JPH0331753A - Method for measuring concentration of chlorine ion in biofluid - Google Patents

Method for measuring concentration of chlorine ion in biofluid

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Publication number
JPH0331753A
JPH0331753A JP16525889A JP16525889A JPH0331753A JP H0331753 A JPH0331753 A JP H0331753A JP 16525889 A JP16525889 A JP 16525889A JP 16525889 A JP16525889 A JP 16525889A JP H0331753 A JPH0331753 A JP H0331753A
Authority
JP
Japan
Prior art keywords
biological fluid
measuring
concentration
electrode
biofluid
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
JP16525889A
Other languages
Japanese (ja)
Inventor
Hisao Osawa
久男 大澤
Katsuhide Suzuki
鈴木 勝英
Akifumi Yamada
明文 山田
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.)
Nippon Filcon Co Ltd
Original Assignee
Nippon Filcon 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 Nippon Filcon Co Ltd filed Critical Nippon Filcon Co Ltd
Priority to JP16525889A priority Critical patent/JPH0331753A/en
Publication of JPH0331753A publication Critical patent/JPH0331753A/en
Pending legal-status Critical Current

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  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)

Abstract

PURPOSE:To make concn. measurement by a sampled biofluid by measuring a change in current generated according to a change in the prescribed potential level of the measuring electrode in the biofluid as the crest value of an oxidation wave and reduction wave and determining the concn. from this value and a calibration curve. CONSTITUTION:The measuring electrode constituted by coating an electrode constituted of a working electrode made of silver a counter electrode made of a stainless steel and a reference electrode constituted of silver/silver chloride with a high-polymer film-like material having the fine pores to allow the passage of chlorine ions and to prohibit the passage of coexisting materials, such as protein, is installed in the biofluid existing in the same chamber. The potential level of the working electrode is cyclically changed in a 0.6Vvs.Ag/AgCl range from -0.6 then in -0.6Vvs.Ag/AgCl from +0.6 with respect to the counter electrode. The change in the current generated according to these voltage changes is measured at the continuously obtd. crest value of the oxidation wave and reduction wave and the concn. of the chlorine ions contained in the biofluid to be inspected is measured from the previously formed calibration curve. The concn. of the chlorine ions contained in the biofluid is obtd. from the crest value obtd. from the figure and the calibration curve shown in the figure in this way.

Description

【発明の詳細な説明】 [産業上の利用分野〕 本発明は、電気化学的な検出法で、生体液中に含有され
る塩素イオンの濃度を定量的に測定する方法に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a method for quantitatively measuring the concentration of chloride ions contained in a biological fluid using an electrochemical detection method.

[従来の技術〕 従来、生体液中に含有される塩素イオンの定量としては
、シャレス−シャレス法  (S c h aIes 
 5chales)−電量滴定法、イオンZ N法、な
ど種々のものがりる。
[Prior Art] Conventionally, the Schales-Chares method has been used to quantify chlorine ions contained in biological fluids.
5chales) - There are various methods such as coulometric titration method and ion ZN method.

しかしながら、いずれも生体液をそのまま使用して塩素
イオンの定置を行うものではなく採取後ただちに生体液
を処理する必要があり、さらに薬物の干渉による誤差が
発生ずる等の問題があり、試料調製の操作が煩雑でその
上化学分析技術の習熟が必要とされる。 特に生体液が
血液の場合は血清を分離しなければならず−このような
余計な操作を必要とし測定法としては複雑にならざるを
得ない欠点がある。
However, these methods do not use biofluids as they are to immobilize chloride ions, and the biofluids must be treated immediately after collection. Furthermore, there are problems such as errors caused by drug interference, and sample preparation is difficult. The operation is complicated and requires proficiency in chemical analysis techniques. In particular, when the biological fluid is blood, serum must be separated - such an extra operation is required, and the measurement method is inevitably complicated.

し・発明が解決しようとする問題点] 前記した様に、従来の生体液の塩素イオンの定置は、試
料の調製を含め定量操作が煩雑なため、迅速性かつ正確
を要求される分析には適さない欠点があるばかりか、繰
り返し分析精度の良い再現性を得るのがむずかしいとい
う問題点を含んでいるので、本発明はこれらの欠点なら
びに問題点を解決したものである。
[Problems to be Solved by the Invention] As mentioned above, the conventional emplacement of chloride ions in biological fluids requires complicated quantitative operations including sample preparation, so it is not suitable for analyzes that require speed and accuracy. The present invention solves these drawbacks and problems, since it not only has disadvantages that it is not suitable, but also that it is difficult to obtain good reproducibility with repeated analysis accuracy.

