Development of a Deep Eutectic Solvent-Assisted Kaempferol Hydrogel: A Promising Therapeutic Approach for Psoriasis-like Skin Inflammation

被引:4
|
作者
Su, Huining [1 ]
Liu, Zhicheng [1 ]
Zhang, Zuoliang [1 ]
Jing, Xunan [2 ]
Meng, Lingjie [1 ,2 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Sch Chem, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, Affiliated Hosp 1, Talent Highland, Xian 710061, Peoples R China
[3] Xi An Jiao Tong Univ, Instrumental Anal Ctr, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
psoriasis; kaempferol; deep eutectic solvent; hydrogel; ROS scavenging; immune regulation; ROS; METHOTREXATE; ANTIOXIDANT; CHEMISTRY;
D O I
10.1021/acs.molpharmaceut.3c00729
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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 G' of DK-pGEL (similar to 14 kPa) hydrogels was significantly lower than the control group (similar to 30 kPa) at 37 degrees C. The DK-pGEL hydrogel exhibited ideal fluidity and viscosity at 37 degrees 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 mu g/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 mu g/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-alpha, 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.
引用
收藏
页码:6319 / 6329
页数:11
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