JP2003159333A - Core material for guide wire for medical treatment and guide wire for medical treatment - Google Patents

Core material for guide wire for medical treatment and guide wire for medical treatment

Info

Publication number
JP2003159333A
JP2003159333A JP2001361033A JP2001361033A JP2003159333A JP 2003159333 A JP2003159333 A JP 2003159333A JP 2001361033 A JP2001361033 A JP 2001361033A JP 2001361033 A JP2001361033 A JP 2001361033A JP 2003159333 A JP2003159333 A JP 2003159333A
Authority
JP
Japan
Prior art keywords
guide wire
core material
wire
medical guide
insertion portion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2001361033A
Other languages
Japanese (ja)
Inventor
Hiroshi Yamada
廣志 山田
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Terumo Corp
Tokusen Kogyo Co Ltd
Original Assignee
Terumo Corp
Tokusen Kogyo Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Terumo Corp, Tokusen Kogyo Co Ltd filed Critical Terumo Corp
Priority to JP2001361033A priority Critical patent/JP2003159333A/en
Publication of JP2003159333A publication Critical patent/JP2003159333A/en
Pending legal-status Critical Current

Links

Abstract

<P>PROBLEM TO BE SOLVED: To provide a high quality and low cost core material for a guide wire for medical treatment having excellent operability by having appropriate suppleness at an inserting part and by providing appropriate rigidity at a guiding part, and the guide wire for medical treatment. <P>SOLUTION: In the core material, the inserting part has form adaptability, and the guiding part has torque transmittance. The inserting part 2 made of a TiNi wire material and the guiding part 3 made of a SUS304 wire material are integrally bonded at a connection part 4 made of a Ni foil. <P>COPYRIGHT: (C)2003,JPO

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、治療や検査を必要
とする血管、消化管、気管、その他体腔(以下、要治療
管という)内に導入する細い管状のカテーテルを案内す
るのに用いる医療用ガイドワイヤ用芯材(以下、芯材と
もいう)及び医療用ガイドワイヤ(以下、ガイドワイヤ
ともいう)に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to medical treatment used for guiding a thin tubular catheter to be introduced into a blood vessel, digestive tract, trachea, or other body cavity (hereinafter referred to as a treatment-necessary tube) that requires treatment or inspection. The present invention relates to a guide wire core material (hereinafter, also referred to as a core material) and a medical guide wire (hereinafter, also referred to as a guide wire).

【0002】[0002]

【従来の技術】ガイドワイヤの構造は用途に応じて種々
のものがあるが、一般的には、図3(a)に示すよう
に、所定長さの芯材10の周囲を合成樹脂11で被覆し
たものと、図3(b)に示すように、所定長さの芯材1
2の周囲をコイルスプリング13で被包したものとがあ
る。そして、図3(a)(b)に示すように、芯材10
と12にはガイドワイヤとしての挿入部分に柔軟性を付
与するため、挿入部10aと12aは次第に断面積が減
少する先細形状に形成されている。
2. Description of the Related Art Although there are various guide wire structures depending on the intended use, generally, as shown in FIG. 3 (a), a synthetic resin 11 surrounds a core material 10 of a predetermined length. As shown in FIG. 3 (b), the coated material and the core material 1 having a predetermined length
There is one in which the circumference of 2 is covered with a coil spring 13. Then, as shown in FIGS. 3A and 3B, the core material 10
Insertions 10a and 12a are formed in a tapered shape whose cross-sectional area gradually decreases in order to give flexibility to the insertion portions as guide wires.

【0003】上記芯材には、ステンレス鋼線またはピア
ノ線が従来から用いられている。しかし、この種の芯材
を用いたガイドワイヤは、先端部分を先細形状にしても
柔軟性に欠け、複雑に蛇行する分岐血管等に対しては適
用し難いという問題があった。
Conventionally, a stainless steel wire or a piano wire has been used as the core material. However, the guide wire using this type of core material has a problem that it is not flexible even if the tip portion is tapered, and it is difficult to apply it to a branching blood vessel that meanders in a complicated manner.

