a top of the second container element, and means for introducing blood to the container element. Means for withdrawing a blood component from each of the container elements;
The container element and the second container element use a parent bag having a volume relationship which is the same as the relationship between the volume of the red blood cell component and the volume of the plasma component of the whole blood, and the parent bag contains whole blood. And centrifuge so that the first container element is of low specific gravity and the second container element is of high specific gravity, the first container element is filled with plasma, the second container element is filled with red blood cells, plasma The surface separating the erythrocytes and erythrocytes is located in the conduit means, and the intermediate layer containing white blood cells is located in the conduit means portion for transferring each blood component through each connection to each child bag. A method for separating blood components, which is characterized in that the parent bag is first folded at the portion of the conduit means, plasma and red blood cells are simultaneously transferred, and the intermediate layer containing white blood cells is left inside the portion of the conduit means of the parent bag.
JP8016532A 1996-02-01 1996-02-01 Separation method for blood components Pending JPH09206371A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8016532A JPH09206371A (en) 1996-02-01 1996-02-01 Separation method for blood components

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8016532A JPH09206371A (en) 1996-02-01 1996-02-01 Separation method for blood components

Publications (1)

Publication Number Publication Date
JPH09206371A true JPH09206371A (en) 1997-08-12

Family

ID=11918885

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8016532A Pending JPH09206371A (en) 1996-02-01 1996-02-01 Separation method for blood components

Country Status (1)

Country Link
JP (1) JPH09206371A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011162547A (en) * 2003-05-21 2011-08-25 Jms Co Ltd Serum preparing method
CN103191015A (en) * 2012-01-09 2013-07-10 金卫医疗科技(上海)有限公司 Separation soft bag for improving separating efficiency during plasma continuous separation

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011162547A (en) * 2003-05-21 2011-08-25 Jms Co Ltd Serum preparing method
US8796017B2 (en) 2003-05-21 2014-08-05 Jms Co., Ltd. Container for preparing serum and regenerative medical process using the same
US8993321B2 (en) 2003-05-21 2015-03-31 Jms Co., Ltd. Container for preparing serum and regenerative medical process using the same
CN103191015A (en) * 2012-01-09 2013-07-10 金卫医疗科技(上海)有限公司 Separation soft bag for improving separating efficiency during plasma continuous separation

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