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JP5437772B2 - Medical treatment tool - Google Patents
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JP5437772B2 - Medical treatment tool - Google Patents

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JP5437772B2
JP5437772B2 JP2009246911A JP2009246911A JP5437772B2 JP 5437772 B2 JP5437772 B2 JP 5437772B2 JP 2009246911 A JP2009246911 A JP 2009246911A JP 2009246911 A JP2009246911 A JP 2009246911A JP 5437772 B2 JP5437772 B2 JP 5437772B2
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rope
medical
operating
wire
treatment
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JP2011092284A (en
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富久 加藤
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Asahi Intecc Co Ltd
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Asahi Intecc Co Ltd
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Description

この発明は、接合部材を用いて操作用ロープと、操作用ロープの先端部、又は手元操作部の連結部材との接合部材を用いた接合における操作用ロープの接合部の機械的強度特性を向上させた医療用処置具等に関する。   The present invention improves the mechanical strength characteristics of the joint portion of the operation rope in the joint using the joint member of the operation rope and the distal end portion of the operation rope or the connecting member of the hand operation portion using the joint member. The present invention relates to a medical treatment tool and the like.

体内へ挿入する医療用処置具の先端部、又は手元操作部は操作用ロープを介して手元操作を先端部へ伝達させる為、連結部材と操作用ロープとの接合部の機械的強度特性を考慮して、病変部治療に際して人体への安全確保を満たさなければならず、この為種々の提案がなされている。   The distal end of the medical treatment instrument to be inserted into the body or the hand operating section transmits the hand operation to the distal end via the operating rope, so the mechanical strength characteristics of the joint between the connecting member and the operating rope are considered. Thus, it is necessary to satisfy the safety of the human body when treating the lesion, and various proposals have been made for this purpose.

特許文献1には、内視鏡として操作ワイヤの先端を、最先端の節輪の内周部にレーザー溶接する接合技術が開示され、局部的な加熱の為の焼きなましによる劣化を極力防止し、接続作業を容易にして、かつ短時間に行うことを目的としている。
しかし、短時間であってもレーザー光による細線の操作ワイヤと節輪との「溶接」であって細線のワイヤは溶け、溶接前の操作ワイヤの機械的強度を維持することはできない。
Patent Document 1 discloses a joining technique of laser welding the tip of an operation wire as an endoscope to the inner periphery of a state-of-the-art node ring, preventing deterioration due to annealing for local heating as much as possible, The purpose is to make the connection work easy and to be done in a short time.
However, even in a short time, it is “welding” between the fine wire operation wire and the node ring by laser light, the fine wire melts and the mechanical strength of the operation wire before welding cannot be maintained.

特許文献2には、内視鏡として湾曲操作ワイヤと挿入先端部とを真空環境下、又は不活性ガス環境下における「ろう付け固着」する接合技術が開示され、錆発生による湾曲操作ワイヤの断線防止を目的としている。

しかし、一般的に、例えばステンレス鋼のろう付けには融点が895℃から1030℃の金ろう(JISZ3266)等が用いられ、かかる場合に湾曲操作ワイヤを撚合構成する金属素線は溶けて溶接され、又かかる特許文献にはろう材の開示はなく、そして、ろう材の溶融温度と湾曲操作ワイヤとの機械的強度特性との相関性については何ら開示はなく、さらに上記いずれの特許文献も「ろう付けを単なる固着手段」として用いる考え方である。
Patent Document 2 discloses a joining technique in which a bending operation wire and an insertion tip are “brazed and fixed” in a vacuum environment or an inert gas environment as an endoscope, and the bending operation wire is disconnected due to the occurrence of rust. The purpose is prevention.

However, in general, for example, gold brazing (JIS Z3266) having a melting point of 895 ° C. to 1030 ° C. is used for brazing stainless steel, and in such a case, the metal strands that constitute the bending operation wire are melted and welded. In addition, there is no disclosure of brazing material in such a patent document, and there is no disclosure about the correlation between the melting temperature of the brazing material and the mechanical strength characteristics of the bending operation wire. This is an idea of using brazing as a simple means of fixing.

特開昭61−293419号公報JP 61-293419 A 特開2001−149307号公報JP 2001-149307 A

従来の医療用内視鏡において、その操作用ロープにステンレス鋼線を用いて操作用ロープと、節輪又は湾曲駒のロープ受けの連結部材とを接合する際、接合部材であるろう材等は単なる固着手段としてのみの技術思想しか存在せず、ステンレス鋼線の加工度の高い強加工の伸線加工した金属素線を複数本撚合構成した操作用ロープと、この強加工した金属素線を用いた操作用ロープの熱影響による機械的強度特性を考慮した、ろう付けやはんだ付けの際の接合部材である共晶合金を用いた接合に関する技術思想は存在していない。
又、後述する医療内視鏡用スネア、医療内視鏡用鉗子等の医療用処置具においても操作用ロープの先端部と連結部材との接合、又は操作用ロープの手元部と連結部材との接合においても同様である。
この発明の目的は、操作用ロープの金属素線にオーステナイト系ステンレス鋼線を用いて強加工の伸線加工を行い、この強加工した金属素線への熱影響による引張破断強度特性向上効果を利用して、前記接合部材を単に固着手段として用いるのみではなく、操作用ロープの引張破断力を向上させながら、かつ接合強度を向上させる新たな接合の技術思想を開示することにより、術者が安全に操作できる医療用処置具を提供することにある。
In a conventional medical endoscope, when joining an operation rope and a connecting member of a rope receiver of a node ring or a bending piece using a stainless steel wire for the operation rope, a brazing material or the like as a joining member is simply There is only a technical idea only as a fixing means, and an operation rope formed by twisting a plurality of high-stretched metal strands with a high degree of processing of stainless steel wire, and this strongly-processed metal strand There is no technical idea regarding joining using a eutectic alloy which is a joining member at the time of brazing or soldering in consideration of the mechanical strength characteristics due to the heat effect of the operating rope used.
Further, in medical treatment instruments such as a medical endoscope snare and medical endoscope forceps described later, the operation rope is joined to the distal end portion of the operation rope and the connection member, or the proximal portion of the operation rope is connected to the connection member. The same applies to bonding.
The object of the present invention is to perform a strong wire drawing process using an austenitic stainless steel wire for the metal wire of the operation rope, and to improve the tensile breaking strength characteristics due to the heat effect on the strongly processed metal wire. By utilizing the joining member not only as a fixing means, but also by disclosing a new joining technical idea that improves the joining strength while improving the tensile breaking force of the operating rope, An object of the present invention is to provide a medical treatment tool that can be operated safely.

請求項1に記載の発明は、可とう性管体に貫挿した操作用ロープの先端処置部の連結部材、又は手元操作部の連結部材と、前記操作用ロープとを接合部材を用いて接合し、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部を動作させる医療用処置具において、前記操作用ロープは、固溶化処理し、且つ、成分にMoを含まないオーステナイト系ステンレス鋼線を用いて、総減面率が80%から99.5%の伸線加工した金属素線を複数本用いて撚合構成して成り、 前記接合部材は、180℃から495℃の溶融温度をもつ共晶合金から成り、又は前記操作用ロープは、固溶化処理し、且つ、成分にMoを含むオーステナイト系ステンレス鋼線を用いて、総減面率が80%から99.5%の伸線加工した金属素線を複数本用いて撚合構成して成り、 前記接合部材は、180℃から525℃の溶融温度をもつ共晶合金から成り、前記操作用ロープと前記連結部材とを、前記接合部材を用いて接合して成ることを特徴とする医療用処置具である。
この構成により、接合部材の溶融熱を利用して接合部での操作用ロープの引張破断力を向上させて高度の機械的強度特性を得て、かつ操作用ロープと連結部材との接合強度を向上させ、術者が安全に操作できる医療用処置具の提供ができる。
According to the first aspect of the present invention, the connecting member of the distal treatment section of the operating rope inserted through the flexible tube or the connecting member of the hand operating section and the operating rope are joined using the joining member. Then, in the medical treatment instrument that operates the distal treatment section by the operation of transmitting the operation force of the operation rope by pushing, pulling, or rotating the hand operation section, the operation rope is solidified. And an austenitic stainless steel wire that does not contain Mo as a component and is formed by twisting a plurality of drawn metal strands having a total area reduction of 80% to 99.5%. The joining member is made of a eutectic alloy having a melting temperature of 180 ° C. to 495 ° C., or the operating rope is subjected to a solution treatment and using an austenitic stainless steel wire containing Mo as a component, Total area reduction is 80% to 99 .5% wire-drawn metal strands are used to form a twisted structure, and the joining member is made of a eutectic alloy having a melting temperature of 180 ° C. to 525 ° C. A medical treatment instrument characterized in that a connecting member is joined using the joining member.
With this configuration, the tensile breaking force of the operation rope at the joint is improved by utilizing the heat of fusion of the joining member to obtain a high mechanical strength characteristic, and the bonding strength between the operation rope and the connecting member is increased. It is possible to improve and provide a medical treatment tool that can be operated safely by an operator.

請求項2に記載の発明は、前記操作用ロープの金属素線は、前記操作用ロープの金属素線の伸線加工における総減面率は90%から99.5%であり、前記連結部材と接合する前記操作用ロープの少なくとも先端処置具の接合部、又は手元操作部の接合部に電解研磨処理、又は前記接合部材と同一の組成成分を含むめっき処理を施したことを特徴とする請求項1に記載の医療用処置具である。
この構成により、接合部での接合部材との濡れ性を向上させて、操作用ロープの引張破断力を向上させながら、かつ接合部の接合強度をより向上させることができる。
According to a second aspect of the present invention, in the metal strand of the operation rope, the total area reduction rate in the wire drawing of the metal strand of the operation rope is 90% to 99.5% , and the connecting member The electropolishing treatment or the plating treatment containing the same composition component as that of the joining member is applied to at least the joint portion of the distal treatment instrument or the joint portion of the hand operation portion of the operation rope to be joined with the joint rope. The medical treatment tool according to Item 1.
With this configuration, it is possible to improve the wettability with the bonding member at the bonded portion and improve the tensile strength of the operating rope while further improving the bonded strength of the bonded portion.

請求項3に記載の発明は、前記操作用ロープは、素線直径が0.008mmから0.200mmの金属素線を芯材と側材に用いて、前記芯材の外周に側材を6本から9本を一方向螺旋状に巻回成形する撚合構成のスパイラルロープから成り、前記芯材の素線直径が前記側材の素線直径の1.07倍から2.12倍とし、前記操作用ロープから成ることを特徴とする請求項1〜2のいずれか一つに記載の医療用処置具である。
この構成により、引張破断力を向上させた操作用ロープを用いて接合部の接合強度をさらに向上させることができ、かつ、特に押し、及び回転操作による先端部への操作力伝達性能をより向上させた医療用処置具の提供ができる。
According to a third aspect of the present invention, in the operation rope, a metal strand having a strand diameter of 0.008 mm to 0.200 mm is used as a core member and a side member, and a side member is provided on the outer periphery of the core member. It is composed of a spiral rope having a twisted configuration in which nine from one are spirally wound in one direction, and the strand diameter of the core material is 1.07 to 2.12 times the strand diameter of the side material, It consists of the said rope for operation, It is a medical treatment tool as described in any one of Claims 1-2.
With this configuration, it is possible to further improve the joint strength of the joint using an operation rope with improved tensile breaking force, and further improve the operating force transmission performance to the tip part, especially by pushing and rotating operations It is possible to provide a medical treatment tool that has been allowed.

請求項4に記載の発明は、前記接合部材である共晶合金が、金、又は銀のいずれかを含む組成から成り、溶融温度が217℃から525℃であることを特徴とする請求項1〜3のいずれか一つに記載の医療用処置具である。
この構成により、接合部材の溶融熱を利用して操作用ロープの引張破断力を向上させ、かつ接合部の接合強度を向上させることができる。
The invention according to claim 4 is characterized in that the eutectic alloy as the joining member is composed of a composition containing either gold or silver and has a melting temperature of 217 ° C. to 525 ° C. It is a medical treatment tool as described in any one of -3.
With this configuration, it is possible to improve the tensile breaking force of the operating rope using the heat of fusion of the joining member, and improve the joining strength of the joined portion.

請求項5に記載の発明は、請求項1〜4のいずれか一つに記載の医療用処置具が、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部の処置用ループを拡縮させ、又は拡縮させた後、前記操作用ロープ、及び前記先端処置部に高周波電流を通電させて患部を切除することを特徴とする医療内視鏡用処置具である医療内視鏡用スネア、又は医療内視鏡用高周波スネアで、又請求項6に記載の発明は、請求項1〜4のいずれか一つに記載の医療用処置具が、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部の生検鉗子の鉗子カップを開閉させて生体組織を採取し、又は前記鉗子カップを開閉させた後、前記操作用ロープ、及び前記鉗子カップに高周波電流を通電させて患部を切除することを特徴とする医療内視鏡用処置具である医療内視鏡用鉗子、又は医療内視鏡用ホットバイオプシー鉗子である。
この構成により、操作用ロープの引張破断強度不足に起因する操作不能状態での術者の手技の中断を防ぎ、先端処置部のループの拡縮、又は生検鉗子カップの開閉作用の円滑化を図り、高度の操作性を維持しながら、かつ高周波通電の際、操作用ロープの通電作用と金、又は銀成分を含む接合部材の高通電作用により患部の切除、又は生体組織の採取、及び止血等の迅速な手技対応ができる医療内視鏡用スネア、医療内視鏡用高周波スネア、並びに、医療内視鏡用鉗子、医療内視鏡用ホットバイオプシー鉗子の医療内視鏡用処置具の提供ができる。
According to a fifth aspect of the present invention, the medical treatment tool according to any one of the first to fourth aspects of the present invention is configured such that the operating force of the operating rope is reduced by pushing, pulling, or rotating the hand operating unit. The medical treatment is characterized in that after the treatment loop of the distal treatment section is expanded or contracted by a transmission action, the affected area is excised by applying a high-frequency current to the operation rope and the distal treatment section. A medical endoscope snare which is a treatment instrument for endoscope or a high frequency snare for medical endoscope, and the invention according to claim 6 is the medical treatment according to any one of claims 1 to 4. The tool pushes, pulls, or rotates the hand operation part to transmit and manipulate the operating force of the operation rope, and opens and closes the forceps cup of the biopsy forceps of the distal treatment part to collect a living tissue, Alternatively, after opening and closing the forceps cup, the operation rope, and The medical endoscope forceps are medical endoscope treatment tool, characterized in that the forcep cups is a high-frequency current to ablate the affected area, or a hot biopsy forceps for medical endoscopes.
This configuration prevents interruption of the operator's procedure in an inoperable state due to insufficient tensile rupture strength of the operating rope, and facilitates the expansion / contraction of the loop of the distal treatment section or the opening / closing action of the biopsy forceps cup. While maintaining high operability and high-frequency energization, excision of the affected area, collection of living tissue, hemostasis, etc. by energizing action of the operating rope and high energizing action of the joining member containing gold or silver components Of medical endoscope snares, medical endoscope high-frequency snares, medical endoscopic forceps, and medical endoscopic hot biopsy forceps it can.