【0004】そこで、芯材として、超弾性合金である、
(1)Ti−Ni−Fe系合金を用いたガイドワイヤ
(例えば、特公平4−2273号公報)、(2)Ti−
Ni系合金を用いたガイドワイヤ(例えば、特公平4−
8065号公報)、(3)Co−Ni−Cr−Fe系合
金を用いたガイドワイヤ(例えば、特開平6−6315
1号公報)等が提案されている。
Therefore, the core material is a superelastic alloy,
(1) A guide wire using a Ti-Ni-Fe alloy (for example, Japanese Patent Publication No. 4-2273), (2) Ti-
A guide wire using a Ni-based alloy (for example, Japanese Patent Publication No. 4-
8065), (3) a guide wire using a Co-Ni-Cr-Fe-based alloy (for example, Japanese Patent Laid-Open No. 6-6315).
No. 1) has been proposed.

【0005】ここで、超弾性とは、特開平6−6315
1号公報第1欄第50行〜第2欄第7行にも記載されて
いるように、回復可能な弾性歪みが数%から数十%と大
きく、しかも歪みが増加しても荷重の大きさが変わらな
いという特性を意味する。
Here, the term "superelasticity" means Japanese Patent Laid-Open No. 6-6315.
As described in column 1, line 50 to column 2, line 7 of Japanese Patent Publication No. 1, the recoverable elastic strain is as large as several% to several tens%, and the load is large even if the strain increases. It means that the characteristics do not change.

【0006】上記超弾性合金からなる芯材は、柔軟でか
なりの範囲までの変形(約8%の歪み)に対しても復元
性を有するため、手元操作中、折れ曲がりが生じ難く、
且つ曲がりぐせがつきにくいなどの利点を有している。
Since the core material made of the above-mentioned superelastic alloy is flexible and has a restoring property to a deformation to a considerable extent (strain of about 8%), it is hard to be bent during the hand operation.
Moreover, it has an advantage that it is hard to bend.

【0007】[0007]

【発明が解決しようとする課題】ところで、ガイドワイ
ヤとして重要な性能は、手元操作によって要治療管内に
スムーズに挿入できて、カテーテルを目的部位に正確に
案内導入できることである。このため、ガイドワイヤに
用いる芯材には、挿入部が複雑に蛇行する要治療管に対
応し、且つ要治療管の内壁を傷つけることなく挿入し得
る形態順応性を備え、これに続く導入部が手元での微妙
な操作量でも挿入部に正確に伝達するトルク伝達性を備
えていることが要求されている。
By the way, the important performance of the guide wire is that it can be smoothly inserted into the treatment-needed tube by manual operation, and the catheter can be accurately guided and introduced into the target site. Therefore, the core material used for the guide wire has a conformability that allows the insertion portion to be complicatedly meandering and needs to be inserted without damaging the inner wall of the treatment-requiring tube. Is required to have torque transmissibility that accurately transmits to the insertion portion even with a delicate operation amount at hand.

【0008】そして、今日、医療技術の発達に応じて、
複雑な分岐血管に対しても適用できるようにするため、
ガイドワイヤの芯材には、挿入部の形態順応性と導入部
のトルク伝達性を、より一層向上することが求められて
いる。
[0008] Today, with the development of medical technology,
In order to be applicable to complex branch vessels,
The core material of the guide wire is required to further improve the conformability of the insertion portion and the torque transmissibility of the introduction portion.

【0009】しかし、上記(1)および(3)の芯材を
用いたガイドワイヤは、芯材が超弾性合金の単一材料か
らなるため、全体として、超弾性があって形態順応性を
充分に備えているが、伝達可能トルク及びねじり剛性が
ステンレス鋼線またはピアノ線に比較して劣るため、導
入部のトルク伝達性に難点がある。
However, in the guide wire using the core material of the above (1) and (3), the core material is made of a single material of a superelastic alloy, so that it has superelasticity as a whole and is sufficiently conformable. However, since the transmissible torque and the torsional rigidity are inferior to those of the stainless steel wire or the piano wire, there is a problem in the torque transmissibility of the introduction portion.

【0010】また、上記(2)の芯材を用いたガイドワ
イヤは、超弾性合金の単一材料で構成した芯材の挿入部
と導入部の熱処理条件を変えることにより、挿入部に形
態順応性を付与し、導入部にトルク伝達性を付与したも
のであるが、高価な超弾性合金を用いて熱処理している
ため、材料コストおよび処理コストが高くなり、製造コ
ストが上昇する。
The guide wire using the core material of the above (2) conforms to the insertion portion by changing the heat treatment conditions of the insertion portion and the introduction portion of the core material made of a single superelastic alloy material. However, since the heat treatment is performed using an expensive superelastic alloy, the material cost and the processing cost increase, and the manufacturing cost increases.

