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
药理学
生物化学
皮肤老化
分散性
维生素C
多酚
维生素E
溶解度
IC50型
色谱法
类黄酮
输送系统
酶
脂质体
阿布茨
脂肪酸
基质(化学分析)
食品科学
作者
Xuemei Gu,Jie Wang,Jing Chen,Zhiyang Lv,Shaohua Wu,Bowen Li,Guanyu Liu,Xiaohui Wang,Tianye Qian,Yu Wu
标识
DOI:10.6084/m9.figshare.31389785
摘要
The natural flavonoids quercetin (Que) and kaempferol (Kae) show great potential for anti-aging applications but suffer from poor solubility and skin permeability. This study aimed to develop a synergistic topical emulsion system to overcome the poor bioavailability of the Que and Kae for enhanced efficacy. The optimal synergistic molar ratio (Que:Kae = 1:2) was first identified via 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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