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JPS59214762A - Liquid chromatography apparatus - Google Patents
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JPS59214762A - Liquid chromatography apparatus - Google Patents

Liquid chromatography apparatus

Info

Publication number
JPS59214762A
JPS59214762A JP8770283A JP8770283A JPS59214762A JP S59214762 A JPS59214762 A JP S59214762A JP 8770283 A JP8770283 A JP 8770283A JP 8770283 A JP8770283 A JP 8770283A JP S59214762 A JPS59214762 A JP S59214762A
Authority
JP
Japan
Prior art keywords
reaction
components
eluted
sample
reactive reagents
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
JP8770283A
Other languages
Japanese (ja)
Inventor
Giichi Yamazaki
義一 山崎
Mitsuo Ito
三男 伊藤
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.)
Hitachi Ltd
Original Assignee
Hitachi 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 Hitachi Ltd filed Critical Hitachi Ltd
Priority to JP8770283A priority Critical patent/JPS59214762A/en
Publication of JPS59214762A publication Critical patent/JPS59214762A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/26Conditioning of the fluid carrier; Flow patterns
    • G01N30/28Control of physical parameters of the fluid carrier
    • G01N30/34Control of physical parameters of the fluid carrier of fluid composition, e.g. gradient
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02Column chromatography
    • G01N30/84Preparation of the fraction to be distributed
    • G01N2030/8429Preparation of the fraction to be distributed adding modificating material

Landscapes

  • Physics & Mathematics (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 Biological Materials (AREA)

Abstract

PURPOSE:To measure many components simultaneously with high accuracy by controlling the quantity and types of reactive reagents in accordance with the components eluted from a separating column tube. CONSTITUTION:A sample from a sampling valve 3 reaches a column 4 with an unsoluble solution 1. An eluted solution and separated components of the sample are mixed with reactive reagents by a mixer 9 and introduced into a detector 12 through a reaction bath 11. The supplying time range, the quantity to be supplied and the types to be supplied of the reactive reagents 5, 5', 5'' are controlled for each separated and eluted component by opening and closing valves 7, 7', 7'' by a program controller 6. Significant time reduction and operation cost savings are achieved and the precious samples such as blood and very fine specimens can be analyzed with the minimum consumption.

Description

【発明の詳細な説明】 〔発明の利用分野〕 本発明は、反応液のボンダにグラジェント@構を用い、
溶出成分に対し最適な反応液を加えることに係り、高感
度または、多種類の成分測定を可能にするに好適な液体
クロマトグラフ装置に関する。
[Detailed Description of the Invention] [Field of Application of the Invention] The present invention uses a gradient @ structure as a bonder for a reaction solution,
The present invention relates to a liquid chromatography device suitable for adding an optimal reaction solution to an eluted component and enabling high sensitivity or measurement of a wide variety of components.

〔発明の背景〕[Background of the invention]

従来の反応ik加える分析法は、反応液の流量および濃
度または、反応液の種類が固定されているために最適な
反応条件または、測ボ成分も限られる大きな欠点があっ
た。
Conventional reaction analysis methods have a major drawback in that the flow rate and concentration of the reaction solution or the type of reaction solution are fixed, which limits the optimal reaction conditions and the components to be measured.

〔発明の目的〕[Purpose of the invention]

本発明の目的は、成分が溶出した溶液に成分に応じて反
応液の量を任意に変更したりまたけ、異質の反応液に変
更するなどして成分を高感度で同時測定を行うもので、
従来は別に行っていた分析が同時測定を可能にする液体
クロマトグラフ装置を枦供することにある。
The purpose of the present invention is to simultaneously measure components with high sensitivity by arbitrarily changing the amount of reaction solution depending on the component, or by changing to a different reaction solution in a solution in which the components have been eluted. ,
The aim is to provide a liquid chromatography device that enables simultaneous measurements of analyzes that were conventionally performed separately.

〔発明の概要〕[Summary of the invention]

本発明の装置は、反応液体クロマトクラフ装置で、反応
液側のポンプ流量や濃度を任意に可変したり、更には分
離カラム管より溶出した成分に依り異質の反応液捷たは
、異質の数種類の反応液全任意の比率で混付してその成
分にr(Q 4な反応条件を任意に且つ容易に設定が出
来る事で高感度で多成分が同時測定出来る事を可能にし
たものでぞ〕る。
The apparatus of the present invention is a reaction liquid chromatograph apparatus, in which the pump flow rate and concentration on the reaction liquid side can be arbitrarily varied, and furthermore, different reaction liquids can be separated depending on the components eluted from the separation column tube, or several types of different types can be generated. By mixing all of the reaction solutions in any ratio and adjusting the reaction conditions for each component (Q4), it is possible to arbitrarily and easily set the reaction conditions, making it possible to simultaneously measure multiple components with high sensitivity. ].

〔発明の実施例〕[Embodiments of the invention]

以下従来の流路糸および本発明の流路系をし1をもとに
説明する。
The conventional channel thread and the channel system of the present invention will be explained below based on 1.

