JP6602293B2 - コネクタの混合構成を備えた血管ステント - Google Patents
コネクタの混合構成を備えた血管ステント Download PDFInfo
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- JP6602293B2 JP6602293B2 JP2016521552A JP2016521552A JP6602293B2 JP 6602293 B2 JP6602293 B2 JP 6602293B2 JP 2016521552 A JP2016521552 A JP 2016521552A JP 2016521552 A JP2016521552 A JP 2016521552A JP 6602293 B2 JP6602293 B2 JP 6602293B2
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- A61F2/82—Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/86—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure
- A61F2/90—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure
- A61F2/91—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes
- A61F2/915—Stents in a form characterised by the wire-like elements; Stents in the form characterised by a net-like or mesh-like structure characterised by a net-like or mesh-like structure made from perforated sheet material or tubes, e.g. perforated by laser cuts or etched holes with bands having a meander structure, adjacent bands being connected to each other
- A61F2002/9155—Adjacent bands being connected to each other
- A61F2002/91575—Adjacent bands being connected to each other connected peak to trough
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- A61L2300/00—Biologically active materials used in bandages, wound dressings, absorbent pads or medical devices
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Description
本発明のステント本体は、生体適合性材料で作製される。これらの材料には、コバルト・クロム、ニッケル、マグネシウム、タンタル、チタン、ステンレス鋼、ニチノール、金、白金、インコネル、イリジウム、銀、タングステン、及び/又は別の生体適合性金属、又はこれらのいずれかの合金;炭素又は炭素繊維;酢酸セルロース、硝酸セルロース、シリコーン、ポリエチレンテラフタレート、ポリウレタン、ポリアミド、ポリエステル、ポリオルトエステル、ポリ無水物、ポリエーテルスルホン、ポリカーボネート、ポリプロピレン、高分子量ポリエチレン、ポリテトラフルオロエチレン、又は別の生体適合性ポリマー材料、又はこれらの混合物若しくはコポリマー;ポリ−L−乳酸、ポリ−DL−乳酸、ポリグリコール酸、又はこれらのコポリマー、ポリ無水物、ポリカプロラクトン、ポリヒドロキシブチレートバレレート、又は別の生分解性ポリマー、又はこれらの混合物若しくはコポリマー;タンパク質、細胞外基質成分、コラーゲン、フィブリン、又は別の生物剤;又はこれらのいずれかの適切な混合物が含まれる。
本発明のステントを製造するための技術的態様は、周知であり、本発明の実施を理解するのにそれほど重要ではない。一般論として、ステントは、開口を設けた壁面を有する管状エンベロープを備えた単なる本体である。ステントの製造には、3つの基本的なアプローチを使用する。1つは、個々のステントに切断された連続管状ブランクからステントを形成することができる。フィラメントを形成する壁面の開口は、レーザ切断、写真製版、電子放出、機械加工などの技法によって形成される。或いはステントは、チューブが形成されるように後で行われるストリップ様要素の閉鎖を目指して、例えば上述の技法によって、開口を持つ領域が形成されたストリップ様本体から生成されてもよく、最後にステントは、例えば微細溶接、ろう付け、のり付け、圧着操作などを用いて、ワイヤのループの連続接続によって成形された金属ワイヤから形成することができる。