請求項7に記載の発明は、請求項1〜4のいずれか一つに記載の医療用処置具が、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部のクリップを離脱させて体内留置することを特徴とする医療内視鏡用処置具である医療内視鏡用クリップ装置である。
この構成により、先端処置部のクリップを複数設けて操作用ロープの引張力が増大しても引張破断強度不足に起因する操作不能を防ぎ、クリップの離脱操作を円滑にさせ、迅速な手技対応ができるクリップ装置の医療内視鏡用処置具の提供ができる。
According to a seventh aspect of the present invention, the medical treatment instrument according to any one of the first to fourth aspects of the present invention is configured such that the operating force of the operating rope is reduced by pushing, pulling, or rotating the hand operating section. A clip device for a medical endoscope, which is a medical endoscope treatment tool, wherein the clip of the distal treatment section is detached and placed in the body by a transmission action.
With this configuration, even if the tension of the rope for operation is increased by providing multiple clips for the distal treatment section, it prevents inoperability due to insufficient tensile breaking strength, smoothing the clip detachment operation, and quick procedure response. It is possible to provide a medical endoscope treatment tool with a clip device.

請求項8に記載の発明は、請求項1〜4のいずれか一つに記載の医療用処置具が、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部のナイフ部を所望の位置へ案内しながら前記操作用ロープ、及び前記ナイフ部へ高周波電流を通電させて患部生体組織を焼灼切開することを特徴とする医療内視鏡用処置具である医療内視鏡用高周波ナイフである。
この構成により、操作用ロープの連結部材との接合部での引張破断強度不足に起因する操作不能状態での術者の手技中断を防ぎ、先端処置部のナイフ部への円滑な操作性を向上させながら、かつ、高周波通電の際、操作用ロープの通電作用と、金、又は銀成分を含む接合部材の高通電作用により、患部の切除、及び止血等の迅速な手技対応ができる高周波ナイフの医療内視鏡用処置具の提供ができる。尚、補足すれば病変部の明瞭な視覚把握の為、生理食塩水の注入に際し、後述する接合部材を任意選択使用することにより、接合部材の黒色化による接合強度不足等を解消することができる。
According to an eighth aspect of the present invention, the medical treatment instrument according to any one of the first to fourth aspects of the present invention is configured to reduce the operating force of the operating rope by pushing, pulling, or rotating the hand operating section. A medical endoscope characterized in that a high-frequency current is applied to the operation rope and the knife portion while a knife portion of the distal treatment portion is guided to a desired position by a transmission action to cauterize and incise the affected living body tissue. This is a high-frequency knife for a medical endoscope that is a treatment instrument for a mirror.
This configuration prevents the operator from interrupting the procedure in an inoperable state due to insufficient tensile break strength at the joint with the connecting member of the operating rope, and improves the smooth operability of the tip treatment section to the knife section Of the high-frequency knife that can respond quickly to procedures such as excision of the affected area and hemostasis by the energizing action of the operating rope and the high energizing action of the joining member containing gold or silver components. A medical endoscope treatment tool can be provided. In addition, if supplemented, a clear visual grasp of the lesioned part can be used to eliminate insufficient bonding strength due to blackening of the bonding member by optionally using a bonding member described later when injecting physiological saline. .

本発明の医療用処置具(医療内視鏡)の全体を示す斜視図。The perspective view which shows the whole medical treatment tool (medical endoscope) of this invention. 本発明の医療用処置具(医療内視鏡)の挿入部先端側を側方からみた断面図。Sectional drawing which looked at the insertion part front end side of the medical treatment tool (medical endoscope) of this invention from the side. 本発明の医療用処置具(医療内視鏡)の先端の湾曲駒、及び操作用ロープの組付図。The assembly | attachment figure of the bending piece of the front-end | tip of the medical treatment tool (medical endoscope) of this invention, and the rope for operation. 他の実施例(管体ロープ受けの連結部材)の医療用処置具(医療用内視鏡)の先端の湾曲駒、及び操作用ロープの組付図。The assembly | attachment figure of the bending piece of the front-end | tip of the medical treatment tool (medical endoscope) of another Example (connecting member of a tubular rope receiver), and the rope for operation. 本発明の医療用処置具に用いる操作用ロープの構成図。The block diagram of the rope for operation used for the medical treatment tool of this invention. 総減面率と引張破断強度特性図。Total area reduction ratio and tensile breaking strength characteristic diagram. 操作用ロープに用いる金属素線の温度と引張破断強度特性図。The temperature and tensile breaking strength characteristic figure of the metal strand used for the rope for operation. 医療内視鏡用スネア、及び医療内視鏡用高周波スネアの構成図。The block diagram of the snare for medical endoscopes, and the high frequency snare for medical endoscopes. 医療内視鏡用鉗子、及び医療内視鏡用ホットバイオプシー鉗子構成図。The forceps for medical endoscopes and the hot biopsy forceps configuration diagram for medical endoscopes. 医療内視鏡用クリップ装置の構成図。The block diagram of the clip apparatus for medical endoscopes. 医療内視鏡用高周波ナイフの構成図。The block diagram of the high frequency knife for medical endoscopes.

この発明の実施形態を図に示すとともに説明する。   An embodiment of the present invention will be described with reference to the drawings.

図1は本発明の実施例1の医療用処置具である医療用内視鏡1の全体の斜視図を示し、医療用内視鏡1は、手元操作部2と、この手元操作部2の先端に接続されて体内へ挿入される細長の挿入部4と、並びに前記操作部2の手元部に医療用内視鏡1の医療内視鏡用処置具11の出入りを可能にした処置具孔10と、及び光源装置(図示せず)に着脱自在に接続されるコネクタ9を備えたユニバーサルコード8から構成されている。又、前記手元操作部2には、先端部を自在に湾曲させる湾曲操作ノブ3、及びビデオプロセッサー(図示せず)をコントロールするリモートスイッチ12が設けられている。
そして挿入部4は、手元部から可とう管部5と、湾曲部6と、先端構成部7を直列に連結した構造となっている。尚、本発明の医療用処置具とは、医療用内視鏡と医療内視鏡用処置具の双方をいい、医療内視鏡用処置具には後述するスネア、鉗子、クリップ、高周波ナイフ等の処置具のことをさす。
FIG. 1 shows an overall perspective view of a medical endoscope 1 that is a medical treatment instrument according to a first embodiment of the present invention. The medical endoscope 1 includes a hand operation unit 2 and a hand operation unit 2. An elongated insertion portion 4 connected to the distal end and inserted into the body, and a treatment tool hole that allows the medical endoscope treatment tool 11 of the medical endoscope 1 to enter and exit from the hand portion of the operation portion 2. 10 and a universal cord 8 having a connector 9 detachably connected to a light source device (not shown). The hand operation unit 2 is provided with a bending operation knob 3 for freely bending the distal end portion and a remote switch 12 for controlling a video processor (not shown).
The insertion portion 4 has a structure in which the flexible tube portion 5, the bending portion 6, and the tip configuration portion 7 are connected in series from the hand portion. The medical treatment tool of the present invention refers to both a medical endoscope and a medical endoscope treatment tool. The medical endoscope treatment tool includes a snare, a forceps, a clip, a high-frequency knife, and the like, which will be described later. Refers to the treatment tool.

図2の先端処置部は、湾曲部6と先端構成部7から成り、湾曲部6は、短円筒状の湾曲駒18を複数個直列に並べてリベット19を介して回動自在に連結し、かつ各湾曲駒18はリベット19の軸方向と概ね直交する部位の短円筒状の軸方向の中間部位で内側へ円弧上に切り曲げて一対のロープ受け22を形成する。
そして操作用ロープ20は、複数の湾曲駒18の内側のロープ受け22内を貫挿し、最先端の先端湾曲駒18aと、先端ロープ受けの連結部材22aにて接合部材21を用いて接合されている。
そして、操作用ロープ20の手元部は、図1に示した手元操作部2の湾曲操作ノブ3まで挿入部4、及び手元操作部2内を貫挿して湾曲操作ノブ3と連動させ、この湾曲操作ノブ3を回動操作することにより操作用ロープ20を押し引き等、牽引操作させて湾曲部6を、図2において上下方向へ湾曲操作が可能な構造となっている。尚、前記図2の上下一対のロープ受け22に対して直交する図2の手前・奥方向へ、もう一対のロープ受けを配設(図示せず)すると、図2の上下方向と手前奥の四方向に湾曲操作が可能な構造となる。かかる構造を用いてもよい。
そして又、湾曲駒18の外周には線材を編組したブレード23と、その外周には合成樹脂から成る外層チューブ24を被覆した構成から成っている。
The distal treatment section in FIG. 2 is composed of a bending section 6 and a distal end constituting section 7. The bending section 6 has a plurality of short cylindrical bending pieces 18 arranged in series and connected rotatably via a rivet 19. Each bending piece 18 is cut inwardly on an arc at an intermediate portion in the axial direction of a short cylinder at a portion substantially orthogonal to the axial direction of the rivet 19 to form a pair of rope receivers 22.
The operation rope 20 is inserted through the rope receivers 22 inside the plurality of bending pieces 18, and is joined using the joining member 21 at the most advanced distal bending piece 18a and the connecting member 22a of the distal rope receiver. Yes.
Then, the proximal portion of the operation rope 20 is inserted through the insertion portion 4 and the proximal operation portion 2 up to the bending operation knob 3 of the proximal operation portion 2 shown in FIG. The bending portion 6 can be bent up and down in FIG. 2 by pulling and pulling the operation rope 20 by rotating the operation knob 3. If another pair of rope receivers (not shown) are arranged in the front and back directions in FIG. 2 orthogonal to the pair of upper and lower rope receivers 22 in FIG. The structure can be bent in four directions. Such a structure may be used.
The outer periphery of the bending piece 18 is constituted by a blade 23 braided with a wire, and the outer periphery thereof is covered with an outer tube 24 made of synthetic resin.

そして先端構成部7は、口金管25内にイメージガイドファイバー26が挿入され、その先端側に対物レンズ27が配設されている。そして接続パイプ29と接続したチャンネルチューブ28は手元操作部2の手元部まで通ずる処置具孔10と連結しており、このチャンネルチューブ28内へ生検鉗子等の鉗子類の他に、高周波スネア、クリップ装置、注射針等の種々の医療内視鏡用処置具11が出入りでき、病変部の治療行為ができる構造となっている。   In the distal end configuration portion 7, an image guide fiber 26 is inserted into the base tube 25, and an objective lens 27 is disposed on the distal end side. The channel tube 28 connected to the connection pipe 29 is connected to the treatment tool hole 10 leading to the hand portion of the hand operation unit 2, and in addition to forceps such as biopsy forceps, a high-frequency snare, Various medical endoscope treatment tools 11 such as a clip device and an injection needle can be moved in and out, so that a lesion can be treated.

図3は、最先端の先端湾曲駒18aと操作用ロープ20の組付図を示し、先端湾曲駒18aの短円筒状の長軸方向の略中間部位で内側へ円弧状に切り曲げて、突起状の一対の先端ロープ受けの連結部材22a内に操作用ロープ20が貫挿され、先端ロープ受けの連結部材22aで接合部材21を用いて操作用ロープ20の先端部20aが接合されている。   FIG. 3 shows an assembled view of the most advanced tip bending piece 18a and the operating rope 20. The tip bending piece 18a is cut in an arc shape inward at a substantially middle portion of the short cylindrical long axis direction to form a protruding shape. The operation rope 20 is inserted into the connecting member 22a of the pair of distal end rope receivers, and the distal end portion 20a of the operating rope 20 is joined using the joining member 21 at the connecting member 22a of the distal end rope receiver.

そして本発明の医療用処置具に用いる操作用ロープ20は、スパイラルロープ、又は後述するストランドロープを用い、図5(A)、(A’)は本発明実施例1の医療用内視鏡に用いる操作用ロープ20のスパイラルロープの実施例を示す。
本発明の実施例の操作用ロープ20は、素線直径が0.008mmから0.200mmの金属素線を複数本用いて撚合構成し、スパイラルロープの実施例Aの操作用ロープ200では、素線直径(線径)が0.13mmの金属素線1本の芯材200Aと、素線直径(線径)が0.11mmの金属素線6本から成る側材200Bを、芯材200Aの外側に側材200Bを撚合させ、撚合方向が長手方向に対して連続して一方向螺旋状の巻回形成とした撚合構成とし、つまり一般にスパイラルロープの撚り構成1×7(芯材1本の外側に6本の側材)とし、撚合後のロープ外径Dは0.35mmで、ロープピッチ(図示P)はロープ外径Dの2.5倍から15倍とする。ここで、スパイラルロープとは、3本以上の金属素線を撚り合わせてストランド(束)としたロープのことをいい、(1×n)の形の呼び名とし、nは金属素線の本数を示す。
And the operation rope 20 used for the medical treatment tool of the present invention uses a spiral rope or a strand rope described later, and FIGS. 5A and 5A show the medical endoscope of the first embodiment of the present invention. An embodiment of the spiral rope of the operation rope 20 to be used will be shown.
The operation rope 20 of the embodiment of the present invention is formed by twisting a plurality of metal strands having a strand diameter of 0.008 mm to 0.200 mm, and in the operation rope 200 of the spiral rope embodiment A, A core material 200A is composed of a core material 200A having one metal strand having a strand diameter (wire diameter) of 0.13 mm and six metal strands having a strand diameter (wire diameter) of 0.11 mm. The side material 200B is twisted on the outside, and the twisting direction is continuous with respect to the longitudinal direction to form a one-way spiral winding, that is, the spiral rope twisting structure 1 × 7 (core The outer rope diameter D after twisting is 0.35 mm, and the rope pitch (P in the drawing) is 2.5 to 15 times the outer rope diameter D. Here, the spiral rope is a rope formed by twisting three or more metal strands into a strand (bundle), and is named (1 × n), where n is the number of metal strands. Show.

そして操作用ロープ200の芯材200Aは、線径が0.46mmの固溶化処理したオーステナイト系ステンレス鋼線を複数のダイスを用いて線径が0.13mmになるまで伸線加工を行い、伸線加工の加工硬化により引張破断強度を約70kgf/mm2 から232kgf/mm2 まで向上させる。
このときの減面率は92.0%となる。又、側材200Bについても概ね前記芯材200Aと同様である。
Then, the core material 200A of the operation rope 200 is drawn by drawing a solidified austenitic stainless steel wire having a wire diameter of 0.46 mm using a plurality of dies until the wire diameter becomes 0.13 mm. The tensile breaking strength is improved from about 70 kgf / mm @ 2 to 232 kgf / mm @ 2 by work hardening of wire processing.
The area reduction rate at this time is 92.0%. Further, the side material 200B is substantially the same as the core material 200A.

