JPS60205346A - Flow-through type analysis device - Google Patents

Flow-through type analysis device

Info

Publication number
JPS60205346A
JPS60205346A JP6463884A JP6463884A JPS60205346A JP S60205346 A JPS60205346 A JP S60205346A JP 6463884 A JP6463884 A JP 6463884A JP 6463884 A JP6463884 A JP 6463884A JP S60205346 A JPS60205346 A JP S60205346A
Authority
JP
Japan
Prior art keywords
specimen
concn
flow rate
sample
specified
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.)
Pending
Application number
JP6463884A
Other languages
Japanese (ja)
Inventor
Masabumi Uejima
上島 正文
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.)
Shimadzu Corp
Shimazu Seisakusho KK
Original Assignee
Shimadzu Corp
Shimazu Seisakusho KK
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 Shimadzu Corp, Shimazu Seisakusho KK filed Critical Shimadzu Corp
Priority to JP6463884A priority Critical patent/JPS60205346A/en
Publication of JPS60205346A publication Critical patent/JPS60205346A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/001Enzyme electrodes
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/28Electrolytic cell components
    • G01N27/30Electrodes, e.g. test electrodes; Half-cells
    • G01N27/327Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
    • G01N27/3271Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Physics & Mathematics (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Immunology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Analytical Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Hematology (AREA)
  • Biotechnology (AREA)
  • Electrochemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)

Abstract

PURPOSE:To enable exact control of specimen concn. with a simple operation by injecting a specimen into a buffer soln. at the flow rate which is made inversely proportional to the concn. of a component in order to analyze a specified amt. of specimen. CONSTITUTION:A specimen is uniformly diffused with a specified flow rate of a buffer soln. during passage through a coil 8 for diffusing sample and arrives at glucose oxidase 11b immobilized to an electrode 11 after dilution to a specified rate when the specimen is injected into a pipe 5 at a specified rate Q0 per unit time at a discharge flow rate V1 from a sample injector 1 while the buffer soln. is fed into said pipe by operating a pump 6. The glucose oxidase generates the hydrogen peroxide proportional to the concn. of glucose while consuming the dissolved oxygen of the buffer soln. by receiving the effect thereof and the signal proportional to said concn. is emitted from the sensitive surface 11a of the electrode formed integrally therewith. When the flow rate is decreased to V2 by decreasing the frequency of an oscillator 2 in the stage of analyzing the specimen at a high concn., the amt. of the specimen decreases and the concn. of the glucose decreases in proportion as well. The specimen is thus detected with high linearity without inducing saturation.

Description

【発明の詳細な説明】 イ、技術の利用分野 本発明は、固定化酵素を使用したフロースル型分析装置
に関する。
DETAILED DESCRIPTION OF THE INVENTION A. Field of Application of the Technology The present invention relates to a flow-through type analyzer using immobilized enzymes.

口、従来技術 電極面に酵素を固定した固定化酵素電極は、保守、管理
が容易なこともあってフロースル型分析装置の検出器と
して数多く使用されている。
2. Description of the Related Art Immobilized enzyme electrodes, in which enzymes are immobilized on the electrode surface, are often used as detectors in flow-through type analyzers because they are easy to maintain and manage.

ところが、固定化酵素電極は、バッファ液に含まれる特
定成分との反応により生成した成分を介して目的成分を
検出するため、限られた濃度範囲においてだけ直線性を
示す。このため、検体をやめ希釈してから分析装置に注
入したり、へンファ流路内に検体を微小場だけ注入して
バッファ液により希釈しながら検出することが行なわれ
るが、前者の手法では、分析に先立って検体を希釈する
ための前処理工程が必要となって自動化の障害となり、
また後者の手法では微小酸の計1の困難性が故に検体の
計量に誤差を含み易く、分析結果の信頼性に低下を来た
すといった問題がある。
However, since the immobilized enzyme electrode detects the target component via a component generated by reaction with a specific component contained in the buffer solution, it exhibits linearity only in a limited concentration range. For this reason, the sample is stopped and diluted before being injected into the analyzer, or the sample is injected into the hemp flow path in a small field and detected while being diluted with a buffer solution, but in the former method, A pretreatment step is required to dilute the sample prior to analysis, which poses an obstacle to automation.
Furthermore, the latter method has the problem that the measurement of the sample is likely to include errors due to the difficulty of measuring small acids, which reduces the reliability of the analysis results.

ハ、目的 本発明はこのような問題に鑑み、固定化酵素電極を使用
して高い分析精度を得ることができるフロースル型分析
装置を提供することを目的とする。
C. Objectives In view of the above-mentioned problems, an object of the present invention is to provide a flow-through type analyzer that can obtain high analysis accuracy using an immobilized enzyme electrode.

