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JPH0437384B2 - - Google Patents
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JPH0437384B2 - - Google Patents

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Publication number
JPH0437384B2
JPH0437384B2 JP56186908A JP18690881A JPH0437384B2 JP H0437384 B2 JPH0437384 B2 JP H0437384B2 JP 56186908 A JP56186908 A JP 56186908A JP 18690881 A JP18690881 A JP 18690881A JP H0437384 B2 JPH0437384 B2 JP H0437384B2
Authority
JP
Japan
Prior art keywords
sample
dilution
measurement
section
reaction
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
Application number
JP56186908A
Other languages
Japanese (ja)
Other versions
JPS5888662A (en
Inventor
Masaki Takeuchi
Shinichi Hasegawa
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.)
Toshiba Corp
Original Assignee
Tokyo Shibaura Electric 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 Tokyo Shibaura Electric Co Ltd filed Critical Tokyo Shibaura Electric Co Ltd
Priority to JP18690881A priority Critical patent/JPS5888662A/en
Publication of JPS5888662A publication Critical patent/JPS5888662A/en
Publication of JPH0437384B2 publication Critical patent/JPH0437384B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
    • G01N35/02Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations
    • G01N35/021Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations having a flexible chain, e.g. "cartridge belt", conveyor for reaction cells or cuvettes
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
    • G01N35/00584Control arrangements for automatic analysers
    • G01N35/00594Quality control, including calibration or testing of components of the analyser
    • G01N35/00603Reinspection of samples

Landscapes

  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Quality & Reliability (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は診断のための医療機器の分野に属し、
自動化学分析装置において検体の化学分析のデー
タ異常が生じた場合の再測定方法に関するもので
ある。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention belongs to the field of medical devices for diagnosis,
The present invention relates to a re-measurement method when an abnormality occurs in the chemical analysis data of a specimen in an automatic chemical analyzer.

(従来の技術) 従来より自動化学分析装置においては、正しい
分析結果が得られないために再測定を行なわなけ
ればならないことがしばしば生じている。正しい
分析結果が得られない原因としては種々考えられ
るが、例えば自動化学分析装置において吸光度を
測定する場合には、検体の高濃度、高単位あるい
は色調等による原因、測定系への気泡の影響、反
応管の汚れ等が考えられる。このような場合、例
えば検体が高濃度であつたと判断された場合は検
体を希釈後再測定を行い、気泡の発生及び反応管
の汚れ等のアクシデントによる場合は、前記原因
を取り除いた状態で再測定を行なう必要がある。
例えば検体が高濃度である為に発色の強度が強す
ぎて装置の使用可能範囲を越え正しい分析結果が
得られない様な場合には、測定者自身がその検体
を生理食塩又は精製水等で一定量希釈したのち検
体サンプルカツプに入れ、自動化学分析装置にセ
ツトして再度測定を行なつていた。
(Prior Art) Conventionally, in automatic chemical analyzers, it has often occurred that correct analysis results cannot be obtained and re-measurement must be performed. There are various reasons why correct analysis results may not be obtained, but for example, when measuring absorbance with an automatic chemical analyzer, there are many reasons such as high concentration, high units, or color of the sample, the effect of air bubbles on the measurement system, Possible causes include dirt in the reaction tube. In such cases, for example, if the sample is determined to have a high concentration, dilute the sample and re-measure it; if it is due to an accident such as the generation of air bubbles or dirt in the reaction tube, re-measure after removing the cause. Measurements need to be taken.
For example, if the intensity of the color development is too strong due to the high concentration of the sample and exceeds the usable range of the device, making it impossible to obtain accurate analysis results, the person performing the measurement should wash the sample with physiological saline or purified water. After diluting a certain amount, the sample was placed in a sample cup, set in an automatic chemical analyzer, and measured again.

近年、自動化学分析装置の自動化が進み、人手
の介入が省略されつつある反面、測定のエラー表
示がなされた検体が生じた場合の対応は測定者自
身の操作に依存している部分が多く、測定者に多
くの負担がかかつている。
In recent years, automated chemical analyzers have become increasingly automated, and manual intervention is being omitted.However, when a sample is displayed as a measurement error, the response to it is still largely dependent on the operator's own operations. This places a lot of burden on the measurer.

