JPS6324164A - Automatic biochemical anlayzing instrument - Google Patents
Automatic biochemical anlayzing instrumentInfo
- Publication number
- JPS6324164A JPS6324164A JP15214286A JP15214286A JPS6324164A JP S6324164 A JPS6324164 A JP S6324164A JP 15214286 A JP15214286 A JP 15214286A JP 15214286 A JP15214286 A JP 15214286A JP S6324164 A JPS6324164 A JP S6324164A
- Authority
- JP
- Japan
- Prior art keywords
- dilution
- standard solution
- sample
- diluted
- analysis
- 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
- 239000012895 dilution Substances 0.000 claims abstract description 62
- 238000010790 dilution Methods 0.000 claims abstract description 62
- 238000004458 analytical method Methods 0.000 claims abstract description 24
- 238000012742 biochemical analysis Methods 0.000 claims abstract description 20
- 238000001514 detection method Methods 0.000 claims abstract description 15
- 239000012086 standard solution Substances 0.000 claims description 52
- 239000000523 sample Substances 0.000 claims description 39
- 238000004364 calculation method Methods 0.000 claims description 16
- 239000012470 diluted sample Substances 0.000 claims description 12
- 238000012360 testing method Methods 0.000 claims description 5
- 238000000034 method Methods 0.000 claims 1
- 239000007788 liquid Substances 0.000 abstract description 8
- 238000012937 correction Methods 0.000 abstract description 6
- 238000007865 diluting Methods 0.000 abstract 1
- 238000005070 sampling Methods 0.000 description 8
- 238000004140 cleaning Methods 0.000 description 5
- 238000010586 diagram Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 238000005457 optimization Methods 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 241000123813 Lutjanus cyanopterus Species 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 239000012472 biological sample Substances 0.000 description 1
- 239000012295 chemical reaction liquid Substances 0.000 description 1
- 238000003113 dilution method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Landscapes
- Automatic Analysis And Handling Materials Therefor (AREA)
Abstract
Description
【発明の詳細な説明】
0産業上の利用分野
この発明は、生化学自動分析装置に関する。さらに詳し
くは、生体試料を一定倍率で希釈した後その所定量を繰
返し生化学分析部へ供給して多項目分析を行なうよう構
成された多項目生化学分析装置に関する。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application This invention relates to an automatic biochemical analyzer. More specifically, the present invention relates to a multi-item biochemical analyzer configured to dilute a biological sample at a constant ratio and then repeatedly supply a predetermined amount of the diluted sample to a biochemical analysis section to perform multi-item analysis.
(ロ)従来の技術
近年、臨床化学検査に用いる生化学自8分析装置として
は、検体の微是化のニーズに応じて検体を希釈した後口
の希釈液をサンプリングして生化学分析部へ供給して分
析する装置が増えており、ことに多項目分析を行なう装
置においては比較的多量の検体を要するため、かかる希
釈方式の装置が用いられている。(B) Conventional technology In recent years, biochemistry automatic 8 analyzers used in clinical chemistry tests have been used to dilute the sample and then sample the diluted solution and send it to the biochemical analysis department. The number of devices that supply and analyze samples is increasing, and in particular, devices that perform multi-item analysis require a relatively large amount of specimen, so such dilution type devices are being used.
このような希釈方式の多項目生化学自動分析装置におい
ては、通常、複数の試料容器を配列した試料ライン及び
これに対応して複数の希釈容器を配列した希釈ラインが
備えられ、試料容器内の試料(検体)は、適当な移動希
釈分注器によって希釈容器内へ所定倍率(通常5〜20
倍)で希釈分注され次いでこの希釈試料が各項目測定毎
に繰返し生化学分析部へ供給されて分析に供される。そ
して、較正用の標準液としては、希釈試料に対応する既
知濃度の希釈標準液が予め調製して用いられ、この希釈
標準液を上記分注器で直接生化学分析部へ供給した際の
検知出力とその標準液濃度に基づいて、各項目について
の試料中の濃度が算出されており、この較正は所定の分
析サイクル毎に更新されている。Such a dilution type multi-item automatic biochemical analyzer is usually equipped with a sample line in which a plurality of sample containers are arranged and a corresponding dilution line in which a plurality of dilution containers are arranged. The sample (specimen) is poured into a dilution container using an appropriate mobile dilution dispenser at a predetermined magnification (usually 5 to 20
This diluted sample is then repeatedly supplied to the biochemical analysis section for analysis for each item measurement. As the standard solution for calibration, a diluted standard solution with a known concentration corresponding to the diluted sample is prepared in advance and used, and detection is performed when this diluted standard solution is directly supplied to the biochemical analysis department using the above-mentioned dispenser. The concentration of each item in the sample is calculated based on the output and its standard solution concentration, and this calibration is updated every predetermined analysis cycle.
