JPH0676963B2 - Particle aggregation pattern determination method - Google Patents
Particle aggregation pattern determination methodInfo
- Publication number
- JPH0676963B2 JPH0676963B2 JP58242163A JP24216383A JPH0676963B2 JP H0676963 B2 JPH0676963 B2 JP H0676963B2 JP 58242163 A JP58242163 A JP 58242163A JP 24216383 A JP24216383 A JP 24216383A JP H0676963 B2 JPH0676963 B2 JP H0676963B2
- Authority
- JP
- Japan
- Prior art keywords
- light receiving
- image
- receiving element
- pattern determination
- microplate
- 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 - Lifetime
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/251—Colorimeters; Construction thereof
- G01N21/253—Colorimeters; Construction thereof for batch operation, i.e. multisample apparatus
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Description
【発明の詳細な説明】 技術分野 本発明は粒子凝集パターンの判定方法、特に免疫学的反
応に基く血球等の粒子の凝集パターンから各種の血液型
の判定や、抗原、抗体の検出を行なう粒子凝集パターン
判定方法に関するものである。TECHNICAL FIELD The present invention relates to a method for determining a particle aggregation pattern, and in particular, particles for determining various blood groups and detecting antigens and antibodies from the aggregation pattern of particles such as blood cells based on immunological reaction. The present invention relates to an aggregation pattern determination method.
従来技術 従来の粒子凝集パターンの判定方法として、反応容器の
底面の像を一次元受光素子列上に結像させることによつ
て走査し、その出力に基いて凝集パターンを判定するよ
うにしたものがある。しかし、この方法では、反応容器
として例えば底面が逆円錐状のものを用いた場合には、
その逆円錐状底面の像の中心と一次元受光素子列の中心
とが一致するように、両者を正確に位置合わせしないと
凝集パターンを正確に判定することができない不具合が
ある。このような不具合は反応容器を同一基板にマトリ
ツクス状に多数形成したマイクロプレートを用いた場合
でも、マイクロプレートすなわち被検反応容器と一次元
受光素子列との相対位置を正確に合わせないと同様に生
じるものである。2. Description of the Related Art A conventional method for determining a particle agglomeration pattern is one in which an image of the bottom surface of a reaction container is imaged on a one-dimensional light-receiving element array for scanning and the agglomeration pattern is determined based on the output. There is. However, in this method, for example, when using a reaction vessel whose bottom surface is an inverted cone,
There is a problem that the aggregation pattern cannot be accurately determined unless the two are accurately aligned so that the center of the image of the inverted conical bottom surface and the center of the one-dimensional light receiving element array coincide with each other. Even when using a microplate in which a large number of reaction vessels are formed on the same substrate in the shape of a matrix, such a problem occurs unless the relative positions of the microplate, that is, the reaction vessel under test and the one-dimensional light receiving element array are accurately aligned. It happens.
このため、かかる判定方法を採用して免疫学的凝集反応
により血液型の判定や、抗原、抗体の検出を自動的に行
なう装置を構成する場合には、反応容器と一次元受光素
子列との正確な位置決め機構が必要となつて構成が複雑
になる不具合がある。Therefore, in the case of adopting such a determination method and configuring an apparatus for automatically determining the blood group by the immunological agglutination reaction and detecting the antigen and the antibody, the reaction container and the one-dimensional light receiving element array are combined. There is a problem that the structure becomes complicated because an accurate positioning mechanism is required.
発明の目的 本発明の目的は、上述した種々の不具合を解決し、反応
容器と測定部との正確な位置合わせを行うことなく、容
器底面上のパターンの中心および周辺を正確に測定で
き、凝集パターンを常に正確に判定できると共に、自動
分析装置に適用した場合に、その構成および制御を簡単
にできる粒子凝集パターン判定方法を提供しようとする
ものである。Object of the invention The object of the present invention is to solve the various problems described above, it is possible to accurately measure the center and periphery of the pattern on the bottom surface of the container without performing accurate alignment between the reaction container and the measurement unit, and An object of the present invention is to provide a particle aggregation pattern determination method capable of always accurately determining a pattern and simplifying the configuration and control when applied to an automatic analyzer.