(発明が解決しようとする課題) 本発明は前記事情に鑑みてなされたものであ
り、自動化学分析装置において測定エラーとなつ
た検体について、速やかに再測定を行うことがで
きる検体の再測定方法を提供することを目的とす
るものである。
(Problems to be Solved by the Invention) The present invention has been made in view of the above-mentioned circumstances, and provides a method for re-measuring a specimen that can promptly re-measure a specimen that has caused a measurement error in an automatic chemical analyzer. The purpose is to provide the following.

(課題を解決するための手段) 前記目的を達成するため、本発明に係る検体の
再測定方法は、測定対象としての検体を収容する
反応管を列状に配置してなる反応ラインと、この
反応ラインに併設された希釈部と、検体を収容し
たサンプルユニツト部と、このサンプルユニツト
部の検体を吸引し、前記希釈部に吐出し、希釈さ
れた検体を再度吸引し、前記反応ラインに分注す
るサンプリング部と、前記反応管に収容された検
体の吸光度を測定する測定部とを備えた自動化学
分析装置における検体の再測定方法であつて、前
記測定部による該検体の測定結果を所定の値と比
較することにより該測定結果が所定の範囲内であ
るか否かを判断し、所定の範囲外である場合には
該測定結果が所定の範囲外となつた原因が該検体
の希釈倍率不適切に起因するものかそれ以外の事
由に起因するものかを該測定結果に基づいて判断
し、該検体の希釈倍率不適切に起因する場合には
該測定結果に基づいて最適希釈倍率を設定し、前
記希釈部において該最適希釈倍率により該検体を
再希釈後前記反応管に分注して再測定を行い、該
検体の希釈倍率不適切以外の事由に起因する場合
には前記希釈部において前回と同一の希釈倍率に
より該検体を再希釈後前記反応管に分注して再測
定を行うようにしたことを特徴とするものであ
る。
(Means for Solving the Problems) In order to achieve the above object, a method for re-assaying a specimen according to the present invention includes a reaction line in which reaction tubes containing a specimen to be measured are arranged in a row; A dilution section attached to the reaction line, a sample unit section containing the sample, the sample from this sample unit section is aspirated and discharged to the dilution section, the diluted sample is aspirated again and separated into the reaction line. A method for re-measuring a sample in an automatic chemical analyzer comprising a sampling section for measuring the absorbance of the sample contained in the reaction tube, and a measuring section for measuring the absorbance of the sample contained in the reaction tube, the method comprising: It is determined whether the measurement result is within a predetermined range by comparing it with the value of Determine whether the problem is due to an inappropriate dilution ratio or other reasons based on the measurement results, and if the problem is caused by an inappropriate dilution ratio for the sample, determine the optimal dilution ratio based on the measurement results. The sample is re-diluted at the optimum dilution ratio in the dilution section and then dispensed into the reaction tube for re-measurement. The method is characterized in that the sample is re-diluted using the same dilution factor as the previous time, and then dispensed into the reaction tube and re-measured.

(作 用) 以上のように構成された本発明に係る検体の再
測定方法にあつては、測定結果に基づいて測定エ
ラーが発生したのかあるいは正しい測定結果が得
られたかを判断し、測定エラーが発生した場合に
は更にその測定結果から検体の希釈倍率不適切に
起因する測定エラーか否か、希釈倍率不適切に起
因する場合にはその測定結果から適切な希釈倍率
が設定されて希釈部用いて再測定が実行されるの
で、測定エラーが発生した検体について、再測定
時の適切な希釈倍率が極めて広い範囲に渡るにも
拘らず貴重な検体を無駄に使用することなく迅速
に再測定を実行することができる。
(Function) In the sample re-measurement method according to the present invention configured as described above, it is determined based on the measurement result whether a measurement error has occurred or whether a correct measurement result has been obtained, and the measurement error is detected. If this occurs, the measurement results will be used to determine whether the measurement error is due to an inappropriate dilution ratio of the sample, and if it is due to an inappropriate dilution ratio, an appropriate dilution ratio will be set based on the measurement results and the dilution section Therefore, even though the appropriate dilution ratio for re-measuring a sample with a measurement error can be re-measured over a very wide range, valuable samples can be quickly re-measured without wasting valuable samples. can be executed.