(ハ)発明が解決しようとする問題点
しかしながら、上記希釈方式の分析装置においては、移
動希釈分注器という橢械的な希釈分注手段を用いている
ため、希釈倍率の態様的誤差ことに系統的誤差が生じ易
く、一定の希釈倍率に対応して調製した前記希釈標準液
をベースとして分析演算を行なった際に、無視し得ない
誤差を生じるという問題点があった。ことに微m試料(
例えば10通程度)を対象して分析を行なった場合、例
えば20倍希釈に設定すると濃度として± 1〜2%程
度の誤差を生じる不都合がある。(c) Problems to be solved by the invention However, since the above-mentioned dilution type analyzer uses a mechanical dilution dispensing means called a moving dilution dispenser, it is prone to errors in the dilution ratio. There is a problem in that systematic errors are likely to occur, and when analytical calculations are performed based on the diluted standard solution prepared in accordance with a fixed dilution ratio, non-negligible errors occur. In particular, micrometer samples (
For example, when an analysis is performed on about 10 samples, for example, if the dilution is set to 20 times, there is an inconvenience that the concentration error will be about ±1 to 2%.
従って、未希釈の標準液を試料容器に導入し、試料と同
条件で分注器による希釈操作を介して分析部へ供給して
較正を行なうのが理想的であるが、この場合には校正時
毎に試料容器への標準液の導入、セットや制御モードの
設定等の操作を要し煩雑であるという問題点があった。Therefore, it is ideal to introduce an undiluted standard solution into a sample container and supply it to the analysis department through a dilution operation using a pipettor under the same conditions as the sample. There is a problem in that operations such as introducing the standard solution into the sample container, setting the set, and control mode are required every time, which is complicated.
この発明は、かかる状況に鑑みなされたものであり、こ
とに簡便な操作で較正の適正化を行ないうる希釈方式の
多項目生化学自動分析装置を提供しようとするものであ
る。The present invention has been made in view of this situation, and it is an object of the present invention to provide a multi-item biochemical automatic analyzer using a dilution method, which allows optimization of calibration with a particularly simple operation.
(ニ)問題点を解決しようとする手段
かくしてこの発明によれば(al複数の試料容器を配グ
1した試料ライン及びこれに対応して複数の希釈容器を
配列した希釈ラインと(b)既知濃度の希釈標準液を貯
留する標準液貯槽と(C)多項目分析を行なう生化学分
析部と(d+上記試料容器内の試料を吸引し希釈容器内
へ所定倍率で希釈分注し次いでこの希釈試料の所定量を
吸引し生化学分析部へ繰返し分別供給すると共に、所定
の分析サイクル毎に上記標準液貯槽中の希釈標準液を吸
引して生化学分析部へ直接供給しうる移動希釈分注手段
とtel希釈標準液の濃度及び生化学分析部への供給時
の検知出力に基づいて各試料中の被検成分の濃度を算出
する演算部とを備え、
上記試料容器内に試料の代わりに未希釈標準液を導入し
移動希釈分注手段による希釈分注操作を介して生化学分
析部へ供給した際の検知出力Aにより、算出演算のベー
スとなる希釈標準液の濃度を各項目について下式: (
■)
C=Co −A/B−−(I>
C式中、Cは補正された希釈標準液の演算用濃度、Co
は実際の希釈標準液の濃度、Bは希釈標準液の検知出力
を示す〕
に基づいて補正する補正演算部を具備したことを特徴と
する生化学自動分析装置が提供される。(d) Means for solving the problem According to the present invention, (a) a sample line in which a plurality of sample containers are arranged and a dilution line in which a plurality of dilution containers are arranged correspondingly; (C) A biochemical analysis section that performs multi-item analysis; A mobile dilution dispenser that can aspirate a predetermined amount of sample and repeatedly separate and supply it to the biochemical analysis department, as well as aspirate the diluted standard solution in the standard solution storage tank and supply it directly to the biochemical analysis department every predetermined analysis cycle. and a calculation unit that calculates the concentration of the test component in each sample based on the concentration of the TEL diluted standard solution and the detection output when supplied to the biochemical analysis unit, Based on the detection output A when the undiluted standard solution is introduced and supplied to the biochemical analysis department through the dilution dispensing operation using the mobile dilution dispensing means, the concentration of the diluted standard solution is calculated for each item, which is the basis for calculation. Formula: (
■) C=Co -A/B--(I>C In the formula, C is the concentration for calculation of the corrected diluted standard solution, Co
represents the actual concentration of the diluted standard solution, and B represents the detection output of the diluted standard solution.
