China Pharmaceutical University, Department of Pharmaceutics, 24 Tongjiaxiang, Nanjing 210009, Jiangsu, China.
China Pharmaceutical University, Department of Pharmaceutics, 24 Tongjiaxiang, Nanjing 210009, Jiangsu, China.
J Control Release. 2024 Aug;372:778-794. doi: 10.1016/j.jconrel.2024.06.060. Epub 2024 Jul 4.
Alopecia areata affects over 140 million people worldwide and causes severe psychological distress. The Janus kinase (JAK) inhibitor, tofacitinib, shows significant potential in therapeutic applications for treating alopecia areata; however, the systemic adverse effects of oral administration and low absorption rate at the target site limit its application. Hence, to address this issue, we designed topical formulations of tofacitinib-loaded cationic lipid nanoparticles (TFB-cNLPs) with particle sizes of approximately 200 nm. TFB-cNLPs promoted percutaneous absorption and hair follicle targeting in an ex vivo pig ear model. TFB-cNLP decreased IFN-γ-induced alopecia areata symptoms in an in vitro follicle model by blocking the Janus kinase/signal transducers and activators of transcription (JAK/STAT) pathway. It also reduced the number of CD8NKG2DT cells in a C3H mouse model of alopecia areata in vivo, thereby inhibiting the progression of alopecia areata and reversing hair loss. These findings suggest that TFB-cNLP enhanced hair follicle targeting and has the potential for topical treatment or prevention of alopecia areata.
斑秃影响全球超过 1.4 亿人,并导致严重的心理困扰。Janus 激酶(JAK)抑制剂托法替尼在治疗斑秃的治疗应用中显示出巨大的潜力;然而,口服的全身不良反应和目标部位的低吸收率限制了其应用。因此,为了解决这个问题,我们设计了载有他克莫司的阳离子脂质纳米粒(TFB-cNLPs)的局部制剂,粒径约为 200nm。TFB-cNLPs 在体外猪耳模型中促进了经皮吸收和毛囊靶向。TFB-cNLP 通过阻断 Janus 激酶/信号转导和转录激活因子(JAK/STAT)通路,抑制 IFN-γ 诱导的体外毛囊模型中的斑秃症状。它还减少了 C3H 斑秃小鼠模型中的 CD8NKG2DT 细胞数量,从而抑制了斑秃的进展并逆转了脱发。这些发现表明,TFB-cNLP 增强了毛囊靶向作用,具有局部治疗或预防斑秃的潜力。