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JPS6252254B2 - - Google Patents

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Publication number
JPS6252254B2
JPS6252254B2 JP54129151A JP12915179A JPS6252254B2 JP S6252254 B2 JPS6252254 B2 JP S6252254B2 JP 54129151 A JP54129151 A JP 54129151A JP 12915179 A JP12915179 A JP 12915179A JP S6252254 B2 JPS6252254 B2 JP S6252254B2
Authority
JP
Japan
Prior art keywords
detector
piston
bellows
sample
chamber
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
JP54129151A
Other languages
Japanese (ja)
Other versions
JPS5652037A (en
Inventor
Shigenori Daito
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.)
Sysmex Corp
Original Assignee
Sysmex 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 Sysmex Corp filed Critical Sysmex Corp
Priority to JP12915179A priority Critical patent/JPS5652037A/en
Publication of JPS5652037A publication Critical patent/JPS5652037A/en
Publication of JPS6252254B2 publication Critical patent/JPS6252254B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、懸濁液中に浮懸する血球などの粒子
を高い精度で検出することができる懸濁粒子検出
装置に関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a suspended particle detection device that can detect particles such as blood cells suspended in a suspension with high accuracy.

〔従来の技術〕[Conventional technology]

従来、生理食塩水などに浮懸する血球に関する
種々のパラメータを自動的に分折する装置におい
て、単位体積中の赤血球数、白血球数などを測定
する際には、血球の浮懸液の吸引量を正確に求め
て生の血液中の血球数に換算する必要があつた。
このため従来は、(1)U字管内の水銀をアンバラン
スな状態にして水銀がバランスされた状態に復帰
するときの水銀の自重によつて試料を吸引し、U
字管の適所に設けた電極と水銀との接触によりス
イツチの作用を生じさせて計数開始信号、計数終
了信号を発生させる方式の装置、(2)定量を行わず
に吸引圧力を一定にして流速を一定と仮定し、単
位時間当りの血球数から換算する方式の装置など
が用いられている。しかし前者の方式は酸化など
により電極との接触不良を生じ易く、また水銀は
公害物質として取扱いに注意を要するなどの欠点
があつた。なお水銀以外に他の遮光性の液体を用
いて自重分に相当する空気圧などによつて光学的
に検知する方法などもあるが、液体の表面は表面
張力や他の要因により物理的に不安定であり、表
面の汚れや装置の震動などの影響も受け易いなど
の欠点があつた。一方、後者の方式は検出器の微
細孔につまりが生じたり汚れが生じたりすると、
流速はもはや一定とはならず、検出器を複数本並
べて精度を上げるとか、他の補償方法に頼る必要
があり、正確な測定法とは言い難い面があつた。
Conventionally, in devices that automatically analyze various parameters related to blood cells suspended in physiological saline, etc., when measuring the number of red blood cells, white blood cells, etc. in a unit volume, the amount of blood cell suspension is aspirated. It was necessary to accurately determine the number of blood cells and convert it to the number of blood cells in raw blood.
For this reason, in the past, (1) the mercury in the U-shaped tube was brought into an unbalanced state, and when the mercury returned to a balanced state, the sample was suctioned by the mercury's own weight;
A device that generates a counting start signal and a counting end signal by creating a switch effect by contacting mercury with electrodes installed at appropriate locations on the tube. A device is used that assumes that the number of blood cells is constant and converts it from the number of blood cells per unit time. However, the former method had drawbacks such as poor contact with the electrodes due to oxidation, etc., and mercury, which is a pollutant, must be handled with care. In addition to mercury, there are other light-shielding liquids that can be used for optical detection using air pressure equivalent to its own weight, but the surface of the liquid is physically unstable due to surface tension and other factors. However, it has drawbacks such as being easily affected by dirt on the surface and vibration of the device. On the other hand, in the latter method, if the fine pores of the detector become clogged or dirty,
The flow velocity was no longer constant, and it was necessary to increase accuracy by lining up multiple detectors or rely on other compensation methods, making it difficult to call it an accurate measurement method.