【0011】本発明は従来の技術の有するこのような問
題点に鑑みてなされたものであって、その目的は、挿入
部に適度の柔軟性を有し且つ導入部に適度の剛性を備え
ることにより優れた操作性を有する、高品質で低コスト
の医療用ガイドワイヤ用芯材および医療用ガイドワイヤ
を提供することにある。
The present invention has been made in view of the above problems of the prior art, and an object thereof is to provide the insertion portion with appropriate flexibility and the introduction portion with appropriate rigidity. Accordingly, it is an object of the present invention to provide a high-quality, low-cost core material for a medical guide wire and a medical guide wire having superior operability.

【0012】[0012]

【課題を解決するための手段】上記目的を達成するため
に本発明の医療用ガイドワイヤ用芯材は、挿入部が形態
順応性を備え、導入部がトルク伝達性を備えた芯材であ
って、上記挿入部と導入部とを化学組成の異なる線材で
構成し、且つ挿入部と導入部を一体に接合したことを特
徴としている。
In order to achieve the above object, the core material for a medical guide wire according to the present invention is a core material in which the insertion part has conformability and the introduction part has torque transmission properties. In addition, the insertion portion and the introduction portion are made of wires having different chemical compositions, and the insertion portion and the introduction portion are integrally joined.

【0013】ここで、形態順応性とは、複雑な分岐血管
にも内壁を傷つけることなく容易に挿入しうる特性を意
味し、トルク伝達性とは、微妙な手元操作量を先端部
(挿入部)に正確に伝達し得る特性を意味し、具体的に
は、挿入部を、Ti−Ni系合金、Cu−Al−Ni系
合金またはFe−Ni−Co−Ti系合金の線材で構成
し、導入部を、ステンレス鋼またはCo−Ni−Cr−
Fe系合金の線材で構成することによって、上記特性を
達成することができる。
Here, the morphological adaptability means a characteristic that even a complicated branch blood vessel can be easily inserted without damaging the inner wall, and the torque transmissibility means a delicate hand operation amount at the tip (insertion portion). ) Means that it can be accurately transmitted, specifically, the insertion portion is composed of a wire rod of Ti-Ni alloy, Cu-Al-Ni alloy or Fe-Ni-Co-Ti alloy, The introduction part is made of stainless steel or Co-Ni-Cr-
The above-mentioned characteristics can be achieved by using a wire of an Fe-based alloy.

【0014】挿入部と導入部とは、各種接着材で接合し
てもよいが、それぞれの部分を構成する線材と親和性を
有するろう接合金を介して接合するのが好ましい。
The insertion portion and the introduction portion may be joined by various adhesives, but it is preferable that they be joined through a brazing filler metal having an affinity with the wire material forming each portion.

【0015】上記ろう接合金としては、Bを含有する銀
ろう、Ni箔、またはBとSiを含有し残部がNiから
なるアモルファス箔が好ましい。
The brazing alloy is preferably silver braze containing B, Ni foil, or amorphous foil containing B and Si with the balance being Ni.

【0016】上記芯材を用いて、合成樹脂や複合材料等
で被覆したり、コイルスプリングで被包することによ
り、医療用ガイドワイヤを構成することができる。
A medical guide wire can be constructed by covering the core material with a synthetic resin, a composite material or the like, or enclosing it with a coil spring.

【0017】[0017]

【発明の実施の形態】本発明の実施の形態を図面に基づ
いて説明する。
BEST MODE FOR CARRYING OUT THE INVENTION Embodiments of the present invention will be described with reference to the drawings.

【0018】図1において、所定の長さ(例えば、20
00〜3000mm)を有する医療用ガイドワイヤ用芯材
1は、挿入部2と導入部3とを接合部4で一体に接合し
てなり、挿入部2と導入部3とは、挿入部2の弾性限度
が導入部3の弾性限度より大きく、導入部3のねじり剛
性が挿入部2のねじり剛性より大きくなるような関係を
満たすように、化学組成の異なる線材で構成されてい
る。
In FIG. 1, a predetermined length (for example, 20
The core material 1 for a medical guide wire having a diameter of 0 to 3000 mm is formed by integrally joining the insertion portion 2 and the introduction portion 3 at the joint portion 4, and the insertion portion 2 and the introduction portion 3 are Wires having different chemical compositions are formed so that the elastic limit is larger than the elastic limit of the introducing portion 3 and the torsional rigidity of the introducing portion 3 is larger than the torsional rigidity of the inserting portion 2.

