JP6311479B2 - Endoscope injection needle and method for manufacturing endoscope injection needle - Google Patents

Endoscope injection needle and method for manufacturing endoscope injection needle Download PDF

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JP6311479B2
JP6311479B2 JP2014127474A JP2014127474A JP6311479B2 JP 6311479 B2 JP6311479 B2 JP 6311479B2 JP 2014127474 A JP2014127474 A JP 2014127474A JP 2014127474 A JP2014127474 A JP 2014127474A JP 6311479 B2 JP6311479 B2 JP 6311479B2
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resin
inner tube
base end
injection needle
endoscope
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JP2016007221A (en
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秀明 松波
秀明 松波
池田 昌夫
昌夫 池田
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Sumitomo Bakelite Co Ltd
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Sumitomo Bakelite Co Ltd
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本発明は、内視鏡用注射針および内視鏡用注射針の製造方法に関する。   The present invention relates to an endoscope injection needle and a method for manufacturing an endoscope injection needle.

内視鏡下に食道、胃、大腸等の粘膜を切除する内視鏡的粘膜切除術(EMR)および内視鏡的粘膜下層剥離術(ESD)施工時に、粘膜と筋層との剥離を要する場合がある。この場合、先端に針体が付設された内管チューブとその内管チューブを挿通自在にする外管チューブとを有した内視鏡用注射針を挿入して、生体組織に生理食塩水や薬液等(以下、単に液体ともいう)を注入することが通常実施されている。
内視鏡用注射針は、例えば1mから2m程度の長尺の内視鏡内に設けられたチャネルに挿入され、所定の生体組織において針体を穿刺する。液体は、内視鏡の基端側から長尺の内管チューブを通して針体の先端から吐出される。
When performing endoscopic mucosal resection (EMR) and endoscopic submucosal dissection (ESD) to remove the mucosa of the esophagus, stomach, large intestine, etc. under the endoscope, separation of the mucosa and muscle layer is required There is a case. In this case, an endoscope injection needle having an inner tube having a needle body attached to the tip and an outer tube that allows the inner tube to be inserted is inserted, and physiological saline or a drug solution is inserted into the living tissue. Etc. (hereinafter, also simply referred to as liquid) is generally practiced.
An endoscope injection needle is inserted into a channel provided in a long endoscope having a length of about 1 to 2 m, for example, and punctures a needle body in a predetermined living tissue. The liquid is discharged from the distal end of the needle body through the long inner tube from the proximal end side of the endoscope.

針体は、穿刺したときの傷を小さくするためにたとえば外径0.65mm以下のものが好適に使用されている。これに対し、注入抵抗を小さくするために内管チューブの内径はたとえば0.8mm以上とすることが好ましい。その結果、針体の外周面と内管チューブの内周面との間には間隙が形成されていた。上記間隙を埋めて、針体と内管チューブとを接続するための接続部材が設けられた内視鏡用注射針が提案されている。   For example, a needle body having an outer diameter of 0.65 mm or less is preferably used in order to reduce the damage when puncturing. On the other hand, in order to reduce the injection resistance, the inner diameter of the inner tube is preferably set to 0.8 mm or more, for example. As a result, a gap was formed between the outer peripheral surface of the needle body and the inner peripheral surface of the inner tube. An endoscope injection needle provided with a connection member for filling the gap and connecting the needle body and the inner tube is proposed.

例えば、下記特許文献1に記載の内視鏡用注射針(以下、従来技術1ともいう)は、針体の先端と反対側の端部にコイル状部材(接続部材)を外嵌して該コイル状部材を該針体に固着し、該コイル状部材に上記内管チューブを外嵌して固着している。
上記コイル状部材が設けられることによって、上記針体と内管チューブとの間の空隙が埋められるとともに両者が接続されている。
特許文献1図4に示されるとおり、上記コイル状部材の基端側の端面は、内管チューブの軸方向に対し略垂直に交差している。
For example, an endoscope injection needle (hereinafter also referred to as conventional art 1) described in Patent Document 1 below has a coiled member (connection member) externally fitted to the end opposite to the tip of the needle body. A coiled member is fixed to the needle body, and the inner tube is externally fixed to the coiled member.
By providing the coil-shaped member, the gap between the needle body and the inner tube is filled and both are connected.
Patent Document 1 As shown in FIG. 4, the end face on the base end side of the coil-shaped member intersects substantially perpendicularly to the axial direction of the inner tube.

特開2009−172029号公報JP 2009-172029 A

しかし従来技術1に例示される針体と内管注射針との間の間隙を埋めて、当該針体と当該内管チューブとを接続する接続部材を有する内視鏡用注射針は、以下の課題を有していた。   However, an endoscope injection needle having a connecting member that fills a gap between the needle body and the inner tube injection needle exemplified in the prior art 1 and connects the needle body and the inner tube tube is as follows. Had problems.

即ち、接続部材の基端面に、強い吐出圧で内管チューブ内を基端側から先端側に流通する液体が接触すると、接続部材が先端側に押圧される。これにより、接続部材の外周面と内管チューブの内周面との接続状態が不良となり、内管チューブ内において接続部材の配置位置が内管チューブの先端側にずれる虞があった。接続部材の配置位置のずれにより当該接続部材に挿通された針体の配置位置もずれるため、設計上予定される針体先端位置よりも実際の針体先端位置が先端側に変異し体内における手技に支障を来たす虞があった。
また接続部材の配置位置が大きく先端側にずれることによって、接続部材およびこれに挿通された針体が、内管チューブの先端側から脱落する虞があった。
That is, when the liquid flowing from the proximal end side to the distal end side in the inner tube tube with a strong discharge pressure comes into contact with the proximal end surface of the connecting member, the connecting member is pressed toward the distal end side. As a result, the connection state between the outer peripheral surface of the connection member and the inner peripheral surface of the inner tube is poor, and the arrangement position of the connection member in the inner tube may be shifted to the tip side of the inner tube. Since the placement position of the needle inserted through the connection member is also displaced due to the displacement of the connection member placement position, the actual needle body tip position is changed to the tip side from the needle tip position planned in the design, and the procedure in the body is performed. There was a risk of causing trouble.
In addition, when the arrangement position of the connecting member is largely displaced toward the distal end side, the connecting member and the needle inserted through the connecting member may fall off from the distal end side of the inner tube.

本発明は上記課題に鑑みてなされたものである。即ち、本発明は、内管チューブを流通する液体の吐出圧により内管チューブに配置された接続部材およびこれに挿通された針体の配置位置が内管チューブの先端側にずれるという上記課題を改善する内視鏡用注射針、および内視鏡用注射針の製造方法を提供する。   The present invention has been made in view of the above problems. That is, the present invention has the above-described problem that the arrangement position of the connecting member arranged in the inner tube and the needle body inserted through the connecting member arranged in the inner tube by the discharge pressure of the liquid flowing through the inner tube deviates to the tip side of the inner tube. Provided are an improved endoscope injection needle and a method for manufacturing an endoscope injection needle.

本発明の内視鏡用注射針は、液体を注入するための内管チューブと、上記内管チューブの先端に設けられた針体と、上記内管チューブの中心軸の方向に貫通し上記針体が挿通する挿通孔を有し、上記内管チューブの内周面と上記針体の外周面との間に配置され上記針体と上記内管チューブとを接続するための接続部材と、上記接続部材の上記基端面より基端側に突出する上記針体の外周面と上記内管チューブの内周面と上記接続部材の上記基端面との間に樹脂部材を充填してなる樹脂充填部と、を有し、内管チューブの内周面に対する切断面であって上記樹脂充填部の基端面の周縁の最近位点および当該周縁の最遠位点を含み上記中心軸と交差するとともに法線と中心軸との交差角が最小となる切断面である第一仮想面の上記法線である第一法線が、上記中心軸に対し傾斜していることを特徴とする。   The endoscope injection needle of the present invention includes an inner tube for injecting a liquid, a needle body provided at a tip of the inner tube, and a needle penetrating in the direction of the central axis of the inner tube. A connecting member for connecting the needle body and the inner tube, which is disposed between the inner peripheral surface of the inner tube and the outer peripheral surface of the needle body, A resin filling portion formed by filling a resin member between the outer peripheral surface of the needle body protruding from the base end surface of the connecting member to the base end side, the inner peripheral surface of the inner tube, and the base end surface of the connecting member. And a cross-sectional surface with respect to the inner peripheral surface of the inner tube, including the most proximal point of the peripheral edge of the base end surface of the resin-filled portion and the most distal point of the peripheral edge and intersecting the central axis The first normal that is the normal line of the first imaginary plane that is the cut surface that minimizes the intersection angle between the line and the central axis Line, and being inclined with respect to the central axis.

本発明の内視鏡用注射針の製造方法は、本発明の内視鏡用注射針を製造する内視鏡用注射針の製造方法であって、上記接続部材における上記挿通孔に上記接続部材の先端側および基端側から突出するよう上記針体を挿通する挿通工程と、上記接続部材の基端側に上記接続部材の外径と略同等の内径を有する型枠部材を外嵌する外嵌工程と、上記型枠部材の内周面と上記針体の外周面と上記接続部材の基端面とに接して上記樹脂部材を上記型枠部材に注入するとともに、先基端方向に対し上記樹脂充填部の基端面が傾斜するよう上記樹脂充填部を形成する樹脂充填部形成工程と、上記接続部材の少なくとも一部および上記樹脂充填部を内包するよう上記内管チューブを設ける内管チューブ取付工程と、を有することを特徴とする。   The method for manufacturing an endoscope injection needle according to the present invention is a method for manufacturing an endoscope injection needle for manufacturing the endoscope injection needle according to the present invention, wherein the connection member is inserted into the insertion hole in the connection member. An insertion step of inserting the needle body so as to protrude from the distal end side and the proximal end side of the outer periphery, and an external fitting of a mold member having an inner diameter substantially equal to the outer diameter of the connection member on the proximal end side of the connection member The resin member is injected into the mold member in contact with the fitting step, the inner peripheral surface of the mold member, the outer peripheral surface of the needle body, and the proximal end surface of the connecting member, and the above-mentioned relative to the proximal end direction A resin filling portion forming step for forming the resin filling portion so that a base end surface of the resin filling portion is inclined, and an inner tube mounting for providing the inner tube so as to enclose at least a part of the connecting member and the resin filling portion. And a process.

本発明の内視鏡用注射針は、内管チューブの内周面に対する切断面であって樹脂充填部の基端面の周縁の最近位点および当該周縁の最遠位点を含み中心軸と交差するとともに法線と中心軸との交差角が最小となる切断面である第一仮想面の法線である第一法線は、中心軸に対し傾斜している。したがって、樹脂充填部に対し内管チューブ内を流通する液体の吐出圧がかかる方向を内管チューブの軸方向からずらすことができる。
樹脂充填部の外周面と内管チューブの内周面との境界に対し液体の吐出圧が軸方向にかかると両者は剥離する虞があり接合状態が不良となる虞がある。これに対し、本発明の内視鏡用注射針は、第一仮想面が中心軸に対し、90°を超えた角度で交差し、上記境界に対しかかる液体の吐出圧の局所的な力が、軸方向に対する側方向にずれやすくなるよう構成される。
そのため、接続部材およびこれに挿通された針体の配置位置が、内管チューブの軸方向の先端側にずれ難い。
The endoscope injection needle of the present invention is a cutting surface with respect to the inner peripheral surface of the inner tube, and includes the most proximal point of the peripheral edge of the proximal end surface of the resin-filled portion and the most distal point of the peripheral edge and intersects the central axis At the same time, the first normal line, which is the normal line of the first imaginary plane, which is the cut surface with the smallest intersection angle between the normal line and the central axis, is inclined with respect to the central axis. Therefore, the direction in which the discharge pressure of the liquid flowing through the inner tube is applied to the resin filling portion can be shifted from the axial direction of the inner tube.
If the liquid discharge pressure is applied in the axial direction to the boundary between the outer peripheral surface of the resin-filled portion and the inner peripheral surface of the inner tube, they may be separated and the bonding state may be poor. In contrast, in the endoscope injection needle of the present invention, the first virtual plane intersects the central axis at an angle exceeding 90 °, and the local force of the liquid discharge pressure is applied to the boundary. It is configured to be easily displaced in the lateral direction with respect to the axial direction.
Therefore, the arrangement position of the connecting member and the needle inserted through the connecting member is not easily shifted to the distal end side in the axial direction of the inner tube.

本発明の内視鏡用注射針の製造方法は、本発明の内視鏡用注射針の製造を可能とする。   The method for manufacturing an endoscope injection needle according to the present invention enables the manufacture of an endoscope injection needle according to the present invention.

(a)は、本発明の第一実施形態の内視鏡用注射針を例示する内視鏡用注射針の全体図であり外管チューブの内部に針体の全体が収納された状態を示しており、(b)は、本発明の第一実施形態の内視鏡用注射針を例示する内視鏡用注射針の全体図であり外管チューブの先端から針体の一部が突出した状態を示している。(A) is the whole endoscope needle which illustrates the endoscope needle of 1st embodiment of this invention, and shows the state by which the whole needle body was accommodated in the inside of an outer tube tube FIG. 5B is an overall view of an endoscope injection needle illustrating the endoscope injection needle according to the first embodiment of the present invention, and a part of the needle body protrudes from the tip of the outer tube. Indicates the state. 図1(b)において破線円で囲む内視鏡用注射針100の先端領域の縦断面図である。It is a longitudinal cross-sectional view of the front-end | tip area | region of the injection needle 100 for endoscopes enclosed with a broken line circle in FIG. 第一実施形態の変形例である内視鏡用注射針の樹脂充填部の基端面および第一仮想面について説明する説明図である。It is explanatory drawing explaining the base end surface and 1st virtual surface of the resin filling part of the injection needle for endoscopes which are the modifications of 1st embodiment. (a)は、本発明の第一実施形態の内視鏡用注射針を説明する説明図であり、(b)は、(a)のIV−IV断面図である。(A) is explanatory drawing explaining the injection needle for endoscopes of 1st embodiment of this invention, (b) is IV-IV sectional drawing of (a). 本発明の第一実施形態の内視鏡用注射針の部分縦断面図である。It is a partial longitudinal cross-sectional view of the injection needle for endoscopes of 1st embodiment of this invention. (a)から(d)は、本発明の第二実施形態の内視鏡用注射針の製造方法を説明する説明図である。(A)-(d) is explanatory drawing explaining the manufacturing method of the injection needle for endoscopes of 2nd embodiment of this invention.