また特公昭38−21547号公報には、計量時間中
プランジヤーが連通する流体の体積の変化によつ
て、計量装置が駆動され、これによつて一定量の
試料の吸引を行う流体計量装置が記載されてい
る。この公報の第5図には、流体圧力を伝達する
装置として、可撓性隔膜または薄膜182を利用
し、計数の始動と停止をメカニカルなスイツチ9
8,100を使つて行うようにした装置が示され
ている。
Furthermore, Japanese Patent Publication No. 38-21547 describes a fluid measuring device in which the measuring device is driven by changes in the volume of fluid communicated with a plunger during the measuring time, thereby aspirating a fixed amount of sample. has been done. In FIG. 5 of this publication, a flexible diaphragm or thin film 182 is used as a device for transmitting fluid pressure, and a mechanical switch 9 is used to start and stop counting.
8,100 is shown.

またこの公報の第6図には、流体圧力を伝達す
る装置として、管状部材74の入口を弾性ゴム状
材料のプラグ242によつて閉鎖するようにした
ものが示されている。
FIG. 6 of this publication also shows a device for transmitting fluid pressure in which the inlet of a tubular member 74 is closed by a plug 242 made of an elastic rubber-like material.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかしながら、上記公報の第5図に示す装置に
おいては、隔膜または薄膜182の劣化によつ
て、プランジヤーの一定量の移動に正確に追従し
ては、隔膜または薄膜182が動かなくなること
があり、このときには定量誤差を生じるという問
題点がある。またメカニカルなスイツチでは、微
妙な定量が行い難く、かつ定量の再現性も悪く、
スイツチの劣化の問題もある。
However, in the device shown in FIG. 5 of the above publication, due to deterioration of the diaphragm or thin film 182, the diaphragm or thin film 182 may stop moving even if it accurately follows a certain amount of movement of the plunger. There is a problem that sometimes quantitative errors occur. In addition, mechanical switches make it difficult to perform delicate quantification, and the reproducibility of quantification is poor.
There is also the problem of deterioration of the switch.

また上記公報の第6図に示す装置においては、
プラグ242のような形状では、プラグ242と
ロツド246との隙間から空気が漏れ、定量誤差
を生じ易いという問題点がある。この隙間を極力
少なくしようとすると、ロツド246の動きが円
滑でなくなる。
Furthermore, in the device shown in FIG. 6 of the above publication,
A problem with the shape of the plug 242 is that air leaks from the gap between the plug 242 and the rod 246, which tends to cause quantitative errors. If an attempt is made to minimize this gap, the movement of the rod 246 will not be smooth.

本発明は上記の諸点に鑑みなされたもので、気
体、ベローズ、固体のピストン、試料の順に駆動
力が伝達されて、微細孔を通じて吸引される試料
を正確に定量することができ、懸濁粒子を高精度
で検出でき、かつ安定な動作をさせることができ
る懸濁粒子検出装置を提供せんとするものであ
る。
The present invention was made in view of the above points, and the driving force is transmitted in this order to gas, bellows, solid piston, and sample, and the sample sucked through the micropores can be accurately quantified, and suspended particles can be accurately quantified. An object of the present invention is to provide a suspended particle detection device that can detect particles with high precision and operate stably.

〔問題点を解決するための手段および作用〕[Means and actions for solving problems]