[発明が解決しようとする課題] 本発明は、前記した従来の測定法の欠点ならびに問題点
を改善し、被検生体液中の塩素イオンの濃度を短時間に
、しかも操作は容易で、要求される繰り返し分析精度で
定量することができる、生体液に含有される塩素イオン
のJ度を測定する方゛法を提供することを、その目的と
する6[課題間を解決するための手段] 本発明は、 「1.  同一槽内にある生体液中に、銀で構成17た
作用電極およびステンレスで構成した対極と、銀/塩化
銀で構成した参照電極とからなる電極を塩素イオンは通
過することができるが、生体液中に含まれる蛋白質など
の共存物質を通過させない、微細多孔を有する高分子膜
状物で覆って構成した測定電極を設置し、作用電極の電
位レベルを対極に対して  −0,6から+〇、6V 
vs、Ag/Ag/AgClに次いで+0,6から一〇
、6V Vs、 A g/A g Cjの範囲でサイク
リックに変化させ、その電圧変化に応じて発生する!?
i変化を連続して得られる酸化波及び還元波の波高値と
して測定して、予め作成した検量線から被検生体液中に
含有されるCIイオンの濃度を測定する方法。
[Problems to be Solved by the Invention] The present invention improves the drawbacks and problems of the conventional measurement methods described above, and enables the concentration of chloride ions in the biological fluid to be measured in a short time, with easy operation, and to meet the requirements. The objective is to provide a method for measuring the degree of J of chloride ions contained in biological fluids, which can be quantified with repeatable analytical accuracy. 6 [Means for solving the problems] The present invention is based on the following points: 1. Chlorine ions pass through an electrode consisting of a working electrode made of silver, a counter electrode made of stainless steel, and a reference electrode made of silver/silver chloride in a biological fluid in the same tank. However, by installing a measuring electrode covered with a polymer membrane with microporous that does not allow coexisting substances such as proteins contained in biological fluids to pass through, the potential level of the working electrode is set relative to the counter electrode. -0,6 to +〇,6V
Vs, Ag/Ag/AgCl, then cyclically changed in the range of +0, 6 to 10, 6V Vs, A g/A g Cj, and generated according to the voltage change! ?
A method of measuring the concentration of CI ions contained in a sample biological fluid from a calibration curve prepared in advance by measuring i changes as the peak values of continuously obtained oxidation waves and reduction waves.

2、生体液が、血液、血清、血漿、リンパ液、髄液、唾
液から選んだ液である請求項Iに記載された、被検生体
液中に含有される塩素イオンの濃度を測定する方法。
2. The method for measuring the concentration of chloride ions contained in a test biological fluid according to claim I, wherein the biological fluid is a fluid selected from blood, serum, plasma, lymph, spinal fluid, and saliva.

3 生体液が、生体液を緩衝液又は蒸溜水で稀釈くしな
液である請求項1に記載された、被検生体液中に含有さ
れる塩素イオンの濃度を測定する方法。
3. The method for measuring the concentration of chloride ions contained in a test biological fluid according to claim 1, wherein the biological fluid is a comb solution obtained by diluting the biological fluid with a buffer solution or distilled water.

4、微細多孔を有する高分子膜状物がポリカーボネート
、セルロースアセテート、から選んだ膜状物である請求
項1ないし3のいずれか1項に記載された、被検生体液
中に含有される塩素イオンの濃度を測定する方法。
4. Chlorine contained in the test biological fluid according to any one of claims 1 to 3, wherein the microporous polymer membrane is selected from polycarbonate and cellulose acetate. A method of measuring the concentration of ions.

5、@細条化を有する高分子膜状物が5〜7ミクロンの
膜厚である、請求項1ないし4のいずれか1項に記載さ
れた、被検生体2α中に含有される塩素イオンの濃度を
測定する方法。
5. Chlorine ions contained in the test organism 2α according to any one of claims 1 to 4, wherein the polymer film having striations has a film thickness of 5 to 7 microns. How to measure the concentration of.

