Multifunctional Bioactive Cu–Sm-Based Nanozyme Systems for Psoriasis Therapy

As a persistent inflammatory dermatological disorder, psoriasis impacts a global population of millions, with existing therapies frequently limited by side effects, high toxicity, and low effectiveness. Herein, we present the design and synthesis of a copper-samarium (Cu-Sm)-based bimetallic nanozyme (CS NPs) with strong antioxidant and anti-inflammatory characteristics for psoriasis therapy. CS NPs imitate natural antioxidant enzymes and efficiently neutralize H<sub>2</sub>O<sub>2</sub>, <sup>•</sup>OH, and O<sub>2</sub><sup>•-</sup>. Characterization investigations have confirmed the nanoparticles' stability, appropriate Sm doping ratio, and catalytic effectiveness. In vitro, CS NPs decrease ROS levels, restrict keratinocyte proliferation, and regulate inflammatory cytokine release through NF-κB pathway inhibition in HaCaT cells activated with IL-17. In vivo, CS NPs ameliorate IMQ-triggered psoriasiform lesions in mouse models through suppression of epidermal acanthosis, immune cell infiltration, and inflammatory marker expression. These results demonstrate the therapeutic potential of Cu-Sm nanozymes to provide biocompatible and effective psoriasis treatment, offering a viable substitute for conventional therapies.

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Publication Details

Journal
ACS Biomaterials Science & Engineering
Published
2025-06-28
DOI
https://doi.org/10.1021/acsbiomaterials.5c00722
Citations
3
Primary Topic
Advanced Nanomaterials in Catalysis
Type
article
Field-Weighted Citation Impact
1.55

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article

Multifunctional Bioactive Cu–Sm-Based Nanozyme Systems for Psoriasis Therapy

Hao Sun, Ting Hu, Jinsheng Liao, Jiayu Chen et al.
3 citations
ACS Biomaterials Science & Engineering
Advanced Nanomaterials in Catalysis
1.55
article

Multifunctional Bioactive Cu–Sm-Based Nanozyme Systems for Psoriasis Therapy

Hao Sun, Ting Hu, Jinsheng Liao, Jiayu Chen, Yuhang Li, Hui Yuan, Xiaofeng Wu, Xiaohua Xie, Can‐Zhong Lu, Peiyuan Wang, Jie Han, Jiangshan Hu
article en
3 citations

Abstract

As a persistent inflammatory dermatological disorder, psoriasis impacts a global population of millions, with existing therapies frequently limited by side effects, high toxicity, and low effectiveness. Herein, we present the design and synthesis of a copper-samarium (Cu-Sm)-based bimetallic nanozyme (CS NPs) with strong antioxidant and anti-inflammatory characteristics for psoriasis therapy. CS NPs imitate natural antioxidant enzymes and efficiently neutralize H<sub>2</sub>O<sub>2</sub>, <sup>•</sup>OH, and O<sub>2</sub><sup>•-</sup>. Characterization investigations have confirmed the nanoparticles' stability, appropriate Sm doping ratio, and catalytic effectiveness. In vitro, CS NPs decrease ROS levels, restrict keratinocyte proliferation, and regulate inflammatory cytokine release through NF-κB pathway inhibition in HaCaT cells activated with IL-17. In vivo, CS NPs ameliorate IMQ-triggered psoriasiform lesions in mouse models through suppression of epidermal acanthosis, immune cell infiltration, and inflammatory marker expression. These results demonstrate the therapeutic potential of Cu-Sm nanozymes to provide biocompatible and effective psoriasis treatment, offering a viable substitute for conventional therapies.

ACS Biomaterials Science & EngineeringVol. 11(7)
City University of Hong Kong (HK), Xiamen University (CN), Chinese Academy of Sciences (CN), First Affiliated Hospital of Xiamen University (CN), Xiamen Institute of Rare-earth Materials (CN), Fujian Institute of Research on the Structure of Matter (CN), University of Chinese Academy of Sciences (CN), Jiangxi University of Science and Technology (CN)
Natural Science Foundation of Xiamen City, National Natural Science Foundation of China, Natural Science Foundation of Fujian Province, Natural Science Foundation of Jiangxi Province
Openalex Percentile: Top 17%
Advanced Nanomaterials in Catalysis
1.55
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