本発明の懸濁粒子検出装置は、図面を参照して
説明すれば、下部に微細孔8を有する検出器7
を、この検出器の下部が試料チヤンバ1内の粒子
懸濁液中に浸漬するように設け、この検出器7の
上部を弁12を介して真空源に接続し、前記試料
チヤンバ1内と検出器7内とに粒子検出用電極1
1,10をそれぞれ設け、一方、検出器の上側に
比較的粘度の高い油などの液体16を常に満たす
ようにしたピストン駆動チヤンバ13を配置し、
このピストン駆動チヤンバの上部に光学的位置検
出装置20,21を備えた管状定量部22を接続
し、この管状定量部の上端を真空源、陽圧源に切
換弁23を介して切換自在に接続し、ピストン駆
動チヤンバ13内の上部に前記陽圧源、真空源に
より伸縮するベローズ14を固定し、さらにこの
ベローズを貫通して上部が管状定量部22内を上
下し下部が検出器7内を上下するように棒状ピス
トン15をベローズ下部に固定し、ピストン駆動
チヤンバ13と検出器7との間の棒状ピストン回
りにパツキング17を設けたことを特徴としてい
る。
The suspended particle detection device of the present invention will be described with reference to the drawings.
is installed such that the lower part of this detector is immersed in the particle suspension in the sample chamber 1, and the upper part of this detector 7 is connected to a vacuum source via a valve 12, so that the inside of the sample chamber 1 and the detection Particle detection electrode 1 inside the container 7
1 and 10 respectively, and on the other hand, a piston drive chamber 13 is arranged above the detector so as to be always filled with a relatively high viscosity liquid 16 such as oil,
A tubular metering section 22 equipped with optical position detection devices 20 and 21 is connected to the top of this piston drive chamber, and the upper end of this tubular metering section is switchably connected to a vacuum source and a positive pressure source via a switching valve 23. A bellows 14 that expands and contracts by the positive pressure source and vacuum source is fixed to the upper part of the piston drive chamber 13, and the bellows 14 is penetrated so that the upper part moves up and down inside the tubular metering part 22 and the lower part moves inside the detector 7. A rod-shaped piston 15 is fixed to the lower part of the bellows so as to move up and down, and a packing 17 is provided around the rod-shaped piston between the piston drive chamber 13 and the detector 7.

本発明の装置においては、ベローズ14に棒状
ピストン15を貫通させて固定し、真空源24に
よりベローズ14を収縮させ、これによつて棒状
ピストン15を駆動し、検出器7内に負圧を発生
させている。また光学的位置検出装置20,21
により、計数のスタート・ストツプ信号を作つて
いる。検出器7内の液はOリングパツキング17
とピストン駆動チヤンバ13内の液体(油)16
によつて密封されている。
In the device of the present invention, the rod-shaped piston 15 is fixed by passing through the bellows 14, and the bellows 14 is contracted by the vacuum source 24, thereby driving the rod-shaped piston 15 and generating negative pressure in the detector 7. I'm letting you do it. Also, the optical position detection devices 20, 21
This creates the start/stop signal for counting. The liquid inside the detector 7 is O-ring packing 17
and the liquid (oil) 16 in the piston drive chamber 13
sealed by.

本発明は上記のような構成、作成により、前記
の公報記載の装置の有する問題点を解決すること
ができる。
The present invention can solve the problems of the apparatus described in the above-mentioned publication by having the structure and production as described above.

