PUBLICATION

A turn-on mitochondria-targeted iridium (Ⅲ) Complex-Based probe for glutathione detection and photodynamic therapy of cancer cells

Authors
Mao, X., Fei, X., Cai, T., Xu, S., Zhang, D., Pu, S., Li, Z.
ID
ZDB-PUB-241218-18
Date
2024
Source
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy   329: 125579 (Journal)
Registered Authors
Keywords
Bioimaging, Fluorescent probe, Glutathione, Iridium complex, Single-linear oxygen
MeSH Terms
  • Animals
  • Cell Line, Tumor
  • Coordination Complexes/chemical synthesis
  • Coordination Complexes/chemistry
  • Coordination Complexes/pharmacology
  • Fluorescent Dyes*/chemistry
  • Fluorescent Dyes*/pharmacology
  • Glutathione*/metabolism
  • HeLa Cells
  • Humans
  • Iridium*/chemistry
  • Iridium*/pharmacology
  • Mitochondria*/drug effects
  • Mitochondria*/metabolism
  • Neoplasms/drug therapy
  • Neoplasms/pathology
  • Photochemotherapy*/methods
  • Photosensitizing Agents/chemistry
  • Photosensitizing Agents/pharmacology
  • Spectrometry, Fluorescence
  • Zebrafish*
PubMed
39689545 Full text @ Spectrochim Acta A Mol Biomol Spectrosc.
Abstract
As one of the most abundant biothiols in cells, glutathione (GSH) usually exists in a dynamic equilibrium of oxidized glutathione (GSSG) and reduces glutathione redox, and plays an essential reducing substance to maintain the REDOX balance of the microenvironment. So, the development of a reliable GSH sensor will be important for living cells and organisms. We fabricated a mitochondria targeted "turn-on" fluorescent sensor based on Ir (III) complex and successfully detected endogenous and exogenous GSH in living cells and zebrafish. For the probe Ir-DINI, a robust electron-withdrawing group 2,4-dinitrobenzoyl was introduced to quench the fluorescence, which could be broken through electrostatic interaction with GSH, following exposing a strong fluorescent Ir (Ⅲ) complex Ir-OH. On the other hand, photodynamic therapy (PDT) has attracted much attention in recent years due to its minimally invasive treatment. We found that singlet oxygen yields of probe Ir-DINI displayed an enhancement before and after the detection of GSH. Additionally, photodynamic studies in living cells illustrated that after reacting with GSH, probe Ir-DINI exhibited more obvious phototoxicity than before the detection of GSH. So the probe Ir-DINI could be served as a GSH sensor and potential GSH-activated photosensitizer for photodynamic therapy.
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Human Disease / Model
Sequence Targeting Reagents
Fish
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