二0発明の構成 すなわち本発明の特徴とするところは、一定量の検体を
分析すべき成分の濃度に反比例させた流速によりバッフ
ァ液中に検体を注入するようにした点にある。
The structure of the present invention, that is, the feature of the present invention is that a fixed amount of the sample is injected into the buffer solution at a flow rate that is inversely proportional to the concentration of the component to be analyzed.

ホ、実施例 そこで、以下に本発明の詳細を図示した実施例に基づい
て説明する。
E. Embodiments The details of the present invention will be explained below based on illustrated embodiments.

第1図は、本発明の実施例を示すものであって、図中符
号1は、試料注入装置で、パルス発振器2からの出力に
より回転駆動されるパルスモータ1aと、このモータの
回転数に比例した流速で吐出するシリンジlbとからな
り、吐出口に分岐管を接続してそれぞれに1弁1c、1
dを介して試ネ111人口3と試料液槽4に適過させ、
パルス発振器2の周波数を調整することにより吐出流速
、つまり単位時間当りの試料注入量を変化できるように
構成されている。5は、一端がポンプ6を介してバッフ
γ液槽7′に、他端が試料拡散用コイル8に接続するバ
ッファ液移送パイプで、試料注入装置lの吐出[1に接
続するパイプを突出させて試ネ;l注入1−13が設け
られている。9は、一端が試料拡散用コイル8の流出側
に、他端が廃液槽10に連通ずるフローセルで、第2図
に示したように退化酸化水素検出電極の感応面11aに
グルコースオキシダーゼ(COD)l l bを固定化
してなるグルコース検出1rL極11を設けて構成され
ている。
FIG. 1 shows an embodiment of the present invention, in which reference numeral 1 indicates a sample injection device, and a pulse motor 1a that is rotationally driven by the output from a pulse oscillator 2, and a pulse motor 1a that is driven to rotate by the output from a pulse oscillator 2. It consists of a syringe lb that discharges at a proportional flow rate, and a branch pipe is connected to the discharge port, and one valve 1c and one valve 1 are connected to the discharge port.
d to test sample 111 population 3 and sample liquid tank 4,
By adjusting the frequency of the pulse oscillator 2, the discharge flow rate, that is, the amount of sample injected per unit time can be changed. 5 is a buffer liquid transfer pipe whose one end is connected to the buffer γ liquid tank 7' via the pump 6 and the other end is connected to the sample diffusion coil 8; Injections 1-13 are provided. Reference numeral 9 denotes a flow cell whose one end communicates with the outflow side of the sample diffusion coil 8 and the other end communicates with the waste liquid tank 10. As shown in FIG. It is configured by providing a glucose detection 1rL pole 11 formed by immobilizing llb.

この実施例において、ポンプ6を作動してバイブ5内に
一定波量によりバッファ液を送給している状態で、試料
注入装置1から一定串Qoの検体を吐出流速v1で単位
時間当り、Qlの検体を注入すると(第3図工)、検体
は試料拡散用コイル8を通る間にパンツγ液に均一に拡
散して一定比率に島釈され、電J4i11に固定化され
ているグルコースオキシダーゼllbに41達する。グ
ルコースオキシダーゼllbに到達した検体中のグルコ
ースは、グルコースオキシダーゼの作用を受け、バッフ
ァ液の溶存酸素を消費しながらグルコース濃度に比例し
た過酸化水素を発生し、一体重に形成された適化酸化水
素電極の感応面11aによりグルコースの濃度に比例し
た信号が出力される。
In this embodiment, while the pump 6 is operated to feed the buffer solution into the vibrator 5 at a constant wave rate, a constant skewer of the sample Qo is discharged from the sample injection device 1 at a flow rate v1 and Ql per unit time. When the sample is injected (Fig. 3), the sample is uniformly diffused into the Pant's γ liquid while passing through the sample diffusion coil 8, and is aliquoted at a constant ratio, and then transferred to the glucose oxidase Ilb immobilized on the electric J4i11. Reach 41. Glucose in the sample that has reached glucose oxidase 1lb is acted upon by glucose oxidase, which consumes dissolved oxygen in the buffer solution and generates hydrogen peroxide in proportion to the glucose concentration. The sensitive surface 11a of the electrode outputs a signal proportional to the glucose concentration.

