JPS5841336A - Particle analyzer - Google Patents
Particle analyzerInfo
- Publication number
- JPS5841336A JPS5841336A JP56139955A JP13995581A JPS5841336A JP S5841336 A JPS5841336 A JP S5841336A JP 56139955 A JP56139955 A JP 56139955A JP 13995581 A JP13995581 A JP 13995581A JP S5841336 A JPS5841336 A JP S5841336A
- Authority
- JP
- Japan
- Prior art keywords
- circuit
- signal
- particle
- particles
- gate
- 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.)
- Granted
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N15/1031—Investigating individual particles by measuring electrical or magnetic effects
- G01N15/12—Investigating individual particles by measuring electrical or magnetic effects by observing changes in resistance or impedance across apertures when traversed by individual particles, e.g. by using the Coulter principle
- G01N15/131—Details
- G01N15/132—Circuits
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N2015/1024—Counting particles by non-optical means
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
- G01N15/10—Investigating individual particles
- G01N2015/103—Particle shape
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating Or Analysing Biological Materials (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、血球などの粒子が浮懸する液を細孔に通過さ
せ、粒子と液との電気的差異に基づく変化を検出し、粒
子の数や平均の大きさなど、とくに完全な球形以外の粒
子の容積をより正確に求めることができる粒子分析装置
に関するものである。Detailed Description of the Invention The present invention allows a liquid in which particles such as blood cells are suspended to pass through pores, detects changes based on electrical differences between the particles and the liquid, and detects changes in the number and average size of particles. In particular, this invention relates to a particle analyzer that can more accurately determine the volume of particles other than perfectly spherical.
従来、粒子計数装置において、測定した粒子の大きさに
関する情報として検出信号のパルス高さを利用してきた
。すなわち第1図に示すように、検出器細孔1を小粒子
2が通過するときの検出信号のパルス高さをh1大粒子
3が通過するときの検出信号のパルス高さをh′とする
と、h′はhより大きくなり、検出器細孔1を通過する
粒子の体積に検出信号のパルス高さが比例していること
を利用していた。このパルス高さの平均高さを測定する
ことにより、血球などの粒子の平均容積を求めていた。Conventionally, particle counting devices have used the pulse height of a detection signal as information regarding the size of a measured particle. That is, as shown in FIG. 1, if the pulse height of the detection signal when a small particle 2 passes through the detector pore 1 is h1, and the pulse height of the detection signal when a large particle 3 passes is h'. , h' are larger than h, and the pulse height of the detection signal is proportional to the volume of particles passing through the detector pore 1. By measuring the average height of this pulse height, the average volume of particles such as blood cells was determined.
たとえば平均赤血球容積(MCV)は次式により求めて
いた。For example, the mean corpuscular volume (MCV) was calculated using the following formula.
MCV=に−h (1)ここでπけ
パルス平均高さ、Kは定数である。MCV=to-h (1) where π times the average pulse height, K is a constant.
しかし赤血球などのような完全な球状でない細胞を測定
する場合、同一体積にもかかわらず検出信号のパルス高
さは変化し誤差を生じさせるという問題点があった。す
カわち第2図に示すように、検出器細孔1に赤血球4が
横向きで通過するときの検出信号のパルス高さをh+、
パルス幅をす、赤血球4が縦向きで通過するときの検出
信号のパルス高さをh2、パルス幅をt2とすると、h
2はb+より大きく、かつtlはt2より大きくなり誤
差が生じていた。However, when measuring cells that are not perfectly spherical, such as red blood cells, there is a problem in that the pulse height of the detection signal changes even though the volume is the same, causing errors. That is, as shown in FIG. 2, the pulse height of the detection signal when the red blood cell 4 passes sideways through the detector pore 1 is h+,
Let the pulse width be h2, the pulse height of the detection signal when the red blood cell 4 passes vertically be h2, and the pulse width be t2, then h
2 was larger than b+, and tl was larger than t2, resulting in an error.
