CLC number:
On-line Access: 2024-12-27
Received: 2023-11-15
Revision Accepted: 2024-10-05
Crosschecked: 2024-12-27
Cited: 0
Clicked: 98
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Abstract: The low temperature, high salt content and bacteria in the seawater environment can induce severe
infections of open wounds, making them difficult to heal. To date, numberous wound dressings have
been developed with functions in repairing injuries and various anti-bacterial functions. However,
ordinary anti-bacterial strategies could not provide long-lasting resistance to infection to promote
wound healing. Here, we reported a strategy to build a durable resistance to seawater immersion wound
infection by killing bacteria and delivering bacterial antigens in situ. Specifically, MXenes-embedded
tannin-Eu3+ particles (M@TA-Eu) were constructed to effectively repair the infected seawater
immersion injuries and fight infection in a lasting manner by forming in situ bacterial vaccines and
immune memory. In the particle, the platform constructed by TA and Eu3+ had pro-vascularization and
antigen presentation effects. The MXenes with near-infrared photothermal effect were introduced to
kill the bacteria and promote the recruitment of antigen presentation cells to enhance vaccination
efficacy. The experimental results showed that the particles not only effectively improved the healing
of injuries by relieving wound inflammation and inhibiting bacteria, but also produced potent
vaccination effect by forming in situ bacterial vaccines. Therefore, the M@TA-Eu particles provided
novel strategy for the development of high-grade dressings for anti-infection.
Open peer comments: Debate/Discuss/Question/Opinion
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