4.7 Article

In-situ forming hydrogel incorporated with reactive oxygen species responsive and antibacterial properties for diabetic infected chronic wound healing

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 450, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.138077

Keywords

Hydrogel; Antibacterial; Chronic wound healing; Reactive oxygen species; e-Poly-Lysine

Funding

  1. National Key RAMP
  2. D Program of China [2018YFA0703000]
  3. Postdoctoral Science Foundation [2020 M681320]
  4. National Natural Science Foundation of China [82072412/81902195]
  5. Translation Medicine National Key Science and Technology Infrastructure (Shanghai) Open Project [TMSK-2020-118]
  6. 2022 Lingang laboratory Seeking Outstanding Youth Program open project [LG-QS-202206-04]
  7. Postdoctoral Fellows Start-up Funding [201901038/202001005]

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In this study, an in-situ gelled and shape-adaptable hydrogel with antibacterial and ROS scavenging properties was developed for chronic diabetic wound healing. The hydrogel provided a physical barrier that protected the wounds from bacteria and promoted wound healing. It exhibited great biocompatibility, antibacterial activity, and the ability to adjust inflammation and promote collagen deposition for wound contraction and healing.
Chronic diabetic wounds are often characterized by oxidative damage due to bacterial infection or pathological interference, representing a major clinical challenge. An in-situ gelled and shape-adaptable hydrogel with antibacterial and reaction oxygen species (ROS) scavenging properties was developed in this study. It was designed and synthesized via progressively adding DL-Dithiothreitol, Poly (ethylene glycol) diacrylate and phe-nylboronic acid modified epsilon-Poly-Lysine to obtain a stock solution before use. Through local light-induced in-situ gelling, this hydrogel can provide a physical barrier that fills wound defects and protects the wounds from bacteria. Moreover, the EPL-PBA modified DPEs exhibited excellent water absorption and outstanding con-sumption of H2O2, which could respond to an overdose of the oxidative micro-environment to promote wound healing. Moreover, the hydrogel displayed great biocompatibility and antibacterial activity, enabling the wound dressing to effectively inhibit bacterial growth and accelerate infected wound healing. Furthermore, an infected diabetic chronic full-thickness skin defect healing test revealed that the wound dressing promoted wound contraction and healing via inflammatory adjustment and collagen deposition. All of these in vitro and in vivo results revealed the capability of DPE2 to the acceleration of infected diabetic wound healing, presenting a viable material for chronic wound healing.

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