6、 高分子膜状物に配設したm細条化の直径が0.0
3ミクロン以下である、請求項1ない!−5のいずれか
1項に記載された。被検生体液中に含有される塩素イオ
ンの濃度を測定する方法、Jである。
6. The diameter of the m strips arranged on the polymer membrane is 0.0.
There is no claim 1, which is 3 microns or less! -5. J is a method for measuring the concentration of chloride ions contained in a sample biological fluid.

生体液には、種々の電解質が含有されているがその中で
もナトリウムイオン、カリウムイオン、塩素イオンが重
要な電解質でありそれらのイオンの量を測定することに
より生体の状態を知ることが出来る。
Biological fluids contain various electrolytes, among which sodium ions, potassium ions, and chloride ions are important electrolytes, and the state of the living body can be determined by measuring the amounts of these ions.

本発明の第1の特徴は採取した′&まの生体液で面接合
まれる塩素イオンの:a反をP1定できることである。
The first feature of the present invention is that it is possible to determine the :a ratio P1 of chloride ions that are brought into contact with each other in the collected biological fluid.

生体液としては、血液、血清、血漿、すンバ湾、N液、
唾液など種々のものがあるが、壺も代表的なものは血液
であるのでこの血液について説明すると採取したそのま
までも、血清、血漿等を適宜分離してから測定すること
もできるし、分離した血清、血漿等について塩素イオン
の濃度を測定することもできるatた、[を液又は蒸溜
水で稀釈して測定することもできる。この様な測定法は
血液に限らずリンパ液、MH1唾液などの全ての生体液
について同様に行うことができる。
Biological fluids include blood, serum, plasma, Sumba Bay, N fluid,
There are various things such as saliva, but blood is the most common type of blood in the jar.To explain about blood, it can be measured as it is, or after separating serum, plasma, etc. as appropriate, or it can be measured after separating serum, plasma, etc. The concentration of chloride ions can be measured in plasma, etc., and can also be measured by diluting it with liquid or distilled water. Such a measurement method can be performed not only for blood but also for all biological fluids such as lymph fluid and MH1 saliva.

本発明は全てのを椎動物、無節を椎動物の生体液ばかり
でなく、植物の生体液についても含有される塩素イオン
の濃度を測定できるのである。
The present invention can measure the concentration of chloride ions contained not only in the biological fluids of all vertebrates and non-vertebrates, but also in the biological fluids of plants.

本発明の第2の特徴は測定電極を生体液中に含まれる蛋
白質などの共存物質を通過させないms多孔を有する高
分子膜状物で覆って構成したことである。高分子膜状物
としては、ポリカーボネート、セルロースアセテ−1−
等から得た膜状物が使用される。S厚は5〜7μmが好
適であり、これより厚くなると塩素イオンの透過が遅く
なるので、測定時間が長くなる欠点が生ずる。微細孔は
直径が0.03μm以下である必要がある。孔がこれよ
り大きいと生体液中に含まれる蛋白質などの共存物質が
通過してしまうので測定結果にS影響を及ぼすからであ
る。この様な特種の膜で測定電極を覆うので採取したま
まの生体液で面接合まれる塩素イオンの濃度を測定でき
るのである。
The second feature of the present invention is that the measurement electrode is covered with a polymeric membrane having ms pores that do not allow coexisting substances such as proteins contained in biological fluids to pass through. Polycarbonate, cellulose acetate-1-
A film-like material obtained from etc. is used. The S thickness is preferably 5 to 7 μm; if it is thicker than this, the permeation of chlorine ions becomes slow, resulting in a disadvantage that the measurement time becomes longer. The micropores need to have a diameter of 0.03 μm or less. This is because if the pores are larger than this, coexisting substances such as proteins contained in the biological fluid will pass through, which will affect the measurement results. By covering the measurement electrode with such a special membrane, it is possible to measure the concentration of chloride ions that are present in the biological fluid as it is collected.

このことを代表的な生体液である血液について詳しく説
明すると高分子膜状物のrR細孔の直径が0゜03μm
これより大きいと血液中に含まれる蛋白質、ヘモグロビ
ンなどの共存物質を通過してしまうのである。
To explain this in detail regarding blood, which is a typical biological fluid, the diameter of the rR pores of the polymer membrane is 0°03 μm.
If it is larger than this, coexisting substances such as proteins and hemoglobin contained in the blood will pass through.

