Telrandhe Umesh B, Hasnain Anjum N, Kothawade Sachin N, Telange Darshan R
Datta Meghe College of Pharmacy, Datta Meghe Institute of Higher Education and Research (DMIHER) (DU), Sawangi Meghe, Wardha, Maharashtra, 442001, India.
SCSSS's Sitabai Thite College of Pharmacy, Near Pune-Nagar Bypass, Behind Hudco Colony, Shirur, Maharashtra, 412210, India.
Discov Nano. 2025 Jul 7;20(1):105. doi: 10.1186/s11671-025-04298-4.
Psoriasis is a chronic inflammatory autoimmune skin disease with enhanced skin cell turnover. Despite the therapies currently available, better and target-oriented therapies are needed. Fisetin is a flavonoid with antioxidant, anti-inflammatory, and immunomodulatory properties. It shows therapeutic potential, but its poor bioavailability and penetration into the skin cannot be used effectively to treat psoriasis. While fisetin-loaded nanoformulations in cancer and other diseases have been explored, their potential as a therapy for psoriasis is unexplored. Most reviews detail the biological activities of fisetin or nanoformulations for psoriasis therapy but not their combination. The review here compiles fisetin's chemical and pharmacological properties along with the problems with conventional drug delivery and fisetin-loaded nanoformulations such as polymeric nanoparticles, liposomes, solid lipid nanoparticles, nanogels, and micelles. It also discusses their mechanisms, preclinical results, and potential for the clinic. Preclinical studies demonstrate fisetin nanoformulations to enhance penetration into the skin, reduce inflammation, promote skin regeneration in psoriasis models, and alleviate symptoms of redness and scaling. Clinical trials are lacking, and studies are needed to assess safety and efficacy. Fisetin nanoformulations are a potential target-oriented psoriasis therapy with better drug delivery and fewer side effects than conventional therapies. Despite formulation stability, scalability, and regulatory issues, the potential for fisetin-loaded nanoformulations is excellent and needs further exploration for their safety and efficacy in patients.
银屑病是一种慢性炎症性自身免疫性皮肤病,皮肤细胞更新加快。尽管目前有多种治疗方法,但仍需要更好的靶向治疗。非瑟酮是一种具有抗氧化、抗炎和免疫调节特性的黄酮类化合物。它显示出治疗潜力,但其较差的生物利用度和皮肤渗透性使其无法有效用于治疗银屑病。虽然已经探索了载有非瑟酮的纳米制剂在癌症和其他疾病中的应用,但它们作为银屑病治疗方法的潜力尚未得到研究。大多数综述详细介绍了非瑟酮或纳米制剂治疗银屑病的生物学活性,但没有涉及它们的联合应用。本文综述汇编了非瑟酮的化学和药理特性,以及传统药物递送和载有非瑟酮的纳米制剂(如聚合物纳米颗粒、脂质体、固体脂质纳米颗粒、纳米凝胶和胶束)存在的问题。还讨论了它们的作用机制、临床前结果以及临床应用潜力。临床前研究表明,非瑟酮纳米制剂可增强皮肤渗透性,减轻炎症,促进银屑病模型中的皮肤再生,并缓解发红和脱屑症状。目前缺乏临床试验,需要开展研究来评估其安全性和有效性。非瑟酮纳米制剂是一种潜在的靶向银屑病治疗方法,与传统疗法相比,具有更好的药物递送效果和更少的副作用。尽管存在制剂稳定性、可扩展性和监管问题,但载有非瑟酮的纳米制剂潜力巨大,需要进一步探索其在患者中的安全性和有效性。