Related Experiment Video
Updated: Sep 9, 2025

Targeted Neuronal Injury for the Non-Invasive Disconnection of Brain Circuitry
Published on: September 27, 2020
Defect-engineered amorphous-like nanointerceptors for T2 MRI-Guided treatment of reperfusion injury
Xiaotong Ma1, Xin Liang2, Yixin Yu3
1Key Laboratory of Biomechanics and Mechanobiology, Key Laboratory of Innovation and Transformation of Advanced Medical Devices, Ministry of Industry and Information Technology, National Medical Innovation Platform for Industry-Education Integration in Advanced Medical Devices (Interdiscipline of Medicine and Engineering), School of Biological Science and Medical Engineering, Beihang University, Ministry of Education, Beihang University, Beijing, 100191, China.
Abstract:
Ischemic reperfusion (I/R) injury is dominated by excessive reactive oxygen species (ROS)-mediated oxidative damage and uncontrolled inflammation, yet effective strategies for simultaneous diagnosis and treatment remain elusive. Herein, we report a defect-engineered amorphous-like MnCeOx nanointerceptor with dual capabilities of magnetic resonance imaging (MRI) -guided stroke diagnosis and ROS-scavenging therapy. The synergistic effect of the amorphous-like structure and Mn-Ce solid solution induces abundant oxygen vacancies and a disordered surface, significantly boosting ROS catalytic removal. Theoretical calculations confirm that Mn doping and oxygen vacancy formation modulate the electronic structure, reduce the adsorption energy of ROS intermediates, and lower catalytic energy barriers, thereby enhancing enzyme-like activity. As a result, MnCeOx exhibits an exceptionally high superoxide radical scavenging efficiency (115-fold higher than CeOx) and superior MRI contrast (r2 = 139 mM⁻¹) for precise lesion localization. In vivo, MnCeOx efficiently alleviates ROS-mediated oxidative stress and neuroinflammation, promoting substantial recovery from I/R injury. This work offers a powerful defect-engineering strategy for developing next-generation diagnostic and therapeutic nanozymes.