【0019】挿入部2の長さは、特に限定されるもので
はないが、通常100〜300mm程度とする。さらに、
挿入部2の形状は導入部3と同一でもよいが、図1に示
すように、先端に向けて断面積が次第に減少する先細形
状に成形すると、より一層柔軟になり形態順応性を向上
することができる。
The length of the insertion portion 2 is not particularly limited, but is usually about 100 to 300 mm. further,
The shape of the insertion portion 2 may be the same as that of the introduction portion 3, but as shown in FIG. 1, if the insertion portion 2 is formed in a tapered shape with the cross-sectional area gradually decreasing toward the tip, it becomes even more flexible and improves the conformability of the shape. You can

【0020】挿入部2を構成する線材としては、Ti−
Ni系合金、Cu−Al−Ni系合金またはFe−Ni
−Co−Ti系合金から選択したいずれかの合金を用い
ることができる。そして、挿入部2としての必要な特性
を考慮すると、Ti−Ni系合金としては、Ni=50
〜52原子%で残部がTiからなるもの、Cu−Al−
Ni系合金としては、Al=13〜15原子%、Ni=
3〜5原子%で残部がCuからなるもの、Fe−Ni−
Co−Ti系合金としては、Ni=32〜34原子%、
Co=10〜15原子%、Ti=3〜6原子%で残部が
Feからなるものが好ましい。
As the wire material forming the insertion portion 2, Ti-
Ni-based alloy, Cu-Al-Ni-based alloy or Fe-Ni
Any alloy selected from -Co-Ti alloys can be used. Then, considering the characteristics required for the insertion portion 2, as the Ti—Ni-based alloy, Ni = 50.
.About.52 atomic% and balance Ti, Cu--Al--
As a Ni-based alloy, Al = 13 to 15 atomic%, Ni =
Fe-Ni-, with 3 to 5 atomic% and the balance being Cu
As a Co-Ti alloy, Ni = 32 to 34 atomic%,
It is preferable that Co = 10 to 15 atomic%, Ti = 3 to 6 atomic%, and the balance being Fe.

【0021】導入部3を構成する線材としては、ステン
レス鋼またはCo−Ni−Cr−Fe系合金を用いるこ
とができる。そして、導入部3としての必要な特性を考
慮すると、ステンレス鋼としては、SUS304、SU
S316、SUS403、SUS410、SUS420
J2、SUS329J1、SUS630、SUS631
などが好ましく、Co−Ni−Cr−Fe系合金として
は、Ni=9〜11原子%、Cr=19〜21原子%、
Fe=3原子%以下で残部がCoからなるものが好まし
い。
As the wire material forming the introducing portion 3, stainless steel or Co-Ni-Cr-Fe alloy can be used. Then, considering the characteristics required for the introduction part 3, as stainless steel, SUS304, SU
S316, SUS403, SUS410, SUS420
J2, SUS329J1, SUS630, SUS631
And the like, and as the Co-Ni-Cr-Fe-based alloy, Ni = 9 to 11 atomic%, Cr = 19 to 21 atomic%,
It is preferable that Fe = 3 atomic% or less and the balance be Co.

【0022】挿入部2と導入部3を構成する線材は、用
途に応じて適宜組み合わせることができるが、Ti−N
i系合金とステンレス鋼(例えば、SUS304)の組
み合わせが低コスト化を図りうる点から好ましい。
The wire rods forming the insertion portion 2 and the introduction portion 3 can be appropriately combined depending on the application, but Ti--N
A combination of an i-based alloy and stainless steel (for example, SUS304) is preferable from the viewpoint of cost reduction.

【0023】挿入部2と導入部3とを溶接によって直接
接合すると、金属間化合物(例えば、FeTi)によ
り、接合部4が脆化することがあるので、挿入部2と導
入部3を構成する両方の線材に対して親和性を有する低
融点のろう接合金を介して挿入部2と導入部3を接合す
るのが好ましい。
If the insertion portion 2 and the introduction portion 3 are directly joined by welding, the joint portion 4 may become brittle due to an intermetallic compound (eg, FeTi). Therefore, the insertion portion 2 and the introduction portion 3 are formed. It is preferable to join the insertion portion 2 and the introduction portion 3 through a low melting point brazing metal having affinity for both wire rods.