この誤差を少なくする方法として、流体力学を利用し血
球を細孔部中心のみに通過させる、いわゆるシース方式
などが考案されているが、構造が複雑となるなどの問題
が生じていた。As a method to reduce this error, a so-called sheath method has been devised that uses fluid dynamics to allow blood cells to pass only through the center of the pore, but this method has had problems such as a complicated structure.
本発明は上記の諸点に鑑みなされたもので、検出器細孔
を粒子が通過する時間が、粒子の通過方向のサイズに比
較的相関があることを利用し、粒子信号の幅を高さの情
報に付加することにより、球形以外の粒子に対してもよ
り正確な測定値を得ることができるような粒子分析装置
を提供せんとするものである。The present invention was developed in view of the above points, and takes advantage of the fact that the time it takes a particle to pass through a detector pore is relatively correlated with the size of the particle in the passing direction, and the width of the particle signal is adjusted to the height. It is an object of the present invention to provide a particle analyzer that can obtain more accurate measurement values even for particles other than spherical by adding information.
以下、本発明の構成を図面に基づいて説明する。Hereinafter, the configuration of the present invention will be explained based on the drawings.
第4図は本発明の粒子分析装置の一例の構成を示し、第
5図は動作を示し、第2図に示すような検出信号から、
次式のような測定を行なう例の場合に基づいたものであ
る。FIG. 4 shows the configuration of an example of the particle analyzer of the present invention, and FIG. 5 shows the operation. From the detection signal shown in FIG.
This is based on an example case in which measurements are performed as shown in the following equation.
体積に比例した情報= h + K t (2)な
おhは検出信号のパルス高さ、Kは定数、tは通過時間
(パルス幅)である。この場合のKは完全球形の粒子の
測定結果に対し、扁平な形状を有する赤血球などの粒子
をさまざまなサイズにわたって測定し、それぞれの粒子
サイズに=Oとして相関図を求めたときに、傾斜が45
°から外れるが、これを45°まで補正するために必要
な補正値を求めてKの値を決定する(第3図参照)。し
たがって測定する粒子の形状によってこのKの値は異な
り、たとえば棒状の外形を有する工業粒子などの場合に
用いるときには、同様に既知の粒子と既知の球形粒子と
により相関図を求め、補正のためのKの値を決定する。Information proportional to volume = h + K t (2) where h is the pulse height of the detection signal, K is a constant, and t is the transit time (pulse width). In this case, K differs from the measurement result of perfectly spherical particles by measuring flat-shaped particles such as red blood cells over various sizes and calculating the correlation diagram with =O for each particle size. 45
The value of K is determined by finding the correction value necessary to correct this to 45° (see FIG. 3). Therefore, the value of K varies depending on the shape of the particle to be measured. For example, when used for industrial particles with a rod-like external shape, a correlation diagram is similarly obtained using known particles and known spherical particles, and the Determine the value of K.
第4図に示すように、本発明の粒子分析装置は、粒子か
浮懸する液を細孔に通過させ粒子と液との電気インピー
ダンスの差または光学的差異に基づいて粒子を検出し粒
子の大きさに比例する電気信号を発生する粒子検出装置
5と、この粒子検出装置5に接続されたピークホールド
回路6およヒ比較回路7と、ピークホールド回路6に接
続されたAD変換回路8と、比較回路7に接続されたゲ
ート回路9、基準電圧発生回路lOおよび計数回路11
と、ゲート回路9およびAD変換回路8に接続された基
準パルス発生回路12および演算回路13と、この演算
回路13に接続された累積回路14と、この累積回路1
4および前記計数回路11に接続された割算回路15と
、累積回路14、割算回路15および計数回路11にそ
れぞれ接続された表°示回路16.17.18とからな
っている。As shown in FIG. 4, the particle analyzer of the present invention detects particles based on the electrical impedance difference or optical difference between the particles and the liquid by passing the liquid in which the particles are suspended through the pores. A particle detection device 5 that generates an electric signal proportional to the size, a peak hold circuit 6 and a comparison circuit 7 connected to the particle detection device 5, and an AD conversion circuit 8 connected to the peak hold circuit 6. , a gate circuit 9 connected to the comparator circuit 7, a reference voltage generation circuit lO, and a counting circuit 11.