そして又、本発明の実施例Bの操作用ロープ201の芯材201Aは、線径が0.76mmの固溶化処理したオーステナイト系ステンレス鋼線を複数のダイスを用いて線径が0.23mmになるまで一次伸線加工を行い、その後450℃で30分の一次低温熱処理を加えた後に、線径が0.168mmまで二次伸線加工を行い、その後前記同様二次低温熱処理(450℃で30分)を加えた後に、線径が0.13mmまで三次伸線加工を行うと総減面率が97.1%となって、より高い引張破断強度を有する芯材201Aを得ることができる。又、側材201Bについても概ね前記芯材201Aと同様である。   Further, the core material 201A of the operation rope 201 according to the embodiment B of the present invention has a wire diameter of 0.23 mm by using a plurality of dies for an austenitic stainless steel wire having a wire diameter of 0.76 mm. After the primary wire drawing process is performed until it becomes, and then the primary low temperature heat treatment is performed at 450 ° C. for 30 minutes, the secondary wire drawing is performed until the wire diameter is 0.168 mm, and then the secondary low temperature heat treatment (at 450 ° C. as described above). 30 minutes), when the wire drawing is performed to a wire diameter of 0.13 mm, the total area reduction is 97.1%, and a core material 201A having higher tensile breaking strength can be obtained. . The side material 201B is substantially the same as the core material 201A.

そして前記実施例Bと同様の製造方法にて総減面率99.5%とする芯材202A、及び側材202Bから成る操作用ロープ202を実施例Cとし、実施例A〜Cの芯材、及び側材の製造工程を整理すると表1、2となる。尚、実施例A〜Bの芯材、及び側材の金属素線の材質は、オーステナイト系ステンレス鋼線のSUS304材を用い、又実施例Cの芯材、及び側材の金属素線の材質は、再溶解材のSUS316材を用いた。又、ここでいう総減面率とは、固溶化処理した線材の線径と伸線加工により伸線工程での最終仕上がり線径との間の断面積差を減少率で表したものをいい、又引張破断強度とは、線材に引張力を加えて破断したときの最大値を線材の断面積で除した値のことをいう。   Then, the rope 202 for operation composed of the core material 202A and the side material 202B having a total area reduction rate of 99.5% by the manufacturing method similar to the above-mentioned Example B is set as Example C, and the core materials of Examples A to C. Tables 1 and 2 summarize the manufacturing process of the side members. The core material of Examples A and B and the material of the metal wire of the side material are SUS304 materials of austenitic stainless steel wire, and the material of the core material of Example C and the metal wire of the side material. Used a SUS316 remelting material. In addition, the total area reduction rate referred to here is a value obtained by expressing the difference in cross-sectional area between the wire diameter of the solidified wire and the final finished wire diameter in the wire drawing process as a reduction rate. In addition, the tensile breaking strength means a value obtained by dividing the maximum value when a tensile force is applied to the wire and the wire is broken by the cross-sectional area of the wire.



表1、2によれば、芯材、及び側材のいずれも総減面率は80%以上で、99.5%の実施例Cにおいて最も高い引張破断強度を示す。
そして本発明の操作用ロープに用いる金属素線の芯材、及び側材は、固溶化処理したオーステナイト系ステンレス鋼線を用いて総減面率が80%から99.5%の伸線加工を行ったことを特徴とする。尚、総減面率が95%以上の強加工伸線においては後述する再溶解材を用いることが望ましい。又、総減面率が80%以上としたのは、80%を境にして引張破断強度が増大する変曲ポイントとなるからである。(図6、ばね第3版丸善株式会社63頁、図2.82参照)
そして、総減面率90%を境にして、さらに急激に引張破断強度が増大する変曲ポイントを見出した。
According to Tables 1 and 2, both the core material and the side material have a total area reduction of 80% or more, and show the highest tensile breaking strength in Example C of 99.5%.
And the core material and side material of the metal strand used for the operation rope of the present invention are drawn to a total area reduction of 80% to 99.5% using a solution-treated austenitic stainless steel wire. It is characterized by having gone. It should be noted that it is desirable to use a remelting material, which will be described later, in the strong work drawing with a total area reduction of 95% or more. The reason why the total area reduction is 80% or more is that it becomes an inflection point where the tensile strength at break increases from 80%. (Refer to Fig. 6, Spring 3rd edition Maruzen Co., Ltd., p. 63, Fig. 2.82)
Then, an inflection point was found at which the tensile strength at breakage increased more rapidly with the total area reduction rate of 90% as a boundary.

表3は前記実施例A又はBと同様の製造方法を用いて総減面率のみ異ならせて温度を450℃加えた後の引張破断強度の比較を示したものである。尚、表中の増加比とは、総減面率が70%のときの最大引張破断強度の値を基準としたときの比を示す。例えば総減面率が90%のとき増加比は1.31(256/196)となる。   Table 3 shows a comparison of the tensile strength at break after adding a temperature of 450 ° C. using only the total area reduction rate using the same manufacturing method as in Example A or B. The increase ratio in the table indicates the ratio based on the value of the maximum tensile breaking strength when the total area reduction is 70%. For example, when the total area reduction is 90%, the increase ratio is 1.31 (256/196).


表3によれば、総減面率80%のときには、総減面率が70%のときの値の1.12倍増加し、さらに総減面率が90%のときには1.31倍となって、明らかに総減面率が80%で引張破断強度が増大する変曲ポイントがみられ、さらに総減面率が90%で急激に引張破断強度が増大する変曲ポイントがみられ、図6に示すような非線形特性を示すと考えられる。
この理由は、総減面率80%以上という強加工による伸線加工により加工度の増大に伴い繊維状組織が現れ、そしてさらに総減面率90%以上においては、この繊維状組織が著しく発達したことによると考えられる。
そして総減面率が99.5%以下としたのは、これを超える伸線加工の強い加工度では、後述する再溶解材を用いても組織内に空隙が生じはじめて脆化し、又伸びの不足により、特に撚合構成時に側材の金属素線の断線が発生し易くなり、これが伸線加工、撚線加工の限界と考えるからである。
従って、後述する接合部材21の共晶合金を用いて溶融熱により操作用ロープに用いて金属素線の引張破断強度を向上させながら接合させる為には、総減面率が80%から99.5%以下が好ましく、より好ましくは、総減面率が90%から99.5%であり、より高い引張破断強度を得て安定して撚合構成する為には、総減面率が90%から99%である。
According to Table 3, when the total area reduction rate is 80%, it increases 1.12 times the value when the total area reduction rate is 70%, and when the total area reduction rate is 90%, it becomes 1.31 times. Clearly, an inflection point at which the tensile strength at break is increased when the total area reduction is 80%, and an inflection point at which the tensile elongation at break is increased at 90% is shown in FIG. It is considered that the nonlinear characteristic as shown in FIG.
The reason for this is that a fibrous structure appears as the degree of processing increases due to wire drawing by strong processing with a total area reduction rate of 80% or more, and when the total area reduction rate is 90% or more, this fibrous structure develops remarkably. This is probably due to the fact that
The reason why the total area reduction is 99.5% or less is that, when the degree of workability is higher than this, even if a remelting material described later is used, voids begin to form in the structure and become brittle, This is because, due to the shortage, breakage of the metal wire of the side material is likely to occur particularly in the twisted configuration, which is considered as the limit of wire drawing and twisting.
Therefore, in order to join the eutectic alloy of the joining member 21, which will be described later, to the operation rope by melting heat while improving the tensile breaking strength of the metal strand, the total area reduction is from 80% to 99.99. 5% or less is preferable, and more preferably, the total area reduction rate is 90% to 99.5%. In order to obtain a higher tensile breaking strength and stably form a twist, the total area reduction rate is 90%. % To 99%.

そして「固溶化処理したオーステナイト系ステンレス鋼線の伸線加工」としたのは、加工性のよいオーステナイト組織を得る為であり、オーステナイト系ステンレス鋼線は変態点を利用した熱処理による結晶粒の微細化ができず、冷間加工によってのみ結晶粒の微細化が可能で、伸線加工により顕著な加工硬化性を示して引張破断強度を向上させることができるからである。又オーステナイト系ステンレス鋼線を用いる理由は、マルテンサイト系ステンレス鋼線では熱処理による焼入硬化性を示して熱影響を受け易く、析出硬化系ステンレス鋼線では靭性が不足して撚線加工時に断線が発生して前記実施例のような細線・極細線の撚合構成はできず、又フェライト系ステンレス鋼線では温度脆性(シグマ脆性)の問題があるからである。   The reason why “Solution-treated austenitic stainless steel wire was drawn” was to obtain an austenitic structure with good workability, and the austenitic stainless steel wire was refined by heat treatment using transformation points. This is because the crystal grains can be refined only by cold working, and the tensile breaking strength can be improved by exhibiting remarkable work hardenability by wire drawing. Also, the reason for using austenitic stainless steel wire is that martensitic stainless steel wire exhibits quench hardenability by heat treatment and is easily affected by heat. This is because the twisted configuration of the fine wire and the extra fine wire cannot be formed as in the above-mentioned embodiment, and the ferritic stainless steel wire has a problem of temperature brittleness (sigma brittleness).

次に図3において操作用ロープ20の先端部20aと、先端湾曲駒18aの先端ロープ受けの連結部材22aとは、接合部材21を溶融加熱して接合させる。
そして接合部材21は、溶融温度が180℃から495℃の共晶合金、又は操作用ロープ20の金属素線が後述するMoを含むオーステナイト系ステンレス鋼線のときには180℃から525℃の共晶合金を用いる。ここでいう共晶合金とは、合金の成分比を変更することにより得られる最低融点(溶融温度)を有する特殊な合金のことをいい、具体的には、金又は銀を含む合金材で金錫系合金材として金80重量%、残部が錫で溶融温度が280℃、又銀錫系合金として銀3.5重量%、残部が錫で溶融温度が221℃、そして、金88重量%、残部がゲルマニウムで溶融温度が356℃、又銀と錫とインジウムから成り、溶融温度が450℃から472℃の共晶合金であり、その代表例を表4に示す。
Next, in FIG. 3, the distal end portion 20a of the operation rope 20 and the connecting member 22a of the distal end rope receiver of the distal bending piece 18a are joined by melting and heating the joining member 21.
The joining member 21 is a eutectic alloy having a melting temperature of 180 ° C. to 495 ° C., or an eutectic alloy having a melting point of 180 ° C. to 525 ° C. when the metal strand of the operation rope 20 includes Mo described later. Is used. The eutectic alloy here refers to a special alloy having the lowest melting point (melting temperature) obtained by changing the component ratio of the alloy, and specifically, an alloy material containing gold or silver. 80% by weight of gold as a tin-based alloy material, the balance being tin and a melting temperature of 280 ° C., and 3.5% by weight of silver as a tin-based alloy, the balance being tin and a melting temperature of 221 ° C., and 88% by weight of gold, The balance is germanium, a melting temperature of 356 ° C., a eutectic alloy composed of silver, tin, and indium and having a melting temperature of 450 ° C. to 472 ° C. Table 4 shows typical examples.


ここで接合部材21として金を用いる理由は、耐食性、展延性向上の為であり、銀を用いる理由は、融点調整等の為であり、錫を用いる理由は、融点を低下させて操作用ロープ20との濡れ性を向上させる為であり、又インジウム、銅を用いる理由も濡れ性向上の為であり、そしてゲルマニウムを用いる理由は、金属間化合物の結晶粒粗大化を抑止して、接合強度の低下防止を図る為である。尚、鉛、アンチモンは人体への不適合性、又加工性の難度等の観点から好ましくない。   The reason why gold is used as the joining member 21 is to improve corrosion resistance and spreadability, the reason why silver is used is to adjust the melting point, and the reason why tin is used is to reduce the melting point and to operate the rope. 20 for improving wettability, and the reason for using indium and copper is to improve wettability, and the reason for using germanium is to suppress the coarsening of the intermetallic compound grains and to increase the bonding strength. This is for the purpose of preventing the decrease in the thickness. Lead and antimony are not preferable from the viewpoints of incompatibility with the human body and difficulty in workability.

そして接合部材21の溶融温度が180℃から495℃、又は180℃から525℃としたのは、180℃を下回ると加工硬化させた操作用ロープ20の引張破断力を接合部材21の溶融温度を利用して向上させることはできず、そして495℃を超えると操作用ロープ20に用いる金属素線のオーステナイト系ステンレス鋼線の特質から、又は525℃を超えるとMoを含むオーステナイト系ステンレス鋼線の特質から、前記各オーステナイト系ステンレス鋼線を520℃、又は540℃を超える800℃に加熱すると鋭敏化現象を生じて、後述するように極端に引張破断強度特性等を低下させることとなり、この現象を防ぎ、操作用ロープ20の機械的強度特性を最大限に発揮させる為である。   The reason why the melting temperature of the joining member 21 is 180 ° C. to 495 ° C., or 180 ° C. to 525 ° C. is that the tensile breaking force of the work rope 20 that has been work-hardened when the temperature falls below 180 ° C. When the temperature exceeds 495 ° C., the characteristics of the austenitic stainless steel wire of the metal strand used for the operation rope 20, or when it exceeds 525 ° C., the austenitic stainless steel wire containing Mo Due to the nature, when each austenitic stainless steel wire is heated to 520 ° C. or 800 ° C. exceeding 540 ° C., a sensitization phenomenon occurs, and as described later, the tensile fracture strength characteristics are extremely lowered, and this phenomenon This is because the mechanical strength characteristics of the operating rope 20 are maximized.

この構造により、以下に述べる特有の作用効果がある。
操作用ロープ20と先端湾曲駒18aの先端ロープ受けの連結部材22aとを前記接合部材21である共晶合金を用いて接合すると、接合時の溶融熱によって操作用ロープ20の芯材、及び側材のような細線を撚合構成したロープであっても引張強度特性等を低下させることなく、むしろこの引張破断強度特性等を向上させて強固接合させることができる。
This structure has the following specific effects.
When the operation rope 20 and the connecting member 22a of the tip rope receiver of the tip bending piece 18a are joined using the eutectic alloy as the joining member 21, the core material and the side of the manipulation rope 20 by the heat of fusion at the time of joining. Even a rope formed by twisting a thin wire such as a material can improve the tensile strength characteristics and the like and can be firmly joined without lowering the tensile strength characteristics.

