Synthesis of novel pyranoflavylium-based dyes as promising photosensitizers for antimicrobial photodynamic inactivation

Amino-substituted dyes have recently been described for their interesting photosensitizing properties in photodynamic therapy against bacterial growth. In the present study, two novel pyranoflavylium-based dyes namely 4′-dimethylamino-10-(4''-(dimethylamino)phenyl)pyranoflavylium (4′,4″N(Me) 2 PyF) and 6-Bromo-4′-dimethylamino-10-(4''-(dimethylamino)phenyl)pyranoflavylium (6Br4′,4″N(Me) 2 PyF) were synthesized through the reactions between salicylaldehyde and acetophenone derivatives to improve the photo-properties of 5-hydroxy-4′-dimethylaminoflavylium (5OH4′N(Me) 2 F), a non-photoactivated flavylium salt previously reported due to the presence of a hydroxyl group in its structure. The presence of a pyranic ring with an additional dimethylaminophenyl group and the insertion of a bromine atom changed the spectroscopic properties of the parent flavylium, causing a red shift of the absorption band, higher molar extinction coefficient, and fluorescence emission. Both pyranoflavylium dyes showed appreciable singlet oxygen production, and phototoxicity studies demonstrated their photoactivable nature, leading to a reduction of >3log in cellular viability of S. aureus ATCC 29213 after 15 min of irradiation (22.5 J/cm 2 ). In conclusion, this study describes a chemical strategy to extend π-conjugation, converting a non-active flavylium dye into photoactivable ones. This approach could be further explored to develop novel solutions for antimicrobial photodynamic inactivation, potentially addressing issues related to antimicrobial resistance. • 4′,4″N(Me) 2 PyF and 6Br4′,4″N(Me) 2 PyF showed significant production of 1 O 2 under red light irradiation. • 4′,4″N(Me)2PyF and 6Br4′,4″N(Me)2PyF yielded photoinactivation of S. aureus (>3-log reduction) at 8 μM. • The accumulation of the pyranoflavylium dyes was around the bacterial cell. • 4′,4″N(Me) 2 PyF and 6Br4′,4″N(Me) 2 PyF do not cause hemolysis at 5 and 10 μM.

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Publication Details

Journal
Dyes and Pigments
Published
2024-10-17
DOI
https://doi.org/10.1016/j.dyepig.2024.112495
Citations
2
Primary Topic
Photodynamic Therapy Research Studies
Type
article
Field-Weighted Citation Impact
0.84

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article

Synthesis of novel pyranoflavylium-based dyes as promising photosensitizers for antimicrobial photodynamic inactivation

Patrícia Correia, Nuno Mateus, Paula Araújo, Víctor de Freitas et al.
2 citations
Dyes and Pigments
Photodynamic Therapy Research Studies
0.84
article

Synthesis of novel pyranoflavylium-based dyes as promising photosensitizers for antimicrobial photodynamic inactivation

Patrícia Correia, Nuno Mateus, Paula Araújo, Víctor de Freitas, Luís Cruz, Iva Fernandes, Joana Oliveira
article en
2 citations

Abstract

Amino-substituted dyes have recently been described for their interesting photosensitizing properties in photodynamic therapy against bacterial growth. In the present study, two novel pyranoflavylium-based dyes namely 4′-dimethylamino-10-(4''-(dimethylamino)phenyl)pyranoflavylium (4′,4″N(Me) 2 PyF) and 6-Bromo-4′-dimethylamino-10-(4''-(dimethylamino)phenyl)pyranoflavylium (6Br4′,4″N(Me) 2 PyF) were synthesized through the reactions between salicylaldehyde and acetophenone derivatives to improve the photo-properties of 5-hydroxy-4′-dimethylaminoflavylium (5OH4′N(Me) 2 F), a non-photoactivated flavylium salt previously reported due to the presence of a hydroxyl group in its structure. The presence of a pyranic ring with an additional dimethylaminophenyl group and the insertion of a bromine atom changed the spectroscopic properties of the parent flavylium, causing a red shift of the absorption band, higher molar extinction coefficient, and fluorescence emission. Both pyranoflavylium dyes showed appreciable singlet oxygen production, and phototoxicity studies demonstrated their photoactivable nature, leading to a reduction of >3log in cellular viability of S. aureus ATCC 29213 after 15 min of irradiation (22.5 J/cm 2 ). In conclusion, this study describes a chemical strategy to extend π-conjugation, converting a non-active flavylium dye into photoactivable ones. This approach could be further explored to develop novel solutions for antimicrobial photodynamic inactivation, potentially addressing issues related to antimicrobial resistance. • 4′,4″N(Me) 2 PyF and 6Br4′,4″N(Me) 2 PyF showed significant production of 1 O 2 under red light irradiation. • 4′,4″N(Me)2PyF and 6Br4′,4″N(Me)2PyF yielded photoinactivation of S. aureus (>3-log reduction) at 8 μM. • The accumulation of the pyranoflavylium dyes was around the bacterial cell. • 4′,4″N(Me) 2 PyF and 6Br4′,4″N(Me) 2 PyF do not cause hemolysis at 5 and 10 μM.

Dyes and PigmentsVol. 233
Universidade do Porto (PT), Rede de Química e Tecnologia (PT)
Fundação para a Ciência e a Tecnologia
Openalex Percentile: Top 23%
Photodynamic Therapy Research Studies
0.84
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