〔実施例〕〔Example〕

以下、本発明の実施例を図面に基づいて説明す
る。第1図および第2図は本発明の懸濁粒子検出
装置の一実施例を示している。1は粒子懸濁液、
たとえば血球の浮懸液を収容するための試料チヤ
ンバで、血球の浮懸液2は弁3を介して試料導入
口4から試料チヤンバ1内に導入され、一方、試
料排出口5から弁6を介して排出される。7は下
部に血球が一個づつ通過できる程度の微細孔8を
有する検出器で、この検出器7の下部が試料チヤ
ンバ1内の血球浮懸液2の液面下に浸漬され、検
出器7の内外に血球検出用電極10,11が設け
られている。これらの電極10,11は微細孔8
を通過する血球を液と血球とのインピーダンスの
差異に基づいて検出するものである。また検出器
7の上部は弁12を介して廃液チヤンバ、真空源
(図示せず)に接続されている。一方、検出器7
の上側にはピストン駆動チヤンバ13が配置され
ている。検出器7の内部にはベローズ14で駆動
される棒状ピストン15が突出しており、ベロー
ズ14を収納するピストン駆動チヤンバ13に
は、比較的粘度の高い油などの液体16が充満さ
れている。この液体16が検出器7の内部に流出
しないように、ピストン駆動チヤンバ13と検出
器7との間の棒状ピストン回りにOリングパツキ
ング17が設けられている。この液体16は定量
誤差をなくす役目を果す。すなわち液体16がな
い場合には、検出器7の内部にパツキング17と
ピストン15との隙間を通じて空気が漏れ、この
ため定量誤差を生じ易い。この液体16はピスト
ン駆動チヤンバ13に連通孔18を介して接続さ
れた補充槽19から補充される。ピストン駆動チ
ヤンバ13の上部には光学的位置検出装置20,
21を備えた管状の定量部22が接続され、この
定量部22を通じてベローズ14内に空気圧など
の気体圧が導入されるように構成されている。す
なわち定量部22の上端は切換弁23を介して真
空源24、陽圧源25に切換自在に接続されてい
る。ピストン15はベローズ14を貫通して定量
部22に達し、光学的位置検出装置20,21に
よりピストンの上端が検出されるように構成され
ている。ピストン15はベローズ14の下部に螺
合などにより固定されている。
Embodiments of the present invention will be described below based on the drawings. 1 and 2 show an embodiment of the suspended particle detection device of the present invention. 1 is a particle suspension;
For example, in a sample chamber for containing a suspension of blood cells, a suspension of blood cells 2 is introduced into the sample chamber 1 from a sample introduction port 4 via a valve 3, and a valve 6 is introduced from a sample discharge port 5. It is discharged through. Reference numeral 7 denotes a detector having a fine hole 8 at its lower part that is large enough to allow one blood cell to pass through. Blood cell detection electrodes 10 and 11 are provided inside and outside. These electrodes 10 and 11 have fine holes 8
Blood cells passing through the blood cell are detected based on the difference in impedance between the fluid and the blood cell. Further, the upper part of the detector 7 is connected via a valve 12 to a waste liquid chamber and a vacuum source (not shown). On the other hand, detector 7
A piston drive chamber 13 is arranged on the upper side. A rod-shaped piston 15 driven by a bellows 14 protrudes inside the detector 7, and a piston drive chamber 13 housing the bellows 14 is filled with a liquid 16 such as relatively high viscosity oil. In order to prevent this liquid 16 from flowing into the inside of the detector 7, an O-ring packing 17 is provided around the rod-shaped piston between the piston drive chamber 13 and the detector 7. This liquid 16 serves to eliminate quantitative errors. That is, when there is no liquid 16, air leaks into the detector 7 through the gap between the packing 17 and the piston 15, which tends to cause a quantitative error. This liquid 16 is replenished from a replenishment tank 19 connected to the piston drive chamber 13 via a communication hole 18. At the top of the piston drive chamber 13, an optical position detection device 20,
A tubular metering section 22 having a tube 21 is connected thereto, and gas pressure such as air pressure is introduced into the bellows 14 through the metering section 22 . That is, the upper end of the metering section 22 is connected to a vacuum source 24 and a positive pressure source 25 via a switching valve 23 so as to be switchable. The piston 15 passes through the bellows 14 to reach the metering portion 22, and is configured such that the upper end of the piston is detected by optical position detection devices 20 and 21. The piston 15 is fixed to the lower part of the bellows 14 by screwing or the like.

