JPS58179339A - Analyzing apparatus of particle - Google Patents

Analyzing apparatus of particle

Info

Publication number
JPS58179339A
JPS58179339A JP6290982A JP6290982A JPS58179339A JP S58179339 A JPS58179339 A JP S58179339A JP 6290982 A JP6290982 A JP 6290982A JP 6290982 A JP6290982 A JP 6290982A JP S58179339 A JPS58179339 A JP S58179339A
Authority
JP
Japan
Prior art keywords
particles
signal
particle
circuit
liquid
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
Application number
JP6290982A
Other languages
Japanese (ja)
Other versions
JPH0257661B2 (en
Inventor
Tokihiro Kosaka
小坂 時弘
Akira Nishigaki
西垣 彰
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
Tao Medical Electronics 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 Sysmex Corp, Tao Medical Electronics Co Ltd filed Critical Sysmex Corp
Priority to JP6290982A priority Critical patent/JPS58179339A/en
Publication of JPS58179339A publication Critical patent/JPS58179339A/en
Publication of JPH0257661B2 publication Critical patent/JPH0257661B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10Investigating individual particles
    • G01N15/1031Investigating individual particles by measuring electrical or magnetic effects
    • G01N15/12Investigating 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

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

PURPOSE:To effectively analyze up to the maximum limit the information concerning minute particles such as a blood corpuscle suspending in a liquid, by sampling so that the number of signals for the analyzing object is made to come within a prescribed range at every measurement and making an operation interval even such as nearly constant. CONSTITUTION:A liquid particles are suspended is passed through a fine pore and the particles are detected basing on the differences of electrical or optical properties between the particles and the liquid and then, an electric signal having the intensity depending on the size of the particles is generated in a particle detecting apparatus 1. The number of signals per unit time is counted 5 at the dead time before beginning of measurement and a sampling interval is selected 7 basing on this counted value. Then, the sampled signal is converted and a histogram is prepared. An AD conversion circuit converting the information of height of an analogue pulse into a digital signal is used for said conversion circuit. This digital signal acts so as to add one to a place of an address of a memory 13 giving its particle size. Such action is performed for a prescribed particle suspension regulated by an apparatus 2 of quantitative determination and in the case where the sampling is carried out for 1/4 of the whole, the original absolute value is obtained by the histogram displayed and printed on a display device 12 or a recording device 11 by quadrupling its number. Accordingly, it is affectively utilized without saturation when nearly a fixed dimension is given to the capacity of the memory.

Description

【発明の詳細な説明】 本発明は液体に浮懸する血球などの微小粒子の分析装置
−詳1−〈は各粒子に関する情報を効率よく−かつ最大
限に分析することを可能にした粒子分析装置に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention is an apparatus for analyzing microparticles such as blood cells suspended in a liquid. It is related to the device.

従来−液体に浮懸する血球などの粒子を分析するには1
粒子を狭い通路に通過させ2粒子と液との電気的または
光学的な差異に基づいて粒子を検出11.さらに検出時
に得られる検出信号を分析することによってなされて因
だ。この分析は一般には2粒子1個1個の情報を所定の
情報群へ分類分けすることによってヒストグラムを作成
し、これらの粒子群の持つ特徴を抽出する方法が取られ
るために1分類分けされた情報の頻度をメモリーを用層
て記憶させる必要がある。また一方では一粒子総個数に
対する相対割合のヒストグラムも必要であるが一粒子を
浮懸する液体の絶対容量に対する個数分布のヒストグラ
ムが必要である。とぐに臨床血液の分野で用すられる血
球の粒度分析などにおりては一赤血球一白血球一血小板
などの同一粒度に対する個数の絶対量−すなわち個数の
分布情報が必要である。
Conventional - To analyze particles such as blood cells suspended in liquid 1
Pass the particles through a narrow channel and detect the particles based on electrical or optical differences between the two particles and the liquid11. This is done by further analyzing the detection signal obtained during detection. In general, this analysis creates a histogram by classifying the information of each particle into predetermined information groups, and extracts the characteristics of these particle groups, so it is divided into one classification. It is necessary to store the frequency of information using memory. On the other hand, a histogram of the relative proportion to the total number of particles is also required, but a histogram of the number distribution to the absolute volume of liquid in which each particle is suspended is also required. In particle size analysis of blood cells, which is used in the field of clinical blood, it is necessary to know the absolute number of particles of the same particle size, such as one red blood cell, one white blood cell, and one platelet, that is, information on the distribution of the number.