くホ)作 用
この発明の装置においては、上記式(I>に基づいて、
所定分析サイクル毎に較正に供される希釈標準液の算出
演算用の濃度が補正される。即ち、未希釈標準液を希釈
分注操作を介して分析部へ供給した際の出力と予め希釈
調製された標準液を供給した際の出力との相違は、希釈
分注手段の希釈操作による設定希釈倍率と実際の希釈倍
率との差異に対応するため、前者の検知出力へを後者の
検知出力Bで除した係数を希釈標準液の設定濃度Coに
乗することにより算出演算に用いる希釈襟準液′a度値
を適正化することができ、希釈分注操作による誤差を解
消することができる。ざらに、かかる適正化のための操
作は、較正毎に行なう必要はなく、長期間(例えば、1
ケ月程度)毎で充分であり、操作上の煩雑さを招くこと
もない。In the device of the present invention, based on the above formula (I>),
The concentration for calculation of the diluted standard solution used for calibration is corrected every predetermined analysis cycle. In other words, the difference between the output when an undiluted standard solution is supplied to the analysis section through the dilution dispensing operation and the output when a pre-diluted standard solution is supplied is due to the setting by the dilution operation of the dilution dispensing means. In order to deal with the difference between the dilution ratio and the actual dilution ratio, the dilution standard used for calculation is calculated by multiplying the set concentration Co of the diluted standard solution by a coefficient obtained by dividing the detection output of the former by the detection output B of the latter. The liquid'a degree value can be optimized, and errors caused by dilution and dispensing operations can be eliminated. In general, such optimization operations do not need to be performed for every calibration, but for a long period of time (e.g.
It is sufficient to do this every month or so, and it does not cause any operational complications.
(へ)実施例
第1図は、この発明の生化学自動分析装置の一実施例を
示す構成説明図であり、第2図はその一部を示す平面構
成説明図である。図において生化学自動分析装置1は、
複数の試料容器21を配列した試料ライン2及び複数の
希釈容器31を配列した希釈ライン3を有するサンプリ
ングテーブル4と、既知濃度の被検成分を各々含有する
希釈標準液の貯槽5と、多項目分析を行なう生化学分析
部6と、試料のサンプリング、希釈、移送等を行なう回
転移動式希釈分注器7と、制御部9と、表示部10とか
ら基本構成されてなる。なお、8は洗浄液貯槽である。(F) Embodiment FIG. 1 is an explanatory diagram showing the configuration of an embodiment of the automatic biochemical analyzer of the present invention, and FIG. 2 is a plan explanatory diagram showing a part of the configuration. In the figure, the biochemical automatic analyzer 1 is
A sampling table 4 having a sample line 2 in which a plurality of sample containers 21 are arranged and a dilution line 3 in which a plurality of dilution containers 31 are arranged, a storage tank 5 for a diluted standard solution each containing a test component of a known concentration, and a multi-item It basically consists of a biochemical analysis section 6 that performs analysis, a rotationally movable dilution dispenser 7 that performs sample sampling, dilution, transfer, etc., a control section 9, and a display section 10. Note that 8 is a cleaning liquid storage tank.