以下、本発明の第一実施形態について、図面を用いて説明する。すべての図面において、同様の構成要素には同一の符号を付し、重複する説明は適宜に省略する。
なお、本実施の形態では図示するように上下の方向を規定して説明する場合がある。しかし、これは構成要素の相対関係を簡単に説明するために便宜的に規定するものであり、本発明を実施する製品の製造時や使用時の方向を限定するものではない。
本発明の内視鏡用注射針およびその製造方法の各種の構成要素は、個々に独立した存在である必要はなく、複数の構成要素が一個の部材として形成されていること、一つの構成要素が複数の部材で形成されていること、ある構成要素が他の構成要素の一部であること、ある構成要素の一部と他の構成要素の一部とが重複していること、等を許容する。
Hereinafter, a first embodiment of the present invention will be described with reference to the drawings. In all the drawings, the same components are denoted by the same reference numerals, and redundant description will be appropriately omitted.
In the present embodiment, there are cases where a vertical direction is defined and illustrated as shown in the figure. However, this is provided for convenience in order to simply explain the relative relationship of the components, and does not limit the direction during the manufacture or use of the product implementing the present invention.
The various components of the endoscope injection needle and the manufacturing method thereof according to the present invention do not have to be independent of each other, and a plurality of components are formed as a single member. Is formed of a plurality of members, a certain component is a part of another component, a part of a certain component overlaps with a part of another component, etc. Allow.

本発明に関し、内視鏡用注射針または内視鏡用注射針を構成する各構成の近位とは、内視鏡用注射針の操作者に近い位置(即ち、内視鏡用注射針の基端側の位置)をいう。また同様に、遠位とは、内視鏡用注射針の操作者に遠い位置(即ち、内視鏡用注射針の先端側の位置)をいう。
また本発明に関し、基端側とは内視鏡用注射針の操作者に近い側をいい、先端側は当該操作者に遠い側、即ち、針体の最先端部の側をいう。
また本発明を説明するにあたり、適宜、内周面または外周面という言葉を用いる場合がある。特段の説明がない場合には、上記内周面は中心軸に対向する面を意味し、上記外周面は、内視鏡用注射針の中心軸に非対向の面を意味する。
また本発明を説明するにあたり、基端側から先端側へ向かう方向又は先端側から基端側へ向かう方向を、適宜、先基端方向という場合がある。
In the context of the present invention, the proximal position of the endoscope needle or the components constituting the endoscope needle is a position close to the operator of the endoscope needle (that is, the position of the endoscope needle). The position on the proximal side). Similarly, the distal means a position far from the operator of the endoscope injection needle (that is, a position on the tip side of the endoscope injection needle).
Further, in the present invention, the proximal end side means a side close to the operator of the endoscope injection needle, and the distal end side means a side far from the operator, that is, the most distal end side of the needle body.
In describing the present invention, the term “inner peripheral surface” or “outer peripheral surface” may be used as appropriate. Unless otherwise specified, the inner peripheral surface means a surface facing the central axis, and the outer peripheral surface means a surface not facing the central axis of the endoscope injection needle.
In the description of the present invention, the direction from the proximal end side to the distal end side or the direction from the distal end side to the proximal end side may be appropriately referred to as a distal proximal end direction.

<第一実施形態>
以下に、本発明の内視鏡用注射針の第一実施形態である内視鏡用注射針100について図1から図5を用いて説明する。
図1(a)は、本発明の第一実施形態の内視鏡用注射針を例示する内視鏡用注射針100の全体図であり外管チューブ30の内部に針体10の全体が収納された状態を示している。図1(b)は、内視鏡用注射針100の全体図であり外管チューブ30の先端から針体10の一部が突出した状態を示している。
図2は、図1(b)において破線円で囲む内視鏡用注射針100の先端領域の縦断面図である。ただし図2において、針体10は側面視している。
図3は、第一実施形態の変形例である内視鏡用注射針100Aの樹脂充填部110の基端面130Aおよび第一仮想面140について説明する説明図である。図3において内管チューブ20は図示省略し、内管チューブ20の内周面11のみを図示する。
図4(a)は、本発明の第一実施形態の内視鏡用注射針100を説明する説明図であり、図4(b)は、図4(a)のIV−IV断面図である。
図5は、本発明の第一実施形態の内視鏡用注射針100の部分縦断面図である。ただし、図5は、針体10、接続部材70、および樹脂充填部110に関し側面視している。
尚、内視鏡用注射針100における接続部材70は、図2に示すとおり接続部本体71および大径部72を有する。ただし、図3から図5および後述する図6では、大径部72を図示省略している。
<First embodiment>
Hereinafter, an endoscope needle 100 which is a first embodiment of an endoscope needle according to the present invention will be described with reference to FIGS. 1 to 5.
FIG. 1A is an overall view of an endoscope injection needle 100 illustrating the endoscope injection needle according to the first embodiment of the present invention, and the entire needle body 10 is accommodated in the outer tube 30. It shows the state that was done. FIG. 1B is an overall view of the endoscope injection needle 100 and shows a state in which a part of the needle body 10 protrudes from the distal end of the outer tube 30.
FIG. 2 is a longitudinal sectional view of the distal end region of the endoscope injection needle 100 surrounded by a broken-line circle in FIG. However, in FIG. 2, the needle body 10 is viewed from the side.
FIG. 3 is an explanatory diagram for explaining the base end surface 130A and the first virtual surface 140 of the resin filling portion 110 of the endoscope injection needle 100A, which is a modification of the first embodiment. In FIG. 3, illustration of the inner tube 20 is omitted, and only the inner peripheral surface 11 of the inner tube 20 is illustrated.
FIG. 4A is an explanatory view illustrating the endoscope injection needle 100 according to the first embodiment of the present invention, and FIG. 4B is a cross-sectional view taken along the line IV-IV in FIG. .
FIG. 5 is a partial longitudinal sectional view of the endoscope injection needle 100 according to the first embodiment of the present invention. However, FIG. 5 is a side view of the needle body 10, the connection member 70, and the resin filling portion 110.
In addition, the connection member 70 in the injection needle 100 for endoscopes has the connection part main body 71 and the large diameter part 72 as shown in FIG. However, in FIG. 3 to FIG. 5 and FIG.

本実施形態にかかる内視鏡用注射針100は、図1(a)および図1(b)に示すとおり、内管チューブ20を内包する外管チューブ30と、基端側に設けられた操作部50とを備える。内視鏡用注射針100における内管チューブ20は、図示省略する内視鏡のチャネルに対し、外管チューブ30とともに挿入可能である。   As shown in FIGS. 1A and 1B, an endoscope injection needle 100 according to the present embodiment includes an outer tube 30 containing the inner tube 20 and an operation provided on the proximal end side. Part 50. The inner tube 20 in the endoscope injection needle 100 can be inserted together with the outer tube 30 into an endoscope channel (not shown).

図2に、内視鏡用注射針100の先端側を中心軸138に沿って切断した切断面を示す。
図2に示すとおり、内視鏡用注射針100は、内管チューブ20と、針体10と、接続部材70と、樹脂充填部110と、を有している。
内管チューブ20は、液体を注入するためのチューブである。針体10は、内管チューブ20の先端に設けられている。接続部材70は、内管チューブ20の中心軸138の方向に貫通し針体10が挿通される挿通孔80を有し、内管チューブ20の内周面と針体10の外周面との間に配置され針体10と内管チューブ20とを接続する。
樹脂充填部110は、接続部材70の基端面73より基端側に突出する針体10の外周面と内管チューブ20の内周面と接続部材70の基端面73との間に樹脂部材を充填してなる。
本実施形態にかかる内視鏡用注射針100は、第一仮想面140の法線である第一法線136が中心軸138に対し傾斜している。第一仮想面140は、内管チューブ20の内周面に対する切断面であって最近位点132および最遠位点134を含み中心軸138と交差するとともに法線と中心軸138との交差角が最小となる切断面である。
本実施形態において、樹脂充填部110の基端面130の周縁は、先基端方向において異なる位置にある最近位点132および最遠位点134を有している。
FIG. 2 shows a cut surface obtained by cutting the distal end side of the endoscope injection needle 100 along the central axis 138.
As shown in FIG. 2, the endoscope injection needle 100 includes an inner tube 20, a needle body 10, a connection member 70, and a resin filling portion 110.
The inner tube 20 is a tube for injecting liquid. The needle body 10 is provided at the tip of the inner tube 20. The connecting member 70 has an insertion hole 80 that penetrates in the direction of the central axis 138 of the inner tube 20 and through which the needle body 10 is inserted, and is between the inner peripheral surface of the inner tube tube 20 and the outer peripheral surface of the needle body 10. The needle body 10 and the inner tube 20 are connected to each other.
The resin filling unit 110 is configured to place a resin member between the outer peripheral surface of the needle body 10 protruding from the base end surface 73 of the connecting member 70 toward the base end side, the inner peripheral surface of the inner tube 20, and the base end surface 73 of the connecting member 70. Filled.
In the endoscope injection needle 100 according to the present embodiment, a first normal line 136 that is a normal line of the first virtual surface 140 is inclined with respect to the central axis 138. The first imaginary surface 140 is a cut surface with respect to the inner peripheral surface of the inner tube 20, and includes the most proximal point 132 and the most distal point 134, intersects the central axis 138, and intersects the normal and the central axis 138. Is the cut surface that minimizes.
In the present embodiment, the peripheral edge of the proximal end surface 130 of the resin filling portion 110 has a nearest point 132 and a most distal point 134 that are at different positions in the distal end direction.

本実施形態において、基端面130の周縁とは、図4(a)に示すとおり、内管チューブ20の内周面と樹脂充填部110の外周面との近位側における交線131を意味する。即ち、基端面130の周縁は、内管チューブ20の内周面と樹脂充填部110の外周面との接合面の近位側における端部が周方向に連続する環状の縁部である。
基端面130は、内管チューブ20の内周面と樹脂充填部110の外周面との近位側における交線よりなる当該周縁によって内包される領域に含まれる樹脂充填部110の基端側の面を指す。
In the present embodiment, the peripheral edge of the base end surface 130 means an intersection line 131 on the proximal side of the inner peripheral surface of the inner tube 20 and the outer peripheral surface of the resin filling portion 110 as shown in FIG. . That is, the peripheral edge of the base end surface 130 is an annular edge portion where the end portion on the proximal side of the joint surface between the inner peripheral surface of the inner tube 20 and the outer peripheral surface of the resin filling portion 110 is continuous in the circumferential direction.
The base end surface 130 is on the base end side of the resin filling portion 110 included in the region enclosed by the peripheral edge formed by the intersection line on the proximal side of the inner peripheral surface of the inner tube 20 and the outer peripheral surface of the resin filling portion 110. Point to the surface.

内視鏡用注射針100における樹脂充填部110の基端面130は、中心軸138に対し直交平坦である面以外の面として構成されている。即ち、基端面130は、湾曲あるいは凹凸を有する面(即ち非平坦な面)であるとともに中心軸138に対し直交する面、および平坦であるが中心軸138に対し90°以外の角度で交差する面を含む。
たとえば基端面130は、図2に示すとおり中心軸138に対し傾斜して交差するとともに、実質的に平滑な面であってもよい。また、樹脂充填部110は、図3に示すとおり、不規則な凹凸を有する面である基端面130Aを備えていてもよい。本実施形態において、樹脂充填部110の基端面130の周縁は、図2に示すように内管チューブ20の内周面に対し周方向に、楕円の軌跡をなしてもよいし、図3に示す基端面130Aのように当該周方向に一周する不規則な軌跡をなしていてもよい。
基端面130Aの外縁は、図3に示す内管チューブ20の内周面11(図3参照)と樹脂充填部110の外周面との近位側における交線131Aである。
上記周縁には、最近位点132および当該周縁の最遠位点134が含まれている。最近位点132とは、当該周縁上であって最も近位側に位置する点である。最遠位点134は、当該周縁上であって最も遠位側に位置する点である。周縁の形状から正円が除かれることによって、最近位点132と最遠位点134とは、中心軸138の伸長方向においてずれた位置に存在する。
そのため、最近位点132および最遠位点134を含み中心軸138と交差する第一仮想面140の法線である第一法線136は、中心軸138に対し傾斜している。
The proximal end surface 130 of the resin filling portion 110 in the endoscope injection needle 100 is configured as a surface other than a surface that is perpendicular to the central axis 138. In other words, the base end face 130 is a curved or uneven surface (that is, a non-flat surface) and is a plane orthogonal to the central axis 138 and is flat but intersects the central axis 138 at an angle other than 90 °. Including faces.
For example, the base end face 130 may be a substantially smooth surface while intersecting with the central axis 138 as shown in FIG. Further, as shown in FIG. 3, the resin filling portion 110 may include a base end surface 130 </ b> A that is a surface having irregular irregularities. In the present embodiment, the peripheral edge of the base end face 130 of the resin filling portion 110 may form an elliptical trajectory in the circumferential direction with respect to the inner peripheral face of the inner tube 20 as shown in FIG. An irregular trajectory that makes one round in the circumferential direction may be formed like a base end face 130A shown.
The outer edge of the base end surface 130 </ b> A is an intersection line 131 </ b> A on the proximal side of the inner peripheral surface 11 (see FIG. 3) of the inner tube 20 shown in FIG. 3 and the outer peripheral surface of the resin filling portion 110.
The peripheral edge includes a nearest point 132 and a distal most point 134 of the peripheral edge. The nearest position point 132 is a point located on the most peripheral side on the periphery. The most distal point 134 is a point located on the peripheral edge and the most distal side. By removing the perfect circle from the shape of the peripheral edge, the closest point 132 and the most distal point 134 are located at positions shifted in the extending direction of the central axis 138.
Therefore, the first normal 136 that is the normal of the first virtual plane 140 that includes the closest point 132 and the most distal point 134 and intersects the central axis 138 is inclined with respect to the central axis 138.

第一仮想面140は、以下のとおり定義することができる。即ち、最近位点132および最遠位点134をとおり中心軸138に沿って切断してなる切断面I(図示省略)を求める。そして内管チューブ20の内周面に対し、上記切断面Iの法線方向であって、最近位点132および最遠位点134を通る位置で切断してなる切断面が、本実施形態における第一仮想面140である。   The first virtual surface 140 can be defined as follows. That is, a cut surface I (not shown) obtained by cutting along the central axis 138 through the most proximal point 132 and the most distal point 134 is obtained. A cut surface obtained by cutting the inner tube tube 20 in a direction normal to the cut surface I and passing through the nearest point 132 and the most distal point 134 with respect to the inner peripheral surface of the inner tube 20 in the present embodiment. This is the first virtual surface 140.