赤血球などの比較的個人差の少ない測定項目にお−では
、情報記憶のためのメモリーの容量は比較的有効に使用
されるが一症例によっては2桁以上の差を生ずる白血球
に対1−ては、その最大数を見越して比較的大容量のメ
モリーを必要とlj−通常の正常人の白血球の分析時に
は一大部分が使用されないまま予備的な使用法を行なっ
ており、無駄を生じていた。また臨床血液検査の分野に
限らす一工業分野においては、同様のノくう・ツキが生
じており一内蔵メモリーの有効使用が行なわれて−ない
現状にある。壕だメモリーがオー/く70−してしまっ
た場合などには一再度試料を希釈し直し。
For measurement items such as red blood cells, which have relatively few individual differences, memory capacity for storing information is used relatively effectively, but for white blood cells, which can vary by more than two orders of magnitude depending on the case, requires a relatively large amount of memory in anticipation of the maximum number of leukocytes, and when analyzing white blood cells in a normal normal person, a large portion of the memory remains unused, resulting in waste. . Furthermore, in the industrial field limited to the field of clinical blood testing, similar problems and difficulties are occurring, and the current situation is that the built-in memory is not being used effectively. If the memory becomes too dark, dilute the sample again.

改めて測定を行なわなければならないなどの手間を必要
とした。さらに大容量のメモリーを周込た場合、ヒスト
グラムを作成する際にメモリーの内容を一度読み出す必
要があり、容量に比例して演算時間が必要であるために
一分析所要時間を多く必要とするなどの欠点があった。
This required time and effort such as having to take measurements again. Furthermore, if a large capacity memory is used, the contents of the memory must be read once when creating a histogram, and the calculation time required is proportional to the capacity, which increases the time required for one analysis. There was a drawback.

本発明は上記の欠点を解消するためになされたもので一
粒子が浮懸する液を′f7&細孔に通過させ粒子と液と
の電気的差異または光学的差異に基づいて粒子を検出し
粒子の大きさに応じた高さの電気信号を発生する粒子検
出装置と、検出測定信号の単位時間当りの信号数を測定
開始前のデッド時間に測定する計数回路と、計数回路の
計数値に基づいてサンプリング間隔を選択する選択回路
と−サンプリングされた信号を変換しヒストグラムを作
成する回路とを備えるように構成することにより一メモ
リ容量を最小限に減らし−かつ有効な利用が行なえるよ
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 made to solve the above-mentioned drawbacks, and the present invention detects particles based on the electrical or optical difference between the particles and the liquid by passing a liquid in which a single particle is suspended through the 'f7 & pores. A particle detection device that generates an electrical signal with a height corresponding to the size of By configuring it to include a selection circuit for selecting a sampling interval based on the sampled signal and a circuit for converting the sampled signal and creating a histogram, the memory capacity can be reduced to a minimum and the particle size can be effectively utilized. The purpose is to provide analytical equipment.

さらに本発明は一従来一単位容積当りの粒子数が少ない
だめに、滑らかなヒストグラムが得られなかった試料に
対しても、効果的に作用1−1有効な分析結果を得るこ
とができる粒子分析装置を提供せんとするものである。
Furthermore, the present invention can effectively work on samples for which a smooth histogram could not be obtained due to the small number of particles per unit volume. 1-1 Particle analysis that can obtain effective analysis results. The aim is to provide the equipment.

