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Elucidating the catalytic mechanism of Prussian blue nanozymes with self-increasing catalytic activity.
Feng, Kaizheng; Wang, Zhenzhen; Wang, Shi; Wang, Guancheng; Dong, Haijiao; He, Hongliang; Wu, Haoan; Ma, Ming; Gao, Xingfa; Zhang, Yu.
Afiliação
  • Feng K; State Key Laboratory of Digital Medical Engineering, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering & Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing, China.
  • Wang Z; Laboratory of Theoretical and Computational Nanoscience, National Center for Nanoscience and Technology of China, Beijing, China.
  • Wang S; State Key Laboratory of Digital Medical Engineering, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering & Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing, China.
  • Wang G; State Key Laboratory of Digital Medical Engineering, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering & Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing, China.
  • Dong H; Nanjing Institute of Measurement and Testing Technology, Nanjing, China.
  • He H; State Key Laboratory of Digital Medical Engineering, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering & Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing, China.
  • Wu H; State Key Laboratory of Digital Medical Engineering, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering & Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing, China.
  • Ma M; State Key Laboratory of Digital Medical Engineering, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering & Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing, China. maming@
  • Gao X; Laboratory of Theoretical and Computational Nanoscience, National Center for Nanoscience and Technology of China, Beijing, China. gaoxf@nanoctr.cn.
  • Zhang Y; State Key Laboratory of Digital Medical Engineering, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Science and Medical Engineering & Basic Medicine Research and Innovation Center of Ministry of Education, Zhongda Hospital, Southeast University, Nanjing, China. zhangyu
Nat Commun ; 15(1): 5908, 2024 Jul 13.
Article em En | MEDLINE | ID: mdl-39003316
ABSTRACT
Although Prussian blue nanozymes (PBNZ) are widely applied in various fields, their catalytic mechanisms remain elusive. Here, we investigate the long-term catalytic performance of PBNZ as peroxidase (POD) and catalase (CAT) mimetics to elucidate their lifespan and underlying mechanisms. Unlike our previously reported Fe3O4 nanozymes, which exhibit depletable POD-like activity, the POD and CAT-like activities of PBNZ not only persist but slightly enhance over prolonged catalysis. We demonstrate that the irreversible oxidation of PBNZ significantly promotes catalysis, leading to self-increasing catalytic activities. The catalytic process of the pre-oxidized PBNZ can be initiated through either the conduction band pathway or the valence band pathway. In summary, we reveal that PBNZ follows a dual-path electron transfer mechanism during the POD and CAT-like catalysis, offering the advantage of a long service life.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oxirredução / Catalase / Peroxidase / Ferrocianetos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oxirredução / Catalase / Peroxidase / Ferrocianetos Idioma: En Ano de publicação: 2024 Tipo de documento: Article