Targeted delivery of Chinese herb pair-based berberine/tannin acid self-assemblies for the treatment of ulcerative colitis

小檗碱 结肠炎 透明质酸 溃疡性结肠炎 单宁酸 中医药 药理学 草本植物 化学 炎症性肠病 医学 免疫学 传统医学 草药 内科学 疾病 病理 替代医学 有机化学 解剖
作者
Shiyun Chen,Zhejie Chen,Yi Wang,Hao Wei,Qin Yuan,Hefeng Zhou,Caifang Gao,Yitao Wang,Xu Wu,Shengpeng Wang
出处
期刊:Journal of Advanced Research [Elsevier]
卷期号:40: 263-276 被引量:35
标识
DOI:10.1016/j.jare.2021.11.017
摘要

Ulcerative colitis (UC) is a chronic recurrent idiopathic disease characterized by damage to the colonic epithelial barrier and disruption of inflammatory homeostasis. At present, there is no curative therapy for UC, and the development of effective and low-cost therapies is strongly advocated. Multiple lines of evidence support that tannic acid (TA) and berberine (BBR), two active ingredients derived from Chinese herb pair (Rhei Radix et Rhizoma and Coptidis Rhizoma), have promising therapeutic effects on colonic inflammation. This study aims to develop a targeted delivery system based on BBR/TA-based self-assemblies for the treatment of UC. TA and BBR self-assemblies were optimized, and hyaluronic acid (HA) was coated to achieve targeted colon delivery via HA-cluster of differentiation 44 (CD44) interactions. The system was systematically characterized and dextran sodium sulfate (DSS)-induced mouse colitis model was further used to investigate the biodistribution behavior, effect and mechanism of the natural system. TA and BBR could self-assemble into stable particles (TB) and HA-coated TB (HTB) further increased cellular uptake and accumulation in inflamed colon lesions. Treatment of HTB inhibited pro-inflammatory cytokine levels, restored expression of tight junction-associated proteins and recovered gut microbiome alteration, thereby exerting anti-inflammatory effects against DSS-induced acute colitis. Our targeted strategy may provide a convenient and powerful platform for UC and reveal new modes of application of herbal combinations.
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