哈卡特
药理学
特应性皮炎
MAPK/ERK通路
抗氧化剂
免疫系统
化学
药品
活性氧
洗剂
细胞因子
医学
水杨酸
免疫学
生物
促炎细胞因子
p38丝裂原活化蛋白激酶
癌症研究
抗生素
碳纤维
细胞毒性
细胞生长
传统医学
作者
Yingnan Jiang,Zhihong Wen,Yue Wu,Xiaoyu He,Tenghui Tian,Mohan Gao,Di Zhang,Ning Tian,Wenfei Ma,Difu Zhu,Ling Li,YoungJoo Lee,Rui Jiang,Quan Lin
标识
DOI:10.1016/j.colsurfb.2026.115754
摘要
Atopic dermatitis (AD) is a chronic and relapsing inflammatory skin disorder with rising global prevalence. Current treatments such as corticosteroids and antibiotics often lead to side effects, drug resistance, and limited long-term safety. Natural compounds, including extracts from Selaginella, offer multi-targeted anti-inflammatory and antioxidant benefits but suffer from poor solubility and low bioavailability. To overcome these limitations, carbon nanodots using selaginella extract as the sole precursor (SSE-CDs) were synthesized. The SSE-CDs (2.5 ± 1.5 nm) possess abundant surface functional groups, negative surface charge and good enzyme-like activity. In vitro, SSE-CDs reduced reactive oxygen species, alleviated inflammation, and promoted proliferation in damaged HaCaT cells. In vivo, in an AD mouse model, SSE-CDs restored immune cell balance and normalized inflammatory cytokine expression. Mechanistic studies revealed that SSE-CDs inhibited phosphorylation of key proteins in the NF-κB and MAPK signaling pathways. Furthermore, a skincare lotion formulated with SSE-CDs showed therapeutic efficacy in an AD mouse model, suggesting its potential for dermatological applications. This study provides a preliminary demonstration of carbon nanodots as a promising anti-inflammatory strategy for AD management.
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