Comparative study of the direct and photocatalytic light activation of platinum(IV) prodrugs.
6 affiliations
- 1Department of Chemistry, King's College London, 7 Trinity Street, London, SE1 1DB, UK. [email protected].
- 2Centre for Host-Microbiome Interactions, King's College London, SE1 1UL, London, UK.
- 3Institute of Biomedical Engineering, Department of Engineering Sciences, Old Road Campus Research Building, University of Oxford, Headington, Oxford, UK.
- 4Graduate School of Health Sciences, Cellular and Molecular Medicine Program, Koç University, Istanbul, 34450, Turkey.
- 5Department of Chemistry, Koç University, Istanbul 34450, Türkiye.
- 6Biomedical Sciences Research Institute, University of Ulster, Coleraine, Northern Ireland, UK. [email protected].
Abstract
Here, we present a comparative study of direct and photocatalyst-mediated photoactivation of reporter-functionalised Pt(IV) prodrugs, Carbo-4NP and CarboNap. Direct blue-light irradiation and green-light activation using the photocatalyst Rose Bengal both achieved rapid and complete Pt(IV) reduction in solution, monitored by UV-Vis and fluorescence spectroscopy. Translation to live cells revealed a marked divergence between the two approaches. Direct blue light (415 nm) photoactivation produced >300-fold enhancement in fluorescence intensities upon probe activation and >10-fold in cytotoxicity. Photocatalytic activation was considerably less effective in cells despite its excellent solution-phase performance. These findings identify direct photoactivation as the superior strategy for intracellular activation of Pt(IV) prodrugs and support the further development of direct light-activated platinum therapeutics.
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BibTeX
@article{mileche2026comparative,
title = {{Comparative study of the direct and photocatalytic light activation of platinum(IV) prodrugs.}},
author = {Kinjal Mileche and Susana M Meza Huaman and Ke Wu and Jake A Vickery and Hannah Coxhead and Alexander N Smith-Xu and Patricia Juhl Allworthy and Jovana Katrinka-Mavrak and Aminesena Baser and Safacan Kolemen and Manuel M Müller and Mahvash Tavassoli and Ismael Diez-Perez and Eleanor Stride and John F Callan and Adam C Sedgwick},
journal = {Dalton transactions (Cambridge, England : 2003)},
year = {2026},
month = oct,
doi = {10.1039/d6dt01745b},
url = {https://europepmc.org/article/MED/42895112},
note = {CC BY},
}
RIS
TY - JOUR
TI - Comparative study of the direct and photocatalytic light activation of platinum(IV) prodrugs.
AU - Kinjal Mileche
AU - Susana M Meza Huaman
AU - Ke Wu
AU - Jake A Vickery
AU - Hannah Coxhead
AU - Alexander N Smith-Xu
AU - Patricia Juhl Allworthy
AU - Jovana Katrinka-Mavrak
AU - Aminesena Baser
AU - Safacan Kolemen
AU - Manuel M Müller
AU - Mahvash Tavassoli
AU - Ismael Diez-Perez
AU - Eleanor Stride
AU - John F Callan
AU - Adam C Sedgwick
PY - 2026
DA - 2026/10/19
JO - Dalton transactions (Cambridge, England : 2003)
DO - 10.1039/d6dt01745b
UR - https://europepmc.org/article/MED/42895112
AB - Here, we present a comparative study of direct and photocatalyst-mediated photoactivation of reporter-functionalised Pt(IV) prodrugs, Carbo-4NP and CarboNap. Direct blue-light irradiation and green-light activation using the photocatalyst Rose Bengal both achieved rapid and complete Pt(IV) reduction in solution, monitored by UV-Vis and fluorescence spectroscopy. Translation to live cells revealed a marked divergence between the two approaches. Direct blue light (415 nm) photoactivation produced >300-fold enhancement in fluorescence intensities upon probe activation and >10-fold in cytotoxicity. Photocatalytic activation was considerably less effective in cells despite its excellent solution-phase performance. These findings identify direct photoactivation as the superior strategy for intracellular activation of Pt(IV) prodrugs and support the further development of direct light-activated platinum therapeutics.
SN - 1477-9226
SN - 1477-9234
ER -