曲酸
体内
药理学
化学
纳米载体
银屑病
米曲霉
赋形剂
透皮
药品
酪氨酸酶
生物化学
皮肤病科
医学
酶
生物
生物技术
作者
Ashaimaa Y. Moussa,Haidy Abbas,Mariam Zewail,Passent M.E. Gaafar,Nehal Ibrahim
标识
DOI:10.1002/ardp.202400410
摘要
Abstract Psoriasis is a skin disorder characterized by impaired epidermal differentiation that is regularly treated by systemic drugs with undesirable side effects. Based on its anti‐inflammatory, antiproliferative and anti‐melanoma attributes, the fungal metabolite kojic acid represents an attractive candidate for anti‐psoriatic research. The present work aims to investigate an efficient topical bio‐friendly vesicular system loaded with kojic acid isolated from Aspergillus oryzae as an alternative way for the management of psoriasis to avoid systemic toxicity. Kojic acid‐loaded spanlastics were prepared by ethanol injection technique, employing span 60 along with brij 35 and cremophor rh40 as edge activators, with the complete in vitro characterization of the developed nanoplatform. The selected formulation displayed a spherical morphology, an optimum particle size of 234.2 ± 1.65 nm, high entrapment efficiency (87.4% ± 0.84%) and significant sustained drug release compared with the drug solution. In vivo studies highlighted the superior relief of psoriasis symptoms and the ability to maintain healthy skin with the least changes in mRNA expression of inflammatory cytokines, achieved by the developed nanoplatform compared to kojic acid solution. Moreover, the in vivo histopathological studies confirmed the safety of the topically applied spanlastics. In addition, the molecular mechanism was approached through in vitro assessment of cathepsin S and PDE‐4 inhibitory activities and in silico investigation of kojic acid docking in several anti‐psoriatic drug targets. Our results suggest that a topically applied vesicular system loaded with kojic acid could lead to an expansion in the dermo‐cosmetic use of kojic acid as a natural bio‐friendly alternative for systemic anti‐psoriatic drugs.
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