本発明のステントは、当業者に公知のポリマーで又は治療用物質で又は1種若しくは複数の治療用物質を含有するポリマーでコーティングされてもよい。1種又は複数の治療用物質は、治療用物質を溶媒に溶解し又は混合し、治療用物質及び溶媒の混合物をステントの表面に付着させることによって、本発明のステントに付加することができる。コーティングは、反管腔側にあっても共形であってもよい。
治療用物質には、抗新生物、抗有糸分裂、抗炎症、抗血小板、抗凝固、抗フィブリン、抗トロンビン、抗増殖、抗生物、抗酸化物、及び抗アレルギー物質、並びにこれらの組合せを含めることができる。
本発明のステントは、いくつかの送達システム及び送達方法によって展開することができる。これらの送達システム及び方法は、ステントが自己拡張によって拡張するのか半径方向の拡張力によって拡張するのかに応じて変わることになる。本発明の方法は、進行したアテローム性動脈硬化疾患の存在に起因して局所的な血管損傷を被った患者又は血管閉塞のリスクがある患者における、再狭窄のリスク及び/又は程度を最小限に抑えるようにデザインされる。
新しいステントの製作
ステントを、コバルト−クロム合金(MP35N)から製作する。そのIDが1.2mmから1.8mmに変わるコバルト−クロム管材からレーザ切断する。広範な拡張直径に順応させるために、ステントは6又は9個のクラウンを有する。6−クラウン・ステント(SV)は3.0mmまで拡張することができ、9−クラウン・ステント(MV)は4.0mmまで拡張することができ、ステントの長さは9.5mmから36.5mmまで変化することができる。各パターンは、共通の長手方向軸に沿って位置合わせされた一連の波形リングから構成される。各リングは、縦方向に位置合わせされた3個のリンク/コネクタによって、隣接するリングに接続される(図1参照)。このステントの独自の特徴は、端部リンク部が真っ直ぐであり、それに対してリンク部の残りの部分が蛇行していることである。
フリップ力測定の詳細及び均一なコネクタを持つステントとの比較
種々のステント・デザインの、フリッピングに対する耐性を評価するのに、新しい試験方法を開発した。図3A〜Cは、試験装置及び試験方法を示す。ステントは、このステントの端部クラウンがマンドレルから突き出るように、マンドレルに圧着させた。これを引張り試験機上に配置し、フォース・ゲージに取着された針(5)を、ステントの露出クラウン上に位置決めした。所与の距離だけクラウンを変位させるのに必要な力を使用して、種々のデザインのフリップ力を比較した。
ステントのフォアショートニングを最小限に抑えること
ステントは、圧着(小さい直径)状態からより大きい直径に拡張したときに、フォアショートニングを引き起こす傾向がある。ステントの端部は最初に拡張し、リンクを軸方向に内向きに押すことができ−ステントのフォアショートニングが引き起こされる。この問題は、軸方向の強度が低い状態でステントがより柔軟になったときに悪化する。本発明のステントの開発中の、1つの予期せぬ発見とは、端部バンドで真っ直ぐなリンクを組み込み、端部−リンクの数を2個から3個に増加させることによって、フォアショートニングがかなり低減されることであった。下記の結果は、端部で3重のリンクと真っ直ぐなリンクとを組み合わせることによって、フォアショートニングを数倍低減させることができることを示す。表2を参照されたい。
ステントの縦方向の圧縮を最小限に抑えること
フォアショートニングに加え、縦方向の圧縮は、ステントがより細くなるにつれてより大きな課題となる。縦方向の圧縮は、ガイドワイヤ、カテーテル、及びバルーンが、引き出し手順の最中に又はその後の介入中にステントの縁部(患者の近位)に捕捉されたときに生ずる歪みである。
Claims (18)
- 円周、遠位端、及び近位端を有する管状本体を有する、放射状に拡張可能なステントであって、コバルト・クロム合金製の前記管状本体は、
長手方向軸を画定する複数の環状セグメントであって、各環状セグメントが、一連の9つのピーク及び9つの谷を形成する実質的にジグザグの形状を有し、前記管状本体の前記遠位及び近位端をそれぞれ画定する遠位及び近位環状端部セグメントと、前記2つの環状端部セグメントの間の内部に位置決めされた少なくとも2つの環状セグメントとを含む複数の環状セグメントと、
前記長手方向軸に平行に位置決めされ、且つ、前記複数の環状セグメントを橋掛けする複数のコネクタ・セグメントであって、前記2つの環状端部セグメントとそれらに隣接する環状内部セグメントとの間のコネクタ・セグメントは真っ直ぐでその数が3つであって、前記真っ直ぐなコネクタ・セグメントの長手方向の長さが、0.1mmから0.5mmの間であり、前記環状内部セグメント間のコネクタ・セグメントは弓形であってその数が3つである、複数のコネクタ・セグメントと
を含み、前記ステントの収縮状態の直径は、0.5mmから2.0mmの間であって、前記ステントは、前記収縮状態において前記遠位端及び前記近位端が歪まないように構成されている、ステント。 - 前記複数の環状セグメントの前記ピーク及び谷が各隣接する環状セグメントと180°位相がずれて、第1又は第3の環状セグメントのピークが、前記第1及び第3のセグメントの間に位置決めされた第2の環状セグメントに向かって延び、且つ、前記第2の環状セグメントの谷に対して長手方向に位置合わせされている、請求項1に記載のステント。