生化学分析部6は、反応キュベツト61を連続的に配列
したターンテーブル62と、この透明の反応キュベツト
61内に所定項目測定用の一種又は二種の試薬を(例え
ば、GOT、CPK、△しP、BtJN等の光学測定用
試薬)を選択して分注する反応試薬分注器63と、光源
、分光手段及び受光器を備え反応キュベツト内の反応液
の所定波長における吸光度を検知する検出器64から構
成されてなる。そして、希釈分注器7は、第2図に示す
ように試料ライン上の試料吸引位置b、希釈ライン上の
希釈試料吐出・吸引位wa、希釈標準液吸引位置C、ノ
ズル71の洗浄位置d及び反応キュベツトへの吐出位置
eの間を移動し、ノズルを上下させて吸引、吐出動作を
行なう。具体的には、試料容器内の試料の吸引(位置b
)→希釈容器内l\の試料の希釈吐出(位置a)→ノズ
ルの洗浄(位置d)→希釈容器内の希釈試料の一部の吸
引(位置a)→反応キュベツトへの希釈試料の吐出(位
置e〉からなる試料サンプリング操作と、希釈標準液の
吸引(位Z、c)→反応キュベツトへの希釈標準液の吐
出(位置e)からなる標準液サンプリング操作を行なう
。標準液サンプリング操作は、ターンテーブル分析毎に
行なわれる。その既知濃度値と検知出力との比亭に基づ
いて試料中の所定項目の濃度が演算され[例えば、m度
−試料の出力×(希釈標準液の出力×希釈倍率/希釈標
準液の出力コ、表示部10で表示される。The biochemical analysis section 6 includes a turntable 62 on which reaction cuvettes 61 are continuously arranged, and one or two types of reagents for measuring a predetermined item (for example, GOT, CPK, A reaction reagent dispenser 63 for selecting and dispensing a reagent for optical measurement such as P, BtJN, etc.; and a detector for detecting the absorbance at a predetermined wavelength of the reaction liquid in the reaction cuvette, which is equipped with a light source, a spectroscopic means, and a light receiver. It consists of 64. As shown in FIG. 2, the dilution dispenser 7 has a sample suction position b on the sample line, a diluted sample discharge/suction position wa on the dilution line, a diluted standard solution suction position C, and a cleaning position d of the nozzle 71. and the discharge position e into the reaction cuvette, and the nozzle is moved up and down to perform suction and discharge operations. Specifically, aspirating the sample in the sample container (position b
) → Discharge of diluted sample in the dilution container l\ (position a) → Cleaning of the nozzle (position d) → Aspiration of a part of the diluted sample in the dilution container (position a) → Discharge of the diluted sample into the reaction cuvette ( Perform the sample sampling operation consisting of position e〉 and the standard solution sampling operation consisting of suction of the diluted standard solution (position Z, c) → discharge of the diluted standard solution into the reaction cuvette (position e).The standard solution sampling operation consists of: The concentration of a predetermined item in the sample is calculated based on the ratio between the known concentration value and the detection output [for example, m degrees - output of the sample x (output of the diluted standard solution x dilution). The output of the magnification/dilution standard solution is displayed on the display unit 10.
一方、制御部9は、サンプリングテーブル、希釈分注器
、生化学分析部等の駆動を予め定められたプログラムに
従ってマイクロコンピュータで制御すると共に、上記所
定項目の濃度を算出する演算部を有し、さらに補正演算
部を備えている。補正演算部は試料の代わりに未希釈標
準液を用いて前記試料サンプリング操作を行なった際に
得られる検知出力により、試料中の濃度の算出演算ベー
スに用いる希釈標準液の濃度を下式(I):%式%
[式中、Cは補正された希釈標準液の演算用濃度、C0
は実際の希釈標準液の濃度、Aは未希釈標準液の検知出
力、Bは希釈標準液の検知出力を示すコ
に基づいて補正を行なう。なお、上記各数値は、複数回
測定による平均値を採用するのが好ましく、通常、3回
の平均値を用いるのが最適である。これらの補正演算及
び平均値モードの採用は、キーボード等による外部入力
により行なわれる。On the other hand, the control unit 9 controls the driving of the sampling table, dilution dispenser, biochemical analysis unit, etc. with a microcomputer according to a predetermined program, and has a calculation unit that calculates the concentration of the above-mentioned predetermined items, Furthermore, it is equipped with a correction calculation section. The correction calculation unit uses the detection output obtained when performing the sample sampling operation using the undiluted standard solution instead of the sample to calculate the concentration of the diluted standard solution used as the calculation base for the concentration in the sample using the following formula (I ):% formula % [In the formula, C is the concentration for calculation of the corrected diluted standard solution, C0
Correction is made based on the actual concentration of the diluted standard solution, A the detection output of the undiluted standard solution, and B the detection output of the diluted standard solution. In addition, it is preferable to adopt the average value of multiple measurements for each of the above-mentioned numerical values, and it is usually optimal to use the average value of three measurements. These correction calculations and adoption of the average value mode are performed by external input using a keyboard or the like.
