摘要
Androgenetic alopecia (AGA) is highly prevalent, yet its treatment is limited by systemic side effects and poor patient compliance. This study aims to develop a topical delivery system for synergistic, effective, safe, and highly compliant AGA treatment. A methacrylated hyaluronic acid (HAMA)-based hydrogel microneedle patch (C-F-HMN) co-loaded with a carbon monoxide-releasing molecule (CORM-401) and finasteride (FIN) was prepared. CORM-401 and FIN were formulated into CORM-401@Pluronic F127 (CO@F127) micelles and FIN@hydroxypropyl-β-cyclodextrin (HP-β-CD) inclusion complexes, respectively. Efficacy, mechanisms, and biocompatibility were evaluated in a testosterone-induced AGA mouse model. C-F-HMN achieved efficient local drug delivery, minimized systemic exposure, and sustained efficacy. FIN reduced dihydrotestosterone (DHT) production by inhibiting 5α-reductase; CORM-401 consumed scalp reactive oxygen species (ROS) and released carbon monoxide (CO) to improve the hair follicle microenvironment. Compared with monotherapy and minoxidil, C-F-HMN showed superior hair regrowth, activated the Wnt/β-catenin pathway, inhibited the transforming growth factor-β (TGF-β)/bone morphogenetic protein (BMP) pathway, and exhibited good biocompatibility without systemic toxicity. This study establishes a novel, effective, safe, and highly patient-compliant topical combination therapy for AGA, overcoming the limitations of traditional treatments and providing a new strategy for clinical AGA management.
危险品化学品经营许可证(带存储)