そして図7は、一般に金属素線の母線にオーステナイト系ステンレス鋼線を用いて総減面率が95%以上の最終伸線加工後の金属素線を熱影響下(各温度30分)での引張破断強度特性を示した図で、SUS304材のときは図示イを、SUS316材のときは図示ロを示す。
これによるとSUS304材は180℃の熱影響により引張破断強度が上昇し始め、概ね450℃近傍で最高の引張破断強度特性を示し、495℃まで引張破断強度特性向上効果が顕著にみられ、そして520℃を超えると常温(20℃)よりも急激に引張破断強度が低下する。又、Moを含むSUS316材は、低温側でSUS304材と同様な傾向を示すが高温側では概ね480℃近傍で最高の引張破断強度特性を示し、525℃まで引張破断強度特性向上効果が顕著にみられ、そして540℃を超えると常温(20℃)よりも急激に引張破断強度が低下する。
この引張破断強度特性が急激に低下する理由は、前述のように、この固溶化処理したオーステナイト系ステンレス鋼線は、前記520℃、540℃を超える温度から800℃に加熱されると、カーボンの析出、クロムの移動の為のエネルギーを必要とし、鋭敏化現象を生じて、特にカーボンが0.08%以下の通常のSUS304のオーステナイト系ステンレス鋼線では、700℃4分から5分程度で、この鋭敏化現象が現れ、引張破断強度が極端に低下するからである。
FIG. 7 shows that, in general, an austenitic stainless steel wire is used as the bus bar of the metal wire, and the metal wire after the final wire drawing with a total area reduction of 95% or more is subjected to heat (each temperature is 30 minutes). The drawing shows the tensile strength at break. In the case of SUS304 material, the illustrated a is shown, and in the case of SUS316 material, the illustrated b is shown.
According to this, SUS304 material began to increase in tensile strength at 180 ° C due to the heat effect, showed the highest tensile strength at about 450 ° C, and the effect of improving tensile strength at 495 ° C was noticeable. If it exceeds 520 ° C., the tensile strength at break will decrease more rapidly than normal temperature (20 ° C.). The SUS316 material containing Mo shows the same tendency as the SUS304 material on the low temperature side, but shows the highest tensile rupture strength characteristics at about 480 ° C. on the high temperature side, and the effect of improving the tensile rupture strength properties to 525 ° C. is remarkable. In addition, when the temperature exceeds 540 ° C., the tensile strength at break decreases more rapidly than normal temperature (20 ° C.).
The reason why the tensile strength at break is abruptly decreased is that, as described above, when the austenitic stainless steel wire subjected to the solution treatment is heated from 800 ° C. to 800 ° C., the carbon This requires energy for precipitation and migration of chromium, causing a sensitization phenomenon. In particular, in an ordinary SUS304 austenitic stainless steel wire having a carbon content of 0.08% or less, the temperature is about 700 ° C. for about 4 to 5 minutes. This is because a sensitization phenomenon appears and the tensile strength at break is extremely reduced.

このような引張破断強度特性を有する為、SUS304材の金属素線の低温熱処理温度範囲は180℃から495℃が望ましく、又Moを含む例えばSUS316材(Moが2重量%〜3重量%)の金属素線の低温熱処理温度範囲は180℃から525℃が望ましい。
従って、接合部材21の溶融温度は、前記望ましい低温熱処理温度範囲と一致させる。 このように本発明は、強加工伸線して総減面率の高いオーステナイト系ステンレス鋼線の温度による引張破断強度特性に着目して、並びに、操作用ロープ20に用いる金属素線は細線・極細線で熱容量小で熱影響を受け易いことに着目して、操作用ロープの金属素線の撚合状態での引張破断強度を、接合部材21の溶融熱を利用して大幅に向上させながら、かつ接合することのできる、新たな技術思想を提供するものである。
In order to have such tensile breaking strength characteristics, the low temperature heat treatment temperature range of the SUS304 metal strand is preferably 180 ° C. to 495 ° C., and for example, SUS316 material containing Mo (Mo is 2 wt% to 3 wt%). The low temperature heat treatment temperature range of the metal wire is desirably 180 ° C. to 525 ° C.
Therefore, the melting temperature of the joining member 21 is matched with the desirable low temperature heat treatment temperature range. As described above, the present invention focuses on the tensile strength at break due to the temperature of the austenitic stainless steel wire with high work drawing and a high total area reduction rate, and the metal strand used for the operation rope 20 is a fine wire, Focusing on the fact that the heat capacity is very small and easy to be affected by heat, the tensile breaking strength in the twisted state of the metal wire of the operation rope is greatly improved by utilizing the heat of fusion of the joining member 21. And a new technical idea that can be joined.

そして、本実施例に用いる金属素線のオーステナイト系ステンレス鋼線の化学成分は、重量%でC:0.15%以下、Si:1%以下、Mn:2%以下、Ni:6%〜16%、Cr:16%〜20%、P:0.045%以下、S:0.030%以下、Mo:3%以下、残部が鉄及び不可避的不純物から成る。このように高珪素ステンレス鋼(Si:3.0%〜5.0%)、又析出硬化系ステンレス鋼線を用いなくても前記工法を用いることにより、高強度のオーステナイト系ステンレス鋼線の金属素線を得ることができる。尚、Cは引張破断強度向上の為には、0.005%以上が望ましく、粒界腐食抑制の観点から0.15%以下が望ましい。   And the chemical component of the austenitic stainless steel wire of the metal strand used for a present Example is C: 0.15% or less, Si: 1% or less, Mn: 2% or less, Ni: 6% -16 in weight%. %, Cr: 16% to 20%, P: 0.045% or less, S: 0.030% or less, Mo: 3% or less, the balance being iron and inevitable impurities. Thus, by using the above method without using high silicon stainless steel (Si: 3.0% to 5.0%) or precipitation hardening stainless steel wire, high strength austenitic stainless steel wire metal. A strand can be obtained. C is preferably 0.005% or more for improving the tensile strength at break, and is preferably 0.15% or less from the viewpoint of suppressing intergranular corrosion.

本発明の医療用内視鏡1の操作用ロープ20に用いる芯材、又は側材の金属素線は、素線直径が0.008mmから0.200mmのオーステナイト系ステンレス鋼線で、特に引張破断強度が300kgf/mm2 以上で、総減面率が95%以上の伸線加工を可能とする為には、再溶解材を用いたSUS304材、又はSUS316材が望ましい。
この理由は、ステンレス鋼線の伸線時の断線原因は、表面疵もさることながら酸化物系介在物であることが最も多く、細線・極細線化するほどこの傾向が著しい。
そしてその化学成分は、介在物生成元素であるAl、Ti、Ca、Oの成分は低く、又硫化物の作用で伸線低下を引き起こすSも低く抑える。具体的なオーステナイト系ステンレス鋼線の化学成分は、重量%で、C:0.08%以下、Si:0.10%以下、Mn:2%以下、P:0.045%以下、S:0.010%以下、Ni:8%〜12%、Cr:16%〜20%、Mo:3%以下、Al:0.0020%以下、Ti:0.10%以下、Ca:0.005%以下、O:0.0020%以下、で残部がFeと不可避的不純物から成る。
そして再溶解材の製造方法としては、ステンレス鋼の溶製後のインゴットにフラックスを用いたエレクトロスラグ再溶解の製造方法等である。トリプル溶解材を用いても前記同様の効果が得られる。
The core material or side metal wire used in the operation rope 20 of the medical endoscope 1 of the present invention is an austenitic stainless steel wire having a strand diameter of 0.008 mm to 0.200 mm, particularly tensile fracture. In order to enable wire drawing with a strength of 300 kgf / mm 2 or more and a total area reduction of 95% or more, SUS304 material or SUS316 material using a remelting material is desirable.
The reason for this is that the cause of disconnection when drawing a stainless steel wire is most often oxide inclusions as well as surface flaws, and this tendency becomes more prominent as the wire becomes finer and finer.
And the chemical component is low in the components of Al, Ti, Ca and O which are inclusion generating elements, and also suppresses S which causes a decrease in wire drawing due to the action of sulfide. The specific chemical components of the austenitic stainless steel wire are, by weight, C: 0.08% or less, Si: 0.10% or less, Mn: 2% or less, P: 0.045% or less, S: 0 0.010% or less, Ni: 8% to 12%, Cr: 16% to 20%, Mo: 3% or less, Al: 0.0020% or less, Ti: 0.10% or less, Ca: 0.005% or less , O: 0.0020% or less, with the balance being Fe and inevitable impurities.
And as a manufacturing method of a remelting material, it is the manufacturing method etc. of the electroslag remelting which used the flux for the ingot after melting of stainless steel. Even when a triple melting material is used, the same effect as described above can be obtained.

そして次に、操作用ロープの実施例A〜C操作用ロープ200〜202と湾曲駒とを接合部材21を用いて接合する際に接合部材21の溶融加熱時間、及び組付時間等を考慮して、温度と引張破断力との関係を表5に示す。尚、時間の5秒は、接合部材21を用いて接合固着するときにロープが180℃以上で溶融加熱される平均時間を示し、又60秒は、再度接合固着作業(やり直し作業)によりロープが180℃以上で再加熱されるのを含む時間を示す。又ここでロープの引張破断力とは、ロープに引張力を加えてロープが破断したときの最大荷重のことをいう。   Then, when the operation ropes A to C of the operation ropes 200 to 202 and the bending pieces are joined using the joining member 21, the melting and heating time of the joining member 21 and the assembling time are taken into consideration. Table 5 shows the relationship between temperature and tensile breaking force. The time of 5 seconds indicates the average time during which the rope is melted and heated at 180 ° C. or higher when it is bonded and fixed using the bonding member 21, and 60 seconds is again due to the bonding and fixing operation (redoing operation). Time including reheating at 180 ° C. or higher is shown. Here, the tensile breaking force of the rope means the maximum load when the rope is broken by applying a tensile force to the rope.


表5によれば、接合部材21の溶融加熱時間を考慮して450℃で5秒間の加熱であっても、操作用ロープ200の引張破断力は16.5kgfから17.1kgfとなって約3.6%増大し、又操作用ロープ201の引張破断力は24.7kgfから25.9kgfとなって約4.9%増大し、さらに操作用ロープ202の引張破断力は25.6kgfから27.0kgfとなって約5.5%増大し、総減面率の増加とともに引張破断力の増加率は増大する傾向となる。
そして前述のように、接合部材21の共晶合金を用いて溶融熱により操作用ロープの引張破断力を向上させながら接合させる為には、操作用ロープに用いる金属素線の総減面率は80%から99.5%が望ましく、好ましくは90%から99.5%以下で、高い引張破断力を有する湾曲操作ロープを安定して得る為には、90%以上99%以下が望ましい。
この理由は、99.5%を超える総減面率を有する金属素線は伸びが不足して撚合時に、側線に用いる金属素線の断線が発生し易いからである。
According to Table 5, considering the melting and heating time of the joining member 21, even when heating is performed at 450 ° C. for 5 seconds, the tensile breaking force of the operating rope 200 is about 16.5 kgf to about 17.1 kgf. .6%, and the tensile breaking force of the operating rope 201 is increased by about 4.9% from 24.7 kgf to 25.9 kgf, and the tensile breaking force of the operating rope 202 is further increased from 25.6 kgf to 25.7 kgf. It becomes 0 kgf and increases by about 5.5%, and the increase rate of the tensile breaking force tends to increase with the increase of the total area reduction rate.
And as mentioned above, in order to join the eutectic alloy of the joining member 21 while improving the tensile breaking force of the operating rope by the heat of fusion, the total area reduction rate of the metal strands used for the operating rope is 80% to 99.5% is desirable, preferably 90% to 99.5% or less, and 90% to 99% is desirable in order to stably obtain a bending operation rope having a high tensile breaking force.
The reason for this is that a metal strand having a total area reduction ratio exceeding 99.5% is insufficient in elongation, and disconnection of the metal strand used for the side wire is likely to occur during twisting.

そして本発明の操作用ロープ20の他のスパイラルロープの実施例を図5(B)〜(E)に示す。図5(B)〜(E)はそれぞれ実施例D〜Gを示し、スパイラルロープの撚り構成は、それぞれ1×8、1×9、1×10、1×19である。又、他の実施例として図示しないが、1×3、1×12等である。
そして、芯材と側材の金属素線の素線直径は、いずれも0.008mmから0.200mmとし、芯材と側材とは同一素線直径の金属素線を撚合構成して用いてもよい。尚、前記実施例D〜F、及び撚り構成1×7の他の実施例の芯材と側材の素線直径(線径)、及び線径比(芯材/側材)を整理すると、表6となる。
An embodiment of another spiral rope of the operation rope 20 of the present invention is shown in FIGS. FIGS. 5B to 5E show Examples D to G, respectively, and the twist configuration of the spiral rope is 1 × 8, 1 × 9, 1 × 10, and 1 × 19, respectively. Further, although not shown as another embodiment, it is 1 × 3, 1 × 12, or the like.
The core diameters of the metal wires of the core material and the side material are both 0.008 mm to 0.200 mm, and the core material and the side material are formed by twisting and forming metal wires having the same wire diameter. May be. In addition, when arranging the wire diameter (wire diameter) and the wire diameter ratio (core material / side material) of the core material and the side material of the other examples of the examples D to F and the twist configuration 1 × 7, Table 6 is obtained.


表6によれば、例えば実施例F(図示(D))は、撚り構成1×10で、芯材は線径が0.18mmの金属素線1本と、側材は線径が0.085mmの金属素線9本からなり、線径比は2.12である。同様に、撚り構成1×7の他の実施例において、芯材は線径が0.122mm、側材の線径は0.114mmで線径比は1.07である。
そして、前記各実施例で示すように、芯材の線径は側材の線径よりも1.07倍から2.12倍の太径線を用いている。芯材も側材も同一線径を用いてもよいが、芯材に太径線を用いる理由は、操作用ロープ20に引張力を加えたとき、芯材1本に加わる引張力の負荷は、数本から成る側材よりもその構造差(側材はスパイラル状で伸び易い構造に対して、芯材はストレート状で直接引張力の負荷が加わり易い構造)から増大する。この為、芯材に太径線を用いて横断面積を増大させて芯材へ加わる引張応力を軽減させて、その結果芯材の早期破断を防いで、ロープとしての引張破断力を向上させる為である。
そして芯材と側材とが同一線径の線径比1.0を下回れば、芯材へ加わる引張力の負荷は増大して芯材の早期破断によるロープの引張破断力を低下させる。又、前記上限値(線径比2.12)を上回れば、芯材の剛性が増大して、耐繰り返し曲げ疲労特性が劣ってくる。尚補足すれば、前記実施例A〜Cの線径比は、1.18である。
従って、線径比(芯材/側材)は、1.0倍から2.12倍が好ましく、より好ましくは1.07倍から2.12倍で、さらに好ましくは、1.18倍から2.12倍である。
According to Table 6, for example, Example F (illustration (D)) has a twist configuration of 1 × 10, the core material is one metal strand having a wire diameter of 0.18 mm, and the side material has a wire diameter of 0.1. It consists of nine 085 mm metal strands and the wire diameter ratio is 2.12. Similarly, in another embodiment of the twisted configuration 1 × 7, the core material has a wire diameter of 0.122 mm, the side material has a wire diameter of 0.114 mm, and the wire diameter ratio is 1.07.
And as shown in the said each Example, the wire diameter of the core material uses the large diameter wire 1.07 times to 2.12 times the wire diameter of the side material. The same wire diameter may be used for both the core material and the side material, but the reason for using a thick wire for the core material is that when a tensile force is applied to the operating rope 20, the tensile force applied to one core material is More than the side material composed of several pieces, the structural difference is greater (the side material is a spiral structure that is easy to elongate, whereas the core material is a straight structure that is easily subjected to a tensile force load). For this reason, a thick wire is used for the core material to increase the cross-sectional area and reduce the tensile stress applied to the core material, thereby preventing the core material from breaking early and improving the tensile breaking force as a rope. It is.
And if a core material and a side material are less than the wire diameter ratio 1.0 of the same wire diameter, the load of the tensile force added to a core material will increase, and the tensile fracture force of the rope by the early fracture | rupture of a core material will be reduced. Moreover, if it exceeds the said upper limit (wire diameter ratio 2.12), the rigidity of a core material will increase and a repeated bending fatigue-proof characteristic will be inferior. Note that the wire diameter ratio of Examples A to C is 1.18.
Therefore, the wire diameter ratio (core material / side material) is preferably 1.0 times to 2.12 times, more preferably 1.07 times to 2.12 times, and still more preferably 1.18 times to 2. .12 times.