上記のように構成された懸濁粒子検出装置にお
いて、まず弁3を開いて被測定液である血球浮懸
液2を試料チヤンバ1内に導入する。ついでベロ
ーズ14内部に真空源24からの吸引圧力を導入
し、第1図に示す状態から第2図に示す状態にベ
ローズ14を収縮させてピストン15を上昇させ
る。ピストン15の上端が下側の光学的位置検出
装置21を通過するときに、スタート信号を生じ
させ、さらにピストン15の上端が上側の光学的
位置検出装置20を通過するときにストツプ信号
を生じさせる。このスタート信号とストツプ信号
との間のゲート信号により血球に関する種々のパ
ラメータを測定し、所定体積当りの測定値とす
る。ピストン15の上昇に伴い、検出器7内部に
突出したピストン15の容積が小さくなり、ピス
トン容積の減少分だけ血球浮懸液が微細孔8を通
じて検出器7内部に導入される。なお予め検出器
7内に弁12を開けて試料を吸引した後、弁12
を閉めておく。一方、ピストン駆動チヤンバ13
内のベローズ14の容積変化により、補充槽19
から液体が連通孔18を通じて自動的にピストン
駆動チヤンバ13内に流入して充満する。測定が
終了した試料は、試料排出口5から弁6を介して
排出し、弁6を閉めておく。ついでベローズ14
内に陽圧を導入し、同時に弁12を開放して検出
器7内部の余分な液を廃液チヤンバ(図示せず)
に排出する。ベローズ14は陽圧により第1図に
示す状態に伸長し、ピストン15の上端が下側の
光学的位置検出装置21の中心部に位置するよう
にして、つぎの測定開始の準備を終了する。
In the suspended particle detection apparatus configured as described above, first, the valve 3 is opened and the blood cell suspension 2, which is a liquid to be measured, is introduced into the sample chamber 1. Next, suction pressure from the vacuum source 24 is introduced into the bellows 14, the bellows 14 is contracted from the state shown in FIG. 1 to the state shown in FIG. 2, and the piston 15 is raised. When the upper end of the piston 15 passes the lower optical position sensing device 21, a start signal is generated, and when the upper end of the piston 15 passes the upper optical position sensing device 20, a stop signal is generated. . Various parameters related to blood cells are measured using a gate signal between the start signal and the stop signal, and are taken as measured values per predetermined volume. As the piston 15 rises, the volume of the piston 15 protruding into the inside of the detector 7 becomes smaller, and the blood cell suspension is introduced into the inside of the detector 7 through the fine holes 8 by the amount of the decrease in the piston volume. Note that after opening the valve 12 in the detector 7 in advance and aspirating the sample, the valve 12
Keep it closed. On the other hand, the piston drive chamber 13
Due to the volume change of the bellows 14 inside, the replenishment tank 19
The liquid automatically flows into the piston drive chamber 13 through the communication hole 18 and fills it. After the measurement has been completed, the sample is discharged from the sample discharge port 5 through the valve 6, and the valve 6 is kept closed. Then bellows 14
At the same time, the valve 12 is opened to drain excess liquid inside the detector 7 into a waste liquid chamber (not shown).
to be discharged. The bellows 14 is expanded by positive pressure to the state shown in FIG. 1, and the upper end of the piston 15 is positioned at the center of the lower optical position detection device 21, thereby completing preparations for starting the next measurement.

第3図は本発明の懸濁粒子検出装置を自動血液
分析装置に使用した一例を示している。26は血
液試料を吸引する吸引パイプで、血液収容容器2
7内に収容された血液28を所定量吸引する。3
0は液体処理装置で、血液はこの液体処理装置3
0内で赤血球計数用試料として5万倍程度に希釈
され、白血球計数用試料として500倍程度に希釈
され、かつ赤血球破壊用の溶血剤を加えて白血球
のみを残留せしめるなどの希釈、撹拌、溶解、試
薬添加などの前処理が行われる。31は本発明の
懸濁粒子検出装置で、血球を血球浮懸液とのイン
ピーダンスの差異に基づいて検出し、線路32を
通じてつぎの検出回路33へ信号が送られる。一
方、懸濁粒子検出装置31の定量部からの信号
は、線路34を通じてゲート信号発生回路35に
送られ、ゲート信号は検出回路33またはつぎの
信号処理回路36へ送られる。信号処理回路36
では、ゲート信号で規制された血球信号に基づい
て、赤血球数、白血球数、血小板数あるいは血球
信号が粒子のサイズに比例することから、ヘマト
クリツト値、MCV(平均赤血球体積)、あるいは
別に設けたヘモグロビン比色測定結果との演算結
果からMCH(平均赤血球ヘモグロビン量)、
MCHC(平均赤血球ヘモグロビン濃度)などの
血球に関するパラメータが分析結果として処理さ
れる。このように血液を吸引させるだけで、自動
的に血液を希釈したり、試薬を分注したり、計算
測定を行つたりすることができ、液体定量部の欠
点を解消してより精度の高い分析を行うことがで
きる。
FIG. 3 shows an example in which the suspended particle detection device of the present invention is used in an automatic blood analyzer. 26 is a suction pipe for aspirating a blood sample, and is connected to the blood storage container 2.
A predetermined amount of blood 28 contained in 7 is aspirated. 3
0 is a liquid processing device, and blood is processed in this liquid processing device 3.
The sample is diluted approximately 50,000 times as a sample for red blood cell counting, and approximately 500 times as a sample for white blood cell counting, and diluted, stirred, and lysed by adding a hemolytic agent to destroy red blood cells so that only white blood cells remain. , pretreatment such as addition of reagents is performed. Reference numeral 31 denotes a suspended particle detection device of the present invention, which detects blood cells based on the difference in impedance from the blood cell suspension, and sends a signal to the next detection circuit 33 through a line 32. On the other hand, the signal from the quantitative unit of the suspended particle detection device 31 is sent to the gate signal generation circuit 35 through the line 34, and the gate signal is sent to the detection circuit 33 or the next signal processing circuit 36. Signal processing circuit 36
Based on the blood cell signal regulated by the gate signal, the number of red blood cells, white blood cells, platelets, or blood cell signals is proportional to the particle size. From the calculation results with the colorimetric measurement results, MCH (mean corpuscular hemoglobin content),
Parameters related to blood cells such as MCHC (mean corpuscular hemoglobin concentration) are processed as analysis results. In this way, just by aspirating blood, it is possible to automatically dilute blood, dispense reagents, and perform calculation measurements, eliminating the drawbacks of liquid metering units and achieving higher accuracy. Analysis can be performed.