本実施形態における第一仮想面140は、内管チューブ20の内周面において最近位点132と最遠位点134とを最短で結ぶ円弧を含み、中心軸138と交差する面である。   The first virtual surface 140 in the present embodiment is a surface that includes an arc connecting the nearest point 132 and the most distal point 134 at the shortest on the inner peripheral surface of the inner tube 20 and intersects the central axis 138.

尚、本実施形態にかかる内視鏡用注射針100は、図2に示すとおり、基端面130と第一仮想面140とが略同一の面をなしている。ただし本実施形態はこれに限定されない。
たとえば図3に示す本実施形態の変形例である内視鏡用注射針100Aのように、基端面130Aと、第一仮想面140とが異なる面をなす態様を本発明は包含する。基端面130Aの周縁は、図3において図示省略する内管チューブ20の内周面に対し周方向に一周する不規則な軌跡をなす。たとえば最遠位点134は、図3に示すとおり、最近位点132に対し、中心軸138(図示省略)を介して対向する位置からはずれた箇所に存在していてもよい。図3に示す第一仮想面140の外縁は、図示省略する内管チューブ20の内周面11において最近位点132と最遠位点134とを結ぶ最短の円弧を含み、中心軸と交差している。
Note that, in the endoscope injection needle 100 according to the present embodiment, the base end surface 130 and the first virtual surface 140 are substantially the same as shown in FIG. However, this embodiment is not limited to this.
For example, the present invention includes an aspect in which the proximal end surface 130A and the first virtual surface 140 are different from each other like an endoscope injection needle 100A which is a modification of the present embodiment shown in FIG. The peripheral edge of the base end surface 130A forms an irregular trajectory that makes one round in the circumferential direction with respect to the inner peripheral surface of the inner tube 20 that is not shown in FIG. For example, as shown in FIG. 3, the most distal point 134 may exist at a location deviated from the position facing the most proximal point 132 via the central axis 138 (not shown). The outer edge of the first virtual surface 140 shown in FIG. 3 includes the shortest arc connecting the nearest point 132 and the most distal point 134 on the inner peripheral surface 11 of the inner tube 20 (not shown), and intersects the central axis. ing.

ここで、内視鏡用注射針100における第一法線136が、中心軸138に対し傾斜しているとは、樹脂充填部110の基端面130が中心軸138に対し実質的に直交している態様を除くことを意味している。本実施形態において、先基端方向における最近位点132および最遠位点134の位置のずれは、製造上の較差に起因して生じる基端面130上の微細な凸部の頂点と微細な凹部の底部との距離を上回る。   Here, the first normal line 136 in the endoscope injection needle 100 is inclined with respect to the central axis 138. That is, the base end surface 130 of the resin filling portion 110 is substantially orthogonal to the central axis 138. It means that the aspect which is is excluded. In the present embodiment, the displacement of the positions of the most proximal point 132 and the most distal point 134 in the direction of the distal end is caused by the fine apex of the fine protrusion on the proximal end surface 130 and the fine recess caused by the manufacturing difference. Beyond the distance to the bottom of the.

樹脂充填部110における基端面130の最近位点132と最遠位点134とから仮定される第一仮想面140は、上述のとおり中心軸138に対し傾斜している。即ち、基端面130は、中心軸138に対し直交する面ではない。そのため内管チューブ20の内部を流通する液体の吐出圧は、基端面130に対し、軸方向とは異なる方向にかかり得る。そのため、樹脂充填部110が当該液体の吐出圧により先端方向に押圧され難く、樹脂充填部110の配置位置が内管チューブ20の先端側にずれ難い構成となっている。
上述する樹脂充填部110を備えることにより、本実施形態は、樹脂充填部110よりも先端側に配置された接続部材70、および接続部材70に挿通された針体10の配置位置が内管チューブ20の先端側にずれるという従来の課題が改善されている。
The first virtual surface 140 assumed from the most proximal point 132 and the most distal point 134 of the base end surface 130 in the resin filling portion 110 is inclined with respect to the central axis 138 as described above. That is, the base end face 130 is not a plane orthogonal to the central axis 138. Therefore, the discharge pressure of the liquid flowing through the inner tube 20 can be applied to the base end surface 130 in a direction different from the axial direction. Therefore, the resin filling part 110 is not easily pressed in the distal direction by the discharge pressure of the liquid, and the arrangement position of the resin filling part 110 is difficult to shift to the distal end side of the inner tube 20.
By providing the resin filling portion 110 described above, in the present embodiment, the connecting member 70 disposed on the distal end side with respect to the resin filling portion 110 and the arrangement position of the needle body 10 inserted through the connecting member 70 are the inner tube tube. The conventional problem of shifting to the tip end side of 20 is improved.

上述する従来の課題の改善の観点からは、第一法線136と中心軸138とが交差する角度である第一交差角α(図2参照)は、0°を超えて90°未満である。第一交差角αは、好ましくは、15°以上90°未満であり、より好ましくは30°以上90°未満であり、特に好ましくは45°以上90°未満である。   From the viewpoint of improving the conventional problem described above, the first intersection angle α (see FIG. 2), which is the angle at which the first normal 136 and the central axis 138 intersect, is greater than 0 ° and less than 90 °. . The first crossing angle α is preferably 15 ° or more and less than 90 °, more preferably 30 ° or more and less than 90 °, and particularly preferably 45 ° or more and less than 90 °.

本実施形態では、図2に示すとおり、第一法線136と中心軸138とが交差する角度である第一交差角αは、接続部材70の基端面73の法線である第二法線738と中心軸138とが交差する角度である第二交差角よりも大きいことが好ましい。
尚、図2において、第二法線738と中心軸138とは、同方向を向く態様を示しており、第二交差角は0°である。
In the present embodiment, as shown in FIG. 2, the first intersection angle α, which is the angle at which the first normal line 136 and the central axis 138 intersect, is the second normal line that is the normal line of the base end face 73 of the connecting member 70. It is preferably larger than the second intersection angle, which is the angle at which 738 and the central axis 138 intersect.
In FIG. 2, the second normal line 738 and the central axis 138 show the same direction, and the second crossing angle is 0 °.

第一交差角αが第二交差角よりも大きく構成されていることにより、第一交差角αと第二交差角が等しい場合と比較して、液体の吐出圧に起因する接続部材70の先端方向への配置位置のずれが良好に回避される。   Since the first crossing angle α is configured to be larger than the second crossing angle, the tip of the connecting member 70 caused by the liquid discharge pressure is compared with the case where the first crossing angle α is equal to the second crossing angle. The displacement of the arrangement position in the direction can be favorably avoided.

尚、接続部材70の基端面73は、中心軸138に対し略直交するとともに平坦状に形成されることが一般的である。したがって第二法線738は、基端面73の主面の法線と理解することができる。ただし、基端面73が、湾曲するなどして平坦な面ではない場合にも、図2に示す第二仮想面736を仮想することにより第一交差角αと第二交差角とを比較することができる。図2では、基端面73が中心軸138に直交する平坦な面であるため、第二仮想面736と同一面として示している。基端面73が、中心軸138に直交する平坦な面以外の面である場合には、第二仮想面736と基端面73とは異なる面として示される(図示省略)。
ここで第二仮想面736は、接続部材70の基端面73の周縁の最近位点731および当該周縁の最遠位点732を含み、中心軸138に交差する面である。基端面73の周縁とは、内管チューブ20の内周面と接続部材70の外周面との近位側における交線である。内管チューブ20と接続部材70との間に任意の層が設けられる場合には、上記交線の代替として、近位側であって接続部材70の外周面が内管チューブ20の内周面に最も近接する縁部の連続を周縁と理解する。
第二仮想面736は、以下のとおり定義することができる。即ち、最近位点731および最遠位点732をとおり中心軸138に沿って切断してなる切断面I(図示省略)を求める。そして内管チューブ20の内周面に対し、上記切断面Iの法線方向であって、最近位点731および最遠位点732を通る位置で切断してなる切断面を、第二仮想面736として扱うことができる。
換言すると、第二仮想面736は、接続部材70の外周面において最近位点731と最遠位点732とを最短で結ぶ円弧を含み、接続部材70または、接続部材70を基端側に延長させてなる仮想接続部材(図示省略)を切断してなる切断面である。
The base end surface 73 of the connecting member 70 is generally formed to be flat and substantially orthogonal to the central axis 138. Therefore, the second normal line 738 can be understood as the normal line of the main surface of the base end face 73. However, even when the base end face 73 is curved and not flat, the first crossing angle α and the second crossing angle are compared by virtualizing the second virtual face 736 shown in FIG. Can do. In FIG. 2, since the base end surface 73 is a flat surface orthogonal to the central axis 138, it is shown as the same surface as the second virtual surface 736. When the base end surface 73 is a surface other than a flat surface orthogonal to the central axis 138, the second virtual surface 736 and the base end surface 73 are shown as different surfaces (not shown).
Here, the second virtual surface 736 is a surface that includes the nearest point 731 at the periphery of the base end surface 73 of the connection member 70 and the most distal point 732 at the periphery and intersects the central axis 138. The peripheral edge of the base end surface 73 is a line of intersection on the proximal side of the inner peripheral surface of the inner tube 20 and the outer peripheral surface of the connection member 70. When an arbitrary layer is provided between the inner tube 20 and the connecting member 70, as an alternative to the intersection line, the outer peripheral surface of the connecting member 70 on the proximal side is the inner peripheral surface of the inner tube 20. The edge sequence closest to is understood as the peripheral edge.
The second virtual surface 736 can be defined as follows. That is, a cut surface I (not shown) obtained by cutting along the central axis 138 through the closest point 731 and the most distal point 732 is obtained. A cut surface obtained by cutting the inner tube tube 20 at a position in the normal direction of the cut surface I and passing through the most proximal point 731 and the most distal point 732 with respect to the inner peripheral surface of the inner tube 20 is a second virtual surface. 736.
In other words, the second virtual surface 736 includes an arc connecting the nearest point 731 and the most distal point 732 at the shortest on the outer peripheral surface of the connection member 70, and extends the connection member 70 or the connection member 70 to the proximal end side. It is a cut surface formed by cutting a virtual connection member (not shown).

本実施形態の好ましい一例として、中心軸138と、樹脂充填部110の基端面130の周縁が形成する平均基端面の法線である第三法線(図示省略)と、が交差する角度である第三交差角(図示省略)を、30°以上90°未満として構成してもよい。   As a preferred example of the present embodiment, an angle at which the central axis 138 intersects with a third normal line (not shown) that is a normal line of the average base end surface formed by the peripheral edge of the base end surface 130 of the resin filling portion 110. The third intersection angle (not shown) may be configured to be 30 ° or more and less than 90 °.

ここで、平均基端面とは、内管チューブ20の内周面の切断面のうち、基端面130の周縁の複数点の座標から最小二乗法で近似して求められる環状の平面である。上記複数点の座標は、基端面130の周縁において、たとえば10か所程度、プロットされた点の各座標である。中心軸138上の一次元座標、および任意の切断面の法線方向を示す2変数である3つの変数を最小二乗法を用いて決定することができる。より具体的には、上記複数点の座標を最も近似する内管チューブ20の内周面の切断面(即ち、平均基端面)を最小二乗法で決定することにより、当該切断面の法線方向を求めることができる。その法線方向と中心軸138との交差角が第三交差角である。
基端面130の平均基端面は、第一仮想面140と実質的に同一となる場合と、異なる場合とを含む。本実施形態にかかる内視鏡用注射針100の上記平均基端面は、第一仮想面140と実質的に同一の面となるよう構成されている。またかかる構成において、内視鏡用注射針100における上記第三法線は、第一法線136と実質的に同一であり、上記第三交差角は、第一交差角αと同一である。
Here, the average base end surface is an annular flat surface obtained by approximating the coordinates of a plurality of points on the periphery of the base end surface 130 among the cut surfaces of the inner peripheral surface of the inner tube 20 by the least square method. The coordinates of the plurality of points are the coordinates of the plotted points at, for example, about 10 points on the periphery of the base end face 130. Three variables, which are two variables indicating one-dimensional coordinates on the central axis 138 and the normal direction of an arbitrary cut surface, can be determined using the least square method. More specifically, by determining the cut surface (that is, the average base end surface) of the inner peripheral surface of the inner tube 20 that most closely approximates the coordinates of the plurality of points by the least square method, the normal direction of the cut surface Can be requested. The intersection angle between the normal direction and the central axis 138 is the third intersection angle.
The average base end surface of the base end surface 130 includes a case where it is substantially the same as the first virtual surface 140 and a case where it is different. The average proximal end surface of the endoscope injection needle 100 according to the present embodiment is configured to be substantially the same surface as the first virtual surface 140. In this configuration, the third normal line in the endoscope injection needle 100 is substantially the same as the first normal line 136, and the third crossing angle is the same as the first crossing angle α.

基端面130から上記平均基端面を求めることによって、たとえば、基端面130が製造上の較差に起因する凹凸を超えた凹凸を有する場合であっても、基端面130を巨視的に認識可能である。平均基端面の法線である第三法線と、中心軸138と、が交差する角度が30°以上90°未満であることによれば、基端面130に対し液体の吐出圧がかかる方向を有意に中心軸138からずらすことができ、本発明の所期の課題を良好に解決することができる。   By obtaining the average base end face from the base end face 130, for example, even when the base end face 130 has irregularities exceeding the irregularities due to manufacturing differences, the base end face 130 can be recognized macroscopically. . When the angle at which the third normal, which is the normal of the average base end face, and the central axis 138 intersect is 30 ° or more and less than 90 °, the direction in which the liquid discharge pressure is applied to the base end face 130 is determined. It can be significantly shifted from the central axis 138, and the desired problem of the present invention can be solved satisfactorily.

ここで内視鏡用注射針100が内視鏡のチャネルに挿通されて用いられることを勘案し、樹脂充填部110はさらに以下の構成を備えることが好ましい。
即ち、図4(a)に示すとおり内視鏡用注射針100における樹脂充填部110は、樹脂充填部110の基端面130の周縁の最近位点132が属する側の半体積が、中心軸138(図2参照)を介して最近位点132と対向する周縁における対向点142が属する半体積よりも大きい。
換言すると、樹脂充填部110を構成する樹脂部材は、最遠位点134の側よりも最近位点132の側に偏在している。
In consideration of the fact that the endoscope injection needle 100 is inserted through the endoscope channel, the resin filling unit 110 preferably further includes the following configuration.
That is, as shown in FIG. 4A, the resin-filled portion 110 in the endoscope injection needle 100 has a half volume on the side to which the nearest point 132 on the peripheral edge of the proximal end surface 130 of the resin-filled portion 110 belongs, and the central axis 138. It is larger than the half volume to which the opposing point 142 at the peripheral edge facing the nearest point 132 via (see FIG. 2) belongs.
In other words, the resin member constituting the resin filling portion 110 is unevenly distributed on the nearest point 132 side rather than the most distal point 134 side.