そして次に、操作用ロープ20の他の実施例としてストランドロープについて説明する。
ここでいうストランドロープとは、3本以上のストランドを撚り合わせたロープのことをいい、(m×n)の呼び名とし、mはストランドの総数、nはストランド内の金属素線の本数を示す。例えば、他のストランドロープの実施例として、前記実施例Aのスパイラルロープの撚り構成1×7を用いて、ストランドの総数が7束のときは、7×7(図示(F))、同様にスパイラルロープの実施例Dの撚り構成1×8を用いて、ストランドの総数が7束のときは7×8(図示せず)となる。
本発明の操作用ロープ20の実施例については、前記スパイラルロープ、及びストランドロープの双方を含み、使用する金属素線は前記各実施例A〜Cと同様である。
そしてスパイラルロープは、医療用処置具の体内挿入時、屈曲蛇行が比較的少なく、高い引張力を要する場合に用いられ、特に押し操作力、及び回転操作力が要求される場合に好適である。これに対してストランドロープは、屈曲蛇行が多くて軽い操作力で、かつ耐曲げ応力を要する場合に用いられ、特に耐繰り返し曲げ疲労特性が要求される場合に好適である。いずれを選択するかは、屈曲蛇行の程度と要求される操作性との関係で決定される。
Next, a strand rope will be described as another embodiment of the operation rope 20.
The strand rope here means a rope in which three or more strands are twisted together, and is called (m × n), where m is the total number of strands and n is the number of metal strands in the strand. . For example, as an example of another strand rope, when the total number of strands is 7 bundles using the spiral rope twist configuration 1 × 7 of Example A, 7 × 7 (illustration (F)), similarly When the total number of strands is 7 bundles using the twist configuration 1 × 8 of Example D of the spiral rope, it becomes 7 × 8 (not shown).
About the Example of the rope 20 for operation of this invention, both the said spiral rope and a strand rope are included, and the metal strand to be used is the same as that of each said Example AC.
The spiral rope is used when the medical treatment instrument is inserted into the body with relatively little meandering and requires a high tensile force, and is particularly suitable when a push operation force and a rotation operation force are required. On the other hand, the strand rope is used when there is a large amount of bending meandering, a light operating force and a high bending stress resistance, and is particularly suitable when a repeated bending fatigue resistance characteristic is required. Which one to select is determined by the relationship between the degree of bending meandering and the required operability.

そして補足すれば、操作用ロープ20は、芯材、及び側材を一定の撚りピッチで撚合構成した後に短時間低温熱処理(380℃から550℃で2秒から10秒)を加えた後、又は撚合構成した後に公知の曲げと捩りの歪を与えるスピナー矯正機、又はローラーレベラー式矯正機等により矯正加工した後に短時間低温熱処理(380℃から550℃で2秒から10秒)を加えた後に、前記接合部材21を用いて接合せても一定の効果を得ることができる。
そして前記工法を用いることにより、操作用ロープの直線性を向上させることができ、医療用処置具の操作性をより向上させることがでる。この理由は、撚合加工後、又は矯正加工後の前記短時間低温熱処理により、操作用ロープに局部的に発生した集中応力を平均化させることによる、と考えることができる。
In addition, after supplementing the core material and the side material at a constant twist pitch, the operation rope 20 is subjected to a short time low temperature heat treatment (from 380 ° C. to 550 ° C. for 2 seconds to 10 seconds), Or after a straightening process using a spinner straightening machine or a roller leveler type straightening machine that applies a known bending and twisting after twisting, a short time low temperature heat treatment (from 380 ° C to 550 ° C for 2 seconds to 10 seconds) is added. After that, even if the joining member 21 is used for joining, a certain effect can be obtained.
And by using the said construction method, the linearity of an operation rope can be improved and the operativity of a medical treatment tool can be improved more. This reason can be considered to be because the concentrated stress generated locally in the operation rope is averaged by the short-time low-temperature heat treatment after twisting or straightening.

そして、この固溶化処理したオーステナイト系ステンレス鋼線を用いて強加工の伸線加工をして引張破断強度特性を向上させた芯材と側材を撚合構成した操作用ロープ20との接合部材21は、操作用ロープ20の引張破断強度向上効果が顕著にみられる温度範囲と同じ温度範囲の、180℃から495℃の溶融温度をもつ共晶合金、又は操作用ロープの金属素線がMoを含むオーステナイト系ステンレス鋼線のときには180℃から525℃の溶融温度をもつ共晶合金を用いる。
これにより共晶合金の溶融熱を利用して引張破断強度を向上させながら接合することが可能となる。尚、接合部材21の溶融温度が180℃から495℃、又は180℃から525℃としたのは、この範囲であれば溶融熱を利用して操作用ロープの引張破断強度を向上させて、湾曲駒18と操作用ロープ20との強固接合が可能となるからである。
And the joining member with the rope 20 for operation which comprised the core material and the side material which carried out the strong wire drawing process and improved the tensile fracture strength characteristic using this solid solution-treated austenitic stainless steel wire, and twisted the side material No. 21 is a eutectic alloy having a melting temperature of 180 ° C. to 495 ° C. in the same temperature range in which the effect of improving the tensile breaking strength of the operating rope 20 is noticeable, or the metal wire of the operating rope is Mo. In the case of an austenitic stainless steel wire containing, an eutectic alloy having a melting temperature of 180 ° C. to 525 ° C. is used.
As a result, it is possible to perform the joining while improving the tensile strength at break using the melting heat of the eutectic alloy. Note that the melting temperature of the joining member 21 is 180 ° C. to 495 ° C. or 180 ° C. to 525 ° C. If the melting temperature of the joining member 21 is within this range, the tensile breaking strength of the operating rope is improved by using the heat of melting, and the bending This is because the piece 18 and the operation rope 20 can be firmly joined.

そして、接合部材21の溶融熱により先端ロープ受けの連結部材22aとの接合部の操作用ロープ20の先端部20aの引張破断強度は増大し、この引張破断強度増大に伴い引張応力は増大し、その結果接合部での操作用ロープの耐繰り返し曲げ疲労特性は向上する。
このことにより、術者の手技中での操作用ロープ20の先端部20aの接合部へ加わる繰り返し曲げ疲労により、操作用ロープ20と先端ロープ受けの連結部材22aとが離脱する危険は生じない。尚、補足すれば、溶融温度が605℃から800℃の銀ろう、溶融温度が895℃から1030℃金ろうを用いた場合には、前述したように芯材、又は側材の鋭敏化現象による脆化、又は、なまし状態となって大幅に引張破断強度が低下し、そして引張破断強度及び曲げ応力の低下に伴い、操作用ロープ20の先端部20aが先端ロープ受けの連結部材22aからの脱落の危険が増大し、湾曲操作ノブ3の操作不能を生じ、医療用内視鏡が操作不能に陥る恐れがある。
そして、溶融温度が約880℃の金74.5重量%から75.5重量%、銀12重量%から13重量%、その他亜鉛、鉄、鉛等0.15重量%以下の金ろうを用いた場合、又溶融温度が780℃の銀72重量%、銅28重量%の銀ろうを用いた場合にも、前記同様の問題が発生し易い。
The tensile breaking strength of the distal end portion 20a of the operating rope 20 at the joint portion with the connecting member 22a of the distal end rope receiver is increased by the melting heat of the joining member 21, and the tensile stress increases with the increase in the tensile breaking strength. As a result, the resistance to repeated bending fatigue of the operating rope at the joint is improved.
Thus, there is no risk that the operation rope 20 and the connecting member 22a of the tip rope receiver are detached due to repeated bending fatigue applied to the joint portion of the tip portion 20a of the operation rope 20 during the operation of the surgeon. In addition, if a silver solder having a melting temperature of 605 ° C. to 800 ° C. and a gold solder having a melting temperature of 895 ° C. to 1030 ° C. are used, as described above, the core material or the side material may be sensitized. The brittle or annealed state significantly reduces the tensile breaking strength, and the lower end of the tensile breaking strength and bending stress causes the distal end portion 20a of the operating rope 20 to move away from the connecting member 22a of the distal end rope receiver. There is a risk that the risk of falling off increases, the bending operation knob 3 becomes inoperable, and the medical endoscope becomes inoperable.
Then, a gold solder having a melting temperature of about 880 ° C. and having a gold content of 74.5 wt. In this case, the same problem as described above is likely to occur when a silver solder having a melting temperature of 780 ° C. of 72% by weight of silver and 28% by weight of copper is used.

そして次に、操作用ロープ20の先端部20aの部分には、先端ロープ受けの連結部材22aの長手方向の長さに添って所定長、例えば先端ロープ受けの連結部材22aの長手方向の長さが2mmであれば、2mmから100mm程度電解研磨を施すことが望ましい。又は、紙やすり等により研磨してもよい。
そして、操作用ロープ20の先端部20aを、接合部材21の共晶合金を溶融する前に研磨する理由は、特に強加工における伸線加工(総減面率90%以上)した金属素線を用いて撚合構成した操作用ロープは、その接合部材21との濡れ性が極端に悪くなり、これを防ぐ為に電解研磨等を用いて酸化皮膜を除去して濡れ性を向上させ、接合部材21による接合性を向上させる為である。又、予め全長にわたって電解研磨等を施した操作用ロープ20を用いてもよい。尚、補足すれば、前記操作用ロープの接合部材21との濡れ性が極端に悪くなる理由は、強加工の伸線加工の加工度増大に伴って現われる金属素線表層部の繊維状組織の発達、及び酸化被膜の形成によるものと考えることができる。
Next, the distal end portion 20a of the operating rope 20 has a predetermined length along the longitudinal length of the connecting member 22a of the distal end rope receiver, for example, the longitudinal length of the connecting member 22a of the distal end rope receiver. Is 2 mm to 100 mm, it is desirable to perform electropolishing. Or you may grind with sandpaper etc.
The reason for polishing the distal end portion 20a of the operation rope 20 before melting the eutectic alloy of the joining member 21 is that the metal wire that has been drawn (particularly the area reduction ratio is 90% or more) in strong working is particularly important. The rope for operation that is twisted and configured to be used has an extremely poor wettability with the joining member 21. In order to prevent this, the oxide film is removed by electrolytic polishing or the like to improve the wettability. This is to improve the bondability by 21. Moreover, you may use the rope 20 for operation which gave electrolytic polishing etc. over the full length beforehand. In addition, if we supplement, the reason why the wettability with the joining member 21 of the operating rope is extremely deteriorated is that the fibrous structure of the surface portion of the metal strand that appears as the degree of processing of the strong wire drawing increases. This can be attributed to the development and formation of an oxide film.

そして又、操作用ロープ20の先端部20aの部分には、先端ロープ受けの連結部材22aの長手方向の長さに添って所定長、例えば先端ロープ受けの連結部材22aの長手方向の長さが2mmであれば、1mmから10mm程度めっき処理、又は接合部材211を芯材と側材との線間間隙に含浸、及び側材の外周に固着させて、その後接合部材21を溶融固着させてもよい。かかる場合、めっき処理に用いる材料は、前記接合部材21の共晶合金と同一の組成成分を含む材料を用いることが望ましく、例えば接合部材21に金、又は銀を含む成分が含まれていれば、めっき処理する材料は、金めっき、又は銀めっきが望ましい。
そして操作用ロープ20の先端部20aの部分に予め含浸・固着させてもよく、かかる場合に用いる接合部材211は、接合部材21と同一又は同種の共晶合金が望ましい。尚、ここでいう同種の共晶合金である接合部材とは、一つ、又は二つの同一の組成成分を合計した重量%が全体の50重量%以上のものをいい、例えば表1で符号A1とA2は同種で、又はA1とB1とは異種である。
Further, the portion of the distal end portion 20a of the operation rope 20 has a predetermined length along the longitudinal length of the connecting member 22a of the distal end rope receiver, for example, the longitudinal length of the connecting member 22a of the distal end rope receiver. If it is 2 mm, a plating process of about 1 mm to 10 mm, or a bonding member 211 may be impregnated in the gap between the core material and the side material and fixed to the outer periphery of the side material, and then the bonding member 21 may be melted and fixed. Good. In such a case, it is desirable to use a material containing the same composition component as the eutectic alloy of the joining member 21 as the material used for the plating process. For example, if the joining member 21 contains a component containing gold or silver The material to be plated is preferably gold plating or silver plating.
Then, the tip portion 20a of the operation rope 20 may be impregnated and fixed in advance, and the joining member 211 used in this case is preferably the same or the same type of eutectic alloy as the joining member 21. In addition, the joining member which is the eutectic alloy of the same kind here means that the weight percent of the total of one or two identical composition components is 50 weight percent or more of the whole. And A2 are the same, or A1 and B1 are different.