発明の概要 本発明は、反応容器に収容した反応溶液中の粒子が沈降
して底面に形成される粒子凝集パターンを光学的に検出
して凝集の有無を判定する粒子凝集パターン判定方法に
おいて、前記反応容器を含む受光範囲を有する光電変換
面によって該受光範囲内の受光像に関する全ての二次元
的出力データを得る工程と、前記受光像の二次元的出力
データから反応容器の輪郭位置を求める工程と、前記輪
郭位置の中心部とその周辺部に対応する各光学的データ
を比較することを特徴とするものである。SUMMARY OF THE INVENTION The present invention is a particle aggregation pattern determination method for determining the presence or absence of aggregation by optically detecting a particle aggregation pattern in which particles in a reaction solution housed in a reaction vessel settle and are formed on the bottom surface, Obtaining all two-dimensional output data relating to a light-receiving image within the light-receiving range by a photoelectric conversion surface having a light-receiving range including the reaction container, and obtaining a contour position of the reaction container from the two-dimensional output data of the light-receiving image. And comparing each optical data corresponding to the central portion of the contour position and its peripheral portion.
実施例 第1図および第2図は本発明を実施する粒子凝集パター
ン判定装置の一例の構成を示すものである。本例では、
多数の反応容器1をマトリツクス状に形成した透明部材
から或るマイクロプレート2を矢印方向に間欠的に移送
し、その移送方向と直交する方向の順次の列の反応容器
1の凝集パターンを検出するものである。このため、所
定の位置において移送方向と直交する方向に延在して設
けた発光部3により一例の反応容器1の底面を照明し、
その像を一列の各反応容器1に対応して設けたレンズ4
を介して二次元受光素子列5上にそれぞれ結像させて走
査する。ここで、各反応容器1に対応する二次元受光素
子列5は、第3図に示すようにレンズ4によって結像さ
せる反応容器1の底面の像6の面積よりも大きな面積か
らなる光電変換面で構成することにより、受光範囲内に
在る受光像に関する全ての二次元的出力データが得られ
るようにする。Example FIG. 1 and FIG. 2 show the configuration of an example of a particle aggregation pattern determination device for carrying out the present invention. In this example,
A certain microplate 2 is intermittently transferred in the arrow direction from a transparent member in which a large number of reaction containers 1 are formed in a matrix, and the agglomeration pattern of the reaction containers 1 in a sequential row in the direction orthogonal to the transfer direction is detected. It is a thing. Therefore, the bottom surface of the reaction container 1 of one example is illuminated by the light emitting unit 3 provided at a predetermined position so as to extend in a direction orthogonal to the transfer direction,
The lens 4 provided with the image corresponding to each reaction container 1 in a row
An image is formed on the two-dimensional light receiving element array 5 via the scanning lines and scanned. Here, the two-dimensional light receiving element array 5 corresponding to each reaction container 1 has a photoelectric conversion surface having an area larger than the area of the image 6 of the bottom surface of the reaction container 1 imaged by the lens 4 as shown in FIG. With this configuration, it is possible to obtain all two-dimensional output data regarding the received light image within the light receiving range.
このようにして、二次元受光素子列5を走査すれば、反
応容器1の底面像を横切る一ラインの受光素子列の出力
分布は、例えば第4図に示すようになり、マイクロプレ
ート2の平坦面の像部分(位置a,b間とc,d間)と反応容
器1の像部分(位置b,c間)とで出力が大きく異なる。
本実施例においては、このようにマイクロプレート2の
平坦面と反応容器1の部分とで出力が異なるのを利用し
て、該二次元受光素子列5上での反応容器1の底面を示
す像の輪郭、すなわち位置を求めると共に、その出力を
適切に処理することにより底面像全体が受光領域内に位
置するようにマイクロプレート2の移動に帰還をかけ
る。このようにして、二次元受光素子列5上での反応容
器1の底面を示す像の輪郭を求めた後、その輪郭内の受
光素子の出力に基いて、例えば底面像の輪郭からその中
心位置を求めて、その中心部のデータと、周辺部のデー
タとの比較に基いて凝集パターンを判定する。When the two-dimensional light receiving element array 5 is scanned in this manner, the output distribution of one line of the light receiving element array that crosses the bottom image of the reaction container 1 becomes as shown in FIG. 4, for example, and the microplate 2 is flat. The output differs greatly between the image portion of the surface (between positions a and b and c and d) and the image portion of reaction container 1 (between positions b and c).
In the present embodiment, an image showing the bottom surface of the reaction container 1 on the two-dimensional light-receiving element array 5 is utilized by utilizing the difference in output between the flat surface of the microplate 2 and the portion of the reaction container 1 as described above. The contour, that is, the position of the microplate 2 is obtained, and the output thereof is appropriately processed to feed back the movement of the microplate 2 so that the entire bottom image is positioned within the light receiving region. In this way, after the contour of the image showing the bottom surface of the reaction vessel 1 on the two-dimensional light receiving element array 5 is obtained, based on the output of the light receiving element within the contour, for example, from the contour of the bottom surface image to the center position thereof. Then, the aggregation pattern is determined based on the comparison between the data of the central part and the data of the peripheral part.