〔発明の効果〕〔Effect of the invention〕

本発明は上記のように構成されているから、気
体、ベローズ、固体のピストン、試料の順に駆動
力が伝達されて、微細孔を通じて吸引される試料
の定量が行われる。この場合被定量液が形状の不
変なピストンという固体によつて定量されるた
め、再現性や精度の面できわめて有効であり、さ
らに弾力のある気体によつてベローズを駆動させ
るために、少々の機械的変動やつまりなどによる
検出孔への無理な力が加わるのを吸収してしまう
ので、安定な動作をさせることができる。さらに
ピストン駆動チヤンバ内の液体の作用により、定
量誤差の原因となる漏れが防止され、かつベロー
ズの振動なども防止されるなどの効果がある。
Since the present invention is configured as described above, the driving force is transmitted to the gas, the bellows, the solid piston, and the sample in this order, and the sample sucked through the micropores is quantified. In this case, the liquid to be measured is quantified using a solid piston that does not change its shape, which is extremely effective in terms of reproducibility and accuracy. Since it absorbs unreasonable force applied to the detection hole due to mechanical fluctuations or clogging, stable operation can be achieved. Furthermore, the action of the liquid in the piston drive chamber has the effect of preventing leakage that would cause a quantitative error, and also preventing vibration of the bellows.

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

第1図および第2図は本発明の懸濁粒子検出装
置の一実施例を示すもので、第1図はベローズが
伸長した状態の断面説明図、第2図はベローズが
収縮した状態の断面説明図、第3図は本発明の懸
濁粒子検出装置を具備した自動血液分析装置の系
統的説明図である。 1……試料チヤンバ、2……血球浮懸液、3…
…弁、4……試料導入口、5……試料排出口、6
……弁、7……検出器、8……微細孔、10,1
1……血球検出用電極、12……弁、13……ピ
ストン駆動チヤンバ、14……ベローズ、15…
…棒状ピストン、16……液体、17……パツキ
ング、18……連通孔、19……補充槽、20,
21……光学的位置検出装置、22……定量部、
23……切換弁、24……真空源、25……陽圧
源、26……吸引パイプ、27……血液収容容
器、28……血液、30……液体処理装置、31
……懸濁粒子検出装置、32……線路、33……
検出回路、34……線路、35……信号発生回
路、36……信号処理回路。
Figures 1 and 2 show an embodiment of the suspended particle detection device of the present invention. Figure 1 is a cross-sectional view of the bellows in an extended state, and Figure 2 is a cross-sectional view of the bellows in a contracted state. The explanatory diagram, FIG. 3, is a systematic explanatory diagram of an automatic blood analyzer equipped with the suspended particle detection device of the present invention. 1...sample chamber, 2...blood cell suspension, 3...
...Valve, 4...Sample inlet, 5...Sample outlet, 6
...Valve, 7...Detector, 8...Minor hole, 10,1
DESCRIPTION OF SYMBOLS 1... Blood cell detection electrode, 12... Valve, 13... Piston drive chamber, 14... Bellows, 15...
... Rod-shaped piston, 16 ... Liquid, 17 ... Packing, 18 ... Communication hole, 19 ... Replenishment tank, 20,
21... Optical position detection device, 22... Quantification unit,
23...Switching valve, 24...Vacuum source, 25...Positive pressure source, 26...Suction pipe, 27...Blood storage container, 28...Blood, 30...Liquid processing device, 31
...Suspended particle detection device, 32...Railway, 33...
Detection circuit, 34...Line, 35...Signal generation circuit, 36...Signal processing circuit.

