Sequential H <sub>2</sub> S‐Triggered Redox Relay Nanoprobes for Self‐Sustained Chem‐Illuminating Cascade Photodynamic Therapy

J Jing Yang Y Yao Lu Y Yutao Zhang (Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, State Key Laboratory of Bioreactor Engineering, State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Center of Photosensitive Chemicals Engineering) X Xiuyan Zhao (Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, State Key Laboratory of Bioreactor Engineering, State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Center of Photosensitive Chemicals Engineering) X Xie Li (Synthetic Biology and Biotechnology Laboratory State Key Laboratory of Bioreactor Engineering Shanghai Collaborative Innovation Center for Biomanufacturing Technology East China University of Science and Technology Shanghai China) C Chenxu Yan (Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, State Key Laboratory of Bioreactor Engineering, State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Center of Photosensitive Chemicals Engineering) Y Yuzheng Zhao W Wei‐Hong Zhu (Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering Shanghai Key Laboratory of Functional Materials Chemistry Feringa Nobel Prize Scientist Joint Research Center Institute of Fine Chemicals Frontiers Science Center For Materiobiology and Dynamic Chemistry School of Chemistry and Molecular Engineering East China University of Science and Technology Shanghai China) Z Zhiqian Guo (Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, State Key Laboratory of Bioreactor Engineering, State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Center of Photosensitive Chemicals Engineering)

Abstract

ABSTRACT Endogenous chemiluminescence offers a transformative approach to photodynamic therapy that circumvents the limited penetration of external light and enables tumor‐selective activation. However, most chemiluminescence‐driven photodynamic therapy (CL‐PDT) systems typically rely on intracellular oxidants (e.g., H 2 O 2 ) as chemiexcitation “fuels”, which conceptually contradicts the primary goal of elevating intratumoral oxidative stress. In this study, we report a sequential H 2 S‐triggered redox relay nano‐photosensitizer, NP‐Rubine, which addresses the fundamental “redox paradox” by decoupling photon generation from oxidation consumption. Composed of an H 2 S‐responsive chemiluminescent probe (Rubine) and a N ‐oxide scaffold (OPDEA‐Ppa), NP‐Rubine is selectively activated by endogenous H 2 S to initiate an efficiency chemiluminescence resonance energy transfer (CRET) cascade for efficient singlet oxygen ( 1 O 2 ) production. Concurrently, the N ‐oxide moiety promotes deep tumor penetration via transcytosis and depletes the intracellular NADPH pool. By synergistically coupling oxidant generation with reductant exhaustion, NP‐Rubine synergistically amplifies intracellular redox imbalance to induce apoptosis. In vivo studies substantiate that NP‐Rubine achieves exceptional deep‐tissue imaging and potent antitumor efficacy in HCT116 xenografts. This bio‐reductant, self‐sustained targeted CL‐PDT strategy circumvents the practical hurdles of oxidation‐fueled systems, offering a robust benchmark for precision nanomedicine in complex redox landscapes.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 07, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (9)

J

Jing Yang

Y

Yao Lu

Y

Yutao Zhang

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, State Key Laboratory of Bioreactor Engineering, State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Center of Photosensitive Chemicals Engineering

X

Xiuyan Zhao

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, State Key Laboratory of Bioreactor Engineering, State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Center of Photosensitive Chemicals Engineering

X

Xie Li

Synthetic Biology and Biotechnology Laboratory State Key Laboratory of Bioreactor Engineering Shanghai Collaborative Innovation Center for Biomanufacturing Technology East China University of Science and Technology Shanghai China

C

Chenxu Yan

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, State Key Laboratory of Bioreactor Engineering, State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Center of Photosensitive Chemicals Engineering

Y

Yuzheng Zhao

W

Wei‐Hong Zhu

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering Shanghai Key Laboratory of Functional Materials Chemistry Feringa Nobel Prize Scientist Joint Research Center Institute of Fine Chemicals Frontiers Science Center For Materiobiology and Dynamic Chemistry School of Chemistry and Molecular Engineering East China University of Science and Technology Shanghai China

Z

Zhiqian Guo

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Institute of Fine Chemicals, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering, State Key Laboratory of Bioreactor Engineering, State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, Center of Photosensitive Chemicals Engineering