Xiang Yu, Fan Beibei, Shang Panpan, Ding Ren, Du Juan, Zhu Tonghe, Zhang Hongmei, Yan Xiaoyu
Department of Sports Medicine, Shanghai Sixth People's Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, 600 Yishan Rd., Shanghai, 200233, P. R. China.
Department of Pharmacy, Shanghai Baoshan District Hospital of Integrated Traditional Chinese and Western Medicine, 181 Youyi Rd., Shanghai, 201999, P. R. China.
Small Methods. 2024 Dec;8(12):e2400273. doi: 10.1002/smtd.202400273. Epub 2024 May 11.
Chronic wounds pose a significant clinical challenge worldwide, which is characterized by impaired tissue regeneration and excessive scar formation due to over-repair. Most studies have focused on developing wound repair materials that either facilitate the healing process or control hyperplastic scars caused by over-repair, respectively. However, there are limited reports on wound materials that can both promote wound healing and prevent scar hyperplasia at the same time. In this study, VR23-loaded dendritic mesoporous bioglass nanoparticles (dMBG) are synthesized and electrospun in poly(ester-curcumin-urethane)urea (PECUU) random composite nanofibers (PCVM) through the synergistic effects of physical adsorption, hydrogen bond, and electrospinning. The physicochemical characterization reveals that PCVM presented matched mechanical properties, suitable porosity, and wettability, and enabled sustained and temporal release of VR23 and BDC with the degradation of PCVM. In vitro experiments demonstrated that PCVM can modulate the functions and polarization of macrophages under an inflammatory environment, and possess effective anti-scarring potential and reliable cytocompatibility. Animal studies further confirmed that PCVM can efficiently promote re-epithelialization and angiogenesis and reduce excessive inflammation, thereby remarkably accelerating wound healing while preventing potential scarring. These findings suggest that the prepared PCVM holds promise as a bidirectional regulatory dressing for effectively promoting scar-free healing of chronic wounds.
慢性伤口在全球范围内构成了重大的临床挑战,其特征是组织再生受损以及由于过度修复导致的瘢痕形成过多。大多数研究分别集中在开发促进愈合过程或控制过度修复引起的增生性瘢痕的伤口修复材料上。然而,关于能够同时促进伤口愈合和预防瘢痕增生的伤口材料的报道有限。在本研究中,通过物理吸附、氢键和静电纺丝的协同作用,合成了负载VR23的树枝状介孔生物玻璃纳米颗粒(dMBG),并将其静电纺丝到聚(酯 - 姜黄素 - 聚氨酯)脲(PECUU)随机复合纳米纤维(PCVM)中。物理化学表征表明,PCVM具有匹配的机械性能、合适的孔隙率和润湿性,并且随着PCVM的降解能够实现VR23和BDC的持续和定时释放。体外实验表明,PCVM可以在炎症环境下调节巨噬细胞的功能和极化,并具有有效的抗瘢痕形成潜力和可靠的细胞相容性。动物研究进一步证实,PCVM可以有效地促进再上皮化和血管生成,并减少过度炎症,从而在防止潜在瘢痕形成的同时显著加速伤口愈合。这些发现表明,所制备的PCVM有望作为一种双向调节敷料,有效促进慢性伤口的无瘢痕愈合。