School of Chemistry, Xi'an Jiaotong University, Xi'an 710049, P. R. China.
Talent Highland, The First Affiliated Hospital, Xi'an Jiaotong University, Xi'an 710061, P. R. China.
Mol Pharm. 2023 Dec 4;20(12):6319-6329. doi: 10.1021/acs.molpharmaceut.3c00729. Epub 2023 Oct 30.
Psoriasis is an incurable inflammatory skin disease that is mediated by the immune system. Although kaempferol has been known for its anti-inflammatory, antioxidant, and anticancer properties, its therapeutic effectiveness is often limited due to its poor water solubility and low bioavailability. To address these challenges, we developed a promising kaempferol hydrogel (DK-pGEL) using Pluronic F127 and a deep eutectic solvent (DES) with varying concentrations of kaempferol. In this study, we first evaluated the rheological properties and viscosity of the DK-pGEL hydrogel. The ' of DK-pGEL (∼14 kPa) hydrogels was significantly lower than the control group (∼30 kPa) at 37 °C. The DK-pGEL hydrogel exhibited ideal fluidity and viscosity at 37 °C, as demonstrated by its shear-thinning behavior. Moreover, the DK-pGEL hydrogel showed controlled release characteristics with a drug release of 97.43 ± 5.37 μg/mL over 60 h. Furthermore, in vitro antioxidant experiments revealed that DK-pGEL exhibited significant radical scavenging ability against the DPPH-radical (96.27 ± 0.37%), ABTS-radical (98.11 ± 0.79%), hydroxyl-radical (66.36 ± 1.01%), and superoxide-radical (90.52 ± 0.79%) at a concentration of 250 μg/mL kaempferol. Additionally, DK-pGEL exhibited notable cellular antioxidant effects by inhibiting reactive oxygen species generation. Cell viability assays (CCK8) and live/dead cell assays were conducted to assess the cytotoxicity of DK-pGEL. The results showed that DK-pGEL could effectively inhibit HaCaT cell proliferation without causing significant cytotoxicity. To evaluate the therapeutic potential of DK-pGEL, an imiquimod (IMQ)-induced mouse model of psoriasis-like lesions was employed. Remarkably, the DK-pGEL hydrogel could significantly reduce the psoriasis area and severity index score, improve the histopathology induced by IMQ, and downregulate the expression of pro-inflammatory cytokines (TNF-α, IL-6, and IL-17A) in the skin tissue. These findings demonstrate that the DES-assisted kaempferol hydrogel holds promise as a topical drug delivery system for psoriasis treatment.
银屑病是一种由免疫系统介导的不可治愈的炎症性皮肤病。尽管山奈酚因其抗炎、抗氧化和抗癌特性而广为人知,但由于其水溶性差和生物利用度低,其治疗效果往往受到限制。为了解决这些挑战,我们使用 Pluronic F127 和具有不同浓度山奈酚的深共晶溶剂 (DES) 开发了一种有前途的山奈酚水凝胶 (DK-pGEL)。在这项研究中,我们首先评估了 DK-pGEL 水凝胶的流变特性和粘度。在 37°C 时,DK-pGEL(约 14 kPa)水凝胶的“η”显著低于对照组(约 30 kPa)。DK-pGEL 水凝胶在 37°C 时表现出理想的流动性和粘度,表现为剪切稀化行为。此外,DK-pGEL 水凝胶具有控制释放特性,在 60 小时内释放 97.43±5.37μg/mL 的药物。此外,体外抗氧化实验表明,DK-pGEL 对 DPPH 自由基(96.27±0.37%)、ABTS 自由基(98.11±0.79%)、羟基自由基(66.36±1.01%)和超氧自由基(90.52±0.79%)具有显著的清除能力,浓度为 250μg/mL 山奈酚。此外,DK-pGEL 通过抑制活性氧的产生表现出显著的细胞抗氧化作用。进行 CCK8 细胞活力测定和死活细胞测定,以评估 DK-pGEL 的细胞毒性。结果表明,DK-pGEL 可以有效抑制 HaCaT 细胞增殖,而不会引起明显的细胞毒性。为了评估 DK-pGEL 的治疗潜力,我们采用咪喹莫特 (IMQ) 诱导的银屑病样病变小鼠模型进行评估。值得注意的是,DK-pGEL 水凝胶可显著降低银屑病面积和严重度指数评分,改善 IMQ 诱导的组织病理学变化,并下调皮肤组织中促炎细胞因子(TNF-α、IL-6 和 IL-17A)的表达。这些发现表明,DES 辅助山奈酚水凝胶有望成为治疗银屑病的局部药物递送系统。