【0024】上記ろう接合金としては、Bを3原子%含
有する銀ろう、Ni箔、または2〜4原子%のBと2〜
4原子%のSiを含有し残部がNiからなるアモルファ
ス箔を用いることができる。これらのうち、挿入部2に
Ti−Ni系合金を用いると、その親和性の点でNi箔
が好ましい。また、ろう接合金の厚みとしては、ねじり
剛性の点から、医療用ガイドワイヤ用芯材1の直径、す
なわち、挿入部2と導入部3の線材の直径(0.2〜
0.7mm程度)の1/3〜1/5程度が好ましい。
As the brazing alloy, silver brazing alloy containing 3 atomic% of B, Ni foil, or 2 to 4 atomic% of B and 2 to 2 atomic% is used.
An amorphous foil containing 4 atomic% of Si and the balance of Ni can be used. Among these, when a Ti—Ni-based alloy is used for the insertion portion 2, Ni foil is preferable from the viewpoint of its affinity. Further, as the thickness of the brazing metal, from the viewpoint of torsional rigidity, the diameter of the medical guidewire core material 1, that is, the diameter of the wire rod of the insertion portion 2 and the introduction portion 3 (0.2 to
It is preferably about 1/3 to 1/5 of about 0.7 mm).

【0025】挿入部2と導入部3との接合手段として
は、レーザ溶接または電子ビーム溶接を使用することが
できる。このうち、特に、通常の光に比較して単色性と
指向性がよく、位相が揃っており、極めて集光性がよい
という性質をもつレーザ光を利用したレーザ溶接が好ま
しい。というのは、エネルギー密度が非常に大きな微小
スポットにより、高精度溶接が可能となるからである。
Laser welding or electron beam welding can be used as a joining means for the insertion portion 2 and the introduction portion 3. Of these, laser welding using laser light, which has a property of having good monochromaticity and directivity, uniform phase, and extremely good light-collecting property as compared with normal light, is particularly preferable. This is because minute spots with a very large energy density enable high-precision welding.

【0026】以上のような芯材を用いた医療用ガイドワ
イヤは、図2(a)に示すように、医療用ガイドワイヤ
用芯材1の全体を合成樹脂5で被覆するか、または、図
2(b)に示すように、挿入部2のみを合成樹脂5で被
覆することによって得ることができる。合成樹脂として
は、ポリエチレン、ポリエステル、ポリプロピレン、ポ
リウレタン、シリコーンゴム等の公知の材料を使用する
ことができる。
In the medical guide wire using the core material as described above, as shown in FIG. 2 (a), the entire core material 1 for the medical guide wire is coated with the synthetic resin 5, or As shown in FIG. 2 (b), it can be obtained by covering only the insertion part 2 with the synthetic resin 5. As the synthetic resin, known materials such as polyethylene, polyester, polypropylene, polyurethane and silicone rubber can be used.

【0027】[0027]

【実施例】以下に、本発明の実施例を説明する。導入部
材として、SUS304組成の合金を真空炉で溶解し、
鍛造後、1100℃以上の温度で熱間圧延を行い、線径
5mmに圧延した。次に、この圧延材を1050℃で焼鈍
後急冷し、加工率20%の冷間伸線と焼鈍を繰り返して
0.7mmの線材とした。その後、1050℃で溶体化処
理後、加工率82%で0.3mmに最終冷間伸線後、50
0℃のAr雰囲気中で30秒間時効処理を施した。
EXAMPLES Examples of the present invention will be described below. As an introduction member, an alloy of SUS304 composition is melted in a vacuum furnace,
After forging, hot rolling was performed at a temperature of 1100 ° C. or higher, and the wire diameter was 5 mm. Next, this rolled material was annealed at 1050 ° C. and then rapidly cooled, and cold drawing and annealing at a working rate of 20% were repeated to obtain a 0.7 mm wire material. Then, after solution heat treatment at 1050 ° C, the final cold drawing to 0.3 mm at a working rate of 82%, and then 50
Aging treatment was performed for 30 seconds in an Ar atmosphere at 0 ° C.

