伤口愈合
光动力疗法
化学
光敏剂
明胶
体内
复合数
纳米颗粒
生物医学工程
镁
矿化(土壤科学)
生物相容性
活性氧
体外
抗生素
生物材料
药理学
磷酸盐
控制释放
作者
Yongpeng Su,ShunYing LIU,Mingdi He,Lingfei Li,Guihong Yang,Xiaohan Liu,Yiting Feng,Hui Tang,Lingbo Li,Jianmin Wu,Z Li,Yi Liang,Chao Qi,Kaiyong Cai,Xia Lei
标识
DOI:10.1016/j.mtbio.2026.102959
摘要
Wound infection remains a significant clinical challenge, exacerbated by the growing prevalence of bacterial resistance due to the overuse of conventional antibiotics. Photodynamic therapy (PDT) offers a promising approach for wound sterilization that circumvents the issue of antibiotic resistance. However, conventional photosensitizers are prone to inactivation and exhibit poor retention at the wound site, limiting their clinical efficacy. To overcome these limitations, we developed a biomimetic mineralization approach to encapsulate the small-molecule photosensitizer chlorin e6 (Ce6) within magnesium phosphate nanoparticles (CMP NPs), preserving its photodynamic activity. This mineralized CMP NPs were further integrated with gelatin and natural moisturizing factor to fabricate a composite hydrogel dressing (CMP/Gel) for infected wound healing. Gelatin functions as a structural matrix that prolongs the local retention of CMP NPs, while the natural moisturizing factor enhances the hydration capacity and mechanical integrity of the dressing. Notably, magnesium ions released during the degradation of CMP NPs contribute to accelerated wound healing through multiple therapeutic effects, including antioxidant, anti-inflammatory, and pro-angiogenic activities following PDT-mediated bacterial eradication. Both in vitro and in vivo experimental results demonstrate that CMP/Gel effectively promotes infected wound repair, highlighting its potential as a novel and multifunctional therapeutic strategy for infected wound management.
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