髓过氧化物酶
催化作用
酶
超氧化物歧化酶
癌症治疗
超氧化物
级联
化学
生物物理学
材料科学
纳米技术
癌症
生物化学
炎症
生物
医学
免疫学
内科学
色谱法
作者
Xiangqin Meng,Huizhen Fan,Lei Chen,Jianxun He,Chaoyi Hong,Jiaying Xie,Yinyin Hou,Kaidi Wang,Xingfa Gao,Lizeng Gao,Xiyun Yan,Kelong Fan
标识
DOI:10.1038/s41467-024-45668-3
摘要
Abstract Developing strategies that emulate the killing mechanism of neutrophils, which involves the enzymatic cascade of superoxide dismutase (SOD) and myeloperoxidase (MPO), shows potential as a viable approach for cancer therapy. Nonetheless, utilizing natural enzymes as therapeutics is hindered by various challenges. While nanozymes have emerged for cancer treatment, developing SOD-MPO cascade in one nanozyme remains a challenge. Here, we develop nanozymes possessing both SOD- and MPO-like activities through alloying Au and Pd, which exhibits the highest cascade activity when the ratio of Au and Pd is 1:3, attributing to the high d-band center and adsorption energy for superoxide anions, as determined through theoretical calculations. The Au 1 Pd 3 alloy nanozymes exhibit excellent tumor therapeutic performance and safety in female tumor-bearing mice, with safety attributed to their tumor-specific killing ability and renal clearance ability caused by ultrasmall size. Together, this work develops ultrasmall AuPd alloy nanozymes that mimic neutrophil enzymatic cascades for catalytic treatment of tumors.
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