第3図は、従来方式に依る反応クロマト分析注出されサ
ンプリングバルブ3に達する。予め試料全添加したサン
プリンクバルブ3全切換よることに依り、試料は、溶離
液と一緒にカラム4に達しカラム充填剤上床部に吸着さ
れる。カラム4を通過した溶出液および、分離した試料
の成分はミキサー9に到達する。この状態の溶出液では
検出しても感度が低かったりまたは、まったく検出出来
ないために溶出した成分を着色捷たは、発螢光物質に変
換する必要が生じる。そのために反応試薬が必要となる
。一定に限られた反応試薬5は、流側゛ヲ同足したポン
プ(B18で吸引、吐出されミキサー9に達し試料が混
入した溶出液と混合する。反応試薬と混・会した溶出液
は、温度コントローラ1゜でj*lJ l1111され
ている反応槽11に達し反応が促進され検出器12に遅
し光吸収または、螢光強度をホトセル捷たは光電管など
で微少電圧に変換し記録第113で記録する。検出器1
2で測定した溶出液は廃液として捨てるの行程で反応ク
ロマト分析法は行なわれる。これらの従来方式の場合、
流量や反応試薬が1分析中固定されているので成分毎に
最適な条件では測定していなかったり、測定する事が不
可能な成分かめる。
FIG. 3 shows a reaction chromatographic analysis according to the conventional method, which is poured out and reaches the sampling valve 3. By fully switching the sample link valve 3 to which all the sample has been added in advance, the sample reaches the column 4 together with the eluent and is adsorbed onto the upper bed of the column packing material. The eluate that has passed through column 4 and the separated sample components reach mixer 9 . If the eluate is in this state, the detection sensitivity is low or it cannot be detected at all, so it becomes necessary to color the eluate or convert it into a fluorescent substance. For this purpose, reaction reagents are required. The reaction reagent 5, which is limited to a certain extent, is sucked and discharged by a pump (B18) on the flow side, and reaches the mixer 9, where it is mixed with the eluate mixed with the sample.The eluate mixed with the reaction reagent is The reaction reaches the reaction tank 11, which is heated by the temperature controller 1°, and the reaction is accelerated, and the detector 12 absorbs the light slowly, or converts the fluorescence intensity into a minute voltage using a photocell or phototube, and records it in No. 113. Record.Detector 1
The reaction chromatography analysis method is carried out in the step of discarding the eluate measured in step 2 as waste liquid. In the case of these conventional methods,
Since the flow rate and reaction reagents are fixed during one analysis, each component may not be measured under optimal conditions, or some components may be impossible to measure.

一方、第2図の木発す」方式の場合には、溶離液1から
ミキサー9までの流れは従来方式と同じだが、反応試薬
S、5/、5//の3神類の選択が分離溶出した成分毎
に、プログラムコントローラ6に依りバルブ7.7/ 
、 7//の開閉に依り任意の時間帯で任意の1′およ
び種類を制御出来る。これらの特徴は、同一成分でも反
応試薬が飽和状態または微′11では著しく感度が異な
り各成分に依って反応状態が違うので本発明の方式では
全成分を有効に測置することが可能になる。
On the other hand, in the case of the method shown in Fig. 2, the flow from eluent 1 to mixer 9 is the same as in the conventional method, but the selection of the three reaction reagents S, 5/, and 5// is separated and eluted. For each component, the program controller 6 sets the valve 7.7/
By opening and closing , 7//, any 1' and type can be controlled at any time. These characteristics are such that even if the components are the same, the sensitivity is markedly different when the reaction reagent is saturated or at a very low temperature.The reaction state differs depending on each component, so the method of the present invention makes it possible to effectively measure all components. .

〔発明の効果〕〔Effect of the invention〕

本発明に依れば、及応夙薬の隼や種類を市11到するこ
とに依り高感度で測雉する事はもとより、従来の固定し
た反応試薬のみでは数回の分析で目的を達していたが、
本発明の方式のように反応試薬をプログラムコン・トロ
ーラでl1flj Iaして、弗゛の可変種類の選択捷
たは、複数の反応試薬を任意の混合比4を作り出す事に
依り1回の分析例で目的ケ達することがt5J能であり
大幅な片1tJJ短縮調・よび運転コストの低減、或い
は、血液、微小試料など貴重な試料を最小限の消費量で
分析出来る効果がある。
According to the present invention, it is possible not only to measure the pheasant with high sensitivity by identifying the types of anti-inflammatory drugs, but also to achieve the purpose with only a few analyzes using conventional fixed reaction reagents. However,
As in the method of the present invention, reaction reagents are controlled by a program controller, and a variety of variable types can be selected, or multiple reaction reagents can be mixed at an arbitrary mixing ratio of 4 to perform a single analysis. For example, achieving the objective is t5J capability, which has the effect of significantly shortening the length of 1tJJ and reducing operating costs, or enabling analysis of valuable samples such as blood and minute samples with minimal consumption.

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

第1図は従来方式に依る反応クロマトグラフ装置の流路
図、第2図は本発明の一実施例に依る反応クロマトグラ
フ装置の流路図である。
FIG. 1 is a flow path diagram of a conventional reaction chromatograph apparatus, and FIG. 2 is a flow path diagram of a reaction chromatography apparatus according to an embodiment of the present invention.

Claims (1)

【特許請求の範囲】[Claims] 1、 溶離液に反応液金加えて測定するクロマト分析法
で反応液の濃度を任意に変更することが出来る手金特徴
とした液体クロマトグラフ装置。
1. A liquid chromatography device characterized by a chromatography method in which gold is added as a reaction liquid to the eluent for measurement, and the concentration of the reaction liquid can be arbitrarily changed.
JP8770283A 1983-05-20 1983-05-20 Liquid chromatography apparatus Pending JPS59214762A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8770283A JPS59214762A (en) 1983-05-20 1983-05-20 Liquid chromatography apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8770283A JPS59214762A (en) 1983-05-20 1983-05-20 Liquid chromatography apparatus

Publications (1)

Publication Number Publication Date
JPS59214762A true JPS59214762A (en) 1984-12-04

Family

ID=13922247

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8770283A Pending JPS59214762A (en) 1983-05-20 1983-05-20 Liquid chromatography apparatus

Country Status (1)

Country Link
JP (1) JPS59214762A (en)

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