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Activatable Lanthanide Nanoprobes with Dye-Sensitized Second Near-Infrared Luminescence for Inflammation Imaging. | LitMetric

Activatable Lanthanide Nanoprobes with Dye-Sensitized Second Near-Infrared Luminescence for Inflammation Imaging.

Anal Chem

National Engineering Research Centre for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, 1037 Luoyu Road, Wuhan 430074, P. R. China.

Published: February 2023

AI Article Synopsis

  • * This study introduces dye-sensitized lanthanide nanoprobes using indocyanine green (ICG), which improves brightness by five times and adjusts the optimal concentration of the activator.
  • * These enhanced nanoprobes can be used for activatable imaging of hypochlorite in a mouse model, showcasing a new approach to improve lanthanide nanoparticles for molecular imaging.

Article Abstract

Lanthanide nanoparticles exhibit unique photophysical properties and thus emerge as promising second near-infrared (NIR-II) optical agents. However, the limited luminescence brightness hampers their construction of activatable NIR-II probes. Herein, we report the synthesis of dye-sensitized lanthanide nanoprobes (NaGdF:Nd/ICG; indocyanine green (ICG)) and their further development for activatable imaging of hypochlorite (ClO). Dye sensitization using ICG not only shifts the optimal doping concentration of Nd from 5 to 20 mol % but also leads to a 5-fold NIR-II enhancement relative to the ICG-free counterpart. Mechanistic studies reveal that such a luminescence enhancement of NaGdF:Nd at high Nd concentration is ascribed to an alleviated cross-relaxation effect due to the broad absorption of ICG and faster energy transfer process. Taking advantage of dye oxidation, the nanoprobes enable activatable NIR-II imaging of hypochlorous acid (ClO) in a drug-induced lymphatic inflammation mouse model. This work thus provides a simple, yet effective luminescence enhancement strategy for constructing lanthanide nanoprobes at higher activator doping concentration toward activatable NIR-II molecular imaging.

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Source
http://dx.doi.org/10.1021/acs.analchem.2c04873DOI Listing

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