本発明の第3の特徴は測定電極の作用電極の電位レベル
を対極に対し −0,6から+0.6V VS、AQ/
AgC1に次いで+0.6から一〇、6V vs、 A
 o/A g /AgClの範囲でサイクリックに変化
させ、その電圧変化に応じて発生する電流変化を連続し
て得られる酸化波及び還元波の波高値として測定して塩
素イオン濃度を測定することである。
The third feature of the present invention is to change the potential level of the working electrode of the measuring electrode from -0.6 to +0.6 V VS, AQ/
AgC1 followed by +0.6 to 10, 6V vs. A
To measure the chloride ion concentration by cyclically changing the voltage in the range o/Ag/AgCl and measuring the current change that occurs in response to the voltage change as the peak value of the continuously obtained oxidation wave and reduction wave. It is.

[作 用] 本発明は、前述のように特種な、微細多孔を有する高分
子膜状物で測定電極を覆い生体液中に含まれる蛋白質な
どの共存物質の通過を防止するので採取したままの生体
液で面接合まれる塩素イオンの濃度を測定できる格別の
作用が奏される。
[Function] As mentioned above, the present invention covers the measurement electrode with a special polymeric membrane having micropores to prevent the passage of coexisting substances such as proteins contained in biological fluids. It has a special ability to measure the concentration of chloride ions that are present in biological fluids.

また、本発明においてはまず測定電極の作用電極の電位
レベルを対極に対し−0,6から+〇、6V vs。
In the present invention, first, the potential level of the working electrode of the measurement electrode is set from -0.6 to +0.6 V vs. the counter electrode.

17/Ag/AgCl!に変化させてAg+CI−Ag
Clモe−の反応による酸化電流を測定しついで、+0
.6から−0,6V VS、/g/AgClにサイクリ
ックに変化させてAgCI +e−−Ag−)−CI−
の反応による還元電流を測定することができる。
17/Ag/AgCl! Change it to Ag+CI-Ag
After measuring the oxidation current due to the reaction of Clmoe-, +0
.. AgCI +e--Ag-)-CI- by cyclically changing from 6 to -0,6V VS, /g/AgCl
The reduction current due to the reaction can be measured.

サイクリックに変化させることにより、A at極に生
成したAgC1を溶解して自動的に電極を洗浄すること
ができる。
By cyclically changing it, AgC1 generated in the A at electrode can be dissolved and the electrode can be automatically cleaned.

[実施S] 以下、本発明の一実施例を第1図ないし第2図に従って
説明する。
[Embodiment S] An embodiment of the present invention will be described below with reference to FIGS. 1 and 2.

第1図に、本発明を実施例について具体的に説明する。In FIG. 1, the present invention will be specifically explained with reference to an embodiment.

第1図は本発明の実施例のボルタモダラムを示+、、作
用電極1として銀電極を用い、被検液として株式会社常
光製の血清を使用したボルタモダラムである。
FIG. 1 shows a volta modalum according to an embodiment of the present invention, in which a silver electrode was used as the working electrode 1 and serum manufactured by Joko Co., Ltd. was used as the test liquid.

第1図の縦軸は波高値を示しそして横軸はVvs。The vertical axis in FIG. 1 shows the peak value, and the horizontal axis shows Vvs.

Ag/AgC1を示す。Indicates Ag/AgC1.

測定電極は膜厚平均5μmで直径はぼ0.03μmの微
細多孔を有するポリカーボネート膜で包まれている。
The measuring electrode is wrapped in a polycarbonate membrane having an average thickness of 5 μm and micropores of approximately 0.03 μm in diameter.

第1図の曲線から明らかなように、作用t%の電位を対
極に対して一〇、6から+G、6V vs、AQ/Ag
C1に変化させると酸化電流が流れてその波形が描かれ
る1次いで40.6から一〇、6V VS、A(+/A
 g C1にサイクリックに変化させると還元電流が流
れてその波形が描かれる。この第1図のボルタモダラム
から波高値を測定する。
As is clear from the curve in Figure 1, the potential of action t% is 10, 6 to +G, 6V vs, AQ/Ag with respect to the opposite electrode.
When changing to C1, an oxidation current flows and its waveform is drawn.
When g C1 is changed cyclically, a reduction current flows and its waveform is drawn. The wave height value is measured from this voltamodrum shown in FIG.