, a reference pulse generation circuit 12 and an arithmetic circuit 13 connected to the gate circuit 9 and the AD conversion circuit 8, an accumulator circuit 14 connected to the arithmetic circuit 13, and an accumulator circuit 1.
4 and a division circuit 15 connected to the counting circuit 11, and display circuits 16, 17, and 18 connected to the accumulation circuit 14, the division circuit 15, and the counting circuit 11, respectively.
粒子検出装置IFi第5図の最上部に示すような粒子信
号を発し、ピークホールド回路6および比較回路7に信
号を送る。AD変換回路8け、ピークホールド回路6で
ホールドされた粒子信号19のピーク値20に対し、鋸
歯状の信号21を発し、ピーク値20と一致した点22
までのゲート信号23を発し、基準パルスAを通過させ
る。この信号がDである。したがって粒子信号19の高
さに応じたパルス数の信号りが得られ、これを累積した
ものが従来の粒子容積の測定に関するものである。一方
、比較回路7は所定の電圧レベル、すなわち基準電圧発
生回路lOの出力電圧24よりも大きい電圧の粒子信号
を通過させ、ゲート信号Cを発生させるものであり、ゲ
ート回路9にゲート信号を送るとともに、計数回路11
で粒子数を計数する。1個の粒子信号についてAD変換
が終ると、リセット信号25を通じてピークホールド回
路6に送る。ゲート回路9に送られる信号Cは信号の幅
に関する情報でもあり、これをゲート信号として基準パ
ルスAを通過させる。すなわち信号幅に応じたパルスE
が得られる。このようにして得られたAD変換の値およ
びゲート回路9の出力値は、演算回路13により前記式
(2)の演算が行なわれ、累積回路14により次々と粒
子信号のそれぞれについての累積が行なわれる。所定の
被測定対象について測定が行なわれ、最終的に得られた
値は粒子の全容積に関する値であるから、粒子数を計数
している計数回路11の値で割算を行なうことにより、
平均の粒子容積が求められる。その値が割算回路15で
得られる。それぞれの値は表示回路16.17.18で
表示される。粒子が赤血球の場合は、表示回路16.1
7.18けそれiぞれヘマトクリット値(HCT )、
平均赤血球容積(MCV)、赤血球数(RBC)を表示
する。Particle detector IFi emits a particle signal as shown at the top of FIG. 5, and sends the signal to peak hold circuit 6 and comparison circuit 7. The AD conversion circuit 8 generates a sawtooth signal 21 in response to the peak value 20 of the particle signal 19 held in the peak hold circuit 6, and detects a point 22 that coincides with the peak value 20.
A gate signal 23 is generated up to and a reference pulse A is passed. This signal is D. Therefore, a signal having a number of pulses corresponding to the height of the particle signal 19 is obtained, and the accumulated signal is related to the conventional particle volume measurement. On the other hand, the comparator circuit 7 passes a particle signal of a predetermined voltage level, that is, a voltage higher than the output voltage 24 of the reference voltage generation circuit IO, and generates a gate signal C, and sends the gate signal to the gate circuit 9. In addition, the counting circuit 11
Count the number of particles. When AD conversion is completed for one particle signal, it is sent to the peak hold circuit 6 via a reset signal 25. The signal C sent to the gate circuit 9 is also information regarding the width of the signal, and is used as a gate signal to allow the reference pulse A to pass. In other words, the pulse E according to the signal width
is obtained. The AD conversion value and the output value of the gate circuit 9 obtained in this way are subjected to the calculation of the above formula (2) by the calculation circuit 13, and the accumulation circuit 14 performs the accumulation of each particle signal one after another. It will be done. Measurements are performed on a predetermined object to be measured, and the final value obtained is a value related to the total volume of particles, so by dividing by the value of the counting circuit 11 that counts the number of particles,
The average particle volume is determined. The value is obtained by the division circuit 15. The respective values are displayed on display circuits 16, 17, 18. If the particle is a red blood cell, the display circuit 16.1
7.18 hematocrit values (HCT),
Displays mean corpuscular volume (MCV) and red blood cell count (RBC).