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1図は本発明を粒度分布測定に応用した例を示し、第
2図は各部の信号波形を示して−る。1は粒子検出装置
で一粒子が浮懸する液を微細孔に通過させ粒子と液との
電気的差異または光学的差異に基づ込て粒子を検出し粒
子の大きさに応じた高さの電気信号を発生する装置であ
る。2は粒子検出装置1を通過する粒子の浮懸液の定量
装置、3は閾回路−4は分周制御信号発生回路−5は計
数回路、6は制御回路−7は選択回路−8はスイ・ソチ
回路−9は変換回路−10は演算回路、11は表示装置
、12は記録装置−16はメモIJ−である。
FIG. 1 shows an example in which the present invention is applied to particle size distribution measurement, and FIG. 2 shows signal waveforms at various parts. 1 is a particle detection device that passes a liquid in which a single particle is suspended through a micropore, detects the particle based on the electrical or optical difference between the particle and the liquid, and detects the particle at a height corresponding to the size of the particle. A device that generates electrical signals. 2 is a device for quantifying suspended particles passing through the particle detection device 1, 3 is a threshold circuit, 4 is a frequency division control signal generation circuit, 5 is a counting circuit, 6 is a control circuit, 7 is a selection circuit, and 8 is a switch. - Sochi circuit-9 is a conversion circuit-10 is an arithmetic circuit, 11 is a display device, 12 is a recording device-16 is a memo IJ-.

粒子検出装置1の出力パルスAは、閾回路乙により矩形
パルスBに変換され一分周制御信号発生回路4および計
数回路5に送られる。制御回路6は演算回路10からの
信号によって駆動され、計数回路5が所定時間だけ計数
を行なうような制御信号Cを計数回路5に送る。一方1
分周制御信号発生回路4は信号Bに基づいて、信号Bの
立上りから立下りまでの信号D1、この信号り、の一つ
おきの信号り、この信号D2の一つおきの信号り、・・
・と因うパラレルの信号群りを選択回路7に送る。
The output pulse A of the particle detection device 1 is converted into a rectangular pulse B by the threshold circuit B and sent to the one-frequency control signal generation circuit 4 and the counting circuit 5. The control circuit 6 is driven by a signal from the arithmetic circuit 10 and sends a control signal C to the counting circuit 5 so that the counting circuit 5 performs counting for a predetermined period of time. On the other hand 1
Based on the signal B, the frequency division control signal generation circuit 4 generates the signal D1 from the rising edge to the falling edge of the signal B, every other signal of this signal, every other signal of this signal D2, and so on.・
・Send the parallel signal group to the selection circuit 7.

信号Cによって規制された所定時間の計数値は、計数回
路5によって求められ、この計数値の大小によって選択
回路7に入力するパラレルの信号群りの中から最適の信
号を選択し一スイツチ回路8にスイッチ信号Eを送る。
The count value for a predetermined time regulated by the signal C is determined by the counting circuit 5, and depending on the magnitude of this count value, the optimum signal is selected from the group of parallel signals input to the selection circuit 7, and one switch circuit 8 Send switch signal E to .

゛スイッチ回路8にけ粒子検出装置1力出力信号Aが送
られており一前記スイッチ信号Eによって選択された信
号間隔で信号Aを通過させるため一信号Fが得られる。
A particle detector output signal A is sent to the switch circuit 8, and a signal F is obtained in order to pass the signal A at the signal interval selected by the switch signal E.

この信号Fを変換回路9で、木実施例におりては一信号
Fの高さを求めるためのAD変換を行ない一演算回路1
0に変換信号を送る。一方一この信号Fは選択回路7で
原信号を何パルス間隔おきにスイッチされたかを知るた
めに一計数回路5からその情報が演算回路10に伝達さ
れるので、変換回路9の変換出力はパルス全体の何割の
情報に該当するかがわかる。さらに定量装置2は演算回
路10に測定開始、測定終了信号を送り、所定試料溶液
中の個数としての絶対測定が行なわれる。
This signal F is subjected to AD conversion in a conversion circuit 9 in order to obtain the height of one signal F in the wooden embodiment.
Send a conversion signal to 0. On the other hand, this signal F is transmitted from the counting circuit 5 to the arithmetic circuit 10 in order to know at what pulse intervals the original signal is switched in the selection circuit 7, so that the conversion output of the conversion circuit 9 is pulsed. You can see what percentage of the information corresponds to the total. Furthermore, the quantitative device 2 sends measurement start and measurement end signals to the arithmetic circuit 10, and absolute measurement is performed as the number of particles in a predetermined sample solution.