【0028】一方、挿入部材として、Ni51原子%で
残部がTiからなるTi−Ni系合金を真空炉で溶解
し、鍛造後、800℃以上の温度で熱間圧延を行い、線
径5mmに圧延した。次に、この圧延材を800℃で焼鈍
後急冷し、加工率20%の冷間伸線と焼鈍を繰り返して
0.4mmの線材とした。その後、800℃で溶体化処理
後、加工率44%で0.3mmに最終冷間伸線後、400
℃のAr雰囲気中で2分間時効処理を施した。
On the other hand, as an insert member, a Ti-Ni alloy containing 51 atomic% of Ni and the balance of Ti was melted in a vacuum furnace, forged, and then hot-rolled at a temperature of 800 ° C. or higher, and rolled to a wire diameter of 5 mm. did. Next, this rolled material was annealed at 800 ° C. and then rapidly cooled, and cold drawing and annealing at a working rate of 20% were repeated to obtain a wire material of 0.4 mm. Then, after solution heat treatment at 800 ℃, final cold drawing to 0.3mm at a working rate of 44%, 400
Aging treatment was performed for 2 minutes in an Ar atmosphere at 0 ° C.

【0029】次に、0.3mmのTiNi線材とSUS3
04線材との間に厚さ0.1mmのNi箔を挿入し、線径
0.3mmのTiNi線材とSUS304線材の両方に対
して、Ni箔に向かって僅かな力を加えてNi箔を固定
し、その上からYAGレーザ溶接機を用いてNi箔を含
む接合部付近にレーザ照射し、TiNi線材とSUS3
04線材とをレーザ溶接により接合し、図1に示すよう
な医療ガイドワイヤ用芯材1を得た。なお、この溶接
時、Ni箔の温度が約1450℃(Niの融点)にな
り、かつTiNi線材とSUS304線材とが直接固溶
しないように、レーザの焦点を多少ぼかして照射した。
Next, 0.3 mm TiNi wire and SUS3
Insert a 0.1 mm thick Ni foil between the 04 wire rod and fix the Ni foil by applying a slight force toward both the NiNi wire rod and the SUS304 wire rod with a wire diameter of 0.3 mm. Then, the vicinity of the joint including the Ni foil is laser-irradiated from above using a YAG laser welding machine, and the TiNi wire and SUS3 are welded.
The No. 04 wire was joined by laser welding to obtain a core material 1 for a medical guide wire as shown in FIG. During this welding, the focus of the laser was slightly blurred so that the temperature of the Ni foil became about 1450 ° C. (melting point of Ni) and the TiNi wire and the SUS304 wire did not directly form a solid solution.

【0030】また、比較例1として、上記と同様の方法
で製造した線径0.3mmのTiNi線材と同じ線径0.
3mmのTiNi線材との間に厚さ0.1mmのNi箔を挿
入し、2本の線径0.3mmのTiNi線材に対して、N
i箔に向かって僅かな力を加えてNi箔を固定し、その
上からYAGレーザ溶接機を用いてNi箔を含む接合部
付近にレーザ照射し、TiNi線材同士をレーザ溶接に
より接合した。なお、この溶接時、Ni箔の温度が約1
450℃(Niの融点)になり、かつTiNi線材が直
接固溶しないように、レーザの焦点を多少ぼかして照射
した。
As Comparative Example 1, a TiNi wire rod having a wire diameter of 0.3 mm and a wire diameter of 0.
Insert a 0.1 mm thick Ni foil between the 3 mm TiNi wire and the two NiNi wires with a diameter of 0.3 mm.
The Ni foil was fixed by applying a slight force toward the i foil, and the vicinity of the joint including the Ni foil was irradiated with laser using a YAG laser welding machine, and the TiNi wires were joined by laser welding. The temperature of the Ni foil was about 1 during this welding.
Irradiation was performed by slightly blurring the laser focus so that the temperature became 450 ° C. (melting point of Ni) and the TiNi wire rod did not directly form a solid solution.

【0031】さらに、比較例2として、上記と同様の方
法で、線径0.3mmのTiNi線材単体のものも製造し
た。
Further, as Comparative Example 2, a TiNi wire alone having a wire diameter of 0.3 mm was manufactured by the same method as described above.

【0032】そして、上記のようにして得た本発明の医
療用ガイドワイヤ用芯材と比較例のものにおいて、伝達
可能トルクとねじり剛性比を測定した結果を以下の表1
に示す。
Then, the results of measuring the transmissible torque and the torsional rigidity ratio of the core material for a medical guide wire of the present invention and the comparative example obtained as described above are shown in Table 1 below.
Shown in.

