4.8 Article

Single-Atom Pd Nanozyme for Ferroptosis-Boosted Mild-Temperature Photothermal Therapy

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 60, Issue 23, Pages 12971-12979

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202101924

Keywords

ferroptosis; heat shock proteins; nanozymes; photothermal therapy; Pd SAzyme

Funding

  1. Chinese Government [2017YFE0132300]
  2. National Natural Science Foundation of China [NSFC 51929201, 51720105015, 52072082, 51972138, 51872263, 51828202]
  3. Science and Technology Development Planning Project of Jilin Province [20190201232JC]
  4. CAS-Croucher Funding Scheme for Joint Laboratories [CAS18204]
  5. Guangdong Natural Science Foundation [2019A1515012214]
  6. Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan People's Hospital [202011-105]
  7. Australian Government [2017YFE0132300]

Ask authors/readers for more resources

Photothermal therapy (PTT) is a promising tumor therapeutic modality, but minimizing damage to healthy tissues while maximizing efficiency is crucial. Utilizing a single-atom nanozyme (SAzyme) can improve the effectiveness of mild PTT by promoting ferroptosis.
Photothermal therapy (PTT) is an extremely promising tumor therapeutic modality. However, excessive heat inevitably injures normal tissues near tumors, and the damage to cancer cells caused by mild hyperthermia is easily repaired by stress-induced heat shock proteins (HSPs). Thus, maximizing the PTT efficiency and minimizing the damage to healthy tissues simultaneously by adopting appropriate therapeutic temperatures is imperative. Herein, an innovative strategy is reported: ferroptosis-boosted mild PTT based on a single-atom nanozyme (SAzyme). The Pd SAzyme with atom-economical utilization of catalytic centers exhibits peroxidase (POD) and glutathione oxidase (GSHOx) mimicking activities, and photothermal conversion performance, which can result in ferroptosis featuring the up-regulation of lipid peroxides (LPO) and reactive oxygen species (ROS). The accumulation of LPO and ROS provides a powerful approach for cleaving HSPs, which enables Pd SAzyme-mediated mild-temperature PTT.

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