Wu Jiaxin, Wang Leyan, Lu Han, Huo Yujia, Guo Zhaoyang, Cheng Yuanyuan, Li Yunan, Wang Yinsong, Li Chunyu
The Province and Ministry Co-Sponsored Collaborative Innovation Center for Medical Epigenetics, Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics (Theranostics), School of Pharmacy, Tianjin Medical University, Tianjin 300070, China.
Department of Integrated Traditional Chinese and Western Medicine, International Medical School, Tianjin Medical University, Tianjin 300070, China.
Mol Pharm. 2025 Sep 1;22(9):5410-5427. doi: 10.1021/acs.molpharmaceut.5c00383. Epub 2025 Aug 20.
Inflammatory bowel disease (IBD) management remains challenging due to the inadequate efficacy and systemic toxicity of conventional therapies. Herein, we developed an inulin hydrogel loaded with self-assembled nanoparticles of curcumin and glycyrrhizic acid (CURG@IN) for IBD treatment. CURG@IN exhibited remarkable gel characteristics and enzyme-responsive drug release behavior. , CURG@IN demonstrated potent antioxidant capabilities, effectively protecting cells from oxidative injury, facilitating wound healing of epithelial cells, and regulating macrophage polarization. Additionally, it exerted inhibitory effects on the NF-κB pathway, thereby reducing the production of inflammatory cytokines. In DSS-induced colitis mice, oral CURG@IN significantly ameliorated disease activity index and restored colonic histological architecture. Gut barrier integrity was reinforced through upregulation of tight junction proteins, while microbiota analysis revealed significant restoration of microbial homeostasis. Notably, no significant toxicity was observed during treatment. Collectively, this oral therapeutic strategy provides a multimechanistic approach combining anti-inflammatory, antioxidative, and microbiota-modulating effects for safe IBD therapy, with the potential for clinical application.
由于传统疗法疗效不足和全身毒性,炎症性肠病(IBD)的管理仍然具有挑战性。在此,我们开发了一种负载姜黄素和甘草酸自组装纳米颗粒的菊粉水凝胶(CURG@IN)用于IBD治疗。CURG@IN表现出显著的凝胶特性和酶响应性药物释放行为。此外,CURG@IN显示出强大的抗氧化能力,有效保护细胞免受氧化损伤,促进上皮细胞伤口愈合,并调节巨噬细胞极化。此外,它对NF-κB通路具有抑制作用,从而减少炎症细胞因子的产生。在DSS诱导的结肠炎小鼠中,口服CURG@IN显著改善了疾病活动指数并恢复了结肠组织学结构。通过上调紧密连接蛋白加强了肠道屏障完整性,而微生物群分析显示微生物稳态得到显著恢复。值得注意的是,治疗期间未观察到明显毒性。总体而言,这种口服治疗策略提供了一种多机制方法,结合抗炎、抗氧化和微生物群调节作用,用于安全的IBD治疗,具有临床应用潜力。