<i>meso</i>-Substituted AB<sub>3</sub>-type phenothiazinyl porphyrins and their indium and zinc complexes photosensitising properties, cytotoxicity and phototoxicity on ovarian cancer cells

New <i>meso</i>-substituted AB<sub>3</sub>-type phenothiazinyl porphyrins and ferrocenylvinyl phenothiazinyl porphyrin were synthesised by Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions, respectively. The free porphyrins were further used in the synthesis of new indium(iii) or zinc(ii) porphyrin complexes. All porphyrins exhibit red fluorescence emission in solution, a property that remains unimpaired following internalisation in ovarian A2780 cancer cells, as evidenced by fluorescence microscopy images. The In(iii) phenothiazinyl porphyrin complexes show a higher quantum yield of fluorescence emission (2a<i>Φ</i> <sub>F</sub> = 30%, 4a<i>Φ</i> <sub>F</sub> = 29%, 5a<i>Φ</i> <sub>F</sub> = 28%) compared to the free base porphyrin precursors, or Zn(ii) complex 4b (<i>Φ</i> <sub>F</sub> = 10%). The potential of novel phenothiazinyl porphyrins to act as photosensitisers was evaluated using two distinct approaches. The first was through the measurement of the singlet oxygen quantum yield <i>Φ</i> <sub>Δ</sub>(<sup>1</sup>O<sub>2</sub>), while the second employed <i>in vitro</i> measurements of metabolic activity, oxidative stress, nuclear factor-erythroid 2 related factor 2 (Nrf-2) activation and tumour necrosis factor-alpha (TNF-α) under both dark and light irradiation conditions. As reflected by the IC<sub>50</sub> values, the most potent cytotoxicity of the phenothiazinyl porphyrins against the A2780 cells was observed for In(iii) ferrocenylvinyl phenothiazinyl porphyrin 4a (36.38 μM), the remaining compounds are less cytotoxic. The reduction in metabolic activity was observed in A2780 ovarian tumour cells treated with 4a and 6a and exposed to light compared to treatment in the absence of light. The oxidative stress, TNF-α and Nrf-2 transcription factor were particularly notable when A2780 cells were treated with 4a and subsequently photoirradiated, the oxidative stress was linked to the highest value of <i>Φ</i> <sub>Δ</sub>(<sup>1</sup>O<sub>2</sub>) recorded for 4a (60%).

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Publication Details

Journal
RSC Medicinal Chemistry
Published
2024-10-28
DOI
https://doi.org/10.1039/d4md00601a
Citations
1
Primary Topic
Porphyrin and Phthalocyanine Chemistry
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article
Field-Weighted Citation Impact
0.12

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article

meso-Substituted AB3-type phenothiazinyl porphyrins and their indium and zinc complexes photosensitising properties, cytotoxicity and phototoxicity on ovarian cancer cells

Emese Gál, Eva Fischer‐Fodor, Ovidiu Bălăcescu, Monica Focşan et al.
1 citations
RSC Medicinal Chemistry
Porphyrin and Phthalocyanine Chemistry
0.12
article

meso-Substituted AB3-type phenothiazinyl porphyrins and their indium and zinc complexes photosensitising properties, cytotoxicity and phototoxicity on ovarian cancer cells

Emese Gál, Eva Fischer‐Fodor, Ovidiu Bălăcescu, Monica Focşan, Patriciu Achimaș-Cădariu, Raluca Borlan, Bianca Stoean, Balázs Brém, E. M. Molnar, Luiza Găină, Adriana Grozav
article en
1 citations

Abstract

New <i>meso</i>-substituted AB<sub>3</sub>-type phenothiazinyl porphyrins and ferrocenylvinyl phenothiazinyl porphyrin were synthesised by Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions, respectively. The free porphyrins were further used in the synthesis of new indium(iii) or zinc(ii) porphyrin complexes. All porphyrins exhibit red fluorescence emission in solution, a property that remains unimpaired following internalisation in ovarian A2780 cancer cells, as evidenced by fluorescence microscopy images. The In(iii) phenothiazinyl porphyrin complexes show a higher quantum yield of fluorescence emission (2a<i>Φ</i> <sub>F</sub> = 30%, 4a<i>Φ</i> <sub>F</sub> = 29%, 5a<i>Φ</i> <sub>F</sub> = 28%) compared to the free base porphyrin precursors, or Zn(ii) complex 4b (<i>Φ</i> <sub>F</sub> = 10%). The potential of novel phenothiazinyl porphyrins to act as photosensitisers was evaluated using two distinct approaches. The first was through the measurement of the singlet oxygen quantum yield <i>Φ</i> <sub>Δ</sub>(<sup>1</sup>O<sub>2</sub>), while the second employed <i>in vitro</i> measurements of metabolic activity, oxidative stress, nuclear factor-erythroid 2 related factor 2 (Nrf-2) activation and tumour necrosis factor-alpha (TNF-α) under both dark and light irradiation conditions. As reflected by the IC<sub>50</sub> values, the most potent cytotoxicity of the phenothiazinyl porphyrins against the A2780 cells was observed for In(iii) ferrocenylvinyl phenothiazinyl porphyrin 4a (36.38 μM), the remaining compounds are less cytotoxic. The reduction in metabolic activity was observed in A2780 ovarian tumour cells treated with 4a and 6a and exposed to light compared to treatment in the absence of light. The oxidative stress, TNF-α and Nrf-2 transcription factor were particularly notable when A2780 cells were treated with 4a and subsequently photoirradiated, the oxidative stress was linked to the highest value of <i>Φ</i> <sub>Δ</sub>(<sup>1</sup>O<sub>2</sub>) recorded for 4a (60%).

RSC Medicinal ChemistryVol. 16(2)
Iuliu Hațieganu University of Medicine and Pharmacy (RO), Babeș-Bolyai University (RO), Institute of Oncology Prof. Dr. Ion Chiricuta (RO)
National Authority for Scientific Research and Innovation, European Commission, Agence Universitaire de la Francophonie, Autoritatea Natională pentru Cercetare Stiintifică, Unitatea Executiva pentru Finantarea Invatamantului Superior, a Cercetarii, Dezvoltarii si Inovarii
Openalex Percentile: Top 59%
Porphyrin and Phthalocyanine Chemistry
0.12
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