この構造により、以下に述べる特有の作用効果がある。つまり、操作用ロープ20の先端部20aと先端のロープ受けの連結部材22aとの接合を強固にさせ、又接合部材211と接合部材21との接合部での溶融一体化固着により、接合強度を大幅に向上させることができる。
そして、操作用ロープ20の先端部20aをめっき処理、又は接合部材211を予め含浸・固着する理由は、前記強加工の伸線加工により濡れ性が極端に悪化した操作用ロープ20の接合部材21との濡れ性を向上させて強固結合を可能とする為である。尚、予め接合部材211を溶融固着した場合には、先端ロープ受けの連結部材22aに貫挿後、溶融固着した接合部材211にレーザー光を照射させて接合部材211を再溶融させて先端ロープ受けの連結部材22aと接合させてもよい。かかる場合、接合部材211は、操作用ロープ20の先端部20aの表面に撚合構成の撚り線の谷間が目視できない程度に厚く形成する必要があり、又本発明の操作用ロープ20の各実施例で用いる接合部材21と同一、又は同種の共晶合金を用いることが望ましい。これにより、接合工程での先端ロープ受けの連結部材22aと操作用ロープ20の先端部20aとの接合の組付作業を簡略化することができる。
This structure has the following specific effects. In other words, the joint strength between the distal end portion 20a of the operating rope 20 and the connecting member 22a of the distal end rope receiver is strengthened, and the joint strength is increased by the fusion-integrated fixation at the joint portion between the joint member 211 and the joint member 21. It can be greatly improved.
The reason why the distal end portion 20a of the operation rope 20 is plated or impregnated and fixed with the joining member 211 in advance is that the joining member 21 of the operation rope 20 whose wettability is extremely deteriorated by the wire drawing of the strong working. This is for improving the wettability and enabling a strong bond. When the joining member 211 is melted and fixed in advance, the joining member 211 is inserted through the connecting member 22a of the tip rope receiver, and then the welding member 211 is irradiated with a laser beam to remelt the joining member 211 to remelt the tip rope receiver. The connecting member 22a may be joined. In such a case, the joining member 211 needs to be formed thick on the surface of the distal end portion 20a of the operation rope 20 to such an extent that the valleys of the twisted strands cannot be seen, and each operation rope 20 of the present invention is implemented. It is desirable to use the same or the same kind of eutectic alloy as the joining member 21 used in the example. Thereby, the assembly | attachment operation | work of joining with the connection member 22a of the tip rope receiver and the tip part 20a of the operation rope 20 in a joining process can be simplified.

そして次に、操作用ロープ20の先端ロープ受けの連結部材22aの構造は、先端湾曲駒18aの内周側先端部へ短小管体の管体ロープ受けの連結部材221を用いて固着させ、操作用ロープ20の先端部20aを貫挿させた後、接合部材21を用いて接合させてもよい。かかる場合、先端湾曲駒18aの先端ロープ受けの連結部材22a、又は管体ロープ受けの連結部材221は、操作用ロープ20と同一、又は同種の材料から形成されることが接合強度向上の観点からより望ましい。ここで同種材料とは、JIS表示でいう鋼種記号のいずれかを問わず(オーステナイト系SUS304かマルテンサイト系SUS403のいずれかを問わず)、前置記号が同一鋼材であれば同種材料のことをいう。従って、ステンレス鋼材とアルミニウム鋼材とは異種材料である。最も好ましいのは、同一材料である。   Next, the structure of the connecting member 22a of the distal end rope receiver of the operating rope 20 is fixed to the inner peripheral side distal end portion of the distal bending piece 18a by using the connecting member 221 of the tubular rope receiver of the short tubular body. After inserting the tip 20a of the rope 20 for use, the joining member 21 may be used for joining. In this case, from the viewpoint of improving the bonding strength, the connecting member 22a of the distal end rope receiver of the distal bending piece 18a or the connecting member 221 of the tubular rope receiver is formed of the same or the same material as the operation rope 20. More desirable. Here, the same kind of material refers to the same kind of material as long as the prefix is the same steel material regardless of any of the steel type symbols in the JIS display (regardless of either austenitic SUS304 or martensitic SUS403). Say. Therefore, the stainless steel material and the aluminum steel material are different materials. Most preferred is the same material.

そして次に、本発明の医療用処置具の他の実施例2〜7について以下説明する。   Next, other examples 2 to 7 of the medical treatment tool of the present invention will be described below.

図8は、本発明の医療内視鏡用処置具である実施例2の医療内視鏡用高周波スネア13Aを示し、図示(A)は先端処置部17を示し、手元操作部2と連結している操作用ロープ20の先端部には、管体ロープ受けの連結部材221が処置用ループ17Aと操作用ロープ20の先端部を管体内、又は管体端部で接合部材21を用いて接合されている。
図示(B)は手元操作部2を示し、手元操作部2はガイド溝2Dと指かけリング2Cを備えた操作部本体2Aと高周波発生装置(図示せず)に接続する端子30を有する平板状の連結部材222を備えたスライダー2Bから構成され、連結部材222は操作用ロープ20の手元端を挿入する穴部32を有して、前記穴部32に操作用ロープ20の手元部を挿入し、穴部32に接合部材21を用いて操作用ロープ20と接合している。尚、操作用ロープ20の手元部の外側には、座屈防止の為補強パイプ2Eが設けられ、スライダー2Bと連結している。尚、図示(C)(D)は、先端処置部17の操作用ロープ20と連結部材221との一部拡大図を示し、又図示(E)(F)は、手元操作部2の操作用ロープ20と連結部材222との一部拡大図を示す。
FIG. 8 shows the medical endoscope high-frequency snare 13A of the second embodiment which is the medical endoscope treatment tool of the present invention. FIG. 8A shows the distal treatment section 17, which is connected to the hand operation section 2. The connecting member 221 of the tubular rope receiver joins the treatment loop 17A and the distal end portion of the operating rope 20 to the distal end portion of the operating rope 20 using the joining member 21 at the tubular body or the tubular body end portion. Has been.
The figure (B) shows the hand operation part 2, and the hand operation part 2 is flat plate shape which has the terminal 30 connected to the operation part main body 2A provided with the guide groove 2D and the finger ring 2C, and the high frequency generator (not shown). The connecting member 222 has a hole portion 32 into which the proximal end of the operation rope 20 is inserted, and the proximal portion of the operation rope 20 is inserted into the hole portion 32. The operation rope 20 is joined to the hole 32 using the joining member 21. A reinforcing pipe 2E is provided outside the hand portion of the operation rope 20 to prevent buckling, and is connected to the slider 2B. In addition, illustration (C) (D) shows the partially expanded view of the rope 20 for operation of the front treatment part 17, and the connection member 221, and illustration (E) and (F) are for operation of the hand operation part 2. A partially enlarged view of the rope 20 and the connecting member 222 is shown.

そしてスライダー2Bをガイド溝2Dに沿って前後方向(図示左右方向)へ移動させることにより、スライダー2Bに連結されている操作用ロープ20に操作力が加わり、処置用ループ17Aをフッ素樹脂等の絶縁材料から成るシース241内へ収納(スライダー2Bを図示右側へ移動)、又はシース241の外へ出して拡張させ(スライダー2Bを図示左側へ移動)、処置用ループ17Aで患部を補足し、端子30に高周波装置と接続して端子30から連結部材222、操作用ロープ20、連結部材221、処置用ループ17Aへ通電させて患部を切除、及び止血等の処置を図っている。   Then, by moving the slider 2B in the front-rear direction (the left-right direction in the drawing) along the guide groove 2D, an operation force is applied to the operation rope 20 connected to the slider 2B, and the treatment loop 17A is insulated with a fluorine resin or the like. It is housed in a sheath 241 made of material (slider 2B is moved to the right side in the figure) or is expanded outside the sheath 241 (slider 2B is moved to the left side in the figure), and the affected part is supplemented by the treatment loop 17A. The terminal 30 is connected to the high-frequency device, and the connection member 222, the operation rope 20, the connection member 221, and the treatment loop 17A are energized to remove the affected area and perform treatment such as hemostasis.

そして、操作用ロープ20と連結部材221、222とは、接合部材21を用いて連結部材221、222の内部、又は端部とで接合している。
かかる構成において、本発明の操作用ロープ20は、固溶化処理したオーステナイト系ステンレス鋼線を用いて強加工の伸線加工した金属素線を撚合構成して成り、強加工した金属素線、及び撚合構成したロープの引張破断強度を向上させる一定温度範囲と合致した溶融温度もつ接合部材21を用いることにより、接合部材21を単に固着手段として用いるのではなく、接合部の操作用ロープ20の引張破断力を向上させながら、かつ接合部の接合強度を向上させることができる。
The operation rope 20 and the connecting members 221 and 222 are joined to each other inside the connecting members 221 and 222 using the joining member 21 or at the end.
In such a configuration, the operation rope 20 of the present invention is formed by twisting a metal wire that has been subjected to strong drawing using a solidified austenitic stainless steel wire, In addition, by using the joining member 21 having a melting temperature that matches a certain temperature range for improving the tensile breaking strength of the twisted rope, the joining member 21 is not simply used as the fixing means, but the operation rope 20 for the joining portion. It is possible to improve the joint strength of the joint portion while improving the tensile rupture force.

そして補足すれば、強加工の伸線加工による接合部材21の濡れ性の低下を、操作用ロープの少なくとも接合部に電解研磨等の処理を施すことによる接合性の向上、及び連結部材221、222にステンレス鋼材を用いて操作用ロープとの同一、又は同種材料を用いることにより相互間の熱膨張差を少なくし、かつ、接合部材との濡れ性を均等化して接合部材との強固な接合性の向上を図ることができる。尚、医療内視鏡用スネア13(実施例3)との差は、主に高周波装置に接合する端子30の有無、及び絶縁性の有無(例えばシース241の材料等)等である。   If supplemented, the reduction in wettability of the joining member 21 due to the strong wire drawing, the improvement of the joining property by performing treatment such as electrolytic polishing on at least the joint portion of the operation rope, and the connecting members 221 and 222. By using the same or the same kind of material as the rope for operation using stainless steel, the difference in thermal expansion between them is reduced, and the wettability with the joining member is equalized to ensure strong joining with the joining member. Can be improved. The difference from the medical endoscope snare 13 (Example 3) is mainly the presence / absence of the terminal 30 joined to the high-frequency device, the presence / absence of insulation (for example, the material of the sheath 241), and the like.

図9は、本発明の医療内視鏡用処置具である実施例4の医療内視鏡用鉗子14を示し、図示(A)は先端処置部17を示し、手元操作部2と連結している操作用ロープ20の先端部には、一対の鉗子カップをパンタグラフ機構から成る生検鉗子17Bと連結する先端側が偏平状で連結ピンの穴部221Z(図示(C))を有し、手元側が略円筒状の連結部材221Aが、操作用ロープ20の先端部と略円筒状の円筒内、又は円筒端部で接合部材21を用いて接合されている。図示(B)は、手元操作部2を示し、手元操作部2はガイド溝2Dと指かけリング2Cを備えた操作部本体2Aと、操作用ロープ20の手元部と連結する略円筒状の連結部材222Aを備えたスラーダー2Bから構成され、略円筒状の連結部材222Aは、操作用ロープ20の手元部と略円筒状の円筒内、又は円筒端部で接合部材21を用いて接合されている。尚、操作用ロープ20の手元部の外側には、座屈防止の為補強パイプ2Eが設けられ、スライダー2Bと連結している。尚、図示(C)(D)は、先端処置部17の操作用ロープ20と連結部材221Aとの一部拡大図を示し、又図示(E)(F)は、手元操作部2の操作用ロープ20と連結部材222Aとの一部拡大図を示す。   FIG. 9 shows the medical endoscope forceps 14 of Example 4 which is the medical endoscope treatment tool of the present invention. FIG. 9A shows the distal treatment section 17, which is connected to the hand operation section 2. The distal end of the operating rope 20 is connected to a biopsy forceps 17B composed of a pantograph mechanism at the distal end thereof, and has a flattened connection pin hole 221Z (illustration (C)). The substantially cylindrical connecting member 221 </ b> A is joined to the distal end portion of the operation rope 20 in the substantially cylindrical cylinder or the cylindrical end portion using the joining member 21. The figure (B) shows the hand operation part 2, and the hand operation part 2 is connected to the operation part main body 2A provided with the guide groove 2D and the finger ring 2C, and the substantially cylindrical connection connected to the hand part of the operation rope 20. The slurder 2B provided with the member 222A, and the substantially cylindrical connecting member 222A is joined to the proximal portion of the operation rope 20 with the joining member 21 in the substantially cylindrical cylinder or at the end of the cylinder. . A reinforcing pipe 2E is provided outside the hand portion of the operation rope 20 to prevent buckling, and is connected to the slider 2B. In addition, illustration (C) (D) shows the partially expanded view of the rope 20 for operation of the front-end | tip treatment part 17, and connection member 221A, and illustration (E) and (F) are for operation of the hand operation part 2. The partially expanded view of the rope 20 and the connection member 222A is shown.

そしてスライダー2Bをガイド溝2Dに沿って前後方向(図示左右方向)へ移動させることにより、スライダー2Bに連結されている操作用ロープ20に操作力が加わり、生検鉗子17Bの鉗子カップを開(スライダー2Bを図示左側へ移動)閉(スライダー2Bを図示右側へ移動)させ、患部を補足し、切除等の処置を図っている。尚、医療内視鏡用鉗子14(実施例4)と、高周波通電による医療用処置具である医療内視鏡用ホットバイオプシー鉗子14A(実施例5)との差は、前記実施例2と3と同様に、主に高周波装置に接合する端子30の有無、及び絶縁性の有無(例えばシース241、242の材料等)等で、実施例5の場合に前記実施例2と同様な端子30をスライダー2B内の連結部材222Aに端子を接続する構造等である。(図8(E)(F)参照)   Then, by moving the slider 2B in the front-rear direction (the left-right direction in the drawing) along the guide groove 2D, an operation force is applied to the operation rope 20 connected to the slider 2B, and the forceps cup of the biopsy forceps 17B is opened ( The slider 2B is moved to the left side in the figure) and closed (the slider 2B is moved to the right side in the figure) to supplement the affected part and perform treatment such as excision. The difference between the forceps 14 for medical endoscope (Example 4) and the hot biopsy forceps 14A for medical endoscope (Example 5), which is a medical treatment instrument using high-frequency energization, is the same as in Examples 2 and 3 described above. In the same manner as in Example 5, in the case of Example 5, the terminal 30 similar to that of Example 2 above is determined by the presence or absence of the terminal 30 to be joined to the high-frequency device and the presence or absence of insulation (for example, the material of the sheaths 241 and 242). For example, the terminal is connected to the connecting member 222A in the slider 2B. (See FIGS. 8E and 8F)

この構成により、実施例4〜5は、前記実施例1〜3と同様に強加工の伸線加工による高強度の引張破断強度特性を有する金属素線を撚合構成した操作用ロープ20を得て、そして接合部材21の溶融熱を利用して接合部の操作用ロープ20の引張破断力を向上させて接合することができ、さらに金、又は銀成分を含む接合部材の高電導特性と併せて、高度の操作性を有する医療内視鏡用処置具の提供ができる。   According to this configuration, Examples 4 to 5 obtain the operation rope 20 in which the metal strands having high strength tensile breaking strength characteristics by the strong wire drawing work are twisted as in Examples 1 to 3 described above. In addition, the heat of fusion of the joining member 21 can be used to improve the tensile breaking force of the operation rope 20 at the joining portion, and the joining member 21 can be joined together with the high conductivity characteristics of the joining member containing a gold or silver component. Thus, it is possible to provide a medical endoscope treatment tool having high operability.

