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Injectable Oxygen-Carrying Microsphere Hydrogel for Dynamic Regulation of Redox Microenvironment of Wounds. | LitMetric

AI Article Synopsis

  • Delayed healing of infected wounds is due to excessive reactive oxygen species (ROS), leading to tissue damage and a lack of oxygen, which fuels inflammation.
  • Existing treatments like hyperbaric oxygen therapy and antibiotics do not sustain oxygen delivery or prevent infections effectively.
  • This study introduces a new hydrogel dressing that scavenges ROS and releases oxygen, enhancing cell survival, promoting healing, and providing drug-free infection resistance by modulating the immune response in wounds.

Article Abstract

The delayed healing of infected wounds can be attributed to the increased production of reactive oxygen species (ROS) and consequent damages to vascellum and tissue, resulting in a hypoxic wound environment that further exacerbates inflammation. Current clinical treatments including hyperbaric oxygen therapy and antibiotic treatment fail to provide sustained oxygenation and drug-free resistance to infection. To propose a dynamic oxygen regulation strategy, this study develops a composite hydrogel with ROS-scavenging system and oxygen-releasing microspheres in the wound dressing. The hydrogel itself reduces cellular damage by removing ROS derived from immune cells. Simultaneously, the sustained release of oxygen from microspheres improves cell survival and migration in hypoxic environments, promoting angiogenesis and collagen regeneration. The combination of ROS scavenging and oxygenation enables the wound dressing to achieve drug-free anti-infection through activating immune modulation, inhibiting the secretion of pro-inflammatory cytokines interleukin-6, and promoting tissue regeneration in both acute and infected wounds of rat skins. Thus, the composite hydrogel dressing proposed in this work shows great potential for dynamic redox regulation of infected wounds and accelerates wound healing without drugs.

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Source
http://dx.doi.org/10.1002/smll.202403781DOI Listing

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