JP2016504066A - パターン化された接着剤層を有する医療用ドレープおよびその製造方法 - Google Patents
パターン化された接着剤層を有する医療用ドレープおよびその製造方法 Download PDFInfo
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Abstract
Description
」の語句は、また、必ずしも傷ついたり欠陥とされていない組織の領域を参照できるが、その代わりに、付加組織の成長を加味あるいは促進することが望ましい。例えば、減圧は、他の組織の場所に採取および移植される付加的な組織を成長させるため、ある組織領域で使用される。いくつかの実施例において、組織部位102は、外皮112を通り、表皮118を通り、および、皮下組織120内に、延びる創傷である。
Claims (54)
- 可とう性フィルム;および
第1のパターンで可とう性フィルムの第1の部分に配置された第1の接着剤、および、第2のパターンで可とう性フィルムの第2の部分に配置された第2の接着剤を備え、
第2のパターンは第1のパターンとともに登録され、第1の部分および第2の部分が可とう性フィルムの実質的に異なる部分を覆うことを特徴とする医療用ドレープ。 - 第2の接着剤が第1の接着剤の粘着性より低い粘着性を有する請求項1に記載の医療用ドレープ。
- 第2の接着剤が第1の接着剤の厚さより大きい厚さを有する請求項1または2に記載の医療用ドレープ。
- 第1の接着剤が約30ミクロンと約65ミクロンとの間の厚さを有し、第2の接着剤が約100ミクロンと約400ミクロンとの間の厚さを有する請求項1〜3のいずれか1項に記載の医療用ドレープ。
- 第1の部分および第2の部分が可とう性フィルムの側面より小さい部分を被覆する請求項1〜4のいずれか1項に記載の医療用ドレープ。
- 第1の部分が複数のセルを備え、
第2の部分が、第1のパターンのセル間の可とう性フィルムを実質的に被覆する、
請求項1〜5のいずれか1項に記載の医療用ドレープ。 - セルが可とう性フィルム上で等間隔に分離されている請求項6に記載の医療用ドレープ。
- 第2のパターンが、可とう性フィルムの端部に平行に伝播する、第2の接着剤の1つ以上の周期的に波形形状のストリップを備える請求項1〜7のいずれか1項に記載の医療用ドレープ。
- 第1のパターンが、可とう性フィルムの端部に平行に伝播する、周期的な波形形状を有する接着剤のストリップを備える請求項1、2、3、4、5または8に記載の医療用ドレープ。
- 接着剤のストリップが、可とう性フィルムの幅と実質的に同様のピークツーピーク振幅を有する請求項9に記載の医療用ドレープ。
- 第1のパターンが:
可とう性フィルムの端部に近接する第1の接着剤の第1の列であって、第1の列が複数のセルを有し、各セルが第1の列の隣接するセルから分離されている第1の列と;
可とう性フィルムの端部から分離した第1の接着剤の第2の列であって、第2の列が第1の列のセルからオフセットして設けられた複数のセルを有し、各セルが第2の列の隣接するセルから分離されている第2の列と;
を備える請求項1、2、3、4、5または8に記載の医療用ドレープ。 - 第2のパターンが第2の接着剤の1つ以上の周期的な波形形状のストリップを備え、周期的な波形形状のストリップがそれぞれ第1および第2の列のセルの中間部分と対応する最大および最小振幅を有し、周期的な波形形状のストリップが、可とう性フィルムの端部に平行に伝播する、第1および第2の列のセルを包含する請求項11に記載の医療用ドレープ。
- 可とう性フィルムがポリウレタンフィルムを備える請求項1〜12のいずれか1項に記載の医療用ドレープ。
- 可とう性フィルムが、約300g/m2/24時間と約14,400g/m2/24時間との間の水蒸気転送速度を有する請求項1〜13のいずれか1項に記載の医療用ドレープ。
- 可とう性フィルムが、約1000g/m2/24時間の水蒸気転送速度を有する請求項14に記載の医療用ドレープ。
- 第1の接着剤がアクリル系接着剤であり、第2の接着剤がシリコーン系接着剤である請求項1〜15のいずれか1項に記載の医療用ドレープ。
- 減圧で組織部位を処置するためのシステムであって、システムが:
組織部位近傍の減圧を分配するためのマニホールドと;
マニホールドに流体的に結合した減圧ソースと;
ドレープと;
ドレープと結合した第1の接着剤および第2の接着剤であって、第2の接着剤が第1の接着剤とともに登録され、第1の接着剤と第2の接着剤がドレープの実質的に異なる部分を被覆する第1の接着剤および第2の接着剤と;
