炎症性肠病
促炎细胞因子
免疫系统
纳米医学
活性氧
炎症
免疫学
背景(考古学)
化学
医学
疾病
生物
细胞生物学
纳米技术
病理
材料科学
纳米颗粒
古生物学
作者
Qingrong Li,Liting Lin,Cong Zhang,Hengguo Zhang,Yan Ma,Haisheng Qian,Xu‐Lin Chen,Xianwen Wang
标识
DOI:10.1186/s12951-023-02246-x
摘要
Abstract There is a growing body of evidence indicating a close association between inflammatory bowel disease (IBD) and disrupted intestinal homeostasis. Excessive production of reactive oxygen species (ROS) and reactive nitrogen species (RNS), along with an increase in M1 proinflammatory macrophage infiltration during the activation of intestinal inflammation, plays a pivotal role in disrupting intestinal homeostasis in IBD. The overabundance of ROS/RNS can cause intestinal tissue damage and the disruption of crucial gut proteins, which ultimately compromises the integrity of the intestinal barrier. The proliferation of M1 macrophages contributes to an exaggerated immune response, further compromising the intestinal immune barrier. Currently, intestinal nanomaterials have gained widespread attention in the context of IBD due to their notable characteristics, including the ability to specifically target regions of interest, clear excess ROS/RNS, and mimic biological enzymes. In this review, we initially elucidated the gut microenvironment in IBD. Subsequently, we delineate therapeutic strategies involving two distinct types of nanomedicine, namely inorganic nanoparticles and natural product nanomaterials. Finally, we present a comprehensive overview of the promising prospects associated with the application of nanomedicine in future clinical settings for the treatment of IBD (graphic abstract). Graphical Abstract
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