JP7382220B2 - 光硬化性接着剤を用いた硬化療法のための組成物およびデバイス - Google Patents
光硬化性接着剤を用いた硬化療法のための組成物およびデバイス Download PDFInfo
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- JP7382220B2 JP7382220B2 JP2019229101A JP2019229101A JP7382220B2 JP 7382220 B2 JP7382220 B2 JP 7382220B2 JP 2019229101 A JP2019229101 A JP 2019229101A JP 2019229101 A JP2019229101 A JP 2019229101A JP 7382220 B2 JP7382220 B2 JP 7382220B2
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2430/00—Materials or treatment for tissue regeneration
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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Description
好ましい態様では、上記組成物は、治療される静脈セグメント100mmにつき、0.001~1.0gの接着剤、好ましくは0.001~0.5、さらに好ましくは、0.001~0.1g/100mmを含む。
より好ましい態様では、上記組成物は、治療される静脈セグメント100mmにつき、0.01~1.0gの接着剤、好ましくは0.05~0.5、さらに好ましくは、0.005~0.1g/100mmを含む。
好ましくは、静脈疾患は静脈不全、膨張静脈、静脈瘤、拡張症または動脈瘤の群から選択される。
さらに好ましい実施形態では、接着剤およびガスは、本発明の注入カテーテル装置に負荷され、その後のボーラスに適用される。好ましくは、接着剤は、薬学的に許容される組織接着剤である。好ましくは、接着剤はまた、光硬化または光活性化接着剤であり、ガスは、静脈内使用のために許容される医療ガスである。
a.より小さい管をより大きな管内に配置して機能ユニットを形成する、大きな管および小さな管であって、
b.両方の管は、任意に再配置可能および取り外し可能であり、
c.両方の管は、両端に開口部を有し、
d.一つの開口部が先端から5mmと40mmとの間の距離に位置する外管の壁に設けられるか、またはいくつかの開口部が先端から5mm~250mmのセグメントに位置し、ここで一つの開口の直径は外管の内径の70%と120%との間であり、またはいくつかの開口部の場合には各開口部につき、外管の内径の30%~60%であり;いくつかの開口部の場合には:サイズ、形状および配給は、(フォーム)硬化薬の均一な展開を提供するように設けられているもの、
e.および光源または光伝導体を含み、
f.内管の外径は0.6mmと2.0mmとの間であり、内径は0.3~1.6mm、より好ましくは0.4~1.0mm、さらにより好ましくは0.5~0.8mmであり、
g.外管の外径は、1.3mmと3.3mmとの間であり、内径は1.1~3.0mm、好ましくは1.1~2.8mm、さらにより好ましくは1.1~2.7mmであり、内管の外壁と外管の内壁との間の距離は、0.1mmから3.0mmとの間であり、好ましくは1.1~2.5mm、さらにより好ましくは0.1~2.0mmである。
・外管の外径:1.3~2.8mm、好ましくは1.5~2.6mm、より好ましくは1.7~2.4mm。
・外管の内径:1.0~2.4mm、好ましくは1.4~2.0mm、より好ましくは1.2~1.8mm。
外管の壁の直径/厚み:0.1~1.5mm、0.1~0.3mm、好ましくは0.125~0.25mm、より好ましくは0.15~0.2mm。
D (mm) = Fr/3または、Fr = D (mm) × 3
Claims (8)
- a)外管(1)
b)光源(3)
c)接着剤の展開のための再配置可能な管(5)を含み、
前記外管(1)が、先端から5mmと40mmとの間の距離に位置する前記外管の壁に一つの開口部を有するか、先端から5mm~250mmのセグメントに位置するいくつかの開口部を有し、
前記光源が前記外管の壁および/または内腔内に一体化されている、二重管注入カテーテルデバイス。 - 前記光源が、光ファイバーまたは他の光伝送素子である請求項1に記載の二重管注入カテーテルデバイス。
- 前記光源が、紫外光、可視光、または赤外光を発生、伝送、または発光し、紫外光は10~380nmの間の波長の光であり、可視光は381~780nmの間の波長の光であり、赤外光は781nm~1mmの間の波長の光である請求項1または2に記載の二重管注入カテーテルデバイス。
- さらに接着剤用の容器を含む請求項1~3のいずれか一項に記載の二重管注入カテーテルデバイス。
- 接着剤の展開のための再配置可能な前記管が、前記外管内の位置に引っ込められる請求項1~4のいずれか一項に記載の二重管注入カテーテルデバイス。
- さらにセンサシステムを含む請求項1~5のいずれか一項に記載の二重管注入カテーテルデバイス。
- 先端まで10cmの遠位の位置での少なくとも1つの前記開口部の大きさが前記外管(1)および/または再配置可能な管(5)の内腔に対して50%の直径を示す請求項1~6のいずれか一項に記載の二重管注入カテーテルデバイス。
- a)薬学的に許容される組織接着剤およびフォームの形態の硬化薬を含む組成物、および
b)請求項1~7のいずれか一項に記載の二重管注入カテーテルデバイス
を含むキット。
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EP14162466 | 2014-03-28 | ||
EP14164393.2 | 2014-04-11 | ||
EP14164393 | 2014-04-11 | ||
JP2017501496A JP2017514642A (ja) | 2014-03-28 | 2015-03-27 | 光硬化性接着剤を用いた硬化療法のための組成物およびデバイス |
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CN115645593A (zh) | 2023-01-31 |
SG11201608010SA (en) | 2016-10-28 |
EP3122390B1 (en) | 2020-04-29 |
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CA2942626C (en) | 2023-06-13 |
ES2806084T3 (es) | 2021-02-16 |
JP2017514642A (ja) | 2017-06-08 |
CN106232152A (zh) | 2016-12-14 |
WO2015144898A9 (en) | 2017-05-26 |
US12036334B2 (en) | 2024-07-16 |
RU2016136850A (ru) | 2018-05-03 |
RU2738739C2 (ru) | 2020-12-16 |
AU2015238215B2 (en) | 2018-12-20 |
EP3122390A2 (en) | 2017-02-01 |
CN115645593B (zh) | 2024-05-14 |
KR102566318B1 (ko) | 2023-08-10 |
JP2020049265A (ja) | 2020-04-02 |
CA2942626A1 (en) | 2015-10-01 |
AU2015238215A1 (en) | 2016-09-29 |
WO2015144898A2 (en) | 2015-10-01 |
RU2016136850A3 (ja) | 2018-10-26 |
KR20160149202A (ko) | 2016-12-27 |
WO2015144898A3 (en) | 2016-02-04 |
SG10201909098PA (en) | 2019-11-28 |
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