4.8 Article

Metal Modulation: An Easy-to Implement Tactic for Tuning Lanthanide Phototheranostics

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 19, Pages 7541-7552

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.1c03041

Keywords

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Funding

  1. National Natural Science Foundation of China [21571007, 21621061, 21778002, 21861162008]
  2. Chemistry and Chemical Engineering Guangdong Laboratory [1932002]
  3. National Institutes of Health [CA 68682]
  4. Robert A. Welch Foundation [F-0018]
  5. High-performance Computing Platform of Peking University

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The study introduces a metal selection approach for fine-tuning the excited state properties and functional features of phototheranostics. Results suggest that the Yb complex designed in the study shows potential for in vivo use in photoacoustic imaging and photothermal/photodynamic therapy.
Phototheranostics constitute an emerging cancer treatment wherein the core diagnostic and therapeutic functions are integrated into a single photosensitizer (PS). Achieving the full potential of this modality requires being able to tune the photosensitizing properties of the PS in question. Structural modification of the organic framework represents a time-honored strategy for tuning the photophysical features of a given PS system. Here we report an easy-to-implement metal selection approach that allows for fine-tuning of excited-state energy dissipation and phototheranostics functions as exemplified by a set of lanthanide (Ln = Gd, Yb, Er) carbazole-containing porphyrinoid complexes. Femto- and nanosecond time-resolved spectroscopic studies, in conjunction with density functional theory calculations, revealed that the energy dissipation pathways for this set of PSs are highly dependent on the energy gap between the lowest triplet excited state of the ligand and the excited states of the coordinated Ln ions. The Yb complex displayed a balance of deactivation mechanisms that made it attractive as a potential combined photoacoustic imaging and photothermal/photodynamic therapy agent. It was encapsulated into mesoporous silica nanoparticles (MSN) to provide a biocompatible construct, YbL@MSN, which displays a high photothermal conversion efficiency (eta = 45%) and a decent singlet oxygen quantum yield (Phi(Delta) = 31%). Mouse model studies revealed that YbL@MSN allows for both photoacoustic imaging and synergistic photothermal- and photodynamic-therapy-based tumor reduction in vivo. Our results lead us to suggest that metal selection represents a promising approach to fine-tuning the excited state properties and functional features of phototheranostics.

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