- 前記2つの環状端部セグメントとそれらに隣接する環状内部セグメントとの間の前記真っ直ぐなコネクタ・セグメントは、前記管状本体の前記円周に沿って互いに等距離離れて位置決めされている、請求項1に記載のステント。
- 前記複数の環状セグメントの前記ピーク及び谷が各隣接する環状セグメントと同位相であって、第1又は第3の環状セグメントのピークが、前記第1及び第3のセグメントの間に位置決めされた第2の環状セグメントに向かって延び、且つ、前記第2の環状セグメントのピークに対して長手方向に位置合わせされる、請求項1に記載のステント。
- 前記遠位環状端部セグメントと、その隣の2つの内部に位置決めされた環状セグメントとの間のコネクタ・セグメントは、真っ直ぐである、請求項1に記載のステント。
- 前記ステントを劇的に変形させるために必要なフリップ力が、0.2ニュートンよりも大きい、請求項1に記載のステント。
- 薬物溶出コーティングをさらに含む、請求項1に記載のステント。
- ラパマイシン、又はラパマイシン誘導体を含む、請求項7に記載のステント。
- 冠動脈を支持するための寸法を有する、請求項1に記載のステント。
- 末梢動脈を支持するための寸法を有する、請求項1に記載のステント。
- 放射状に拡張可能なステントであって、円周、遠位端、及び近位端を備えるコバルト・クロム合金製の管状本体を有するステントを製造する方法であって、
長手方向軸を画定する複数の環状セグメントを有する前記ステントの前記管状本体を形成するステップであって、各環状セグメントが、一連の9つのピーク及び9つの谷を形成する実質的にジグザグの形状を有し、前記複数の環状セグメントが、前記管状本体の前記遠位及び近位端をそれぞれ画定する遠位及び近位環状端部セグメントと、前記2つの環状端部セグメントの間の内部に位置決めされた少なくとも2つの環状セグメントとを含み、複数のコネクタ・セグメントが、前記長手方向軸に平行に位置決めされ、且つ、前記複数の環状セグメントを橋掛けし、前記2つの環状端部セグメントとそれらに隣接する環状内部セグメントとの間のコネクタ・セグメントは真っ直ぐでその数が3つであって、前記真っ直ぐなコネクタ・セグメントの長手方向の長さが、0.1mmから0.5mmの間であり、前記環状内部セグメント間のコネクタ・セグメントは弓形であってその数は3つである、ステップ
を含み、前記ステントの収縮状態の直径は、0.5mmから2.0mmの間であって、前記ステントは、前記収縮状態において前記遠位端及び前記近位端が歪まないように構成されている、方法。 - 前記複数の環状セグメントの前記ピーク及び谷が各隣接する環状セグメントと180°位相がずれて、第1又は第3の環状セグメントのピークが、前記第1及び第3のセグメントの間に位置決めされた第2の環状セグメントに向かって延び、且つ、前記第2の環状セグメントの谷に対して長手方向に位置合わせされている、請求項11に記載の方法。
- 前記2つの環状端部セグメントとそれらに隣接する環状内部セグメントとの間の前記真っ直ぐなコネクタ・セグメントは、前記管状本体の前記円周に沿って互いに等距離離れて位置決めされている、請求項11に記載の方法。
- 前記複数の環状セグメントの前記ピーク及び谷が各隣接する環状セグメントと同位相であって、第1又は第3の環状セグメントのピークが、前記第1及び第3のセグメントの間に位置決めされた第2の環状セグメントに向かって延び、且つ、前記第2の環状セグメントのピークに対して長手方向に位置合わせされている、請求項11に記載の方法。
- 前記遠位環状端部セグメントと、その隣の2つの内部に位置決めされた環状セグメントとの間のコネクタ・セグメントは、真っ直ぐである、請求項11に記載の方法。
- 前記ステントを劇的に変形させるために必要なフリップ力が、0.2ニュートンよりも大きい、請求項11に記載の方法。
- 薬物溶出コーティングをさらに含む、請求項11に記載の方法。
- 前記コーティングは、ラパマイシン、又はラパマイシン誘導体を含む、請求項17に記載の方法。
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Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP6622914B2 (ja) * | 2015-07-23 | 2019-12-18 | オプティメド メディツィニッシェ インストゥルメンテ ゲーエムベーハーOptimed Medizinische Instrumente Gmbh | ステント |
CN106361478B (zh) * | 2016-11-02 | 2018-08-21 | 江苏大学 | 一种混合型球囊扩张式血管支架 |
US10835398B2 (en) * | 2017-11-03 | 2020-11-17 | Covidien Lp | Meshes and devices for treating vascular defects |
KR102221074B1 (ko) * | 2018-12-24 | 2021-03-02 | 부산대학교 산학협력단 | 생분해성 고분자 및 니티놀을 포함하는 스텐트 및 이의 제조방법 |