【0033】[0033]

【表1】 [Table 1]

【0034】「伝達可能トルク」とは、素材の先端をト
ルク計で保持し、基端部からねじり変形を与えた後、こ
の変形を解除して永久ねじり変形が発生していないこと
を確認した後、さらに大きな変形を与えることを繰り返
して、永久ねじり変形が発生しない最大トルクをいう。
The term "transmittable torque" means that the tip of the material is held by a torque meter, and after the base end is twisted and deformed, this deformation is released to confirm that permanent twisting is not generated. After that, the maximum torque at which permanent torsional deformation does not occur is repeated by further applying a larger deformation.

【0035】「ねじり剛性比」とは、所定のトルクを加
えたときのねじれ角度を、比較例1を1としたときの指
数で示したものである。
The "torsional rigidity ratio" is an index when the torsion angle when a predetermined torque is applied is set to 1 in Comparative Example 1.

【0036】表1に明らかなように、本発明の医療用ガ
イドワイヤ用芯材は、比較例1、2のものに比べて伝達
可能トルクとねじり剛性比が極めて大きく、トルク伝達
性に優れていることが分かる。
As is clear from Table 1, the core material for a medical guide wire of the present invention has an extremely large transmissible torque and torsional rigidity ratio as compared with those of Comparative Examples 1 and 2, and is excellent in torque transmissibility. I know that

【0037】[0037]

【発明の効果】本発明によれば、挿入部に適度の柔軟性
を有し且つ導入部に適度の剛性を備えることにより優れ
た操作性を有する、高品質で低コストの医療用ガイドワ
イヤ用芯材および医療用ガイドワイヤを提供することが
できる。
EFFECTS OF THE INVENTION According to the present invention, a medical guide wire of high quality and low cost, which has an excellent operability by having an appropriate flexibility in the insertion portion and an appropriate rigidity in the introduction portion, is provided. A core material and a medical guide wire can be provided.

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

【図1】本発明の医療用ガイドワイヤ用芯材の断面図で
ある。
FIG. 1 is a cross-sectional view of a core material for a medical guide wire according to the present invention.

【図2】図2(a)、(b)は本発明の医療用ガイドワ
イヤの断面図である。
2 (a) and 2 (b) are cross-sectional views of the medical guide wire of the present invention.

【図3】従来の医療用ガイドワイヤの断面図である。FIG. 3 is a cross-sectional view of a conventional medical guide wire.

【符号の説明】[Explanation of symbols]

1…医療用ガイドワイヤ用芯材 2…挿入部 3…導入部 4…接合部 5…合成樹脂 1 ... Core material for medical guide wire 2 ... insertion part 3 ... Introduction 4 ... Joint 5 ... Synthetic resin

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4C081 AC08 BB04 BB07 BB08 CA022 CA162 CA212 CA272 CG03 CG04 CG05 CG07 DA03 DC03 DC05 4C167 AA28 BB02 BB03 BB11 BB14 BB20 BB38 BB47 CC08 CC20 CC21 CC22 CC23 FF03 GG02 GG03 GG05 GG06 GG08 GG14 GG21 GG22 GG23 GG24 HH03 HH17    ─────────────────────────────────────────────────── ─── Continued front page    F-term (reference) 4C081 AC08 BB04 BB07 BB08 CA022                       CA162 CA212 CA272 CG03                       CG04 CG05 CG07 DA03 DC03                       DC05                 4C167 AA28 BB02 BB03 BB11 BB14                       BB20 BB38 BB47 CC08 CC20                       CC21 CC22 CC23 FF03 GG02                       GG03 GG05 GG06 GG08 GG14                       GG21 GG22 GG23 GG24 HH03                       HH17

Claims (8)

