JPS58138464A - Sampling of high density blood component - Google Patents

Sampling of high density blood component

Info

Publication number
JPS58138464A
JPS58138464A JP57021772A JP2177282A JPS58138464A JP S58138464 A JPS58138464 A JP S58138464A JP 57021772 A JP57021772 A JP 57021772A JP 2177282 A JP2177282 A JP 2177282A JP S58138464 A JPS58138464 A JP S58138464A
Authority
JP
Japan
Prior art keywords
blood
blood cells
collected
rotor
plasma
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
JP57021772A
Other languages
Japanese (ja)
Inventor
中川 隆郷
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.)
Koki Holdings Co Ltd
Original Assignee
Hitachi Koki Co Ltd
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 Hitachi Koki Co Ltd filed Critical Hitachi Koki Co Ltd
Priority to JP57021772A priority Critical patent/JPS58138464A/en
Publication of JPS58138464A publication Critical patent/JPS58138464A/en
Pending legal-status Critical Current

Links

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、供血者の血液中から顆粒球や血小板など採取
しようとする成分を高密度に含む血液成分を採取する方
法に関するものである。    ・第1図に従来の血液
成分採取方法を示しである。第1図において、ローラポ
ンプ19により供血者すから採取した血液は、血液流入
口lより開口部12を経て遠心分離ロータ30室内に導
かれる。血液流入口l及び流出口2と一体をなす静止シ
ール4は、遠心分離ロータ3と一体をなす回転シール5
とともに気密を保つ構造になっている。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for collecting blood components containing a high density of components to be collected, such as granulocytes and platelets, from blood of a blood donor. - Figure 1 shows a conventional blood component collection method. In FIG. 1, blood collected from a donor by a roller pump 19 is introduced into a centrifugal rotor 30 chamber from a blood inlet 1 through an opening 12. A stationary seal 4 that is integral with the blood inlet 1 and an outlet 2 is a rotating seal 5 that is integral with the centrifugal rotor 3.
It also has a structure that maintains airtightness.

回転する遠心ロータ3の室内では、外周外より赤血球9
、白血球lO1血漿11の11に分離層が形成される。
Inside the rotating centrifugal rotor 3, red blood cells 9 are collected from outside the outer periphery.
, a separate layer is formed between the white blood cells 101 and 11 of the plasma 11.

−口部13の上に白血球lOの層が位置する状態のとき
ローラポンプ19を停止させ、ローラポンプ7を回転さ
せて白血球lOを開口部13から吸い出し、血液バック
8に溜めたのちポンプ7を停止させる。ロータ3の室内
に残った血液は、ローラポンプ6により供血者15へ返
す。以上の手順を複数回くり返して血液バック8に沢山
の白血球幻を採取する。
- When a layer of white blood cells 10 is located above the mouth 13, stop the roller pump 19, rotate the roller pump 7 to suck out the white blood cells 10 from the opening 13, collect it in the blood bag 8, and then turn off the pump 7. make it stop. Blood remaining in the chamber of the rotor 3 is returned to the blood donor 15 by the roller pump 6. The above procedure is repeated several times to collect a large number of white blood cells into the blood bag 8.

しかし、−この従来方法には次の欠点がある。それは、
白血球io (この附近は白血球を主とするパッフイコ
ートと呼ばれる部分)Fi極めて微蓋で分離層中がせま
いため、これだけ取り出すことは困難でありその附の赤
血球9や血漿11をも大量に含んたものτ採取し7うる
にすぎない。従って、その採取成分の白血球留部は極め
て低いものになる。
However, this conventional method has the following drawbacks. it is,
White blood cells io (This area is called the puffy coat, which is mainly composed of white blood cells) Fi is extremely thin and the separation layer is narrow, so it is difficult to extract this much, and it also contains a large amount of red blood cells 9 and plasma 11. The amount of τ sampled is only 7. Therefore, the leukocyte retention area of the collected component is extremely low.

ましてや、バッフィコートの一部である顆粒球を局側0
(採取することとか、血小板を高密度に採取することは
困難である。
Moreover, the granulocytes, which are part of the buffy coat, are removed from the local side.
(It is difficult to collect platelets or collect platelets at a high density.

