植物由来材料を用いた感染予防創傷被覆材を開発(Plant-based wound dressing fights infection before it takes hold)

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2026-07-14 バース大学

英国バース大学の研究チームは、植物由来の天然多糖類を用いた新しい創傷被覆材(創傷ドレッシング)を開発し、感染が成立する前に細菌の増殖を抑制できることを示した。材料には植物由来のバイオポリマーを利用し、傷口を適度に湿潤な状態に保ちながら、抗菌成分を持続的に放出することで細菌の定着やバイオフィルム形成を防ぐ仕組みを採用している。実験では、創傷感染の原因となる細菌に対して高い抗菌効果を示すとともに、哺乳類細胞への毒性は低く、創傷治癒を妨げないことが確認された。また、植物由来材料を使用するため、生分解性や持続可能性にも優れ、従来の抗菌剤や抗生物質への依存を減らし、薬剤耐性菌対策にも貢献する可能性がある。研究チームは今後、臨床応用に向けた性能評価を進める予定であり、本技術は慢性創傷や術後創部など感染リスクの高い創傷管理への応用が期待されている。

<関連情報>

抗菌性創傷治療のためのバイオベースフランポリアミド製ヤヌス型電界紡糸ナノファイバー膜 Janus electrospun nanofiber membranes from bio-based furan polyamides for antibacterial wound care

Xiang Ding, Naing Tun Thet, Carmelo Herdes, Edward Chaloner, Mikal Negasi, Ioanna Kontou, Maisem Laabei, Ute Jungwirth, Dominic Savage, Muhammad Kamran, Michael Zachariadis, Toby Jenkins, Matthew G. Davidson, Hannah S. Leese
Bioactive Materials  Available online: 24 June 2026
DOI:https://doi.org/10.1016/j.bioactmat.2026.06.022

植物由来材料を用いた感染予防創傷被覆材を開発(Plant-based wound dressing fights infection before it takes hold)

Highlights

  • Sustainable Janus nanofiber membranes are fabricated from bio-based furan polyamides.
  • Electrospinning amplifies subtle chain-length-dependent wettability differences.
  • Asymmetric PA8F/PA10F membranes enable rapid local antibiotic delivery with high cytocompatibility.
  • Antibacterial efficacy is validated in biofilm and ex vivo porcine wound models.

Abstract

Early-stage bacterial contamination and rapid biofilm growth are critical barriers to effective wound healing, highlighting the need for dressing materials that enable prompt, localised antibacterial intervention while maintaining cytocompatibility and sustainability. Here, we report a sustainable electrospun Janus nanofiber membrane based on two bio-derived semi-aromatic furan polyamides, poly(octamethylene furanamide) (PA8F) and poly(decamethylene furanamide) (PA10F), for antibacterial wound dressing applications. Although PA8F and PA10F differ only by two methylene units and show modest wettability differences as dense films, electrospinning into nanofiber networks amplifies this subtle molecular contrast into a pronounced, robust wettability asymmetry that enables a Janus dressing architecture without chemical surface modification. Tetracycline was physically dispersed within the hydrophilic PA8F, prior to electrospinning, to localise antibiotic delivery at the wound-material interface. The Janus membrane exhibits uniform, bead-free nanofibrous morphology and pronounced interfacial wettability asymmetry. Molecular dynamics simulations reveal distinct polymer-water interaction behaviours that underpin the experimentally observed hydration contrast between PA8F and PA10F. Drug release studies demonstrate rapid antibiotic availability, reaching ∼20 μg mL−1 in phosphate-buffered saline within 4 h. The Janus membranes achieve ∼1 log and ∼2 log reductions against Pseudomonas aeruginosa and Staphylococcus aureus colony biofilms, respectively, and produce ∼0.5 log bacterial reduction in an ex vivo porcine burn wound infection model. This study establishes the first use of sustainable furan-based semi-aromatic polyamides as electrospun wound dressings and demonstrates how electrospinning-induced asymmetry can translate subtle molecular differences into efficient, localised antibacterial delivery for advanced wound care.

医療・健康
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