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Apremilast Microemulsion as Topical Therapy for Local Inflammation: Design Characterization and Efficacy Evaluation

机译:Apremilast微乳液作为局部炎症的局部治疗:设计表征和疗效评估

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摘要

Apremilast (APR) is a selective phosphodiesterase 4 inhibitor administered orally in the treatment of moderate-to-severe plaque psoriasis and active psoriatic arthritis. The low solubility and permeability of this drug hinder its dermal administration. The purpose of this study was to design and characterize an apremilast-loaded microemulsion (APR-ME) as topical therapy for local skin inflammation. Its composition was determined using pseudo-ternary diagrams. Physical, chemical and biopharmaceutical characterization were performed. Stability of this formulation was studied for 90 days. Tolerability of APR-ME was evaluated in healthy volunteers while its anti-inflammatory potential was studied using in vitro and in vivo models. A homogeneous formulation with Newtonian behavior and droplets of nanometric size and spherical shape was obtained. APR-ME released the incorporated drug following a first-order kinetic and facilitated drug retention into the skin, ensuring a local effect. Anti-inflammatory potential was observed for its ability to decrease the production of IL-6 and IL-8 in the in vitro model. This effect was confirmed in the in vivo model histologically by reduction in infiltration of inflammatory cells and immunologically by decrease of inflammatory cytokines IL-8, IL-17A and TNFα. Consequently, these results suggest that this formulation could be used as an attractive topical treatment for skin inflammation.
机译:Apremilast(APR)是一种选择性磷酸二酯酶4抑制剂,用于口服施用中度至重度斑块牛皮癣和活性银屑病关节炎。该药物的低溶解度和渗透性阻碍了其皮肤给药。本研究的目的是设计和表征可满足载荷的微乳液(APR-ME)作为局部皮肤炎症的局部治疗。使用伪三元图测定其组合物。进行物理,化学和生物制药表征。研究了该制剂的稳定性90天。在健康的志愿者评估APR-ME的可耐受性,而在体外和体内模型中研究其抗炎潜力。获得了牛顿行为和纳米尺寸和球形液滴的均匀配方。 APR-ME在一阶动力学后释放了掺入的药物,并促进了皮肤潴留,确保了局部效果。观察到抗炎潜力的能力降低了在体外模型中减少IL-6和IL-8的能力。通过减少炎性细胞的渗透和免疫炎症细胞因子IL-8,IL-17A和TNFα的降低,在体内模型中在体内模型中确认了该效果。因此,这些结果表明该配方可以用作皮肤炎症的有吸引力的局部治疗方法。

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