図4(a)において、基端面130の周縁の最近位点132、および中心軸138を介して最近位点132と対向する周縁上の対向点142とを結んでなる第一線分154を示す。図4(a)に示す内視鏡用注射針100は、対向点142が最遠位点134となっている。
ここで、最近位点132が属する側の半体積とは、第一線分154に直交し、且つ、中心軸138に沿って縦方向に分割されてなる樹脂充填部110であって最近位点132を含んだ側である第一分割部144の体積である。また、対向点142が属する側の半体積とは、上述のとおり縦方向に分割されてなる樹脂充填部110であって対向点142を含んだ側である第二分割部146の体積である。
上述する第一分割部144の体積および第二分割部146の体積の和は、それぞれ接続部材70の基端面73よりも基端側に位置する樹脂充填部110の体積を示す。
FIG. 4A shows a first line segment 154 formed by connecting the nearest point 132 on the periphery of the base end face 130 and an opposing point 142 on the periphery facing the nearest point 132 via the central axis 138. . In the endoscope injection needle 100 shown in FIG. 4A, the opposite point 142 is the most distal point 134.
Here, the half volume on the side to which the nearest point 132 belongs is the resin filling portion 110 that is orthogonal to the first line segment 154 and divided in the vertical direction along the central axis 138, and is the nearest point. This is the volume of the first divided portion 144 on the side including 132. Further, the half volume on the side to which the facing point 142 belongs is the volume of the second divided portion 146 on the side including the facing point 142 in the resin filling portion 110 divided in the vertical direction as described above.
The sum of the volume of the first divided portion 144 and the volume of the second divided portion 146 described above indicates the volume of the resin filling portion 110 located on the proximal end side with respect to the proximal end surface 73 of the connecting member 70.

樹脂充填部110を構成する樹脂部材が最近位点132側に偏在する内視鏡用注射針100によれば、屈曲する内視鏡のチャネル内を先基端方向に摺動する際、樹脂部材の偏在量が小さい第二分割部146の方が第一分割部144よりも屈曲しやすい。そのため、図5に示すとおり、屈曲するチャネル(図示省略)内の経路において、第二分割部146(図4(a)参照)が内周側に自然と位置する傾向にある。即ち、最遠位点134が内視鏡用注射針100の屈曲する経路の内周側に自然と位置する傾向にある。
このように樹脂充填部110において屈曲し易い側が自然と内周側に位置することにより、内視鏡用注射針100は、屈曲する内視鏡のチャネル内において屈曲しながら摺動する動作が円滑である。
According to the endoscope injection needle 100 in which the resin member constituting the resin filling portion 110 is unevenly distributed on the closest point 132 side, when sliding in the proximal end direction in the channel of the bending endoscope, the resin member The second divided portion 146 having a small amount of uneven distribution is easier to bend than the first divided portion 144. Therefore, as shown in FIG. 5, the second divided portion 146 (see FIG. 4A) tends to be naturally positioned on the inner peripheral side in the path in the bending channel (not shown). That is, the most distal point 134 tends to be naturally located on the inner peripheral side of the path of bending of the endoscope injection needle 100.
As described above, the side that is easily bent in the resin-filled portion 110 is naturally positioned on the inner peripheral side, whereby the endoscope injection needle 100 smoothly moves while being bent in the channel of the bending endoscope. It is.

基端面130の周縁の最近位点132が属する側の半体積が、中心軸138を介して最近位点132と対向する周縁における対向点142が属する半体積よりも大きい樹脂充填部110を備える内視鏡用注射針100は、さらに以下の構成を備えることが好ましい。
即ち、図4(a)および図4(b)に示すとおり、本実施形態にかかる内視鏡用注射針100は、針体10の先端面152が、中心軸138に対して傾斜しており、先端面152の最先端部Xが、樹脂充填部110の基端面130の周縁の最近位点132が属する側に配置されている。最先端部Xは、上面視上、第一分割部144側に配置されている。ここで上面視とは、内視鏡用注射針100を基端側から先端側に向けて観察することを意味する。
An inner portion of the base end face 130 is provided with a resin filling portion 110 in which the half volume on the side to which the nearest point 132 belongs is larger than the half volume to which the opposite point 142 on the periphery facing the nearest point 132 via the central axis 138 belongs. The endoscope injection needle 100 preferably further comprises the following configuration.
That is, as shown in FIGS. 4A and 4B, the endoscope injection needle 100 according to the present embodiment has the distal end surface 152 of the needle body 10 inclined with respect to the central axis 138. The most distal portion X of the distal end surface 152 is arranged on the side to which the nearest point 132 on the periphery of the base end surface 130 of the resin filling portion 110 belongs. The most advanced portion X is disposed on the first divided portion 144 side in a top view. Here, the top view means that the endoscope injection needle 100 is observed from the proximal end side toward the distal end side.

かかる最先端部Xの配置によれば、図5に示すとおり、屈曲する内視鏡のチャネル内を先端方向に内視鏡用注射針100が摺動する際、最先端部Xは、屈曲する外管チューブ30の外周側に位置する傾向となる。かかる最先端部Xは、当該外周側の外管チューブ30の内周面の付近に位置しつつも、屈曲方向に向かって摺動する。そのため、外管チューブ30の内周面に最先端部Xが接触して外管チューブ30の先端方向に対する針体10の摺動が不良となり、または外管チューブ30の先端から針体10の突出動作が不良となるといった問題を低減することができる。   According to the arrangement of the most advanced portion X, as shown in FIG. 5, when the endoscope injection needle 100 slides in the distal direction in the channel of the bending endoscope, the most advanced portion X bends. It tends to be located on the outer peripheral side of the outer tube 30. The most advanced portion X slides in the bending direction while being located near the inner peripheral surface of the outer tube 30 on the outer peripheral side. Therefore, the most distal portion X comes into contact with the inner peripheral surface of the outer tube 30 and the sliding of the needle body 10 with respect to the distal direction of the outer tube 30 becomes poor, or the needle body 10 protrudes from the tip of the outer tube 30 Problems such as poor operation can be reduced.

比較として、針体10の最先端部Xが、基端面130の周縁の最遠位点134が属する側に配置された針体10Bを仮想線として図5に示した。針体10Bの最先端部Xは、外管チューブ30の屈曲する経路の内周側に位置しつつ、屈曲方向に向かって摺動するため、外管チューブ30の内周面に近接し、当接する虞がある。   For comparison, the most distal portion X of the needle body 10 is shown in FIG. 5 with the needle body 10B arranged on the side to which the most distal point 134 of the peripheral edge of the base end face 130 belongs as an imaginary line. Since the most distal portion X of the needle body 10B slides in the bending direction while being positioned on the inner peripheral side of the path where the outer tube 30 bends, it is close to the inner peripheral surface of the outer tube 30 and There is a risk of contact.

次に、内視鏡用注射針100における各構成の詳細について説明する。   Next, the detail of each structure in the injection needle 100 for endoscopes is demonstrated.

図1(a)および図1(b)に示すとおり、本実施形態にかかる内視鏡用注射針100は、内管チューブ20を進退可能に内包する外管チューブ30を備えている。進退可能とは、先基端方向において摺動可能という意味である。
外管チューブ30は、内管チューブ20および針体10を収納可能な長尺のチューブである。外管チューブ30は、外管チューブ30の任意の箇所に設けられた開口から突出可能に針体10を収納可能である。そのため、たとえば体腔内の生体組織において処置をするタイミングで外管チューブ30の上記開口から針体10を突出させるとともに、針体10が生体組織に到達するまでの間は針体10を内包して針体10の先端が体腔に接触することを回避可能である。外管チューブ30の詳細は後述する。
As shown in FIGS. 1A and 1B, an endoscope injection needle 100 according to this embodiment includes an outer tube 30 that encloses the inner tube 20 so as to be able to advance and retreat. “Advancing and retracting” means being slidable in the proximal direction.
The outer tube 30 is a long tube that can accommodate the inner tube 20 and the needle body 10. The outer tube 30 can store the needle body 10 so as to protrude from an opening provided at an arbitrary position of the outer tube 30. Therefore, for example, the needle body 10 is protruded from the opening of the outer tube 30 at the timing of treatment in the body tissue in the body cavity, and the needle body 10 is included until the needle body 10 reaches the body tissue. It is possible to avoid the tip of the needle body 10 from contacting the body cavity. Details of the outer tube 30 will be described later.

内視鏡用注射針100は、基端部においてさらに操作部50を有している。
本実施形態において、操作部50は外筒グリップ40、内筒グリップ60を含む。操作部50は、内視鏡用注射針100の操作者によって把持される部位である。
また、操作部50は内筒グリップ60の基端側に付設されたコネクタ51を含み、シリンジ(図示せず)を連結できる。内管チューブ20は、コネクタ51に連結されたシリンジ(図示せず)から注液された液体の流路となる。操作者が操作部50を操作することによって、針体10を被験者の生体組織に刺すことができる。また、針体10の先端には開口(図示せず)が設けられ、作業者がシリンジ(図示せず)を操作することによって液体を生体組織に注入可能となっている。
The endoscope injection needle 100 further includes an operation unit 50 at the proximal end portion.
In the present embodiment, the operation unit 50 includes an outer cylinder grip 40 and an inner cylinder grip 60. The operation unit 50 is a part that is held by an operator of the endoscope injection needle 100.
The operation unit 50 includes a connector 51 attached to the proximal end side of the inner cylinder grip 60, and can connect a syringe (not shown). The inner tube 20 serves as a flow path for liquid injected from a syringe (not shown) connected to the connector 51. When the operator operates the operation unit 50, the needle body 10 can be inserted into the body tissue of the subject. Moreover, an opening (not shown) is provided at the tip of the needle body 10, and an operator can inject a liquid into a living tissue by operating a syringe (not shown).

内筒グリップ60は、外管チューブ30の内外に針体10を進退操作する。内管チューブ20は、針体10を有し、外管チューブ30の中に摺動可能に挿入されている。
ここで、外管チューブ30の内外に針体10を進退操作するとは、外管チューブ30の何処かに設けられた開口から針体10の少なくとも一部が突出する状態(突出状態、図1(b)参照)と、開口の中に針体10を当該突出状態より収納する状態(収納状態、図1(a)参照)のいずれか一方から他方へと移行させることである。
本実施形態では、外管チューブ30の先端に開口が設けられるように図示したが、これは一例であって、他の位置に開口が設けられる形態であっても構わない。
The inner cylinder grip 60 moves the needle body 10 back and forth inside and outside the outer tube 30. The inner tube 20 has a needle body 10 and is slidably inserted into the outer tube 30.
Here, when the needle body 10 is moved back and forth inside and outside the outer tube 30, a state in which at least a part of the needle body 10 protrudes from an opening provided somewhere in the outer tube 30 (protruding state, FIG. b)), and shifting the needle body 10 from one of the protruding states to the other (the stored state, see FIG. 1A).
In the present embodiment, the opening is provided at the tip of the outer tube 30, but this is only an example, and an opening may be provided at another position.

内筒グリップ60は、基端側から先端側へ又は先端側から基端側へと摺動可能なように外筒グリップ40の中に収納されている。また、外筒グリップ40の側面には案内溝41が設けられており、内筒グリップ60の突出部61が摺動可能なように案内溝41の中に嵌め込まれている。   The inner cylinder grip 60 is accommodated in the outer cylinder grip 40 so as to be slidable from the proximal end side to the distal end side or from the distal end side to the proximal end side. Further, a guide groove 41 is provided on the side surface of the outer cylinder grip 40, and the protrusion 61 of the inner cylinder grip 60 is fitted into the guide groove 41 so as to be slidable.

本実施形態では、外筒グリップ40と外管チューブ30とが連結し、内筒グリップ60と内管チューブ20と針体10とが連結している。従って、内視鏡用注射針100の操作者は、外筒グリップ40と内筒グリップ60とを互いに軸方向にスライドさせることによって、針体10を軸方向に進退させることができる。
さらに詳細には、外筒グリップ40に設けた案内溝41の基端側に突出部61を位置させるとき収納状態となり、案内溝41の先端側に突出部61を位置させるとき、針体10が外管チューブ30から突出状態となる(図1(b))。
In this embodiment, the outer cylinder grip 40 and the outer tube 30 are connected, and the inner cylinder grip 60, the inner tube 20 and the needle body 10 are connected. Therefore, the operator of the endoscope injection needle 100 can advance and retract the needle body 10 in the axial direction by sliding the outer cylinder grip 40 and the inner cylinder grip 60 in the axial direction.
More specifically, when the protruding portion 61 is positioned on the proximal end side of the guide groove 41 provided in the outer cylinder grip 40, the needle body 10 is in the retracted state, and when the protruding portion 61 is positioned on the distal end side of the guide groove 41, the needle body 10 is It protrudes from the outer tube 30 (FIG. 1B).

一般的に、操作部50は収納状態または突出状態の少なくとも一方を固定する構造を備えている。本実施形態では、案内溝41の基端側と先端側に突出部61を嵌めて固定する固定用の溝を設けている。そして、突出部61が案内溝41の基端側または先端側に位置するときに、内筒グリップ60と外筒グリップ40とを回転方向にスライドさせることで、固定用溝に突出部61を嵌めることができる。これは上記収納状態または上記突出状態を固定するための一例であり、他の形態を用いても構わない。   In general, the operation unit 50 has a structure for fixing at least one of a stored state and a protruding state. In the present embodiment, a fixing groove for fitting and fixing the protruding portion 61 on the proximal end side and the distal end side of the guide groove 41 is provided. And when the protrusion part 61 is located in the base end side or the front end side of the guide groove 41, the protrusion part 61 is fitted in the fixing groove by sliding the inner cylinder grip 60 and the outer cylinder grip 40 in the rotation direction. be able to. This is an example for fixing the storage state or the protruding state, and other forms may be used.

図2に突出状態である内視鏡用注射針100の先端領域の断面図を示す。外管チューブ30の先端には、針体10が突出可能な開口が設けられている。当該開口を有する先端は、たとえば、径方向の内向きに屈曲して先細状に形成されている。換言すると、外管チューブ30の先細状の先端の開口径は、内管チューブ20の先端の外径または接続部材70の先端の外径よりも小さい。当該先細状の先端の内周面と内管チューブ20の先端または接続部材70の先端とが当接することによって、内管チューブ20および接続部材70の先端方向への移動を制限可能である。   FIG. 2 shows a cross-sectional view of the distal end region of the endoscope injection needle 100 in a protruding state. An opening through which the needle body 10 can project is provided at the distal end of the outer tube 30. The tip having the opening is, for example, formed in a tapered shape by bending inward in the radial direction. In other words, the opening diameter of the tapered tip of the outer tube 30 is smaller than the outer diameter of the tip of the inner tube 20 or the outer diameter of the tip of the connecting member 70. When the inner peripheral surface of the tapered tip contacts the tip of the inner tube 20 or the tip of the connecting member 70, the movement of the inner tube 20 and the connecting member 70 in the tip direction can be restricted.

