摘要
The exposed bone wound is defined as a kind of wound with bone denuded of periosteum and the deficiency of full-thickness skin and muscles. The wound have no matrix microenvironment and is prone to infection and, hence, hard to heal. Granulation tissue is significant during wound healing, providing a matrix and resisting infection. 3D printing is adopted to fabricate dermis and epidermis regeneration. However, the porosity of most 3D-printed scaffolds is low, leading to a poor drug-loading capacity. To address these limitations, this study developed an alginate-based hierarchical porous scaffold fabricated via cryogenic bi-nozzle 3D printing, enabling dual-factor spatial delivery of VEGF and LL-37 to simultaneously promote angiogenesis and immunomodulation. The alternating dual nozzle printing allows the scaffolds to carry two biological factors with spatial distribution while maintaining the structure integrity. In vitro studies demonstrated enhanced tube formation and endothelial migration, while in vivo implantation in rabbit exposed bone wounds revealed accelerated granulation tissue regeneration and re-epithelialization. The drug-loaded scaffolds can induce the tube formation of vascular endothelial cells, assist inflammatory cells in resisting infection, and ultimately form a fully functional granulation tissue. These results demonstrate the potential clinical applicability of this immunomodulatory dual-factor scaffold for challenging exposed bone wound repair.
危险品化学品经营许可证(带存储)