Zirconium‐Based Metal‐Organic Framework Capable of Binding Proinflammatory Mediators in Hydrogel Form Promotes Wound Healing Process through a Multiscale Adsorption Mechanism

The regulation of proinflammatory mediators has been explored to promote natural healing without abnormal inflammation or autoimmune response induced by their overproduction. However, most efforts to control these mediators have relied on pharmacological substances that are directly engaged in biological cycles. It is believed that functional porous materials removing target mediators provide a new way to promote the healing process using their adsorption mechanisms. In this study, the Zr‐based metal‐organic frameworks (MOF)‐808 (Zr6O4(OH)4(BTC)2(HCOO)6) crystals are found to be effective at removing proinflammatory mediators, such as nitric oxide (NO), cytokines, and reactive oxygen species (ROS) in vitro and in vivo, because of their porous structure and surface affinity. The MOF‐808 crystals are applied to an in vivo skin wound model as a hydrogel dispersion. Hydrogel containing 0.2 wt% MOF‐808 crystals shows significant improvement in terms of wound healing efficacy and quality over the corresponding control. It is also proven that the mode of action is to remove the proinflammatory mediators in vivo. Moreover, the application of MOF‐808‐containing hydrogels promotes cell activation, proliferation and inhibits chronic inflammation, leading to increased wound healing quality. These findings suggest that Zr‐based MOFs may be a promising drug‐free solution for skin problems related to proinflammatory mediators. Zr‐based metal‐organic frameworks (MOF)‐808 promote wound healing by removing proinflammatory mediators, such as nitric oxide (NO), cytokines, and reactive oxygen species (ROS), using their porous structure and surface affinity. Application of the MOF‐808‐containing hydrogel improves the wound healing efficacy and quality, as proven in vivo. It is also shown that MOF‐808 promote cell activation and proliferation while inhibiting chronic inflammation.