次に図10は、本発明の医療内視鏡用処置具である実施例6の医療内視鏡用クリップ装置15を示し、先端処置部17のクリップ17Cを導入管33内へ収納させた状態で体内へ挿入し、その後手元操作部2のスライダー部2Bをガイド溝2Dに沿って図示右方向へ移動させることにより、スライダー2B内の連結部材222Bと接合部材21により接合されている操作用ロープ20に操作力が加わり、操作用ロープの先端部と接合部材21により接合されているフック状の連結部材221Bへ力が伝わり、フック状の連結部材221Bからクリップ17Cが外れて離脱し、患部を補足して血管を閉じて止血処置を図っている。尚、図(C)は、クリップ17Cによる血管34のクリップ状態を示す縦断面図である。   Next, FIG. 10 shows the medical endoscope clip device 15 of Example 6 which is the medical endoscope treatment tool of the present invention, and the clip 17C of the distal treatment section 17 is housed in the introduction tube 33. Then, the operating rope joined to the connecting member 222B in the slider 2B and the joining member 21 by moving the slider 2B of the hand operating part 2 to the right in the figure along the guide groove 2D. 20, an operating force is applied, and the force is transmitted to the hook-shaped connecting member 221B joined to the distal end portion of the operating rope by the joining member 21, and the clip 17C is detached from the hook-shaped connecting member 221B and detached, and the affected part is removed. In addition, the blood vessels are closed to stop the hemostasis. Incidentally, FIG. (C) is a longitudinal sectional view showing a clip state of the blood vessel 34 by the clip 17C.

そして次に図11は、本発明の医療内視鏡用処置具である実施例7の医療内視鏡用高周波ナイフ16を示し、先端処置部17のナイフ部17Dを体内へ挿入して患部へ近づけた後、手元操作部2のスライダー部2Bをガイド溝2Dに沿って図示左方向へ移動させることにより、スライダー2B内の高周波装置と接続できる端子30を有する連結部材222Cと接合部材21により接合されている操作用ロープ20に操作力が加わる。
そして操作用ロープ20の先端部と接合部材21により接合している略円筒状連結部材221Cへ力が加わり、連結部材221Cの先端側と連結している棒状電極部172Dと平板状電極部171Dとから成るナイフ部17Dの平板状電極部171Dを患部へ接触させて生体組織を焼灼切開の処置を図っている。尚、前記実施例7の医療用処置具は、シリンジ31より生理食塩水をシース243の内部空間243Aへ通過させて先端処置部17より噴出させ、出血部分を明確にさせる機能を備えている。
そして、実施例6、7において、接合部材21を用いて操作用ロープ20と連結部材221B、222B、221C、222Cとの接合法は前記実施例1〜5と同様である。
Next, FIG. 11 shows the medical endoscope high-frequency knife 16 of Example 7 which is the medical endoscope treatment tool of the present invention, and the knife portion 17D of the distal treatment section 17 is inserted into the body to the affected area. After approaching, the slider portion 2B of the hand operation portion 2 is moved in the left direction in the figure along the guide groove 2D, so that the connecting member 222C having the terminal 30 that can be connected to the high frequency device in the slider 2B and the joining member 21 are joined. An operating force is applied to the operating rope 20 that is being operated.
A force is applied to the substantially cylindrical connecting member 221C joined to the distal end portion of the operating rope 20 by the joining member 21, and the rod-like electrode portion 172D and the flat electrode portion 171D joined to the distal end side of the connecting member 221C The plate-like electrode portion 171D of the knife portion 17D made of the above is brought into contact with the affected area to treat the living tissue for cautery incision. Note that the medical treatment instrument of the seventh embodiment has a function of causing the physiological saline to pass through the internal space 243A of the sheath 243 from the syringe 31 and ejecting from the distal treatment section 17 to clarify the bleeding part.
And in Example 6, 7, the joining method of the rope 20 for operation and connection member 221B, 222B, 221C, 222C using the joining member 21 is the same as that of the said Examples 1-5.

この構成により、実施例6、7は、前記実施例1〜5と同様に強加工の伸線加工による高強度の引張破断強度特性を有する金属素線を撚合構成した操作用ロープ20を得て、そして接合部材21の溶融熱を利用して接合部の操作用ロープ20の引張破断力を向上させて接合することができ、さらに金、又は銀成分を含む接合部材の高電導特性と併せて、高度の操作性を有する医療内視鏡用処置具の提供ができる。   By this structure, Example 6, 7 obtains the operation rope 20 which twisted and comprised the metal strand which has the high strength tensile breaking strength characteristic by the strong wire drawing like the said Examples 1-5. In addition, the heat of fusion of the joining member 21 can be used to improve the tensile breaking force of the operation rope 20 at the joining portion, and the joining member 21 can be joined together with the high conductivity characteristics of the joining member containing a gold or silver component. Thus, it is possible to provide a medical endoscope treatment tool having high operability.

そして生理食塩水を用いた医療用処置具においては、銀成分を含む接合部材を用いたとき、生理食塩水との接触により硫化銀等が形成されて黒色化が始まり、時間の経過とともに黒色化がさらに進んで腐食が進行して接合強度が低下する。この為、腐食進行による接合強度低下防止、及び黒色化防止の観点から金系共晶合金の接合部材21を用いることが、より望ましい接合形態である。このことは、医療用内視鏡のチャンネルチューブ等の内孔から生理食塩水を通過させて先端部の対物レンズの洗浄、又病変部の把握明確化等の為に病変部へ生理食塩水を噴射させる場合にも同様の問題が発生し、医療用内視鏡、及び医療内視鏡用処置具に共通する技術課題である。前記方法により、この技術課題を解消することができる。   In a medical treatment instrument using physiological saline, when a joining member containing a silver component is used, silver sulfide or the like is formed by contact with physiological saline, and blackening starts. However, the corrosion progresses further and the bonding strength decreases. For this reason, it is a more desirable joining form to use the joining member 21 of a gold eutectic alloy from the viewpoint of preventing the joining strength from being lowered due to the progress of corrosion and preventing blackening. This is because the physiological saline is passed through the inner hole of the channel tube of the medical endoscope, and the objective lens at the tip is washed, and the physiological saline is applied to the lesion to clarify the lesion. The same problem also occurs when spraying, which is a technical problem common to medical endoscopes and medical endoscope treatment tools. By this method, this technical problem can be solved.

そしてさらに補足すれば、特に実施例6、7において、手元操作部の押し操作、及び回転操作により先端処置部17のクリップ17C、又はナイフ部17Dを所望の患部位置へコントロールし易い操作用ロープ20は、ストランドロープよりもスパイラルロープが望ましく、さらに望ましいのはスパイラルロープのうち前記したように側材よりも芯材のほうが一定の範囲の太径線を用いた態様である。
この理由は、手元操作部の押し操作、及び回転操作は操作用ロープの、特にストレート状の芯材の特性に大きく影響され、例えば押し操作の場合には、耐座屈荷重は断面二次モーメントに比例し、芯材の素線直径の太いものほどこの値は大きくなって耐座屈荷重は向上し、押し操作力は向上する。又、回転操作の場合には、捩り抵抗モーメントは断面二次極モーメントに比例し、素線直径の太いものほどこの値は大きくなり、その結果先端部への回転伝達性能を向上させることができるからである。
Further, in addition, particularly in the sixth and seventh embodiments, the operation rope 20 that makes it easy to control the clip 17C or the knife portion 17D of the distal treatment section 17 to a desired affected position by pushing and rotating the hand operation section. The spiral rope is more desirable than the strand rope, and more preferable is an aspect in which the core material uses a large diameter wire in a certain range rather than the side material as described above.
The reason for this is that the pushing operation and rotating operation of the hand operating part are greatly influenced by the characteristics of the rope for operation, particularly the straight core material. The larger the core wire diameter is, the larger this value is, so that the buckling resistance is improved and the pushing operation force is improved. In addition, in the case of rotational operation, the torsional resistance moment is proportional to the cross-sectional secondary pole moment, and this value increases as the wire diameter increases, and as a result, the ability to transmit rotation to the tip can be improved. Because.

そして次に、本発明の医療用処置具の製造方法について以下に説明する。
可とう性管体に貫挿した操作用ロープの先端処置部の連結部材、又は手元操作部の連結部材と、前記操作用ロープとを接合部材を用いて接合し、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部を動作させる医療用処置具の製造方法において、前記操作用ロープは、固溶化処理したオーステナイト系ステンレス鋼線を用いて総減面率が90%から99.5%の伸線加工した金属素線を複数本用いて撚合構成したロープから成る工程と、前記撚合構成したロープを電解研磨した後に所定長切断する工程と、又は前記撚合構成したロープを所定長切断した後に電解研磨する工程と、その後切断した前記操作用ロープの先端部を前記先端処置部の連結部材の穴部へ挿入する工程と、又はその後切断した前記操作用ロープの手元部を前記手元操作部の連結部材の穴部へ挿入する工程と、前記連結部材内へ挿入した前記操作用ロープとの接合部に、180℃から1 495℃の溶融温度をもつ共晶合金から成る前記接合部材を溶融させ、又は前記操作用ロープの金属素線がMoを含むオーステナイト系ステンレス鋼線のときには、180℃から525℃の溶融温度をもつ共晶合金からなる前記接合部材を溶融させ、前記連結部材と前記操作用ロープとを前記接合部材を用いて接合する工程から成ることを特徴とする医療用処置具の製造方法である。
この構成により、強加工の伸線加工した金属素線を複数本用いて撚合構成して操作用ロープを形成し、又強加工伸線による接合部材との濡れ性を向上させ、かつ連結部材との接合において、オーステナイト系ステンレス鋼線の強加工と低温熱処理の引張破断強度との相関性に着目して、強加工伸線による高度の引張破断強度を有する操作用ロープの引張破断強度を接合時の接合部材の溶融熱を利用して、より引張破断強度を向上させて接合できる、新たな技術思想から成る医療用処置具の製造ができる。
Next, a method for manufacturing the medical treatment tool of the present invention will be described below.
Join the connecting member of the distal treatment section of the operating rope inserted through the flexible tube, or the connecting member of the hand operating section and the operating rope using the joining member, and press the hand operating section, In the method of manufacturing a medical treatment tool for operating the distal treatment portion by pulling or rotating and operating the operating force of the operating rope, the operating rope is a solution treated austenitic stainless steel wire A process comprising a rope formed by twisting a plurality of metal strands having a total area reduction ratio of 90% to 99.5% using a wire, and a predetermined after electropolishing the twisted rope. A step of long cutting, a step of electropolishing after cutting the twisted rope by a predetermined length, and a step of inserting the cut end of the operating rope into the hole of the connecting member of the tip treatment portion And or In the step of inserting the proximal portion of the operation rope that has been cut later into the hole portion of the connecting member of the proximal operation portion and the joint portion of the operating rope inserted into the connecting member, 180 ° C. to 1 495 When the joining member made of a eutectic alloy having a melting temperature of 0 ° C. is melted or the metal element wire of the operating rope is an austenitic stainless steel wire containing Mo, the joint member having a melting temperature of 180 ° C. to 525 ° C. A method for manufacturing a medical treatment instrument comprising the steps of melting the joining member made of a crystal alloy and joining the connecting member and the operating rope using the joining member.
With this configuration, a plurality of metal wires that have been subjected to strong wire drawing are twisted together to form an operation rope, and wettability with a joining member by strong wire drawing is improved, and a connecting member Focusing on the correlation between strong working of austenitic stainless steel wire and tensile breaking strength of low-temperature heat treatment, joining the tensile breaking strength of an operating rope with a high tensile breaking strength due to strong work drawing By utilizing the heat of fusion of the joining member at the time, it is possible to manufacture a medical treatment instrument composed of a new technical idea that can be joined with further improved tensile fracture strength.

そして又、可とう性管体に貫挿した操作用ロープの先端処置部の連結部材、又は手元操作部の連結部材と、前記操作用ロープとを接合部材を用いて接合し、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部を動作させる医療用処置具の製造方法において、前記操作用ロープは、固溶化処理したオーステナイト系ステンレス鋼線を用いて総減面率が90%から99.5%の伸線加工した金属素線を複数本用いて撚合構成したロープから成る工程と、前記撚合構成したロープを電解研磨した後に所定長切断する工程と、又は前記撚合構成したロープを所定長切断した後に電解研磨する工程と、その後切断した前記操作用ロープの先端部を前記先端処置部のステンレス鋼材から成る連結部材の穴部へ挿入する工程と、又はその後切断した前記操作用ロープの手元部を前記手元操作部のステンレス鋼材から成る連結部材の穴部へ挿入する工程と、前記連結部材内へ挿入した前記操作用ロープとの接合部に180℃から495℃の溶融温度をもつ共晶合金から成る前記接合部材を溶融させ、又は前記操作用ロープの金属素線がMoを含むオーステナイト系ステンレス鋼線のときには、180℃から525℃の溶融温度をもつ共晶合金からなる前記接合部材を溶融させ、同一、又は同種の材料から成る前記連結部材と前記操作用ロープとを、前記接合部材により接合する工程からなることを特徴とする医療用処置具の製造方法である。
この構成により、操作用ロープと連結部材との接合において、オーステナイト系ステンレス鋼線の強加工伸線と低温熱処理の引張破断強度との相関性に着目して、強加工伸線による高度の引張破断強度を有する操作用ロープの引張破断強度を、接合時の接合部材の溶融熱を利用して、より引張破断強度を向上させ、さらに操作用ロープと連結部材とが同一、又は同種材料を用いることにより、相互間の熱膨張差を少なくし、かつ操作用ロープと接合部材との濡れ性、及び連結部材と接合部材との濡れ性を接合面で概ね均一にさせることにより、又接合部の部材間の接合力を均一にさせることにより、より高い接合部の接合強度を得ることができる。
Further, the operating member inserted into the flexible tube is joined to the connecting member of the distal treatment section or the operating member of the hand operating part and the operating rope using a joining member, and the hand operating part In the method of manufacturing a medical treatment instrument for operating the distal treatment section by transmitting, operating, pushing, pulling, or rotating the operating force of the operating rope, the operating rope is a solution treated austenite A process comprising a rope formed by twisting a plurality of metal strands drawn with a stainless steel wire with a total area reduction of 90% to 99.5%, and the twisted rope is electropolished. A step of cutting a predetermined length after cutting, a step of electrolytic polishing after cutting the twisted rope by a predetermined length, and then connecting the distal end portion of the operating rope cut by the stainless steel material of the distal treatment section A step of inserting into the hole portion of the material, or a step of inserting the proximal portion of the operating rope cut thereafter into the hole portion of the connecting member made of stainless steel material of the proximal operating portion, and the step of inserting into the connecting member When the joining member made of a eutectic alloy having a melting temperature of 180 ° C. to 495 ° C. is melted at the joint with the operation rope, or the metal strand of the operation rope is an austenitic stainless steel wire containing Mo From the step of melting the joining member made of a eutectic alloy having a melting temperature of 180 ° C. to 525 ° C. and joining the connecting member made of the same or the same kind of material and the rope for operation by the joining member. It is the manufacturing method of the medical treatment tool characterized by becoming.
With this configuration, in joining the operating rope and the connecting member, paying attention to the correlation between the strong work drawing of the austenitic stainless steel wire and the tensile break strength of the low temperature heat treatment, the high tensile breaking by the strong work drawing The tensile breaking strength of the operating rope having strength is improved by utilizing the heat of fusion of the joining member at the time of joining, and the operating rope and the connecting member are made of the same or the same material. By reducing the difference in thermal expansion between them, and making the wettability between the rope for operation and the joining member, and the wettability between the connecting member and the joining member substantially uniform on the joining surface, the member of the joining part By making the bonding force between them uniform, higher bonding strength of the bonding portion can be obtained.

