JPS582737A - Ion concentration analysing apparatus - Google Patents

Ion concentration analysing apparatus

Info

Publication number
JPS582737A
JPS582737A JP56100565A JP10056581A JPS582737A JP S582737 A JPS582737 A JP S582737A JP 56100565 A JP56100565 A JP 56100565A JP 10056581 A JP10056581 A JP 10056581A JP S582737 A JPS582737 A JP S582737A
Authority
JP
Japan
Prior art keywords
ion
liquid
electrode
selective
sending
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
Application number
JP56100565A
Other languages
Japanese (ja)
Other versions
JPS6352701B2 (en
Inventor
Tetsuya Katayama
潟山 哲哉
Kenichi Sugano
菅野 憲一
Masao Koyama
小山 昌夫
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
Toshiba Corp
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 Toshiba Corp, Tokyo Shibaura Electric Co Ltd filed Critical Toshiba Corp
Priority to JP56100565A priority Critical patent/JPS582737A/en
Publication of JPS582737A publication Critical patent/JPS582737A/en
Publication of JPS6352701B2 publication Critical patent/JPS6352701B2/ja
Granted legal-status Critical Current

Links

Classifications

    • 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

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Molecular Biology (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)
  • Sampling And Sample Adjustment (AREA)

Abstract

PURPOSE:To use a titled apparatus in a maintenance-free state for a long period, by sending a sample solution, a standard solution, and a regenerating liquid of an ion selective electrode to a cell room selectively. CONSTITUTION:Only standard solutions 6 and 6' are sent to a cell room 1 by actuating a liquid sending pump 10 and operating sending liquid switching means 8 and 8' and an ion selective electrode 2 is calibrated. Next, only a sample solution 5 is introduced into the room 1 by switching the means 8 and the ion concentration is measured. Next, only a regenerating liquid 7 is introduced into the room 1 by switching the means 8 and 8' and is allowed to stand in the room for a prescribed time and then, regenerating treatment of the electrode 2 is carried out. This liquid 7 is a plasticizer of the same kind as that for constituting an ion selective film of the electrode 2.

Description

【発明の詳細な説明】 本発明はイオン選択性電極を用いえイオ/濃度分析装置
、更に詳しくは、イオン選択性電極O再生Jal1手段
を備え、長期に亘ヤメインテナンスフリーで使用できる
イオン一度分析装置に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention is an ion/concentration analyzer using an ion-selective electrode, more specifically, an ion/concentration analyzer that uses an ion-selective electrode and is equipped with an ion-selective electrode O regeneration means, which allows for one-time ion analysis that can be used for a long period of time without maintenance. Regarding equipment.

生化学や医療の分野では1体液中に存在する多くO化学
物質の中から目的とする化学物質を選別し、そoat−
1−側室することがしばしば行なわれる。たとえば、患
者の1清中に存在するナトリウム、カリウム、カルシウ
ムあるいは塩素などの電解質成分や贋自質中鴫分O濃度
を知ることによって、病気の診断に役立てる揚台がある
。現代医学は急速に進歩してお如、前記の血清中に存在
する化学物質を分析する事に関しても、非常に多種11
0化学物質を分析する事が必要となった。従来血清中O
化学物質測定には。
In the fields of biochemistry and medicine, a target chemical substance is selected from among the many O chemicals present in body fluids, and the soat-
1 - Concubinage is often practiced. For example, there is a system that is useful for diagnosing diseases by knowing the electrolyte components such as sodium, potassium, calcium, or chlorine that are present in a patient's blood, and the O concentration in fake blood. As modern medicine is rapidly progressing, it is becoming increasingly difficult to analyze the chemical substances present in serum.
It became necessary to analyze 0 chemical substances. Conventional serum O
For measuring chemical substances.

化学分析による方法中炎光光f法、螢光@光法、等O方
法が行なわれていえ。しかし、最近、患者の緊急検査時
に即応可能で操作中保!管運0簡単な分析装置が要望さ
れ、その中でも電解質成分分析用としてこれらO要望に
対応可能なイオン選択性電極を使用しえ臨床検査用自動
化学分析装置が実用化されている。
Chemical analysis methods such as flame light f method, fluorescence @ light method, etc. have been used. However, recently, we have been able to respond immediately and operate the center during emergency examinations of patients! There is a demand for an analyzer that is easy to operate, and among these, automatic chemical analyzers for clinical tests have been put into practical use that use ion-selective electrodes that can meet these requirements for electrolyte component analysis.