本発明の目的は、上iビ従米技術の欠点をなくしλ血液
中に微量しか含まれない白血球を高密度に含A、だ血豫
、成分を採取することにある。白血球を代表例にとって
説明するが\実際に必要な顆粒球を高密度に含む成分や
、血小板を高@鞭に含む成分を採取する場合も同様であ
る。
The object of the present invention is to eliminate the drawbacks of the above-mentioned and conventional techniques and to collect leukocyte-containing components at a high density, which are contained in minute amounts in lambda blood. The explanation will be given using white blood cells as a typical example, but the same applies when collecting actually necessary components containing a high density of granulocytes or components containing a high density of platelets.

本発明は、はじめに複数回の粗分離を行った後、複数回
分の粗分離物を1回以上再分離して精分離物を得ようと
するものである。採取しようとするものを白血球に限定
して説明する。遠心分離ロータ内で形成される分離層は
、外周側より赤血球、白血球、血漿の順となり、それぞ
れの量をRlwXpzとすれば、Wの分k I’m I
I]は非常にせまいが若干の赤血球(△R)と血漿(A
Pf )をも抽出してよいとすれば容易に採取できる。
In the present invention, after first performing a plurality of rough separations, the crude separators from the plurality of times are re-separated one or more times to obtain a purified product. The explanation will be limited to white blood cells as what is to be collected. The separation layer formed inside the centrifugal rotor consists of red blood cells, white blood cells, and plasma in this order from the outer circumferential side, and if the amount of each is RlwXpz, then the amount of W is k I'm I
I] is very narrow but contains some red blood cells (△R) and plasma (A
If Pf ) can also be extracted, it can be easily collected.

この工程を1回繰り返せば、粗分離物として?L(ΔR
+W +t2j−)が得られこれを一担外部容器に溜め
る。
If you repeat this process once, will it produce a crude separated product? L(ΔR
+W +t2j-) is obtained and stored in an external container.

この粗分離物をもう一部ロータ室に戻して分離層を形成
させると第2図のように赤血球(−、ΔR)h1白血球
(n 、W ) 17、血漿(?L、、べ以)18とな
って、とくに白血球17の層が全血分離のときのn倍に
なるので、白血球のみの採取が容易になる。若干量の赤
血球△Rと血漿へP1を同時に抽出したとして(△R−
1−n 、W十人阿)なる棺分離物が容易に得られる。
Another part of this crude separation is returned to the rotor chamber to form a separation layer, and as shown in Fig. 2, red blood cells (-, ΔR) h1 white blood cells (n, W) 17, plasma (?L,, Bei) 18 In particular, since the layer of white blood cells 17 is n times as large as that in whole blood separation, collection of only white blood cells becomes easy. Assuming that P1 is simultaneously extracted into a small amount of red blood cells △R and plasma (△R-
A coffin isolate of 1-n, 1-n, and 1-n is easily obtained.

従来方法によって採取される血液成分に対する白血球の
含有率は、W/(ΔR−) W −)−JJ )である
が、本発明によるときは4・2ΔR十n 、W、−f−
tsPi )となる。
The content rate of white blood cells in blood components collected by the conventional method is W/(ΔR-) W-)-JJ), but in the case of the present invention, it is 4.2ΔRn,W,-f-
tsPi).

白血球含有率の改善比は、次式のようになる。The improvement ratio of white blood cell content is expressed by the following formula.

すなわち、本発明により採取される血液成分の白血球含
有率は、粗分離回数ルが増えるほど高率になる。
That is, the white blood cell content of the blood components collected according to the present invention increases as the number of times of rough separation increases.

次に本発明を第2図゛、第3図Krり詳細に説明する。Next, the present invention will be explained in detail with reference to FIGS. 2 and 3.

供血者すからローラポンプ19で採血し、血液抗凝固剤
26が一建比率になるようにローラポンプ25の!!1
1転数を設定し、通電の生理笈塩水27を加えて一担血
赦バツク21に溜める。仄にローラポンプ24? 1O
IL、て血散流人口lより開口部犯を経て遠心分附ロー
タ3′に適量の血液を入れたらポンプ24JI−i停止
させる。遠心分離ロータ3内の血液は(ロ)転数の2乗
′と同転半径に比例した遠心力により、外周より赤血球
9、血球球引、血漿11の順に分離層を形by、する。
Blood is collected from the blood donor using the roller pump 19, and the roller pump 25 is adjusted so that the blood anticoagulant 26 is in a uniform ratio. ! 1
One rotation number is set, and energized saline saline 27 is added and stored in one blood tank 21. Roller pump 24? 1O
After pouring an appropriate amount of blood into the centrifugal rotor 3' from the blood sprinkling volume 1 through the opening, the pump 24JI-i is stopped. The blood in the centrifugal rotor 3 forms separation layers in the order of red blood cells 9, blood cells, and plasma 11 from the outer periphery due to the centrifugal force proportional to the square of the rotation number and the radius of rotation.