を備えることを特徴とするシステム。 - マニホールドを含むシールされたスペースを形成するために、第1の接着剤は組織部位近傍のドレープを接合するよう構成され、第2の接着剤は組織部位近傍のドレープをシールするよう構成される請求項17に記載のシステム。
- 第2の接着剤が、第1の接着剤の厚さより大きい厚さを有する請求項17または18に記載のシステム。
- 第2の接着剤が、第1の接着剤の粘着性よりも小さい粘着性を有する請求項17〜19のいずれか1項に記載のシステム。
- ドレープが可とう性フィルムを備え、第1の接着剤および第2の接着剤が、可とう性フィルムの側面を実質的に被覆する請求項17〜20のいずれか1項に記載のシステム。
- 第1の接着剤および第2の接着剤が、ドレープの側面より小さい部分を被覆する請求項17〜21のいずれか1項に記載のシステム。
- 第1の接着剤が約30ミクロンと約65ミクロンとの間の厚さを有し、第2の接着剤が約100ミクロンと約400ミクロンとの間の厚さを有する請求項17〜22のいずれか1項に記載のシステム。
- 第1の接着剤が複数のセルを備え、第2の接着剤が複数のセルの間のドレープを実質的に被覆する請求項17〜23のいずれか1項に記載のシステム。
- 第1の接着剤のセルが第1の接着剤の隣接するセルから等間隔で分離される請求項24に記載のシステム。
- 第2の接着剤が、ドレープの端部に平行に伝播する、第2の接着剤の1つ以上の周期的な波形形状のストリップを備える請求項17〜25のいずれか1項に記載のシステム。
- 第1の接着剤が、ドレープの端部に平行に伝播する、周期的な波形形状を有する接着剤のストリップを備える請求項17〜23のいずれか1項または26に記載のシステム。
- 接着剤のストリップが、ドレープの幅と実質的に同等のピークツーピーク振幅を有する請求項27に記載のシステム。
- 第1の接着剤が:
ドレープの外側の端部に近接するセルの第1の列であって、第1の列が複数のセルを有し、各セルが第1の列の隣接するセルから分離されている第1の列と;
ドレープの端部から分離されたセルの第2の列であって、第2の列が第1の列のセルからオフセットして設けられた複数のセルを有し、各セルが第2の列の隣接するセルから分離されている第2の列と;
を備えている請求項17〜23のいずれか1項または26に記載のシステム。 - 第2の接着剤が1つ以上の周期的な波形形状のストリップを備え、周期的な波形形状のストリップがそれぞれ第1および第2の列のセルの中間部分と対応する最大および最小振幅を有し、周期的な波形形状のストリップが第1および第2の列のセルを包含する請求項29に記載のシステム。
- 第1の接着剤がアクリル系接着剤であり、第2の接着剤がシリコン系接着剤である請求項17〜30のいずれか1項に記載のシステム。
- 可とう性フィルムがポリウレタンフィルムを備える請求項17〜31のいずれか1項に記載のシステム。
- 可とう性フィルムが、約300g/m2/24時間と約14,400g/m2/24時間との間の水蒸気転送速度を有する請求項17〜32のいずれか1項に記載のシステム。
- 可とう性フィルムが、約1000g/m2/24時間の水蒸気転送速度を有する請求項33に記載のシステム。
- 第1の接着剤がアクリル系接着剤であり、第2の接着剤がシリコン系接着剤である請求項17〜34のいずれか1項に記載のシステム。
- 医療用ドレープを製造する方法であって、方法が:
可とう性フィルムを提供する工程と;
第1のパターンで可とう性フィルムの側面上に第1の接着剤を配置する工程と;
第2のパターンで可とう性フィルムの側面上に第2の接着剤を配置する工程と;
を備え、第1の接着剤および第2の接着剤が可とう性フィルムの実質的に異なる部分を被覆し、第2の接着剤が第1の接着剤の粘着性より小さい粘着性を有することを特徴とする医療用ドレープを製造する方法。 - 第1の接着剤および第2の接着剤を配置する工程が、第1の接着剤および第2の接着剤で可とう性フィルムの側面を実質的に被覆する工程を備える請求項36に記載の方法。
- 第1の接着剤および第2の接着剤を配置する工程が、可とう性フィルムの側面の部分を被覆する工程を備える請求項36または37に記載の方法。
- 第1のパターンで可とう性フィルムの側面上に第1の接着剤を配置する工程が:
回転部材を通って可とう性フィルムを移動する工程であって、可とう性フィルムが回転部材に対し直線的に移動している間、可とう性フィルムが回転部材の外部の部分と接触する工程と;
第1の接着剤を回転部材の内部に供給する工程と;
第1の接着剤を回転部材の開口を介して可とう性フィルム上に押し付ける工程であって、開口が第1のパターンで回転部材の外側表面に形成されている工程と;