(実施例) 以下本発明の一実施例を第1図を参照して説明
する。
(Example) An example of the present invention will be described below with reference to FIG.

第1図は本発明に係る検体の再測定方法に用い
られる自動化学分析装置の一例を示す図である。
FIG. 1 is a diagram showing an example of an automatic chemical analyzer used in the sample remeasurement method according to the present invention.

第1図において、測定対象としての検体が分注
される反応管1は駆動ベルト2に適宜に取り付け
られ、図示矢印E方向に間欠的に移動可能であ
る。尚、駆動方向Eに対して並列に取り付けられ
た反応管1のうち、1本のラインは検体を希釈す
るための検体希釈ラインであり、残りの例えば4
本のラインが測定に供される反応ラインとする。
18はサンプリングノズル3及び希釈用ノズル3
aを具備したサンプリングユニツトであり、駆動
プーリ19aと従動プーリ19bとに張り渡され
た無端ベルト20の一部に適宜に固定され、スラ
イド部21に沿つて図示矢印F方向に往復運動可
能である。前記サンプリングノズル3及び希釈用
ノズル3aはサンプリングユニツト18に対して
図面の表面より裏面方向へと往復動可能であり、
かつその他端部は、サンプリングポンプ5及び希
釈水ビン6に接続された希釈用ポンプ5aにそれ
ぞれ連結されている。9aはサンプルユニツトで
あり、その上に個々の検体サンプル9を縦横に配
置し、図示矢印G方向に駆動可能である。11は
試薬ノズルであり、反応ラインに属する反応管1
に試薬を所定量分注可能である。前記の駆動を要
するサンプリングノズル3、希釈用ノズル3a、
サンプリングポンプ5、希釈用ポンプ5a、駆動
プーリ19a、サンプルユニツト9a、及び試薬
ノズル11は、入力装置17への入力に基づいて
駆動制御部16によりその駆動が制御されてい
る。更に、図では省略してあるが、入力装置17
はデータ処理部14に連結されている。また、吸
光度を測定する測定部(図示省略)はデータ処理
部14に順次データを送り、その測定値を演算処
理した後、出力装置(図示省略)よりその分析値
を得る構成を有しているものとする。
In FIG. 1, a reaction tube 1 into which a sample to be measured is dispensed is appropriately attached to a drive belt 2 and can be moved intermittently in the direction of arrow E in the figure. Note that among the reaction tubes 1 installed in parallel with the driving direction E, one line is a sample dilution line for diluting the sample, and the remaining lines, for example, 4
The book line is the reaction line used for measurement.
18 is a sampling nozzle 3 and a dilution nozzle 3
It is a sampling unit equipped with a, and is appropriately fixed to a part of an endless belt 20 stretched between a driving pulley 19a and a driven pulley 19b, and is capable of reciprocating along a sliding portion 21 in the direction of arrow F in the figure. . The sampling nozzle 3 and the dilution nozzle 3a are capable of reciprocating with respect to the sampling unit 18 from the front side of the drawing toward the back side,
The other end is connected to a dilution pump 5a connected to a sampling pump 5 and a dilution water bottle 6, respectively. Reference numeral 9a denotes a sample unit, on which individual specimen samples 9 are arranged vertically and horizontally, and can be driven in the direction of arrow G in the figure. 11 is a reagent nozzle, and reaction tube 1 belonging to the reaction line
A predetermined amount of reagent can be dispensed. The sampling nozzle 3 that requires the above-mentioned drive, the dilution nozzle 3a,
The driving of the sampling pump 5, dilution pump 5a, drive pulley 19a, sample unit 9a, and reagent nozzle 11 is controlled by a drive control section 16 based on input to an input device 17. Furthermore, although omitted in the figure, an input device 17
is connected to the data processing section 14. In addition, a measurement unit (not shown) that measures absorbance sequentially sends data to the data processing unit 14, and after processing the measured values, obtains the analysis value from an output device (not shown). shall be taken as a thing.

