Hayati Rima, Lukitaningsih Endang, Sulaiman Teuku Nanda Saifullah, Earlia Nanda, Idroes Rinaldi
Graduate School of Mathematics and Applied Sciences, Universitas Syiah Kuala, Banda Aceh, 23111, Indonesia.
Department of Pharmacy, Poltekkes Kemenkes Aceh, Aceh Besar, 23231, Indonesia.
Arch Dermatol Res. 2025 Jan 28;317(1):313. doi: 10.1007/s00403-025-03824-9.
Atopic dermatitis (AD) is a chronic inflammatory skin condition characterized by dry skin, severe itching, redness, and inflammation. Its complex etiology, involving genetic, immunological, and environmental factors, necessitates innovative therapeutic approaches. This study investigates nanostructured lipid carriers (NLCs) formulated with traditional fermented coconut (Cocos nucifera L.) oil from Aceh (pliek oil). The NLC was optimized using Box-Behnken Design and prepared through high shear homogenization and ultrasonication. The optimized formula consisted of 8% w/w lipid phase, 2 min sonication time, and 6% Tween 80, resulting in a particle size of 207.1 ± 0.93 nm, a polydispersity index of 0.275 ± 0.005, and a zeta potential of - 30.2 ± 0.78 mV. A 1:1 ratio of Tween 80 and Span 20 ensured stable NLC. The NLC of Pliek oil (NLC-PL) gel met EuroGuiDerm standards for AD treatment, with a pH of 5.62 ± 0.06, indicating skin compatibility. Histological analysis demonstrated that the NLC-PL gel (2.5% w/w pliek oil) significantly reduced MC903-induced ear thickness and inflammation compared to the negative control (p < 0.05), and suppressed mast cell numbers, comparable to the positive control (p > 0.05). Enzyme-Linked Immunosorbent Assay (ELISA) confirmed its role as a c-jun N-terminal kinase 1 (JNK1) inhibitor, supporting its potential as targeted topical therapy for AD. This study aligns with the study's objective to develop innovative treatments for AD.
特应性皮炎(AD)是一种慢性炎症性皮肤病,其特征为皮肤干燥、剧烈瘙痒、发红和炎症。其复杂的病因涉及遗传、免疫和环境因素,因此需要创新的治疗方法。本研究调查了用来自亚齐的传统发酵椰子(Cocos nucifera L.)油(普利克油)配制的纳米结构脂质载体(NLC)。使用Box-Behnken设计对NLC进行优化,并通过高剪切均质化和超声处理制备。优化后的配方包含8%(w/w)脂质相、2分钟超声处理时间和6%吐温80,所得粒径为207.1±0.93nm,多分散指数为0.275±0.005,ζ电位为-30.2±0.78mV。吐温80和司盘20的比例为1:1可确保NLC的稳定性。普利克油的NLC(NLC-PL)凝胶符合欧洲皮肤病学指南中AD治疗的标准,pH值为5.62±0.06,表明具有皮肤相容性。组织学分析表明,与阴性对照相比,NLC-PL凝胶(2.5%(w/w)普利克油)显著降低了MC903诱导的耳部厚度和炎症(p<0.05),并且抑制了肥大细胞数量,与阳性对照相当(p>0.05)。酶联免疫吸附测定(ELISA)证实其作为c-jun氨基末端激酶1(JNK1)抑制剂的作用,支持其作为AD靶向局部治疗的潜力。本研究符合该研究开发AD创新治疗方法的目标。