次に、高い濃度でグルコースを含む検体の分析に当って
は、パルス発振器2の発振周波数をドげて試ネ;]注入
装置lからの検体の吐出波速を■2に才で下げる。これ
により八ツファ液単位体積当りの検体量が低下しく同図
II)、これに比例してグルコースの濃度も検出に適し
た濃度にまで低下し、飽和を起すことなく高い直線性を
もって検出電極11により検出される。
Next, when analyzing a sample containing a high concentration of glucose, try lowering the oscillation frequency of the pulse oscillator 2;] lower the wave velocity of the sample ejected from the injection device 1 to 2; As a result, the amount of sample per unit volume of Yatsufa liquid decreases (Fig. Detected by

なお、この実施例においては、グルコースの分析に例を
採って説明したが、他の固定化酸素、例えばユリアーゼ
を利用した尿素の分析に対しても、同様の作用により高
い直線性を持って分析することができる。また、この実
施例においては、モータの回転数を制御して吐出流速を
調整するようにしたが、無段変速機構を使用してもよく
、さらには回転型ポンプを使用しても同様の作用を奏す
ることは言うまでもない。
Although this example has been explained using the analysis of glucose as an example, the same effect can be applied to the analysis of urea using other fixed oxygen, such as urea, with high linearity. can do. In addition, in this embodiment, the discharge flow rate was adjusted by controlling the rotation speed of the motor, but a continuously variable transmission mechanism may be used, or even a rotary pump may be used to achieve the same effect. Needless to say, it plays.

へ、効果 以上、説明したように本発明によれば、フローセルにバ
ッファ液を給送する管路へ検体を注入するに際し、一定
量の検体を被分析成分の濃度に反比例した吐出流速によ
り検体を八ツファ液流中に吐出させるようにしたので、
ポンプの用出樋を調整するという筒中な操作により検体
連成をIF確に調節することができ、酵素反応を使用し
た分析を高い信頼性をもって行なうことができる。
As described above, according to the present invention, when a sample is injected into the conduit for supplying the buffer solution to the flow cell, a fixed amount of the sample is discharged at a flow rate inversely proportional to the concentration of the analyte component. Since it was made to be discharged into the Yatsufa liquid flow,
Specimen coupling can be accurately controlled at IF by adjusting the pump outlet, and analysis using enzymatic reactions can be performed with high reliability.

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

第1図は、本発明の一実施例をなす装置の構成図、第2
図は、検出電極の一例を示す断面図、第3図(I)(T
I)は、それぞれ同」二装置の動作を示す説明図である
。 ■・・・・試料注入装置 3・・・・試才1汀入ロア・
・・・バッファ11 9・・・・フローセル11・・・
・固定化酵素電極 出願人 株式会社島津製作所 代理人 弁理士 西 川 慶 治 同 木 村 勝 彦
Fig. 1 is a configuration diagram of a device constituting an embodiment of the present invention;
The figure is a cross-sectional view showing an example of the detection electrode, Figure 3 (I) (T
I) is an explanatory diagram showing the operation of the two devices, respectively. ■...Sample injection device 3...Test sample 1 lower entry point
...Buffer 11 9...Flow cell 11...
・Immobilized enzyme electrode applicant Shimadzu Corporation Representative Patent attorney Haruto Nishikawa Katsuhiko Kimura

Claims (1)

【特許請求の範囲】[Claims] 固定化酵素電極を備えた流路に検体を注入してバッファ
液により希釈しながら移送するフロースル型分析装置に
おいて、吐出波速を調整することができる試ネ4注入手
段により検体を前記流路に注入するようにしたことを特
徴とするフロースル型分析装置。
In a flow-through type analyzer in which a sample is injected into a channel equipped with an immobilized enzyme electrode and transferred while being diluted with a buffer solution, the sample is injected into the channel using a sample 4 injection means that can adjust the discharge wave speed. A flow-through type analyzer characterized by:
JP6463884A 1984-03-30 1984-03-30 Flow-through type analysis device Pending JPS60205346A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6463884A JPS60205346A (en) 1984-03-30 1984-03-30 Flow-through type analysis device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6463884A JPS60205346A (en) 1984-03-30 1984-03-30 Flow-through type analysis device

Publications (1)

Publication Number Publication Date
JPS60205346A true JPS60205346A (en) 1985-10-16

Family

ID=13264008

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6463884A Pending JPS60205346A (en) 1984-03-30 1984-03-30 Flow-through type analysis device

Country Status (1)

Country Link
JP (1) JPS60205346A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6126851A (en) * 1984-07-17 1986-02-06 Snow Brand Milk Prod Co Ltd Method and instrument for automatic measurement of glucose

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58135949A (en) * 1982-02-08 1983-08-12 Omron Tateisi Electronics Co Solidified enzyme film for flow type enzyme electrode

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58135949A (en) * 1982-02-08 1983-08-12 Omron Tateisi Electronics Co Solidified enzyme film for flow type enzyme electrode

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6126851A (en) * 1984-07-17 1986-02-06 Snow Brand Milk Prod Co Ltd Method and instrument for automatic measurement of glucose
JPH0462022B2 (en) * 1984-07-17 1992-10-02 Snow Brand Milk Prod Co Ltd

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