次に゛ローラポンプ24を回しロータ室外周に全血(図
示省略)を送り込み、同時に弁22を開けば血液バッグ
加に血漿Uが流れでる。白血球10が血液流出口2に出
たら弁22を閉じ、弁加を開ければ白血球(が血液バッ
グ8に流れでる。前配白皿球10の流出妓図示し7ない
センサによって行われ、該センサに応答して一部 22
 Fi閉じられる。血液バッグ8に赤血球9が出かかっ
たら弁(資)を閉じ、遠心ロータ3の回転を停止させる
。1紀赤血球9の流出も同様に図示しない別のセンサで
検出され、該センサに応答してロータ3は回転を停止す
る。
Next, the roller pump 24 is turned to feed whole blood (not shown) to the outer periphery of the rotor chamber, and at the same time the valve 22 is opened, allowing plasma U to flow out in addition to the blood bag. When the white blood cells 10 come out to the blood outflow port 2, the valve 22 is closed, and when the valve is opened, the white blood cells (white blood cells) flow out into the blood bag 8. Part 22 in response to
Fi is closed. When the red blood cells 9 begin to appear in the blood bag 8, the valve is closed and the rotation of the centrifugal rotor 3 is stopped. The outflow of primary red blood cells 9 is similarly detected by another sensor (not shown), and the rotor 3 stops rotating in response to the sensor.

残った血液は溜部14内に赤血球が下層で血漿が上層に
なって溜る。ロータ3の(ロ)転停止に連動し7て直ち
にローラポンプ23が回転して残部血液を血液バッグ加
に溜めること忙より、混入した空気をバッグ20の上部
に逃がし、空気の混らない血液を生理食塩水28で適当
に薄めながらローラポンプ6によりzイルタ29を通し
7て供血者15に返血する。以上の動作を1回繰り返す
と、血液バッグ、8内にけ粗す離成分が九(△R−)−
W+ΔpL)だけ溜る。
The remaining blood accumulates in the reservoir 14 with red blood cells in the lower layer and plasma in the upper layer. When the rotor 3 (b) stops rolling, the roller pump 23 immediately rotates and collects the remaining blood in the blood bag, allowing the mixed air to escape to the upper part of the bag 20 and allowing the blood to remain air-free. While appropriately diluting the blood with physiological saline 28, the blood is returned to the donor 15 through the Z filter 29 using the roller pump 6. When the above operation is repeated once, the amount of separated components in the blood bag 8 will be reduced to 9 (△R-)-
W+ΔpL) is accumulated.

次に、ローラポンプ7を回して再びロータ3′に粗分離
成分を戻し、遠心分離を行い、第2図のように赤血球1
6 (九、△R)、白血球17 (九、w)、血漿18
(?L、ΔPj) O°順5白血球の巾が広い分離層が
得られる。ローラポンプ24により血液バッグ21の全
血(゛図示せず)を遠心ロータ室9外周に押し込み弁2
2を開けば、開口部31より血漿18が血液バッグ加に
出ていく。つづく白血球17が血液流出口2にきたら弁
22を閉じ弁30を開いて、血液バッグ8に血漿侶の若
干量ΔP1を伴った白血球17の全量Wを導く0次に赤
面116の若干量△Rが血液バッグ8に入ったところで
弁(資)を閉じれば梢分離成分として(ΔR十九、W+
Δpz)が採取できる。
Next, the roller pump 7 is turned to return the crudely separated components to the rotor 3', and centrifugation is performed.
6 (9, △R), white blood cells 17 (9, w), plasma 18
(?L, ΔPj) O° order 5 A wide separation layer of white blood cells is obtained. The roller pump 24 pushes whole blood (not shown) from the blood bag 21 into the outer periphery of the centrifugal rotor chamber 9 and the valve 2
2, plasma 18 comes out from the opening 31 into the blood bag. When the white blood cells 17 reach the blood outflow port 2, the valve 22 is closed and the valve 30 is opened to introduce the total amount W of the white blood cells 17 into the blood bag 8 along with a small amount ΔP1 of plasma particles. When the valve (supply) is closed when the blood enters the blood bag 8, it becomes a separated component (ΔR19, W+
Δpz) can be collected.