尚、データ処理部14は、入力装置17への入
力に伴いその演算方法の修正が可能なものとす
る。又、入力装置17は、再測定時に検体の番号
を入力する操作キーと、再測定時の希釈倍率を入
力する操作キーとを具備している。
Note that the data processing unit 14 is capable of modifying its calculation method in response to input to the input device 17. The input device 17 also includes an operation key for inputting the sample number at the time of re-measurement, and an operation key for inputting the dilution factor at the time of re-measurement.

上記のように構成された装置の作用について説
明する。入力装置17より入力されたデータに基
づき、先ず駆動プーリ19a及びサンプルユニツ
ト9aが作動し、サンプリングユニツト18のサ
ンプリングノズル3が指定された検体サンプル9
の真上に移動する。その後、サンプリングノズル
3が移動してその先端が検体サンプル9中に浸さ
れ、サンプリングポンプ5の作動により所定の検
体を吸引し、再び駆動プーリ19aが作動してサ
ンプリングユニツト18が検体希釈ライン上に移
動する。ここで、吸引した検体をサンプリングノ
ズル3より反応管1内に吐出し、さらに希釈用ポ
ンプ5aが作動して希釈用ノズル3aを介して希
釈水が吐出される。このようにして、検体希釈ラ
イン上の反応管に1:1の割合で混合された検体
と希釈水は、再びサンプリングノズル3に吸引さ
れ、反応ライン上の各反応管1に、その検査項目
に応じて所定量分注される。その後駆動ベルト2
が間欠移動し、上記と同じ作用により、指定され
た次の検体が反応ライン上の反応管1に分注され
る。順次検体が分注された反応管1は、図示矢印
E方向に移動して、試薬ノズル11より検査項目
に応じた試薬が分注され、測定部(図示省略)に
移動して所定波長の光を照射することにより吸光
度測定が行われ、その測定値がデータ処理部14
にて演算された後、出力装置(図示省略)より検
体の番号とその分析結果とがプリントされて出力
される。測定者はその分析結果より、先ず標準血
清の分析値とその標準血清の既知である吸光度と
を比較し、装置が正常に作動していることを確認
した後、他の個々の検体について測定のエラー表
示が出力されているか否かをチエツクする。測定
エラー(以下測定不可能ともいう)であるか否か
の判断は、第2図に示す上限吸光度あるいは下限
吸光度の範囲外であるか否かをデータ処理部14
において判断することにより行なわれる。第2図
において、は上昇反応における測定可能な吸光
度であり、図示測定点で上限吸光度以下の吸光度
を示している。これに対して′は同じ上昇反応
でありながら、測定点での吸光度は上限吸光度以
上の値を示しているので測定不可能であると判断
できる。は下降反応における測定可能な吸光度
であり、測定点で下限吸光度以上の吸光度を示し
ているが′の測定点での吸光度は下限吸光度以
下の値を示し、測定不可能とみなすことができ
る。上記のような判断基準及び測定中の吸光度の
変動が一定の基準値を越える様な場合、個々の検
体は、データのエラー表示がなされ、その検体番
号と共に出力される。測定不可能の原因としては
前記に掲げたものが考えられるが、大きく分けて
二つに大別することができる。
The operation of the device configured as above will be explained. Based on the data input from the input device 17, first the drive pulley 19a and the sample unit 9a are operated, and the sampling nozzle 3 of the sampling unit 18 picks up the specified specimen sample 9.
Move directly above. After that, the sampling nozzle 3 is moved so that its tip is immersed in the specimen sample 9, and the sampling pump 5 is activated to aspirate a predetermined specimen, and the drive pulley 19a is activated again to move the sampling unit 18 onto the specimen dilution line. Moving. Here, the aspirated specimen is discharged into the reaction tube 1 from the sampling nozzle 3, and the dilution pump 5a is activated to discharge dilution water through the dilution nozzle 3a. In this way, the sample and dilution water mixed at a ratio of 1:1 in the reaction tube on the sample dilution line are sucked into the sampling nozzle 3 again, and are transferred to each reaction tube 1 on the reaction line for that test item. A predetermined amount is dispensed accordingly. Then drive belt 2
moves intermittently, and the next designated sample is dispensed into the reaction tube 1 on the reaction line by the same action as above. The reaction tube 1 into which the samples have been sequentially dispensed moves in the direction of the arrow E shown in the figure, and the reagent according to the test item is dispensed from the reagent nozzle 11.The reaction tube 1 then moves to the measurement section (not shown) and is exposed to light of a predetermined wavelength. Absorbance measurement is performed by irradiating the
After the calculation is performed, the sample number and the analysis result are printed and output from an output device (not shown). Based on the analysis results, the measurer first compares the analytical value of the standard serum with the known absorbance of that standard serum, and after confirming that the device is working properly, performs measurements on other individual samples. Check whether an error message is output. To determine whether there is a measurement error (hereinafter also referred to as measurement impossible), the data processing unit 14 determines whether the absorbance is outside the upper limit absorbance or lower limit absorbance range shown in FIG.
This is done by making a judgment in the following. In FIG. 2, is the measurable absorbance in the rising reaction, and indicates the absorbance below the upper limit absorbance at the illustrated measurement point. On the other hand, although ' is the same increasing reaction, the absorbance at the measurement point shows a value greater than the upper limit absorbance, so it can be determined that measurement is impossible. is the measurable absorbance in the descending reaction, and the absorbance at the measurement point is above the lower limit absorbance, but the absorbance at the measurement point '' is below the lower limit absorbance and can be considered to be impossible to measure. If the above-mentioned judgment criteria and absorbance fluctuations during measurement exceed a certain standard value, a data error is displayed for each sample and output together with the sample number. The causes of inability to measure can be considered to be the ones listed above, but they can be broadly divided into two.

