摘要:由于miR-301a抑制剂(anti-miR-301a,简称anti-iR)对与炎症性肠病(IBD)病程显著相关的miR-301a具有显著抑制作用,其在IBD治疗中的应用已被广泛探索。然而,anti-iR的口服治疗效果有限,且无法调控炎症结肠中活性氧(ROS)
期刊导读
Journal Guide
1
An anti-miR-301a and zinc coordination driven nanozyme loaded in nanoparticle for oral therapy of inflammatory bowel disease based on colitis microenvironment regulation
由于miR-301a抑制剂(anti-miR-301a,简称anti-iR)对与炎症性肠病(IBD)病程显著相关的miR-301a具有显著抑制作用,其在IBD治疗中的应用已被广泛探索。然而,anti-iR的口服治疗效果有限,且无法调控炎症结肠中活性氧(ROS)和硫化氢(H₂S)的过度表达。在本研究中,基于锌(Zn)配位的辅助优势,我们开发了一种anti-iR与Zn配位驱动的纳米酶(anti-iR−Zn,简称R-Z),可在促进anti-iR转染的同时调控ROS和H₂S。此外,我们还制备了由R-Z和ROS响应脂质体组成的口服纳米颗粒(R-Z@iPS),以克服复杂的胃部环境,并在结肠炎症区域富集。在结肠炎小鼠模型中,R-Z@iPS可通过调控ROS和H₂S减轻结肠炎症指数,修复受损的紧密连接和黏液层。此外,该纳米颗粒可下调miR-301a水平,抑制核因子kappa-B信号通路,并增加Smad核相互作用蛋白1和B细胞易位基因1的表达,从而逆转结肠炎症。R-Z@iPS还可通过增加益生菌丰度、减少有害菌丰度来协调结肠炎微环境,恢复肠道菌群平衡。综上,本研究开发了一种具有良好安全性的新型口服纳米颗粒,在结肠炎的综合临床管理中具有潜力,并可能改变其他miR-301a相关疾病的反义寡核苷酸治疗模式。
(信息以英文摘要为准)
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文章介绍:
上述研究工作的成功实施,主要依托于上海市细胞代谢光遗传学技术前沿科学研究基地,国家重点研发计划,国家自然科学基金,和中央高校基本科研业务费等项目的资助和支持。
期刊介绍
《Chemical Engineering Journal》是 Elsevier 旗下化学工程与环境科学领域的国际权威期刊,2023年影响因子达 15.1,JCR与中科院分区均为 Q1/1区Top期刊,覆盖催化、环境治理、新能源材料、绿色工艺等方向,强调跨学科应用与创新。
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