Claims (1)

【特許請求の範囲】[Claims] 1 下部に微細孔を有する検出器を、この検出器
の下部が試料チヤンバ内の粒子懸濁液中に浸漬す
るように設け、この検出器の上部を弁を介して真
空源に接続し、前記試料チヤンバ内と検出器内と
に粒子検出用電極をそれぞれ設け、一方、検出器
の上側に比較的粘度の高い油などの液体を常に満
たすようにしたピストン駆動チヤンバを配置し、
このピストン駆動チヤンバの上部に光学的位置検
出装置を備えた管状定量部を接続し、この管状定
量部の上端を真空源、陽圧源に切換弁を介して切
換自在に接続し、ピストン駆動チヤンバ内の上部
に前記陽圧源、真空源により伸縮するベローズを
固定し、さらにこのベローズを貫通して上部が管
状定量部内を上下し下部が検出器内を上下するよ
うに棒状ピストンをベローズ下部に固定し、ピス
トン駆動チヤンバと検出器との間の棒状ピストン
回りにパツキングを設けたことを特徴とする懸濁
粒子検出装置。
1. A detector with micropores in its lower part is provided such that the lower part of the detector is immersed in the particle suspension in the sample chamber, the upper part of the detector is connected via a valve to a vacuum source, and the Particle detection electrodes are provided inside the sample chamber and inside the detector, while a piston-driven chamber is placed above the detector so as to be constantly filled with a liquid such as oil with relatively high viscosity.
A tubular metering section equipped with an optical position detection device is connected to the top of this piston drive chamber, and the upper end of this tubular metering section is connected to a vacuum source and a positive pressure source via a switching valve so that the piston drive chamber can be switched freely. A bellows that is expanded and contracted by the positive pressure source and vacuum source is fixed to the upper part of the inside, and a rod-shaped piston is inserted into the lower part of the bellows so that the upper part moves up and down inside the tubular metering section and the lower part moves up and down inside the detector. What is claimed is: 1. A suspended particle detection device, characterized in that the device is fixed and provided with packing around a rod-shaped piston between a piston drive chamber and a detector.
JP12915179A 1979-10-05 1979-10-05 Detector of suspended particle Granted JPS5652037A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12915179A JPS5652037A (en) 1979-10-05 1979-10-05 Detector of suspended particle

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12915179A JPS5652037A (en) 1979-10-05 1979-10-05 Detector of suspended particle

Publications (2)

Publication Number Publication Date
JPS5652037A JPS5652037A (en) 1981-05-09
JPS6252254B2 true JPS6252254B2 (en) 1987-11-04

Family

ID=15002392

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12915179A Granted JPS5652037A (en) 1979-10-05 1979-10-05 Detector of suspended particle

Country Status (1)

Country Link
JP (1) JPS5652037A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01152170U (en) * 1988-04-12 1989-10-20

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01152170U (en) * 1988-04-12 1989-10-20

Also Published As

Publication number Publication date
JPS5652037A (en) 1981-05-09

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