Li Yu, Qian Lu, Liu Fei, Xu Shilong, Zhou Lian, Wei Chenxi, Zhang Yanqin, Zhai Yuewen, Gu Yueqing, Li Siwen
Department of Biomedical Engineering, School of Engineering, China Pharmaceutical University, No. 639 Longmian Avenue, Jiangning District, Nanjing, 211198, Jiangsu Province, China.
Department of Biomedical Engineering, Nanjing University of Aeronautics and Astronautics, No. 29 Jiangjun Avenue, Jiangning District, Nanjing, 211100, Jiangsu Province, China.
Nano Lett. 2025 Jun 4;25(22):9098-9109. doi: 10.1021/acs.nanolett.5c01747. Epub 2025 May 23.
Small extracellular vesicles (sEV) derived from mesenchymal stem cells hold promise for anti-skin aging, yet their clinical application is hindered by poor transdermal permeability. Herein, we report an innovative light-controlled sEV-based spherical nucleic acid nanomotor (NM-ESNA). This nanosystem was composed of an sEV core and an MMP1-targeting siRNA shell, forming a 3D penetrative nanostructure. In addition, asymmetrically modified light-responsive gas-generating molecules were integrated into the nanomotor, enabling efficient dermal delivery. The light-controlled and enhanced transdermal delivery guaranteed synergistic anti-skin aging therapy through sEV-mediated paracrine effects and gene therapy targeting MMP1 in the dermis. On the basis of this deep transdermal delivery technology and the synergistic therapy strategy, NM-ESNA demonstrated outstanding anti-skin aging effects in a mouse model. This biocompatible nanosystem (NM-ESNA) enabled light-controlled and deep transdermal delivery, establishing a therapeutic platform with significant potential for sEV-based noninvasive anti-skin aging therapy.
间充质干细胞衍生的小细胞外囊泡(sEV)具有抗皮肤衰老的潜力,但其临床应用受到经皮渗透性差的阻碍。在此,我们报告了一种基于sEV的创新光控球形核酸纳米马达(NM-ESNA)。该纳米系统由一个sEV核心和一个靶向基质金属蛋白酶1(MMP1)的小干扰RNA(siRNA)外壳组成,形成一种三维穿透性纳米结构。此外,不对称修饰的光响应产气分子被整合到纳米马达中,实现高效的真皮递送。光控增强经皮递送通过sEV介导的旁分泌作用和靶向真皮中MMP1的基因治疗,保证了协同抗皮肤衰老治疗。基于这种深度经皮递送技术和协同治疗策略,NM-ESNA在小鼠模型中表现出显著的抗皮肤衰老效果。这种生物相容性纳米系统(NM-ESNA)实现了光控和深度经皮递送,建立了一个具有巨大潜力的基于sEV的非侵入性抗皮肤衰老治疗平台。