CN110279501A (zh) * | 2019-07-18 | 2019-09-27 | 中科益安医疗科技(北京)股份有限公司 | 一种医用植入冠脉支架 |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5133732A (en) | 1987-10-19 | 1992-07-28 | Medtronic, Inc. | Intravascular stent |
US5292331A (en) | 1989-08-24 | 1994-03-08 | Applied Vascular Engineering, Inc. | Endovascular support device |
US5843175A (en) * | 1997-06-13 | 1998-12-01 | Global Therapeutics, Inc. | Enhanced flexibility surgical stent |
US6071308A (en) * | 1997-10-01 | 2000-06-06 | Boston Scientific Corporation | Flexible metal wire stent |
US6309414B1 (en) | 1997-11-04 | 2001-10-30 | Sorin Biomedica Cardio S.P.A. | Angioplasty stents |
US6623521B2 (en) | 1998-02-17 | 2003-09-23 | Md3, Inc. | Expandable stent with sliding and locking radial elements |
CA2322973C (en) | 1998-03-05 | 2011-04-12 | Boston Scientific Limited | Intraluminal stent |
US20020173839A1 (en) | 1998-07-24 | 2002-11-21 | Leopold Eric W. | Intravascular flow modifier and reinforcement device with connected segments |
JP4799738B2 (ja) * | 1999-05-19 | 2011-10-26 | ノイス,マルテ | 放射状に拡大可能な管支持物 |
US6409754B1 (en) | 1999-07-02 | 2002-06-25 | Scimed Life Systems, Inc. | Flexible segmented stent |
WO2001021101A1 (en) | 1999-09-22 | 2001-03-29 | Andrei Vladimirovich Karev | Flexible expandable stent and method for manufacturing the same |
US6331189B1 (en) | 1999-10-18 | 2001-12-18 | Medtronic, Inc. | Flexible medical stent |
US8034097B2 (en) | 2000-05-22 | 2011-10-11 | Malte Neuss | Radially expandable vessel support |
US6818013B2 (en) | 2001-06-14 | 2004-11-16 | Cordis Corporation | Intravascular stent device |
US20060004437A1 (en) * | 2001-08-29 | 2006-01-05 | Swaminathan Jayaraman | Structurally variable stents |
US7025777B2 (en) | 2002-07-31 | 2006-04-11 | Unison Therapeutics, Inc. | Flexible and conformable stent and method of forming same |
US7331987B1 (en) * | 2002-08-16 | 2008-02-19 | Advanced Cardiovascular Systems, Inc. | Intravascular stent and method of use |
US6786922B2 (en) | 2002-10-08 | 2004-09-07 | Cook Incorporated | Stent with ring architecture and axially displaced connector segments |
US6896697B1 (en) * | 2002-12-30 | 2005-05-24 | Advanced Cardiovascular Systems, Inc. | Intravascular stent |
US20050080479A1 (en) | 2003-09-29 | 2005-04-14 | Feng James Q. | Expandable endovascular stent |
