Xu Peng, Xu Kun, Li Jiayin, Liu Aoxue, Xiao Wei, Sun Lin
Department of Zhuhai Campus of Zunyi Medical University, Zhuhai 519041, China; Department of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China.
Department of Zhuhai Campus of Zunyi Medical University, Zhuhai 519041, China.
Int J Pharm. 2025 Apr 30;675:125528. doi: 10.1016/j.ijpharm.2025.125528. Epub 2025 Mar 27.
Psoriasis, a prevalent immunoinflammatory skin condition, is characterized by abnormal skin thickening, which complicates traditional topical drug delivery and hinders drug penetration. Our goal is to enhance the efficacy of psoriasis treatment by developing a transdermal drug formulation. Microneedles (MNs) can improve treatment outcomes by increasing the absorption of topical medications through skin penetration. Curcumin (Cur), a natural anti-inflammatory, antioxidant, and immunomodulatory small molecule with water-insoluble properties, shows promise for psoriasis relief. In this research, three Cur nano-formulations (NFs) were screened and prepared using antisolvent and ethanol injection methods, with one being dispersed into hyaluronic acid (HA) dissolving MNs. A transdermal nano-MNs delivery system was constructed using a double-layer centrifugation technique. This co-delivery system overcame Cur's solubility issues, poor absorption, and instability, allowing targeted and efficient delivery of Cur-NFs to the skin without being hindered by the skin barrier. In vitro studies demonstrated that Cur-NF dissolving MNs possess adequate mechanical properties for skin implantation, exhibit rapid dissolution, and achieve an effective drug release rate of 73 % within 6 h. Pharmacodynamic evaluations demonstrated that the MNs system effectively ameliorated key psoriatic skin manifestations. Notably, MNs treatment significantly reduced the Psoriasis Area and Severity Index (PASI) score from 12.0 ± 0.0 (model group) to 4.7 ± 0.5 (p < 0.05), alongside a marked suppression of pro-inflammatory cytokines, including TNF-α, IL-17, IL-22, and IL-23, compared to untreated psoriatic controls. Therefore, the composite dissolving MNs delivery system loaded with Cur-NFs represents a promising approach for psoriasis treatment.
银屑病是一种常见的免疫炎症性皮肤病,其特征是皮肤异常增厚,这使得传统局部给药变得复杂,并阻碍药物渗透。我们的目标是通过开发一种透皮给药制剂来提高银屑病的治疗效果。微针(MNs)可以通过增加局部药物经皮肤渗透的吸收来改善治疗效果。姜黄素(Cur)是一种具有抗炎、抗氧化和免疫调节作用的天然小分子,不溶于水,有望缓解银屑病症状。在本研究中,采用反溶剂法和乙醇注入法筛选并制备了三种Cur纳米制剂(NFs),其中一种分散在溶解于透明质酸(HA)的微针中。采用双层离心技术构建了一种透皮纳米微针给药系统。这种共递送系统克服了Cur的溶解度问题、吸收不良和稳定性问题,使Cur-NFs能够靶向、高效地递送至皮肤,而不受皮肤屏障的阻碍。体外研究表明,Cur-NF溶解微针具有适合皮肤植入的机械性能,溶解迅速,在6小时内有效药物释放率达到73%。药效学评价表明,微针系统有效地改善了银屑病的关键皮肤表现。值得注意的是,与未治疗的银屑病对照组相比,微针治疗显著降低了银屑病面积和严重程度指数(PASI)评分,从12.0±0.0(模型组)降至4.7±0.5(p<0.05),同时显著抑制了包括TNF-α、IL-17、IL-22和IL-23在内的促炎细胞因子。因此,负载Cur-NFs的复合溶解微针给药系统是一种很有前景的银屑病治疗方法。