この場合、イオン選択性電極の試料ll1IE中の特定
イオンに対する検出端は、イオン選択性膜で構成されて
いる。このイオン選択性膜は、電極を試験溶液中に浸漬
し九場合、該試料St中に存在する分析対象の特定イオ
ンにのみ選択的に作用するものであ)、他の成分に対し
ては作用し&い可撓性高分子膜である。このような高分
子膜は1分析対象とする電解質成分に対応する疎水性0
=ニートツルキヤリア(例えば、対象がNa”0場舎は
毫ネンシン、対象かに+O場揚台パリノマイシン等)と
ジオクチルアジペート。
In this case, the detection end of the ion-selective electrode for specific ions in the sample ll1IE is constituted by an ion-selective membrane. When the electrode is immersed in a test solution, this ion-selective membrane acts selectively only on specific ions to be analyzed that are present in the sample St), but does not act on other components. It is a soft and flexible polymer membrane. Such a polymer membrane has a hydrophobicity of 0 corresponding to the electrolyte component to be analyzed.
= Neat Tsurukiyaria (for example, if the target is Na"0, the target is Nensin, if the target is Na"0, palinomycin, etc.) and dioctyl adipate.

ジオクチルフタレートなどの可塑剤とをポリ塩化ビニル
、ポリカーボネートなどのプラスチック材KIR定量含
有せしめ良後膜形成して構成されている。
It is constructed by adding a plasticizer such as dioctyl phthalate to a plastic material such as polyvinyl chloride or polycarbonate in a fixed amount and then forming a film.

しかしX&から従来のイオン濃度分析装置にありては、
血液中血清をナンプルとして使用しえ場合、高分子膜形
イオン選択性電極Oイオン選択性膜中O可履剤が血液中
車11によって溶出され−に如、洗浄液、標準−液中に
拡散し九シして。
However, from X& to conventional ion concentration analyzers,
When blood serum can be used as a sample, the polymer membrane type ion-selective electrode O ion-selective membrane O lubricant is eluted by the blood serum 11 and diffused into the cleaning solution and standard solution. Do nine.

イオン選択性膜中の可塑剤含有量が減少すゐえめ、イオ
ン選択物質としてのニエートフルキャリアーの活性が低
下する。即ちイオン選択性電極の劣化が促進され、その
寿命が値くなるという欠点があった。ζO橡な鳩舎、従
来のイオン濃度分析装置は高価なイオン選択性電極の交
換、イオン選択性電極のイオン選択性110貼換えなど
の作業を類繁に行なわなければならなかつえ。
As the plasticizer content in the ion-selective membrane decreases, the activity of the neat full carrier as an ion-selective substance decreases. That is, there was a drawback that the deterioration of the ion-selective electrode was accelerated and its life span was shortened. In conventional ion concentration analyzers, operations such as replacing the expensive ion selective electrode and replacing the ion selective electrode 110 with the ion selective electrode must be performed frequently.

本尭明者らは、高分子膜形イオン選択性電極を履込んに
イオン濃1ILll定装置における上記のような欠点を
解消するえめに鋭意研究を重ねえ結果、活性の劣化し九
イオン選択性膜を絨膜〇−成分である可塑剤と同種の可
塑剤に所定時間etasせると、鉄膜は再びその#A性
を俵元するとの事実を見出し、腋事実に基づ龜本尭―装
置を一発するK11つえ。
The authors of this study conducted extensive research to solve the above-mentioned drawbacks of the ion concentration 1ILll determination device by incorporating a polymer membrane type ion-selective electrode. It was discovered that when the film is exposed to the same type of plasticizer as the plasticizer that is the component of the chorion for a predetermined period of time, the iron film regains its #A properties. K11 cane that fires once.

本発明は、高分子膜形イオン選択、性電極61%生処層
手段を備え、長期にI)メインテナンス79−で使用で
きるイオン濃度分析装置の提供を目的とする。
An object of the present invention is to provide an ion concentration analyzer that is equipped with a polymer membrane type ion selection and a 61% active electrode and can be used for a long period of time without maintenance.

