JPS6029134A - Production of living body electrode - Google Patents
Production of living body electrodeInfo
- Publication number
- JPS6029134A JPS6029134A JP58137573A JP13757383A JPS6029134A JP S6029134 A JPS6029134 A JP S6029134A JP 58137573 A JP58137573 A JP 58137573A JP 13757383 A JP13757383 A JP 13757383A JP S6029134 A JPS6029134 A JP S6029134A
- Authority
- JP
- Japan
- Prior art keywords
- plastic substrate
- solution
- electrode
- biological
- silver
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000000758 substrate Substances 0.000 claims description 34
- 229920003023 plastic Polymers 0.000 claims description 31
- HAAYBYDROVFKPU-UHFFFAOYSA-N silver;azane;nitrate Chemical compound N.N.[Ag+].[O-][N+]([O-])=O HAAYBYDROVFKPU-UHFFFAOYSA-N 0.000 claims description 10
- 229910052709 silver Inorganic materials 0.000 claims description 6
- 239000004332 silver Substances 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 4
- GTKRFUAGOKINCA-UHFFFAOYSA-M chlorosilver;silver Chemical compound [Ag].[Ag]Cl GTKRFUAGOKINCA-UHFFFAOYSA-M 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 description 13
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 12
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 229910001961 silver nitrate Inorganic materials 0.000 description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 239000003365 glass fiber Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229910000108 silver(I,III) oxide Inorganic materials 0.000 description 2
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 241001311547 Patina Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 238000001802 infusion Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
Landscapes
- Measurement And Recording Of Electrical Phenomena And Electrical Characteristics Of The Living Body (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は生体用電極の製造方法に関するものであり、更
に詳しくは生体用電極の形状に成型されたプラスチック
基体の表面が銀−塩化銀（Ａｇ−ｈｇＯ））で被覆され
た生体用電極の製造方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a biological electrode, and more specifically, the surface of a plastic substrate molded into the shape of a biological electrode is coated with silver-silver chloride (Ag-hgO). The present invention relates to a method of manufacturing a biological electrode.
生体用電極として、Ａｇ−Ａメソを素材とするものが広
く用いられている。これは静止電極電位、分極電圧、安
定性等の点で優れているからである。As biological electrodes, those made of Ag-A meso are widely used. This is because they are excellent in terms of static electrode potential, polarization voltage, stability, etc.
しかし生体用電極をすべてＡｇ−ＡｇＣ／で形成された
ものは、重くかつ高価である。このため最近では生体用
電極の形状に成型されたプラスチック等の基体の表面を
Ａｇ−Ａｇｏノで被覆した生体用電極が用いられるよう
になった。このような生体用電極は耐久性に欠けるが軽
量であシ安価であるから、いわゆる使い捨て電極として
きわめて有用である。However, a biomedical electrode made entirely of Ag-AgC is heavy and expensive. For this reason, recently, biomedical electrodes have been used in which the surface of a base material such as plastic molded into the shape of a biomedical electrode is coated with Ag-Ago. Although such biological electrodes lack durability, they are lightweight and inexpensive, so they are extremely useful as so-called disposable electrodes.
一般にプラスチ、り基体表面を金属で被覆する方法とし
て、真空蒸着法、スパッタリング法等があるがこれらは
設備、費用の点で問題がある。そこで現在生体用電極の
製造には主に、次の２つの方法が用いられている。Generally, there are vacuum evaporation methods, sputtering methods, etc. as methods for coating the surface of plastic substrates with metals, but these methods have problems in terms of equipment and costs. Therefore, the following two methods are currently used to manufacture biological electrodes.
第１は、生体用電極の形に成型されたプラスチ、り基体
の表面に銀ペースト（銀塗料）を塗布する方法である。The first method is to apply silver paste (silver paint) to the surface of a plastic substrate molded into the shape of a biological electrode.
第２は、生体用電極の形に成型されたプラスチック基体
の表面を化学エツチング法等で凹凸を設け、その凹部を
埋めるようにＮｉ、Ｃｕ等を付着させて（溶液メッキで
折力う）下地を作り、この下地の上にＡｇを電気メッキ
する方法である。Second, the surface of a plastic substrate molded into the shape of a biological electrode is made uneven by chemical etching, etc., and Ni, Cu, etc. are attached to fill the indentations (reinforced by solution plating), and a base layer is formed. This method involves making a substrate and electroplating Ag on top of this substrate.
