Engineered targeted Ce-based MOF nanozymes for ROS scavenging and inflammatory Reprogramming in chronic pancreatitis
Yongkang Lai, Yongliang Ouyang, Xiaojing Yin, Tao Yu, Jianhua Wan, Xueyang Li, Yi Hu, Xu Shu, Huan Wang

TL;DR
Researchers developed a nanosystem to target and reduce inflammation in chronic pancreatitis by scavenging harmful molecules and suppressing inflammation.
Contribution
A novel Ce-based MOF nanozyme system is introduced for targeted ROS scavenging and inflammation modulation in chronic pancreatitis.
Findings
HC@CeMOF nanosystem effectively scavenges ROS through Ce3+/Ce4+ redox cycling.
Curcumin release from HC@CeMOF suppresses NF-κB signaling and reduces inflammatory cytokines.
The nanosystem shows favorable safety and accumulates selectively in inflamed pancreatic tissue.
Abstract
Chronic pancreatitis (CP) is a lifelong progressive fibrotic inflammatory disorder for which no effective cure is currently available. Persistent and recurrent inflammatory stimulation induced by reactive oxygen species (ROS) is a key driver of pancreatic fibrogenesis, making oxidative stress a promising therapeutic target to halt disease progression. In this study, we developed a nanosystem, HC@CeMOF, consisting of a small-sized cerium-based metal–organic framework (CeMOF) core loaded with curcumin and coated with hyaluronic acid (HA), enabling precise targeting of inflamed pancreatic tissue. HC@CeMOF exhibits a small-sized particle size along with favorable cellular and biological safety profiles. Once administered in vivo, the nanosystem exploits the specific binding affinity of HA to CD44 receptors on macrophages to selectively accumulate at inflamed pancreatic sites. Subsequently,…
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Taxonomy
TopicsPancreatitis Pathology and Treatment · Pancreatic and Hepatic Oncology Research · Advanced Nanomaterials in Catalysis