本尭明装置け、ニエートフルキャリアと可塑剤を含有す
る高分子膜Oイオン選択性膜を有するイオン選択性電極
及び比較電IIO電極llFが配置され九セhas該セ
ル富に試料sii及び標準**を送液するえめ0送液手
段;並びに、皺電極群からO電気出力信号を処理する丸
めの信号処理手段とから成るイオン濃度分析装置におい
て、鋏送液手段に、該イオン選択性電極(R1虫濠を透
液する手段;並びに、腋試料−筐、鍍標準S*及び皺再
生液をそれぞれ選択的に#セル童に送液する送波切換え
手段な付酸しえ構造であることを特徴とする。
In this device, an ion-selective electrode with an ion-selective membrane containing a polymer membrane containing a nate full carrier and a plasticizer, and a comparative electrode IIO are placed in the sample SI and the standard. **In an ion concentration analyzer comprising a liquid feeding means for feeding liquid; and a rounded signal processing means for processing an electric output signal from a group of wrinkled electrodes, the scissors liquid feeding means includes the ion-selective electrode. (Means for permeating liquid through the R1 insect moat; and means for selectively sending the armpit sample-housing, sill standard S*, and wrinkle regenerating liquid to the #cell child. It is characterized by

以下に、本li@装置を第1図に期し九−実施例に基づ
き更に詳細に説明する。第1図は1本発明義置O−実施
例O概略模式■である。
In the following, the present li@ device will be explained in more detail based on a ninth embodiment shown in FIG. FIG. 1 is a schematic diagram of one embodiment of the present invention.

111に&%Aて、lはセル富で、該セル寅にはイオン
選択性電極2及び比較電極3が配置される。
111, &%A, l is the cell depth, and the ion selective electrode 2 and the comparison electrode 3 are arranged in the cell depth.

これら全体は70−セル4の中に収納され、試料溶液、
標準溶液及び再生液は図中左から右へと*h111内を
過flfb。5−is試料11m1.6゜6′は標準溶
液、7が再生液である。再生液7は。
All of these are stored in 70-cell 4, and the sample solution,
The standard solution and regeneration solution pass through *h111 from left to right in the figure. 5-is sample 11ml 1.6°6' is the standard solution, and 7 is the regenerated solution. The regeneration liquid 7 is.

イオン選択性電極2のイオン選択性膜を構成する可塑剤
を主成分とする。8は試料S液5及び標準111118
’0例えdl!方コック弁′から威る送液切換え手段で
、サンプリング用配管! 、 I’。
The main component is a plasticizer that constitutes the ion-selective membrane of the ion-selective electrode 2. 8 is sample S solution 5 and standard 111118
'0 analogy dl! Sampling piping with liquid feeding switching means controlled from the side cock valve! , I'.

9″を介してそれぞれの溶液に連結する。8′はサンプ
リング用配管9″′を介して再生液7と接続する例えば
三方コック弁のような送波切換え手段で島る。図では、
送波切換え手12sと8′を別々に配置し喪が、4)種
sniが渦合す為ことなくセル皇IK選択的に導入でき
るような手段であればどのような手段であってもよい。
9'' to each solution. 8' is connected to the regenerating liquid 7 via a sampling pipe 9'', and is connected to a transmission switching means such as a three-way cock valve. In the diagram,
4) Any means may be used as long as the transmitter switching devices 12s and 8' can be placed separately and the cell IK can be selectively introduced without causing any merging of the species SNI. .

これらO送液切換え手段を適宜にセットし。Set these O liquid feeding switching means appropriately.

送液ポンプWを作動讐しめて所定の淑をセル意l内に導
入し、iw定後それを排出する。
The liquid feed pump W is turned off, a predetermined amount of liquid is introduced into the cell, and after the amount of liquid is determined, it is discharged.

11はイオン選択性電極2と比較電113011に発生
する電位差出力O増@器、12はその出力をイオン濃度
に換算する演算器、口はイオン1lIiWIO表示器で
全体として信号処理手段を構成する。
Reference numeral 11 denotes a potential difference output O intensifier generated between the ion-selective electrode 2 and the comparison voltage 113011, 12 an arithmetic unit for converting the output into an ion concentration, and an ion 1lIiWIO indicator, all of which constitute a signal processing means.

以上のような本発−装置を用いて市販のコントー−ル真
情中ox”oイオン濃度の分析試験を行なつえ。
Using the apparatus of the present invention as described above, an analysis test of the concentration of ox''o ions in commercially available control was conducted.

装置の配管はいずれも外II ”/isイ/テOテ7一
ンチェープを用い、送液切換え手段8.I′と70−セ
ル40間の長さはできるだけ短くした。
All of the piping of the apparatus was made of pipes, and the length between the liquid feeding switching means 8.I' and 70-cell 40 was made as short as possible.

送液ポンプWはしごき4ンプを用い良。なお。You can use liquid transfer pump W ladder 4 pump. In addition.