本発明の粒子分析装置は上記のように構成されているか
ら、赤血球のような球形以外の粒子に対してもより正確
な粒子容積に関する情報を得ることができ、流体系(粒
子の検出装置)に改良を加えずに、回路的な改良による
ものであるから、従来の血球計数器のような粒子計数回
路に容易に内蔵させることができるという利点を有して
いる。Since the particle analyzer of the present invention is configured as described above, it is possible to obtain more accurate particle volume information even for non-spherical particles such as red blood cells, and the fluid system (particle detection device) Since this method is based on a circuit improvement without making any improvements, it has the advantage that it can be easily incorporated into a particle counting circuit such as a conventional hemocytometer.
第1図は検出器細孔に小粒子が通過するときの検出信号
、および大粒子が通過するときの検出信号を示す説明図
、第2図は検出器細孔に赤血球が横向きで通過するとき
の検出信号、および赤血球が縦向きで通過するときの検
出信号を示す説明図、第3図は定数Kを求めるための説
明図、第4図は本発明の粒子分析装置の一実施態様を示
す系統的説明図、第5図は動作の説明図である。
1・・・検出器細孔、2・・・小粒子、3・・・大粒子
、4・・・赤血球、5・・・粒子検出装置、6・・・ピ
ークホールド回路、7・・・比較回路、8・・・AD変
換回路、9・・・ゲート回路、10・・・基準電圧発生
回路、11・・・計数回路、12・・・基準パルス発生
回路、13・・・演算回路、14・・・累積回路、15
・・・割算回路、16.17.18・・・表示回路、1
9・・・粒子信号、20・・・ピーク値、21・・・鋸
歯状信号、22・・・一致点、23・・・ゲート信号、
24・・・出力電圧、25・・・リセット信号
特許出願人 東亜医用電子株式会社第2図Figure 1 is an explanatory diagram showing the detection signal when a small particle passes through the detector pore and the detection signal when a large particle passes through it, and Figure 2 shows the detection signal when a red blood cell passes sideways through the detector pore. FIG. 3 is an explanatory diagram showing the detection signal when a red blood cell passes vertically, FIG. 3 is an explanatory diagram for determining the constant K, and FIG. 4 is an embodiment of the particle analyzer of the present invention. Systematic explanatory diagram, FIG. 5 is an explanatory diagram of operation. 1...Detector pore, 2...Small particle, 3...Large particle, 4...Red blood cell, 5...Particle detection device, 6...Peak hold circuit, 7...Comparison Circuit, 8... AD conversion circuit, 9... Gate circuit, 10... Reference voltage generation circuit, 11... Counting circuit, 12... Reference pulse generation circuit, 13... Arithmetic circuit, 14 ...cumulative circuit, 15
...Division circuit, 16.17.18...Display circuit, 1
9... Particle signal, 20... Peak value, 21... Sawtooth signal, 22... Match point, 23... Gate signal,
24... Output voltage, 25... Reset signal Patent applicant Toa Medical Electronics Co., Ltd. Figure 2
Claims (1)
気的差異または光学的差異に基づいて粒子を検出し粒子
の大きさに比例する電気信号を発生する粒子検出装置と
、この粒子検出装置に接続されたビークホー・レド回路
および比較回路と、ピークホールド回路に接続されたA
D変換回路と、比較回路に接続されたゲート回路、基準
電圧発生回路および計数回路と、ゲート回路およびAD
変換回路に接続された基準パルス発生回路および演算回
路と、この演算回路に接続された累積回路と、この累積
回路および前記計数回路に接続された割算回路と、累積
回路、割算回路および計数回路にそれぞれ接続された表
示回路とからなることを特徴とする粒子分析装置。1 A particle detection device that detects particles by passing a liquid in which particles are suspended through pores based on electrical or optical differences between the particles and the liquid and generates an electric signal proportional to the size of the particles; A peak hold circuit and a comparison circuit connected to the particle detection device, and an A connected to the peak hold circuit.
