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Synthesis and In Vitro Studies of a Gd(DOTA)–Porphyrin Conjugate for Combined MRI and Photodynamic Treatment

Sébastien Jenni, Frédéric Bolze, Célia S. Bonnet, Agnès Pallier, Angélique Sour, Éva Tóth, Barbara Ventura, Valérie Heitz

2020Inorganic Chemistry30 citationsDOIOpen Access PDF

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.

Topics & Concepts

ChemistryPhotodynamic therapyConjugateSinglet oxygenHeLaPhotosensitizerPorphyrinMoleculeDOTAMRI contrast agentSmall moleculeBovine serum albuminIn vitroGadoliniumPhotochemistryNuclear magnetic resonanceChelationOxygenBiochemistryInorganic chemistryOrganic chemistryMathematicsPhysicsMathematical analysisNanoplatforms for cancer theranosticsPorphyrin and Phthalocyanine ChemistryPhotodynamic Therapy Research Studies
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