第2図は、予め作成した検量線を示す、第1図から得た
波高値と第2図の検量線から含有される塩素イオンの濃
度が得られるのである。
FIG. 2 shows a calibration curve prepared in advance, and the concentration of chlorine ions contained can be obtained from the peak value obtained from FIG. 1 and the calibration curve of FIG.

試験結果 次に、表1に本発明による株式会社常光製の1漬の塩素
イオンの濃度再現性を示す。
Test Results Next, Table 1 shows the reproducibility of the concentration of chlorine ions in a single dip made by Joko Co., Ltd. according to the present invention.

測定例 [注J 回  数 平均値 =1 慨準変差=0 変動係数−〇 表  1 塩素イオンの4度 (m  mol/1) 100.9 ioo、1 100.9 100.4 99.8 101.1 101.0 100.4 98.9 99.2 0 00、 27 、 7689 、767% 測定は同一反応槽内で電極を洗浄しないで連続測定した
Measurement example [Note J Number of times average value = 1 Standard deviation = 0 Coefficient of variation - Table 1 4 degree of chloride ion (m mol/1) 100.9 ioo, 1 100.9 100.4 99.8 101 .1 101.0 100.4 98.9 99.2 0 00, 27, 7689, 767% Measurements were carried out continuously in the same reaction tank without cleaning the electrodes.

比較例 次に比較のために同一試料について測定電極を膜厚平均
10μmで直径はぼ0.05〜l Q )1mの細孔を
有するポリカーボネート膜で包んで測定した結果を表2
に示す。
Comparative Example Next, for comparison, the same sample was measured by wrapping the measurement electrode in a polycarbonate membrane with an average thickness of 10 μm and a diameter of approximately 0.05 to 1 m (Q) pores, and the results are shown in Table 2.
Shown below.

表 塩素イオンの1度 (m  mol/I) 101.4 85.7 79.2 74.4 72.0 測定例 以上のように本発明は優れた反復再現性を示すが本発明
の構成を欠く比較例は全く反復再現性がなく本発明の優
れた作用効果が理解できる。他の生体液を使用しても同
様に優れた反復再現性がえられる。
1 degree of surface chlorine ion (m mol/I) 101.4 85.7 79.2 74.4 72.0 Measurement example As described above, the present invention shows excellent repeatability, but lacks the structure of the present invention The comparative examples showed no reproducibility at all, and the excellent effects of the present invention can be understood. Similar excellent reproducibility is obtained using other biological fluids.

[発明の効果] 本発明は、上記したような簡便な操作で、且つ迅速に、
しかも精度よく生体液中の塩素イオンの濃度を測定する
方法を提供するものである。この方法により被検体の状
態を適確迅速に検出できる優れた効果が奏される。
[Effects of the Invention] The present invention provides simple and quick operations as described above.
Moreover, it provides a method for accurately measuring the concentration of chloride ions in biological fluids. This method provides an excellent effect of accurately and quickly detecting the condition of the subject.

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

第1図は本発明の実験結果を示すボルタモダラムである
。第2図は検1線を示すグラフである。
FIG. 1 is a voltamodalum showing the experimental results of the present invention. FIG. 2 is a graph showing the test line.

Claims (1)