かかる生化学自動分析装置1において、各試料ライン2
に血清等の試料が導入された試料容器21が順次配列さ
れ、かつ希釈ライン3に空の希釈容器31を配列した状
態で、希釈分注器7は位置Cにおいて希釈標準液く未希
釈標準液の20倍希釈液)を吸引し位置eでキュベツト
61内へ分注し、これにより分析部6で得られる検知出
力が外部入力される希釈標準液の濃度と共に演算部内に
記憶される。これは各項目について行なわれる。In such an automatic biochemical analyzer 1, each sample line 2
With the sample containers 21 into which samples such as serum have been introduced are arranged in sequence, and the empty dilution containers 31 are arranged in the dilution line 3, the dilution dispenser 7 dispenses the diluted standard solution and undiluted standard solution at position C. A 20-fold diluted solution) is aspirated and dispensed into the cuvette 61 at position e, and the detection output obtained by the analysis section 6 is stored in the calculation section together with the concentration of the diluted standard solution inputted from the outside. This is done for each item.
次いでノズル洗浄の後、位置すにおいて試料の吸引、位
置aにおける希釈分注(設定希釈倍数は上記と同じで2
0倍)、続いてノズル洗浄後の位置aにおける希釈吸引
及び位置eにおける希釈試料の吐出(分注)が行なわれ
、これが繰返されて多項目に対応する数の希釈試料がキ
ュベラ1−61に連続的に導入され、分析部6で前記希
釈標準液の′&1度及び出力に基づいて各項目について
の濃度か算出される。所定数の試料について分析を行な
った後、再び希釈標準液による較正が行なわれ、この較
正も所定分析サイクル毎に行なわれるが、さらに所定の
較正回数毎に前記式<I>による希釈標準液の濃度値の
補正が各項目について行なわれ、希釈分注操作による希
釈誤差が是正されることとなる。かかる補正は、通常の
病院のルーチン検査においては1力月に一度程度で充分
であり、これにより正確度の高い多項目分析を簡便に行
なうことかできることとなる。Next, after cleaning the nozzle, the sample is aspirated at position a, and the diluted sample is dispensed at position a (the set dilution factor is the same as above, 2).
After cleaning the nozzle, the diluted sample is suctioned at position a and the diluted sample is discharged (dispensed) at position e, and this is repeated until a number of diluted samples corresponding to the multiple items are transferred to Cubera 1-61. The diluted standard solution is introduced continuously, and the concentration of each item is calculated in the analysis section 6 based on the diluted standard solution'&1 degree and the output. After analyzing a predetermined number of samples, calibration is performed again using a diluted standard solution, and this calibration is also performed every predetermined analysis cycle. Concentration values are corrected for each item, and dilution errors due to dilution and dispensing operations are corrected. It is sufficient to perform such a correction once a month in routine examinations at a normal hospital, and this makes it possible to easily perform multi-item analysis with high accuracy.
(ト)発明の効果
この発明の生化学自動分析装置によれば、較正毎に標準
液の試料容器への導入することなく、正確度の高い多項
目分析を行なうことができる。従って、大量の試料の多
項目生化学分析を行なうルーチン検査用の分析装置とし
て極めて有用である。(G) Effects of the Invention According to the automatic biochemical analyzer of the present invention, highly accurate multi-item analysis can be performed without introducing a standard solution into a sample container for each calibration. Therefore, it is extremely useful as an analyzer for routine testing that performs multi-item biochemical analysis of a large amount of samples.
第1図は、この発明の生化学自動分析装置の一実施例を
示す構成説明図、第2図は同じくその一部を示す平面構
成説明図である。
1・・・・・・生化学自動分析装置、2・・・・・・試
料ライン、3・・・・・・希釈ライン、4・・・・・・
サンプリングテーブル、5・・・・・・標準液貯蔵、6
・・・・・・生化学分析部、7・・・・・・回転移動式
希釈分注器、9・・・・・・制御部、21・・・・・・
試料容器、31・・・・・・希釈容器。FIG. 1 is a structural explanatory diagram showing one embodiment of an automatic biochemical analyzer of the present invention, and FIG. 2 is a planar structural explanatory diagram showing a part of the same. 1... Biochemical automatic analyzer, 2... Sample line, 3... Dilution line, 4...