針体10は、内視鏡用注射針に設けられる針を適宜選択して用いることができる。穿刺したときの傷を小さくするために、たとえば外径0.65mm以下のものが好ましく選択されるが、これに限定されない。本発明は接続部材70を有するため、針体10の外周面と内管チューブ20との間に有意な距離を有していても接続部材70を介して針体10と内管チューブ20とを接続することができる。換言すると、接続部材70の厚みを調節することにより、定型の内径を有する内管チューブ20に対し、所望の外径を有する針体10を適宜選択して用いることができる。   As the needle body 10, a needle provided in an endoscope injection needle can be appropriately selected and used. In order to reduce the damage at the time of puncture, for example, an outer diameter of 0.65 mm or less is preferably selected, but is not limited thereto. Since the present invention has the connecting member 70, the needle body 10 and the inner tube 20 can be connected via the connecting member 70 even if there is a significant distance between the outer peripheral surface of the needle 10 and the inner tube 20. Can be connected. In other words, by adjusting the thickness of the connection member 70, the needle body 10 having a desired outer diameter can be appropriately selected and used for the inner tube 20 having a fixed inner diameter.

内管チューブ20は、その先端側に針体10が取り付けられ、外管チューブ30の中を進退可能に挿通している。
本実施形態では、内管チューブ20の最先端に針体10を取り付けているように図示したが、これに限定されるものでなく、内視鏡用注射針100に必要な機能を阻害しない程度に取り付け位置が変更されてもよい。
The inner tube 20 has a needle body 10 attached to the distal end thereof, and is inserted through the outer tube 30 so as to be able to advance and retreat.
In the present embodiment, the needle body 10 is illustrated as being attached to the forefront of the inner tube 20, but the present invention is not limited to this, and does not hinder the functions necessary for the endoscope injection needle 100. The attachment position may be changed.

内管チューブ20の構成部材は、特に限定されないが、外管チューブ30内を摺動するため、一定の低摩擦性・非粘着性を有することが好ましく、さらに耐薬品性が高いと良い。一般的には、上記部材として、テトラフルオロエチレン重合体(PTFE)やテトラフルオロエチレン・パーフルオロアルコキシエチレン共重合体(PFA)等のフッ素樹脂、ポリアミド樹脂(ナイロン樹脂)などを用いることができる。
内管チューブ20の外径および内径は特に限定されないが、例えば、外径は1.2mm以上1.7mm以下、内径は0.5mm以上1mm以下の範囲とすることができる。
The constituent members of the inner tube 20 are not particularly limited. However, since the inner tube 20 slides in the outer tube 30, it is preferable that the inner tube 20 has a certain low friction property and non-adhesiveness, and further has high chemical resistance. In general, a fluororesin such as tetrafluoroethylene polymer (PTFE) or tetrafluoroethylene / perfluoroalkoxyethylene copolymer (PFA), polyamide resin (nylon resin), or the like can be used as the member.
The outer diameter and inner diameter of the inner tube 20 are not particularly limited. For example, the outer diameter can be in the range of 1.2 mm to 1.7 mm, and the inner diameter can be in the range of 0.5 mm to 1 mm.

外管チューブ30は、基端側の一部が、外筒グリップ40の内面に接合されている。
なお、本実施形態では外筒グリップ40の内面と外管チューブ30の外面とが接合するように図示したが、外筒グリップ40の外面と外管チューブ30の内面とが接合する構成であっても構わない。また、外管チューブ30と外筒グリップ40の接合には、図示しない留め具が使われてもよいし、接着剤が用いられてもよい。
A portion of the outer tube 30 on the base end side is joined to the inner surface of the outer cylinder grip 40.
In the present embodiment, the inner surface of the outer tube grip 40 and the outer surface of the outer tube tube 30 are illustrated as being joined, but the outer surface of the outer tube grip 40 and the inner surface of the outer tube tube 30 are bonded. It doesn't matter. For joining the outer tube 30 and the outer cylinder grip 40, a fastener (not shown) may be used, or an adhesive may be used.

外管チューブ30の構成部材は、特に限定されないが、内視鏡の処置具挿通チャンネルの中に挿通して用いるため一定の低摩擦性・非粘着性を有することが好ましい。一般的には、上記構成部材として、ポリオレフィン樹脂、ポリアミド樹脂(ナイロン樹脂)、ポリウレタン樹脂等を用いることができる。また、上述のフッ素樹脂が外管チューブ30の構成部材として用いられてもよい。   Although the constituent member of the outer tube 30 is not particularly limited, it is preferable that the outer tube 30 has a certain low friction and non-adhesiveness because it is inserted into the treatment instrument insertion channel of the endoscope. In general, polyolefin resin, polyamide resin (nylon resin), polyurethane resin, or the like can be used as the constituent member. Moreover, the above-mentioned fluororesin may be used as a constituent member of the outer tube 30.

外管チューブ30の内部において内管チューブ20がスムーズに摺動可能なよう、外管チューブ30の内周面と内管チューブ20の外周面との間には適度なクリアランスが設けられている。たとえば、外管チューブ30の外径および内径は特に限定されないが、たとえば外径は2mm以上2.6mm以下、内径は1.3mm以上1.9mm以下の範囲とすることができる。   An appropriate clearance is provided between the inner peripheral surface of the outer tube 30 and the outer peripheral surface of the inner tube 20 so that the inner tube 20 can slide smoothly inside the outer tube 30. For example, the outer diameter and inner diameter of the outer tube 30 are not particularly limited. For example, the outer diameter can be in the range of 2 mm to 2.6 mm, and the inner diameter can be in the range of 1.3 mm to 1.9 mm.

本実施形態における接続部材70は、略均一の内径を有している。接続部材70の内径は、針体10の外径と略同等である。ここで略同等とは、接続部材70の内周面と針体10の外周面との間に任意で薄厚の樹脂層が形成可能な程度の差異を含むという意味である。当該樹脂層は、針体10と接続部材70との接合を果たすものであることが好ましく、たとえば後述する樹脂接続部90が相当する。当該樹脂層は、針体10と接続部材70との間の水密性を向上させる機能を有していてもよい。
接続部材70は、筒状体であって、たとえば円筒体である。
The connection member 70 in this embodiment has a substantially uniform inner diameter. The inner diameter of the connecting member 70 is substantially the same as the outer diameter of the needle body 10. Here, “substantially equivalent” means that there is a difference that allows an optional thin resin layer to be formed between the inner peripheral surface of the connecting member 70 and the outer peripheral surface of the needle body 10. It is preferable that the said resin layer fulfill | performs joining of the needle body 10 and the connection member 70, for example, the resin connection part 90 mentioned later corresponds. The resin layer may have a function of improving water tightness between the needle body 10 and the connection member 70.
The connection member 70 is a cylindrical body, for example, a cylindrical body.

本実施形態における接続部材70は、図2に示すとおり、基端側に接続部本体71を有するとともに、接続部本体71よりも先端側に、接続部本体71の外径よりも大きい外径を備える大径部72を有している。たとえば大径部72の外径は、内管チューブ20の内径よりも大きく、内管チューブ20の外径よりも小さい。接続部本体71の外径は、内管チューブ20の内径と略同等である。
本実施形態では、接続部本体71および大径部72はいずれも外形が円筒形状である。ただし本実施形態における接続部材70はこれに限定されず、少なくとも接続部本体71を有し、大径部72が省略されてもよい。
As shown in FIG. 2, the connection member 70 in the present embodiment has a connection portion main body 71 on the proximal end side, and has an outer diameter larger than the outer diameter of the connection portion main body 71 on the distal end side than the connection portion main body 71. A large-diameter portion 72 is provided. For example, the outer diameter of the large diameter portion 72 is larger than the inner diameter of the inner tube 20 and smaller than the outer diameter of the inner tube 20. The outer diameter of the connecting portion main body 71 is substantially the same as the inner diameter of the inner tube 20.
In this embodiment, both the connection part main body 71 and the large diameter part 72 have a cylindrical outer shape. However, the connection member 70 in the present embodiment is not limited to this, and may include at least the connection portion main body 71 and the large diameter portion 72 may be omitted.

接続部材70には、針体10を挿通するための挿通孔80が設けられている。本実施形態において針体10は先端側の端部および基端側の端部のそれぞれが挿通孔80の両端から突出している。針体10は、挿通孔80に挿通されるとともに、接続部材70に保持される。接続部材70において針体10を保持するための保持手段は特に限定されない。   The connection member 70 is provided with an insertion hole 80 for inserting the needle body 10. In the present embodiment, the needle body 10 has a distal end and a proximal end protruding from both ends of the insertion hole 80. The needle body 10 is inserted into the insertion hole 80 and held by the connection member 70. The holding means for holding the needle body 10 in the connecting member 70 is not particularly limited.

たとえば、接続部材70がインサート成形などにより樹脂部材で構成される場合には、上記保持手段として以下のような例を挙げることができる。即ち、針体10が挿通した接続部材70の外周面の周方向に熱収縮部材を配置し、当該熱収縮部材を加熱して接続部材70を径方向の内向きに締め付けることができる(以下、熱収縮保持手段ともいう)。これにより挿通孔80に挿通された状態の針体10が、挿通孔80から脱落し難くなり、良好に接続部材70に保持され得る。
また、接続部材70が金属材料よりなる場合には、針体10が挿通する接続部材70をかしめて針体10の外周面の一部と接続部材70の内周面の一部とを物理的に当接させることにより、針体10を保持させることもできる(以下、かしめ保持手段ともいう)。
For example, when the connecting member 70 is formed of a resin member by insert molding or the like, the following examples can be given as the holding means. That is, a heat shrinkable member can be arranged in the circumferential direction of the outer peripheral surface of the connecting member 70 through which the needle body 10 is inserted, and the heat shrinkable member can be heated to tighten the connecting member 70 inward in the radial direction (hereinafter, Also called heat shrinkage retention means). As a result, the needle body 10 inserted through the insertion hole 80 is unlikely to fall out of the insertion hole 80 and can be satisfactorily held by the connection member 70.
When the connection member 70 is made of a metal material, the connection member 70 through which the needle body 10 is inserted is caulked to physically connect a part of the outer peripheral surface of the needle body 10 and a part of the inner peripheral surface of the connection member 70. The needle body 10 can also be held by being brought into contact with (hereinafter also referred to as caulking holding means).

接続部材70の構成部材は特に限定されない。たとえば接続部材70は、インサート成形により形成された樹脂部材よりなる態様、金属の線状部材を螺旋状に巻き回してなるコイル、または、ステンレスなどの金属材料からなる壁面が湾曲かつ略平坦な筒状体よりなる態様を含む。   The constituent members of the connecting member 70 are not particularly limited. For example, the connecting member 70 is an aspect made of a resin member formed by insert molding, a coil formed by spirally winding a metal linear member, or a tube having a curved and substantially flat wall surface made of a metal material such as stainless steel. The aspect which consists of a shape body is included.

次に、樹脂充填部110について説明する。内視鏡用注射針100は、接続部材70の基端面73より基端側に突出する針体10の外周面と内管チューブ20の内周面と接続部材70の基端面73との間に樹脂部材を充填してなる樹脂充填部110を備える。
本実施形態における樹脂充填部110は、中心軸138を中心として周方向に連続している。樹脂充填部110における第一仮想面140の法線である第一法線136が、中心軸138に対し傾斜していることは上述のとおりである。
Next, the resin filling unit 110 will be described. The endoscope injection needle 100 is formed between the outer peripheral surface of the needle body 10 protruding from the base end surface 73 of the connection member 70 to the base end side, the inner peripheral surface of the inner tube 20, and the base end surface 73 of the connection member 70. A resin filling unit 110 is provided that is filled with a resin member.
The resin filling part 110 in the present embodiment is continuous in the circumferential direction around the central axis 138. As described above, the first normal line 136 that is the normal line of the first virtual surface 140 in the resin filling portion 110 is inclined with respect to the central axis 138.

本実施形態における樹脂充填部110は、先基端方向において最遠位点134を含む位置から接続部材70の基端面73までの間は、内管チューブ20の内周面と針体10の外周面との間に、実質的に、中実の状態で樹脂部材が充填されている。   In the present embodiment, the resin filling portion 110 has an inner peripheral surface of the inner tube 20 and an outer periphery of the needle body 10 between the position including the most distal point 134 in the distal proximal direction and the proximal end surface 73 of the connecting member 70. Between the surfaces, the resin member is substantially filled in a solid state.

ここで、図4(a)に示すとおり、本実施形態では、樹脂充填部110の基端面130の周縁の最遠位点134から、接続部材70の基端面73の周縁までの距離Yが、針体10の外周面と内管チューブ20の内周面との距離Z以上となるよう構成されている。そのため、樹脂充填部110よりも先端側に液体が浸出し難く、内管チューブ20の水密性に優れる。   Here, as shown to Fig.4 (a), in this embodiment, the distance Y from the most distal point 134 of the periphery of the base end surface 130 of the resin filling part 110 to the periphery of the base end surface 73 of the connection member 70 is the following. The distance between the outer peripheral surface of the needle body 10 and the inner peripheral surface of the inner tube 20 is greater than or equal to Z. Therefore, it is difficult for the liquid to permeate to the tip side of the resin filling part 110 and the water tightness of the inner tube 20 is excellent.

樹脂充填部110を構成する樹脂材料は特に限定されないが、たとえば、エポキシ樹脂、ウレタン樹脂、シアノアクリレート樹脂などの接着剤として使用可能な樹脂部材、あるいは、ABS樹脂やポリアミド樹脂、ウレタン樹脂などの熱可塑性樹脂を挙げることができる。   Although the resin material which comprises the resin filling part 110 is not specifically limited, For example, it is resin members which can be used as adhesives, such as an epoxy resin, a urethane resin, and a cyanoacrylate resin, or heat, such as ABS resin, a polyamide resin, and a urethane resin A plastic resin can be mentioned.