上記第１の方法は、銀粉を混入した塗料を使うためコス
ト高となるという欠点がある。一方上記第２の方法は、
経済的には優れているが異種金属が接することになるか
ら、電気的、化学的安定性に欠は心電図等の生体信号に
雑音が混入する原因となる。またこの第２の方法で製造
された電極は、被覆材であるＡｇにピンホールがあると
、下地のＣｕ。The first method described above has the disadvantage of being expensive because it uses a paint containing silver powder. On the other hand, the second method above is
Although it is economically superior, since different metals come into contact with each other, it lacks electrical and chemical stability, which causes noise to be mixed into biological signals such as electrocardiograms. Further, in the electrode manufactured by this second method, if there is a pinhole in the Ag coating material, the Cu underlying layer will be removed.
Ｎｉが表出するためその部分から酸化が進みいわゆる静
止電極電位が不安定となる。特にＣｕが酸化される（緑
青となる）と有害でちる。Since Ni is exposed, oxidation progresses from that part and the so-called resting electrode potential becomes unstable. In particular, when Cu is oxidized (becomes patina), it is harmful.
本発明は上記欠点に鑑みなされたものでその目的は、す
べてがＡｇ −Ａｇ （Ｍで作製された生体用電極と同
様な電気的化学的特性を有しかつ軽量で安価な生体用電
極を製造する方法を提供することである。The present invention was made in view of the above-mentioned drawbacks, and its purpose is to produce a lightweight and inexpensive biomedical electrode that has electrochemical properties similar to biomedical electrodes made entirely of Ag-Ag (M). The goal is to provide a method to do so.
そこで本発明では、生体用電極の形状に成型されたプラ
スチック基体をアンモニア性硝酸銀溶液中に浸漬しこの
溶液中に還元性有機物を添加して上記プラスチ、り基体
の表面に銀を付着させた後、表面に銀を付着された上記
プラスチック基体を陽極に用いてＭａｉｌ溶液を電気分
解し上記プラスチック基体の表面をＡｇ−Ａｇｏ）にし
て生体用電極を製造した。Therefore, in the present invention, a plastic substrate molded into the shape of a biological electrode is immersed in an ammoniacal silver nitrate solution, and a reducing organic substance is added to this solution to adhere silver to the surface of the plastic substrate. A biological electrode was manufactured by electrolyzing the Mail solution using the plastic substrate with silver adhered to its surface as an anode to make the surface of the plastic substrate Ag-Ago.
本発明の方法は２つの過程から成り立っている。The method of the invention consists of two steps.
まず第１の過程は、いわゆる鋼装反応を利用して、あら
かじめ生体用電極の形に成型されているプラスチック基
体の表面をＡｇで神覆するものである。In the first step, the surface of a plastic substrate, which has been previously formed into the shape of a biological electrode, is coated with Ag using a so-called steel-cladding reaction.
まず硝酸銀溶液にアンモニア水を注入し、当初できる沈
殿物Ａｇ２Ｏが完全に溶解する寸で加える。First, aqueous ammonia is poured into the silver nitrate solution until the Ag2O precipitate that is initially formed is completely dissolved.
このときの溶液がアンモニア性硝酸銀溶液である。The solution at this time is an ammoniacal silver nitrate solution.
次に、あらかじめ生体用電極の形に成型しである清浄な
プラスチック基体を、前記のアンモニア性硝酸銀溶液と
ホルマリン等の還元性有機物（以下単に還元剤という）
との混合液に浸漬する。こうしてプラスチック基体の表
面にＡｇが析出する。Next, a clean plastic substrate, which has been previously molded into the shape of a biological electrode, is mixed with the ammoniacal silver nitrate solution and a reducing organic substance such as formalin (hereinafter simply referred to as a reducing agent).
Soak in a mixture of In this way, Ag is deposited on the surface of the plastic substrate.