(A) 検体の異常(検体の高濃度、高単位、色調不
良等) (B) 検体以外の異常(分注時又は撹拌時の気泡発
生、反応管の汚れ等) 原因(B)の場合は突発的なアクシデントであり、
検体サンプル9より一定量の検体を再度取り出し
再測定を行えばよい。尚、図には示していない
が、反応管1は測定終了後、試料が排出され、そ
の後洗浄されているので、再度反応管の汚れに起
因して測定のエラー表示がなされることはないと
考えてよい。
(A) Abnormalities in the sample (high concentration of the sample, high units, poor color tone, etc.) (B) Abnormalities other than the sample (formation of bubbles during dispensing or stirring, staining of the reaction tube, etc.) In case of cause (B) It was a sudden accident,
It is sufficient to take out a certain amount of the specimen again from the specimen sample 9 and perform the re-measurement. Although it is not shown in the figure, the sample is discharged from the reaction tube 1 after the measurement is completed, and the sample is then washed, so there is no possibility that a measurement error will be displayed again due to dirt in the reaction tube. You can think about it.

原因(A)の場合は、同じ条件で再測定しても結果
は同じであるので、検体の条件をかえて再測定し
なければならない。したがつて測定者は測定不可
能の原因を判断した後、原因(B)に起因して測定の
エラー表示がなされた検体に対してはその検体番
号の操作キーを、原因(A)に起因して測定のエラー
表示がなされた検体に対しては、その検体番号及
び希釈倍率を決定する操作キーをそれぞれ操作し
て入力装置17にインプツトする。
In the case of cause (A), the results are the same even if remeasured under the same conditions, so it is necessary to change the sample conditions and remeasure. Therefore, after determining the cause of the inability to measure, the operator should press the operation key corresponding to the sample number for the sample for which a measurement error was displayed due to cause (B), and then press the operation key corresponding to the sample number due to cause (A). For a sample for which a measurement error has been displayed, the operation keys for determining the sample number and dilution factor are input into the input device 17 by operating the respective operation keys.

以上の操作を行うと、反応ラインの全測定が終
了した後、再測定が指定された検体が再び検体希
釈ラインの反応管に分注れ、希釈倍率が指定され
ない場合には再び1:1に希釈し、希釈倍率が指
定された場合には、希釈倍率に応じて例えば1:
10に希釈して再測定が行われる。又、データ処理
での演算処理も希釈倍率が指示されたものに対し
ては、入力装置17より入力された希釈倍率がデ
ータ処理部に入力し、その値が考慮されて行われ
る。
By performing the above operation, after all measurements in the reaction line are completed, the sample for which re-measurement is specified will be dispensed into the reaction tube of the sample dilution line again, and if the dilution ratio is not specified, the sample will be 1:1 again. If diluted and a dilution rate is specified, for example 1:
The sample is diluted to 10 and remeasured. In addition, when the dilution factor is specified, the arithmetic processing in the data processing is performed by inputting the dilution factor input from the input device 17 to the data processing section and taking that value into consideration.