ローラポンプ19.25を停止し、供血者6からの採血
を終了し、生理食塩水27の滴下も停止させ、血液バッ
グ21が空になるまでローラポンプ24ヲ回す。ロータ
3′の回転を止めると残血は溜部14に集まり、開口部
稔よ、リローラボンブ23で血液バッグlに導いて気泡
を抜いたのち必要に応じて生理食塩水28を添加しなが
らローラポンプ6によりフィルタ29を経て供血者15
4C返血する。血液バッグ20が供血者6より十分高所
にあれば、ローラポンプ6を省略してもよい。
The roller pumps 19 and 25 are stopped, blood collection from the donor 6 is completed, and dripping of the physiological saline 27 is also stopped, and the roller pump 24 is rotated until the blood bag 21 is empty. When the rotation of the rotor 3' is stopped, the residual blood collects in the reservoir 14, and is guided to the blood bag l using the reroller bomb 23 through the opening, and after removing air bubbles, the roller pump adds physiological saline 28 as necessary. 6 to the donor 15 via the filter 29
4C Return blood. If the blood bag 20 is located sufficiently higher than the donor 6, the roller pump 6 may be omitted.

以−ヒは白血球の例で説明したが、一般には赤血球と血
漿の境界部分のバクフィコートと叶ばれる層が採威され
るのである。厳密にいうと、顆粒球や血小板が要求され
ることが多い。しかし、その場合でも粗分離方法と返血
方法は共通で樗分離方法が異なるたけである。
The following has been explained using the example of white blood cells, but in general, the layer that forms the bucficoat at the boundary between red blood cells and plasma is collected. Strictly speaking, granulocytes and platelets are often required. However, even in that case, the crude separation method and the blood return method are common, and the only difference is the chestnut separation method.

顆粒球の稍分離は、バッフィコートの赤血球寄りを採取
すればよい。従来技術によると、白血球lOO層巾層巾
くて採取困難であるが、本発明によれば層中が1倍に拡
げられるので次の採取方法が容易になる。すなわち、ロ
ーラポンプ鴎により遠心ロータ室外周に全血を送り込み
弁22を開けば開口部31よね血液バッグ加へ血漿侶が
押し出される。つづいて白血球17−が若干入ったとこ
ろで弁22を閉じ弁間を開き血液バック8に送りこみ、
若干の赤血球が入ったところで弁間を閉じローラポンプ
冴を停止させれば、顆粒球を高密度に含む精分離面液成
分(n 、W+?FL 、△R)ただしn ) mが採
取できる。
Granulocytes can be isolated by collecting the buffy coat near the red blood cells. According to the prior art, the white blood cell layer is so wide that it is difficult to collect it, but according to the present invention, the layer is expanded by a factor of 1, making the next collection method easier. That is, when whole blood is sent to the outer periphery of the centrifugal rotor chamber by a roller pump and the valve 22 is opened, plasma is pushed out through the opening 31 and into the blood bag. Next, when some white blood cells 17- have entered, the valve 22 is closed and the gap between the valves is opened to send them into the blood bag 8.
When some red blood cells have entered, the valve gap is closed and the roller pump is stopped, and the purified surface liquid component (n, W+?FL, ΔR) containing granulocytes at a high density can be collected.

血小板の精分離は、バラフィコ−1トの血漿寄りを採取
すればよい。同様にして白血球17が血液流出口2に押
しだされたとき弁型を閉じ弁30を開き、血液流出p2
に赤血球16が出たらすぐ升30を閉〜・、 。
For fine separation of platelets, it is sufficient to collect blood plasma from platelets. Similarly, when the white blood cells 17 are pushed out to the blood outflow port 2, the valve mold is closed and the valve 30 is opened, and the blood outflow p2
As soon as 16 red blood cells appear, close square 30.

じローラポンプ24を停;止させれば、血小板を高密度
に含む稍分離血液−分(?L 、 W−1−?FL 、
ΔPj)が採取できる。(?L>?FL) 本発明によれば、供血者の全血中から白血球を高奮度に
含む血液成分を採取することが容易かつ確実にできるば
かりでなく、顆粒球を高密度に含むものの採取も容易確
実であり、また血小板を高密度に含むものの採取も容易
確実に行うこと力量できる。そのことは、供血者から大
量の血液をとりだし、微量しか含まれない上記血液成分
だけとりだし、残血は供血者に戻す場合に、高効率の採
取ができることは供血者の負担を軽減するという意味で
も効果が大きい。
When the roller pump 24 is stopped, the separated blood containing platelets at a high density (?L, W-1-?FL,
ΔPj) can be collected. (?L>?FL) According to the present invention, it is possible not only to easily and reliably collect a blood component containing a high concentration of white blood cells from the whole blood of a blood donor, but also to collect a blood component containing a high concentration of granulocytes. It is easy and reliable to collect things, and it is also possible to collect things that contain platelets at a high density. This means that when a large amount of blood is taken from a donor, only trace amounts of the above blood components are taken out, and the remaining blood is returned to the donor, high efficiency collection reduces the burden on the donor. But the effect is great.

