| Literature DB >> 32960580 |
Sébastien Jenni1, Frédéric Bolze2, Célia S Bonnet3, Agnès Pallier3, Angélique Sour1, Éva Tóth3, Barbara Ventura4, Valérie Heitz1.
Abstract
With the aim of developing new molecular theranostic agents, a π-extended Zn(II) porphyrin as photosensitizer for photodynamic therapy (PDT) linked to two GdDOTA-type complexes for magnetic resonance imaging (MRI) detection was synthesized. The relaxivity studies revealed a much higher relaxivity value per Gd ion for this medium sized molecule (19.32 mM-1 s-1 at 20 MHz and 298 K) compared to clinical contrast agents-a value which strongly increases in the presence of bovine serum albumin, reaching 25.22 mM-1 s-1. Moreover, the photophysical studies showed the strong ability of the molecule to absorb light in the deep red (670 nm, ε ≈ 60000 M-1 cm-1) and in the near-infrared following two-photon excitation (920 nm, σ2 ≈ 650 GM). The conjugate is also able to generate singlet oxygen, with a quantum yield of 0.58 in DMSO. Promising results were obtained in cellular studies, demonstrating that the conjugate is internalized in HeLa cells at micromolar concentration and leads to 70% of cell death following 30 min irradiation at 660 nm. These results confirm the potential of the designed molecule as an imaging and therapeutic agent.Entities:
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Year: 2020 PMID: 32960580 DOI: 10.1021/acs.inorgchem.0c02189
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165