ここでアンモニア性硝酸銀溶液の濃度は、０．３ｍｊｉ
／ｌ〜８ｍｏＶ１の範囲が良い。この濃度が低いと反応
速度が小さくなりプラスチック基体の表面′に必要量の
Ａｇが付着する才で長時間を要する。またこの濃度が高
いと、例えば溶解度の限界近くまで高ければ、プラスチ
ック基体の表面に付着するＡｇはむらを生じる。同様に
還元剤の５・も、少なければプラスチック基体表面にＡ
ｇが付着する効率が悪くなり、多ければプラスチ、り基
体表面に付着するＡｇはむらを生じる。Here, the concentration of the ammoniacal silver nitrate solution is 0.3 mji
A range of /l to 8moV1 is preferable. If this concentration is low, the reaction rate will be low and it will take a long time to deposit the required amount of Ag on the surface of the plastic substrate. Also, if this concentration is high, for example close to the solubility limit, the Ag deposited on the surface of the plastic substrate will become uneven. Similarly, if there is less reducing agent 5, A
The efficiency with which Ag adheres becomes poor, and if too much Ag adheres to the surface of the plastic substrate, the Ag adheres to the surface of the substrate becomes uneven.
第２の過程は上記のようにして表面にＡｇを付着された
プラスチック基体をＨＢＯ＃溶液に浸漬し、これを陽極
としてＮａＣｊノ ！液を電気分解しプラスチック基体
表面をＡｇ −Ａｇ ０１とするものである。In the second step, the plastic substrate with Ag adhered to its surface as described above is immersed in an HBO# solution, and this is used as an anode to generate NaCjNO! The liquid is electrolyzed to make the surface of the plastic substrate Ag-Ag 01.
このとき陰極にはｐｔ板を用いる。At this time, a PT plate is used as the cathode.
ここで例えばＮａｏ４′溶液の濃度が０．９俤であると
き、電流密度は０．１ｍＶｃＪ〜６．５ｍＡ／ｃｒｙと
し、通電時間は６０分〜３分とすれば良好である。For example, when the concentration of the Nao4' solution is 0.9, it is preferable to set the current density to 0.1 mVcJ to 6.5 mA/cry and to set the current application time to 60 minutes to 3 minutes.
なお、プラスチック基体の材質の軸頚は問わずメッキは
可能であるが、Ａｇが剥離しやすく生体用電極として実
用にｌえないものもある。ナチュラルＡＢＳ樹脂、ガラ
ス繊維入りＡＢＳ樹脂等巳ｇが良く付着しており、生体
用電極として十分使用可能である。Although plating is possible regardless of the material of the plastic substrate, there are some that cannot be used as biological electrodes because the Ag tends to peel off easily. Natural ABS resin, glass fiber-containing ABS resin, etc. have good adhesion and can be used as biological electrodes.
本発明によれば、プラスチック基体表面に直接付着した
ＡｇをＡｇ −Ａｇｃｚとすることができるので電気的
化学的特性が安５１了シた生体用１打極を作製すること
ができる。また、このような方法によれば、従来ノ化学
エッヂング管の前処理を必要とする方法と比べ、工程が
簡略化されるので製造が簡単でかつ経済的である。According to the present invention, since the Ag directly attached to the surface of the plastic substrate can be made into Ag-Agcz, it is possible to produce a single electrode for biological use with excellent electrochemical properties. Further, according to such a method, the manufacturing process is simpler and more economical than the conventional method which requires pre-treatment of the chemically etched pipe because the process is simplified.
本発明により製造された生体用電極は、プラスチック基
体をＡｇあるいはＡｇ−ＡｇＣ！ノで被覆しだ構造の従
来型電極がもつ利点（軽量、安価、電気的化学的に安定
等）をすべて備えている。The biomedical electrode manufactured according to the present invention has a plastic base made of Ag or Ag-AgC! It has all the advantages of conventional electrodes with a sheathed structure (light weight, low cost, electrochemical stability, etc.).
以下実施例を示す。Examples are shown below.
