纳米颗粒
凝聚
胃肠道
材料科学
药理学
涂层
药物输送
纳米技术
治疗指标
小肠
生物医学工程
胃肠上皮
渗透(战争)
治疗效果
氧化铈
抗氧化剂
口服
肠粘膜
药品
作者
Yunjung Lee,Y. M. Kim,Seokjun Kwon,Ok Kyu Park,Gyeong Ho Min,Jinyoung Chu,Yubeen Kim,Johyun Yoon,Hyochul Lee,H. S. Kim,Min Soh,N Lee,Hojeong Jeon,Yu‐Chan Kim,Junchul Kim,Ki Baek Yeo,Seung Hong Choi,Sang Ho Jun,Yuhan Lee,Taeghwan Hyeon
标识
DOI:10.1002/adma.202514708
摘要
Oral delivery of therapeutic nanoparticles offers a non-invasive approach for treating gastrointestinal diseases, but achieving localized and sustained mucosal exposure while avoiding systemic toxicity remains a major challenge. Here, a Sucralfate-based oral formulation is developed that incorporates therapeutic nanoparticles and transforms into a paste-like coacervate upon contact with intestinal fluid, uniformly coating the entire gastrointestinal tract within 6 h, and clearing through fecal transit by 12 h. Systematic investigation shows that nanoparticle hydrophobicity is essential for stable incorporation into Sucralfate-based formulation, supporting compatibility with a wide range of nanoparticle types. The incorporated nanoparticles are stabilized by strong non-covalent interactions, which limit gastric leaching and reduce cellular uptake by 0.044% compared with PEGylated nanoparticles. As a representative example, antioxidant cerium oxide nanoparticles are tested in two distinct oxidative stress-related models of intestinal injury, including immune-mediated colitis and radiation-induced enteropathy. In DSS colitis, our system reduced weight loss from 17.2% to 2.2% and restored colon structure and oxidative-stress injury. In radiation-induced enteropathy, our system attenuated weight loss from 25.5% to 11.4%, doubled villus length, and markedly enhanced epithelial regeneration. The formulation also accommodates nanoparticles with imaging capability, demonstrating versatility for both therapeutic and diagnostic applications in gastrointestinal diseases.
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