【特許請求の範囲】[Claims] 【請求項1】 挿入部が形態順応性を備え、導入部がト
ルク伝達性を備えた芯材であって、上記挿入部と導入部
とを化学組成の異なる線材で構成し、且つ挿入部と導入
部を一体に接合したことを特徴とする医療用ガイドワイ
ヤ用芯材。
1. A core material in which the insertion portion has conformability and the introduction portion has torque transmission properties, and the insertion portion and the introduction portion are made of wire rods having different chemical compositions, and A core material for a medical guide wire, wherein the introduction portion is integrally joined.
【請求項2】 挿入部を構成する線材が、Ti−Ni系
合金、Cu−Al−Ni系合金またはFe−Ni−Co
−Ti系合金であり、導入部を構成する線材が、ステン
レス鋼またはCo−Ni−Cr−Fe系合金である請求
項1記載の医療用ガイドワイヤ用芯材。
2. The wire material constituting the insert portion is a Ti—Ni based alloy, a Cu—Al—Ni based alloy or a Fe—Ni—Co alloy.
The core material for a medical guide wire according to claim 1, which is a -Ti-based alloy and the wire material constituting the introduction portion is stainless steel or a Co-Ni-Cr-Fe-based alloy.
【請求項3】 挿入部と導入部とを、それぞれの部分を
構成する線材と親和性を有するろう接合金を介して接合
した請求項1または2記載の医療用ガイドワイヤ用芯
材。
3. The core material for a medical guide wire according to claim 1 or 2, wherein the insertion portion and the introduction portion are joined via a brazing filler metal having an affinity with the wire material forming each portion.
【請求項4】 ろう接合金が、Bを含有する銀ろう、N
i箔、またはBとSiを含有し残部がNiからなるアモ
ルファス箔である請求項3記載の医療用ガイドワイヤ用
芯材。
4. The braze alloy is a silver braze containing B, N.
The core material for a medical guide wire according to claim 3, which is an i foil or an amorphous foil containing B and Si with the balance being Ni.
【請求項5】 請求項1記載の芯材を用いた医療用ガイ
ドワイヤ。
5. A medical guide wire using the core material according to claim 1.
【請求項6】 請求項2記載の芯材を用いた医療用ガイ
ドワイヤ。
6. A medical guide wire using the core material according to claim 2.
【請求項7】 請求項3記載の芯材を用いた医療用ガイ
ドワイヤ。
7. A medical guide wire using the core material according to claim 3.
【請求項8】 請求項4記載の芯材を用いた医療用ガイ
ドワイヤ。
8. A medical guide wire using the core material according to claim 4.
JP2001361033A 2001-11-27 2001-11-27 Core material for guide wire for medical treatment and guide wire for medical treatment Pending JP2003159333A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
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Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
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Publications (1)

Publication Number Publication Date
JP2003159333A true JP2003159333A (en) 2003-06-03

Family

ID=19171756

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Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2003159333A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
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JP2009172229A (en) * 2008-01-25 2009-08-06 Kanai Hiroaki Guide wire core, manufacturing method of this core, and medical guide wire using this core
US7892187B2 (en) 2002-08-23 2011-02-22 Terumo Kabushiki Kaisha Guide wire
JP2011041612A (en) * 2009-08-19 2011-03-03 Patentstra Co Ltd Medical guide wire, method of manufacturing the same and assembly of medical guide wire and microcatheter or balloon catheter and guiding catheter
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US8206837B2 (en) * 2007-01-12 2012-06-26 Terumo Kabushiki Kaisha Interventional medical device
US8487210B2 (en) 2010-06-11 2013-07-16 W. C. Hereaus GmbH Joined dissimilar materials and method
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KR101153506B1 (en) * 2003-12-18 2012-06-11 테루모 가부시키가이샤 Guide wire
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KR101326997B1 (en) * 2003-12-18 2013-11-14 테루모 가부시키가이샤 Guide wire
US8206837B2 (en) * 2007-01-12 2012-06-26 Terumo Kabushiki Kaisha Interventional medical device
US8568470B2 (en) 2007-05-09 2013-10-29 Japan Science And Technology Agency Guide wire and stent
US8052620B2 (en) 2007-05-09 2011-11-08 Japan Science And Technology Agency Guide wire and stent
JP2009172229A (en) * 2008-01-25 2009-08-06 Kanai Hiroaki Guide wire core, manufacturing method of this core, and medical guide wire using this core
JP2011041612A (en) * 2009-08-19 2011-03-03 Patentstra Co Ltd Medical guide wire, method of manufacturing the same and assembly of medical guide wire and microcatheter or balloon catheter and guiding catheter
US8835799B2 (en) 2009-12-22 2014-09-16 Heraeus Precious Metals Gmbh & Co. Kg Method of joining dissimilar materials
US8487210B2 (en) 2010-06-11 2013-07-16 W. C. Hereaus GmbH Joined dissimilar materials and method
DE102011102986B4 (en) 2010-06-11 2023-01-12 Heraeus Deutschland GmbH & Co. KG Interconnected disparate materials and processes
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