このように、反応容器1の底面の像をレンズ4を介し
て、その結像位置において底面像の面積よりも大きい受
光面積を有する二次元受光素子列5上に結像させるよう
にすれば、発光部3、レンズ4および二次元受光素子列
5を有する測定部と、反応容器1すなわちマイクロプレ
ート2との厳密な位置合わせが不要となり、かつ二次元
受光素子列5の出力を基いてマイクロプレート2の微調
整も容易にできると共に、凝集パターンを常に正確に判
定することができる。Thus, if the image of the bottom surface of the reaction container 1 is formed through the lens 4 on the two-dimensional light receiving element array 5 having a light receiving area larger than the area of the bottom surface image at the image forming position, Strict alignment between the measuring unit having the light emitting unit 3, the lens 4, and the two-dimensional light receiving element array 5 and the reaction container 1, that is, the microplate 2, is unnecessary, and the microplate is based on the output of the two-dimensional light receiving element array 5. The second fine adjustment can be easily performed, and the aggregation pattern can always be accurately determined.
第5図および第6図は本発明を実施する粒子凝集パター
ン判定装置の他の例の構成を示すものである。本例では
発光部7によりマイクロプレート2の底面全体を照明
し、その全体の像を一つのレンズ8を介して二次元受光
素子列9に結像させ、この二次元受光素子列9を走査す
ることにより各反応容器1の底面像の輪郭を求めてその
輪郭内の受光素子の出力に基いて凝集パターンを判定す
るようにしたものである。したがつて、本実施例におい
ても上述した実施例と同様、発光部7、レンズ8および
二次元受光素子列9を有する測定部と、マイクロプレー
ト2とを厳密に位置合わせしなくても常に正確に凝集パ
ターンを判定することができる。FIG. 5 and FIG. 6 show the configuration of another example of the particle agglomeration pattern determination device embodying the present invention. In this example, the entire bottom surface of the microplate 2 is illuminated by the light emitting unit 7, the entire image is formed on the two-dimensional light receiving element array 9 through one lens 8, and the two-dimensional light receiving element array 9 is scanned. Thus, the contour of the bottom image of each reaction container 1 is obtained, and the aggregation pattern is determined based on the output of the light receiving element within the contour. Therefore, in the present embodiment as well, similar to the above-described embodiments, the measurement unit having the light emitting unit 7, the lens 8 and the two-dimensional light receiving element array 9 and the microplate 2 are not always accurately aligned with each other. The aggregation pattern can be determined.
なお、本発明は上述した実施例にのみ限定されるもので
はなく、幾多の変形または変更が可能である。例えば第
1図および第2図に示す実施例においては発光部3、レ
ンズ4および二次元受光素子列5を有する測定部をマイ
クロプレート2に対して間欠的に移送させるようにして
もよい。また二次元受光素子列5はマイクロプレート2
の一例の反応容器1の個々に対して必ずしも分離する必
要はなく、連続するものであっても良い。更に第5図お
よび第6図に示す実施例いおいては、マイクロプレート
2上に位置検出用のマーカを設けることにより、マイク
ロプレート2および反応容器1の絶対位置を知ることも
できる。また、第5図および第6図の実施例では、マイ
クロプレート2の各反応容器1に対応してその底面像よ
りも大きい受光面積を有する二次元受光素子を分離して
設けてもよい。更にまた、上述した各実施例において、
マイクロプレートを上方から照明して反応容器の底面像
をマイクロプレートの下方において二次元受光素子列に
結像させてもよい。更に本発明はマイクロプレートのみ
でなく、個々に分離された反応容器を用いる場合でも有
効に適用することができる。It should be noted that the present invention is not limited to the above-described embodiments, and various modifications and changes can be made. For example, in the embodiment shown in FIGS. 1 and 2, the measuring section having the light emitting section 3, the lens 4 and the two-dimensional light receiving element array 5 may be intermittently transferred to the microplate 2. The two-dimensional light receiving element array 5 is the microplate 2
It is not always necessary to separate each of the reaction vessels 1 of one example, and they may be continuous. Further, in the embodiment shown in FIGS. 5 and 6, by providing a position detecting marker on the microplate 2, the absolute positions of the microplate 2 and the reaction container 1 can be known. Further, in the embodiment of FIGS. 5 and 6, a two-dimensional light receiving element having a light receiving area larger than the bottom surface image may be separately provided corresponding to each reaction container 1 of the microplate 2. Furthermore, in each of the embodiments described above,
The bottom surface image of the reaction container may be imaged on the two-dimensional light receiving element array below the microplate by illuminating the microplate from above. Further, the present invention can be effectively applied not only to the microplate but also to the case of using individually separated reaction vessels.
