银屑病
透皮
甲氨蝶呤
活性氧
药品
药理学
二苯甲酚
药物输送
化学
医学
材料科学
皮肤病科
纳米技术
生物化学
免疫学
作者
Duohang Bi,Fei Qu,Wanyue Xiao,Jiaxin Wu,Pei Liu,Hongyao Du,Youwei Xie,Hongmei Liu,Lianbin Zhang,Juan Tao,Yijing Liu,Jintao Zhu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-02-27
卷期号:17 (5): 4346-4357
被引量:46
标识
DOI:10.1021/acsnano.2c08979
摘要
Psoriasis is an inflammatory skin disease. Microneedle (MN) patches can improve psoriasis treatment outcomes by increasing local drug content in the skin. As psoriasis frequently relapses, developing intelligent MN-based drug delivery systems with prolonged therapeutic drug levels and improved treatment efficiency is of great significance. Here, we designed detachable H2O2-responsive gel-based MN patches containing methotrexate (MTX) and epigallocatechin gallate (EGCG) by using EGCG as both cross-linkers for needle-composited materials and anti-inflammatory drugs. The gel-based MNs had dual-mode drug release kinetics, which quickly released MTX diffusively and sustainably released EGCG in an H2O2-responsive way. Compared with dissolving MNs, the gel-based MNs extended skin retention of EGCG, leading to prolonged reactive oxygen species (ROS) scavenging effects. The ROS-responsive MN patches that transdermally delivered antiproliferative and anti-inflammatory drugs improved treatment outcomes in both psoriasis-like and prophylactic psoriasis-like animal models.
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