Nanozymes with multi-enzymatic activity in biomedical fields have gained significant attention. However, the effects of metal-doping elements on the structure-activity relationship of many nanomaterials remain insufficiently understood. Herein, we selected NiFe-LDH as the base material to systematically investigate how varying Mn doping ratios and specific Mn doping sites within the NiFe-LDH lattice influences peroxidase (POD), oxidase (OXD), and catalase (CAT) activities.
View Article and Find Full Text PDFPrimary liver cancer remains a significant global health challenge, with the majority of patients diagnosed at an unresectable stage, further complicated by liver dysfunction due to cirrhosis. To address these clinical hurdles, nanozyme-based catalytic therapy has emerged as a promising strategy. However, its therapeutic efficacy is often limited by self-protective mechanisms associated with the tumor microenvironment (TME), particularly the overexpression of glutathione (GSH) and hypoxia-induced metabolic adaptation.
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