Freeze‐Thawing Chitosan/Ions Hydrogel Coated Gauzes Releasing Multiple Metal Ions on Demand for Improved Infected Wound Healing
Imbalance of metal ions in the wound microenvironment is a key factor that leads to delayed wound healing. However, single metal administration to enhance wound repair is usually not enough due to the overlapping nature of the wound healing phases. Herein, a facile freeze‐thawing strategy is develop...
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Veröffentlicht in: | Advanced healthcare materials 2021-03, Vol.10 (6), p.e2001591-n/a |
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Sprache: | eng |
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Zusammenfassung: | Imbalance of metal ions in the wound microenvironment is a key factor that leads to delayed wound healing. However, single metal administration to enhance wound repair is usually not enough due to the overlapping nature of the wound healing phases. Herein, a facile freeze‐thawing strategy is developed to incorporate chitosan/ions hydrogel into medical gauzes to realize on‐demand release of multiple ions to accelerate wound healing. In vitro study reveals that the gauzes can temporally release multiple metal ions on demand, and the released metal ions show effectiveness in killing bacteria and expediting cell migration. In vivo studies demonstrate that the metal ions loaded gauzes can efficiently enhance infected wound healing. Further histological analysis find that these metal ion‐loaded gauzes accelerate wound healing by promoting granulation formation, collagen deposition and maturation, re‐epithelization, angiogenesis, and inhibiting inflammation via regulating the expression of inflammatory factors (e.g., tumor necrosis factor‐α) and polarization of macrophages. Thus, this novel metal ions delivery system has great potential in infected tissue repair and antibacterial applications.
Chitosan/metal ions hydrogels are coated to medical gauzes through a simple freeze‐thawing strategy to realize on‐demand release of multiple metal ions for improved wound healing by promoting granulation formation, collagen deposition and maturation, re‐epithelization, angiogenesis, and inhibiting inflammation via regulating the expression of inflammatory factors (e.g., tumor necrosis factor‐α ) and polarization of macrophages. |
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ISSN: | 2192-2640 2192-2659 |
DOI: | 10.1002/adhm.202001591 |