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Methacrylated gelatin-based microneedles loaded with Polygonatum kingianum-derived extracellular vesicles for the protection against Ultraviolet B induced photoaging

Journal 2026 · IF 8.7 · 发表于 2026 年 7 月 9 日
作者: Qiong'e Sun,Qiqi Li,Dandan Zhao,Ziyue Li,Yikun Shang,Yu Sun,Meijing Wang,Jiasen Lin,Kun Yu,Xiang Su,Yu Mao,Yan He,Xin Cheng,Xujie Liu
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摘要

GelMA microneedles enhance the transdermal delivery of PDEVs. • PkEVs were efficiently encapsulated and released from GelMA MNs. • Pk@MN attenuates oxidative stress and ROS in skin cells. • Pk@MN effectively alleviate UVB-induced photoaging in vitro and in vivo . Ultraviolet B (UVB) exposure is a major extrinsic factor inducing skin photoaging, while conventional photoprotective strategies are often limited by insufficient skin penetration and poor compliance. In this study, a methacrylated gelatin (GelMA)-based microneedle system was developed for the efficient transdermal delivery of extracellular vesicles derived from Polygonatum kingianum (PkEVs) to prevent UVB-induced skin photoaging. The PkEVs exhibited a typical spherical morphology, with an average diameter of 168.2 ± 10.1 nm, and were successfully incorporated into a GelMA-based microneedle system (Pk@MN) for transdermal delivery. Pk@MN exhibited sufficient mechanical strength, with a breaking force of approximately 0.36 N per needle, and showed a rapid PkEV release profile, with approximately 90% of PkEVs released within 10 min. In vitro , Pk@MN effectively inhibited UVB-induced oxidative stress and cellular senescence in HaCaT cells, as indicated by reduced intracellular reactive oxygen species (ROS) levels and decreased senescence-associated β-galactosidase (SA-β-Gal) positive cells. Pk@MN also suppressed LPS-induced inflammatory responses in RAW264.7 cells. In vivo , pretreatment with Pk@MN markedly inhibited UVB-induced skin photoaging in mice, maintained skin elasticity by suppressing epidermal thickening, and promote dermal collagen deposition, with a 2.1-fold increase in collagen density compared with the Model group. Moreover, Pk@MN significantly suppressed the expression of the proinflammatory cytokine interleukin-6 (IL-6), approaching the level observed in the Control group. Transcriptome sequencing analysis further suggested that the protective effects of Pk@MN were associated with the regulation of pathways related to inflammation, oxidative stress, and tissue repair. This study highlights a GelMA-based microneedle platform for efficient transdermal delivery of plant-derived extracellular vesicles and provides a promising strategy for preventing UVB-induced skin photoaging.

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