このポンプとしてはチェック弁を備ええ往復動式ポンプ
又はシリンジ式ポンプを用いることもできる。
As this pump, a reciprocating pump or a syringe pump equipped with a check valve can also be used.

高分子形イオン選択性電極2としては、ポジ塩化ビニル
を基材とし、アジピン酸ジオタチルを可塑剤とし、パリ
ノマイシンをイオン選択性物質とし、これらをテトツヒ
ドロ7ランKml解・温合し大後シートに成形したカリ
ウムイオン選択性膜を有するカリウムイオン選択性膜極
を用いえ、比較電極は銀−塩化銀電極であった。
The polymeric ion-selective electrode 2 is made of polyvinyl chloride as a base material, diotatyl adipate as a plasticizer, and palinomycin as an ion-selective substance, which are dissolved and heated in 7-run Kml to form a large sheet. A potassium ion selective membrane electrode with a molded potassium ion selective membrane was used and the reference electrode was a silver-silver chloride electrode.

標準11116 ハ10−’M[CJlli[、榔阜霞
諌6′はl G−”MやE)溶液で、再生液7はアジピ
ン酸ジオタチルであった。
The standard 11116 was a 10-'M[CJlli[, 榔阜霞諌6'was a l G-''M or E) solution, and the regenerating solution 7 was diotatyl adipate.

まず、送液ポンプWを作動し、送液切換え手段8.8′
を操作して標準溶液6及び6’0みをそれぞれセルl[
lK送入して電極2のネルンスト応答O頷斜を求め電極
の校正を行なっ九。ついで切換え手段8を切換えて試料
溶液5の拳を竜ル童IK導入して電極2の電位を測定し
良。校正の動作は、11定前と5時間後とした。
First, the liquid feeding pump W is operated, and the liquid feeding switching means 8.8'
to add standard solutions 6 and 6'0 to cell l [
Calibrate the electrode by injecting lK to obtain the Nernst response O nod of electrode 2. Next, switch the switching means 8, introduce the fist of the sample solution 5 into the Ryurudo IK, and measure the potential of the electrode 2. The calibration operation was performed before 11 hours and after 5 hours.

測定終了前に1回、切換え手段8.8′を切換えて再生
I[7のみをセル*IK導入し該室内KW分間存在せし
めて電極20再生処1を行なり九。そのIl、再生液を
#液しえ。
Before the end of the measurement, the switching means 8.8' is switched once to introduce only the regenerating I[7 into the cell*IK and leaving it present in the room KW for the electrode 20 regenerating process 9. Then, add the regenerating solution.

以上の作動様式で本’11@懺置を1日mesm稼動し
九〇し良がって、校正動作211/日、再生処環操作1
回/日となる。
With the above operating mode, I operated the book '11 @ Mesm for 1 day and it worked fine for 90 days, calibration operation 211/day, regeneration processing operation 1
times/day.

電極出力のネルンスト傾斜(t11力感[j鳳:mV)
()装置稼動日数に対す為変化を嬉=−に示しえ。比較
の丸め従来装置の場合O結!&も示し丸。図でaは従来
装置、bは本発―義置O曽果である。
Nernst slope of electrode output (t11 force sensation [jho: mV)
() Indicate the change in terms of the number of days the equipment has been in operation. Comparison rounding: O result for conventional equipment! & is also indicated by a circle. In the figure, a is the conventional device, and b is the original device.

膳か−ら明らかなように1本実@装置の優位性は明らか
である。すなわち、従来のイオン811分析装置では分
析−始30日ぐらいで!l初fiOmVO出力感度:ノ
Eが低下しはじめ50日にしてノ鼠−48mVと亀つ九
のに対し、高分子膜形イオン選択性電@0再生鶏運機構
を備え九本俺116イオン濃度分析鋏置は、稼動日数9
0日でもノ冨−315mVであ)その出力感度低下は極
めてわずかで血清の分析KPiらの支障も生じなかつ丸
As can be seen from the table, the superiority of the single real @ device is obvious. In other words, with the conventional ion 811 analyzer, analysis can be completed in about 30 days! Initial fiOmVO output sensitivity: After 50 days, the E started to decrease -48 mV, whereas the 116 ion concentration with polymer membrane type ion-selective electricity @ 0 regeneration mechanism was achieved. The analytical scissors holder is in operation for 9 days.
Even on day 0, the output sensitivity was -315 mV) The decrease in output sensitivity was extremely slight, and there was no problem with serum analysis KPi et al.