発明の効果 以上述べたように、本発明によれば反応容器と測定部と
の正確な位置合わせを行なうことなく、容器底面上のパ
ターンの中心および周辺を正確に測定でき、凝集パター
ンを常に正確に判定できると共に、本発明を免疫学的凝
集反応による自動分析装置に適用すればその構成および
制御を簡単にできる。EFFECTS OF THE INVENTION As described above, according to the present invention, the center and periphery of the pattern on the bottom surface of the container can be accurately measured without performing accurate alignment between the reaction container and the measurement unit, and the agglomeration pattern is always accurate. If the present invention is applied to an automatic analyzer based on an immunological agglutination reaction, the configuration and control can be simplified.
第1図および第2図は本発明を実施する粒子凝集パター
ン判定装置の一例の構成を示す平面図および断面図、 第3図は反応容器の底面像と二次元受光素子列との関係
を示す図、 第4図は二次元受光素子列の一列の出力分布を示す図、 第5図および第6図は本発明を実施する粒子凝集パター
ン判定装置の他の例の構成を示す平面図および断面であ
る。 1……反応容器、2……マイクロプレート 3,7……発光部、4,8……レンズ 5,9……二次元受光素子列 6……底面像。1 and 2 are a plan view and a cross-sectional view showing an example of the structure of a particle agglomeration pattern determination apparatus for carrying out the present invention, and FIG. 3 shows a relationship between a bottom image of a reaction container and a two-dimensional light receiving element array. FIG. 4 is a diagram showing the output distribution of one row of a two-dimensional light receiving element array, and FIGS. 5 and 6 are plan views and cross sections showing the configuration of another example of the particle aggregation pattern determination device embodying the present invention. Is. 1 ... Reaction container, 2 ... Microplate 3,7 ... Light emitting part, 4,8 ... Lens 5,9 ... Two-dimensional light receiving element array 6 ... Bottom image.
Claims (1)
降して底面に形成される粒子凝集パターンを光学的に検
出して凝集の有無を判定する粒子凝集パターン判定方法
において、前記反応容器を含む受光範囲を有する光電変
換面によって該受光範囲内の受光像に関する全ての二次
元的出力データを得る工程と、前記受光像の二次元的出
力データから反応容器の輪郭位置を求める工程と、前記
輪郭位置の中心部とその周辺部に対応する各光学的デー
タを比較することを特徴とする粒子凝集パターン判定方
法。1. A particle agglomeration pattern determination method for optically detecting a particle agglomeration pattern formed by sedimentation of particles in a reaction solution contained in a reaction vessel on the bottom surface to determine the presence or absence of aggregation, wherein the reaction vessel A step of obtaining all two-dimensional output data relating to a light-receiving image in the light-receiving range by a photoelectric conversion surface having a light-receiving range, and a step of obtaining the contour position of the reaction container from the two-dimensional output data of the light-receiving image, A particle agglomeration pattern determination method characterized by comparing respective optical data corresponding to a central portion of the contour position and its peripheral portion.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58242163A JPH0676963B2 (en) | 1983-12-23 | 1983-12-23 | Particle aggregation pattern determination method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58242163A JPH0676963B2 (en) | 1983-12-23 | 1983-12-23 | Particle aggregation pattern determination method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60135748A JPS60135748A (en) | 1985-07-19 |
| JPH0676963B2 true JPH0676963B2 (en) | 1994-09-28 |
Family
ID=17085265
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58242163A Expired - Lifetime JPH0676963B2 (en) | 1983-12-23 | 1983-12-23 | Particle aggregation pattern determination method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0676963B2 (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62105031A (en) * | 1985-11-01 | 1987-05-15 | Fujirebio Inc | Decision device for particle flocculation |
| JP2897027B2 (en) * | 1988-10-27 | 1999-05-31 | スズキ株式会社 | Immunological agglutination detector |
| JP2525487B2 (en) * | 1989-09-22 | 1996-08-21 | 東レ株式会社 | Particle aggregation pattern determination method |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57182651A (en) * | 1981-05-07 | 1982-11-10 | Olympus Optical Co Ltd | Detection apparatus of particle agglomeration pattern |
| JPS57186169A (en) * | 1981-05-12 | 1982-11-16 | Olympus Optical Co Ltd | Detector for particle coagulation pattern |
| JPS5832142A (en) * | 1981-08-19 | 1983-02-25 | Olympus Optical Co Ltd | Microplate illumination device |
| JPH0230470B2 (en) * | 1981-10-09 | 1990-07-06 | Olympus Optical Co | RYUSHIGYOSHUPATAANKENSAHOHOOYOBISOCHI |
-
1983
- 1983-12-23 JP JP58242163A patent/JPH0676963B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60135748A (en) | 1985-07-19 |
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| EXPY | Cancellation because of completion of term |