Development of a Nucleoside Photosensitizer Efficiently Activated by One- or Two-Photon Absorption in the Optical Therapeutic Window

High Resolution Image Download MS PowerPoint Slide Developing DNA/RNA nucleoside prodrugs that absorb in the red-to-near-infrared is crucial for applications requiring deep-tissue penetration. This study reports the rational design and synthesis of a novel thiocarbonyl analog, 5-(5-(4-(dimethylamino)phenyl)thiophen-2-yl)-2′,3′,5′-tri- O -benzoyl-6-aza-2,4-dithiouridine (DATU), efficiently activated through one- and two-photon absorption in the red-to-near-infrared spectrum. We report DATU’s electronic structure and its photophysical and triplet-state properties under both excitation, comparing these results to its carbonyl counterpart, 5-(5-(4-(dimethylamino)phenyl)thiophen-2-yl)-2’,3′,5′-tri- O -benzoyl-6-azauridine (DAU). DATU exhibits strong visible one-photon absorption, with ε 522 = (0.73 ± 0.02) × 10 4 M –1 cm –1 in aqueous solution, extending to ∼750 nm. Additionally, it features a triplet-state lifetime of 1.7 ± 0.1 μs and a singlet-oxygen quantum yield of 56% in benzene. Photoexcited DATU generates both singlet oxygen and hydroxyl radicals in solvents of varying polarity (water, methanol, acetonitrile, and benzene), functioning as both a type I and type II photosensitizer depending on the cellular environment. Notably, replacing carbonyl with thiocarbonyl groups increases the two-photon absorption cross section at 800 nm 3-fold, from 55 ± 5 GM for DAU to 160 ± 20 GM for DATU, the largest reported for a nucleoside analog. In vitro investigations using 4T1 murine mammary carcinoma cells confirm that DATU exhibits significant photocytotoxicity under one-photon (525 nm, 6 μM) and two-photon (800 nm, 25 μM) activation, with negligible dark toxicity. Together, these findings position DATU as the most promising nucleoside photosensitizer for deep-tissue photodynamic therapy (PDT) to date, laying the foundation for future mechanistic/ in vivo studies while broadly guiding the development of next-generation thiocarbonyl photosensitizers for PDT, bioimaging, and photocatalysis.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2026-06-08
DOI
https://doi.org/10.1021/jacs.6c00216
Primary Topic
Photodynamic Therapy Research Studies
Type
article
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article

Development of a Nucleoside Photosensitizer Efficiently Activated by One- or Two-Photon Absorption in the Optical Therapeutic Window

Sourav Kanti Seth, Sean J. Hoehn, Carlos E. Crespo‐Hernández, Chris Acquah et al.
Journal of the American Chemical Society
Photodynamic Therapy Research Studies
article

Development of a Nucleoside Photosensitizer Efficiently Activated by One- or Two-Photon Absorption in the Optical Therapeutic Window

Sourav Kanti Seth, Sean J. Hoehn, Carlos E. Crespo‐Hernández, Chris Acquah, Liraz Levi
article en

Abstract

High Resolution Image Download MS PowerPoint Slide Developing DNA/RNA nucleoside prodrugs that absorb in the red-to-near-infrared is crucial for applications requiring deep-tissue penetration. This study reports the rational design and synthesis of a novel thiocarbonyl analog, 5-(5-(4-(dimethylamino)phenyl)thiophen-2-yl)-2′,3′,5′-tri- O -benzoyl-6-aza-2,4-dithiouridine (DATU), efficiently activated through one- and two-photon absorption in the red-to-near-infrared spectrum. We report DATU’s electronic structure and its photophysical and triplet-state properties under both excitation, comparing these results to its carbonyl counterpart, 5-(5-(4-(dimethylamino)phenyl)thiophen-2-yl)-2’,3′,5′-tri- O -benzoyl-6-azauridine (DAU). DATU exhibits strong visible one-photon absorption, with ε 522 = (0.73 ± 0.02) × 10 4 M –1 cm –1 in aqueous solution, extending to ∼750 nm. Additionally, it features a triplet-state lifetime of 1.7 ± 0.1 μs and a singlet-oxygen quantum yield of 56% in benzene. Photoexcited DATU generates both singlet oxygen and hydroxyl radicals in solvents of varying polarity (water, methanol, acetonitrile, and benzene), functioning as both a type I and type II photosensitizer depending on the cellular environment. Notably, replacing carbonyl with thiocarbonyl groups increases the two-photon absorption cross section at 800 nm 3-fold, from 55 ± 5 GM for DAU to 160 ± 20 GM for DATU, the largest reported for a nucleoside analog. In vitro investigations using 4T1 murine mammary carcinoma cells confirm that DATU exhibits significant photocytotoxicity under one-photon (525 nm, 6 μM) and two-photon (800 nm, 25 μM) activation, with negligible dark toxicity. Together, these findings position DATU as the most promising nucleoside photosensitizer for deep-tissue photodynamic therapy (PDT) to date, laying the foundation for future mechanistic/ in vivo studies while broadly guiding the development of next-generation thiocarbonyl photosensitizers for PDT, bioimaging, and photocatalysis.

Journal of the American Chemical Society
Cell Medica (Switzerland) (CH), Case Western Reserve University (US)
Openalex Percentile: Top 6%
Photodynamic Therapy Research Studies
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