を備える請求項36、37または38に記載の方法。 - 第2のパターンで可とう性フィルムの側面上に第2の接着剤を配置する工程が:
回転部材を通って可とう性フィルムを移動する工程であって、可とう性フィルムが回転部材に対し直線的に移動している間、可とう性フィルムが回転部材の外部の部分と接触する工程と;
第2の接着剤を回転部材の内部に供給する工程と;
第2の接着剤を回転部材の開口を介して可とう性フィルム上に押し付ける工程であって、開口が第2のパターンで回転部材の外側表面に形成されている工程と;
を備える請求項36、37、38または39に記載の方法。 - 第1のパターンで可とう性フィルムの側面上に第1の接着剤を配置する工程が:
第1の接着剤を受け取るよう構成されるとともに第1の接着剤を可とう性フィルム上に押出する操作が可能な1つ以上の押出機を提供する工程と;
押出機に対し可とう性フィルムを移動させる工程と;
可とう性フィルムが押出機を通って直線的に移動している間、第1の接着剤を可とう性フィルム上に押し出すように押出機を作動させる工程と;
を備える請求項36、37または38に記載の方法。 - 第2のパターンで可とう性フィルムの側面上に第2の接着剤を配置する工程が:
第2の接着剤を受け取るよう構成されるとともに第2の接着剤を可とう性フィルム上に押し出すよう構成された1つ以上の押出機を提供する工程と;
押出機に対し第1の方向に可とう性フィルムを移動させる工程と;
可とう性フィルムの移動に対し垂直な第2の方向に押出機を直線的に移動させる工程であって、その移動が可とう性フィルムの第1の端部と可とう性フィルムの第2の端部との間で周期的である工程と:
可とう性フィルムが押出機を通って移動している間、第2の接着剤を押出機により可とう性フィルムの第1の端部上に押し出すように押出機を作動させる工程と;
を備える請求項36、37、38、39または41に記載の方法。 - 第1のパターンで可とう性フィルムの側面上に第1の接着剤を配置する工程が:
第1の接着剤を受け取るよう構成されるとともに第1の接着剤を可とう性フィルム上に押し出すよう構成された1つ以上の押出機を提供する工程と;
押出機に対し可とう性フィルムを直線的に移動させる工程と;
可とう性フィルムが押出機を通って直線的に移動している間、第1の接着剤を押出機により可とう性フィルム上に押し出すように押出機を作動させる工程と;
可とう性フィルムの移動に対し垂直で直線的に押出機を移動させる工程であって、その移動が可とう性フィルムの第1の端部と可とう性フィルムの第2の端部との間で周期的である工程と:
可とう性フィルムを押出機に垂直に移動させる工程であって、第1のパターンがそれに応じた周期的な波形形状のストリップである工程と;
を備える請求項36、37、38、40または42に記載の方法。 - 第1のパターンで可とう性フィルムの側面上に第1の接着剤を配置する工程が:
移送シリンダーの外部上に彫刻された第1のパターンを有する移送シリンダーを提供する工程と;
移送シリンダーを第1の接着剤で被覆する工程と;
第1の接着剤を可とう性フィルム上に堆積させるために、可とう性フィルムが移送シリンダーを通って直線的に移動する間、移送シリンダーを可とう性フィルム上にプレスする工程と;
可とう性フィルム上の第1の接着剤を加硫する工程と;
を備える請求項36、37、38、40または42に記載の方法。 - 第2のパターンで可とう性フィルムの側面上に第2の接着剤を配置する工程が:
移送シリンダーの外部上に彫刻された第2のパターンを有する移送シリンダーを提供する工程と;
移送シリンダーを第2の接着剤で被覆する工程と;
第2の接着剤を可とう性フィルム上に堆積させるために、可とう性フィルムが移送シリンダーを通って直線的に移動する間、移送シリンダーを可とう性フィルム上にプレスする工程と;
可とう性フィルム上の第2の接着剤を加硫する工程と;
を備える請求項36、37、38、39、41、43または44に記載の方法。 - 減圧で組織部位を処置するための方法であって、方法が:
組織部位近傍の減圧を分配するためのマニホールドを配置する工程と;
マニホールドに減圧ソースを流体的に結合する工程と;
組織部位の上に医療用ドレープを配置する工程であって、医療用ドレープが医療用ドレープと結合した第1の接着剤および第2の接着剤を有し、第2の接着剤が第1の接着剤とともに登録され、第1および第2の接着剤が医療用ドレープの実質的に異なる部分を被覆する工程と;
ドレープと組織部位との間のシール用結合を形成するために、組織部位に第2の接着剤を貼り付ける工程と;
ドレープを位置決めする工程と;
ドレープと組織部位との間の接合用接結合を形成するために、第1の接着剤に力を加える工程と;