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

第1図は従来の血液成分採取方法を示す説明図、第2図
、第3図は本発明になる血液成分採取方法を示す説明図
であるう lは血液流入口、2は血液流出口、3.3′は遠心分1
11’−タ、4はシール、5はシール、6はローラポン
プ、7はローラポンプ、8け血液ノ(ラグ、9は赤血球
、lOは白血球、llは血漿、稔は開口部、13は開口
部、賛は溜部、15け供血者、迅は赤血球、17は白血
球、梠は血漿、台はローラポンプ、別は血液バッグ、2
1Fi血液バツグ、22は弁、nはローラポンプ、24
はローラポンプ、25はローラポンプ、届は血液抗峡固
剤、27は生理食塩水、路は生理食塩水、29はフィル
タ、3oIfi弁、31は開口部である。 特許出願人の名称  日立工機株式会社千1図 千2図 寸3図 0
FIG. 1 is an explanatory diagram showing a conventional blood component collection method, and FIGS. 2 and 3 are explanatory diagrams showing a blood component collection method according to the present invention. 1 is a blood inlet, 2 is a blood outlet, 3.3' is centrifugal fraction 1
11'-ta, 4 is a seal, 5 is a seal, 6 is a roller pump, 7 is a roller pump, 8 is a blood cell (lug, 9 is a red blood cell, 10 is a white blood cell, 11 is a plasma, Minoru is an opening, 13 is an opening Department, support is Tamabe, 15 blood donors, Jin is red blood cells, 17 are white blood cells, Kakashi is plasma, stand is roller pump, another is blood bag, 2
1Fi blood bag, 22 is valve, n is roller pump, 24
25 is a roller pump, 25 is a blood anticoagulant, 27 is physiological saline, 29 is a filter, 3 o Ifi valve, 31 is an opening. Name of patent applicant Hitachi Koki Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 供血者から採血した血液をローター室内に注入して遠心
分離層を形成させ、顆粒球又は血小板など採取しようと
する血液成分とそれに近接する赤血球や血漿を若干蓋含
んだ粗分離血液成分を外部容器に溜め、ローター内に残
った血液は供血者に戻す、という動作を複数回繰り返し
、この複数回分の粗分離血液成分を再びローター室内に
戻し、同様の分離採取動作を1回以上繰り返して、顆粒
球又は血小板などの採取しようとする血液成分を高密度
に含んだ槍分離血液成分を採取する方法。
Blood collected from a donor is injected into the rotor chamber to form a centrifugal separation layer, and the crudely separated blood components containing the blood components to be collected, such as granulocytes or platelets, and some adjacent red blood cells and plasma are transferred to an external container. The blood remaining in the rotor is collected in the rotor, and the blood remaining in the rotor is returned to the donor. This operation is repeated multiple times, and the crudely separated blood components from multiple times are returned to the rotor chamber. The same separation and collection operation is repeated one or more times to form granules. A method for collecting separated blood components containing a high density of blood components to be collected, such as spheres or platelets.
JP57021772A 1982-02-13 1982-02-13 Sampling of high density blood component Pending JPS58138464A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57021772A JPS58138464A (en) 1982-02-13 1982-02-13 Sampling of high density blood component

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57021772A JPS58138464A (en) 1982-02-13 1982-02-13 Sampling of high density blood component

Publications (1)

Publication Number Publication Date
JPS58138464A true JPS58138464A (en) 1983-08-17

Family

ID=12064360

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57021772A Pending JPS58138464A (en) 1982-02-13 1982-02-13 Sampling of high density blood component

Country Status (1)

Country Link
JP (1) JPS58138464A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62116736U (en) * 1986-01-17 1987-07-24
JP2015536719A (en) * 2012-11-05 2015-12-24 ヘモネティクス・コーポレーションHaemonetics Corporation System and method for continuous separation of whole blood

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62116736U (en) * 1986-01-17 1987-07-24
JP2015536719A (en) * 2012-11-05 2015-12-24 ヘモネティクス・コーポレーションHaemonetics Corporation System and method for continuous separation of whole blood

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