本実施形態において、さらに、接続部材70の内周面と針体10の外周面との間に位置し接続部材70と針体10とを接続する樹脂材料からなる樹脂接続部90を設けてもよい。図2に示すとおり、樹脂接続部90は、樹脂充填部110と連続するよう設けることができる。   In the present embodiment, a resin connection portion 90 made of a resin material that is located between the inner peripheral surface of the connection member 70 and the outer peripheral surface of the needle body 10 and that connects the connection member 70 and the needle body 10 may be further provided. Good. As shown in FIG. 2, the resin connection portion 90 can be provided so as to be continuous with the resin filling portion 110.

樹脂接続部90を設けることによって、接続部材70と針体10とを良好に接合することができる。そのため、接続部材70から針体10の脱落防止が図られる。
ここで本実施形態における内視鏡用注射針100は、樹脂充填部110を備えることによって、内管チューブ20内における接続部材70の配置位置が、液体の吐出圧によって先端側にずれることが防止されていることは上述のとおりである。しかして、先端方向に配置位置がずれることが防止された接続部材70に良好に接合された針体10は、接続部材70とともに、設計当初に予定された先基端方向における配置位置を良好に維持可能である。
By providing the resin connection part 90, the connection member 70 and the needle body 10 can be favorably joined. Therefore, the needle body 10 can be prevented from dropping from the connecting member 70.
Here, the endoscope injection needle 100 according to the present embodiment includes the resin filling portion 110, thereby preventing the arrangement position of the connecting member 70 in the inner tube 20 from shifting to the distal end side due to the discharge pressure of the liquid. This is as described above. Thus, the needle body 10 that is favorably joined to the connecting member 70 that is prevented from being displaced in the distal end direction, together with the connecting member 70, has a favorable arrangement position in the proximal end direction that is initially planned. It can be maintained.

また樹脂接続部90が設けられることによって、接続部材70の内周面と針体10の外周面との間における空隙が塞がれ得るため、接続部材70と針体10との間の水密性が向上する。   Further, since the resin connecting portion 90 is provided, a gap between the inner peripheral surface of the connecting member 70 and the outer peripheral surface of the needle body 10 can be closed, so that the water tightness between the connecting member 70 and the needle body 10 is achieved. Will improve.

樹脂接続部90を構成する樹脂部材は、特に限定されないが、例えば樹脂充填部110を構成するための樹脂部材と同様の樹脂部材であってよい。
樹脂接続部90と樹脂充填部110とは、同一の樹脂部材より構成されていてもよく、両者が同一の樹脂により一体的に形成されていてもよい。また別の態様として、樹脂接続部90と樹脂充填部110とは、異なる樹脂部材により構成されていてもよい。たとえば、本実施形態における樹脂接続部90は、樹脂充填部110を構成する工程と同工程において、樹脂充填部110を構成する樹脂部材と同一の樹脂部材により、樹脂充填部110と一体的に形成されてもよい。
Although the resin member which comprises the resin connection part 90 is not specifically limited, For example, the resin member similar to the resin member for comprising the resin filling part 110 may be sufficient.
The resin connection part 90 and the resin filling part 110 may be comprised from the same resin member, and both may be integrally formed with the same resin. Moreover, as another aspect, the resin connection part 90 and the resin filling part 110 may be comprised by the different resin member. For example, the resin connecting portion 90 in the present embodiment is formed integrally with the resin filling portion 110 by the same resin member as the resin member constituting the resin filling portion 110 in the same step as the step constituting the resin filling portion 110. May be.

本実施形態にかかる内視鏡用注射針100は、さらに大径部72の基端側面と内管チューブ20の先端面との間に、図示省略する第二樹脂接続部が設けられてもよい。上記第二樹脂接続部が設けられることにより、接続部材70と内管チューブ20の先端との接合性をより確実にすることができる。これにより、内管チューブ20を流れる液体が内管チューブ20の先端側から体腔に漏れ出ることを防止するとともに、体液が体腔側から内管チューブ20と接続部材70との間に侵入することが防止される。   In the endoscope injection needle 100 according to the present embodiment, a second resin connection portion (not shown) may be provided between the proximal end side surface of the large diameter portion 72 and the distal end surface of the inner tube 20. . By providing the second resin connection portion, it is possible to further ensure the bondability between the connection member 70 and the distal end of the inner tube 20. This prevents the liquid flowing through the inner tube 20 from leaking from the distal end side of the inner tube 20 into the body cavity, and allows body fluid to enter between the inner tube 20 and the connection member 70 from the body cavity side. Is prevented.

またさらに、本実施形態にかかる内視鏡用注射針100は、接続部材70の外周面と内管チューブ20の内周面の間に図示省略する第三樹脂接続部が設けられてもよい。第三樹脂接続部は、上述する第二樹脂接続部と連続的に設けられてもよい。第二樹脂接続部と連続して設けられた第三樹脂接続部であれば、接続部材70の外周面と内管チューブ20の内周面との間に第三樹脂接続部が確実に形成されていることを、第二樹脂接続部を目視確認することで、確認可能である。第三樹脂接続部が設けられることによって、内管チューブ20と接続部材70との接続性が向上するとともに、内管チューブ20と接続部材70との間の水密性が向上する。   Furthermore, in the endoscope injection needle 100 according to the present embodiment, a third resin connecting portion (not shown) may be provided between the outer peripheral surface of the connecting member 70 and the inner peripheral surface of the inner tube 20. The third resin connection portion may be provided continuously with the second resin connection portion described above. If the third resin connection portion is provided continuously with the second resin connection portion, the third resin connection portion is reliably formed between the outer peripheral surface of the connection member 70 and the inner peripheral surface of the inner tube 20. It can be confirmed by visually confirming the second resin connecting portion. By providing the third resin connecting portion, the connectivity between the inner tube 20 and the connecting member 70 is improved, and the water tightness between the inner tube 20 and the connecting member 70 is improved.

上述する第二樹脂接続部および第三樹脂接続部を構成する樹脂部材は特に限定されないが、たとえば、樹脂充填部110を構成するための樹脂部材と同様の樹脂部材であってよい。
第二樹脂接続部および第三樹脂接続部は、たとえば、樹脂充填部110を構成する工程と同工程において、樹脂充填部110を構成する樹脂部材と同一の樹脂部材により、樹脂充填部110と一体的に形成されてもよい。あるいは、別の態様として、樹脂充填部110の形成工程とは別工程において、樹脂充填部110を構成する樹脂と同一の樹脂あるいは異なる樹脂によって形成されてもよい。内視鏡用注射針100は、樹脂充填部110と第二樹脂接続部と第三樹脂接続部とが連続的に設けられることによって、優れた水密性を発揮し得る。
Although the resin member which comprises the 2nd resin connection part mentioned above and the 3rd resin connection part is not specifically limited, For example, the resin member similar to the resin member for comprising the resin filling part 110 may be sufficient.
For example, the second resin connection portion and the third resin connection portion are integrated with the resin filling portion 110 by the same resin member as the resin member constituting the resin filling portion 110 in the same step as the step of constituting the resin filling portion 110. It may be formed automatically. Alternatively, as another aspect, the resin filling part 110 may be formed of the same resin as the resin constituting the resin filling part 110 or a different resin in a process different from the process of forming the resin filling part 110. The endoscope injection needle 100 can exhibit excellent water-tightness by continuously providing the resin filling portion 110, the second resin connection portion, and the third resin connection portion.

<第二実施形態>
次に本発明の第二実施形態である内視鏡用注射針の製造方法(以下、単に「本製造方法」ともいう)について図6(a)から図6(d)を用いて説明する。図6(a)から図6(d)は、本製造方法をいくつかの工程に分けて説明する説明図である。本製造方法について、内視鏡用注射針100を製造する方法を例に説明する。
<Second embodiment>
Next, a method for manufacturing an endoscope injection needle (hereinafter also simply referred to as “the present manufacturing method”) according to a second embodiment of the present invention will be described with reference to FIGS. 6 (a) to 6 (d). FIG. 6A to FIG. 6D are explanatory views for explaining the manufacturing method divided into several steps. This manufacturing method will be described taking a method of manufacturing the endoscope injection needle 100 as an example.

本製造方法は、挿通孔80(図示省略)に針体10を挿通する挿通工程と、接続部材70に対し型枠部材300を外嵌する外嵌工程と、樹脂充填部110を形成する樹脂充填部形成工程と、内管チューブ20を取り付ける内管チューブ取付工程と、を有する。
挿通工程は、接続部材70における挿通孔80に接続部材70の先端側および基端側から突出するよう針体10を挿通させる工程である。
外嵌工程は、接続部材70の基端側に接続部材70の外径と略同等の内径を有する型枠部材300を外嵌する工程である。
樹脂充填部形成工程は、型枠部材300の内周面と針体10の外周面と接続部材70の基端面73とに接して樹脂部材を型枠部材300に注入するとともに、先基端方向に対し樹脂充填部110の基端面130が傾斜するよう樹脂充填部110を形成する工程である。
内管チューブ取付工程は、接続部材の少なくとも一部および樹脂充填部110を内包するよう上記内管チューブを設ける工程である。
This manufacturing method includes an insertion step of inserting the needle body 10 into an insertion hole 80 (not shown), an external fitting step of externally fitting the mold member 300 to the connection member 70, and a resin filling for forming the resin filling portion 110. A part forming step and an inner tube attaching step for attaching the inner tube 20.
The insertion step is a step of inserting the needle body 10 into the insertion hole 80 in the connection member 70 so as to protrude from the distal end side and the proximal end side of the connection member 70.
The external fitting process is a process of externally fitting a mold member 300 having an inner diameter substantially equal to the outer diameter of the connection member 70 to the proximal end side of the connection member 70.
In the resin filling portion forming step, the resin member is injected into the mold member 300 in contact with the inner peripheral surface of the mold member 300, the outer peripheral surface of the needle body 10, and the proximal end surface 73 of the connecting member 70, and the proximal direction In contrast, the resin filling portion 110 is formed so that the base end face 130 of the resin filling portion 110 is inclined.
The inner tube attaching step is a step of providing the inner tube so as to enclose at least a part of the connecting member and the resin filling portion 110.

本製造方法によれば、樹脂充填部110を備える内視鏡用注射針100を製造することができる。
以下に、本製造方法の各工程について、適宜、図6(a)から図6(d)を用いて詳細に説明する。
According to this manufacturing method, the injection needle 100 for endoscope provided with the resin filling part 110 can be manufactured.
Below, each process of this manufacturing method is demonstrated in detail suitably using FIG. 6 (a)-FIG.6 (d).

まず、挿通工程を実施するために、針体10および接続部材70を準備し、図6(a)において接続部材70に設けられた挿通孔80(図示省略)に針体10を挿通させる。挿通工程において、図6(a)に示すとおり、針体10を接続部材70の先端側および基端側から突出するよう挿通する。針体10が接続部材70から突出する突出長さは特に限定されないが、基端側における針体10の突出長さは、後工程で形成される樹脂充填部110の軸長よりも長いことが望ましい。
挿通工程において、あるいは挿通工程の後、適宜、針体10を接続部材70に保持させるための保持工程をさらに実施してもよい。保持工程としては、たとえば第一実施形態において説明した熱収縮保持手段、またはかしめ保持手段の実施が挙げられるがこれに限定されない。
尚、本実施形態に用いられる針体10は、先端面が、中心軸に対して傾斜しており、最先端部Xを有している。
First, in order to carry out the insertion step, the needle body 10 and the connection member 70 are prepared, and the needle body 10 is inserted into an insertion hole 80 (not shown) provided in the connection member 70 in FIG. In the insertion step, the needle body 10 is inserted so as to protrude from the distal end side and the proximal end side of the connecting member 70 as shown in FIG. Although the protrusion length from which the needle body 10 protrudes from the connection member 70 is not particularly limited, the protrusion length of the needle body 10 on the proximal end side may be longer than the axial length of the resin filling portion 110 formed in a later step. desirable.
In the insertion step or after the insertion step, a holding step for holding the needle body 10 on the connecting member 70 may be further performed as appropriate. Examples of the holding step include, but are not limited to, implementation of the heat shrinkage holding means or the caulking holding means described in the first embodiment.
In addition, the needle body 10 used in the present embodiment has a distal end surface that is inclined with respect to the central axis and has the most advanced portion X.

図示省略するが、上記挿通工程の後工程において樹脂接続部90(図2参照)を形成ししてもよい。この場合、挿通工程または挿通工程実施後、針体10の外周面と接続部材70の内周面との間に基端面73から先端方向に連通する空隙を予め形成しておくとよい。当該空隙は、たとえば接続部材70をインサート成形により形成する場合には、当該空隙を確保するための所定厚みのくさび部材を針体10の外周面と樹脂部材からなる接続部材70の内周面との境界に打ち込み、これを抜去することにより形成することができる。あるいは、針体10が挿通された金属材料からなる接続部材70に対し、かしめ処理することによって当該空隙を設けることもできる。即ち、かしめた箇所において接続部材70の内周面の一部と針体10の外周面の一部とを当接させるとともに、当該箇所から基端面73までの間に当該空隙を形成することができる。   Although not shown in the drawing, the resin connection portion 90 (see FIG. 2) may be formed in a step subsequent to the insertion step. In this case, after the insertion step or the insertion step, a gap communicating in the distal direction from the proximal end surface 73 may be formed in advance between the outer peripheral surface of the needle body 10 and the inner peripheral surface of the connection member 70. For example, when the connection member 70 is formed by insert molding, the gap includes a wedge member having a predetermined thickness for securing the gap, and an outer peripheral surface of the needle body 10 and an inner peripheral surface of the connection member 70 made of a resin member. It can be formed by driving it into the boundary and removing it. Alternatively, the gap can be provided by caulking the connection member 70 made of a metal material into which the needle body 10 is inserted. That is, a part of the inner peripheral surface of the connection member 70 and a part of the outer peripheral surface of the needle body 10 are brought into contact with each other at the caulked portion, and the gap is formed between the portion and the base end surface 73. it can.

次に、外嵌工程について説明する。まず、接続部材70の外径と略同等の内径を有する型枠部材300を準備する。ここで略同等とは、接続部材70の外径と型枠部材300の内径とが実質的に同一である場合と、接続部材70の外周面に上記第三樹脂接続部を形成可能な隙間を確保可能な程度に、型枠部材300の内径が接続部材70の外径より大きい場合とを包含する趣旨である。
かかる型枠部材300を、接続部材70の少なくとも基端側に外嵌することにより外嵌工程が実施される。図6(a)では、型枠部材300が、接続部材70の基端側の一部領域を覆って接続部材70に対し嵌合された態様を示したが、これに限定されず、型枠部材300は接続部材70の外周面全体を覆うよう嵌合されてもよい。
Next, the external fitting process will be described. First, a mold member 300 having an inner diameter substantially equal to the outer diameter of the connection member 70 is prepared. Here, “substantially equivalent” means that the gap where the outer diameter of the connecting member 70 and the inner diameter of the mold member 300 are substantially the same and the gap where the third resin connecting portion can be formed on the outer peripheral surface of the connecting member 70. This is intended to encompass the case where the inner diameter of the mold member 300 is larger than the outer diameter of the connecting member 70 to the extent that it can be secured.
The external fitting process is performed by externally fitting the mold member 300 to at least the base end side of the connecting member 70. FIG. 6A shows a mode in which the mold member 300 is fitted to the connection member 70 so as to cover a partial region on the proximal end side of the connection member 70. However, the present invention is not limited to this. The member 300 may be fitted so as to cover the entire outer peripheral surface of the connection member 70.