を備えることを特徴とする方法。 - 第2の接着剤が第1の接着剤の厚さより大きい厚さを有する請求項46に記載の方法。
- 第1の接着剤が約30ミクロンと約65ミクロンとの間の厚さを有し、第2の接着剤が約100ミクロンと約400ミクロンとの間の厚さを有する請求項46または47に記載の方法。
- 第1の接着剤がアクリル系接着剤であり、第2の接着剤がシリコン系接着剤である請求項46、47または48に記載の方法。
- 可とう性フィルムがポリウレタンフィルムを備える請求項46、47、48または49に記載の方法。
- 可とう性フィルムが、約300g/m2/24時間と約14,400g/m2/24時間との間の水蒸気転送速度を有する請求項46、47、48、49または50に記載の方法。
- 可とう性フィルムが、約1000g/m2/24時間の水蒸気転送速度を有する請求項51に記載の方法。
- 第2の接着剤が、第1の接着剤の粘着性より小さい粘着性を有する請求項46、47、48、49、50、51、52または53に記載の方法。
- 実質的にここに示されるか記載された、装置、システムおよび方法。
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JP2009219869A (ja) * | 2008-03-13 | 2009-10-01 | Tyco Healthcare Group Lp | 可変の性能ゾーンを備える真空創傷治療の創傷ドレッシング |
JP2009297434A (ja) * | 2008-06-17 | 2009-12-24 | Nitto Denko Corp | 粘着テープもしくはシート |
JP2014518651A (ja) * | 2011-04-21 | 2014-08-07 | スミス アンド ネフュー ピーエルシー | 閉塞管理 |
WO2013009239A1 (en) * | 2011-07-08 | 2013-01-17 | Mölnlycke Health Care Ab | Self-adhesive wound care product |
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CA2892465A1 (en) | 2014-05-22 |
EP3669842A1 (en) | 2020-06-24 |
EP4279094A3 (en) | 2024-02-28 |
JP6324983B2 (ja) | 2018-05-16 |
AU2013344686A1 (en) | 2015-06-04 |
EP2919730A1 (en) | 2015-09-23 |
US20140155791A1 (en) | 2014-06-05 |
US11395785B2 (en) | 2022-07-26 |
US20200237605A1 (en) | 2020-07-30 |
US10842707B2 (en) | 2020-11-24 |
EP4279094A2 (en) | 2023-11-22 |
BR112015011271A8 (pt) | 2019-10-22 |
CN105050558B (zh) | 2020-09-08 |
BR112015011271B1 (pt) | 2022-03-03 |
WO2014078518A1 (en) | 2014-05-22 |
CN111991092A (zh) | 2020-11-27 |
KR20150085837A (ko) | 2015-07-24 |
US11839529B2 (en) | 2023-12-12 |
BR112015011271A2 (pt) | 2017-07-11 |
EP3092990B1 (en) | 2020-03-11 |
EP3092990A1 (en) | 2016-11-16 |
SG11201503860RA (en) | 2015-06-29 |
US20230404816A1 (en) | 2023-12-21 |
AU2013344686B2 (en) | 2018-06-21 |
EP3669842B1 (en) | 2023-09-27 |
CN105050558A (zh) | 2015-11-11 |
EP2919730B1 (en) | 2016-06-01 |
US20220257452A1 (en) | 2022-08-18 |
CA2892465C (en) | 2020-10-27 |
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