透明质酸
间充质干细胞
生物医学工程
材料科学
伤口愈合
体内
聚乙烯醇
药理学
人体皮肤
纤维蛋白
药物输送
自愈水凝胶
细胞外基质
脚手架
炎症
药品
干细胞
硫代硫酸钠
战场
疤痕
人造皮肤
纳米纤维
脐带
透皮
皮肤刺激
氮芥
细胞外
组织工程
细胞外小泡
机械强度
作者
Weiqian Jiang,Qinghe Meng,Ketong Liu,Ang Li,Chaoying Jin,Bing Zhu,Ji Zhu,Minliang Wu,Qingqiang Xu,Chunyu Xue
标识
DOI:10.1021/acsami.6c12383
摘要
Nitrogen mustard (NM) induces severe, refractory skin injuries lacking specific available therapeutics. Considering that extracellular vesicles (EVs) show promising effects in wound healing, we developed a split-type microneedle (MN-EVs@miR) loaded with miR-125b-enriched engineered EVs (EVs@miR) to treat NM-induced skin injury. EVs were isolated from human umbilical cord mesenchymal stem cells (hUMSCs), loaded with miR-125b via transfection, and then conjugated to hyaluronic acid methacryloyl (HAMA) hydrogel using acrylic acid-polyethylene glycol-N-hydroxysuccinimide (AC-PEG-NHS) to prepare microneedle tips, with polyvinyl alcohol (PVA) and sodium thiosulfate constituting the substrate. The prepared MN-EVs@miR exhibited sufficient mechanical strength (0.34 N/needle), sustained EVs@miR release over 21 days, and long-term in vivo retention (>21 days) with excellent biocompatibility. In vitro, EVs@miR enhanced cell viability, inhibited apoptosis, regulated inflammation (downregulating TNF-α, IL-1β, and IL-6; upregulating IL-10), and promoted angiogenesis. In vivo, MN-EVs@miR significantly mitigated NM-induced skin blistering and necrosis, with superior wound healing efficacy compared to that of EVs@miR injection and blank MNs. In conclusion, the split-type MN-EVs@miR provides a promising preventive and therapeutic strategy for NM-induced skin injuries with potential battlefield and clinical applications.
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