Development of ginger-derived extracellular vesicles thermosensitive gel for UVA-induced photodamage of skin

细胞外 活力测定 真皮成纤维细胞 抗氧化剂 细胞凋亡 成纤维细胞 活性氧 细胞外基质 化学 渗透(战争) 体外 生物物理学 生物化学 生物 运筹学 工程类
作者
Jinghuang Wang,Bo Ran,Wuzhen Ma,Yupu Teng,Mubarak G. Bello,Lihua Chen,Jiwen Zhang,Jin Sun,Xiaohong Ren,Li Wu
出处
期刊:Journal of Drug Delivery Science and Technology [Elsevier BV]
卷期号:96: 105649-105649 被引量:1
标识
DOI:10.1016/j.jddst.2024.105649
摘要

Due to an increase in outdoor activities, UV radiation exposure has grown recently, leading to an increase in the occurrence of illnesses associated to photodamage. The necessity of developing skin photodamage restoration technology has drawn attention. Herein, a temperature-sensitive gel was designed to load ginger-derived extracellular vesicles (gEVs) for UVA-induced skin inflammatory injury. Traditional medicine has used ginger extracts as natural therapeutic agents, however, no study has looked into how gEVs might be used in drug development or regenerative medicine. The average particle size of gEVs purified by sucrose density gradient centrifugation was 231.20±25.30 nm, with a tea leaf-like structure and discriminative features. The proliferative and migratory effects of gEVs on epithelial and dermal fibroblast cells were demonstrated. The protective effect of gEVs on in vitro photodamage model was investigated, based on its potent performance in antioxidant capacity that gEVs pretreated cells had a good inhibitory effect on cell viability, UVA-induced apoptosis and reactive oxygen species (ROS). The targeted treatment of specific skin injury sites can be realized by temperature-sensitive gel. The optimal prescription of gel was P407 22.5% and P188 4% screened by gelling temperature and time. The gel with more than 75% water content and 50 μm porous diameter can provide a transient extracellular matrix for cell adhesion and penetration, and well support the gEVs. Within three days, the 12.5% and 25.0% gEVs@Gel exhibited a mending role by gradually releasing 37.4±4.5% and 48.7±2.9% gEVs, respectively. Overall, this study proposes a novel approach to inflammatory skin healing that may serve as a safe substitute for UVA-induced skin photodamage.
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