化学
抗氧化剂
山奈酚
生物利用度
乳状液
槲皮素
药品
氧化应激
药物输送
生物化学
药理学
皮肤老化
分散性
维生素E
维生素C
多酚
溶解度
色谱法
IC50型
类黄酮
输送系统
脂质体
酶
阿布茨
脂肪酸
基质(化学分析)
食品科学
维生素
作者
Xuemei Gu,Yì Wáng,Jing Chen,Zhiyang Lv,Shaohua Wu,Bowen Li,Guanyu Liu,Xiaohui Wang,Tianye Qian,Yelin Wu
标识
DOI:10.1080/10837450.2026.2635734
摘要
1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging and cellular assays. The drugs were then loaded into milk-derived exosomes (mExo) using a Box-Behnken design (BBD), achieving high encapsulation (>69%), a size of ∼120 nm, and a polydispersity index (PDI) of 0.180. This complex was incorporated into an oil-in-water emulsion, with its formulation also BBD-optimized for stability. In a D-galactose-induced skin aging mouse model, the final Que/Kae-mExo@Eml formulation significantly outperformed control groups (free drug mixture, blank exosome emulsion, and vitamin C). It most effectively reduced oxidative stress (malondialdehyde, MDA), enhanced antioxidant enzymes (superoxide dismutase, SOD and glutathione, GSH), suppressed matrix metalloproteinase-1 (MMP-1), promoted collagen I (Col I) synthesis, and improved skin histology, elasticity, and hydration. In conclusion, an optimized, stable emulsion leveraging a synergistic 1:2 drug ratio and an mExo delivery system was successfully developed, demonstrating superior comprehensive efficacy against skin aging.
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