US20050149168A1 (en) * | 2003-12-30 | 2005-07-07 | Daniel Gregorich | Stent to be deployed on a bend |
US7578840B2 (en) | 2004-03-31 | 2009-08-25 | Cook Incorporated | Stent with reduced profile |
US20050222671A1 (en) | 2004-03-31 | 2005-10-06 | Schaeffer Darin G | Partially biodegradable stent |
US20060190072A1 (en) | 2005-01-28 | 2006-08-24 | Das Gladwin S | Flexible cells for axially interconnecting stent components |
US7637939B2 (en) | 2005-06-30 | 2009-12-29 | Boston Scientific Scimed, Inc. | Hybrid stent |
WO2007134222A2 (en) | 2006-05-12 | 2007-11-22 | Cordis Corporation | Baloon expandable bioabsorbable drug eluting stent |
GB0616579D0 (en) | 2006-08-21 | 2006-09-27 | Angiomed Ag | Self-expanding stent |
US7988720B2 (en) * | 2006-09-12 | 2011-08-02 | Boston Scientific Scimed, Inc. | Longitudinally flexible expandable stent |
US7842082B2 (en) * | 2006-11-16 | 2010-11-30 | Boston Scientific Scimed, Inc. | Bifurcated stent |
RU2566225C2 (ru) * | 2009-02-09 | 2015-10-20 | ЭВИЗИО МЕДИКАЛ ДЕВАЙСИЗ ЮЭлСи | Стент |
US8568471B2 (en) * | 2010-01-30 | 2013-10-29 | Abbott Cardiovascular Systems Inc. | Crush recoverable polymer scaffolds |
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2014
- 2014-06-18 SG SG11201510447PA patent/SG11201510447PA/en unknown
- 2014-06-18 CN CN201480045953.8A patent/CN105722480A/zh active Pending
- 2014-06-18 ES ES14814637.6T patent/ES2694006T3/es active Active
- 2014-06-18 US US14/307,723 patent/US10548749B2/en active Active
- 2014-06-18 JP JP2016521552A patent/JP6602293B2/ja active Active
- 2014-06-18 WO PCT/US2014/043018 patent/WO2014205124A1/en active Application Filing
- 2014-06-18 EP EP14814637.6A patent/EP3010452B1/en active Active
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2016
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US11648136B2 (en) | 2023-05-16 |
CN105722480A (zh) | 2016-06-29 |
EP3010452A1 (en) | 2016-04-27 |
HK1222115A1 (zh) | 2017-06-23 |
US20140379073A1 (en) | 2014-12-25 |
EP3010452B1 (en) | 2018-08-01 |
WO2014205124A1 (en) | 2014-12-24 |
US20200253758A1 (en) | 2020-08-13 |
JP2016524944A (ja) | 2016-08-22 |
EP3010452A4 (en) | 2017-01-04 |
ES2694006T3 (es) | 2018-12-17 |
SG11201510447PA (en) | 2016-01-28 |
US10548749B2 (en) | 2020-02-04 |
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