Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2026 Mar 25:e72857.
doi: 10.1002/adma.72857. Online ahead of print.

Reengineering Aligned D-Orbital Energy Levels in FeMn Dual-Atom Nanozyme Inhibits Pyroptosis for Effective Alleviation of Inflammatory Diseases

Affiliations

Reengineering Aligned D-Orbital Energy Levels in FeMn Dual-Atom Nanozyme Inhibits Pyroptosis for Effective Alleviation of Inflammatory Diseases

Jianfeng Guo et al. Adv Mater. .

Abstract

Pyroptosis inhibition via Fe single-atom nanozymes is promising for inflammation therapy, but the common Fe-N4 configuration restricts oxygen intermediate desorption and lacks cooperative sites, thus limiting catalytic performance. To overcome this, we develop a FeMn dual-atom nanozyme supported on oxygen-nitrogen-doped bamboo-like carbon nanotubes (FeMnDA/BCNT). Through the precise alignment of Fe and Mn 3dz2 orbital energy levels by the electron-delocalized BCNT support in the FeMn-N/O active center, thereby lowering the dissociation energy barrier for *O2 or *H2O molecules, promoting O─O bond cleavage to bypass toxic ─OOH species, and thus accelerating the enzyme-like kinetics. Combined with a hierarchical porous bamboo-like structure of the BCNT that enhances high specific surface, atom exposure, and mass transfer, the FeMnDA/BCNT nanozymes exhibit potent superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPx)-like activities. Further encapsulation with a macrophage membrane ([MM]FeMnDA/BCNT) confers excellent biocompatibility and active targeting ability toward inflammatory sites. The resulting [MM]FeMnDA/BCNT nanozymes target the inflammatory microenvironment, scavenges ROS, restores mitochondrial function, and suppresses NLRP3 inflammasome activation, thereby inhibiting pyroptosis. In vivo, [MM]FeMnDA/BCNT nanozymes show good biocompatibility and efficacy in treating osteoarthritis, acute liver injury, and acute kidney injury. This work provides a novel strategy for inflammatory disease therapy using a biomimetic dual-atom nanozyme.

Keywords: FeMn dual‐atom nanozymes; aligned d‐orbital; bamboo‐like carbon nanotubes; inflammatory; pyroptosis.

PubMed Disclaimer

References

    1. Y. Liu, R. Pan, Y. Ouyang, et al., “Pyroptosis in Health and Disease: Mechanisms, Regulation and Clinical Perspective,” Signal Transduction and Targeted Therapy 9, no. 1 (2024): 245, https://doi.org/10.1038/s41392‐024‐01958‐2.
    1. B. Zhou, Z.‐H. Jiang, M.‐R. Dai, et al., “Full‐Length GSDME Mediates Pyroptosis Independent From Cleavage,” Nature Cell Biology 26, no. 9 (2024): 1545–1557, https://doi.org/10.1038/s41556‐024‐01463‐2.
    1. T. Ye, C. Wang, J. Yan, et al., “Lysosomal Destabilization: A Missing Link Between Pathological Calcification And Osteoarthritis,” Bioactive Materials 34 (2024): 37–50, https://doi.org/10.1016/j.bioactmat.2023.12.001.
    1. H. Li, Y. Wu, L. Xiang, et al., “A20 Attenuates Oxidized self‐DNA‐Mediated Inflammation in Acute Kidney Injury,” Signal Transduction and Targeted Therapy 10, no. 1 (2025): 154, https://doi.org/10.1038/s41392‐025‐02194‐y.
    1. Y. Wang, X. Liu, K. Li, et al., “Self‐Sulfhydrated, Nitro‐Fixed Albumin Nanoparticles as a Potent Therapeutic Agent for the Treatment of Acute Liver Injury,” ACS Nano 18, no. 31 (2024): 20772–20791, https://doi.org/10.1021/acsnano.4c07297.

LinkOut - more resources