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Programmed pH-responsive core-shell nanoparticles for precisely targeted therapy of ulcerative colitis

机译:程序化pH响应性核壳纳米颗粒用于溃疡性结肠炎的精确靶向治疗

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pH-Responsive nanotherapeutics were recently developed for the treatment of ulcerative colitis (UC). However, they target the entire colon rather than the UC site, which leads to insufficient accumulation in inflamed colon lesions and causes side effects. Core-shell nanoparticles exhibit unique advantages in improving the precision of targeted delivery. In this study, Eudragit? EPO and L100, two pH-sensitive materials, were coated on nano-sized curcumin to fabricate core-shell nanoparticles. The developed CNs@EPO@L100 exhibited programmed pH-responsive drug release behavior, improved in vitro anti-inflammatory ability, and enhanced accumulation at the site of inflammation in the colon. Furthermore, after oral administration, CNs@EPO@L100 significantly ameliorated the inflammatory symptoms in mice. Taken together, this study provides insights into programmed release through the rational application of pH-sensitive materials and offers strategies for a precisely targeted therapy of UC using core-shell nanoparticles.
机译:pH-Responsive纳米疗法最近治疗溃疡性结肠炎的开发(加州大学)。而不是加州大学网站,从而导致在结肠发炎积累不足病变,引起副作用。纳米粒子表现出独特的优势提高目标的精度。这项研究中,Eudragit吗?pH-sensitive材料,涂层在纳米级姜黄素制备核壳纳米粒子。发达CNs@EPO@L100编程展出pH-responsive药物释放行为,改善体外抗炎能力,和增强在炎症的积累结肠。CNs@EPO@L100显著改善炎症小鼠的症状。本研究为编程提供了见解通过rational applicationpH-sensitive材料并提供策略加州大学使用的精确的靶向治疗核壳纳米粒子。

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