D conversion circuit, gate circuit connected to comparison circuit, reference voltage generation circuit and counting circuit, gate circuit and AD
a reference pulse generation circuit and an arithmetic circuit connected to a conversion circuit, an accumulation circuit connected to this arithmetic circuit, a division circuit connected to this accumulation circuit and the counting circuit, an accumulation circuit, a division circuit, and a counting circuit; A particle analysis device comprising a display circuit connected to each circuit.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56139955A JPS5841336A (en) | 1981-09-04 | 1981-09-04 | Particle analyzer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56139955A JPS5841336A (en) | 1981-09-04 | 1981-09-04 | Particle analyzer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5841336A true JPS5841336A (en) | 1983-03-10 |
| JPH026019B2 JPH026019B2 (en) | 1990-02-07 |
Family
ID=15257557
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56139955A Granted JPS5841336A (en) | 1981-09-04 | 1981-09-04 | Particle analyzer |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5841336A (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61178643A (en) * | 1985-02-05 | 1986-08-11 | Toa Medical Electronics Co Ltd | Particle analyser |
| US5078011A (en) * | 1988-04-25 | 1992-01-07 | Krivorozhsky Gornorudny Institut | Method of monitoring parameters of solid phase of suspension and device therefor |
| US5308990A (en) * | 1991-05-15 | 1994-05-03 | Hitachi, Ltd. | Method for measuring microparticles, quantitative measuring method therefor and instrument for measuring microparticles |
| JP2009102076A (en) * | 2009-01-05 | 2009-05-14 | Masayuki Makita | Bottle cap |
| CN106525675A (en) * | 2016-10-27 | 2017-03-22 | 合肥福瞳光电科技有限公司 | Online monitoring device of atmospheric particulate matter concentration |
| WO2017110753A1 (en) * | 2015-12-25 | 2017-06-29 | 国立大学法人大阪大学 | Number analyzing method, number analyzing device, and storage medium for number analysis |
| US11781099B2 (en) | 2015-12-25 | 2023-10-10 | Aipore Inc. | Number analyzing method, number analyzing device, and storage medium for number analysis |
-
1981
- 1981-09-04 JP JP56139955A patent/JPS5841336A/en active Granted
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61178643A (en) * | 1985-02-05 | 1986-08-11 | Toa Medical Electronics Co Ltd | Particle analyser |
| US5078011A (en) * | 1988-04-25 | 1992-01-07 | Krivorozhsky Gornorudny Institut | Method of monitoring parameters of solid phase of suspension and device therefor |
| US5308990A (en) * | 1991-05-15 | 1994-05-03 | Hitachi, Ltd. | Method for measuring microparticles, quantitative measuring method therefor and instrument for measuring microparticles |
| JP2009102076A (en) * | 2009-01-05 | 2009-05-14 | Masayuki Makita | Bottle cap |
| WO2017110753A1 (en) * | 2015-12-25 | 2017-06-29 | 国立大学法人大阪大学 | Number analyzing method, number analyzing device, and storage medium for number analysis |
| JPWO2017110753A1 (en) * | 2015-12-25 | 2018-10-25 | 国立大学法人大阪大学 | Piece analysis method, piece analysis apparatus, and storage medium for piece analysis |
| US11597898B2 (en) | 2015-12-25 | 2023-03-07 | Aipore Inc. | Number analyzing method, number analyzing device, and storage medium for number analysis |
| US11781099B2 (en) | 2015-12-25 | 2023-10-10 | Aipore Inc. | Number analyzing method, number analyzing device, and storage medium for number analysis |
| CN106525675A (en) * | 2016-10-27 | 2017-03-22 | 合肥福瞳光电科技有限公司 | Online monitoring device of atmospheric particulate matter concentration |
| CN106525675B (en) * | 2016-10-27 | 2019-01-22 | 合肥福瞳光电科技有限公司 | A kind of atmosphere particle concentration on-Line Monitor Device |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH026019B2 (en) | 1990-02-07 |
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