活性氧
化学
抗氧化剂
催化作用
生物物理学
体内
氧化应激
体外
纳米技术
细胞生物学
再生(生物学)
硒
氧气
激进的
铈
纳米材料
氧化磷酸化
原位
软骨
作者
Ziyan Liu,X. Wang,Ziyang Liu,Jing Jiang,Xiao Lin,Zhe Xiao,Ping Zhang,Huan Zhou,Lei Yang
标识
DOI:10.1002/adhm.202505174
摘要
ABSTRACT Precise control of reactive oxygen species (ROS) is indispensable during tissue repairing. Inorganic nanozymes such as cerium dioxide (CeO 2 ) have emerged as potent ROS modulators, however, their fixed catalytic activity prevents on‐demand adaptation to the rapidly changing immune microenvironment. Here, we reported a magnetically responsive dynamic antioxidant system that autonomously tunes its ROS‐scavenging capacity on demand. Selenium (Se) doping was first exploited to engineer high‐density oxygen vacancies (Vo) in the CeO 2 lattice, enabling the nanozyme intrinsic antioxidant activity enhancement. Its catalytic efficiency could be further amplified under a static magnetic field (SMF). In vitro analysis revealed that Se‐CeO 2 under SMF significantly promoted the polarization of macrophages toward the pro‐regenerative M2 phenotype. The as‐prepared Se‐CeO 2 was subsequently loaded into a sodium alginate–hyaluronic acid hydrogel (SCSH‐Gel), witnessed to protect chondrocytes and fibroblasts from oxidative stress in vitro. Followed in vivo tests found SMF and Se‐CeO 2 synergistically accelerate neocartilage formation in a cartilage defect model and promoted re‐epithelialization in a full‐thickness skin‐wound model. Collectively, our results demonstrated that Se doping coupled with magnetic actuation enables inorganic nanozymes to dynamically modulate ROS homeostasis, offering a versatile strategy for precisely programming the microenvironment to facilitate tissue regeneration.
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