実施例１
硝酸銀５ｇを純水２５ｃｃ・に入れて完全に溶解させ硝
酸銀溶液を作る。この硝酸銀溶液に１０チのアンモニア
水を徐々に点滴すると当初この溶液は褐色になる。更に
１０チアンモニア水を点滴して溶液が透明になったとこ
ろで点滴を止める。この溶液がアンモニア性硝酸銀溶液
である。次に電極の形状に成型されたナチュラルＡＢＳ
樹脂をホルマリンに浸した後、上記のアンモニア性硝酸
銀溶液に浸漬する。浸漬してから５分後、更にホルマリ
ンをＱ、５ＣＣ１゛追加する。このときプラスチック（
ナチュラルＡＢＳ樹脂）基体表面にＡｇが析出する。ア
ンモニア性硝酸銀溶液に浸漬してから７分後、プラスチ
、り基体を取シ出して水洗いをして乾燥させる。次に表
面にＡｇを付着されたこのプラスチ、り基体を０．９チ
のＮａＯΔ溶液に浸漬し、これを陽極としてＮａＯノ溶
液を電気分解する。このとき陰極はｐｔ板とする。そし
て５臥の直流電流を約３分間流すとプラスチ、り基体表
面はＡｇ−Ａｇ０＃となる。Example 1 A silver nitrate solution was prepared by adding 5 g of silver nitrate to 25 cc of pure water and completely dissolving it. When 10 g of aqueous ammonia is gradually dripped into this silver nitrate solution, the solution initially turns brown. Furthermore, 10 thiammonia water is instilled, and the infusion is stopped when the solution becomes clear. This solution is an ammoniacal silver nitrate solution. Next, natural ABS molded into the shape of the electrode
After the resin is immersed in formalin, it is immersed in the ammoniacal silver nitrate solution described above. 5 minutes after immersion, add Q, 5CC1'' of formalin. At this time, plastic (
(Natural ABS resin) Ag is deposited on the substrate surface. After 7 minutes of immersion in the ammoniacal silver nitrate solution, the plastic substrate is removed, washed with water, and dried. Next, this plastic substrate with Ag adhered to its surface is immersed in a 0.9 inch NaOΔ solution, and the NaO solution is electrolyzed using this as an anode. At this time, the cathode is a PT plate. Then, when 5 degrees of direct current is passed for about 3 minutes, the surface of the plastic substrate becomes Ag-Ag0#.
このようにして製造された生体用電極を実際に心電計に
接続して作成した心電図は、従来の生体用電極を同様に
して用いて作成した心電図と比べ何等異なることはなか
った。また、このようにして製造された生体用電極を取
り扱うとき、プラスチ、り基体表面のＡｇ−ＡｇＧＪが
剥離する等の不都合は生じなかった。An electrocardiogram created by actually connecting the biological electrode manufactured in this manner to an electrocardiograph was not different from an electrocardiogram created using a conventional biological electrode in the same manner. Further, when handling the biomedical electrode manufactured in this manner, no problems such as peeling of Ag-AgGJ on the surface of the plastic substrate occurred.
実施例２
硝酸銀５ｇを純水ＩＱＱ＋ｃｃに入れて完全に溶解させ
硝酸鋼溶液を作る。この硝酸銀溶液に２８係のアンモニ
ア水を徐々に点滴し、実施例１と同様に溶液が透明にな
ったところで点滴を止めアンモニア性硝酸銀溶液を作る
。次に電極の形状に成型されたガラス繊維入りＡＢＳ樹
脂をアンモニア性硝酸銀溶液に入れ、アセトンを２ＣＣ
入れて１時間浸漬する。このときプラスチック（ガラス
繊維入、９ＡＢＳ樹脂）基体表面にＡｇが析出する。そ
してプラスチ、り基体を溶液から取り出して水洗いをし
た後乾燥させる。次に、表面にｈｉを付着されたこのプ
ラスチック基体を０，９チのＮａＣ１溶液に浸漬し、こ
れを陽極に用いてＮａ（１７溶液を電気分解する。この
とき陰極はｐｔ板とする。そして０．５１１’ＬＡの直
流電流を３０分流すとプラスチ、り基体表面はＡｇ−Ａ
ｇ０１となる。Example 2 5 g of silver nitrate was completely dissolved in pure water IQQ+cc to prepare a nitric acid steel solution. Aqueous ammonia No. 28 was gradually dripped into this silver nitrate solution, and as in Example 1, when the solution became transparent, the dripping was stopped to prepare an ammoniacal silver nitrate solution. Next, the glass fiber-containing ABS resin molded into the shape of an electrode was placed in an ammoniacal silver nitrate solution, and 2cc of acetone was added.
Pour in and soak for 1 hour. At this time, Ag is deposited on the surface of the plastic (glass fiber-containing, 9ABS resin) substrate. The plastic substrate is then removed from the solution, washed with water, and then dried. Next, this plastic substrate with hi adhered to the surface is immersed in a 0.9-inch NaCl solution, and this is used as an anode to electrolyze the Na(17 solution). At this time, a PT plate is used as the cathode. When a DC current of 0.511'LA is applied for 30 minutes, the substrate surface becomes Ag-A.
It becomes g01.