そして又、前記医療用処置具の製造方法の連結部材と操作用ロープとを接合する工程が、真空環境下、又は不活性ガス環境下における接合工程から成ることがより望ましい。
この理由は、医療用処置具のオートクレープ滅菌後であっても、フラックス残留に起因する高強度を有する操作用ロープの引張破断強度の低下を防いで接合させることができるからである。
Further, it is more desirable that the step of joining the connecting member and the operating rope in the method for manufacturing the medical treatment instrument comprises a joining step in a vacuum environment or an inert gas environment.
This is because even after the autoclave sterilization of the medical treatment instrument, the operation rope having high strength due to residual flux can be joined while preventing a decrease in tensile breaking strength.

次に図1、2を用いて医療用処置具である処置具孔10を有する医療用内視鏡1と、前記実施例2〜7の医療内視鏡用処置具との組立体について説明する。
前記組立体は、先端処置部17が湾曲駒18を複数個連結し、先端側の前記湾曲駒18aと前記操作用ロープ20の先端部とを前記接合部材21、211を用いて接合した湾曲部6から成り、手元操作部2を操作して前記操作用ロープ20の操作力の伝達作用により、前記湾曲部6を湾曲変形させ、かつ前記手元操作部2に処置具孔10を有する請求項1〜4のいずれか一つに記載の医療用処置具である医療用内視鏡1と、前記実施例2〜7の医療内視鏡用処置具1を前記処置具孔10より出入りさせて病変部治療を行うことを特徴とする医療用内視鏡1と、医療内視鏡用処置具との組立体である。
この構成により、操作用ロープの引張破断強度不足、及び接合部での引張破断強度不足に起因する医療用内視鏡、及び医療内視鏡用処置具の操作不能状態での手技の中断を防ぎ、高度の操作性を有しながら、円滑、かつ迅速な病変部の多様な手技対応ができる組立体の提供ができる。そして補足すれば、操作用ロープに、芯材が側材よりも一定範囲の径大の金属素線を用いることによる医療内視鏡用処置具の押し操作性、及び回転操作の操作性のより向上、又高周波通電させて患部を処置する高通電特性を有する接合部材の使用による通電特性の向上、さらに補足すれば、対物レンズの洗浄、又は病変部の正確認識等の為、医療用内視鏡のチャンネルチューブ等、又は医療内視鏡用処置具のシース内の内孔から生理食塩水を通過させることによる接合部での黒色化防止の為の金成分を含む接合部材の選択使用等により高度の操作性を有する組立体の提供ができる。
Next, an assembly of the medical endoscope 1 having the treatment instrument hole 10 which is a medical treatment instrument and the medical endoscope treatment instrument according to the second to seventh embodiments will be described with reference to FIGS. .
The assembly includes a bending portion in which a distal end treatment portion 17 connects a plurality of bending pieces 18, and the bending piece 18 a on the distal end side and the distal end portion of the operation rope 20 are joined using the joining members 21 and 211. 6, the bending portion 6 is bent and deformed by the operation of transmitting the operating force of the operation rope 20 by operating the hand operation portion 2, and the treatment tool hole 10 is provided in the hand operation portion 2. The medical endoscope 1 that is the medical treatment instrument according to any one of 4 to 4 and the medical endoscopic treatment instrument 1 according to Examples 2 to 7 are caused to enter and exit from the treatment instrument hole 10. This is an assembly of a medical endoscope 1 and a medical endoscope treatment tool characterized by performing partial therapy.
This configuration prevents the interruption of the procedure when the medical endoscope and the treatment tool for medical endoscope are inoperable due to insufficient tensile breaking strength of the operating rope and insufficient tensile breaking strength at the joint. Thus, it is possible to provide an assembly capable of handling various procedures for a lesioned part smoothly and quickly while having high operability. And, supplementally, the operation rope can be pushed more easily and the operability of the rotation operation can be improved by using a metal wire having a diameter larger than that of the side material. Improvement of current-carrying characteristics by using a joint member with high-current-carrying characteristics that improves the treatment of the affected area by applying high-frequency current, and, in addition, medical endoscope for cleaning the objective lens or accurately recognizing the lesion. By selecting and using a joining member containing a gold component for preventing blackening at the joint by passing physiological saline through the inner tube in the sheath of a treatment tube for a medical endoscope, etc. An assembly having a high degree of operability can be provided.

[発明の効果]
以上説明のとおり、本発明の医療用処置具は、強加工の伸線加工した引張破断強度の高い金属素線を複数本用いて撚合構成し、引張破断力の高い操作用ロープを備え、そして強加工伸線により引張破断強度が向上する温度範囲と一致させた溶融温度範囲をもつ接合部材である共晶合金の溶融熱を利用して、前記操作用ロープの引張破断力をより向上させながら、連結部材との強固な接合を可能とするものである。
[Effect of the invention]
As described above, the medical treatment tool of the present invention is formed by twisting using a plurality of high-strength drawn metal strands having high tensile breaking strength, and includes an operation rope having high tensile breaking strength. Further, by using the heat of fusion of the eutectic alloy, which is a joining member having a melting temperature range matched with the temperature range in which the tensile breaking strength is improved by strong work drawing, the tensile breaking force of the operating rope is further improved. However, it is possible to firmly join the connecting member.

そして又、処置具孔を備えた本発明の医療用内視鏡を用いて、処置具孔より各医療内視鏡用処置具を出入りさせ、病変部の状況に対応した治療を行う為の術者へ高度の操作性を有する医療用処置具の組立体の提供ができ、迅速治療に大きく寄与することができる。以上の諸効果がある。   Further, using the medical endoscope of the present invention provided with a treatment tool hole, each medical endoscope treatment tool is moved in and out of the treatment tool hole, and a treatment corresponding to the condition of the lesioned part is performed. It is possible to provide a medical treatment instrument assembly having a high degree of operability to a person, and can greatly contribute to rapid treatment. There are the above various effects.

1 医療用内視鏡
2 操作部
3 湾曲操作ノブ
4 挿入部
5 可とう管部
6 湾曲部
7 先端構成部
10 処置具孔
13 医療内視鏡用スネア
13A 医療内視鏡用高周波スネア
14 医療内視鏡用鉗子
14A 医療内視鏡用ホットバイオプシー鉗子
15 医療内視鏡用クリップ装置
16 医療内視鏡用高周波ナイフ
18 湾曲駒
20 操作用ロープ
20a 操作用ロープの先端部
21 接合部材
22 ロープ受け
22a 先端ロープ受けの連結部材
221 管体ロープ受けの連結部材
DESCRIPTION OF SYMBOLS 1 Medical endoscope 2 Operation part 3 Bending operation knob 4 Insertion part 5 Flexible tube part 6 Bending part 7 Tip structure part 10 Treatment tool hole 13 Snare 13A for medical endoscopes High frequency snare 14 for medical endoscopes Endoscopic forceps 14A Medical endoscope hot biopsy forceps 15 Medical endoscope clip device 16 High-frequency knife for medical endoscope 18 Bending piece 20 Operation rope 20a Operation rope tip 21 Joining member 22 Rope receiver 22a Connecting member 221 for the tip rope receiver Connecting member for the tubular rope receiver

Claims (8)

可とう性管体に貫挿した操作用ロープの先端処置部の連結部材、又は手元操作部の連結部材と、前記操作用ロープとを接合部材を用いて接合し、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部を動作させる医療用処置具において、
前記操作用ロープは、固溶化処理し、且つ、成分にMoを含まないオーステナイト系ステンレス鋼線を用いて、総減面率が80%から99.5%の伸線加工した金属素線を複数本用いて撚合構成して成り、 前記接合部材は、180℃から495℃の溶融温度をもつ共晶合金から成り、又は
前記操作用ロープは、固溶化処理し、且つ、成分にMoを含むオーステナイト系ステンレス鋼線を用いて、総減面率が80%から99.5%の伸線加工した金属素線を複数本用いて撚合構成して成り、 前記接合部材は、180℃から525℃の溶融温度をもつ共晶合金から成り、
前記操作用ロープと前記連結部材とを、前記接合部材を用いて接合して成ることを特徴とする医療用処置具。
Join the connecting member of the distal treatment section of the operating rope inserted through the flexible tube, or the connecting member of the hand operating section and the operating rope using the joining member, and press the hand operating section, In the medical treatment instrument for operating the distal treatment section by transmitting or operating the pulling or rotating operation force of the operating rope,
The operating rope is a plurality of metal strands that have been subjected to solid solution treatment and drawn using an austenitic stainless steel wire that does not contain Mo as a component, with a total area reduction of 80% to 99.5%. The joining member is made of a eutectic alloy having a melting temperature of 180 ° C. to 495 ° C.
The operation rope is a plurality of metal strands that have been subjected to a solid solution treatment and drawn using an austenitic stainless steel wire containing Mo as a component and having a total area reduction of 80% to 99.5%. The joining member is made of a eutectic alloy having a melting temperature of 180 ° C. to 525 ° C.
A medical treatment instrument comprising the operation rope and the connecting member joined together using the joining member.
前記操作用ロープの金属素線の伸線加工における総減面率は90%から99.5%であり、
前記連結部材と接合する前記操作用ロープの少なくとも先端処置具の接合部、又は手元操作部の接合部に電解研磨処理、又は前記接合部材と同一の組成成分を含むめっき処理を施したことを特徴とする請求項1に記載の医療用処置具。
The total area reduction ratio in the wire drawing of the metal wire of the operation rope is 90% to 99.5% ,
Electrolytic polishing treatment or plating treatment containing the same composition component as that of the joining member is applied to at least the joint portion of the distal treatment tool or the joint portion of the hand operation portion of the operation rope to be joined to the connecting member. The medical treatment tool according to claim 1.
前記操作用ロープは、素線直径が0.008mmから0.200mmの金属素線を芯材と側材に用いて、前記芯材の外周に側材を6本から9本を一方向螺旋状に巻回成形する撚合構成のスパイラルロープから成り、
前記芯材の素線直径が前記側材の素線直径の1.07倍から2.12倍とし、前記操作用ロープから成ることを特徴とする請求項1〜2のいずれか一つに記載の医療用処置具。
The rope for operation uses a metal wire having a wire diameter of 0.008 mm to 0.200 mm as a core material and a side material, and 6 to 9 side materials are unidirectionally spiraled on the outer periphery of the core material. It consists of a spiral rope with a twisted configuration that is wound around
The strand diameter of the core material is 1.07 to 2.12 times the strand diameter of the side member, and the operation rope is used. Medical treatment tool.
前記接合部材である共晶合金が、金、又は銀のいずれかを含む組成から成り、溶融温度が217℃から525℃であることを特徴とする請求項1〜3のいずれか一つに記載の医療用処置具。   The eutectic alloy which is the said joining member consists of a composition containing either gold | metal | money or silver, and a melting temperature is 217 degreeC to 525 degreeC, It is any one of Claims 1-3 characterized by the above-mentioned. Medical treatment tool. 請求項1〜4のいずれか一つに記載の医療用処置具が、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部の処置用ループを拡縮させ、又は拡縮させた後、前記操作用ロープ、及び前記先端処置部に高周波電流を通電させて患部を切除する医療内視鏡用処置具の医療内視鏡用スネア、又は医療内視鏡用高周波スネアであることを特徴とする医療用処置具。   The medical treatment tool according to any one of claims 1 to 4, wherein the distal operation unit is pushed, pulled, or rotated to transmit the operation force of the operation rope. A medical endoscope snare of a medical endoscope treatment tool for enlarging or contracting a treatment loop and then excising an affected area by energizing a high-frequency current to the operation rope and the distal treatment section, or A medical treatment instrument characterized by being a high-frequency snare for a medical endoscope. 請求項1〜4のいずれか一つに記載の医療用処置具が、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部の生検鉗子の鉗子カップを開閉させて生体組織を採取し、又は前記鉗子カップを開閉させた後、前記操作用ロープ、及び前記鉗子カップに高周波電流を通電させて患部を切除する医療内視鏡用処置具の医療内視鏡用鉗子、又は医療内視鏡用ホットバイオプシー鉗子であることを特徴とする医療用処置具。   The medical treatment tool according to any one of claims 1 to 4, wherein the distal operation unit is pushed, pulled, or rotated to transmit the operation force of the operation rope. A medical endoscope that opens and closes a forceps cup of a biopsy forceps and collects a living tissue, or opens and closes the forceps cup, and then excises the affected part by energizing a high-frequency current to the operation rope and the forceps cup. A medical treatment instrument characterized by being a medical endoscopic forceps for a medical treatment instrument or a hot biopsy forceps for a medical endoscope. 請求項1〜4のいずれか一つに記載の医療用処置具が、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部のクリップを離脱させて体内留置する医療内視鏡用処置具の医療内視鏡用クリップ装置であることを特徴とする医療用処置具。   The medical treatment tool according to any one of claims 1 to 4, wherein the distal operation unit is pushed, pulled, or rotated to transmit the operation force of the operation rope. A medical treatment instrument characterized by being a medical endoscope clip device for a medical endoscope treatment instrument in which a clip is detached and placed in the body. 請求項1〜4のいずれか一つに記載の医療用処置具が、前記手元操作部を押し、引き、又は回転操作して前記操作用ロープの操作力の伝達作用により、前記先端処置部のナイフ部を所望の位置へ案内しながら前記操作用ロープ、及び前記ナイフ部へ高周波電流を通電させて患部生体組織を焼灼切開する医療内視鏡用処置具の医療内視鏡用高周波ナイフであることを特徴とする医療用処置具。

The medical treatment tool according to any one of claims 1 to 4, wherein the distal operation unit is pushed, pulled, or rotated to transmit the operation force of the operation rope. A high-frequency knife for a medical endoscope of a treatment instrument for medical endoscope that cauterizes and incises an affected living body tissue by applying a high-frequency current to the knife portion while guiding the knife portion to a desired position. A medical treatment instrument characterized by that.

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