樹脂充填部形成工程は、型枠部材300の内周面と針体10の外周面と接続部材70の基端面73とに接するよう樹脂部材を型枠部材300に注入するとともに、先基端方向に対し樹脂充填部110の基端面130が傾斜するよう樹脂充填部110を形成する工程である。ここで基端面130が傾斜するとは、図6(b)に示すように略平滑な面である基端面130が軸方向に対し傾斜する態様に限定されない。樹脂充填部形成工程は、図2を用いて第一実施形態において説明したとおり、内管チューブ20の内周面に対する切断面であって樹脂充填部110の基端面130の周縁の最近位点132および当該周縁の最遠位点134を含み中心軸138と交差するとともに法線と中心軸138との交差角が最小となる切断面である第一仮想面140の法線である第一法線136が、中心軸138に対し傾斜するよう樹脂充填部110を形成する。   In the resin filling portion forming step, the resin member is injected into the mold member 300 so as to be in contact with the inner peripheral surface of the mold member 300, the outer peripheral surface of the needle body 10, and the proximal end surface 73 of the connecting member 70, and the proximal direction In contrast, the resin filling portion 110 is formed so that the base end face 130 of the resin filling portion 110 is inclined. Here, the fact that the base end surface 130 is inclined is not limited to a mode in which the base end surface 130 that is a substantially smooth surface is inclined with respect to the axial direction as shown in FIG. As described in the first embodiment with reference to FIG. 2, the resin filling portion forming step is a cut surface with respect to the inner peripheral surface of the inner tube 20 and the nearest point 132 on the periphery of the proximal end surface 130 of the resin filling portion 110. In addition, the first normal line that is the normal line of the first virtual plane 140 that includes the most distal point 134 of the peripheral edge and intersects the central axis 138 and has a minimum crossing angle between the normal line and the central axis 138. The resin filling portion 110 is formed so that 136 inclines with respect to the central axis 138.

樹脂充填部形成工程の好ましい態様の一例としては以下の工程を挙げることができる。
即ち、図6(a)に示すとおり、樹脂充填部形成工程において、樹脂部材を型枠部材300の内側に注入するための注入チューブ400の先端を型枠部材300の内周面に寄せて設置する。次いで、図6(b)に示すとおり、樹脂部材を型枠部材300に注入する。これにより形成される樹脂充填部110の基端面130を軸方向に対し傾斜させることが可能である。
The following processes can be mentioned as an example of the preferable aspect of a resin filling part formation process.
That is, as shown in FIG. 6A, in the resin filling portion forming step, the tip of the injection tube 400 for injecting the resin member into the inside of the mold member 300 is placed close to the inner peripheral surface of the mold member 300. To do. Next, as shown in FIG. 6B, the resin member is poured into the mold member 300. It is possible to incline the base end surface 130 of the resin filling part 110 formed by this with respect to an axial direction.

型枠部材300を重力方向に対し、略平行に配置して樹脂充填部形成工程を行う場合には、たとえば以下の点に留意することが好ましい。即ち、注入チューブ400により型枠部材300に注入された樹脂部材の基端面が均される前に、注入された当該樹脂部材を少なくとも半乾燥し、または樹脂部材の基端面が短時間で均され難い程度に樹脂部材の粘度を調整するとよい。
上述する樹脂充填部形成工程を実施することにより、容易に基端面130を備える樹脂充填部110を形成することができる。
When the mold filling member 300 is arranged substantially parallel to the direction of gravity and the resin filling portion forming step is performed, it is preferable to pay attention to the following points, for example. That is, before the base end surface of the resin member injected into the mold member 300 by the injection tube 400 is leveled, the injected resin member is at least semi-dried, or the base end surface of the resin member is leveled in a short time. It is preferable to adjust the viscosity of the resin member to such an extent that it is difficult.
By performing the resin filling part formation process mentioned above, the resin filling part 110 provided with the base end face 130 can be formed easily.

さらに樹脂充填部形成工程において、注入チューブ400の先端の配置位置に関し、以下の点を留意することが好ましい。
即ち、樹脂充填部形成工程において、上面視上、注入チューブ400の先端を針体10の最先端部Xが配置された側に寄せて配置する。そして、本工程において形成される樹脂充填部110(図6(c)参照)の最近位点132が属する側の半体積が、対向点142が属する半体積よりも大きくなるよう樹脂部材を注入するとよい。
ここで上面視とは、型枠部材300の開口側から針体10の最先端部X方向を観察することを意味し、たとえば、型枠部材300を重量方向に対し略平行に配置した場合には、重量方向における上方向から観察することを意味する。
尚、最近位点132が属する側の半体積および対向点142が属する半体積に関する説明は、適宜、第一実施形態に関する説明を参照することができる。
Furthermore, in the resin filling portion forming step, it is preferable to pay attention to the following points regarding the arrangement position of the tip of the injection tube 400.
That is, in the resin filling portion forming step, the top end of the injection tube 400 is arranged close to the side on which the most distal portion X of the needle body 10 is arranged in top view. Then, when the resin member is injected so that the half volume on the side to which the closest point 132 of the resin filling portion 110 (see FIG. 6C) formed in this step belongs is larger than the half volume to which the opposite point 142 belongs. Good.
Here, the top view means observing the foremost portion X direction of the needle body 10 from the opening side of the mold member 300. For example, when the mold member 300 is arranged substantially parallel to the weight direction. Means to observe from above in the weight direction.
For the description of the half volume on the side to which the closest point 132 belongs and the half volume to which the opposing point 142 belongs, the description on the first embodiment can be referred to as appropriate.

このように、注入チューブ400の先端の配置位置と針体10の最先端部Xの配置位置に留意することによって、容易に、図6(c)に示されるように、針体10の最先端部Xを、基端面130の周縁の最近位点132が属する側に配置することが可能である。   Thus, by paying attention to the arrangement position of the distal end of the injection tube 400 and the arrangement position of the most distal end portion X of the needle body 10, as shown in FIG. It is possible to arrange the portion X on the side to which the nearest point 132 on the periphery of the base end face 130 belongs.

尚、樹脂充填部工程において、型枠部材300に対し注入チューブ400から樹脂部材を注入する際に、針体10と接続部材70との間に形成された空隙にも当該樹脂部材を充填することにより樹脂接続部90(図示省略)を、形成することができる。また同様に、接続部材70と型枠部材300との間に形成された空隙に当該樹脂部材を注入することにより第三樹脂接続部(図示省略)を、形成することができる。
樹脂充填部形成工程において、樹脂充填部110の形成とともに樹脂接続部90および/または第三樹脂接続部を形成することによって、樹脂充填部110と、樹脂接続部90および/または第三樹脂接続部とを、一体的に形成することができる。
In the resin filling portion process, when the resin member is injected from the injection tube 400 into the mold member 300, the resin member is also filled in the gap formed between the needle body 10 and the connection member 70. Thus, the resin connection portion 90 (not shown) can be formed. Similarly, a third resin connection portion (not shown) can be formed by injecting the resin member into a gap formed between the connection member 70 and the mold member 300.
In the resin filling portion forming step, the resin filling portion 110 and the resin connecting portion 90 and / or the third resin connecting portion are formed by forming the resin connecting portion 90 and / or the third resin connecting portion together with the formation of the resin filling portion 110. Can be formed integrally.

樹脂充填部形成工程後に、図6(d)に示すとおり、内管チューブ取付工程を実施する。
内管チューブ取付工程は、接続部材70の少なくとも一部および樹脂充填部110を内包するよう内管チューブ20を設ける工程である。
より具体的には、たとえば、樹脂充填部形成工程後に、型枠部材300を接続部材70から抜き取り(図6(c)参照)、形成された樹脂充填部110および接続部材70の少なくとも基端側を覆うよう内管チューブ20を外嵌する。
After the resin filling portion forming step, as shown in FIG. 6D, an inner tube tube attaching step is performed.
The inner tube mounting step is a step of providing the inner tube 20 so as to enclose at least a part of the connecting member 70 and the resin filling portion 110.
More specifically, for example, after the resin filling portion forming step, the mold member 300 is extracted from the connecting member 70 (see FIG. 6C), and at least the proximal end side of the formed resin filling portion 110 and the connecting member 70 The inner tube 20 is externally fitted to cover

たとえば、樹脂充填部110が半硬化の状態において、内管チューブ取付工程を実施し、その後に、樹脂充填部110を完全に硬化させることにより、内管チューブ20の内周面と樹脂充填部110の外周面とを接合することができる。   For example, when the resin filling portion 110 is semi-cured, the inner tube tube mounting step is performed, and then the resin filling portion 110 is completely cured, whereby the inner peripheral surface of the inner tube 20 and the resin filling portion 110 are cured. Can be joined to the outer peripheral surface.

以上のとおり、本製造方法を実施することによって、内視鏡用注射針100を製造することができる。   As described above, the endoscope injection needle 100 can be manufactured by carrying out this manufacturing method.

以上に本発明の第一実施形態および第二実施形態について説明した。本発明は上述の実施形態に限定されるものではなく、本発明の目的が達成される限りにおける種々の変形、改良等の態様も含む。各実施形態において説明された事項は適宜、他の実施形態に適用することが可能である。
また第二実施形態における各工程の説明の順序は、本製造方法を限定するものではない。所期の内視鏡用注射針を製造できる範囲において、工程順は適宜入れ替え可能である。また説明する各工程の前または後または一の工程と他の工程との間に、適宜任意の工程をさらに追加してもよい。
また第二実施形態において説明した本製造方法は、本発明の内視鏡用注射針の製造方法の好適な例を示すものであるが、本発明の内視鏡用注射針の製造方法を何ら限定するものではない。
The first embodiment and the second embodiment of the present invention have been described above. The present invention is not limited to the above-described embodiment, and includes various modifications and improvements as long as the object of the present invention is achieved. The matters described in each embodiment can be applied to other embodiments as appropriate.
Moreover, the order of description of each process in 2nd embodiment does not limit this manufacturing method. As long as the desired endoscope injection needle can be manufactured, the order of the steps can be appropriately changed. Moreover, you may further add arbitrary processes suitably before or after each process demonstrated, or between one process and another process.
Moreover, although this manufacturing method demonstrated in 2nd embodiment shows the suitable example of the manufacturing method of the injection needle for endoscopes of this invention, what is the manufacturing method of the injection needle for endoscopes of this invention? It is not limited.

