Macao Centre for Research and Development in Chinese Medicine, State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao, 999078, China.
College of Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, 611137, China.
Adv Healthc Mater. 2023 Oct;12(26):e2300946. doi: 10.1002/adhm.202300946. Epub 2023 Jun 25.
Ulcerative colitis (UC) is a high incidence disease worldwide and clinically presents as relapsing and incurable inflammation of the colon. Bilirubin (BR), a natural antioxidant with significant anti-colitic effects, is utilized in preclinical studies as an intestinal disease therapy. Due to their water-insolubility, the design of BR-based agents usually involves complicated chemosynthetic processes, introducing various uncertainties in BR development. After screening numerous materials, it is identified that chondroitin sulfate can efficiently mediate the construction of BR self-assembled nanomedicine (BSNM) via intermolecular hydrogen bonds between dense sulfate and carboxyl of chondroitin sulfate and imino groups of BR. BSNM exhibits pH sensitivity and reactive oxygen species responsiveness, enabling targeted delivery to the colon. After oral administration, BSNM significantly inhibits colonic fibrosis and apoptosis of colon and goblet cells; it also reduces the expression of inflammatory cytokines. Moreover, BSNM maintains the normal level of zonula occludens-1 and occludin to sustain the integrity of intestinal barrier, regulates the macrophage polarization from M1 to M2 type, and promotes the ecological recovery of intestinal flora. Collectively, the work provides a colon-targeted and transformable BSNM that is simple to prepare and is useful as an efficient targeted UC therapy.
溃疡性结肠炎(UC)是一种全球高发疾病,临床上表现为结肠反复发作且无法治愈的炎症。胆红素(BR)是一种具有显著抗结肠炎作用的天然抗氧化剂,在临床前研究中被用作肠道疾病的治疗药物。由于其不溶于水,BR 基制剂的设计通常涉及复杂的化学合成过程,这给 BR 的开发带来了各种不确定性。经过大量材料的筛选,发现硫酸软骨素可以通过硫酸软骨素中密集的硫酸盐和羧基与 BR 的亚氨基之间的分子间氢键,有效地介导 BR 自组装纳米药物(BSNM)的构建。BSNM 具有 pH 敏感性和活性氧响应性,能够靶向递送到结肠。口服 BSNM 后,能显著抑制结肠纤维化和结肠及杯状细胞的凋亡,降低炎症细胞因子的表达。此外,BSNM 维持着紧密连接蛋白-1 和闭合蛋白的正常水平,以维持肠道屏障的完整性,调节巨噬细胞从 M1 型向 M2 型极化,并促进肠道菌群的生态恢复。总之,这项工作提供了一种具有结肠靶向性和可转化性的 BSNM,其制备简单,是一种有效的 UC 靶向治疗方法。