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Preparation of Polyoxometalate-based Photo-responsive Membranes for the Photo-activation of Manganese Oxide Catalysts
Published on: August 7, 2018
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Water-Soluble Mn(III)-Porphyrins with High Relaxivity and Photosensitization.
Tamas Nemeth1, Agnès Pallier2, Çetin Çelik1
1Department of Chemistry and Applied Biosciences, ETH Zürich, Vladimir-Prelog-Weg 3, CH-8093 Zürich, Switzerland.
Chemical & Biomedical Imaging
|January 31, 2025
Summary
New manganese(III)-porphyrin complexes show promise for combined magnetic resonance imaging (MRI) and photodynamic therapy (PDT). These water-soluble agents exhibit high relaxivity and efficient photoinduced DNA cleavage, with potential applications in cancer treatment.
Area of Science:
- Coordination Chemistry
- Biomedical Imaging
- Photodynamic Therapy
Background:
- Development of novel contrast agents for Magnetic Resonance Imaging (MRI).
- Exploration of photosensitizers for Photodynamic Therapy (PDT).
- Need for multimodal agents combining diagnostic and therapeutic capabilities.
Purpose of the Study:
- Synthesize and characterize water-soluble Mn(III)-porphyrin complexes.
- Evaluate their potential as dual-action agents for MRI and PDT.
- Investigate their interaction with G4 DNA and photocytotoxicity.
Main Methods:
- Synthesis of three Mn(III)-porphyrin complexes with varying side chains.
- Measurement of water relaxivity at different frequencies and temperatures.
- Assessment of photoinduced DNA cleavage and singlet oxygen generation.
- G4 DNA binding studies and photocytotoxicity assays on HeLa cells.
Main Results:
- Synthesized water-soluble Mn(III)-porphyrin complexes (Mn-1, Mn-2, Mn-3) with high relaxivity (10-15 mM⁻¹s⁻¹), exceeding Gd(III) agents.
- Para-substituted complexes (Mn-2, Mn-3) showed efficient photoinduced DNA cleavage and singlet oxygen generation.
- Mn-3 demonstrated G4 DNA binding and stabilizing activity, with significant photocytotoxicity on HeLa cells in a light-dependent manner.
Conclusions:
- Water-soluble Mn(III)-porphyrins are promising multimodal agents for MRI and PDT.
- Complexes with para-substituted carboxylate or alcoholic side chains exhibit enhanced performance.
- Further development could lead to novel theranostic agents for cancer treatment.