上記実施形態は、以下の技術思想を包含するものである。
(1)液体を注入するための内管チューブと、
前記内管チューブの先端に設けられた針体と、
前記内管チューブの中心軸の方向に貫通し前記針体が挿通する挿通孔を有し、前記内管チューブの内周面と前記針体の外周面との間に配置され前記針体と前記内管チューブとを接続するための接続部材と、
前記接続部材の基端面より基端側に突出する前記針体の外周面と前記内管チューブの内周面と前記接続部材の前記基端面との間に樹脂部材を充填してなる樹脂充填部と、
を有し、
前記内管チューブの内周面に対する切断面であって前記樹脂充填部の基端面の周縁の最近位点および当該周縁の最遠位点を含み前記中心軸と交差するとともに法線と中心軸との交差角が最小となる切断面である第一仮想面の前記法線である第一法線が、前記中心軸に対し傾斜していることを特徴とする内視鏡用注射針。
(2)前記内管チューブを進退可能に内包する外管チューブを備える上記(1)に記載の内視鏡用注射針。
(3)前記第一法線と前記中心軸とが交差する角度である第一交差角は、前記接続部材の前記基端面の法線である第二法線と前記中心軸とが交差する角度である第二交差角よりも大きい上記(1)または(2)に記載の内視鏡用注射針。
(4)前記中心軸と、前記樹脂充填部の前記基端面の前記周縁が形成する平均基端面の法線である第三法線と、が交差する角度である第三交差角は、30°以上90°未満である上記(1)から(3)のいずれか一項に記載の内視鏡用注射針。
(5)前記樹脂充填部は、前記樹脂充填部の前記基端面の前記周縁の前記最近位点が属する側の半体積が、前記中心軸を介して前記最近位点と対向する前記周縁における対向点が属する半体積よりも大きい上記(1)から(4)のいずれか一項に記載の内視鏡用注射針。
(6)前記針体の先端面は、前記中心軸に対して傾斜しており、
前記先端面の最先端部が、前記樹脂充填部の前記基端面の前記周縁の前記最近位点が属する側に配置されている上記(5)に記載の内視鏡用注射針。
(7)前記樹脂充填部の前記基端面の前記周縁の前記最遠位点から、前記接続部材の前記基端面の前記周縁までの距離が、前記針体の外周面と前記内管チューブの内周面との距離以上である上記(1)から(6)のいずれか一項に記載の内視鏡用注射針。
(8)前記接続部材の内周面と前記針体の外周面との間に位置し前記接続部材と前記針体とを接続する樹脂材料からなる樹脂接続部を有し、
前記樹脂接続部と前記樹脂充填部とが連続している上記(1)から(7)のいずれか一項に記載の内視鏡用注射針。
(9)上記(1)から(8)に記載の内視鏡用注射針を製造する内視鏡用注射針の製造方法であって、
前記接続部材における前記挿通孔に前記接続部材の先端側および基端側から突出するよう前記針体を挿通する挿通工程と、
前記接続部材の基端側に前記接続部材の外径と略同等の内径を有する型枠部材を外嵌する外嵌工程と、
前記型枠部材の内周面と前記針体の外周面と前記接続部材の基端面とに接して前記樹脂部材を前記型枠部材に注入するとともに、先基端方向に対し前記樹脂充填部の基端面が傾斜するよう前記樹脂充填部を形成する樹脂充填部形成工程と、
前記接続部材の少なくとも一部および前記樹脂充填部を内包するよう前記内管チューブを設ける内管チューブ取付工程と、を有することを特徴とする内視鏡用注射針の製造方法。
(10)前記樹脂充填部形成工程において、前記樹脂部材を前記型枠部材の内側に注入するための注入チューブの先端を前記型枠部材の内周面に寄せて設置し、前記樹脂部材を前記型枠部材に注入することにより、形成される前記樹脂充填部の前記基端面を軸方向に対し傾斜させる上記(9)に記載の内視鏡用注射針の製造方法。
(11)前記樹脂充填部形成工程において、上面視上、注入チューブの先端を前記針体の最先端部が配置された側に寄せ、形成される前記樹脂充填部の前記最近位点が属する側の前記半体積が、前記対向点が属する前記半体積よりも大きくなるよう樹脂部材を注入する上記(10)に記載の内視鏡用注射針の製造方法。
The above embodiment includes the following technical idea.
(1) an inner tube for injecting liquid;
A needle provided at the tip of the inner tube,
There is an insertion hole that penetrates in the direction of the central axis of the inner tube and passes through the needle body, and is disposed between the inner peripheral surface of the inner tube tube and the outer peripheral surface of the needle body, A connecting member for connecting the inner tube,
A resin filling portion formed by filling a resin member between the outer peripheral surface of the needle body protruding from the base end surface of the connection member to the base end side, the inner peripheral surface of the inner tube, and the base end surface of the connection member. When,
Have
A cutting surface with respect to the inner peripheral surface of the inner tube, which includes the most proximal point of the peripheral edge of the base end surface of the resin-filled portion and the most distal point of the peripheral edge and intersects the central axis, and a normal line and a central axis An endoscope needle, wherein a first normal, which is the normal of the first virtual plane, which is a cut surface having a minimum crossing angle, is inclined with respect to the central axis.
(2) The injection needle for endoscope according to (1), further including an outer tube that encloses the inner tube so as to be able to advance and retreat.
(3) The first intersection angle, which is the angle at which the first normal line and the central axis intersect, is the angle at which the second normal line, which is the normal line of the base end surface of the connection member, and the central axis intersect. The endoscope injection needle according to (1) or (2) above, which is larger than the second crossing angle.
(4) The third intersection angle, which is an angle at which the central axis and the third normal line that is the normal line of the average base end surface formed by the peripheral edge of the base end surface of the resin-filled portion, is 30 °. The endoscope needle according to any one of (1) to (3), which is less than 90 °.
(5) The resin filling portion is opposed to the peripheral edge where the half volume on the side to which the nearest point of the peripheral edge of the base end surface of the resin filling portion belongs is opposed to the nearest point via the central axis. The injection needle for endoscope according to any one of (1) to (4), wherein the needle is larger than a half volume to which the point belongs.
(6) The tip surface of the needle body is inclined with respect to the central axis,
The injection needle for endoscope according to (5), wherein the most distal end portion of the distal end surface is disposed on a side to which the nearest point of the peripheral edge of the base end surface of the resin filling portion belongs.
(7) The distance from the most distal point of the peripheral edge of the base end surface of the resin filling portion to the peripheral edge of the base end surface of the connection member is the distance between the outer peripheral surface of the needle body and the inner tube. The endoscope needle according to any one of (1) to (6), which is equal to or greater than a distance from a peripheral surface.
(8) having a resin connection portion made of a resin material located between the inner peripheral surface of the connection member and the outer peripheral surface of the needle body and connecting the connection member and the needle body;
The endoscope needle according to any one of (1) to (7), wherein the resin connection portion and the resin filling portion are continuous.
(9) A method for manufacturing an endoscope needle for manufacturing the endoscope needle according to (1) to (8) above,
An insertion step of inserting the needle body so as to protrude from the distal end side and the proximal end side of the connection member into the insertion hole in the connection member;
An external fitting step of externally fitting a mold member having an inner diameter substantially equal to the outer diameter of the connection member on the proximal end side of the connection member;
The resin member is injected into the mold member in contact with the inner peripheral surface of the mold member, the outer peripheral surface of the needle body, and the proximal end surface of the connecting member, and the resin filling portion A resin filling portion forming step of forming the resin filling portion so that the base end face is inclined;
An inner tube tube mounting step of providing the inner tube so as to enclose at least a part of the connecting member and the resin filling portion.
(10) In the resin filling portion forming step, the tip of an injection tube for injecting the resin member into the inside of the mold member is placed close to the inner peripheral surface of the mold member, and the resin member is The method for manufacturing an endoscope injection needle according to (9), wherein the base end surface of the resin filling portion to be formed is inclined with respect to the axial direction by being injected into a mold member.
(11) In the resin filling portion forming step, the top end of the injection tube is brought close to the side where the most distal end portion of the needle body is arranged in top view, and the closest point of the resin filling portion to be formed belongs to The method for manufacturing an endoscope injection needle according to (10), wherein the resin member is injected so that the half volume of the is larger than the half volume to which the opposing point belongs.

10、10B・・・針体
11・・・内周面
20・・・内管チューブ
30・・・外管チューブ
40・・・外筒グリップ
41・・・案内溝
50・・・操作部
51・・・コネクタ
60・・・内筒グリップ
61・・・突出部
70・・・接続部材
71・・・接続部本体
72・・・大径部
73・・・基端面
80・・・挿通孔
90・・・樹脂接続部
100、100A・・・内視鏡用注射針
110・・・樹脂充填部
130、130A・・・基端面
131、131A・・・交線
132・・・最近位点
134・・・最遠位点
136・・・第一法線
138・・・中心軸
140・・・第一仮想面
142・・・対向点
144・・・第一分割部
146・・・第二分割部
152・・・先端面
154・・・第一線分
300・・・型枠部材
400・・・注入チューブ
731・・・最近位点
732・・・最遠位点
736・・・第二仮想面
738・・・第二法線
α・・・第一交差角
X・・・最先端部
Y・・・距離
Z・・・距離
DESCRIPTION OF SYMBOLS 10, 10B ... Needle body 11 ... Inner peripheral surface 20 ... Inner tube tube 30 ... Outer tube tube 40 ... Outer cylinder grip 41 ... Guide groove 50 ... Operation part 51- ··· Connector 60 ··· Inner cylinder grip 61 ··· Projection portion 70 ··· Connection member 71 ··· Connection portion main body 72 ··· Large diameter portion 73 ··· Base end surface 80 ··· Insertion hole 90 · ···································································································· Endoscope injection needle 110 ··· resin filled portion 130, 130A ... proximal end surface 131, 131A ... · Distal point 136 ··· First normal line 138 ··· Central axis 140 ··· First imaginary plane 142 · · · Point 144 ··· First division portion 146 ··· Second division portion 152 ... tip end surface 154 ... first line segment 300 ... formwork member 400 ... injection tube 731 ... Proximal point 732 ... Distal point 736 ... Second imaginary plane 738 ... Second normal α ... First crossing angle X ... Most advanced portion Y ... Distance Z ... ·distance

Claims (11)

液体を注入するための内管チューブと、
前記内管チューブの先端に設けられた針体と、
前記内管チューブの中心軸の方向に貫通し前記針体が挿通する挿通孔を有し、前記内管チューブの内周面と前記針体の外周面との間に配置され前記針体と前記内管チューブとを接続するための接続部材と、
前記接続部材の基端面より基端側に突出する前記針体の外周面と前記内管チューブの内周面と前記接続部材の前記基端面との間に樹脂部材を充填してなる樹脂充填部と、
を有し、
前記内管チューブの内周面に対する切断面であって前記樹脂充填部の基端面の周縁の最近位点および当該周縁の最遠位点を含み前記中心軸と交差するとともに法線と中心軸との交差角が最小となる切断面である第一仮想面の前記法線である第一法線が、前記中心軸に対し傾斜していることを特徴とする内視鏡用注射針。
An inner tube for injecting liquid;
A needle provided at the tip of the inner tube,
There is an insertion hole that penetrates in the direction of the central axis of the inner tube and passes through the needle body, and is disposed between the inner peripheral surface of the inner tube tube and the outer peripheral surface of the needle body, A connecting member for connecting the inner tube,
A resin filling portion formed by filling a resin member between the outer peripheral surface of the needle body protruding from the base end surface of the connection member to the base end side, the inner peripheral surface of the inner tube, and the base end surface of the connection member. When,
Have
A cutting surface with respect to the inner peripheral surface of the inner tube, which includes the most proximal point of the peripheral edge of the base end surface of the resin-filled portion and the most distal point of the peripheral edge and intersects the central axis, and a normal line and a central axis An endoscope needle, wherein a first normal, which is the normal of the first virtual plane, which is a cut surface having a minimum crossing angle, is inclined with respect to the central axis.
前記内管チューブを進退可能に内包する外管チューブを備える請求項1に記載の内視鏡用注射針。   The injection needle for endoscope according to claim 1, further comprising an outer tube that encloses the inner tube so as to be able to advance and retreat. 前記第一法線と前記中心軸とが交差する角度である第一交差角は、前記接続部材の前記基端面の法線である第二法線と前記中心軸とが交差する角度である第二交差角よりも大きい請求項1または2に記載の内視鏡用注射針。   The first intersection angle, which is the angle at which the first normal line and the central axis intersect, is the angle at which the second normal line, which is the normal line of the base end surface of the connecting member, and the central axis intersect. The injection needle for an endoscope according to claim 1 or 2, which is larger than a two-intersection angle. 前記中心軸と、前記樹脂充填部の前記基端面の前記周縁が形成する平均基端面の法線である第三法線と、が交差する角度である第三交差角は、30°以上90°未満である請求項1から3のいずれか一項に記載の内視鏡用注射針。   A third intersection angle, which is an angle at which the central axis and a third normal line that is a normal line of an average base end surface formed by the peripheral edge of the base end surface of the resin-filled portion, is 30 ° or more and 90 °. The injection needle for an endoscope according to any one of claims 1 to 3, wherein the injection needle is less than the number. 前記樹脂充填部は、前記樹脂充填部の前記基端面の前記周縁の前記最近位点が属する側の半体積が、前記中心軸を介して前記最近位点と対向する前記周縁における対向点が属する半体積よりも大きい請求項1から4のいずれか一項に記載の内視鏡用注射針。   The resin-filled portion has an opposing point at the periphery where the half volume on the side to which the nearest point of the base end surface of the resin-filled portion belongs is opposed to the nearest point via the central axis. The injection needle for endoscope according to any one of claims 1 to 4, wherein the injection needle is larger than a half volume. 前記針体の先端面は、前記中心軸に対して傾斜しており、
前記先端面の最先端部が、前記樹脂充填部の前記基端面の前記周縁の前記最近位点が属する側に配置されている請求項5に記載の内視鏡用注射針。
The tip surface of the needle body is inclined with respect to the central axis,
6. The endoscope injection needle according to claim 5, wherein a most distal end portion of the distal end surface is arranged on a side to which the nearest point of the peripheral edge of the base end surface of the resin filling portion belongs.
前記樹脂充填部の前記基端面の前記周縁の前記最遠位点から、前記接続部材の前記基端面の前記周縁までの距離が、前記針体の外周面と前記内管チューブの内周面との距離以上である請求項1から6のいずれか一項に記載の内視鏡用注射針。   The distance from the most distal point of the peripheral edge of the base end surface of the resin filling portion to the peripheral edge of the base end surface of the connecting member is the outer peripheral surface of the needle body and the inner peripheral surface of the inner tube. The injection needle for an endoscope according to any one of claims 1 to 6, which is equal to or greater than the distance. 前記接続部材の内周面と前記針体の外周面との間に位置し前記接続部材と前記針体とを接続する樹脂材料からなる樹脂接続部を有し、
前記樹脂接続部と前記樹脂充填部とが連続している請求項1から7のいずれか一項に記載の内視鏡用注射針。
A resin connecting portion made of a resin material that is located between the inner peripheral surface of the connecting member and the outer peripheral surface of the needle body and connects the connecting member and the needle body;
The endoscope injection needle according to any one of claims 1 to 7, wherein the resin connection portion and the resin filling portion are continuous.
請求項1から8に記載の内視鏡用注射針を製造する内視鏡用注射針の製造方法であって、
前記接続部材における前記挿通孔に前記接続部材の先端側および基端側から突出するよう前記針体を挿通する挿通工程と、
前記接続部材の基端側に前記接続部材の外径と略同等の内径を有する型枠部材を外嵌する外嵌工程と、
前記型枠部材の内周面と前記針体の外周面と前記接続部材の基端面とに接して前記樹脂部材を前記型枠部材に注入するとともに、先基端方向に対し前記樹脂充填部の基端面が傾斜するよう前記樹脂充填部を形成する樹脂充填部形成工程と、
前記接続部材の少なくとも一部および前記樹脂充填部を内包するよう前記内管チューブを設ける内管チューブ取付工程と、を有することを特徴とする内視鏡用注射針の製造方法。
An endoscope injection needle manufacturing method for manufacturing the endoscope injection needle according to claim 1,
An insertion step of inserting the needle body so as to protrude from the distal end side and the proximal end side of the connection member into the insertion hole in the connection member;
An external fitting step of externally fitting a mold member having an inner diameter substantially equal to the outer diameter of the connection member on the proximal end side of the connection member;
The resin member is injected into the mold member in contact with the inner peripheral surface of the mold member, the outer peripheral surface of the needle body, and the proximal end surface of the connecting member, and the resin filling portion A resin filling portion forming step of forming the resin filling portion so that the base end face is inclined;
An inner tube tube mounting step of providing the inner tube so as to enclose at least a part of the connecting member and the resin filling portion.
前記樹脂充填部形成工程において、前記樹脂部材を前記型枠部材の内側に注入するための注入チューブの先端を前記型枠部材の内周面に寄せて設置し、前記樹脂部材を前記型枠部材に注入することにより、形成される前記樹脂充填部の前記基端面を軸方向に対し傾斜させる請求項9に記載の内視鏡用注射針の製造方法。   In the resin filling portion forming step, a tip of an injection tube for injecting the resin member into the inside of the mold member is placed close to an inner peripheral surface of the mold member, and the resin member is installed in the mold member The method for manufacturing an endoscope injection needle according to claim 9, wherein the base end surface of the resin filling portion to be formed is inclined with respect to the axial direction by being injected into the endoscope. 前記樹脂充填部形成工程において、上面視上、注入チューブの先端を前記針体の最先端部が配置された側に寄せ、形成される前記樹脂充填部の前記最近位点が属する側の前記半体積が、前記対向点が属する前記半体積よりも大きくなるよう樹脂部材を注入する請求項10に記載の内視鏡用注射針の製造方法。   In the resin filling portion forming step, the top end of the injection tube is brought close to the side where the most distal portion of the needle body is arranged in top view, and the half of the side where the nearest point of the resin filling portion to be formed belongs The method for manufacturing an endoscope injection needle according to claim 10, wherein the resin member is injected so that a volume becomes larger than the half volume to which the opposing point belongs.
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