以上本発明の一実施例について詳述したが、本
発明はデイスクリート方式に限らず、フロー方式
等の各種自動化学分析装置に適用可能である。
又、上記の実施例は生化学反応を例にあげ測定不
可能となる原因の中で頻度の高い、分析に供され
る検体の濃度が高すぎた場合に対処できるように
希釈装置を構成し、再測定の能率向上を図つた
が、他の種々の測定では測定不可能となる原因も
種々様々である。従つて、他の種々の自動化学分
析装置に関しては、測定不可能となる原因のそれ
ぞれに対応した付属装置を具備させて、再測定の
能率向上を図ることが望ましい。例えばサンプル
の容量不足に起因して測定のエラー表示がなされ
た場合には、再測定時にサンプルの容量を増加さ
せる付属装置例えば分注装置を具備させることも
できる。尚、測定不可能となる原因が限られ、か
つデータ処理部14の判断回路において、その再
測定時の条件が判断可能である場合には、その信
号を自動的に入力装置17にフイードバツクし、
人手の介入を要さずに、全自動的に再測定を行う
ことも可能である。
Although one embodiment of the present invention has been described in detail above, the present invention is applicable not only to discrete type but also to various automatic chemical analyzers such as flow type.
In addition, in the above embodiment, the dilution device is configured to deal with the case where the concentration of the sample to be analyzed is too high, which is a frequent cause of failure to measure, taking biochemical reactions as an example. , we have tried to improve the efficiency of re-measurement, but there are various reasons why measurements cannot be made in other various measurements. Therefore, with regard to other various automatic chemical analyzers, it is desirable to improve the efficiency of re-measurement by equipping them with auxiliary devices corresponding to each of the causes of inability to measure. For example, if a measurement error is displayed due to insufficient sample volume, an accessory device such as a dispensing device may be provided to increase the sample volume during re-measurement. In addition, if the cause of the inability to measure is limited and the conditions for re-measuring can be determined in the judgment circuit of the data processing section 14, the signal is automatically fed back to the input device 17,
It is also possible to perform remeasurement fully automatically without requiring manual intervention.

本発明は、前記実施例に限定されるものではな
く、この発明の要旨の範囲で種々の変形例を包含
することは言うまでもない。
It goes without saying that the present invention is not limited to the embodiments described above, and includes various modifications within the scope of the invention.

(発明の効果) 以上説明したように本発明により、自動化学分
析装置において測定エラーが発生した検体につい
て、再測定時の適切な希釈倍率が極めて広い範囲
に渡るにも拘らず貴重な検体を無駄に使用するこ
となく迅速に再測定を行うことができる検体の再
測定方法を提供することができる。
(Effects of the Invention) As explained above, according to the present invention, valuable specimens are wasted despite the fact that the appropriate dilution ratio for re-measuring a specimen for which a measurement error has occurred in an automatic chemical analyzer is over a very wide range. It is possible to provide a method for re-measuring a specimen, which allows rapid re-measurement without using the sample.

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

第1図は本発明に係る検体の再測定方法に用い
られる自動化学分析装置の一例を示す図、第2図
は時間と吸光度との関係を示し、測定値の異常を
判断する特性図である。 1…反応管、2…駆動ベルト、3…サンプリン
グノズル、3a…希釈用ノズル、5…サンプリン
グポンプ、5a…希釈用ポンプ、6…希釈水ビ
ン、9…検体サンプル、9a…サンプルユニツ
ト、11…試薬ノズル、14…データ処理部、1
6…駆動制御装置、17…入力装置、18…サン
プリングユニツト、19a…駆動プーリ、19b
…従動プーリ、20…無端ベルト、21…スライ
ド部。
FIG. 1 is a diagram showing an example of an automatic chemical analyzer used in the sample remeasurement method according to the present invention, and FIG. 2 is a characteristic diagram showing the relationship between time and absorbance and determining abnormalities in measured values. . DESCRIPTION OF SYMBOLS 1... Reaction tube, 2... Drive belt, 3... Sampling nozzle, 3a... Dilution nozzle, 5... Sampling pump, 5a... Dilution pump, 6... Dilution water bottle, 9... Specimen sample, 9a... Sample unit, 11... Reagent nozzle, 14...data processing section, 1
6... Drive control device, 17... Input device, 18... Sampling unit, 19a... Drive pulley, 19b
...Followed pulley, 20...Endless belt, 21...Slide portion.