【特許請求の範囲】 1、同一槽内にある生体液中に、銀で構成した作用電極
およびステンレスで構成した対極と、銀/塩化銀で構成
した参照電極とからなる電極を塩素イオンは通過するこ
とができるが、生体液中に含まれる蛋白質などの共存物
質を通過させない、微細多孔を有する高分子膜状物で覆
つて構成した測定電極を設置し、作用電極の電位レベル
を対極に対して−0.6から+0.6Vvs.Ag/A
gClに次いで+0.6から−0.6Vvs.Ag/A
gClの範囲でサイクリックに変化させ、その電圧変化
に応じて発生する電流変化を連続して得られる酸化波及
び還元波の波高値として測定して、予め作成した検量線
から被検生体液中に含有される塩素イオンの濃度を測定
する方法。 2、生体液が、血液、血清、血漿、リンパ液、髄液、唾
液から選んだ液である請求項1に記載された、被検生体
液中に含有される塩素イオンの濃度を測定する方法。 3、生体液が、生体液を緩衝液又は蒸溜水で稀釈くした
液である請求項1に記載された、被検生体液中に含有さ
れる塩素イオンの濃度を測定する方法。 4、微細多孔を有する高分子膜状物がポリカーボネート
、セルロースアセテート、から選んだ膜状物である請求
項1ないし3のいずれか1項に記載された、被検生体液
中に含有される塩素イオンの濃度を測定する方法。 5、微細多孔を有する高分子膜状物が5〜7ミクロンの
膜厚である、請求項1ないし4のいずれか1項に記載さ
れた、被検生体液中に含有される塩素イオンの濃度を測
定する方法。 6、高分子膜状物に配設した微細多孔の直径が0.03
ミクロン以下である、請求項1ないし5のいずれか1項
に記載された、被検生体液中に含有される塩素イオンの
濃度を測定する方法。
[Claims] 1. Chlorine ions pass through an electrode consisting of a working electrode made of silver, a counter electrode made of stainless steel, and a reference electrode made of silver/silver chloride in a biological fluid in the same tank. However, by installing a measuring electrode covered with a polymer membrane with microporous that does not allow coexisting substances such as proteins contained in biological fluids to pass through, the potential level of the working electrode is set relative to the counter electrode. -0.6 to +0.6V vs. Ag/A
gCl then +0.6 to -0.6V vs. Ag/A
gCl is cyclically changed in the range of voltage, and the current change that occurs in response to the voltage change is measured as the peak value of the continuously obtained oxidation wave and reduction wave. A method to measure the concentration of chloride ions contained in. 2. The method for measuring the concentration of chloride ions contained in a test biological fluid according to claim 1, wherein the biological fluid is a fluid selected from blood, serum, plasma, lymph, spinal fluid, and saliva. 3. The method for measuring the concentration of chloride ions contained in a test biological fluid according to claim 1, wherein the biological fluid is a liquid obtained by diluting the biological fluid with a buffer solution or distilled water. 4. Chlorine contained in the test biological fluid according to any one of claims 1 to 3, wherein the microporous polymer membrane is selected from polycarbonate and cellulose acetate. A method of measuring the concentration of ions. 5. Concentration of chloride ions contained in the biological fluid to be tested according to any one of claims 1 to 4, wherein the polymer membrane having micropores has a thickness of 5 to 7 microns. How to measure. 6. The diameter of the micropores arranged in the polymer membrane is 0.03
The method for measuring the concentration of chloride ions contained in a test biological fluid according to any one of claims 1 to 5, which is less than a micron.
JP16525889A 1989-06-29 1989-06-29 Method for measuring concentration of chlorine ion in biofluid Pending JPH0331753A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16525889A JPH0331753A (en) 1989-06-29 1989-06-29 Method for measuring concentration of chlorine ion in biofluid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16525889A JPH0331753A (en) 1989-06-29 1989-06-29 Method for measuring concentration of chlorine ion in biofluid

Publications (1)

Publication Number Publication Date
JPH0331753A true JPH0331753A (en) 1991-02-12

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Application Number Title Priority Date Filing Date
JP16525889A Pending JPH0331753A (en) 1989-06-29 1989-06-29 Method for measuring concentration of chlorine ion in biofluid

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Country Link
JP (1) JPH0331753A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0643300A1 (en) * 1993-09-09 1995-03-15 Kodak Limited Method and apparatus for measuring silver ion activity
US11217714B2 (en) 2018-09-13 2022-01-04 Kabushiki Kaisha Toshiba Evaluation method on anion permeability of graphene-containing membrane and photoelectric conversion device

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0643300A1 (en) * 1993-09-09 1995-03-15 Kodak Limited Method and apparatus for measuring silver ion activity
US11217714B2 (en) 2018-09-13 2022-01-04 Kabushiki Kaisha Toshiba Evaluation method on anion permeability of graphene-containing membrane and photoelectric conversion device
US11682740B2 (en) 2018-09-13 2023-06-20 Kabushiki Kaisha Toshiba Evaluation method on anion permeability of graphene-containing membrane and photoelectric conversion device

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