Sub 20 nm Upconversion Photosensitizers for Near‐Infrared Photodynamic Theranostics

Author:

Nsubuga Anne1,Morice Korentin2,Fayad Nour1,Pini Federico134,Josserand Véronique5,Le Guével Xavier5,Alhabi Abdallah5,Henry Maxime5,Puchán Sánchez Dario2,Plassais Nathan2,Josse Pierre2,Boixel Julien6,Blanchard Philippe2,Cabanetos Clément27,Hildebrandt Niko89ORCID

Affiliation:

1. Univ Rouen, CNRS, INSA Rouen, Normandie Université Laboratoire COBRA Rouen 76000 France

2. Univ Angers, CNRS, MOLTECH‐ANJOU SFR MATRIX Angers 49000 France

3. Istituto di Chimica della Materia Condensata e Tecnologie per l'Energia (ICMATE) Consiglio Nazionale delle Ricerche (CNR) Padova 35131 Italy

4. Dipartimento di Scienze Chimiche Università di Padova Padova 35131 Italy

5. University of Grenoble Alpes, Institute for Advanced Biosciences INSERM‐U1209/CNRS‐UMR5309 Grenoble 38700 France

6. Univ Rennes CNRS UMR6226 Rennes F‐35042 France

7. Building Blocks for Future Electronics Laboratory (2BFUEL), IRL CNRS 2002 Yonsei University Seoul 03722 South Korea

8. Department of Chemistry Seoul National University Seoul 08826 South Korea

9. McMaster University Department of Engineering Physics Hamilton ON M8S 4K1 Canada

Abstract

AbstractEfficient type II photodynamic therapy (PDT) requires stable and biocompatible photosensitizers (PS) that present low dark cytotoxicity, are photo‐excitable in deep tissue regions, and can efficiently penetrate and kill cells via in situ singlet oxygen production. Here, heavy‐metal‐free organic PS are combined with near‐infrared (NIR)‐excitable small (<20 nm) upconversion nanoparticles (UCNPs) into UCNP‐PS nanohybrids for accomplishing such advanced PDT conditions. UCNP‐to‐PS energy transfer efficiencies between 11% and 42% and 1O2 generation quantum yields between 74% and 86% resulted in efficient NIR‐sensitized PDT. HeLa cells incubated with UCNP‐PS can be efficiently destroyed via 808 nm laser irradiance at 140 mW cm−2 for 3 min (<30% cell viability) or 3.2 W cm−2 for 6 min (<10% cell viability). Theranostic functionality of UCNP‐PS is demonstrated via live cell in situ imaging of intracellular UCNP‐PS‐mediated 1O2 production, which resulted in cell death, most probably via apoptosis. Preliminary in vivo experiments are also performed and the consequences for a detailed in vivo study toward clinical translation are discussed. The combined PDT and deep‐tissue imaging properties of the nanomolecular PS present a large potential for future implementation into advanced in vivo photodynamic theranostics.

Funder

Région Normandie

Université de Rouen

Centre National de la Recherche Scientifique

European Regional Development Fund

Ministry of Science and ICT, South Korea

National Research Foundation of Korea

Canada Excellence Research Chairs, Government of Canada

Agence Nationale de la Recherche

H2020 Marie Skłodowska-Curie Actions

Publisher

Wiley

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