以上のように1本発明装置Kあっては、試料溶液のイオ
ン濃度の分析時に、イオン選択性膜から可塑剤−1Ih
iI筐中に拡散して損失しても、それを定期的に再生液
を供給することによって補充できるので、電極の出力感
度を長期に夏って維持することがてきる。
As described above, in the device K of the present invention, when analyzing the ion concentration of a sample solution, the plasticizer-1Ih is removed from the ion-selective membrane.
Even if it is lost due to diffusion into the iI casing, it can be replenished by periodically supplying regenerating liquid, so the output sensitivity of the electrode can be maintained over a long period of time.

し丸がって1本発明装置は、従来の様Kjllli価な
イオン選択性電極の交換中イオン選択性電極のイオン選
択性膜を貼換える作11.勢を■繁に行なう事なく、長
期メンテナンスフリーで使用で龜ゐOで有用である。
11. The device of the present invention is capable of replacing the ion-selective membrane of the ion-selective electrode during the replacement of the conventional ion-selective electrode. It is useful for long-term maintenance-free use without frequent maintenance.

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

1Ii1図は1本実@装置0−夾施例の概略模式■、1
12111は従来0イオン濃度分IfiI&置と本俺―
のイオンam分析装置をIl!刑して1雪の分析をし九
時の装置稼動日数に対するイオン選択性電極O出力感度
の変化を示し丸■である。
1Ii1 Figure is a schematic diagram of one actual @device 0-Example ■, 1
12111 is conventionally 0 ion concentration IfiI & place and book -
Il!'s ion am analyzer! The circle ``■'' shows the change in the ion-selective electrode O output sensitivity with respect to the number of days the device was in operation at 9:00 a.m. after analyzing 1 snow.

Claims (1)

【特許請求の範囲】 1、=エートラルキャリアと可履剤を含有する高分子層
のイオン選択性層を有するイオン選択性゛電極及び比較
電fiの電極#*配装されえセル篇; 鋏セルIIK試料*ii及び標準1)[を送液する丸め
の送液手段廖並びに、 皺電極群からの電気約出力信号を処理する丸めの信号鶏
瀾手段;とかも成るイオン濃度分析装置K>いて。 該送液手段K。 皺イオン選択性電Iiの再生液を送液する手段募並びK
、 該試料溜i[、皺標準溶液及び該再生波をそれぞれ選択
的に皺童ル重に送液する送液切換え手段 を付設した構造のイオン濃度分析装置。 ′LIIII!再生派が、腋写生派と同種O可朧剤を特
徴とする特許請求OSS菖1項記載Oイオンam分析懺
置装
[Scope of Claims] 1. = Ion-selective electrode having an ion-selective layer of a polymer layer containing an ethral carrier and a lubricant; Cell IIK sample *ii and standard 1) [Ion concentration analyzer K, which also consists of a round liquid sending means for sending the liquid, and a round signal sending means for processing the electrical output signal from the wrinkled electrode group; Stay. The liquid feeding means K. Recruitment of means for feeding the regenerating solution of Wrinkle Ion Selective Electron Ii
An ion concentration analyzer having a structure including a liquid feeding switching means for selectively feeding the sample reservoir i[, the wrinkle standard solution and the regenerated wave to the wrinkle standard solution, respectively. 'LIII! The O ion am analysis device described in Patent Claim OSS Iris Paragraph 1, in which the reproduction group is characterized by the same type of O obfuscating agent as in the armpit sketch group.
JP56100565A 1981-06-30 1981-06-30 Ion concentration analysing apparatus Granted JPS582737A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56100565A JPS582737A (en) 1981-06-30 1981-06-30 Ion concentration analysing apparatus

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56100565A JPS582737A (en) 1981-06-30 1981-06-30 Ion concentration analysing apparatus

Publications (2)

Publication Number Publication Date
JPS582737A true JPS582737A (en) 1983-01-08
JPS6352701B2 JPS6352701B2 (en) 1988-10-19

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP56100565A Granted JPS582737A (en) 1981-06-30 1981-06-30 Ion concentration analysing apparatus

Country Status (1)

Country Link
JP (1) JPS582737A (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5426791A (en) * 1977-08-01 1979-02-28 Hitachi Ltd Activating and regenerating method for ion electrode

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5426791A (en) * 1977-08-01 1979-02-28 Hitachi Ltd Activating and regenerating method for ion electrode

Also Published As

Publication number Publication date
JPS6352701B2 (en) 1988-10-19

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