Claims (1)

【特許請求の範囲】[Claims] 1 測定対象としての検体を収容する反応管を列
状に配置してなる反応ラインと、この反応ライン
に併設された希釈部と、検体を収容したサンプル
ユニツト部と、このサンプルユニツト部の検体を
吸引し、前記希釈部に吐出し、希釈された検体を
再度吸引し、前記反応ラインに分注するサンプリ
ング部と、前記反応管に収容された検体の吸光度
を測定する測定部とを備えた自動化学分析装置に
おける検体の再測定方法であつて、前記測定部に
よる該検体の測定結果を所定の値と比較すること
により該測定結果が所定の範囲内であるか否かを
判断し、所定の範囲外である場合には該測定結果
が所定の範囲外となつた原因が該検体の希釈倍率
不適切に起因するものかそれ以外の事由に起因す
るものかを該測定結果に基づいて判断し、該検体
の希釈倍率不適切に起因する場合には該測定結果
に基づいて最適希釈倍率を設定し、前記希釈部に
おいて該最適希釈倍率により該検体を再希釈後前
記反応管に分注して再測定を行い、該検体の希釈
倍率不適切以外の事由に起因する場合には前記希
釈部において前回と同一の希釈倍率により該検体
を再希釈後前記反応管に分注して再測定を行うよ
うにした検体の再測定方法。
1. A reaction line consisting of reaction tubes arranged in a row for containing a sample to be measured, a dilution section attached to this reaction line, a sample unit section containing the sample, and a sample unit section for disposing the sample in the sample unit section. An automatic device comprising: a sampling section for aspirating the sample, discharging it into the diluting section, aspirating the diluted sample again, and dispensing it into the reaction line; and a measuring section for measuring the absorbance of the sample contained in the reaction tube. A method for re-measuring a sample in a chemical analyzer, in which it is determined whether the measurement result is within a predetermined range by comparing the measurement result of the sample by the measurement section with a predetermined value, and If the measurement result is outside the specified range, it is determined based on the measurement result whether the cause of the measurement result being outside the specified range is due to an inappropriate dilution ratio of the sample or other reasons. If this is due to an inappropriate dilution ratio of the specimen, set an optimal dilution ratio based on the measurement results, re-dilute the specimen according to the optimal dilution ratio in the dilution section, and then dispense it into the reaction tube. Perform re-measurement, and if the dilution rate of the sample is due to reasons other than inappropriateness, re-dilute the sample at the same dilution rate as the previous time in the dilution section, dispense it into the reaction tube, and perform re-measurement. How to re-measure the sample.
JP18690881A 1981-11-24 1981-11-24 Automatic chemical analyzer Granted JPS5888662A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18690881A JPS5888662A (en) 1981-11-24 1981-11-24 Automatic chemical analyzer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18690881A JPS5888662A (en) 1981-11-24 1981-11-24 Automatic chemical analyzer

Publications (2)

Publication Number Publication Date
JPS5888662A JPS5888662A (en) 1983-05-26
JPH0437384B2 true JPH0437384B2 (en) 1992-06-19

Family

ID=16196782

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18690881A Granted JPS5888662A (en) 1981-11-24 1981-11-24 Automatic chemical analyzer

Country Status (1)

Country Link
JP (1) JPS5888662A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60114764A (en) * 1983-11-28 1985-06-21 Fujikura Ltd Measurement of oxygen concentration
JP4083339B2 (en) * 1999-03-30 2008-04-30 オリンパス株式会社 Analysis equipment

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55122157A (en) * 1979-03-14 1980-09-19 Olympus Optical Co Ltd Automatic analyzer
JPS56108957A (en) * 1980-02-01 1981-08-28 Hitachi Ltd Automatic chemical analytical apparatus

Also Published As

Publication number Publication date
JPS5888662A (en) 1983-05-26

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