桉树油
Zeta电位
药剂师
分散性
化学
伊米奎莫德
体内
银屑病
离体
药理学
色谱法
医学
皮肤病科
体外
生物化学
材料科学
免疫学
病理
生物
有机化学
纳米技术
生物技术
纳米颗粒
作者
Mohamed Ashraf,Hossam S. El‐Sawy,Ghada M. El-Zaafarany,Mona M.A. Abdel-Mottaleb
标识
DOI:10.1002/ardp.202400557
摘要
Abstract Psoriasis is a chronic inflammatory skin disease that affects patients' quality of life. This study aimed to enhance the efficacy of topical application of fluticasone propionate (FP) using a eucalyptus oil‐based nanoemulsion, an oil possessing anti‐inflammatory activity and extracted from the leaves, fruits, and buds of Eucalyptus globulus or Eucalyptus maidenii , to improve the skin deposition of FP and aid its anti‐inflammatory effect. Box‐Behnken design was employed to optimize NE formulations, which were characterized for globule size, zeta potential, polydispersity index, rheological behavior, microscopic morphology, ex vivo skin permeation/deposition, and in vivo efficacy using imiquimod‐induced psoriatic lesions. The optimized formulation depicted a droplet size of 188 ± 22.4 nm, a zeta potential of −17.63 ± 1.66 mV, and a viscosity of 204.9 mPa s. In addition to the increased FP retention in different skin layers caused by the NE and the reduced PASI score compared to the marketed cream, the levels of inflammatory cytokines IL‐1α, IL‐6, IL17a were markedly lowered, indicating the improved anti‐psoriatic curable efficacy of the optimized formulation in comparison to the FP‐marketed product.
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