JP2018511410A5 - - Google Patents

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JP2018511410A5
JP2018511410A5 JP2017551593A JP2017551593A JP2018511410A5 JP 2018511410 A5 JP2018511410 A5 JP 2018511410A5 JP 2017551593 A JP2017551593 A JP 2017551593A JP 2017551593 A JP2017551593 A JP 2017551593A JP 2018511410 A5 JP2018511410 A5 JP 2018511410A5
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film
layer
film according
active agent
implantation
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JP2017551593A
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JP6824188B2 (ja
JP2018511410A (ja
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Priority claimed from GBGB1505527.0A external-priority patent/GB201505527D0/en
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Priority to JP2021002539A priority Critical patent/JP7376520B2/ja
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Publication of JP6824188B2 publication Critical patent/JP6824188B2/ja
Priority to JP2023181875A priority patent/JP2024010067A/ja
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Claims (20)

  1. 活性剤の制御された、持続的な放出のための、対象の体の手術部位への移植用のフィルムであって、前記フィルムは:
    上位層および下位層、ここで、前記上位層および下位層のそれぞれは、生分解性ポリマーおよび放出剤からなる;および、
    前記上位層と下位層の間の中位層、ここで、前記中位層は生分解性ポリマー、放出剤、および、活性剤を含み、ここで、前記活性剤は、前記中位層の40〜80wt%を構成する、
    を含み、
    前記上位層および下位層は、少なくとも移植前は活性剤を含まず、および、
    前記フィルムは、移植後3から14日の期間にわたって前記手術部位において前記活性剤を放出するように設計される、
    フィルム。
  2. 請求項1に記載のフィルムであって、
    前記活性剤が、麻酔薬を含む、
    フィルム。
  3. 請求項1に記載のフィルムであって、
    前記フィルムは、細長い一片(strip)である、
    フィルム。
  4. 請求項1に記載のフィルムであって、
    前記放出剤は、少なくとも、ポリソルベート20、ポリソルベート60、および、ポリソルベート80の少なくとも1つを含む放出剤である、
    フィルム。
  5. 請求項1に記載のフィルムであって、
    少なくとも移植前は、前記上位層は前記中位層の上表面を覆い、前記下位層は前記中位層の下表面を覆い、および、前記中位層の周囲(perimeter)は、前記手術部位に移植される際に、前記中位層の周囲が前記手術部位の体液に直接接触するように、前記上位および下位層から露出している、
    フィルム。
  6. 請求項1に記載のフィルムであって、
    前記フィルムの厚さが、約1μm〜約2000μmである、
    フィルム。
  7. 請求項1に記載のフィルムであって、
    少なくとも10wt%の前記活性剤が、前記フィルムの移植の24時間以内に放出され、および、残りの放出剤は、移植後3から14日の期間にわたって前記フィルムから放出される、
    フィルム。
  8. 請求項1に記載のフィルムであって、
    前記フィルムの前記上位、中位、および/または、下位層の厚さが、0.01μm〜1000μmであってよい、
    フィルム。
  9. 請求項1に記載のフィルムであって、
    前記フィルムの前記上位、中位、および/または、下位層の厚さが、0.01μm〜200μmであってよい、
    フィルム。
  10. 請求項1に記載のフィルムであって、
    前記放出剤は、前記上位および下位層のそれぞれの、約0.1wt%〜約50wt%を構成する、
    フィルム。
  11. 請求項1に記載のフィルムであって、
    前記放出剤は、前記中位層の、約0.1wt%〜約50wt%を構成する、
    フィルム。
  12. 活性剤の制御された、持続的な放出のための、対象の体の手術部位への移植用のフィルムであって、前記フィルムは:
    複数の積層された層、ここで、それぞれの層は生分解性ポリマーおよび放出剤を含み、前記複数の層は、2つの最外層、および、前記最外層の間に挟まれた少なくとも1つの中間層を含み、前記中間層は活性剤を含み、および、前記活性剤は前記中間層の40〜80wt%を構成し、
    ここで、前記フィルムは、少なくとも10wt%の前記活性剤を、前記手術部位における前記フィルムの移植の24時間以内に放出し、および、残りの放出剤が、移植後3から14日の期間にわたって前記フィルムから放出されるように設計される、
    フィルム。
  13. 請求項12に記載のフィルムであって、
    前記活性剤が、麻酔薬を含む、
    フィルム。
  14. 請求項12に記載のフィルムであって、
    前記フィルムは、細長い一片(strip)である、
    フィルム。
  15. 請求項12に記載のフィルムであって、
    前記放出剤は、少なくとも、ポリソルベート20、ポリソルベート60、および、ポリソルベート80の少なくとも1つを含む放出剤である、
    フィルム。
  16. 請求項12に記載のフィルムであって、
    少なくとも移植前は、前記上位層は前記中位層の上表面を覆い、前記下位層は前記中位層の下表面を覆い、および、前記中位層の周囲は、前記手術部位に移植される際に、前記中位層の周囲が前記手術部位の体液に直接接触するように、前記上位および下位層から露出している、
    フィルム。
  17. 請求項12に記載のフィルムであって、
    前記フィルムの厚さが、約1μm〜約2000μmである、
    フィルム。
  18. 請求項12に記載のフィルムであって、
    前記フィルムの前記上位、中位、および/または、下位層の厚さが、0.01μm〜1000μmであってよい、
    フィルム。
  19. 請求項12に記載のフィルムであって、
    前記フィルムの前記上位、中位、および/または、下位層の厚さが、0.01μm〜200μmであってよい、
    フィルム。
  20. 請求項12に記載のフィルムであって、
    前記放出剤は、前記中位層の、約0.1wt%〜約50wt%を構成する、
    フィルム。
JP2017551593A 2015-03-31 2016-03-31 弾性の抗菌フィルムおよびそれから作られるソケット Active JP6824188B2 (ja)

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JP2021002539A JP7376520B2 (ja) 2015-03-31 2021-01-12 弾性の抗菌フィルムおよびそれから作られるソケット
JP2023181875A JP2024010067A (ja) 2015-03-31 2023-10-23 弾性の抗菌フィルムおよびそれから作られるソケット

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GBGB1505527.0A GB201505527D0 (en) 2015-03-31 2015-03-31 Composition
GB1505527.0 2015-03-31
PCT/SG2016/050158 WO2016159885A1 (en) 2015-03-31 2016-03-31 Elastic antimicrobial film and socket made therefrom

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JP2018511410A JP2018511410A (ja) 2018-04-26
JP2018511410A5 true JP2018511410A5 (ja) 2019-05-09
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US (3) US20180193537A1 (ja)
EP (3) EP4129350A1 (ja)
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CN (2) CN107921180A (ja)
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