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ROS 清除和炎症靶向聚多巴胺纳米颗粒调节炎症性肠病中的肠道免疫和菌群治疗。

ROS Scavenging and inflammation-directed polydopamine nanoparticles regulate gut immunity and flora therapy in inflammatory bowel disease.

机构信息

Central Laboratory, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, 301# Yanchang Middle Road, Shanghai, 200072, China.

Department of Urology Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, 200060, China.

出版信息

Acta Biomater. 2023 Apr 15;161:250-264. doi: 10.1016/j.actbio.2023.02.026. Epub 2023 Mar 1.

Abstract

Dysfunction of the intestinal mucosal immune system and dysbiosis of the intestinal microflora can induce inflammatory bowel disease. However, drug-mediated clinical treatment remains a challenge due to its poor therapeutic efficacy and severe side effects. Herein, a ROS scavenging and inflammation-directed nanomedicine is designed and fabricated by coupling polydopamine nanoparticles with mCRAMP, an antimicrobial peptide, while wrapping macrophage membrane in the outer layer. The designed nanomedicine reduced the secretion of pro-inflammatory cytokines and elevate the expression of anti-inflammatory cytokine in vivo and in vitro inflammation models, demonstrating its significant ability of improving inflammatory responses. Importantly, the macrophage membrane encapsulated nanoparticles exhibit the obviously enhanced targeting performance in local inflamed tissues. Furthermore, the 16S rRNA sequencing of fecal microorganisms showed that probiotics increased and pathogenic bacteria were inhibited after oral delivery the nanomedicine, indicating that the designed nano platform played a significant role in optimizing intestinal microbiome. Taken together, the designed nanomedicine are not only easy to prepare and exhibit high biocompatibility, but also show the inflammatory targeting property, anti-inflammatory function and positive regulation of intestinal flora, thus providing a new idea for the intervention and treatment of colitis. STATEMENT OF SIGNIFICANCE: Inflammatory bowel disease (IBD), a chronic and intractable disease, may lead to colon cancer in severe cases without effective treatment. However, clinical drugs are largely ineffective owing to insufficient therapeutic efficacies and side effects. Herein, we constructed a biomimetic polydopamine nanoparticle for oral administration to treat the IBD by modulating mucosal immune homeostasis and optimizing intestinal microorganisms. In vitro and in vivo experiments showed that the designed nanomedicine not only exhibits the anti-inflammatory function and inflammatory targeting property but also positively regulate the gut microflora. Taken together, the designed nanomedicine combined immunoregulation and intestinal microecology modulation to significantly enhance the therapeutic effect on colitis in mice, thus providing a new approach for the clinical treatment of colitis.

摘要

肠道黏膜免疫系统功能障碍和肠道微生物菌群失调可诱导炎症性肠病。然而,由于其疗效差和副作用严重,药物介导的临床治疗仍然是一个挑战。在此,通过将多巴胺纳米粒子与抗菌肽 mCRAMP 偶联,并在外层包裹巨噬细胞膜,设计并制备了一种 ROS 清除和炎症靶向的纳米药物。在体内和体外炎症模型中,所设计的纳米药物减少了促炎细胞因子的分泌,并提高了抗炎细胞因子的表达,证明了其改善炎症反应的显著能力。重要的是,巨噬细胞膜包裹的纳米粒子在局部炎症组织中表现出明显增强的靶向性能。此外,粪便微生物 16S rRNA 测序结果表明,口服给予纳米药物后,益生菌增加,致病菌受到抑制,表明所设计的纳米平台在优化肠道微生物组方面发挥了重要作用。总之,所设计的纳米药物不仅易于制备,具有较高的生物相容性,而且还表现出炎症靶向特性、抗炎功能和对肠道菌群的正向调节作用,为干预和治疗结肠炎提供了新的思路。

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