Sampling table, 5...Standard solution storage, 6
...Biochemical analysis department, 7...Rotating and moving dilution dispenser, 9...Control section, 21...
Sample container, 31... Dilution container.
Claims (1)
れに対応して複数の希釈容器を配列した希釈ラインと(
b)既知濃度の希釈標準液を貯留する標準液貯槽と(c
)多項目分析を行なう生化学分析部と(d)上記試料容
器内の試料を吸引し希釈容器内へ所定倍率で希釈分注し
次いでこの希釈試料の所定量を吸引し生化学分析部へ繰
返し分別供給すると共に、所定の分析サイクル毎に上記
標準液貯槽中の希釈標準液を吸引して生化学分析部へ直
接供給しうる移動希釈分注手段と(e)希釈標準液の濃
度及び生化学分析部への供給時の検知出力に基づいて各
試料中の被検成分の濃度を算出する演算部とを備え、上
記試料容器内に試料の代わりに未希釈標準液を導入し移
動希釈分注手段による希釈分注操作を介して生化学分析
部へ供給した際の検知出力Aにより、算出演算のベース
となる希釈標準液の濃度を各項目について下式:( I
) C=Co・A/B……( I ) 〔式中、Cは補正された希釈標準液の演算用濃度、Co
は実際の希釈標準液の濃度、Bは希釈標準液の検知出力
を示す〕 に基づいて補正する補正演算部を具備したことを特徴と
する生化学自動分析装置。[Scope of Claims] 1. (a) A sample line in which a plurality of sample containers are arranged, a dilution line in which a plurality of dilution containers are arranged correspondingly, and (
b) A standard solution storage tank for storing a diluted standard solution of known concentration;
) A biochemical analysis department that performs multi-item analysis; and (d) the sample in the sample container is aspirated, diluted and dispensed at a predetermined ratio into a dilution container, and then a predetermined amount of this diluted sample is aspirated and repeated to the biochemical analysis department. A mobile dilution/dispensing means that can separately supply the diluted standard solution and aspirate the diluted standard solution in the standard solution storage tank for each predetermined analysis cycle and directly supply it to the biochemical analysis section; and (e) the concentration and biochemistry of the diluted standard solution. It is equipped with a calculation unit that calculates the concentration of the test component in each sample based on the detection output when it is supplied to the analysis unit, and an undiluted standard solution is introduced in place of the sample into the sample container, allowing for mobile dilution and dispensing. Based on the detection output A when supplied to the biochemical analysis department through the dilution and dispensing operation using the method, the concentration of the diluted standard solution, which is the basis for calculation, can be calculated using the following formula for each item: (I
) C=Co・A/B...(I) [In the formula, C is the concentration for calculation of the corrected diluted standard solution, Co
represents the actual concentration of the diluted standard solution, and B represents the detection output of the diluted standard solution.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15214286A JPS6324164A (en) | 1986-06-27 | 1986-06-27 | Automatic biochemical anlayzing instrument |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15214286A JPS6324164A (en) | 1986-06-27 | 1986-06-27 | Automatic biochemical anlayzing instrument |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6324164A true JPS6324164A (en) | 1988-02-01 |
JPH0363025B2 JPH0363025B2 (en) | 1991-09-27 |
Family
ID=15533952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15214286A Granted JPS6324164A (en) | 1986-06-27 | 1986-06-27 | Automatic biochemical anlayzing instrument |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6324164A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010025951A (en) * | 2009-11-02 | 2010-02-04 | Hitachi High-Technologies Corp | Autoanalyzer and operating method for autoanalyzer |
US8758685B2 (en) | 2007-09-10 | 2014-06-24 | Hitachi High-Technologies Corporation | Automatic analyzer and operating method for same |
-
1986
- 1986-06-27 JP JP15214286A patent/JPS6324164A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8758685B2 (en) | 2007-09-10 | 2014-06-24 | Hitachi High-Technologies Corporation | Automatic analyzer and operating method for same |
JP2010025951A (en) * | 2009-11-02 | 2010-02-04 | Hitachi High-Technologies Corp | Autoanalyzer and operating method for autoanalyzer |
Also Published As
Publication number | Publication date |
---|---|
JPH0363025B2 (en) | 1991-09-27 |
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