以上のような構成および動作をする装置において一定量
装置2がリセットされ測定開始信号を発するまでのデッ
ドタイムを利用し一信号Cに基づく初期設定のだめの計
数測定が行なわれる。すなわち−パルス間隔が非常に短
かい高濃度の試料においては、パルスを所定のパルス間
隔でサンプリングするように初期選択がなされ−スイッ
チ信号が発生する。このスイッチ信号によって変換回路
(たとえばAD変換回路)に送られる信号が常にどの測
定においても所定の間隔になる。
In the apparatus configured and operated as described above, the initial setting count measurement based on one signal C is performed using the dead time from when the fixed amount device 2 is reset to when the measurement start signal is issued. That is, - in highly concentrated samples with very short pulse intervals, an initial selection is made to sample the pulses at a predetermined pulse interval - and a switch signal is generated. This switch signal causes signals sent to a conversion circuit (for example, an AD conversion circuit) to always be at predetermined intervals in any measurement.

実施例の一つとして粒度分布を得る装置においては、変
換回路はアナログパルス高さの情報をディジタル信号に
変換するAD変換回路が用いられ。
In an apparatus for obtaining a particle size distribution as one of the embodiments, an AD conversion circuit that converts analog pulse height information into a digital signal is used as the conversion circuit.

このディジタル信号はメモリー16のその粒度を示す番
地の所に1個を加えるように動作する。以上の動作は定
量装置2で規制される所定の粒子浮懸液に対して行なわ
れ、サンプリングが全体の1/4に対して行なわれだ場
合には1表示装置11や記録装置12に表示印字される
ヒストグラムは、その個数を4倍することによってもと
の絶対値を得ることができる。したがってメモリーの容
量はほぼ一定の大きさがあれば一飽和することもなく有
効利用することができる。さらに実施例においては1粒
度のヒストグラムを得る装置につ−て説明1−だが、他
の実施例として、粒子検出装置を光学的な検出信号を発
する色分析装置とし1色彩による粒子の分類分析などに
も適用することができる。
This digital signal operates to add one to the memory 16 at the address indicating the granularity. The above operations are performed on a predetermined particle suspended liquid regulated by the quantitative device 2, and when sampling is performed for 1/4 of the total, the display is printed on the display device 11 and the recording device 12. The original absolute value of the histogram can be obtained by multiplying the number by four. Therefore, if the memory capacity is approximately constant, it can be used effectively without reaching saturation. Furthermore, in the embodiment, a device for obtaining a histogram of one particle size is explained (1), but in other embodiments, the particle detection device is a color analysis device that emits an optical detection signal, and particle classification analysis using one color, etc. It can also be applied to

すなわち計数回路5に計数される信号を白黒信号とし、
スイッチ回路8を赤−緑、青の3系列とし一3系列の信
号のサンプリングを行ない一変換回路9および演算回路
10によって分類を行なって一メモリー16に分類後の
粒子数を記憶させ一最後にサンプリング割合で補正する
ことにより一原液中のそれぞれ力粒子個数の絶対値を得
ることができる。
That is, the signal counted by the counting circuit 5 is a black and white signal,
The switch circuit 8 is set to three systems of red, green, and blue, and the signals of the three systems are sampled, the conversion circuit 9 and the arithmetic circuit 10 perform classification, and the number of particles after classification is stored in the memory 16. By correcting the sampling rate, it is possible to obtain the absolute value of the number of force particles in each stock solution.

以上説明L−だように、本発明の粒子分析装置において
は1分析対象の信号数が測定の都度−所定の範囲になる
ようにサンプリングされるため一演算間隔がほぼ一定と
平均化され、低速の演算回路でも十分に追従することが
でき、まだメモリーの容量を必要最小限とすることがで
き−さらに有効に使用することができる。1−たがって
本発明の装置は一血液中の比較的数の変動の大きい白血
球や血小板の粒度分布曲線の測定装置−あるい(寸工業
分野で数の一定でない粒子の粒度分布ヒストグラムの測
定などのほかに一光学的な粒子分類測定装置などとして
用いるのに適している。
As explained above, in the particle analyzer of the present invention, the number of signals for one analysis target is sampled within a predetermined range each time the measurement is performed, so the calculation interval is averaged almost constant, and the speed is low. It is possible to sufficiently follow up even with an arithmetic circuit of 1, and the memory capacity can still be kept to the minimum necessary - and it can be used more effectively. 1- Therefore, the device of the present invention is a device for measuring the particle size distribution curve of white blood cells and platelets whose numbers fluctuate relatively widely in blood, or (in the industrial field, measuring particle size distribution histograms of particles whose number is not constant, etc.) It is also suitable for use as an optical particle classification and measurement device.