このようにして製造された生体用電極は、実施例１と同
様充分実用に耐えるものであシ、従来の電極と比べ電気
的あるいは化学的特性は異なるところがない。The biological electrode manufactured in this way is sufficiently usable as in Example 1, and there is no difference in electrical or chemical properties compared to conventional electrodes.
Claims (1)
モニア性硝酸銀溶液中に浸漬し該溶液中に還元性有機物
を添加して前記プラスチ、り基体表面に銀を付着した後
、表面に銀を付着された前記プラスチック基体を陽極に
して塩化ナトリウム溶液を電気分解し前記グラ・スナッ
ク基体の表面を銀−塩化銀とすることを特徴とする生体
用電極の製造方法。A plastic substrate molded into the shape of a biological electrode is immersed in an ammoniacal silver nitrate solution, and a reducing organic substance is added to the solution to adhere silver to the surface of the plastic substrate. A method for producing a biological electrode, characterized in that a sodium chloride solution is electrolyzed using the plastic substrate as an anode to make the surface of the glass-snack substrate silver-silver chloride.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58137573A JPS6029134A (en) | 1983-07-29 | 1983-07-29 | Production of living body electrode |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58137573A JPS6029134A (en) | 1983-07-29 | 1983-07-29 | Production of living body electrode |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS6029134A true JPS6029134A (en) | 1985-02-14 |
Family
ID=15201875
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58137573A Pending JPS6029134A (en) | 1983-07-29 | 1983-07-29 | Production of living body electrode |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6029134A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63132632A (en) * | 1986-11-26 | 1988-06-04 | フクダ電子株式会社 | Electrode element for living body induction electrode and its production |
| JPH024324A (en) * | 1988-06-13 | 1990-01-09 | Fukuda Denshi Co Ltd | Organism induction electrode for chest |
| JPH024322A (en) * | 1988-06-13 | 1990-01-09 | Fukuda Denshi Co Ltd | Organism induction electrode for four limbs |
| JPH024320A (en) * | 1988-06-13 | 1990-01-09 | Fukuda Denshi Co Ltd | Organism induction electrode for four limbs |
| JPH024325A (en) * | 1988-06-13 | 1990-01-09 | Fukuda Denshi Co Ltd | Organism induction electrode for four limbs |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55130647A (en) * | 1979-03-02 | 1980-10-09 | Tokyo Tokushu Densen Kk | Silverrsilver chloride compound material for electrode and its preparation |
| JPS5729336A (en) * | 1980-07-31 | 1982-02-17 | Fujikura Kasei Kk | Conductive resin electrode for living body |
| JPS587227A (en) * | 1981-07-02 | 1983-01-17 | ティーディーケイ株式会社 | Preparation of electrode for live body |
-
1983
- 1983-07-29 JP JP58137573A patent/JPS6029134A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55130647A (en) * | 1979-03-02 | 1980-10-09 | Tokyo Tokushu Densen Kk | Silverrsilver chloride compound material for electrode and its preparation |
| JPS5729336A (en) * | 1980-07-31 | 1982-02-17 | Fujikura Kasei Kk | Conductive resin electrode for living body |
| JPS587227A (en) * | 1981-07-02 | 1983-01-17 | ティーディーケイ株式会社 | Preparation of electrode for live body |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS63132632A (en) * | 1986-11-26 | 1988-06-04 | フクダ電子株式会社 | Electrode element for living body induction electrode and its production |
| JPH0230249B2 (en) * | 1986-11-26 | 1990-07-05 | Fukuda Denshi Kk | |
| JPH024324A (en) * | 1988-06-13 | 1990-01-09 | Fukuda Denshi Co Ltd | Organism induction electrode for chest |
| JPH024322A (en) * | 1988-06-13 | 1990-01-09 | Fukuda Denshi Co Ltd | Organism induction electrode for four limbs |
| JPH024320A (en) * | 1988-06-13 | 1990-01-09 | Fukuda Denshi Co Ltd | Organism induction electrode for four limbs |
| JPH024325A (en) * | 1988-06-13 | 1990-01-09 | Fukuda Denshi Co Ltd | Organism induction electrode for four limbs |
| JPH059094B2 (en) * | 1988-06-13 | 1993-02-04 | Fukuda Denshi Kk | |
| JPH0513662B2 (en) * | 1988-06-13 | 1993-02-23 | Fukuda Denshi Kk | |
| JPH0581133B2 (en) * | 1988-06-13 | 1993-11-11 | Fukuda Denshi Kk |
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