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

第1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2図は各部の信号波形の説明図である。 1・・粒子検出装置、2・・定量装置、6・、閾回路。 4・・分周制御信号発生回路−5・・・計数回路、6・
・制御回路−7・・選択回路−′8・・スイ・ソチ回路
、9・・変換回路、10・・−演算回路−11・・表示
装置。 1291、記録装置−13・・・メモリー特許出願人 
東亜医用電子株式会社
FIG. 1 is a systematic explanatory diagram showing one embodiment of the particle analyzer of the present invention, and FIG. 2 is an explanatory diagram of signal waveforms of each part. 1. Particle detection device, 2. Quantification device, 6. Threshold circuit. 4... Frequency division control signal generation circuit-5... Counting circuit, 6...
-Control circuit-7...Selection circuit-'8...Sui-Sochi circuit, 9...Conversion circuit, 10...-Arithmetic circuit-11...Display device. 1291, Recording device-13...Memory patent applicant
Toa Medical Electronics Co., Ltd.

Claims (1)

【特許請求の範囲】[Claims] 1 粒子が浮懸する液を微細孔に通過させ粒子と液との
電気的差異または光学的差異に基づいて粒子を検出し粒
子の大きさに応じた高さの電気信号を発生する粒子検出
装置と、検出測定信号の単位時間当りの信号数を測定開
始前のデッド時間に測定する計数回路と、計数回路の計
数値に基づいてサンプリング間[−選択する選択回路と
、サンプリングされた信号を変換[2ヒヌトグラムを作
成する回路とを備えてなることを特徴とする粒子分析装
置。
1 A particle detection device that passes a liquid in which particles are suspended through micropores, detects particles based on electrical or optical differences between the particles and the liquid, and generates an electrical signal with a height corresponding to the size of the particles. , a counting circuit that measures the number of detected measurement signals per unit time during the dead time before the start of measurement, a selection circuit that selects between sampling based on the count value of the counting circuit, and a selection circuit that converts the sampled signal. [2] A particle analysis device comprising: a circuit for creating a hinutogram;
JP6290982A 1982-04-14 1982-04-14 Analyzing apparatus of particle Granted JPS58179339A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6290982A JPS58179339A (en) 1982-04-14 1982-04-14 Analyzing apparatus of particle

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6290982A JPS58179339A (en) 1982-04-14 1982-04-14 Analyzing apparatus of particle

Publications (2)

Publication Number Publication Date
JPS58179339A true JPS58179339A (en) 1983-10-20
JPH0257661B2 JPH0257661B2 (en) 1990-12-05

Family

ID=13213846

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6290982A Granted JPS58179339A (en) 1982-04-14 1982-04-14 Analyzing apparatus of particle

Country Status (1)

Country Link
JP (1) JPS58179339A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0435166A2 (en) * 1989-12-22 1991-07-03 Hitachi, Ltd. Particle analyzing method and device for realizing same
CN113811754A (en) * 2018-08-30 2021-12-17 贝克顿·迪金森公司 Characterization and sorting of particle analyzers

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0435166A2 (en) * 1989-12-22 1991-07-03 Hitachi, Ltd. Particle analyzing method and device for realizing same
US5166537A (en) * 1989-12-22 1992-11-24 Hitachi, Ltd. Particle analyzing method and device for realizing same
CN113811754A (en) * 2018-08-30 2021-12-17 贝克顿·迪金森公司 Characterization and sorting of particle analyzers

Also Published As

Publication number Publication date
JPH0257661B2 (en) 1990-12-05

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